Water Treatment, Metal and Mining Chemicals

TRIMETHYLOLPROPANE TRIACRYLATE
TRIMETHYLOLPROPANE TRIISOSTEARATE N° CAS : 68541-50-4 Nom INCI : TRIMETHYLOLPROPANE TRIISOSTEARATE Nom chimique : 2-Ethyl-2-[[(1-oxoisooctadecyl)oxy]methyl]-1,3-propanediyl bis(isooctadecanoate) N° EINECS/ELINCS : 271-347-5 Ses fonctions (INCI) Emollient : Adoucit et assouplit la peau Agent d'entretien de la peau : Maintient la peau en bon état
TRIMETHYLOLPROPANE TRIISOSTEARATE
cas no : 9005-70-3, Emsorb 6903; Glycosperse TO-20; Liposorb TO-20; polyethyleneglycol sorbitan trioleate; Polyoxyethylene (20) sorbitan trioleate; Polyoxyethylene sorbitan trioleate; Polysorbate 85; Protasorb TO-20; Sorbimacrogol trioleate 300; Sorbitan, tri-(9Z)-9-octadecenoate, poly(oxy-1,2-ethanediyl) derivs.; Sorbitan, tri-9-octadecenoate, poly(oxy-1,2-ethanediyl) derivs.; Sorbitan, trioleate polyoxyethylene deriv.; Tween 85; Ses fonctions (INCI) Agent émulsifiant : Favorise la formation de mélanges intimes entre des liquides non miscibles en modifiant la tension interfaciale (eau et huile) Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation
TRIOCTYLAMINE
DESCRIPTION:
Trioctylamine is a clear and colorless chemical compound in the group of aliphatic amines and tertiary amines.
Trioctylamine can easily soluble in chloroform.
Trioctylamine has a form of low melting crystalline mass, and Trioctylamine has the color of white to off-white.

CAS Number: 1116-76-3
EC Number: 214-242-1
IUPAC name: N,N-Di(octyl)octan-1-amine
Molecular Formula: C24H51N


PHYSICAL AND CHEMICAL PROPERTIES OF TRIOCTYLAMINE:
Chemical formula: C24H51N
Molar mass: 353.679 g•mol−1
Density: 0.81 g/cm3[1]
Melting point: −34.6 °C (−30.3 °F; 238.6 K)
Solubility in water: 0.050 mg/l
Viscosity: 7.862 mPa.s
Molecular Weight: 353.7
XLogP3-AA: 10.5
Hydrogen Bond Donor Count: 0
Hydrogen Bond Acceptor Count: 1
Rotatable Bond Count: 21
Exact Mass: 353.402150631
Monoisotopic Mass: 353.402150631
Topological Polar Surface Area: 3.2 Ų C
Heavy Atom Count: 25
Formal Charge: 0
Complexity: 188
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes
Density: 0.81 g/cm3 (20 °C)
Flash point: 168 °C
Ignition temperature: 315 °C
Melting Point: -39 °C
Vapor pressure: Solubility: Appearance (Clarity): Clear
Appearance (Colour): Pale yellow
Appearance (Form): Liquid
Assay (T): min. 95%
Density (g/ml) @ 20°C: 0.809-0.810
Refractive Index (20°C): 1.448-1.450
Water (KF): max. 0.1%
Melting point: 34 °C
Boiling point: 164-168 °C/0.7 mmHg (lit.) 365-367 °C (lit.)
Density: 0.809 g/mL at 25 °C (lit.)
vapor pressure: refractive index :n20/D 1.449(lit.)
Flash point: >230 °F
storage temp.: Store below +30°C.
solubility: chloroform: 0.1 g/mL, clear, colorless
form: Low Melting Crystalline Mass
pka: 10.08±0.50(Predicted)
Specific Gravity: 0.811 (20/4℃)
Color: White to off-white
Water Solubility: Miscible with chloroform. Immiscible with water.
Sensitive: Air Sensitive
Trioctylamine is a clear colorless method and can be converted to the amine hydrochloride etherate which is recrystallized four times from diethyl ether at -30 °C.
Neutralization of this salt regenerates the free amine which distilled under high vacuum.
Trioctylamine has melting point of −34 °C; boiling point of 164-168 °C at 0.7 mmHg and 365-367 °C at 1 atm; density of 0.810 g/mL at 20 °C; refractive index of n20/D 1.449; flash point of >230 °F; storage temperature is below 30 °C.

Trioctylamine is miscible with chloroform but immiscible with water.
Trioctylamine is air sensitive.
There is a safety hazard for this chemical compound.

Trioctylamine can cause skin irritation, serious eye irritation, and respiratory irritation.
Trioctylamine can damage fertility or the unborn child and cause damage to organs through prolonged or repeated exposure.
Trioctylamine is very toxic to aquatic life with long lasting effects.


PRODUCTION METHOD OF TRIOCTYLAMINE:
Ammoniation is carried out in the presence of aluminum trichloride catalyst using n-octanol as raw material.
The reaction is carried out in a condensation kettle, ammonia is introduced into the kettle, and the reaction is carried out at 400 ℃.
Then remove the excess n-octanol and filter out the catalyst to obtain the finished trioctylamine.
Raw material consumption (kg/t) n-octanol 1217 trialumina 685.


APPLICATION OF TRIOCTYLAMINE:
Trioctylamine is used to extract organic acids such as succinic acid and acetic acid, and also precious metals.
A formulation containing metoxuron mixed with an emulsion containing trioctylamine 50%, atlox 4851 B 15%, and isopropanol 35% was active as a potato defoliant.
Trioctylamine can be used to extract monocarboxylic acid for equilibria and correlation of apparent reactive equilibrium constant.

Liquid-liquid equilibria for aqueous solutions of carboxylic acids with trioctylamine in various diluents was determined at various trioctylamine concentrations.
The loading of trioctylamine for a given carboxylic acid depends on the nature of the solute and its concentration.
The apparent extraction equilibrium constants depend on the hydrophobicity and acidity of the carboxylic acid, as well as the specific basicity of trioctylamine.
Trioctylamine production can be used as a mineral extraction reagent, an extractant for reactor fuel processing, and its use as an extractant for identification of dyes may result in its release to the environment through various waste streams.

USES OF TRIOCTYLAMINE:
Trioctylamine is used as a precious metal extractant.
In the metallurgical industry, Trioctylamine is used to extract and separate cobalt, nickel, actinides and lanthanides.
Trioctylamine is used in organic synthesis.

Trioctylamine is a heat-resistant, solvent-resistant, polymeric rubber antioxidant.
Trioctylamine is the intermediate amine extractant for synthesizing NAPM.
Trioctylamine has good extraction performance for actinides such as thorium and uranium.

Moreover, Trioctylamine can extract and separate non-ferrous metals, rare and scattered metals and platinum elements in different systems.
Trioctylamine is used in the production of phase transfer catalysts, rubber additives and corrosion inhibitors.

Trioctylamine is used as surfactant and extractant.
Tri-n-octylamine is used as an extractant for organic acids and precious metals.
Tri-n-octylamine is used as an extractant for organic acids like trichloroacetic acid, succinic acid, acetic acid and precious metals.
Trioctylamine is also used as a solvent and an intermediate in the manufacture of pharmaceuticals.

Further, Trioctylamine is employed in the preparation of quaternary ammonium compounds, agrochemicals, surfactants, lubricant additives, corrosion inhibitors, vulcanization accelerators and dyes.
Trioctylamine is used as an extractant for organic acids (such as TCA, succinic acid, and acetic acid), and precious metals.

SAFETY INFORMATION ABOUT TRIETHYLAMINE:
First aid measures:
Description of first aid measures:
General advice:
Consult a physician.
Show this safety data sheet to the doctor in attendance.
Move out of dangerous area:

If inhaled:
If breathed in, move person into fresh air.
If not breathing, give artificial respiration.
Consult a physician.
In case of skin contact:
Take off contaminated clothing and shoes immediately.
Wash off with soap and plenty of water.
Consult a physician.

In case of eye contact:
Rinse thoroughly with plenty of water for at least 15 minutes and consult a physician.
Continue rinsing eyes during transport to hospital.

If swallowed:
Do NOT induce vomiting.
Never give anything by mouth to an unconscious person.
Rinse mouth with water.
Consult a physician.

Firefighting measures:
Extinguishing media:
Suitable extinguishing media:
Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.
Special hazards arising from the substance or mixture
Carbon oxides, Nitrogen oxides (NOx), Hydrogen chloride gas

Advice for firefighters:
Wear self-contained breathing apparatus for firefighting if necessary.
Accidental release measures:
Personal precautions, protective equipment and emergency procedures
Use personal protective equipment.

Avoid breathing vapours, mist or gas.
Evacuate personnel to safe areas.

Environmental precautions:
Prevent further leakage or spillage if safe to do so.
Do not let product enter drains.
Discharge into the environment must be avoided.

Methods and materials for containment and cleaning up:
Soak up with inert absorbent material and dispose of as hazardous waste.
Keep in suitable, closed containers for disposal.

Handling and storage:
Precautions for safe handling:
Avoid inhalation of vapour or mist.

Conditions for safe storage, including any incompatibilities:
Keep container tightly closed in a dry and well-ventilated place.
Containers which are opened must be carefully resealed and kept upright to prevent leakage.
Storage class (TRGS 510): 8A: Combustible, corrosive hazardous materials

Exposure controls/personal protection:
Control parameters:
Components with workplace control parameters
Contains no substances with occupational exposure limit values.
Exposure controls:
Appropriate engineering controls:
Handle in accordance with good industrial hygiene and safety practice.
Wash hands before breaks and at the end of workday.

Personal protective equipment:
Eye/face protection:
Tightly fitting safety goggles.
Faceshield (8-inch minimum).
Use equipment for eye protection tested and approved under appropriate government standards such as NIOSH (US) or EN 166(EU).

Skin protection:
Handle with gloves.
Gloves must be inspected prior to use.
Use proper glove
removal technique (without touching glove's outer surface) to avoid skin contact with this product.
Dispose of contaminated gloves after use in accordance with applicable laws and good laboratory practices.
Wash and dry hands.

Full contact:
Material: Nitrile rubber
Minimum layer thickness: 0.11 mm
Break through time: 480 min
Material tested:Dermatril (KCL 740 / Aldrich Z677272, Size M)
Splash contact
Material: Nitrile rubber
Minimum layer thickness: 0.11 mm
Break through time: 480 min
Material tested:Dermatril (KCL 740 / Aldrich Z677272, Size M)
It should not be construed as offering an approval for any specific use scenario.

Body Protection:
Complete suit protecting against chemicals, The type of protective equipment must be selected according to the concentration and amount of the dangerous substance at the specific workplace.
Respiratory protection:
Where risk assessment shows air-purifying respirators are appropriate use a fullface respirator with multi-purpose combination (US) or type ABEK (EN 14387) respirator cartridges as a backup to engineering controls.

If the respirator is the sole means of protection, use a full-face supplied air respirator.
Use respirators and components tested and approved under appropriate government standards such as NIOSH (US) or CEN (EU).
Control of environmental exposure
Prevent further leakage or spillage if safe to do so.
Do not let product enter drains.
Discharge into the environment must be avoided.

Stability and reactivity:
Chemical stability:
Stable under recommended storage conditions.
Incompatible materials:
Strong oxidizing agents:
Hazardous decomposition products:
Hazardous decomposition products formed under fire conditions.
Carbon oxides, Nitrogen oxides (NOx), Hydrogen chloride gas.

Disposal considerations:
Waste treatment methods:
Product:
Offer surplus and non-recyclable solutions to a licensed disposal company.
Contact a licensed professional waste disposal service to dispose of this material.
Contaminated packaging:
Dispose of as unused product.


SYNONYMS OF TRIOCTYLAMINE:
MeSH Entry Terms:
tri-N-octylamine
trioctylamine
Depositor-Supplied Synonyms:
Trioctylamine
1116-76-3
TRI-N-OCTYLAMINE
Tricaprylamine
Tricaprylylamine
1-Octanamine, N,N-dioctyl-
Tri-n-caprylylamine
Farmin 08
Alamine 336
Alamine 336S
N,N-dioctyloctan-1-amine
Alamine 3365
Alamine 308
336S
NSC 11034
TOA
NSC-11034
I40965UY86
HSDB 5786
EINECS 214-242-1
BRN 1210618
trioctyl amine
AI3-17998
UNII-I40965UY86
Trioctylamine, 98%
1-Octanamine,N-dioctyl-
SCHEMBL36609
TRICAPRYLAMINE [HSDB]
N,N-Dioctyl-1-octanamine #
CHEMBL3222022
DTXSID3047635
WLN: 8N8&8
AMY21907
NSC11034
ZINC6920427
MFCD00009560
AKOS015915431
CS-W011849
SB83655
Trioctylamine, purum, >=98.0% (GC)
BS-14388
Trioctylamine, SAJ first grade, >=99.0%
FT-0600026
FT-0655520
I0362
T0502
EN300-74244
D70441
A802393
W-108670
Q27280370
Z1167043198



TRIOLÉATE DE SORBITAN 20 EO ( tween 85)
TRIOLÉATE DE SORBITAN, cas no : 26266-58-0; Span 85 (=Sorbitan Trioleate); Span 85; Span 85V, Anhydro-D-glucitol trioleate; Nom INCI : SORBITAN TRIOLEATE; Nom chimique : Anhydro-D-glucitol trioleate; N° EINECS/ELINCS : 247-569-3; Agent émulsifiant : Favorise la formation de mélanges intimes entre des liquides non miscibles en modifiant la tension interfaciale (eau et huile)
TRIOLÉATE DE SORBITAN N
TRIOLEYL CITRATE, N° CAS : 175831-77-3, Nom INCI : TRIOLEYL CITRATE, Nom chimique : 1,2,3-Propanetricarboxylic acid, 2-hydroxy-, tri-9-octadecenyl ester (all-Z)-, Ses fonctions (INCI) Emollient : Adoucit et assouplit la peau, Agent plastifiant : Adoucit et rend souple une autre substance qui autrement ne pourrait pas être facilement déformée, dispersée ou être travaillée, Agent d'entretien de la peau : Maintient la peau en bon état
TRIOLEIN
Triolein is a symmetrical triglyceride derived from glycerol and three units of the unsaturated fatty acid oleic acid.
Triolein, known widely as Glyceryl trioleate, is an oily liquid that is a main constituent of some nondrying oils and fats.
Triolein is also known as glyceryl trioleate and is one of the two components of Lorenzo's oil.

CAS Number: 122-32-7
EC Number: 204-534-7
Chemical formula: C57H104O6
Molecular Weight: 885.43

(9Z)9-Octadecenoic acid 1,2,3-propanetriyl ester, 1,2,3-Tri(cis-9-octadecenoyl)glycerol, Glycerol trioleate, Glycerol triolein, Oleic acid triglyceride, Oleic triglyceride, TG(18:1(9Z)/18:1(9Z)/18:1(9Z)), Triolein, GLYCERYL TRIOLEATE, Glycerol trioleate, 122-32-7, Oleic triglyceride, Olein, Trioleoylglycerol, Glycerol triolein, Oleic acid triglyceride, Trioleoylglyceride, Glycerin trioleate, Oleyl triglyceride, Raoline, Glyceryl-1,2,3-trioleate, Aldo TO, Emery 2423, Olein, tri-, Emery oleic acid ester 2230, Glycerol, tri(cis-9-octadecenoate), 1,2,3-Propanetriyl trioleate, HSDB 5594, Triglyceride OOO, Edenor NHTi-G, Kaolube 190, sn-Glyceryl trioleate, 1,2,3-tri-(9Z-octadecenoyl)-glycerol, Actor LO 1, Kemester 1000, UNII-O05EC62663, Emerest 2423, 9-Octadecenoic acid (Z)-, 1,2,3-propanetriyl ester, 9-Octadecenoic acid (9Z)-, 1,2,3-propanetriyl ester, Estol 1433, Radia 7363, 1,2,3-Tri(cis-9-octadecenoyl)glycerol, 1,2,3-tri-oleoyl-glycerol, 1,2,3-Propanetriol tri(9-octandecenoate), CHEBI:53753, TG(18:1(9Z)/18:1(9Z)/18:1(9Z)), 2,3-bis[[(Z)-octadec-9-enoyl]oxy]propyl (Z)-octadec-9-enoate, 9-Octadecenoic acid, 1,2,3-propanetriyl ester, MFCD00137563, O05EC62663, propane-1,2,3-triyl (9Z,9'Z,9''Z)tris-octadec-9-enoate, glycerine trioleate, 1,3-bis[(9Z)-octadec-9-enoyloxy]propan-2-yl (9Z)-octadec-9-enoate, TG 54:3, (9Z)9-Octadecenoic acid 1,2,3-propanetriyl ester, EINECS 204-534-7, CCRIS 8687, tri-Olein, 9-Octadecenoic-9,10-t2 acid, 1,2,3-propanetriyl ester, (Z,Z,Z)- (9CI), C57H104O6, triolein C18:1, Triolein, tech grade, GLYCERYLTRIOLEATE, tri(cis-9-octadecenoate), Epitope ID:117714, 1,2,3-propanetriyl ester, EC 204-534-7, Glyceryl trioleate, ~65% SCHEMBL23730, Glyceryl trioleate, >=99%, 9-Octadecenoic acid (9Z)-, 1,1',1''-(1,2,3-propanetriyl) ester, CHEMBL4297656, DTXSID3026988, HY-N1981, Triolein, [9,10-3H(N)]-, LMGL03010250, s3590, ZINC85545180, AKOS024437536, DB13038, Glyceryl trioleate, >=97.0% (TLC), 1,2,3-tri-(9Z-octadecenoyl)-sn-glycerol, CS-0018302, G0089, V0255, Glyceryl trioleate, technical, >=60% (GC), (Z)-1,2,3-propanetriyl ester 9-Octadecenoate, (9Z)-1,2,3-propanetriyl ester 9-Octadecenoate, Glyceryl trioleate, analytical reference material, Q413929, (9Z)-1,2,3-propanetriyl ester 9-Octadecenoic acid, (Z)-1,2,3-propanetriyl ester 9-Octadecenoic acid, (Z)-9-Octadecenoic acid, 1,2,3-propanetriyl ester, J-004788, propane-1,2,3-triyl tris[(9Z)-octadec-9-enoate], AC7B54B8-0E34-455F-A1E0-442F3ECD69EA, Triolein, European Pharmacopoeia (EP) Reference Standard, TG(18:1(9Z)/18:1(9Z)/18:1(9Z))[iso], UNII-2GQR19D8A4 component PHYFQTYBJUILEZ-IUPFWZBJSA-N, UNII-4PC054V79P component PHYFQTYBJUILEZ-IUPFWZBJSA-N, (9Z)-1,1',1''-(1,2,3-propanetriyl) ester 9-Octadecenoate, (9Z)-1,1',1''-(1,2,3-propanetriyl) ester 9-Octadecenoic acid, 9-octadecenoic acid, 1,2,3-propanetriyl ester, (9Z,9'Z,9''Z)-, Triolein (18:1 TG), 1,2,3-tri-(9Z-octadecenoyl)-glycerol, neat oil, (9Z)9-Octadecenoic acid 1,2,3-propanetriyl ester, (9Z,9'Z,9''Z)Tris(-9-octadécénoate) de 1,2,3-propanetriyle, 1,2,3-Propanetriyl (9Z,9'Z,9''Z)tris(-9-octadecenoate), 1,2,3-Propantriyl-(9Z,9'Z,9''Z)tris(-9-octadecenoat), 1,2,3-tri-(9Z-octadecenoyl)-sn-glycerol, 1,2,3-Tri(cis-9-octadecenoyl)glycerol, 1,2,3-Trioleoyl Glycerol, 122-32-7, 204-534-7, 9-Octadecenoic acid (9Z)-, 1,2,3-propanetriyl ester, 9-Octadecenoic acid (Z)-, 1,2,3-propanetriyl ester, 9-Octadecenoic acid, 1,2,3-propanetriyl ester, (9Z,9'Z,9''Z)-, Glycerin trioleate, Glycerine trioleate, Glycerol trioleate, Glycerol triolein, Glycerol, tri(cis-9-octadecenoate), glyceryl trioleate, Glyceryl-1,2,3-trioleate, MFCD00137563, Oleic acid triglyceride, Oleic triglyceride, Olein, tri-, Propane-1,2,3-triyl (9Z,9'Z,9''Z)tris-octadec-9-enoate, Triolein, (9Z)-1,1',1''-(1,2,3-propanetriyl) ester 9-Octadecenoate, (9Z)-1,1',1''-(1,2,3-propanetriyl) ester 9-Octadecenoic acid, (9Z)-1,2,3-propanetriyl ester 9-Octadecenoate, (9Z)-1,2,3-propanetriyl ester 9-Octadecenoic acid, (9Z)-9-Octadecenoic acid 1,2,3-propanetriyl ester, (Z)-1,2,3-propanetriyl ester 9-Octadecenoate, (Z)-1,2,3-propanetriyl ester 9-Octadecenoic acid, (Z)-9-Octadecenoic acid, 1,2,3-propanetriyl ester, 1,2,3-Propanetriol tri(9-octandecenoate), 1,2,3-Propanetriyl trioleate, 1,2,3-tri-(9Z-octadecenoyl)-glycerol, 1,2,3-Trioleoyl-rac-glycerol, 1,3-bis[(9Z)-octadec-9-enoyloxy]propan-2-yl (9Z)-octadec-9-enoate, 124330-00-3, 1257300-52-9, 1-oleoyl-2-oleoyl-3-oleoyl-glycerol, 2,3-bis[[(Z)-octadec-9-enoyl]oxy]propyl (Z)-octadec-9-enoate, 24016-60-2, 247-038-6, 25496-72-4, 41755-78-6, 9-Octadecenoic acid, 1,2,3-propanetriyl ester, Aldo TO, Edenor NHTi-G, GLYCERYL OLEATE, Kaolube 190, olein, Oleyl triglyceride, propane-1,2,3-triyl trioleate, propane-1,2,3-triyl tris[(9Z)-octadec-9-enoate], Raoline, sn-Glyceryl trioleate, TAG(18:1,18:1,18:1), TAG(54:3), TG(54:3), Tracylglycerol(54:3), Triglyceride, trioctadecenoin, Tri-Olein, Triolein (18:1 TG), Triolein, [9,10-3H(N)]-, trioleína, Trioleoylglyceride, Trioleoylglycerol

Triolein is derived from glycerol.
Triolein is composed of three oleic acid units and is an unsaturated triglyceride.

Triolein, known widely as Glyceryl trioleate, is an oily liquid that is a main constituent of some nondrying oils and fats.
Triolein occurs in many natural fats and oils, including sunflower oil, palm oil, cacao butter, and, most notably, olive oil.

In 1941, Thomas P. Hilditch and L. Maddison at the University of Liverpool (UK) crystallized olive oils from Italy and Palestine at temperatures down to –30 °C to resolve them into several components.
They found that olive oil from Palestine contained ≈30% triolein, whereas the Italian oil contained only ≈5%.

Eight years later, M. L. Meara, also at Liverpool, resolved cacao butter into 11 fractions “by exhaustive crystallization”.
For his efforts, only 1.1% of the fat turned out to be Triolein.
From 1940 to 1961, several chemists devised syntheses of triolein by esterifying glycerol and oleic acid.

Sacramental uses of olive oil are strongly connected to Christian and Jewish traditions, especially Hanukkah.

During the period of the Hanukkah story (168 BCE), only pure olive oil blessed by the high priest could be used to light the Temple menorah, which had to be lit continuously.
After their victorious battle over the Syrian Greeks, the Maccabees could find only enough holy oil to last for one day.
The Hanukkah miracle is that the oil lasted eight days, enough time for more oil to be prepared and sanctified.

Olive oil was the major component of anointing oils and lamp fuel that date to biblical times.
Kings were anointed with oil as a mark of their official status; and one title for Jesus is the Anointed One.
References are found throughout the Hebrew and Christian scriptures about the use of oil as part of fasting and healing rituals.

Triolein is a symmetrical triglyceride derived from glycerol and three units of the unsaturated fatty acid oleic acid.
Most triglycerides are unsymmetrical, being derived from mixtures of fatty acids.
Triolein represents 4–30% of olive oil.

Triolein is also known as glyceryl trioleate and is one of the two components of Lorenzo's oil.

The oxidation of triolein is according to the formula:
C57H104O6 + 80 O2 → 57 CO2 + 52 H2O

This gives a respiratory quotient of 57/80 or 0.7125.
The heat of combustion is 8,389 kcal (35,100 kJ) per mole or 9.474 kcal (39.64 kJ) per gram.
Per mole of oxygen Triolein is 104.9 kcal (439 kJ).

Triolein is derived from glycerol.
Triolein is composed of three oleic acid units and is an unsaturated triglyceride.

Triolein (glycerol trielaidate, or trielaidin) is a triglyceride formed by esterification of the three hydroxy groups of glycerol with elaidic acid.

Triolein or Glyceryl trioleate is a triglyceride formed by esterification of the three hydroxy groups of glycerol with oleic acid.
Triolein is one of the two components of Lorenzo's oil.

Triolein has a role as a plant metabolite.
Triolein derives from an oleic acid.
Triolein can be found as a clear colorless liquid.

Constituent of olive oil and other vegetable oils TG(18:1(9Z)/18:1(9Z)/18:1(9Z)) or Triolein is a monoacid triglyceride.
Triglycerides (TGs) are also known as triacylglycerols or triacylglycerides.

TGs are fatty acid triesters of glycerol and may be divided into three general types with respect to their acyl substituents.
They are simple or monoacid if they contain only one type of fatty acid, diacid if they contain two types of fatty acids and triacid if three different acyl groups.

Chain lengths of the fatty acids in naturally occurring triglycerides can be of varying lengths and saturations but 16, 18 and 20 carbons are the most common.
TGs are the main constituent of vegetable oil and animal fats.

TGs are major components of very low density lipoprotein (VLDL) and chylomicrons, play an important role in metabolism as energy sources and transporters of dietary fat.
They contain more than twice the energy (9 kcal/g) of carbohydrates and proteins.

In the intestine, triglycerides are split into glycerol and fatty acids (this process is called lipolysis) (with the help of lipases and bile secretions), which can then move into blood vessels.
The triglycerides are rebuilt in the blood from their fragments and become constituents of lipoproteins, which deliver the fatty acids to and from fat cells among other functions.

Various tissues can release the free fatty acids and take them up as a source of energy.
Fat cells can synthesize and store triglycerides.

When the body requires fatty acids as an energy source, the hormone glucagon signals the breakdown of the triglycerides by hormone-sensitive lipase to release free fatty acids.
As the brain cannot utilize fatty acids as an energy source, the glycerol component of triglycerides can be converted into glucose for brain fuel when Triolein is broken down.

TAGs can serve as fatty acid stores in all cells, but primarily in adipocytes of adipose tissue.
The major building block for the synthesis of triacylglycerides, in non-adipose tissue, is glycerol.

Adipocytes lack glycerol kinase and so must use another route to TAG synthesis.
Specifically, dihydroxyacetone phosphate (DHAP), which is produced during glycolysis, is the precursor for TAG synthesis in adipose tissue. DHAP can also serve as a TAG precursor in non-adipose tissues, but does so to a much lesser extent than glycerol.

The use of DHAP for the TAG backbone depends on whether the synthesis of the TAGs occurs in the mitochondria and ER or the ER and the peroxisomes.
The ER/mitochondria pathway requires the action of glycerol-3-phosphate dehydrogenase to convert DHAP to glycerol-3-phosphate. Glycerol-3-phosphate acyltransferase then esterifies a fatty acid to glycerol-3-phosphate thereby generating lysophosphatidic acid.

The ER/peroxisome reaction pathway uses the peroxisomal enzyme DHAP acyltransferase to acylate DHAP to acyl-DHAP which is then reduced by acyl-DHAP reductase.
The fatty acids that are incorporated into TAGs are activated to acyl-CoAs through the action of acyl-CoA synthetases.

Two molecules of acyl-CoA are esterified to glycerol-3-phosphate to yield 1,2-diacylglycerol phosphate (also known as phosphatidic acid). The phosphate is then removed by phosphatidic acid phosphatase (PAP1), to generate 1,2-diacylglycerol.
This diacylglycerol serves as the substrate for addition of the third fatty acid to make TAG.

Intestinal monoacylglycerols, derived from dietary fats, can also serve as substrates for the synthesis of 1,2-diacylglycerols.
Triolein is a triglyceride and unsaturated fat formed from oleic acid.
Triolein is found in fats and oils, almond, and peach.

Applications of Triolein:

Triolein has been used:
Triolein used as an experimental diet along with fat-free basal mix and corn oil and then to access the dietary fat absorption among mice

Triolein used as an interfering substance to test Triolein effect on human serum in the approach to develop rapid enzyme immunoassay for the detection of retinol-binding protein
Triolein used as a standard in the determination of triglyceride concentration, colorimetrically using liver tissue sample from cows

Uses of Triolein:
A major component of oils and fats, e.g., olive oil.
Triolein used as lubricant (e.g. for cosmetics, drugs, and textiles), emulsifier (e.g. for water/oil mixtures), intermediate for radioactive iodine derivatives, and plasticizer.
Triolein used in sweet almond oil for medicines and cosmetics.

Industry Uses:
Intermediates
Lubricants and lubricant additives

Consumer Uses:
Lubricants and greases
Non-TSCA use

Therapeutic Uses:
The aim of this study was to identify asymptomatic boys with X-linked adrenoleukodystrophy who have a normal magnetic resonance image (MRI), and to assess the effect of 4:1 Triolein-glyceryl trierucate (Lorenzo's oil) on disease progression.
Eighty-nine boys (mean +/- SD baseline age, 4.7 +/- 4.1 years; range, 0.2-15 years) were identified by a plasma very long-chain fatty acids assay used to screen at-risk boys.

All were treated with Lorenzo's oil and moderate fat restriction.
Plasma fatty acids and clinical status were followed for 6.9 +/- 2.7 years.

Changes in plasma hexacosanoic acid levels were assessed by measuring the length-adjusted area under the curve, and a proportional hazards model was used to evaluate association with the development of abnormal MRI results and neurological abnormalities.
Of the 89 boys, 24% developed MRI abnormalities and 11% developed both neurological and MRI abnormalities.

Abnormalities occurred only in the 64 patients who were aged 7 years or younger at the time therapy was started.
There was significant association between the development of MRI abnormalities and a plasma hexacosanoic acid increase.

(For a 0.1-ug/mL increase in the length-adjusted area under the curve for the hexacosanoic acid level, the hazard ratio for incident MRI abnormalities in the whole group was 1.36; P = .01; 95% confidence interval, 1.07-1.72.)
Results for patients aged 7 years or younger were similar (P = .04).

In this single-arm study, hexacosanoic acid reduction by Lorenzo's oil was associated with reduced risk of developing MRI abnormalities.
We recommend Lorenzo's oil therapy in asymptomatic boys with X-linked adrenoleukodystophy who have normal brain MRI results.

X-linked adrenoleukodystrophy (X-ALD) is an inherited disorder of peroxisomal metabolism, biochemically characterized by deficient beta-oxidation of saturated very long chain fatty acids (VLCFA).
The consequent accumulation of these fatty acids in different tissues and in biological fluids is associated with a progressive central and peripheral demyelination, as well as with adrenocortical insufficiency and hypogonadism.

Seven variants of this disease have been described, cerebral childhood being the most frequent.
The recommended therapy consists of the use of the glyceroltrioleate/glyceroltrierucate mixture known as Lorenzo's Oil (LO), combined with a VLCFA-poor diet, but only in asymptomatic patients will this treatment prevent the progression of the symptomatology.

In the present study we evaluated the biochemical course of patients with cerebral childhood (CCER) and asymptomatic clinical forms of X-ALD treated with LO associated with a VLCFA-restricted diet.
We observed that hexacosanoic acid plasma concentrations and hexacosanoic/docosanoic ratio were significantly reduced in CCER patients during treatment when compared with diagnosis.

Hexacosanoic acid plasma level was significantly reduced when compared with that at diagnosis and achieved the normal levels only in asymptomatic patients under LO treatment.
In asymptomatic patients the magnitude of hexacosanoic acid decrease was higher than that of the CCER patients.

These results show the good biochemical response of LO treatment in asymptomatic X-ALD patients.
Triolein is possible to suppose that this could be correlated with the prevention of the appearance of neurological signals in this group of patients treated with LO.

Investigated the possible therapeutic effect of decreasing plasma levels of very-long-chain fatty acids (C26:0) with a synthetic oil containing trioleate and trielucate (Lorenzo's oil) as well as increasing docosahexaenoic acid (DHA) in red blood cells (RBC) with DHA ethyl ester in four patients with Zellweger syndrome.
Investigated serial changes of plasma C26:0 levels and DHA levels in RBC membranes by gas-liquid chromatography/mass spectrometry (GC/MS). After death, the fatty acid composition of each patient's cerebrum and liver was studied.

Dietary administration of Lorenzo's oil diminished plasma C26:0 levels.
Earlier administration of Lorenzo's oil was more effective and the response did not depend on the duration of administration.

DHA was incorporated into RBC membrane lipids when administrated orally, and Triolein level increased for several months.
The final DHA level was correlated with the duration of administration and was not related to the timing of initiation of treatment.

DHA levels in the brains and livers of treated patients were higher than in untreated patients.
Early initiation of Lorenzo's oil and the long-term administration of DHA may be useful for patients with Zellweger syndrome.

Pharmacology and Biochemistry of Triolein:

Absorption, Distribution and Excretion:
In the small intestine, most triglycerides are split into monoglycerides, free fatty acids, and glycerol, which are absorbed by the intestinal mucosa.
Within the epithelial cells, resynthesized triglycerides collect into globules along with cholesterol and phospholipids and are encased in a protein coat as chylomicrons.

Chylomicrons are transported in the lymph to the thoracic duct and eventually to the venous system.
The chylomicrons are removed from the blood as they pass through the capillaries of adipose tissue.
Fat is stored in adipose cells until Triolein is transported to other tissues as free fatty acids which are used for cellular energy or incorporated into cell membranes.

When (14)C-labeled long-chain triglycerides are administered intravenously, 25% to 30% of the radiolabel is found in the liver within 30 to 60 minutes, with less than 5% remaining after 24 hours.
Lesser amounts of radiolabel are found in the spleen and lungs.

After 24 hours, nearly 50% of the radiolabel has been expired in carbon dioxide, with 1% of the carbon label remaining in the brown fat.
The concentration of radioactivity in the epididymal fat is less than half that of the brown fat.

Human Metabolite Information of Triolein:

Cellular Locations:
Extracellular
Membrane

Manufacturing Methods of Triolein:
Preparation by esterification of oleic acid.

Triolein is the predominating constituent in expressed almond oil, in lard oil, & in many of the more fluid animal oils & those of vegetable origin.
Triolein is separated & purified by cold expression, the other constituents being retained by their lack of fluidity at low temp.

The triglyceride of oleic acid, occurring in most fats and oils.
Triolein constitutes 70-80% of olive oil

Reaction of refined oil, eg, olive oil, with glycerol followed by fractional distillation; reaction of oleic acid with glycerol; separation & purification from fats & oils as liquid phase by cold expression.

General Manufacturing Information of Triolein:

Industry Processing Sectors:
Textiles, apparel, and leather manufacturing
Transportation equipment manufacturing

Stable water-in-oil emulsions (with a high water content) for cosmetics are prepared by dissolving the neutral oil & 5-50% lecithin emulsifier at less than or equal to 70 °C, cooling to 0-12 °C, & adding water to a concentration of 50-83%.
The neutral oil can be a glycerol, such as Triolein, or propylene glycol ester of a carbon 8-12 fatty acid or isopropyl myristate.

Ecological Information of Triolein:

Environmental Fate/Exposure Summary of Triolein:
Triolein's production and use as textile lubricant and plasticizer may result in Triolein release to the environment through various waste streams.
Triolein is found in cacao butter and accounts for 70-80% of olive oil.

If released to air, an estimated vapor pressure range of 5X10-5 mm Hg to 1.1X10-9 mm Hg at 25 °C indicates triolein may exist in both the vapor and particulate phases in the atmosphere.
Vapor-phase triolein will be degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals; the half-life for this reaction in air is estimated to be 1.7 hours.

Vapor-phase triolein will also be degraded in the atmosphere by reaction with ozone; the half-life for this reaction in air is estimated to be 0.7 hours.
Particulate-phase triolein will be removed from the atmosphere by wet or dry deposition.

If released to soil, triolein is expected to have no mobility based upon an estimated Koc of 1X10+10.
Volatilization from moist soil surfaces may be an important fate process based upon an estimated Henry's Law constant of 9.6X10-4 atm-cu m/mole; however, soil adsorption will attenuate the importance of volatilization.

14C-Labeled triolein biodegraded to CO2 at a rate of 63.5% to 84% over 140 days in a sewage sludge-amended soil, suggesting that biodegradation may occur in the soil environment.
If released into water, triolein is expected to adsorb to suspended solids and sediment based upon the estimated Koc.

Volatilization from water surfaces is expected to be an important fate process based upon this compound's estimated Henry's Law constant.
Estimated volatilization half-lives for a model river and model lake are 11 hours and 13 days, respectively.

However, volatilization from water surfaces is expected to be attenuated by adsorption to suspended solids and sediment in the water column.
The estimated volatilization half-life from a model pond is 5.1X10+5 years if adsorption is considered.

An estimated BCF of 3.2 suggests the potential for bioconcentration in aquatic organisms is low.
An estimated base-catalyzed second-order hydrolysis rate constant of 0.15 L/mole-sec corresponds to half-lives of 1.5 years and 55 days at pH values of 7 and 8, respectively.

In respirometry tests, triolein had a biodegradation rate constant of 0.0025 per hour which corresponds to a half-life of 11.6 days; bioavailability was restricted due to the presence of double bonds and an autoxidation process occurring in the allylic chains resulting in the production of hydroperoxides, but the non-oxidized fractions were readily mineralized.
Occupational exposure to triolein may occur through dermal contact with this compound at workplaces where triolein is produced or used. Monitoring data indicate that the general population may be exposed to triolein via ingestion of food products containing triolein as well as via dermal contact with consumer products containing triolein.

Stability and Reactivity of Triolein:

Hazardous Reactivities and Incompatibilities of Triolein:
Triolein (major skin lipid) was irradiated with 300-nm ultraviolet (UV) light, and the conditions for exposure approximated those at the skin surface exposed to sunlight.
Using gas chromatography, the irradiated samples were analyzed for the presence of acrolein, formaldehyde, and acetaldehyde.

The maximum amount of acrolein (1.05 nmol/mg Triolein) was formed after 6 hours of irradiation.
Maximum amounts of formaldehyde (6 nmol/mg Triolein) and acetaldehyde (2.71 nmol/mg Triolein) were formed after 12 hours of irradiation.

Disposal Methods of Triolein:
The most favorable course of action is to use an alternative chemical product with less inherent propensity for occupational exposure or environmental contamination.
Recycle any unused portion of the material for Triolein approved use or return Triolein to the manufacturer or supplier. Ultimate disposal of the chemical must consider: the material's impact on air quality; potential migration in soil or water; effects on animal, aquatic, and plant life; and conformance with environmental and public health regulations.

Antidote and Emergency Treatment of Triolein:

Immediate first aid:
Ensure that adequate decontamination has been carried out.
If patient is not breathing, start artificial respiration, preferably with a demand valve resuscitator, bag-valve-mask device, or pocket mask, as trained.

Perform CPR if necessary.
Immediately flush contaminated eyes with gently flowing water.

Do not induce vomiting.
If vomiting occurs, lean patient forward or place on the left side (head-down position, if possible) to maintain an open airway and prevent aspiration.

Keep patient quiet and maintain normal body temperature.
Obtain medical attention.

Basic treatment: Establish a patent airway (oropharyngeal or nasopharyngeal airway, if needed).
Suction if necessary.
Watch for signs of respiratory insufficiency and assist ventilations if needed.

Administer oxygen by nonrebreather mask at 10 to 15 L/min.
Monitor for pulmonary edema and treat if necessary.

Monitor for shock and treat if necessary.
Anticipate seizures and treat if necessary.

For eye contamination, flush eyes immediately with water.
Irrigate each eye continuously with 0.9% saline (NS) during transport.

Do not use emetics.
For ingestion, rinse mouth and administer 5 mL/kg up to 200 mL of water for dilution if the patient can swallow, has a strong gag reflex, and does not drool.
Cover skin burns with dry sterile dressings after decontamination.

Advanced treatment: Consider orotracheal or nasotracheal intubation for airway control in the patient who is unconscious, has severe pulmonary edema, or is in severe respiratory distress.
Positive-pressure ventilation techniques with a bag valve mask device may be beneficial. Consider drug therapy for pulmonary edema.

Consider administering a beta agonist such as albuterol for severe bronchospasm.
Monitor cardiac rhythm and treat arrhythmias as necessary.

Use 0.9% saline (NS) or lactated Ringer's if signs of hypovolemia are present.
For hypotension with signs of hypovolemia, administer fluid cautiously.

Watch for signs of fluid overload.
Treat seizures with diazepam or lorazepam.
Use proparacaine hydrochloride to assist eye irrigation.

Identifiers of Triolein:
CAS Number: 122-32-7
ChEBI: CHEBI:53753
ChemSpider: 4593733
ECHA InfoCard: 100.004.123
MeSH: Triolein
PubChem CID: 5497163
UNII: O05EC62663
CompTox Dashboard (EPA): DTXSID3026988
InChI:
InChI=1S/C57H104O6/c1-4-7-10-13-16-19-22-25-28-31-34-37-40-43-46-49-55(58)61-52-54(63-57(60)51-48-45-42-39-36-33-30-27-24-21-18-15-12-9-6-3)53-62-56(59)50-47-44-41-38-35-32-29-26-23-20-17-14-11-8-5-2/h25-30,54H,4-24,31-53H2,1-3H3/b28-25-,29-26-,30-27- check
Key: PHYFQTYBJUILEZ-IUPFWZBJSA-N check
InChI=1/C57H104O6/c1-4-7-10-13-16-19-22-25-28-31-34-37-40-43-46-49-55(58)61-52-54(63-57(60)51-48-45-42-39-36-33-30-27-24-21-18-15-12-9-6-3)53-62-56(59)50-47-44-41-38-35-32-29-26-23-20-17-14-11-8-5-2/h25-30,54H,4-24,31-53H2,1-3H3/b28-25-,29-26-,30-27-
Key: PHYFQTYBJUILEZ-IUPFWZBJBN
SMILES: O=C(OCC(OC(=O)CCCCCCC\C=C/CCCCCCCC)COC(=O)CCCCCCC\C=C/CCCCCCCC)CCCCCCC\C=C/CCCCCCCC

Properties of Triolein:
Biological source: plant (sunflower)
Quality Level: 200
Assay: ≥99%
Form: oil
bp: 235-240 °C/18 mmHg (lit.)
Density: 0.91 g/mL (lit.)
Functional group: ester
Shipped in: ambient
Storage temp.: −20°C
SMILES string: [H]C(COC(CCCCCCC/C=C\CCCCCCCC)=O)(OC(CCCCCCC/C=C\CCCCCCCC)=O)COC(CCCCCCC/C=C\CCCCCCCC)=O
InChI: 1S/C57H104O6/c1-4-7-10-13-16-19-22-25-28-31-34-37-40-43-46-49-55(58)61-52-54(63-57(60)51-48-45-42-39-36-33-30-27-24-21-18-15-12-9-6-3)53-62-56(59)50-47-44-41-38-35-32-29-26-23-20-17-14-11-8-5-2/h25-30,54H,4-24,31-53H2,1-3H3/b28-25-,29-26-,30-27-
InChI key: PHYFQTYBJUILEZ-IUPFWZBJSA-N

Chemical formula: C57H104O6
Molar mass: 885.432 g/mol
Appearance: Colourless viscous liquid
Density: 0.9078 g/cm3 at 25 °C
Melting point: 5 °C; 41 °F; 278 K
Boiling point: 554.2 °C; 1,029.6 °F; 827.4 K
Solubility: Chloroform 0.1g/mL

Molecular Weight: 885.4
XLogP3-AA: 22.4
Hydrogen Bond Donor Count: 0
Hydrogen Bond Acceptor Count: 6
Rotatable Bond Count: 53
Exact Mass: 884.78329103
Monoisotopic Mass: 884.78329103
Topological Polar Surface Area: 78.9 Ų
Heavy Atom Count: 63
Complexity: 1010
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 3
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes

Hazards of Triolein:
Flash point: 302.6 °C (576.7 °F; 575.8 K)

Thermochemistry of Triolein:
Std enthalpy of formation (ΔfH⦵298): 1.97*105 kJ/kmol
Gibbs free energy (ΔfG˚): -1.8*105 kJ/kmol
Std enthalpy of combustion (ΔcH⦵298): 8,389 kcal (35,100 kJ) /mole

Specifications of Triolein:
Density: 0.9130g/mL
Color: Colorless to Yellow
Boiling Point: 235.0°C to 240.0°C (18.0mmHg)
Assay Percent Range: 98.5% min. (GC)
Infrared Spectrum: Authentic
Linear Formula: (C17H33COOCH2)2CHOCOC17H33
Beilstein: 02,IV,1664
Packaging: Glass bottle
Merck Index: 15,9904
Refractive Index: 1.4680 to 1.4700
Quantity: 1mL
Solubility Information: Solubility in water: insoluble in water. Other solubilities: soluble in chloroform, ether, ccl4, slightly soluble in alcohol
Specific Gravity: 0.913
Formula Weight: 885.45
Physical Form: Liquid
Percent Purity: 99%
Chemical Name or Material: Glycerine trioleate

Names of Triolein:

Preferred IUPAC name:
Propane-1,2,3-triyl tri[(9Z)-octadec-9-enoate]
TRIOLEYL CITRATE
TRIOLEYL PHOSPHATE, N° CAS : 3305-68-8, Nom INCI : TRIOLEYL PHOSPHATE, Nom chimique : Trioleyl phosphate, N° EINECS/ELINCS : 221-983-4. Ses fonctions (INCI) Emollient : Adoucit et assouplit la peau. Agent plastifiant : Adoucit et rend souple une autre substance qui autrement ne pourrait pas être facilement déformée, dispersée ou être travaillée, Agent d'entretien de la peau : Maintient la peau en bon état. Produits qui en contiennent
TRIOLEYL PHOSPHATE
TRIPEPTIDE-10 Nom INCI : TRIPEPTIDE-10 Ses fonctions (INCI) Agent d'entretien de la peau : Maintient la peau en bon état
TRIPALMITIN

Tripalmitin is a triglyceride composed of three palmitic acid molecules esterified to a glycerol backbone.
Tripalmitin is a white, waxy solid with a powdery texture.
Tripalmitin is odorless and tasteless.

CAS number: 555-44-2
EC number: 209-008-0



APPLICATIONS


Tripalmitin (glycerin tripalmitate) finds applications in various industries. Here are some of its key applications:

Food Industry:
Tripalmitin is used as a food additive and ingredient.
Tripalmitin functions as a texturizer, stabilizer, and emulsifier in processed foods, baked goods, confectionery, and dairy products.

Cosmetics and Skincare:
Tripalmitin is used in cosmetics and skincare products as an emollient, moisturizer, and thickening agent.
Tripalmitin helps improve the texture, spreadability, and stability of creams, lotions, lip balms, and other personal care formulations.

Pharmaceuticals:
Tripalmitin is employed in the pharmaceutical industry for various applications. It is used as a carrier for lipophilic drugs, facilitating their delivery and absorption.
Tripalmitin can be incorporated into solid oral dosage forms, transdermal patches, and suppositories.

Industrial Lubricants:
Tripalmitin is utilized in the production of industrial lubricants and metalworking fluids due to its lubricating properties.
Tripalmitin helps reduce friction and wear in machinery and improves overall performance.

Candle Making:
Tripalmitin is a common ingredient in candle making.
Tripalmitin serves as a wax component, contributing to the candle's structure, hardness, and burn characteristics.

Personal Care Products:
Tripalmitin is used in various personal care products, including lipsticks, lip balms, sunscreens, and hair care formulations.
Tripalmitin provides texture, moisturizing properties, and stability to these products.

Coatings and Polishes:
Tripalmitin can be found in coatings, polishes, and wax-based products.
Tripalmitin enhances the gloss, smoothness, and protective properties of surfaces, such as wood, leather, and metal.

Industrial Applications:
Tripalmitin is employed in industrial applications, such as mold release agents, plasticizers, and lubricant additives.
Tripalmitin helps reduce friction, improve flow, and enhance the performance of various materials and processes.

Research and Development:
Tripalmitin is commonly used in laboratories for research and development purposes.
Tripalmitin serves as a model compound to study lipid metabolism, drug delivery systems, and formulation development.

Nutraceuticals:
Tripalmitin is used in the formulation of nutraceutical products, including dietary supplements and functional foods.
Tripalmitin provides a source of energy and serves as a carrier for fat-soluble vitamins and bioactive compounds.

Animal Feed:
Tripalmitin can be incorporated into animal feed formulations as an energy source for livestock and poultry.
Tripalmitin helps improve the caloric density of the feed and supports healthy growth.

Biomedical Research:
Tripalmitin is utilized in biomedical research, particularly in lipid studies and drug delivery systems.
Tripalmitin serves as a representative model for studying triglycerides and their behavior in biological systems.

Microencapsulation:
Tripalmitin is employed in microencapsulation techniques to protect sensitive ingredients, such as flavors, fragrances, and pharmaceutical compounds.
Tripalmitin helps enhance stability, control release, and improve the shelf life of encapsulated substances.

Fuel Additive:
Tripalmitin can be used as a renewable fuel additive in biodiesel production.
Its chemical structure and properties make it suitable for blending with biodiesel fuels, improving their combustion characteristics.

Analytical Chemistry:
Tripalmitin is utilized in analytical chemistry as a calibration standard for various instrumental techniques, such as gas chromatography and mass spectrometry.
Tripalmitin helps validate and quantify analytical measurements.

Surfactant Systems:
Tripalmitin is sometimes employed as a surfactant or emulsifier in formulations.
Tripalmitin aids in the formation and stabilization of emulsions, foams, and dispersed systems.

Nanotechnology:
Tripalmitin is explored in nanotechnology applications, including nanoparticle synthesis and drug delivery systems.
Tripalmitin can be used as a matrix material or a component in nanoparticle formulations.

Bioplastics:
Tripalmitin is investigated as a potential ingredient in biodegradable and renewable bioplastics.
Its compatibility with other biopolymers offers possibilities for environmentally friendly packaging materials.

Veterinary Medicine:
Tripalmitin may have applications in veterinary medicine, such as in the formulation of animal pharmaceuticals, topical preparations, and nutritional supplements.


Tripalmitin is widely used as a texturizer, stabilizer, and emulsifier in processed foods, contributing to their texture and stability.
Tripalmitin is commonly found in baked goods, confectionery, margarine, and other food products.

Tripalmitin serves as an energy source in animal feed, providing essential calories for livestock and poultry.
In the cosmetics industry, tripalmitin acts as an emollient, enhancing the moisturizing properties of skincare products.
Tripalmitin is a key ingredient in lip balms, lipsticks, and moisturizing creams.
Tripalmitin is employed in the pharmaceutical field as a carrier for lipophilic drugs, aiding their absorption and bioavailability.

Tripalmitin is utilized in transdermal patches, solid oral dosage forms, and suppositories.
Tripalmitin is an essential component in industrial lubricants, improving the performance and durability of machinery.
Tripalmitin helps reduce friction, wear, and heat generation in moving parts.
Candle manufacturers use tripalmitin as a primary ingredient in wax formulations, enabling the production of high-quality candles with desirable burning characteristics.
Tripalmitin contributes to the hardness, structure, and fragrance retention of candles.

Tripalmitin finds application in the formulation of coatings and polishes, providing gloss, protection, and ease of application.
Tripalmitin is used in the production of wood polishes, leather conditioners, and metal protective coatings.
Tripalmitin is employed in the creation of industrial mold release agents, ensuring smooth and efficient mold release in manufacturing processes.
Tripalmitin acts as a plasticizer in certain materials, enhancing their flexibility and workability.

Tripalmitin is utilized in research and development as a model compound for studying lipid metabolism, drug delivery systems, and formulation development.
Tripalmitin is a valuable tool in lipid and bioactive compound studies.

Tripalmitin is employed in microencapsulation techniques to protect sensitive ingredients, such as flavors, fragrances, and pharmaceutical compounds.
Tripalmitin helps enhance stability, control release, and improve the shelf life of encapsulated substances.

Tripalmitin can serve as a renewable fuel additive in biodiesel production, improving the combustion properties of biodiesel fuels.
Tripalmitin aids in reducing emissions and enhancing the overall performance of biodiesel.
Analytical chemists utilize tripalmitin as a calibration standard in gas chromatography and mass spectrometry for accurate quantification of compounds.
Tripalmitin acts as a surfactant in formulations, aiding in the formation and stabilization of emulsions and foams.

Tripalmitin finds applications in nanotechnology, serving as a matrix material or component in nanoparticle formulations for drug delivery and other applications.
Veterinary medicine explores the use of tripalmitin in animal pharmaceuticals, topical preparations, and nutritional supplements.
Tripalmitin is used as a coating material in the production of confectionery items like chocolates and candy coatings, providing a smooth and glossy finish.

Tripalmitin acts as a binding agent in the manufacturing of tablets and pills, ensuring the cohesive integrity of the dosage forms.
Tripalmitin is employed in the production of nutritional supplements, particularly those containing fat-soluble vitamins and essential fatty acids.
Tripalmitin serves as a source of energy in energy bars and sports nutrition products.
Tripalmitin is utilized in the production of emulsified meat products such as sausages and processed meats, helping improve their texture and juiciness.

Tripalmitin is used in the formulation of dairy products like ice cream and whipped toppings to provide stability, smoothness, and enhanced mouthfeel.
Tripalmitin finds application in the production of bakery products like cookies and pastries, contributing to their texture, mouthfeel, and shelf life.
Tripalmitin is employed in the creation of cosmetic powders and pressed powders, enhancing their smoothness, adhesion, and blendability.

Tripalmitin is used as a film-forming agent in cosmetic and personal care products, providing a protective barrier on the skin or hair.
Tripalmitin finds application in the production of solid perfumes and fragrance sticks, ensuring the controlled release of fragrance over time.
Tripalmitin is utilized in the formulation of liposomal drug delivery systems, enabling the targeted and controlled release of therapeutic compounds.

Tripalmitin is explored in the field of tissue engineering and regenerative medicine as a scaffold material for cell growth and tissue regeneration.
Tripalmitin is employed in the creation of biodegradable packaging materials, reducing the environmental impact of plastic waste.
Tripalmitin is used as a lubricant in various industries, including automotive, manufacturing, and machinery, to reduce friction and wear.

Tripalmitin is employed in the production of adhesive tapes, providing adhesion and smooth unwinding properties.
Tripalmitin is used as a component in hair care products like conditioners and serums, providing nourishment, shine, and manageability.
Tripalmitin finds application in the formulation of sunscreens and sun protection products, aiding in the dispersion and stability of UV filters.

Tripalmitin is utilized in the creation of pet care products like shampoos and conditioners, offering moisturizing and nourishing benefits to animal fur and skin.
Tripalmitin is explored in the field of drug delivery systems for targeted and sustained release of therapeutic compounds in cancer treatment.
Tripalmitin finds application in the creation of bio-based lubricants and greases, providing effective lubrication while reducing environmental impact.
Tripalmitin is used in the production of nutritional infant formulas, contributing to the energy content and nutritional profile of the product.

Tripalmitin is employed in the creation of high-performance coatings for applications in aerospace, marine, and industrial sectors, providing protection against corrosion and wear.
Tripalmitin finds application in the formulation of solid-state phase change materials, used for thermal energy storage and management in various industries.
Tripalmitin is utilized in the production of dietary supplements for weight management, as it provides a source of long-lasting energy.
Tripalmitin is explored in the field of gene delivery systems, offering a potential carrier for the delivery of genetic material in gene therapy applications.



DESCRIPTION


Tripalmitin, also known as glycerin tripalmitate, is a chemical compound classified as a triglyceride.
Tripalmitin is formed by the esterification of glycerol (also called glycerin) with three molecules of palmitic acid.
Its chemical formula is C₅₃H₁₀₀O₆, and its molecular weight is approximately 853.43 g/mol.

Tripalmitin is a solid substance that appears as a white or off-white powder or crystalline material.
Tripalmitin is odorless and insoluble in water.
However, Tripalmitin is soluble in organic solvents such as ethanol, chloroform, and ether.

This triglyceride is naturally found in various fats and oils, including palm oil and animal fats.
Tripalmitin serves as an energy storage molecule in organisms and is a major component of dietary fats.
Tripalmitin is commonly used in the food industry as a fat source, emulsifier, and stabilizer.
Tripalmitin is also employed in the formulation of cosmetics, pharmaceuticals, and personal care products due to its desirable properties as an emollient and thickening agent.

Tripalmitin is a triglyceride composed of three palmitic acid molecules esterified to a glycerol backbone.
Tripalmitin is a white, waxy solid with a powdery texture.
Tripalmitin is odorless and tasteless.
Tripalmitin has a melting point around 63-65 degrees Celsius.

The compound is insoluble in water but soluble in organic solvents.
Tripalmitin is derived from natural sources such as palm oil and animal fats.

Tripalmitin is commonly found in dietary fats and oils.
Tripalmitin serves as an energy reservoir in living organisms.
Tripalmitin is a major constituent of many food products.

Tripalmitin acts as a natural emollient, providing moisturizing properties to skincare products.
Tripalmitin has a long shelf life and is resistant to oxidation.
Tripalmitin is stable under normal storage and handling conditions.
Tripalmitin has low volatility, making it suitable for various formulations.

Tripalmitin is used as a thickening agent in cosmetics and personal care products.
Tripalmitin helps improve the texture and consistency of formulations.
Tripalmitin is widely utilized in the pharmaceutical industry for drug delivery systems.
Tripalmitin can serve as a carrier for lipophilic drugs.

Tripalmitin has good compatibility with many active ingredients.
Tripalmitin exhibits excellent stability in different formulations and environments.
Tripalmitin is biodegradable and poses minimal environmental impact.
Tripalmitin is an FDA-approved ingredient for various food applications.
Tripalmitin contributes to the smoothness and mouthfeel of food products.



PROPERTIES


Physical Properties:

Molecular Formula: C51H98O6
Molecular Weight: 807.36 g/mol
Appearance: White to off-white solid
Odor: Odorless
Melting Point: Approximately 63-65°C (145-149°F)
Boiling Point: Decomposes before boiling
Solubility: Insoluble in water, soluble in organic solvents (e.g., ethanol, acetone)

Chemical Properties:

Chemical Formula: C3H5(C16H31O2)3
Chemical Structure: Tripalmitin is a triglyceride consisting of glycerol linked to three palmitic acid molecules.
Lipid Type: Saturated triglyceride
Hydrophobicity: Tripalmitin is hydrophobic (water-insoluble) due to its long hydrocarbon chains.



FIRST AID


Inhalation:

If tripalmitin particles or dust are inhaled, remove the affected person to a well-ventilated area.
If respiratory symptoms develop, such as coughing or difficulty breathing, seek medical attention immediately.
Provide supportive care, such as fresh air, rest, and reassurance.


Skin Contact:

In case of contact with tripalmitin on the skin, immediately remove contaminated clothing.
Gently wipe or blot away any excess tripalmitin from the skin surface.
Wash the affected area thoroughly with mild soap and water.
If skin irritation, redness, or rash occurs and persists, seek medical advice.
Apply a suitable skin moisturizer or emollient to help alleviate dryness or discomfort.


Eye Contact:

In the event of contact with tripalmitin in the eyes, immediately flush the eyes with gently flowing water for at least 15 minutes, ensuring thorough rinsing of the eye surfaces.
If wearing contact lenses, remove them during the rinsing process.
Seek immediate medical attention and bring the Safety Data Sheet (SDS) or product container for reference.


Ingestion:

If tripalmitin is accidentally ingested, do not induce vomiting unless directed to do so by medical professionals.
Rinse the mouth with water to remove any residual product.
Do not give anything by mouth to an unconscious or convulsing person.
Seek immediate medical attention, and provide the healthcare professional with relevant information, including the quantity and time of ingestion.



HANDLING AND STORAGE


Handling:

Personal Protective Equipment (PPE):
When handling tripalmitin, wear appropriate PPE, including gloves, safety goggles, and protective clothing, to minimize the risk of skin contact and eye irritation.

Ventilation:
Ensure proper ventilation in the working area to prevent the buildup of airborne particles or vapors.

Avoid Heat Sources: Keep tripalmitin away from open flames, sparks, and direct heat sources, as it may melt or ignite at high temperatures.

Prevent Contamination:
Take precautions to prevent cross-contamination with incompatible substances, such as strong oxidizing agents or reactive chemicals.

Good Hygiene Practices:
Wash hands thoroughly with soap and water after handling tripalmitin, especially before eating, drinking, or smoking.


Storage:

Store in a Cool, Dry Place:
Keep tripalmitin containers tightly closed in a cool, dry, and well-ventilated area to prevent moisture absorption and degradation.

Temperature Control:
Maintain storage temperatures below the melting point of tripalmitin (approximately 63-65°C or 145-149°F) to ensure its solid-state and prevent product degradation.

Protect from Light:
Store tripalmitin in opaque containers or areas protected from direct sunlight or strong UV radiation, as exposure to light may lead to color changes or degradation.

Segregation:
Store tripalmitin away from strong oxidizing agents, acids, and reactive substances to prevent potential chemical reactions.

Keep Away from Ignition Sources:
Store tripalmitin away from ignition sources, such as open flames, sparks, or heat-producing equipment, to minimize the risk of fire hazards.

Proper Labeling:
Clearly label containers with the product name, batch number, date of receipt, and any relevant hazard information.



SYNONYMS


Glycerol tripalmitate
Glycerin tripalmitate
Glyceryl tripalmitate
Palmitin triglyceride
Glyceryl palmitate triester
Tripalmitin glyceride
Triglyceride of palmitic acid
Palmitic acid triglyceride
Palm oil glyceride
Glyceryl ester of palmitic acid
Glycerol ester of palmitic acid
Glyceryl palmitate
Palmitin
Palmitic triglyceride
Glycerol palmitate
Palmitoyl glycerol
Palmitic acid ester of glycerol
Tripalmitin ester
Glyceryl palmitin
Palmitate ester of glycerol
Glyceride of palmitic acid
Trihexadecanoin
1,2,3-Trihexadecanoylglycerol
1-Palmitoyl-2,3-dipalmitin
Hexadecanoic acid ester with glycerol
Tripalmitoylglycerol
Glycerol palmitate ester
Glyceryl palmitate triglyceride
Palmitic acid glycerol ester
1,2,3-Propanetriyl palmitate
Glycerol tris(hexadecanoate)
Triglycerol palmitate
1,3-Dihydroxypropan-2-yl hexadecanoate
Palmitic acid glyceride
Hexadecanoyl glycerol
Glycerol trihexadecanoate
Tris(hexadecanoyloxy)methyl propane
Glycerin tris(palmitate)
Tri(hexadecanoyl)glycerol
Glycerol trihexadecanoate
Tris(palmitoyloxy)methyl propane
1,3-Bis(hexadecanoyloxy)propan-2-yl palmitate
Glycerol 1,2,3-tripalmitate
Palmitic acid glyceryl ester
1,2,3-Tri(hexadecanoyloxy)propane
Tris(hexadecanoyloxy)methylpropane
Glycerin tris(palmitin)
Trihexadecyl glycerol
1,2,3-Tri(hexadecanoyloxy)propane
Hexadecyl 1,2,3-tripalmitate
Triglycerol palmitate
Glyceryl palmitate tripalmitate
Trihexadecanoyl glycerol
Glycerol trihexadecanoate
Hexadecyl palmitate
Glycerol tris(hexadecanoic acid ester)
Glycerol tripalmitate ester
1,2,3-Propanetriyl palmitate
Tris(hexadecanoyl)glycerol
Trihexadecylglycerol
Hexadecanoate ester of glycerol
1,2,3-Trihexadecanoylglycerol
Glycerin trihexadecanoate
Glycerol tris(palmitic acid ester)
Trihexadecyl glyceryl ester
Hexadecanoate glycerol ester
Glycerol 1,2,3-trihexadecanoate
Tris(palmitoyloxy)methylpropane
1,3-Dihydroxypropan-2-yl palmitate
1,3-Bis(hexadecanoyloxy)propan-2-yl palmitate
Hexadecyl 1,2,3-trihexadecanoate
Glycerin tris(palmitoyl ester)
1,2,3-Tri(hexadecanoyloxy)propane
Trihexadecanoyl glyceryl ester
Glycerol trihexadecanoylate
TRIPEPTIDE-10
TRIPHENYL PHOSPHATE, N° CAS : 115-86-6, Nom INCI : TRIPHENYL PHOSPHATE, Nom chimique : Phosphoric acid, triphenyl ester, N° EINECS/ELINCS : 204-112-2, Ses fonctions (INCI) Agent plastifiant : Adoucit et rend souple une autre substance qui autrement ne pourrait pas être facilement déformée, dispersée ou être travaillée
TRIPHENYL PHOSPHATE
T 309; tris(phe;NSC 57867; TRIPHENYLTHIOPHOSPHATE; T 309 (antiwear additive); Triphenyl Phosphorothioate; O,O,O-Triphenylthiophosphat; Triphenoxyphosphine sulfide; TRIPHENYL PHOSPHOROTHIONATE; O,O,O-Triphenyl thiophosphate CAS NO:597-82-0
TRIPHENYL PHOSPHATE (TPP)
Triphenyl phosphate (TPP) is colorless, crystalline powder with a phenol-like odor.
Triphenyl phosphate (TPP) has a role as a flame retardant and a plasticiser.


CAS Number: 115-86-6
EC Number: 204-112-2
MDL number: MFCD00003031
Linear Formula: (C6H5O)3PO
Chemical formula: C18H15O4P



SYNONYMS:
triphenylphosphate, phosphoric acid, triphenyl ester, disflamoll tp, triphenoxyphosphine oxide, celluflex tpp, phosflex tpp, trifenylfosfat, phenyl phosphate pho 3po, phosphoric acid triphenyl ester, trifenylfosfat czech, TPP, TPPA, Tripheyl phosphate, TRIPHENYL PHOSPHATE (TPP), PHOSPHORIC ACID TRIPHENYL ESTER, Phosflex TPP, Triphenyl hosphate, Altal, Dymel, Wako TPP, Phosphoric acid,triphenyl ester, Celluflex TPP, Triphenyl phosphate, Phenyl phosphate ((PhO)3PO), Triphenoxyphosphine oxide, Disflamoll TP, TP, Phosflex TPP, TPP, TPPA, Reofos TPP, S 4, S 4 (phosphate), TTP, Sumilizer TPP, Wako TPP, NSC 57868, Phoscon FR 903N, TFF, WSFR-TPP, Triphenol phosphate, TTP (triphenyl phosphate), DHPF 005, Antioxidant TTP, UN 3077, Disflamoll TPP, FR 3031, 402955-02-6, Triphenyl phosphate, TPP, Phosphoric acid, triphenyl ester, Celluflex TPP, Disflamoll TP, Phenyl phosphate ((PhO)3PO), Phosflex TPP, Triphenoxyphosphine oxide, TP, Trifenylfosfat, Altal, Dymel, Kronitex TPP, Phenyl phosphate, Triphenyl phosphoric acid ester, NSC 57868, TPhP, Triphénylphosphate, Trifenilfosfato, TPP, Phosphoric acid, triphenyl ester, Celluflex TPP, Disflamoll TP, Phenyl phosphate ((PhO)3PO), Phosflex TPP, Triphenoxyphosphine oxide, TP, Trifenylfosfat, Altal, Kronitex TPP, Phenyl phosphate, Triphenyl phosphoric acid ester, NSC 57868, phenyl phosphate, TPP, triphenyl ester of phosphoric acid, Celluflex TPP, Disflamoll TP, Phenyl phosphate ((PhO)3PO), Phosflex TPP, Phosphoric acid, triphenyl ester, TP (VAN), TPP, Trifenylfosfat [Czech], Triphenoxyphosphine oxide, Triphenyl phosphate, Triphenylphosphate, [ChemIDplus], phenyl phosphate, TPP, Phosphoric acid triphenyl ester, triphenyl phosphoric acid ester, celluflex tpp, TRIPHENYL PHOSPHATE, 115-86-6, Triphenylphosphate, Phosphoric acid, triphenyl ester, Disflamoll TP, Celluflex TPP, Phosflex TPP, Triphenoxyphosphine oxide, Trifenylfosfat, Phenyl phosphate ((PhO)3PO), Phosphoric Acid Triphenyl Ester, NSC 57868, TPPA, CCRIS 4888, HSDB 2536, UNII-YZE19Z66EA, EINECS 204-112-2, YZE19Z66EA, BRN 1888236, DTXSID1021952, CHEBI:35033, AI3-04491, NSC-57868, Triphenyl phosphoric acid ester, DTXCID201952, EC 204-112-2, 4-06-00-00720 (Beilstein Handbook Reference), Triphenyl Phosphate 1000 microg/mL in Acetone, Triphenyl phosphate 10 microg/mL in Ethyl acetate, Trifenylfosfat [Czech], Triphenyl phosphate 500 microg/ml in Methyl-tert-butyl ether, Reofos TPP, CAS-115-86-6, TPHP, C18H15O4P, Triphenyl Phosphate (TPP), Altal, Kronitex TPP, Reolube TPP, Reomol TPP, TPP; TPHP, NCIOpen2_007435, Triphenyl Phosphate, Reagent, SCHEMBL18116, Phenyl phosphate, (PhO)3PO, BIDD, , Triphenyl phosphate, >=99%, CHEMBL454511, TRIPHENYL PHOSPHATE [MI], WLN: ROPO & OR & OR, Triphenyl phosphate (TPP, TPhP), TRIPHENYL PHOSPHATE [HSDB], NSC57868, Tox21_201511, Tox21_300504, MFCD00003031, STL280499, AKOS015888630, Triphenyl phosphate, analytical standard, NCGC00164033-01, NCGC00164033-02, NCGC00164033-03, NCGC00254408-01, NCGC00260671-01, AC-19461, CS-0017793, NS00010271, P0272, A803498, Q418573, J-003328, Triphenyl phosphate, TraceCERT(R), 31P-qNMR Standard, Triphenyl phosphate (TPP) 500 microg/mL in Methyl tert-butyl ether



Triphenyl phosphate (TPP) is a solid phosphate ester which imparts good flame retardance to a large number of polymers.
Triphenyl phosphate (TPP) is a clear liquid, used as a performance additive to improve the colour and clarity of alkyd resin, unsaturated polyester resin and various industrial oils during their manufacture.


The manufacture of various resins involves the use of high temperatures, usually in excess of 150° C.
At these temperature the reaction mass tends to get coloured due to oxidation.
Triphenyl phosphate (TPP), n°115-86-6 is determined by GC-MS. Sample material must be taken using special equipment.


Triphenyl phosphate (TPP) is found in the photography industry. It is also a fire retardant.
Triphenyl phosphate (TPP) is a solid phosphate ester which imparts good flame retardance to a large number of polymers.
Triphenyl phosphate (TPP) is an aryl phosphate resulting from the formal condensation of phosphoric acid with 3 mol eq. of phenol.


Triphenyl phosphate (TPP) has a role as a flame retardant and a plasticiser.
Triphenyl phosphate (TPP) is functionally related to a phenol.
Triphenyl phosphate (TPP) is a colorless, crystalline solid widely and safely used by many industries around the world.


Triphenyl phosphate (TPP) provides many benefits to consumer products – from preventing electrical and automobile fires to increasing flexibility and durability of such products as photographic films.
Triphenyl phosphate (TPP) is colorless, crystalline powder with a phenol-like odor.


Triphenyl phosphate (TPP) is one of many chemical compounds that are part of multicomponent substances based on phosphorus esters.
Due to the adverse effects of this chemical compound on the environment, low Triphenyl phosphate (TPP) solutions are required in some applications.
Following the requirements of the market and in the interests of human health and environmental health, the PCC Group has developed a technology to obtain phosphorus esters with low levels of Triphenyl phosphate (TPP).


This group of chemicals includes products bearing the sign “Low TPP”.
Triphenyl phosphate (TPP) available as white flake or crystal.
Triphenyl phosphate (TPP) acts as a flame retardant, non-flammable plasticizer or additive in cellulose for photographic film, polyester and polyurethane.


Triphenyl phosphate (TPP) exhibits insolubility in water and solubility in benzene, chloroform, ether and acetone.
Triphenyl phosphate (TPP) is a colorless solid.
The primary uses for Triphenyl phosphate (TPP) are as a flame retardant or solvent in chemical and plastics manufacturing.


Information from the 2016 Chemical Data Reporting (CDR) for Triphenyl phosphate (TPP) indicates the reported production volume is between 1 million and 10 million lbs/year (manufacture and import).
Triphenyl phosphate (TPP), in the form of a white, odorless crystalline powder, is a flame-retardant plasticizer.


Its crystallization point begins above 47 degrees Celsius, and Triphenyl phosphate (TPP) contains less than .1 mg of potassium hydroxide per gram.
Triphenyl phosphate (TPP) is a non-halogen flame retardant plasticizer.
Triphenyl phosphate (TPP) is present as a white flaky crystal.


Compatible with phenolic resins, cellulose resin, vinyl resin and rubber, and some engineering plastics such as PPO.
Triphenyl phosphate (TPP) is the chemical compound with the formula OP(OC6H5)3.
Triphenyl phosphate (TPP) is the simplest aromatic organophosphate.


This colourless solid, Triphenyl phosphate (TPP), is the ester (triester) of phosphoric acid and phenol.
Nail polish has received particular interest as a source of exposure to Triphenyl phosphate (TPP).
Triphenyl phosphate (TPP) appears as colorless crystals.


Triphenyl phosphate (TPP) is an aryl phosphate resulting from the formal condensation of phosphoric acid with 3 mol eq. of phenol.
Triphenyl phosphate (TPP) has a role as a flame retardant and a plasticiser.
Triphenyl phosphate (TPP) is functionally related to a phenol.


Triphenyl phosphate (TPP) is an organophosphate flame retardant.
Triphenyl phosphate (TPP) is part of the group of Non-Halogenated Aromatic Phosphates.
Triphenyl phosphate (TPP) is part of the group of Organophosphate Flame Retardants (OPFRs).


Triphenyl phosphate (TPP) is a chemical compound in the form of a colourless solid.
Triphenyl phosphate (TPP) is the ester (triester) of phosphoric acid and phenol.
Triphenyl phosphate (TPP) is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 100 tonnes per annum.



USES and APPLICATIONS of TRIPHENYL PHOSPHATE (TPP):
Triphenyl phosphate (TPP) can be used as flame retardant plasticizer for cellulose resin, vinyl resin, natural rubber and synthetic rubber, with low flame retardant efficiency, excellent mechanical retention, transparency, softness and strong toughness.
Triphenyl phosphate (TPP) is used in nitrocellulose, various coatings, rigid polyurethane foam plastics, engineering plastics plasticizers, and flame retardant additives.


Triphenyl phosphate (TPP) is mainly used as a flame retardant plasticizer for engineering plastics and phenolic resin laminates;
Triphenyl phosphate (TPP) is used as softener of synthetic rubber and raw material of trimethyl phosphate;
Triphenyl phosphate (TPP) is used as a plasticizer, fire-retardant, and substitute for camphor in celluloid; also used in lubricating oils and hydraulic fluids.


Triphenyl phosphate (TPP) acts as an anti-oxidant and prevents colour formation of the finished product, as a result of which better quality resins are obtained.
Triphenyl phosphate (TPP) is used paint, Coating, Ink


Triphenyl phosphate (TPP) is used as stabilizer
Triphenyl phosphate (TPP) is used polymers (including) Adhesives, Styrenics, Engineering, Thermoplastics, Polymers.
Triphenyl phosphate (TPP) is used to regulate Viscosity and improve colour stability


Polyolefins: Triphenyl phosphate (TPP) is used as catalyst
Polyurethane hot melt adhesives, SBR Rubber, Epoxies
Triphenyl phosphate (TPP) is used to prevent scorching during curing and improve colour stability


Triphenyl phosphate (TPP) is a commonly used flame retardant and plasticizer in various industries.
Triphenyl phosphate (TPP) is used for this analysis, the lab adopts the following method: Inhouse.
Triphenyl phosphate (TPP) is used Flame Retardants, Plastic, Resin & Rubber, Plasticizers


Triphenyl phosphate (TPP) is used as flame retardant and processing aid in cellulose acetate, cellulose acetate butyrate and vinyl copolymer compounds which are used in moulding applications.
Other important applications of Triphenyl phosphate (TPP) are coatings based on nitrocellulose, phenolic resins, ABS/PC and HIPS/PPE compounds.


Studies support the safe use of Triphenyl phosphate (TPP) in its different applications.
Triphenyl phosphate (TPP) is used in some nail polish and nail enamels, basecoats and undercoats, and manicuring products.
Triphenyl phosphate (TPP) is used in very low concentrations, primarily to increase the flexibility and durability of nail polish products, and improve adhesion of the product to the nail plate.


Triphenyl phosphate (TPP) is known as a product with manifold fields of applications regarding its qualities in particular as a flame retardant.
One primary use of Triphenyl phosphate (TPP) is as a flame retardant in phenolic- and phenylene oxide-based resins for the manufacture of electrical and automobile components, for auto upholstery, and as a nonflammable plasticizer in cellulose acetate for photographic films.


Triphenyl phosphate (TPP) has also been used to impregnate roofing paper.
Triphenyl phosphate (TPP) occurs as a plasticizer in various lacquers and varnishes, and as a component of lubricating oil and hydraulic fluids.
Triphenyl phosphate (TPP) is used in the insecticidal composition.


Triphenyl phosphate (TPP) is also used in hydraulic liquids, and adhesives, inks, coatings, as a plasticizer in lacquers and varnishes, and as a substitute for camphor in celluloid materials to make the latter stable and fireproof.
Triphenyl phosphate (TPP) can be used in coatings, nitrocellulose applications, and rigid polyurethane foams.


Triphenyl phosphate (TPP) is used in many plastics and resins (such as phenolic resin, cellulose resin, epoxy resin, PVC, PP, PC, ABS and PC/ABS).
Triphenyl phosphate (TPP) is used as an internal standard in the screening and quantification of agrochemical residues in vegetables and fruits.
Triphenyl phosphate (TPP) is used in plastic processing and molding of plastic flow and performance.


Triphenyl phosphate (TPP) is used as an internal standard in the screening and quantification of agrochemical residues in vegetables and fruits.
Triphenyl phosphate (TPP) is used in plastic processing and molding of plastic flow and performance.
Triphenyl phosphate (TPP) is used as a plasticiser in a wide variety of fields and objects.


Triphenyl phosphate (TPP) is also used as a flame retardant for certain materials including electronic equipment, PVC, hydraulic fluids, glues, nail polishes and moulding resins.
To be effective as a flame retardant, Triphenyl phosphate (TPP) acts as follows: phosphoric acid is formed during thermal decomposition.


This reacts to form pyrophosphoric acid.
In Triphenyl phosphate (TPP)'s condensed phase, pyrophosphoric acid acts to block heat transfer.
Triphenyl phosphate (TPP) is active in the gas phase.


The gradual phase-out of PBDEs may explain the increased use of triphenyl phosphate.
Triphenyl phosphate (TPP) has been added as a flame retardant to a variety of products, such as foam used in upholstered furniture, children’s products, and electronic equipment.


Triphenyl phosphate (TPP) is also used in some nail polish and as an additive to increase the durability and flexibility of some plastics.
Triphenyl phosphate (TPP) is also used as a plasticizer in lacquers, varnishes, and hydraulic fluids.
Triphenyl phosphate (TPP) has been used widely as a flame retardant and plasticizer.


Triphenyl phosphate (TPP) has been used as a flame retardant for a variety of materials, including electronic equipment, PVC, hydraulic fluids, glues, in nail polishes, and casting resins.
Triphenyl phosphate (TPP)'s mechanism of action as a flame retardant is as follows: first, during thermal decomposition, phosphoric acid is formed.



This reacts to form pyrophosphoric acid, which, when in Triphenyl phosphate (TPP)'s condensed phase, acts to block heat transfer.
One of the most effective flame retardants for certain polymers, Triphenyl phosphate (TPP) is only active as an additive flame retardant in its gas phase.
Phase out of PBDEs may have increased the use of Triphenyl phosphate (TPP) in recent years.


Triphenyl phosphate (TPP) is used as a plasticizer and a fire retardant in a wide variety of settings and products.
Triphenyl phosphate (TPP) is used by consumers, in articles, by professional workers (widespread uses), in formulation or re-packing, at industrial sites and in manufacturing.


Triphenyl phosphate (TPP) is used in the following products: adhesives and sealants, coating products and cosmetics and personal care products.
Other release to the environment of Triphenyl phosphate (TPP) is likely to occur from: indoor use and outdoor use resulting in inclusion into or onto a materials (e.g. binding agent in paints and coatings or adhesives).


Release to the environment of Triphenyl phosphate (TPP) can occur from industrial use: industrial abrasion processing with low release rate (e.g. cutting of textile, cutting, machining or grinding of metal).


Other release to the environment of Triphenyl phosphate (TPP) is likely to occur from: outdoor use in long-life materials with low release rate (e.g. metal, wooden and plastic construction and building materials) and indoor use in long-life materials with low release rate (e.g. flooring, furniture, toys, construction materials, curtains, foot-wear, leather products, paper and cardboard products, electronic equipment).


Triphenyl phosphate (TPP) can be found in complex articles, with no release intended: vehicles and machinery, mechanical appliances and electrical/electronic products (e.g. computers, cameras, lamps, refrigerators, washing machines).


Triphenyl phosphate (TPP) can be found in products with material based on: fabrics, textiles and apparel (e.g. clothing, mattress, curtains or carpets, textile toys), paper (e.g. tissues, feminine hygiene products, nappies, books, magazines, wallpaper) and plastic (e.g. food packaging and storage, toys, mobile phones).


Triphenyl phosphate (TPP) is used in the following products: adhesives and sealants, coating products and laboratory chemicals.
Triphenyl phosphate (TPP) is used in the following areas: scientific research and development.


Other release to the environment of Triphenyl phosphate (TPP) is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners) and outdoor use resulting in inclusion into or onto a materials (e.g. binding agent in paints and coatings or adhesives).


Triphenyl phosphate (TPP) is used in the following products: polymers and cosmetics and personal care products.
Release to the environment of Triphenyl phosphate (TPP) can occur from industrial use: formulation in materials and formulation of mixtures.
Triphenyl phosphate (TPP) is used in the following products: polymers.


Triphenyl phosphate (TPP) is used in the following areas: scientific research and development.
Triphenyl phosphate (TPP) is used for the manufacture of: plastic products, textile, leather or fur, electrical, electronic and optical equipment and machinery and vehicles.


Release to the environment of Triphenyl phosphate (TPP) can occur from industrial use: in the production of articles.
Release to the environment of Triphenyl phosphate (TPP) can occur from industrial use: manufacturing of the substance.



CONDITIONS OF USE OF TRIPHENYL PHOSPHATE (TPP):
In the final scope, EPA identified conditions of use associated with the importing; processing; distribution in commerce; industrial, commercial and consumer uses; and disposal of Triphenyl phosphate (TPP), for example:

*The flame retardant is processed as a reactant, incorporated into a formulation, mixture, or reaction products, and incorporated into articles;
*Triphenyl phosphate (TPP) is reportedly used in commercial paints and coatings and for plastic and rubber products; and
*Several consumer uses were reported, including foam seating and bedding products.
*The above listed conditions of use are ways that a person or the environment could be potentially exposed to this chemical.



PREPARTION OF TRIPHENYL PHOSPHATE (TPP):
Triphenyl phosphate (TPP) is prepared by reacting phosphorus pentoxide and phenol, or by reacting phosphorus oxychloride and phenol.
On a larger scale phosphorus oxychloride and phenol are reacted in an esterification tank with heating.
The HCL formed is trapped and condensed, while the crude Triphenyl phosphate (TPP) runs into a large tank where it is purified.



REACTIVITY PROFILE OF TRIPHENYL PHOSPHATE (TPP):
Organophosphates, such as Triphenyl phosphate (TPP), are susceptible to formation of highly toxic and flammable phosphine gas in the presence of strong reducing agents such as hydrides.
Partial oxidation by oxidizing agents may result in the release of toxic phosphorus oxides.



PREPARTION OF TRIPHENYL PHOSPHATE (TPP):
Triphenyl phosphate (TPP) is prepared by the SN2 reaction of phosphorus oxychloride and phenol.



CHEMICAL PROPERTIES OF TRIPHENYL PHOSPHATE (TPP):
Triphenyl phosphate (TPP) is a colorless crystalline powder with a faint, phenol-like odor.
Triphenyl phosphate (TPP) is practically insoluble in water at 1.9 × 10 7 mg/l at 24 °C.

Triphenyl phosphate (TPP) is very soluble in carbon tetrachloride and is soluble in most lacquers, solvents, thinners, and oils, as well as in alcohol, benzene, ether, chloroform, and acetone.

Triphenyl phosphate (TPP) begins to decompose at about 600 °C in inert gas, and in a large excess of air, complete combustion to carbon dioxide occurs in the range 800–900 °C.
Hydrolysis of Triphenyl phosphate (TPP) occurs very slowly in acidic or neutral solutions, but occurs rapidly in alkaline solutions.



CHEMICAL/PHYSICAL PROPERTIES OF TRIPHENYL PHOSPHATE (TPP):
When an aqueous solution containing Triphenyl phosphate (TPP) (0.1 mg/L) and chlorine (3 to 1,000 mg/L) was stirred in the dark at 20 °C for 24 h, the benzene ring was substituted with one to three chlorine atoms.
The reported hydrolysis half-lives at pH values of 8.2 and 9.5 were 7.5 and 1.3 d, respectively.
Triphenyl phosphate (TPP) decomposes at temperatures greater than 410 °C



SOLUBILITY OF TRIPHENYL PHOSPHATE (TPP):
Triphenyl phosphate (TPP) reacts with water.



NOTES OF TRIPHENYL PHOSPHATE (TPP):
Triphenyl phosphate (TPP) is incompatible with oxidizing agents and moisture.
Store Triphenyl phosphate (TPP) under dry inert gas.
Protect Triphenyl phosphate (TPP) from humidity and water.



FEATURES OF TRIPHENYL PHOSPHATE (TPP):
Triphenyl phosphate (TPP)is useful for plastic, which is of cellulose ester radical, and it is insoluble in gas, nonflammable and it has good light stability.

Plastic uses of Triphenyl phosphate (TPP): Acrylonitrile, butadienestyrene copolymer, acetate fibre, cellulose nitrate, polyester, polyvinyl chloride, polyvinyl acetate, polyolepine, polyaminoester (PU soft).

Triphenyl phosphate (TPP) noncombustable substitute for camphor in celluloid.
Triphenyl phosphate (TPP) is used plasticizer in plastics (e.g., cellulose acetate) lacquers, varnishes, etc.
Triphenyl phosphate (TPP) is also used in impregnating roofing paper.



TRANSPORTATION PRECAUTIONS OF TRIPHENYL PHOSPHATE (TPP):
1. The package of Triphenyl phosphate (TPP) shall be complete and the loading shall be safe.
During transportation, ensure that containers do not leak, collapse, fall or damage.

Triphenyl phosphate (TPP) is strictly prohibited to mix with oxidant and transport.
During transportation, Triphenyl phosphate (TPP) shall be protected from sun exposure, rain and high temperature;


2. Storage precautions:
store Triphenyl phosphate (TPP) in a cool and ventilated warehouse.
Keep away from fire and heat.

Triphenyl phosphate (TPP) should be stored separately from the oxidant, avoiding mixed storage.
Fire fighting equipment of corresponding variety and quantity shall be provided.
The storage area shall be equipped with appropriate materials to contain the leakage.



SOLUBILITY OF TRIPHENYL PHOSPHATE (TPP):
Triphenyl phosphate (TPP) is insoluble in water, easily hydrolyzed to free phenol in case of moisture, soluble in organic solvents such as alcohol, ether, benzene and acetone, which has absorption effect on ultraviolet rays.



PHYSICAL and CHEMICAL PROPERTIES of TRIPHENYL PHOSPHATE (TPP):
Chemical Formula: C₁₈H₁₅O₄P
Molar Mass: 326.288 g·mol⁻¹
Molecular Weight: 326.3 g/mol
Exact Mass: 326.07079595 g/mol
Monoisotopic Mass: 326.07079595 g/mol
Physical Properties
Appearance: Colorless solid
Density: 1.184 g/mL
Melting Point: 48 to 50 °C (118 to 122 °F; 321 to 323 K)
Boiling Point: 244 °C (471 °F; 517 K) at 10 mmHg
Vapor Pressure: 1 mmHg at 193 °C
Chemical Characteristics
XLogP3: 4.6

Hydrogen Bond Donor Count: 0
Hydrogen Bond Acceptor Count: 4
Rotatable Bond Count: 6
Topological Polar Surface Area: 44.8 Ų
Heavy Atom Count: 23
Formal Charge: 0
Complexity: 325
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes

CAS Number: 115-86-6
EC Number: 204-112-2
Hill Formula: C₁₈H₁₅O₄P
Chemical Formula: (C₆H₅O)₃PO
Molar Mass: 326.29 g/mol
HS Code: 2919 90 30
Physical Properties
Physical State: Flakes
Color: White
Odor: No data available
Melting Point/Freezing Point: 48 - 50 °C (lit.)
Boiling Point: 220 °C (5 hPa)
Density: 1.2 g/cm³ (50 °C)
Relative Density: 1.21 at 50 °C

Bulk Density: 650 kg/m³
Flash Point: 220 °C (closed cup)
Ignition Temperature: >500 °C
Decomposition Temperature: No data available
pH: No data available
Viscosity: No data available (kinematic and dynamic)
Water Solubility: 0.0019 g/L at 20 °C (slightly soluble)
Vapor Pressure: 1.73 hPa at 200 °C; 0.1 hPa at 150 °C
Relative Vapor Density: No data available
Partition Coefficient (n-octanol/water): log Pow: 4.63 at 20 °C (Potential bioaccumulation)
Additional Properties
Refractive Index: 1.563 at 50 °C

Specific Gravity: 1.185-1.202
Acid Value: ≤0.1 mg KOH/g
Free Phenol: ≤50 mg/kg
Water Content: ≤0.1%
Color (APHA): ≤80
Phosphorus Content: 9.5% (calculated)
Hazen Color Value: ≤50 (in melt)
Log Pow: 4.6 at 20 °C
Safety and Stability
Flammability: Combustible Solid
Explosive Properties: No data available
Oxidizing Properties: None
Storage Conditions: Store below +30°C

Autoignition Temperature: No data available
Decomposition Temperature: No data available
General Information
Chemical Name: Phosphoric acid triphenyl ester; Triphenyl Phosphate (TPP)
CAS Number: 115-86-6
EINECS Number: 204-112-2
Molecular Formula: C₁₈H₁₅O₄P
Molecular Weight: 326.29 g/mol
Physical Properties
Appearance: White flakes or pellets; colorless crystal powder or needles
Color (APHA): ≤ 80
Odor: Odorless

Density: 1.205 g/cm³ at 50 °C; 1.185-1.202 (specific gravity)
Refractive Index: 1.555 at 50 °C; 1.550
Melting Point: 48-50 °C
Freezing Point: 48-50 °C
Boiling Point: 245 °C at 11 mmHg
Flash Point: 220 °C (428 °F) - closed cup
Viscosity at 50 °C: 11 mPa·s
Chemical Characteristics
Acid Value: ≤ 0.1 mg KOH/g; ≤ 0.05 mg KOH/g (specific grades)
Free Phenol: ≤ 50 mg/kg; 0.03 MAX
Water Content: ≤ 0.1%
Phosphorus Content: 9.5% (calculated)

Solubility and Stability
Solubility: Insoluble in water
Storage Conditions: 2-8 °C
Hazen Color Value: ≤ 50 (in melt)
Additional Information
Content: ≥ 99.0%
Flash Point (cc): 220 °C
Molecular Weight: 326.28-326.29 g/mol
Chemical Formula: C₁₈H₁₅O₄P
Molecular Weight: 326.28300 g/mol
Exact Mass: 326.28 g/mol

CAS Number: 115-86-6
EC Number: 204-112-2
HS Code: 2919 90 30
Hill Formula: C₁₈H₁₅O₄P
Physical Properties:
Appearance: Colorless crystals or flakes
Color: White (Colorless to faint yellow in some formulations)
Odor: Odorless
Density: 1.2055 g/cm³ at 50 °C
Specific Gravity: 1.268 at 50 °C; 1.180-1.186 at 25 °C
Melting Point: 49-50 °C
Boiling Point: 245 °C at 11 mmHg (lit.)
Flash Point: 220 °C (428 °F) - closed cup

Refractive Index: 1.563 (at 50 °C), 1.580-1.589 (at 25 °C)
Water Solubility: Insoluble (0.0019 g/L at 20 °C)
Vapor Pressure: 1.3 mm Hg at 200 °C
Vapor Density: 1.19 (Air = 1)
Flammability: Combustible Solid
Chemical Characteristics:
Partition Coefficient (log Pow): 4.6
Topological Polar Surface Area (PSA): 54.57 Ų
Hydrogen Bond Donor Count: 0
Hydrogen Bond Acceptor Count: 4
Rotatable Bond Count: 6
Safety and Storage:

Storage Conditions: 2-8 °C
Autoignition Temperature: >500 °C
Stability: Stable
Decomposition Temperature: No data available
Solubility:
Solvents: Benzene, chloroform, ether, acetone, lacquers, solvents, thinners, oil
Additional Information:
Phosphorus Content: 9.8-10.1%
Acidic Value: ≤ 0.5 mg KOH/g
Freezing Point: 22-24 °C
Chemical Name: Phosphoric acid triphenyl ester; Triphenyl Phosphate (TPP)
Chemical Name: Triphenyl phosphate

CAS Number: 115-86-6
EC Number: 204-112-2
Hill Formula: C₁₈H₁₅O₄P
Chemical Formula: (C₆H₅O)₃PO
Molecular Weight: 326.3 g/mol
Formula Weight: 326.29 g/mol
HS Code: 2919 90 30
Physical Properties
Appearance: Colorless, crystalline powder with a phenol-like odor
Color: White
Physical State: Flakes
Odor: Odorless

Melting Point/Freezing Point: 48 - 52 °C (118 - 124 °F)
Boiling Point: 244 - 250 °C (473 °F at 11 mmHg)
Density: 1.2055 g/cm³ (1.184 g/mL at 50 °C)
Specific Gravity: 1.185 - 1.202
Flash Point: 220 - 435 °F (220 °C to 433 °F)
Vapor Pressure: 1 - 1.73 hPa (1 mmHg at 193-200 °C)
Refractive Index: 1.550 - 1.563
Vapor Density: 11.3 (vs air)
Viscosity: 11 mm²/s at 50 °C
Henry's Law Constant: 5.88 at 20 °C (approximate)
Water Solubility: 0.0019 g/L at 20 °C (insoluble)
Storage Temperature: Store below +30°C

Chemical Properties
XLogP3: 4.6
Topological Polar Surface Area (PSA): 44.8 Ų
Log Pow: 4.6 at 20 °C
Hydrogen Bond Donor Count: 0
Hydrogen Bond Acceptor Count: 4
Rotatable Bond Count: 6
Complexity: 325
Defined/Undefined Stereocenter Count: 0
Covalently-Bonded Unit Count: 1

Safety and Regulations
UN Number: UN3077
Beilstein Reference: 1888236
Merck Index: 14,9742
TLV-TWA Exposure Limit: 3 mg/m³ (ACGIH, OSHA, NIOSH)
FDA 21 CFR: 175.105
FDA UNII: YZE19Z66EA
EPA Substance Registry System: Triphenyl phosphate (115-86-6)
EWG's Food Scores: 5
Additional Information
InChIKey: XZZNDPSIHUTMOC-UHFFFAOYSA-N
CAS DataBase Reference: 115-86-6
BRN: 1888236



FIRST AID MEASURES of TRIPHENYL PHOSPHATE (TPP):
-Description of first-aid measures
*General advice:
Show this material safety data sheet to the doctor in attendance.
*If inhaled:
After inhalation:
Fresh air.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with
water/ shower.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Call in ophthalmologist.
Remove contact lenses.
*If swallowed:
After swallowing:
Immediately make victim drink water (two glasses at most).
Consult a physician.
-Indication of any immediate medical attention and special treatment needed.
No data available



ACCIDENTAL RELEASE MEASURES of TRIPHENYL PHOSPHATE (TPP):
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Observe possible material restrictions.
Take up dry.
Dispose of properly.
Clean up affected area.



FIRE FIGHTING MEASURES of TRIPHENYL PHOSPHATE (TPP):
-Extinguishing media:
*Suitable extinguishing media:
Carbon dioxide (CO2)
Foam
Dry powder
*Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Prevent fire extinguishing water from contaminating surface water or the ground water system.



EXPOSURE CONTROLS/PERSONAL PROTECTION of TRIPHENYL PHOSPHATE (TPP):
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Safety glasses
*Body Protection:
protective clothing
*Respiratory protection:
Recommended Filter type: Filter A
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of TRIPHENYL PHOSPHATE (TPP):
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
Dry.



STABILITY and REACTIVITY of TRIPHENYL PHOSPHATE (TPP):
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .
-Possibility of hazardous reactions:
No data available


TRIPHENYL PHOSPHOROTHIONATE
TRIPROPYLENE GLYCOL, N° CAS : 24800-44-0, Nom INCI : TRIPROPYLENE GLYCOL, Nom chimique : Propanol, [(1-methyl-1,2-ethanediyl)bis(oxy)]bis-, N° EINECS/ELINCS : 246-446-0 Classification : Glycol, Ses fonctions (INCI), Antioxydant : Inhibe les réactions favorisées par l'oxygène, évitant ainsi l'oxydation et la rancidité, Stabilisateur d'émulsion : Favorise le processus d'émulsification et améliore la stabilité et la durée de conservation de l'émulsion, Humectant : Maintient la teneur en eau d'un cosmétique dans son emballage et sur la peau
TRIPOTASSIUM CITRATE MONOHYDRATE
TRIPOTASSIUM CITRATE MONOHYDRATE = TRIPOTASSIUM CITRATE = TPC


CAS Number: 6100-05-6
EC-Number : 212-755-5
MDL number: MFCD00150442
E Number: E332
Empirical Formula (Hill Notation): C6H5K3O7 · xH2O / C6H7K3O8


Tripotassium Citrate Monohydrate (also known as tripotassium citrate) is a potassium salt of citric acid.
Tripotassium Citrate Monohydrate is a white, hygroscopic crystalline powder.
Tripotassium Citrate Monohydrate is odorless with a saline taste.
Tripotassium Citrate Monohydrate contains 38.3% potassium by mass.


Tripotassium Citrate Monohydrate is white/clear crystalline powder
Tripotassium Citrate Monohydrate is transparent prismatic crystals or a white, granular powder.
Tripotassium Citrate Monohydrate is hygroscopic and odorless, and has a cooling, saline taste.
In the monohydrate form Tripotassium Citrate Monohydrate is highly hygroscopic and deliquescent.


Tripotassium Citrate Monohydrate is a hydrate that is the monohydrate form of potassium citrate.
Tripotassium Citrate Monohydrate has a role as a diuretic.
Tripotassium Citrate Monohydrate contains a potassium citrate (anhydrous).
Tripotassium Citrate Monohydrate is the potassium salt form of citrate with alkalinizing property.


Following absorption, potassium citrate causes increased plasma bicarbonate concentration, thereby raising blood and urinary pH.
A simultaneous decrease in calcium ion activity occurs as a result of increasing calcium complex formation with dissociated anions.
Levels of urinary citrate are increased due to modification of the renal handling of citrate.
By promoting excretion of free bicarbonate ion and by increasing urinary pH in addition to an increased ionization of uric acid to more soluble urate ions, this agent exerts the alkalizing and anti-urolithic effect.


Tripotassium Citrate Monohydrate is powder that dissolves in water, which is administered orally and is used as a diuretic, expectorant, systemic alkalizer, and electrolyte replenishes.
Tripotassium Citrate Monohydrate is the common tribasic potassium salt of citric acid, also known as potassium citrate.
Tripotassium Citrate Monohydrate is produced by complete neutralization of citric acid with a high purity potassium source and subsequent crystallisation.


Tripotassium Citrate Monohydrate reduces sensitivity of teeth in oral care products.
Tripotassium Citrate Monohydrate is a non-toxic, slightly alkaline salt with low reactivity.
Tripotassium Citrate Monohydrate is chemically stable if stored at ambient temperatures.
In Tripotassium Citrate Monohydrate's monohydrate form it is very hygroscopic and must be protected from exposure to humidity.


Tripotassium Citrate Monohydrate occurs as transparent crystals or a white, granular powder.
Tripotassium Citrate Monohydrate is an odourless substance with a cooling, salty taste.
Tripotassium Citrate Monohydrate is slightly deliquescent when exposed to moist air, freely soluble in water and almost insoluble in ethanol (96%).
Tripotassium Citrate Monohydrate is one of the popular food additives and ingredients in most countries.


Tripotassium Citrate Monohydrate is the common tribasic potassium salt of citric acid, also known as potassium citrate.
Tripotassium Citrate Monohydrate is produced by complete neutralisation of citric acid with a high purity potassium source and subsequent crystallisation.
Tripotassium Citrate Monohydrate is one of the three potassium salts of citric acid.
Tripotassium Citrate Monohydrate appears as white crystalline powder with a salty taste.


Tripotassium Citrate Monohydrate is slightly deliquescent when in contact with moisture.
Tripotassium Citrate Monohydrate is very soluble in water and almost insoluble in ethanol.
Tripotassium Citrate Monohydrate is very hygroscopic and must be protected from humidity.
Tripotassium Citrate Monohydrate is non-toxic and fully biodegradable.


Tripotassium Citrate Monohydrate is a slightly alkaline salt with low reactivity at ambient temperatures.
Tripotassium Citrate Monohydrate is widely distributed in plants and in animal tissues and fluids and exist in greater than grace amounts in variety of fruits and vegetables, most notably in citrus fruits such as lemon and limes.
Tripotassium Citrate Monohydrate is also a metabolite of Dimethyl Fumarate (D464965), a compound.
Tripotassium Citrate Monohydrate is a source of citric acid, which is an alpha-hydroxy acid.


Tripotassium Citrate Monohydrate is widely distributed in plants and in animal tissues and fluids and exist in greater than grace amounts in variety of fruits and vegetables, most notably in citrus fruits such as lemon and limes.
Tripotassium Citrate Monohydrate is a hydrate that is the monohydrate form of potassium citrate.
Tripotassium Citrate Monohydrate is a potassium salt that has been reported to be efficient in forming aqueous two-phase system (ATPS) with UCON 50-HB-5100, a random copolymer.


Tripotassium Citrate Monohydrate is a sequestrant and buffer that exists as crystals or powder.
Tripotassium Citrate Monohydrate is slightly hygroscopic and possesses the advantageous properties of citric acid without having its acid reaction.
a 1% solution has a ph of 7.5–9.0.
Tripotassium Citrate Monohydrate reacts with metal ions such as calcium, magnesium, and iron to form a complex.


Tripotassium Citrate Monohydrate is soluble in water with a solubility of 1.8 g in 1 ml of 20°c water and 2 g in 1 ml of 80°c water.
Tripotassium Citrate Monohydrate is also termed tripotassium citrate.
Tripotassium Citrate Monohydrate is soluble in water and glycerol.
Tripotassium Citrate Monohydrate is insoluble in alcohol


Tripotassium Citrate Monohydrate is soluble in 0-65ml of water, slowly soluble in 2-5ml of glycerol, insoluble in ethanol.
Tripotassium Citrate Monohydrate is generally immediately available in most volumes.
High purity, submicron and nanopowder forms of Tripotassium Citrate Monohydrate may be considered.
Tripotassium Citrate Monohydrate is a white, granulated powder or colourless crystals.


Tripotassium Citrate Monohydrate is very easily soluble in water and hardly soluble in alcohol.
Tripotassium Citrate Monohydrate is a potassium salt of the citric acid and is formed by neutralisation of citric acid with potassium.
Tripotassium Citrate Monohydrate is a pure white granular powder and has no fillers or binders, additives or preservatives.
Tripotassium Citrate Monohydrate is created by combining Potassium Bicarbonate with Citric Acid and evaporating the solution until the granular form remains.


Tripotassium Citrate Monohydrate (also known as tripotassium citrate) is a potassium salt of citric acid with the molecular formula K3C6H5O7.
Tripotassium Citrate Monohydrate is a white, hygroscopic crystalline powder.
Tripotassium Citrate Monohydrate is odorless with a saline taste.
Tripotassium Citrate Monohydrate contains 38.28% potassium by mass.


In the monohydrate form Tripotassium Citrate Monohydrate is highly hygroscopic and deliquescent.
Tripotassium Citrate Monohydrate has no smell.
Tripotassium Citrate Monohydrate's taste is salty and cool.
Tripotassium Citrate Monohydrate's hygroscopic.


Tripotassium Citrate Monohydrate is loss of crystal water at 180 ℃.
1 aqueous solution is alkaline to litmus, pH is about 8.5.
Tripotassium Citrate Monohydrate is white crystalline granules or powder.
1g of Tripotassium Citrate Monohydrate is soluble in 0.65mL water, slowly soluble in 2.5ml glycerol, insoluble in ethanol.


Tripotassium Citrate Monohydrate's aqueous solution is alkaline to litmus.
The pH value of Tripotassium Citrate Monohydrate is about 8.5.
Tripotassium Citrate Monohydrate has loss of water of crystallization at 180 °c.
As a food additive, Tripotassium Citrate Monohydrate is used to regulate acidity and is known as E number E332.



USES and APPLICATIONS of TRIPOTASSIUM CITRATE MONOHYDRATE:
Tripotassium Citrate Monohydrate is rapidly absorbed when given by mouth and is excreted in the urine.
Since Tripotassium Citrate Monohydrate is an alkaline salt it is effective in reducing the pain and frequency of urination when these are caused by highly acidic urine.
Tripotassium Citrate Monohydrate is used for this purpose in dogs and cats, but is chiefly employed as a non-irritating diuretic.


Tripotassium Citrate Monohydrate is used food, Beverages, Tablets, Personal Care and Technical Applications.
In food industry: Tripotassium Citrate Monohydrate is used buffering agent, chelating agent, yeast food, emulsifying salt, and synergistic agent of anti-oxidation.
In chemical industry: Tripotassium Citrate Monohydrate is used tripotassium phosphate is used in the manufacture of liquid soap, refined gasoline, high-quality paper, metal surface treatment, biological hydration treatment, phosphorus-potassium fertilizers.


Tripotassium Citrate Monohydrate is the common tribasic potassium salt of citric acid, also known as potassium citrate.
Tripotassium Citrate Monohydrate is used in foods, beverages, personal care and technical applications as buffering, sequestering or emulsifying agent.
Tripotassium Citrate Monohydrate usually replaces trisodium citrate whenever a low sodium content is desired.
Tripotassium Citrate Monohydrate is used in foods, beverages, and technical applications as buffering, sequestering or emulsifying agent.


Tripotassium Citrate Monohydrate usually replaces trisodium citrate whenever a low sodium content is desired.
In pharmaceuticals Tripotassium Citrate Monohydrate is used as potassium source and as active ingredient to treat urinary duct stones.
When added to oral care products, Tripotassium Citrate Monohydrate is the active ingredient to reduce the sensitivity of the teeth.
In contrary to other potassium salts, Tripotassium Citrate Monohydrate is less bitter and thus can be used at higher concentration levels.


The food-approved substance is safe and easy in handling.
Furthermore, Tripotassium Citrate Monohydrate is one of the few fully biodegradable and non-toxic flame retardants.
Tripotassium Citrate Monohydrate is used in food and beverage industries.
Tripotassium Citrate Monohydrate finds application as buffering, sequestering or emulsifying agent.


Tripotassium Citrate Monohydrate is also used as a potassium source in pharmaceuticals and an active ingredient to treat urinary duct stones.
Tripotassium Citrate Monohydrate is added to oral care products to reduce the teeth sensitivity.
Tripotassium Citrate Monohydrate is used in foods, beverages, cosmetics, agrochemicals and as buffering agents and emulsifying agents.
Tripotassium Citrate Monohydrate is used in place of Sodium Citrate where low sodium content is required.


Tripotassium Citrate Monohydrate is used in manufacturing method of printed circuit board for autonomous vehicle to perform recognition, judgment, determination and execution.
Tripotassium Citrate Monohydrate is a weak organic acid that is known as a commodity chemical, as more than a million tonnes are produced every year by mycological fermentation on an industrial scale using crude sugar solutions, such as molasses and strains of Aspergillus niger.


Tripotassium Citrate Monohydrate is mainly used as an acidifier, flavoring agent and chelating agent.
Tripotassium Citrate Monohydrate is used in the laboratory as a buffering agent and chelator.
In renal function studies, potassium citrate is used as an alkanizing agent where the citric acid is a metabolic substrate in renal cells.
Studies have shown that potassium citrate may increase bone density, it is therefore used in research experiments related to the treatment of osteoporosis.


Tripotassium Citrate Monohydrate is used in foods, beverages, and other applications as a buffering, sequestering or emulsifying ingredient.
Tripotassium Citrate Monohydrate is the potassium salt of citric acid and it usually replaces trisodium citrate whenever a low sodium content is desired.
An organic acid naturally found in citrus fruits, Tripotassium Citrate Monohydrate is a natural preservative and is also used to add an acidic (sour) taste to foods and soft drinks.


Tripotassium Citrate Monohydrate can be added to ice cream to keep fat globules separated and be added to recipes in place of fresh lemon juice.
Tripotassium Citrate Monohydrate used in food industry, pharmaceutical industry and laboratory analytical reagents.
In the food industry Tripotassium Citrate Monohydrate can be used as buffer, chelating agents, stabilizer etc.
Tripotassium Citrate Monohydrate can be used for milk and dairy products, jellies, jams, meat, cheese emulsification, citrus preservation etc.


In the pharmaceutical industry Tripotassium Citrate Monohydrate’s used for hypokalaemia, potassium deficiency and alkaline urine.
Tripotassium Citrate Monohydrate can also be used for chemical analysis reagent.
Tripotassium Citrate Monohydrate is found in artificially sweetened jelly and in certain milk and meat products.
Tripotassium Citrate Monohydrate uses include processed cheese, pud- dings, and dietetic foods in which sodium is undesirable.


Tripotassium Citrate Monohydrate is used in foods and beverages as buffering, sequestering or emulsifying agent.
Tripotassium Citrate Monohydrate is used in manufacturing method of printed circuit board for autonomous vehicle to perform recognition, judgment, determination and execution.
Tripotassium Citrate Monohydrate is a weak organic acid that is known as a commodity chemical, as more than a million tonnes are produced every year by mycological fermentation on an industrial scale using crude sugar solutions, such as molasses and strains of Aspergillus niger.


Tripotassium Citrate Monohydrate is mainly used as an acidifier, flavoring agent and chelating agent.
Tripotassium Citrate Monohydrate is used in beverages, foods, and oral pharmaceutical formulations as a buffering and alkalizing agent.
Tripotassium Citrate Monohydrate is also used as a sequestering agent and as a therapeutic agent to alkalinize the urine and to relieve the painful irritation caused by cystitis.
Tripotassium Citrate Monohydrate is used in food (sequestrant, emulsifier, and stabilizer) and in medicine as an alkalinizing agent and antiurolithic.


Tripotassium Citrate Monohydrate is used as a flavoring agent, nutritional supplement, pH control agent, and sequestrant for foods
Tripotassium Citrate Monohydrate is used in food industry (E-332), antioxidant, preservative agent, laboratory reagent, in pharma industry.
Tripotassium Citrate Monohydrate is used as a flavoring, stabilizing agent and acidulant in food Industry.
Tripotassium Citrate Monohydrate is also used as an alkalizing agent in the treatment of mild urinary tract infections such as cystitis.


Tripotassium Citrate Monohydrate is used as a pharmaceutical aid in veterinary practice.
Tripotassium Citrate Monohydrate is also used in many pharmacopoeia and other preparations like potassium hydroxide solution, Cresol solution, Soap solution etc.
Tripotassium Citrate Monohydrate works as a buffer for juices like real, R-cola etc
Tripotassium Citrate Monohydrate is used in food, beverage, cosmetics, and many other applications.


Tripotassium Citrate Monohydrate is used in buffer solution preparation, electroplating and pharmaceutical industry.
Medicinally, Tripotassium Citrate Monohydrate may be used to control kidney stones derived from either uric acid or cystine.
Tripotassium Citrate Monohydrate is an effective way to treat/manage gout and arrhythmia if the patient is hypokalemic.
Tripotassium Citrate Monohydrate is widely used to treat urinary calculi (kidney stones) and is often used by patients with cystinuria.


A study of 500 patients with recurrent stones found that it reduced the frequency of stones from 2 per year to a half per year.
Tripotassium Citrate Monohydrate is also used as an alkanizing agent in the treatment of mild urinary tract infections such as cystitis.
Tripotassium Citrate Monohydrate is also used in many soft drinks as a buffering agent.
Tripotassium Citrate Monohydrate is a food additive and has other household and health uses as well.
Tripotassium Citrate Monohydrate may be added to foods and beverages or smoothies and green drinks.


Tripotassium Citrate Monohydrate provides bright plate in alkaline baths.
Tripotassium Citrate Monohydrate may act as sequestering agent in some metal plating
Tripotassium Citrate Monohydrate is used to adjust pH and forms metallic complexes in photo chemicals
Tripotassium Citrate Monohydrate is used as a buffer, sequestrant or emulsifier.
Tripotassium Citrate Monohydrate is used as a source of potassium in pharmaceuticals and an active ingredient for the treatment of urinary tract stones.



BENEFITS of TRIPOTASSIUM CITRATE MONOHYDRATE:
*Provides overall health and wellness
*Promotes healthy skin, hair, and nails
*Used to increase blood flow and circulation
*Stabilizes naturally produced chemicals in the body
*USP Grade Powder – 100% Pure



PRODUCTION METHODS of TRIPOTASSIUM CITRATE MONOHYDRATE:
Tripotassium Citrate Monohydrate is prepared by adding either potassium bicarbonate or potassium carbonate to a solution of citric acid until effervescence ceases.
The resulting solution is then filtered and evaporated to dryness to obtain Tripotassium Citrate Monohydrate.



FUNCTIONS of TRIPOTASSIUM CITRATE MONOHYDRATE:
1. Acidity Regulator / Buffering Agent - Changes or maintains the acidity or basicity of food/cosmetics.
2. Binder / Stabilizer - Retains the physical characteristics of food/cosmetics and ensure the mixture remains in an even state.
Tripotassium Citrate Monohydrate is a potassium salt of citric acid.
Tripotassium Citrate Monohydrate is a white, hygroscopic crystalline powder.
Tripotassium Citrate Monohydrate is odorless with a saline taste.
As a food additive, potassium citrate is used to regulate acidity and is known as E number E332.
Tripotassium Citrate Monohydrate is also used in many soft drinks as a buffering agent.



PHYSICAL and CHEMICAL PROPERTIES of TRIPOTASSIUM CITRATE MONOHYDRATE:
Molecular Weight: 306.39 (anhydrous basis)
Physical state: solid
Color: white
Odor: No data available
Melting point/freezing point: 275 °C
Initial boiling point and boiling range: No data available
Flammability (solid, gas): No data available
Upper/lower flammability or explosive limits: No data available
Flash point: No data available
Autoignition temperature: No data available
Decomposition temperature: No data available
pH: 8,0 - 9,5
Viscosity
Viscosity, kinematic: No data available
Viscosity, dynamic: No data available

Water solubility: No data available
Partition coefficient: n-octanol/water: No data available
Vapor pressure: No data available
Density: 1,98 g/cm3 at 20 °C
Relative density: No data available
Relative vapor density: No data available
Particle characteristics: No data available
Explosive properties: No data available
Oxidizing properties: No data available
Other safety information:
Bulk density: ca.950 kg/m3
Min. Purity Spec: 99%
Physical Form (at 20°C): Solid
Melting Point: 275°C

Long-Term Storage: Store long-term in a cool, dry place
Molecular Weight: 324.41
Hydrogen Bond Donor Count: 2
Hydrogen Bond Acceptor Count: 8
Rotatable Bond Count: 2
Exact Mass: 323.9052116
Monoisotopic Mass: 323.9052116
Topological Polar Surface Area: 142 Ų
Heavy Atom Count: 17
Formal Charge: 0
Complexity: 211
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0

Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 5
Compound Is Canonicalized: Yes
Water Solubility: 39.4 mg/mL
logP: -0.7
logP: -1.3
logS: -0.89
pKa (Strongest Acidic): 3.05
pKa (Strongest Basic): -4.2
Physiological Charge: -3
Hydrogen Acceptor Count: 7
Hydrogen Donor Count: 1
Polar Surface Area: 140.62 Å2

Rotatable Bond Count: 5
Refractivity: 68.14 m3·mol-1
Polarizability: 14.23 Å3
Number of Rings: 0
Bioavailability: 1
Rule of Five: Yes
Ghose Filter: No
Veber's Rule: No
MDDR-like Rule: No
Melting point: 275 °C (dec.)(lit.)
Density: 1.98

storage temp.: Inert atmosphere,Room Temperature
solubility: H2O: 1 M at 20 °C, clear, colorless
form: Granular
Specific Gravity: 1.98
color: White crystalline
Odor: Odorless
PH Range: 8 - 9.5
PH: 7.5-9.0 (25℃, 50mg/mL in H2O)
Water Solubility: Soluble in water and glycerol.
Practically insoluble in alcoholSoluble in water and glycerol.
Insoluble in alcohol
Merck: 14,7623
BRN: 3924344
Stability: Stable.



FIRST AID MEASURES of TRIPOTASSIUM CITRATE MONOHYDRATE:
-Description of first-aid measures:
*If inhaled:
After inhalation:
Fresh air.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with water/ shower.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Remove contact lenses.
*If swallowed:
After swallowing:
Make victim drink water (two glasses at most).
Consult doctor if feeling unwell.
-Indication of any immediate medical attention and special treatment needed:
No data available



ACCIDENTAL RELEASE MEASURES of TRIPOTASSIUM CITRATE MONOHYDRATE:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Take up dry.
Dispose of properly.



FIRE FIGHTING MEASURES of TRIPOTASSIUM CITRATE MONOHYDRATE:
-Extinguishing media:
*Suitable extinguishing media:
Water
Foam
Carbon dioxide (CO2)
Dry powder
*Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Prevent fire extinguishing water from contaminating surface water or the ground water system.



EXPOSURE CONTROLS/PERSONAL PROTECTION of TRIPOTASSIUM CITRATE MONOHYDRATE:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use Safety glasses.
*Skin protection:
Full contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min
Splash contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of TRIPOTASSIUM CITRATE MONOHYDRATE:
-Conditions for safe storage, including any incompatibilities:
*Storage conditions
Tightly closed.
Dry.



STABILITY and REACTIVITY of TRIPOTASSIUM CITRATE MONOHYDRATE:
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature).
-Possibility of hazardous reactions:
no information available
-Conditions to avoid:
no information available
-Incompatible materials:
No data available



SYNONYMS:
tri-Potassium citrate monohydrate
Tripotassium citrate
Citric acid potassium salt
2-Hydroxy-1,2,3-Propanetriccarboxylic Acid
Potassium citrate monohydrate
6100-05-6
Tripotassium citrate monohydrate
UROCIT-K
Potassium citrate tribasic monohydrate
K-cit-v
Kalii citras
MFCD00150442
EE90ONI6FF
Potassium citrate (monohydrate)
1,2,3-Propanetricarboxylic acid, 2-hydroxy-, tripotassium salt, monohydrate
Hydroxycitric acid (tripotassium hydrate)
Potassium 2-hydroxypropane-1,2,3-tricarboxylate hydrate
INS NO.332(II)
INS-332(II)
E-332(II)
NSC-760107
CCRIS 6543
Urocit-K (TN)
potassium citrate.H2O
Citric acid, tripotassium salt, monohydrate
UNII-EE90ONI6FF
Potassium Citrate, granular
CHEMBL3989822
DTXSID8042501
POTASSIUM CITRATE
CHEBI:64746
Tripotassium 2-hydroxy-1,2,3-propanetricarboxylate monohydrate
Citric acid potassium salt monohydrate
NSC 760107
D05578
Q27133400
ADV-7103 COMPONENT POTASSIUM CITRATE MONOHYDRATE
ADV7103 COMPONENT POTASSIUM CITRATE MONOHYDRATE
Potassium citrate tribasic monohydrate, puriss., 99.5%
Potassium citrate tribasic monohydrate, cell culture tested
Potassium citrate tribasic solution, BioUltra, 1 M in H2O
Potassium citrate tribasic monohydrate, >=98% (GC/titration)
Potassium citrate tribasic monohydrate, purum p.a., >=99.0% (NT)
Potassium citrate tribasic monohydrate, SAJ special grade, >=99.0%
Potassium citrate tribasic monohydrate, tested according to Ph.Eur.
tripotassium 2-hydroxypropane-1,2,3-tricarboxylate--water (1/1)
Potassium citrate tribasic monohydrate, meets USP testing specifications
Potassium citrate tribasic monohydrate, Vetec(TM) reagent grade, 98%
Potassium citrate, United States Pharmacopeia (USP) Reference Standard
Citric acid tripotassium salt
Tripotassium citrate
Tripotassium citrate hydrate
Tripotassium citrate monohydrate
Potassium citrate
Citric acid tripotassium salt monohydrate
Citric acid potassium salt monohydrate
Potassium citrate tribasic monohydrate
Tripotassium 2-hydroxypropane-1,2,3-tricarboxylate monohydrate
Kalii citras
Tripotassium citrate monohydrate
Potassium citrate tribasic monohydrate
Citric acid tripotassium salt monohydrate
Tripotassium 2-hydroxypropane-1,2,3-tricarboxylate monohydrate
TRIPOTASSIUM CITRATE MONOHYDRATE
Urocit-K
Hydroxycitric acid (tripotassium hydrate)
CITRIC ACID TRIPOTASSIUM SALT MONOHYDRATE
KALII CITRAS
tri-Potassium citrate
TrikaliumcitratH2O,BP
Tri-PotassiumCitrateGr
PotassiuM Citrate (AS)
Tri-PotassiumCitrateA.R.
1,2,3-Propanetricarboxylic acid, 2-hydroxy-, tripotassium salt, monohydrate
Citric acid, tripotassium salt, monohydrate
Potassium citrate
Potassium citrate monohydrate
Tripotassium 2-hydroxy-1,2,3-propanetricarboxylate monohydrate
Urocit-K
K-CIT-V
Potassium citrate tribasic monohydrate
Tripotassium citrate monohydrate
Potassium 2-hydroxy-1, 2, 3-propanetricarboxylate hydrate (3:1:1)
1, 2, 3-propanetricarboxylic acid, 2-hydroxy-, potassium salt, hydrate (1:3:1)
2-Hydroxy-1, 2, 3-propanetricarboxylic acid tripotassium salt monohydrate
Potassium 2-hydroxypropane-1, 2, 3-tricarboxylate hydrate (3:1:1)
Citric acid tripotassium salt
KALII CITRAS
TRI-POTASSIUM CITRATE H2O
POTASSIUM CITRATE TRIBASIC
POTASSIUM CITRATE-1-HYDRATE
Potassium citrate monohydrate
POTASSIUM CITRATE, MONOHYDRATE
TRIPOTASSIUM CITRATE MONOHYDRATE
tripotassium citrate monohydrate
tri-Potassium citrate monohydrate
POTASSIUM CITRATE TRIBASIC HYDRATE
POTASSIUM CITRATE, TRIBASIC MONOHYDRATE
Potassium citrate, tribasic monohydrate
citric acid tripotassium cell culture*tested monohydrate
tripotassium 2-hydroxypropane-1,2,3-tricarboxylate hydrate
tripotassium 2-hydroxypropane-1,2,3-tricarboxylate dihydrate
tripotassium 2-hydroxypropane-1,2,3-tricarboxylate monohydrate




TRIPROPYLENE GLYCOL
Tributoxy Ethyl Phosphate; Tri-butoxyethyl phosphate; TRIBUTOXYETHYL PHOSPHATE;Phosphoric acid, tributoxyethyl ester; TRIS(2-BUTOXYETHYL) PHOSPHATE, N° CAS : 78-51-3, Nom INCI : TRIS(2-BUTOXYETHYL) PHOSPHATE; Noms français : 2-BUTOXYETHANOL PHOSPHATE (3:1); 2-BUTOXYETHANOL, PHOSPHATE; PHOSPHATE DE TRI(BUTOXY-2 ETHANOL); PHOSPHATE DE TRI(BUTOXY-2 ETHYLE); Phosphate de tri(butoxyéthyle); PHOSPHATE DE TRIS(BUTOXYETHYLE) ; PHOSPHORIC ACID, TRIS(2-BUTOXYETHYL) ESTER; TRI(2-BUTOXYETHYL) PHOSPHATE; TRIS(2-BUTOXYETHYL) PHOSPHATE. Noms anglais : ETHANOL, 2-BUTOXY-, PHOSPHATE (3:1); Tri(butoxyethyl) phosphate; TRIBUTOXYETHYL PHOSPHATE; TRIBUTOXYETHYLPHOSPHATE; TRIBUTYL CELLOSOLVE PHOSPHATE; TRIS(2-BUTOXYETHYL) ESTER OF PHOSPHORIC ACID. Utilisation et sources d'émission; Agent plastifiant, agent antimousse; Tris(2-butoxyethyl) phosphate; CAS names: Ethanol, 2-butoxy-, 1,1',1''-phosphate. IUPAC names : TBEP; Tris(2-butoxyethyl)phosphate. Trade names: 2-butoxyethanol phosphate; Kronitex KP-140; KP-140; Phosflex T-BEP; Phosflex 176C; Amgard TBEP; TBOP; TBEP; TBXP ; tri(2-butoxyethanol)phosphate; tri(2-butylethylether) phosphate; tributoxyethyl phosphate; tributyl cellosolve phosphate; tris(2-n-butoxyethyl)phosphate; tris(butylglycol) phosphate; 201-122-9 ; [EINECS]; 4-01-00-02422 (Beilstein Handbook Reference) [Beilstein]; 78-51-3 [RN]; KJ9800000; MFCD00009456; Phosphate de tris(2-butoxyéthyle) [French]; phosphoric acid tris(2-butoxyethyl) ester; Phosphoric acid, tri(butoxyethyl) ester; Phosphoric acid, tributoxyethyl ester; Phosphoric acid, tris(2-butoxyethyl) ester; Tris(2-butoxyethyl) phosphate [ACD/IUPAC Name]; Tris-(2-butoxyethyl)fosfat [Czech]; Tris(2-butoxyethyl)phosphat [German] [ACD/IUPAC Name]; tris(2-n-butoxyethyl) phosphate; 1716010 [Beilstein]; 2-butoxyethanol phosphate; 2-Butoxy-ethanol phosphate (3:1); 2-BUTOXYETHANOL PHOSPHATE (3:1); 2-Butoxyethanol, phosphate; 4O2OPO&O2O4&O2O4 [WLN]; Amgard TBEP; EINECS 201-122-9; Ethanol, 2-butoxy-, 1,1',1''-phosphate ; ETHANOL, 2-BUTOXY-, PHOSPHATE (3:1); Kronitex KP-140; NCGC00091600-02; Phosflex T-be; Phosflex T-bep; phosphoric acid tris-(2-butoxyethyl) ester; Phosphoric acid tris(2-n-butoxyethyl) ester; Phosphoric acid, tri-(2-butoxyethyl) ester; pTri(2-butoxyethanol) phosphate; TBEP; Tri(2-butoxyethanol) phosphate; Tri(2-butoxyethanol)phosphate; TRI(2-BUTOXYETHYL) PHOSPHATE TRI-(2-BUTOXYETHYL)-PHOSPHATE; Tri-(2-Butoxyethyl)phosphate (en); Tri(butoxyethyl) phosphate; TRI-2-BUTOXYETHYL PHOSPHATE; Tributoxy Ethyl Phosphate; Tri-butoxyethyl phosphate ; TRIBUTOXYETHYL PHOSPHATE; Tributyl cellosolve phosphate; Tris(2-butoxyethyl)ester phosphoric acid; Tris-(2-butoxyethyl)fosfat [Czech]; tris(2-butoxyethyl)phosphate; Tris-(2-butoxyethyl)phosphate; Tris(2-butyloxyethyl)phosphate; Tris(butoxyethyl) phosphate; Tris(butoxyethyl)phosphate; tris[2-(butyloxy)ethyl] phosphate; Tris-2-butoxyethyl phosphate; WLN: 4O2OPO&O2O4&O2O4
TRIPROPYLENE GLYCOL N-BUTYL ETHER
CAS: 57499-93-1
EC Number:259-910-3
Molecular Weight: 248.36
IUPAC Name: 1-[1-(1-butoxypropan-2-yloxy)propan-2-yloxy]propan-2-ol
Molecular Formula: C13H28O4

DESCRIPTION:
Tripropylene glycol n-butyl ether (TBPE) is a fatty acid that belongs to the group of polyoxyethylene-based nonionic surfactants.
Tripropylene glycol n-butyl ether is soluble in water and has detergent properties.
Tripropylene glycol n-butyl ether has been shown to have a high affinity for cationic surfactants, such as p-hydroxybenzoic acid, and can be used to remove them from wastewater during sewage treatment.

The toxicity of Tripropylene glycol n-butyl ether has been studied in rats and mice, showing that Tripropylene glycol n-butyl ether does not cause any significant toxic effects.
Studies have also shown that Tripropylene glycol n-butyl ether can be used as a film-forming polymer in the production of films with antimicrobial activity.
Tripropylene glycol n-butyl ether is also combined with other compounds, such as sodium citrate or dodecyl glycol ethers, to form detergent compositions for removing oil and grease from surfaces or water.
Tripropylene glycol n-butyl ether is a cleaning agent that can also be found in other laundry pre-treaters.
Tripropylene glycol n-butyl ether works by dissolving stains and soils.




CHEMICAL AND PHYSICAL PROPERTIES OF TRIPROPYLENE GLYCOL N-BUTYL ETHER:
Molecular Weight: 248.36
XLogP3-AA: 1.6
Hydrogen Bond Donor Count: 1
Hydrogen Bond Acceptor Count: 4
Rotatable Bond Count: 11
Exact Mass: 248.19875937
Monoisotopic Mass: 248.19875937
Topological Polar Surface Area: 47.9 Ų
Heavy Atom Count: 17
Formal Charge: 0
Complexity: 164
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 3
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes
Assay: ≥95%
refractive index: n20/D 1.432 (lit.)
bp: 276 °C (lit.)
Mp: −75 °C (lit.)
Density: 0.932 g/mL at 25 °C (lit.)
Application: Cleaners, Coatings, Inks and Adhesives
Boiling Point (°C @760mmHg): 274
CAS#: 55934-93-5
Chemical Name: Tripropylene glycol mono n-butyl ether
Density (25°C) at lb/gal (g/cc): 7.73 (0.927)
Evaporation Rate (n-butyl acetate=1.0): 0.0004
Flash Point, Closed Cup: 126 °C
Freezing Point °F(°C): Hansen Solubility Parameter, dD (joules/cm3)1/2: 14.8
Hansen Solubility Parameter, dH (joules/cm3)1/2: 7.9
Hansen Solubility Parameter, dP (joules/cm3)1/2: 1.7
Low Vapor Pressure (Molecular Weight: 248.4 g/mol
Series: P-Series
Solubility in Water (25°C): 4.5 wt%
Solubility Water in (25°C): 8 wt%
Specific Gravity (25°C):0.93
Surface Tension (1% actives, 25 °C):29.7 dynes/cm
Vapor Pressure (mmHg @ 20°C): 0.002
Viscosity (25°C):7 cP

USES OF TRIPROPYLENE GLYCOL N-BUTYL ETHER:
Tripropylene Glycol N-Butyl Ether is used in Cleaners
Tripropylene Glycol N-Butyl Ether is used in Textiles
Tripropylene Glycol N-Butyl Ether is used in Cosmetics
Tripropylene Glycol N-Butyl Ether is used in Resins
Tripropylene Glycol N-Butyl Ether is used in Coating formulation and application
Tripropylene Glycol N-Butyl Ether is used in Industrial, automotive and architectural coatings


SAFETY INFORMATION ABOUT TRIPROPYLENE GLYCOL N-BUTYL ETHER:
First aid measures:
Description of first aid measures:
General advice:
Consult a physician.
Show this safety data sheet to the doctor in attendance.
Move out of dangerous area:

If inhaled:
If breathed in, move person into fresh air.
If not breathing, give artificial respiration.
Consult a physician.
In case of skin contact:
Take off contaminated clothing and shoes immediately.
Wash off with soap and plenty of water.
Consult a physician.

In case of eye contact:
Rinse thoroughly with plenty of water for at least 15 minutes and consult a physician.
Continue rinsing eyes during transport to hospital.

If swallowed:
Do NOT induce vomiting.
Never give anything by mouth to an unconscious person.
Rinse mouth with water.
Consult a physician.

Firefighting measures:
Extinguishing media:
Suitable extinguishing media:
Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.
Special hazards arising from the substance or mixture
Carbon oxides, Nitrogen oxides (NOx), Hydrogen chloride gas

Advice for firefighters:
Wear self-contained breathing apparatus for firefighting if necessary.
Accidental release measures:
Personal precautions, protective equipment and emergency procedures
Use personal protective equipment.

Avoid breathing vapours, mist or gas.
Evacuate personnel to safe areas.

Environmental precautions:
Prevent further leakage or spillage if safe to do so.
Do not let product enter drains.
Discharge into the environment must be avoided.

Methods and materials for containment and cleaning up:
Soak up with inert absorbent material and dispose of as hazardous waste.
Keep in suitable, closed containers for disposal.

Handling and storage:
Precautions for safe handling:
Avoid inhalation of vapour or mist.

Conditions for safe storage, including any incompatibilities:
Keep container tightly closed in a dry and well-ventilated place.
Containers which are opened must be carefully resealed and kept upright to prevent leakage.
Storage class (TRGS 510): 8A: Combustible, corrosive hazardous materials

Exposure controls/personal protection:
Control parameters:
Components with workplace control parameters
Contains no substances with occupational exposure limit values.
Exposure controls:
Appropriate engineering controls:
Handle in accordance with good industrial hygiene and safety practice.
Wash hands before breaks and at the end of workday.

Personal protective equipment:
Eye/face protection:
Tightly fitting safety goggles.
Faceshield (8-inch minimum).
Use equipment for eye protection tested and approved under appropriate government standards such as NIOSH (US) or EN 166(EU).

Skin protection:
Handle with gloves.
Gloves must be inspected prior to use.
Use proper glove
removal technique (without touching glove's outer surface) to avoid skin contact with this product.
Dispose of contaminated gloves after use in accordance with applicable laws and good laboratory practices.
Wash and dry hands.

Full contact:
Material: Nitrile rubber
Minimum layer thickness: 0.11 mm
Break through time: 480 min
Material tested:Dermatril (KCL 740 / Aldrich Z677272, Size M)
Splash contact
Material: Nitrile rubber
Minimum layer thickness: 0.11 mm
Break through time: 480 min
Material tested:Dermatril (KCL 740 / Aldrich Z677272, Size M)
It should not be construed as offering an approval for any specific use scenario.

Body Protection:
Complete suit protecting against chemicals, The type of protective equipment must be selected according to the concentration and amount of the dangerous substance at the specific workplace.
Respiratory protection:
Where risk assessment shows air-purifying respirators are appropriate use a fullface respirator with multi-purpose combination (US) or type ABEK (EN 14387) respirator cartridges as a backup to engineering controls.

If the respirator is the sole means of protection, use a full-face supplied air respirator.
Use respirators and components tested and approved under appropriate government standards such as NIOSH (US) or CEN (EU).
Control of environmental exposure
Prevent further leakage or spillage if safe to do so.
Do not let product enter drains.
Discharge into the environment must be avoided.

Stability and reactivity:
Chemical stability:
Stable under recommended storage conditions.
Incompatible materials:
Strong oxidizing agents:
Hazardous decomposition products:
Hazardous decomposition products formed under fire conditions.
Carbon oxides, Nitrogen oxides (NOx), Hydrogen chloride gas.

Disposal considerations:
Waste treatment methods:
Product:
Offer surplus and non-recyclable solutions to a licensed disposal company.
Contact a licensed professional waste disposal service to dispose of this material.
Contaminated packaging:
Dispose of as unused product.











SYNONYMS OF TRIPROPYLENE GLYCOL N-BUTYL ETHER:
57499-93-1
Tripropylene glycol mono-n-butyl ether
ppg-3 butyl ether
1-[1-(1-butoxypropan-2-yloxy)propan-2-yloxy]propan-2-ol
1-((1-((1-Butoxypropan-2-yl)oxy)propan-2-yl)oxy)propan-2-ol
1-({1-[(1-BUTOXYPROPAN-2-YL)OXY]PROPAN-2-YL}OXY)PROPAN-2-OL
2-Propanol, 1-(2-(2-butoxy-1-methylethoxy)-1-methylethoxy)-
2-Propanol, 1-[2-(2-butoxy-1-methylethoxy)-1-methylethoxy]-
Dowanol 66B
BRN 1704643
DOWANOL TPnB
SCHEMBL15374
DTXSID90973032
1-(2-(2-Butoxy-1-methylethoxy)-1-methylethoxy)-2-propanol
K0N34Z34O8
PPG-3 BUTYL ETHER [INCI]
POLYOXYPROPYLENE (3) BUTYL ETHER
AS-63503
POLYPROPYLENE GLYCOL (3) BUTYL ETHER
Propanol, [(butoxymethylethoxy)methylethoxy]-
5,8-Dimethyl-4,7,10-trioxatetradecane-2-ol
D93141
A905620
Q27896607
TPBGE
Dowanol TPnB
Tripropylene glycol butyl ether
((Butoxymethylethoxy)methylethoxy)propan-1-ol
Propanol, (2-(2-butoxymethylethoxy)methylethoxy)-
Tripropylene glycol (mono) n-butyl ether
1-(2-(2-Butoxy-1-methylethoxy)-1-methylethoxy)-2-propanol
DOWANOL TPNB CLYCOL ETHER
Tripropylene glycol monobutyl ether


TRIS (2-HYDROXYETHYL) ISOCYANURATE (THEIC)
1,3,5-tris(2-hydroxyethyl)triazine-2,4,6-trione is a white powder. Industry Uses Chemical additive used in heat stabilizers for PVC applications Flame retardants Ingredient in polyester-type resins Paint additives and coating additives not described by other categories Process regulators Processing aids, not otherwise listed Processing aids, specific to petroleum production THEIC is a white crystalline powder that is soluble in water, THF and hot lower alcohols. It is insoluble in other common organic solvents. This symmetrical triol undergoes reactions typical of unhindered, primary hydroxyl groups. Tris (2-Hydroxyethyl) isocyanurate (THEIC) is a white crystalline powder that is soluble in water. THEIC is used in coating industry for heat resistant wire enamels, electrical insulatings, alkyd resins, urethanes, water-soluble stoving enamels and polyesters. It is also used as an intermediate for the synthesis of dyes, agrochemicals, pharmaceuticals and plasticizers. Chemical Group is a long-experienced distributor of Tris (2-Hydroxyethyl) Isocyanurate.worldwide company who imports and supplies Tris (2-Hydroxyethyl) Isocyanurate in over four continents. As a supplier of Tris (2-Hydroxyethyl) Isocyanurate with a wide distribution network, customers in numerous industries rely for their supply of Tris (2-Hydroxyethyl) Isocyanurate. We have the capability and know-how as a importer, supplier, and distributor of Tris (2-Hydroxyethyl) Isocyanurate to provide your business with value-added supply chain solutions. supplies Tris (2-Hydroxyethyl) Isocyanurate to users/customers for Plastic, Resin & Rubber. This product is also known as THEIC. CAS Number 839-90-7 Formula C9-H15-N3-O6 Major Category Plastics & Rubber 1,3,5-Tris(2-hydroxyethyl) isocyanurate formula graphical representation Synonyms 1,3,5-Triazine-2,4,6(1H,3H,5H)-trione, 1,3,5-tris(2-hydroxyethyl)-; 1,3,5-Tris(2-hydroxyethyl) isocyanuric acid; 1,3,5-Tris(2-hydroxyethyl)isocyanuric acid; 1,3,5-Tris(2-hydroxyethyl)triazine-2,4,6-trione; Isocyanuric acid tris(2-hydroxyethyl) ester; N,N',N''-Tris(2-hydroxyethyl) isocyanurate; N,N',N''-Tris(2-hydroxyethyl)isocyanurate; THEIC; Tris(2-hydroxyethyl) isocyanurate; Tris(2-hydroxyethyl)-s-triazine-2,4,6-trione; Tris(2-hydroxyethyl)cyanurate; Tris(2-hydroxyethyl)isocyanurate; Tris(beta-hydroxyethyl) isocyanurate; Tris(hydroxyethyl) cyanurate; s-Triazine-2,4,6(1H,3H,5H)-trione, 1,3,5-tris(2-hydroxyethyl)-; [ChemIDplus] Category Other Monomers Description White solid; [HSDB] White powder; [MSDSonline] Sources/Uses Used as a plastics additive to impart thermal stability; [HSDB] Used as a monomer to make polyesters (thermosetting varnishes and paints for metal) and as a polymer stabilizer; [Reference #1] Triazine is the chemical species of six-membered heterocyclic ring compound with three nitrogens replacing carbon-hydrogen units in the benzene ring structure. The names of the three isomers indicate which of the carbon-hydrogen units on the benzene ring position of the molecule have been replaced by nitrogens, called 1,2,3-triazine, 1,2,4-triazine, and 1,3,5-triazine respectively. Symmetrical 1,3,5-triazine is the common. Triazines are prepared from 2-azidocyclopropene through thermal rearrangement (1,2,3-triazine), from 1,2-dicarbonyl compound with amidrazone by condensation reaction (1,2,4-triazine) and from cyanic acid amide by trimerization (1,3,5-triazine). Pyridine is the aromatic nitrogen heterocycle compound having only one nitrogen, and diazines are with 2 nitrogen atoms and tetrazines are with 4 nitrogen atoms on the benzene ring system. Triazines are weak base. Triazines have much weaker resonance energy than benzene, so nucleophilic substitution is preferred than electrophilic substitution. Triazines are basic structure of herbicides, examples are amitole (CAS #: 61-82-5), atrazine (CAS #: 1912-24-9), cyanazine (CAS #: 21725-46-2), simazine (CAS #: 122-34-9), trietazine (CAS #: 1912-26-1). Large volume of triazines are used in the manufacture of resin modifiers such as melamine and benzoguanamine. Melamine (1,3,5-Triazine-2,4,6-triamine) is reacted with formaldehyde to from a very durable thermoset resin. Benzoguanamine (2,4-Diamino-6-phenyl-1,3,5-triazine) is used to increase thermoset properties of alkyd, acrylic and formaldehyde resins. Triazines are also useful as chromophore groups in colorants and Chlorine attached in Triazine compounds undergo nucleophilic substitution reactions well with with hydroxyl groups in cellulose fibres. Some triazine family compounds are used in pharmaceutical industry as coupling agent for the synthesis of peptide in solid phase as well as solution and as side chain of antibiotics. Triazine compounds are used in formulating bactericide and fungicide. They are used as preservatives in oil field applications. They are used as disinfectant, industrial deodorant and biocide in water treatment. They are used as a bleaching agents. Tris(2-hydroxyethyl) isocyanurate (THEIC) has the symmetrical triol structure and thus it can undergo polymerization reactions. It is used as a monomer for the synthesis of polyesters which are industrially used in a variety of coatings (thermosetting paints, magnet wire enamels, electrical insulating varnishes). Because of its trifunctionality, THEIC is used as a precursor to crosslinking agents for rigid urethane foams and postforming laminating resins. THEIC is used as a stabilizer and heat resistant flame retardant of polymers. One of the uses of such polymer is as exterior building material. It is also used as an intermediate for the synthesis of dyes, agrochemicals, pharmaceuticals and plasticizers.Tris (2-hydroxyethyl) isocyanurate (THEIC) was decomposed by means of chemical treatment. NMR analysis showed that the products contained large amounts of 2-oxazolidinone. The effects of potassium hydroxide as an additive, reaction temperature and time, and solvent were investigated. The decomposition of THEIC with potassium hydroxide in dimethylformamide (DMF) at 130°C for 4 hours gave a quantitative amount of 2-oxazolidinone. These results indicate that THEIC decomposed under mild reaction conditions in the presence of potassium hydroxide. DESCRIPTION AND USES Tris(2-hydroxyethyl) isocyanurate is used in costing industry for heat resistant wire enamels, electrical insulatings, alkyd resins, urethanes, water-soluble stoving enamels and polyesters. It is also used as an intermediate for the synthesis of dyes, agrochemicals, pharmaceuticals and plasticizers. APPLICATIONS Agrochemicals, Dyes, Electrical insulatings, Electronics, Enamels, Pharmaceuticals, Plastizisers, Polyesters, Resins, Alkyd, Urethanes, Wire enamel INDUSTRIES Agrochemicals, Electrical, Electronics, Pharmaceuticals PRODUCT DETAILS Product group Speciality Synonym product Tris(2-Hydroxyethyl)-s-Triazine-2,4,6-trione Package Bulk and Packed Materials Statistics number 2933-69-80(-90) Cas number 839-90-7 Cus number N/A EC number 212-660-9 RID/ADR number N/A UN number N/A Structure N/A A macromolecular homopolymer (named as Homo-THEIC) was synthesized through self-etherification of tris(2-hydroxyethyl) isocyanurate (THEIC) molecules and used as charring agent. Its chemical structure was characterized by FTIR and 13C-NMR. The charring agent was mixed with ammonium polyphosphate (APP) and applied in flame retarded polypropylene (PP). Results of UL-94, LOI, and cone calorimeter test showed that the LOI of flame retarded PP can reach 32.8% and UL-94 V-0 rating can be achieved at 30 wt % loading. The heat release rate and smoke production rate during the combustion of PP were substantially reduced. TGA results indicated that the synergistic effect between APP and Homo-THEIC existed and the addition of intumescent flame retardant (IFR) dramatically enhanced the thermal stability of PP. According to the results of TGA, SEM, TG-FTIR, FTIR, and Raman, the char forming process of IFR can be separated into three stages: the formation of viscous phosphate ester (Tonset−330 °C), the expanding process along with the decomposition of phosphate ester and the release of a large amount of gases (330–480 °C), and the final formation of graphitic-like char without any expanding feature (480–670 °C). Used as an important raw material for the production of heat-resistant wire enamels and surface coatings with extremely good mechanical properties, diverse polyurethane plastic. water-base stoving enamels. unsaturated polyester resins, As organic intermediates for insecticide, plasticizing agent, dyestuffs and phar-maceuticals etc.Tris 2-Hydroxyethyl isocyanurate (THEIC) is a white crystalline powder that is soluble in water. THEIC is used in coating industry for heat resistant wire enamels, electrically insulating, alkyd resins, urethanes, water-soluble stoving enamels, and polyesters. Product name: Tris(2-hydroxyethyl)Isocyanurate(THEIC) CAS: 839-90-7 Molecular weight: 224.2546 Molecular formula: C9H15N3O6 Applications: Used as an important raw material for the production of heat-resistant wire enamels and surface coatings with extremely good mechanical properties, diverse polyurethane plastic. water-base stoving enamels. unsaturated polyester resins, As organic intermediates for insecticide, plasticizing agent, dyestuffs and phar-maceuticals etc. A method of preparing tris(2-hydroxyethyl)isocyanurate (THEIC) is disclosed. The method comprises the step of heating a mixture of ethylene carbonate and isocyanuric acid in the presence of a catalyst at a temperature between about 160° C. and 170° C. The molar ratio of ethylene carbonate to isocyanuric acid is at least about 3 to 1, and the catalyst has at least one amine functional group. THEIC produced by the disclosed method can be used without purification as a cross-linking agent in polyester-based magnet wire enamels. In view of the problem of low combustion performance of polymer, two charring agents tris (2-hydroxyethyl) isocyanurate terephthalate ester (T-ester43 and T-ester45) with different degree of esterification were synthesized by using tris (2-hydrooxyethyl) isocyanurate (THEIC) and purified terephthalic acid (PTA) as raw materials. Two kinds of intumescent flame retardants (IFR43 and IFR45) were prepared by combination of T-ester and ammonium polyphosphate (APP).The preformed IFR were melt blended with four commercial thermoplastics to obtain flame retardant polymer blends. It is found that, after esterification, the decomposition temperature of charring agent increased up to 300℃ and char residue at 700 ℃ increases up to 10% from 1%. With 20% mass loading of IFR43 into PA6, PET, PLA, and PP, the char residue increased by 14.97%, 9.69%, 11.59%, and 7.25%, respectively. Correspondingly, the limiting oxygen index (LOI) value of polymers enhanced by 6%~7%. The melt drops during LOI test decreased. In addition, crystallization acceleration effect is found in the sample of PLA after addition of IFR. THEIC is mainly be used as an important raw material for the production of heat-resistant wire enamels and PVC heat stabilizer for improving the heat-resistant of wire enamels and PVC processing temperature and performance. Besides these two major application, THEIC also be used in the production of various polyurethane plastics, water-based baking lacquer, unsaturated polyester resins, pesticide, plastic accelerator, dye staffs and intermediate for organic synthesis. Tris (2-Hydroxyethyl) isocyanurate (THEIC) is a white crystalline powder that is soluble in water. THEIC is used in coating industry for heat resistant wire enamels, electrical insulatings, alkyd resins, urethanes, water-soluble stoving enamels and polyesters. It is also used as an intermediate for the synthesis of dyes, agrochemicals, pharmaceuticals and plasticizers. 1,3,5-Tris(2-hydroxyethyl)isocyanurate (THEIC) is a triazine derivative with three nitrogen atoms in its structure. It can be used as a stabilizer and can be a useful material in applications that require flame-retardancy and water durability. THEIC can be used to functionalize graphene magnetic nanoparticles to form a catalyst that facilitates the synthesis of benzimidazole compounds.[2] It may also be used in the synthesis of hyperbranched epoxy resin by UV-initiated thiolene click reaction, which finds potential application in the fabrication of insulating materials. Tris 2-hydroxyethyl isocyanurate. Derived from cyanuric acid (1, 3, 5-triazine-2, 4, 6-triol) which is a cyclic trimer. It is usually a white, odorless solid. Used as a raw material for synthetic resins. THEIC, also known as Tris (2-Hydroxyethyl) Isocyanurate, has applications in modified polyimide insulating varnish, paint for the base plate of automobiles, the manufacture of high-quality heat-resisting alcohol acid and plasticizer, and in the printing, textile, plastics, and photo industries.
TRIS(2-BUTOXYETHYL) PHOSPHATE
Tris(2-Butoxyethyl) Phosphate is an organic flame retardant.
Tris(2-Butoxyethyl) Phosphate is a trialkyl phosphate in which the alkyl group specified is 2-butoxyethyl.


CAS Number: 78-51-3
EC Number: 201-122-9
MDL number: MFCD00009456
Linear Formula: [CH3(CH2)3OCH2CH2O]3P(O)
Molecular Formula: C18H39O7P



SYNONYMS:
TBEP, TRI(BUTOXYETHYL)PHOSPHATE, TRIS(BUTOXYETHYL) PHOSPHATE, TBXP, kp140, KP 140, KP-140, 2-butoxy, Amgard TBEP, phosflext-bep, tris 2-butoxyethyl phosphate, tbep, phosflex t-bep, tris butoxyethyl phosphate, tributoxyethyl phosphate, tri butoxyethyl phosphate, kronitex kp-140, tributyl cellosolve phosphate, ethanol, 2-butoxy-, phosphate 3:1, tri 2-butoxyethyl phosphate, 2-Butoxyethanol, phosphate, Ethanol, 2-butoxy-, phosphate (3:1), KP 140, Kronitex KP-140, Phosflex T-BEP, Phosphoric acid, tributoxyethyl ester, Phosphoric acid, tris(2-butoxyethyl) ester, TBEP, Tri(2-butoxyethanol) phosphate, Tri(2-butoxyethanol)phosphate, Tributoxyethyl phosphate, Tributyl cellosolve phosphate, Tris(2-butoxyethyl) phosphate, Tris(butoxyethyl) phosphate, Tris-(2-butoxyethyl)fosfat, Tbep, Tris(Butoxyethyl)Phosphate, Phosflex T-Bep, Kronitex Kp-140, Tributyl Cellosolve Phosphate, Tri(2-Butoxyethanol)Phosphate, Tris-(2-Butoxyethyl)Fosfat, Tributoxyethyl phosphate, Phosphoric acid, tris(2-butoxyethyl) ester, Tris(butoxyethyl)phosphate, Phosphoric acid, tributoxyethyl ester, Tris[2-(butyloxy)ethyl] phosphate, Phosphoric acid tris(2-butoxyethyl) ester, Phosflex T-bep, Kronitex KP-140, 2-Butoxyethanol phosphate, KP 140, Phosphoric acid, tributoxyethyl ester, Tri(butoxyethyl) phosphate, Tri(2-butoxyethyl) phosphate, Tributyl cellosolve phosphate, Tris(butoxyethyl) phosphate, Tris(2-butoxyethyl) phosphate, TBEP, Phosphoric acid, tris(2-butoxyethyl) ester, 2-Butoxyethanol phosphate, Kronitex KP-140, Phosflex T-bep, Tri(2-butoxyethanol)phosphate, Tris-(2-butoxyethyl)fosfat, 2-Butoxy-ethanol phosphate (3:1), Amgard TBEP, Tris(2-butoxyethyl)ester phosphoric acid, Phosphoric acid, tri-(2-butoxyethyl) ester, Ethanol, 2-butoxy-, 1,1',1''-phosphate, NSC 4839, 31227-66-4, 19040-50-7, Phosphoric acid tris(2-butoxyethyl) ester, Tris(2-butoxyethyl) phosphate, 78-51-3, TBEP, Tributoxyethyl phosphate, TRI(2-BUTOXYETHYL) PHOSPHATE, Phosflex T-bep, Tris(butoxyethyl) phosphate, tris(2-butoxyethyl)phosphate, KP 140, Kronitex KP-140, Tributyl cellosolve phosphate, Ethanol, 2-butoxy-, phosphate (3:1), Tri(butoxyethyl) phosphate, Phosphoric acid, tributoxyethyl ester, Phosphoric acid, tris(2-butoxyethyl) ester, Tri(2-butoxyethanol)phosphate, NSC 4839, Tris-(2-butoxyethyl)fosfat, Phosphoric Acid Tris(2-butoxyethyl) Ester, 2-Butoxyethanol phosphate, Tris(butoxyethyl)phosphate, Ethanol, 2-butoxy-, 1,1',1''-phosphate, DTXSID5021758, CHEBI:35038, RYA6940G86, tris[2-(butyloxy)ethyl] phosphate, NSC-4839, TBEP; KP 140; Hostaphat B 310, NSC-62228, Phosphoric acid, tri-(2-butoxyethyl) ester, Ethanol, phosphate (3:1), Tris(2-butyloxyethyl)phosphate, DTXCID201758, WLN: 4O2OPO&O2O4&O2O4, 2-Butoxyethanol, phosphate, CAS-78-51-3, Phosphoric acid, tri(butoxyethyl) ester, TBOEP, CCRIS 5942, Tri(2-butoxyethanol) phosphate, HSDB 2564, 2-Butoxyethanol phosphate (3:1), EINECS 201-122-9, Tris(2-butoxyethyl) phosphate, C18H39O7P, 78-51-3, BRN 1716010, tris-2-butoxyethyl phosphate, UNII-RYA6940G86, AI3-04596, Amgard TBEP, MFCD00009456, EC 201-122-9, NCIOpen2_007840, SCHEMBL37268, 4-01-00-02422 (Beilstein Handbook Reference), Tri-(2-Butoxyethyl)phosphate, BIDD, CHEMBL1534811, NSC4839, NSC62228, 2-Butoxy-ethanol phosphate (3:1), Tox21_201593, Tox21_302891, Tris(2-butoxyethyl) phosphate, 94%, AKOS015839670, NCGC00091600-01, NCGC00091600-02, NCGC00091600-03, NCGC00256553-01, NCGC00259142-01, Tris(2-butoxyethyl)ester phosphoric acid, AS-59809, Phosphoric acid tris(2-n-butoxyethyl)ester, CS-0066127, FT-0689063, NS00010389, P0683, Phosphoric acid tris(2-n-butoxyethyl) ester, TRI(2-BUTOXYETHYL) PHOSPHATE [HSDB], F71229, A915093, Tris(2-butoxyethyl) phosphate, analytical standard, W-104277, Q27116378, Tris(2-butoxyethyl) phosphate, tri(butoxyethyl)phosphate, KP-140, TBEP, Phosphoric acid tris(2-Butoxyethyl)ester, 2-butoxy-ethanol phosphate (3:1), Tris(2-butoxyethyl)phosphate, TBEP, 2-butoxy, 2-Butoxy-ethanol phosphate (3:1), 2-Butoxy-ethanolphosphate(3:1), 2-butoxy-ethanophosphate(3:1), Amgard TBEP, Ethanol, 2-butoxy-, phosphate (3:1), tri(butoxyethyl), TBXP, TBEP, KP-140, Tributoxy Ethyl Phosphate, Tris(butoxyethyl) Phosphate, Tris(2-butoxyethyl)phosphate, Tris(2-butoxyethyl) phosphate, Phosphoric acid tris(2-n-butoxyethyl) ester, 2-BUTOXYETHANOL PHOSPHATE, PHOSPHORIC ACID TRIS (2-N-BUTOXYETHYL) ESTER, PHOSPHORIC ACID TRIS (2-BUTOXYETHYL) ESTER, TBEP, TRI (BUTOXYETHYL) PHOSPHATE, TRIS (BUTOXYETHYL) PHOSPHATE, TRIS (2-BUTOXYETHYL) PHOSPHATE, 2-Butoxy, Phosphoric acid, tri-(2-butoxyethyl) ester, Tributoxyethyl phosphate, 2-Butoxyethanol phosphate, Ethanol, 2-butoxy-, phosphate (31), TBEP, Tris (2-butoxyethyl) phosphate



Tris(2-Butoxyethyl) Phosphate acts as an additive flame retardant and plasticizer in plastics and synthetic rubbers.
Tris(2-Butoxyethyl) Phosphate appears as a colorless clear liquid having molecular weight of 398.47.
Tris(2-Butoxyethyl) Phosphate is a phosphorothioate that is used to inhibit the activity of the enzyme polymerase chain reaction.


Tris(2-Butoxyethyl) Phosphate has been shown to induce apoptosis in vitro, which may be due to its ability to decrease mitochondrial membrane potential and interfere with signal pathways.
Tris(2-Butoxyethyl) Phosphate has not been shown to affect human serum α1-acid glycoprotein or dimethyl fumarate levels.


Tris(2-Butoxyethyl) Phosphate is an efficient inhibitor of DNA polymerase activity and mitochondrial DNA synthesis in vivo, but it does not significantly affect mitochondrial membrane potential or cell proliferation.
Tris(2-Butoxyethyl) Phosphate is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 1 000 to < 10 000 tonnes per annum.


Tris(2-Butoxyethyl) Phosphate is a trialkyl phosphate in which the alkyl group specified is 2-butoxyethyl.
Tris(2-Butoxyethyl) Phosphate is an organic flame retardant.
Tris(2-Butoxyethyl) Phosphate shows PXR agonistic activity.


Tris(2-Butoxyethyl) Phosphate was detected and quantified during the analysis of herring gull eggs by liquid chromatography-electrospray ionization(+)-tandem mass spectrometry.
Tris(2-Butoxyethyl) Phosphate is a slightly yellow viscous liquid.


Tris(2-Butoxyethyl) Phosphate is a trialkyl phosphate in which the alkyl group specified is 2-butoxyethyl.
Tris(2-Butoxyethyl) Phosphate has a role as an environmental contaminant and a flame retardant.
Tris(2-Butoxyethyl) Phosphate is slightly yellow liquid with a sweetish odor.


Tris(2-Butoxyethyl) Phosphate is an organic flame retardant.
Tris(2-Butoxyethyl) Phosphate shows PXR agonistic activity.
Tris(2-Butoxyethyl) Phosphate was detected and quantified during the analysis of herring gull eggs by liquid chromatography-electrospray ionization(+)-tandem mass spectrometry.



USES and APPLICATIONS of TRIS(2-BUTOXYETHYL) PHOSPHATE:
Tris(2-Butoxyethyl) Phosphate is used by consumers, in articles, by professional workers (widespread uses), in formulation or re-packing and at industrial sites.
Tris(2-Butoxyethyl) Phosphate is used in the following products: washing & cleaning products, polishes and waxes, plant protection products and water treatment chemicals.


Other release to the environment of Tris(2-Butoxyethyl) Phosphate is likely to occur from: indoor use as processing aid and outdoor use as processing aid.
Release to the environment of Tris(2-Butoxyethyl) Phosphate can occur from industrial use: as processing aid and of substances in closed systems with minimal release.


Other release to the environment of Tris(2-Butoxyethyl) Phosphate is likely to occur from: indoor use as processing aid, indoor use in long-life materials with low release rate (e.g. flooring, furniture, toys, construction materials, curtains, foot-wear, leather products, paper and cardboard products, electronic equipment), outdoor use as processing aid and outdoor use in long-life materials with low release rate (e.g. metal, wooden and plastic construction and building materials).


Tris(2-Butoxyethyl) Phosphate can be found in products with material based on: wood (e.g. floors, furniture, toys), plastic (e.g. food packaging and storage, toys, mobile phones) and paper (e.g. tissues, feminine hygiene products, nappies, books, magazines, wallpaper).
Tris(2-Butoxyethyl) Phosphate is used in the following products: plant protection products, hydraulic fluids, lubricants and greases, metal working fluids, washing & cleaning products and polishes and waxes.


Tris(2-Butoxyethyl) Phosphate has an industrial use resulting in manufacture of another substance (use of intermediates).
Tris(2-Butoxyethyl) Phosphate is used in the following areas: agriculture, forestry and fishing and formulation of mixtures and/or re-packaging.
Tris(2-Butoxyethyl) Phosphate is used for the manufacture.


Other release to the environment of Tris(2-Butoxyethyl) Phosphate is likely to occur from: outdoor use as processing aid and indoor use as processing aid.
Tris(2-Butoxyethyl) Phosphate is used in the following products: polymers and textile treatment products and dyes.
Release to the environment of Tris(2-Butoxyethyl) Phosphate can occur from industrial use: formulation in materials and formulation of mixtures.


Tris(2-Butoxyethyl) Phosphate is used in the following products: polymers, textile treatment products and dyes and washing & cleaning products.
Tris(2-Butoxyethyl) Phosphate is used for the manufacture of: plastic products and textile, leather or fur.
Release to the environment of Tris(2-Butoxyethyl) Phosphate can occur from industrial use: in the production of articles, as processing aid and in processing aids at industrial sites.


Tris(2-Butoxyethyl) Phosphate is a fire-resistant and light-stable plasticizer for food-contact products, resins & elastomers in floor finishes and waxes.
Tris(2-Butoxyethyl) Phosphate is a useful research chemical suitable for rubber stoppers in blood specimen containers.
Tris(2-Butoxyethyl) Phosphate emits toxic fumes of phosphorous oxides when heated to decomposition.


Tris(2-Butoxyethyl) Phosphate can be used as a resin solvent, plastisol viscosity modifier, and antifoam agent for synthetic rubber, plastics & lacquers.
Tris(2-Butoxyethyl) Phosphate is used as a plasticizer for resins and elastomers, in floor finishes and waxes, as a flame retardant, as a plasticizer for rubber stoppers in blood specimen containers, and as a fire-resistant and light-stable plasticizer for products intended for food contact; Occupational exposure is likely to be by skin absorption during production and from floor polishes.


Tris(2-Butoxyethyl) Phosphate is used as solvent for resins, a viscosity modifier in plastisols, and an antifoam agent for synthetic rubber, plastics, and lacquers.
Tris(2-Butoxyethyl) Phosphate is used in a mixed solvent/aqueous system as a defoamer during production and as a secondary plasticiser in many polymers.


The above properties in combination with inherent flame retardancy makes Tris(2-Butoxyethyl) Phosphate a real multifunctional additive essential to many polymer formulations.
Tris(2-Butoxyethyl) Phosphate is a phosphate ester that, thanks to its structure, can be used in many applications including plasticisation, solvation, flame retardancy and defoaming.


Tris(2-Butoxyethyl) Phosphate is in fact a multifunctional additive that may be used to modify the properties of many polymer systems and is a particularly good levelling aid and coalescent additive for emulsion polymers.


Tris(2-Butoxyethyl) Phosphate may be used as an analytical reference standard for the quantification of the analyte in herring gull eggs, house dust, and urine samples using liquid chromatography technique.
Tris(2-Butoxyethyl) Phosphate is used primary plasticizer for most resins and elastomers, floor finishes and waxes, flame-retarding agent.



CHEMICAL PROPERTIES OF TRIS(2-BUTOXYETHYL) PHOSPHATE:
Tris(2-Butoxyethyl) Phosphate is slightly yellow, oily liquid.
Tris(2-Butoxyethyl) Phosphate is insoluble or limited solubility in glycerol, glycols, and certain amines; soluble in most organic liquids.



AIR AND WATER REACTIONS OF TRIS(2-BUTOXYETHYL) PHOSPHATE:
Tris(2-Butoxyethyl) Phosphate is water soluble.



REACTIVITY PROFILE OF TRIS(2-BUTOXYETHYL) PHOSPHATE:
Organophosphates, such as Tris(2-Butoxyethyl) Phosphate, are susceptible to formation of highly toxic and flammable phosphine gas in the presence of strong reducing agents such as hydrides.
Partial oxidation by oxidizing agents may result in the release of toxic phosphorus oxides.
Tris(2-Butoxyethyl) Phosphate may react with oxidizers.



PHYSICAL and CHEMICAL PROPERTIES of TRIS(2-BUTOXYETHYL) PHOSPHATE:
CAS Number: 78-51-3
Molecular Weight: 398.47
EC Number: 201-122-9
MDL number: MFCD00009456
CBNumber: CB1312263
Molecular Formula: C18H39O7P
Molecular Weight: 398.47
MDL Number: MFCD00009456
MOL File: 78-51-3.mol
Melting point: -70°C
Boiling point: 215-228 °C (4 mm Hg, lit.)
Density: 1.006 g/mL at 25 °C (lit.)
Vapor density: 13.7 (vs air)
Vapor pressure: 0.03 mm Hg (150 °C)

Refractive index: n20/D 1.438 (lit.)
Flash point: >230 °F
Storage temp.: Store at -20°C
Solubility: Chloroform (Slightly), DMSO (Slightly),
Ethyl Acetate (Slightly), Methanol (Slightly)
Form: Liquid
Color: Clear colorless to very slightly yellow
Water Solubility: Soluble
Stability: Stable.
Incompatible with strong oxidizing agents.
InChIKey: WTLBZVNBAKMVDP-UHFFFAOYSA-N
LogP: 3.75 at 20℃

CAS DataBase Reference: 78-51-3 (CAS DataBase Reference)
Indirect Additives used in Food Contact Substances: TRIBUTOXYETHYL PHOSPHATE
FDA 21 CFR: 175.105
EWG's Food Scores: 1
FDA UNII: RYA6940G86
NIST Chemistry Reference: Phosphoric acid, tri-(2-butoxyethyl) ester (78-51-3)
EPA Substance Registry System: Tris(2-butoxyethyl) phosphate (78-51-3)
Appearance Form: liquid
Color: colorless
Odor: No data available
Odor Threshold: No data available
pH: No data available
Melting point/range: < -70 °C - (ECHA)
Initial boiling point and boiling range: 215 - 228 °C at 5 hPa - lit.

Flash point: ca.159 °C at ca.1.014,6 hPa - closed cup - ISO 1523
Evaporation rate: No data available
Flammability (solid, gas): No data available
Upper/lower flammability or explosive limits: No data available
Vapor pressure: 0,04 hPa at 150 °C
Vapor density: 13,75 - (Air = 1.0)
Density: 1,006 g/cm3 at 25 °C - lit.
Relative density: 1,02 at 20 °C
Water solubility: 0,66 g/l at 25 °C
Partition coefficient: n-octanol/water log Pow: 3,75
Autoignition temperature: 322 °C at 1.013 hPa
Decomposition temperature: No data available

Viscosity
Viscosity, kinematic: No data available
Viscosity, dynamic: 12,4 mPa.s at 20 °C
Explosive properties: No data available
Oxidizing properties: none
Surface tension: 32,7 mN/m at 20,2 °C
Relative vapor density: 13,75 - (Air = 1.0)
Appearance: colorless transparent liquid
Acidity (mgKOH/ g): ≤0.1
Refractive index (nD25): 1.4320 —1.4380
Specific gravity (20/20℃): 1.012-1.023
Color (Pt-Co): ≤ 50
Moisture: ≤0.1%
Appearance: colorless transparent liquit
Acid value(mgKOH/g): ≤0.1

Refractive index(nD25): 1.4320-1.4380
Specific gravity(20/20℃): 1.012-1.023
Chroma(Pt-Co): ≤60
Moisture(Pt-Co): ≤0.2%
Cas No: 78-42-2
Molecular Formula: C24H51O4P
Molecular Weight: 434.64
Appearance: Colorless Transparent Liquid
Molecular Formula: C18H39O7P
Molar Mass: 398.47
Melting Point: -70℃
Boling Point: 215-228℃4 mm Hg(lit.)
Water Solubility: Soluble
Appearance: Transparent liquid
Storage Condition: 2-8℃
MDL: MFCD00009456

melting point: -70°C
boiling point: 215-228 °C4mm Hg(lit.)
density: 1.006 g/mL at 25 °C(lit.)
vapor density: 13.7 (vs air)
Vapor pressure: 0.03mm Hg ( 150 °C)
refractive index: n20/D 1.438(lit.)
flash point: >230 °F
morphology: Liquid
color: Clear colorless to very slightly yellow
water solubility: Soluble
stability: Stable.
Incompatible with strong oxidizing agents.
InChIKey: WTLBZVNBAKMVDP-UHFFFAOYSA-N

Molecular Weight: 398.5 g/mol
XLogP3-AA: 2.8
Hydrogen Bond Donor Count: 0
Hydrogen Bond Acceptor Count: 7
Rotatable Bond Count: 21
Exact Mass: 398.24334058 g/mol
Monoisotopic Mass: 398.24334058 g/mol
Topological Polar Surface Area: 72.4 Ų
Heavy Atom Count: 26
Formal Charge: 0
Complexity: 281
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0

Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes
CAS Number: 78-51-3
Formula: C18H39O7P
Molecular weight: 398.48 g/mol
MDL Number: MFCD00009456
InChI Key: WTLBZVNBAKMVDP-UHFFFAOYSA-N
PubChem CID: 6540
ChEBI: CHEBI:35038
IUPAC Name: tris(2-butoxyethyl) phosphate
SMILES: CCCCOC(COCCOC)OP(=O)(OCCOCCCC)OCCOCCCC
Color: Colorless to Yellow

Density: 1.0000 g/mL
Boiling Point: 215°C to 228°C (4.0 mmHg)
Flash Point: 132°C
Infrared Spectrum: Authentic
Assay Percent Range: 94% min. (GC)
Packaging: Glass bottle
Linear Formula: [CH3(CH2)3OCH2CH2O]3P(O)
Refractive Index: 1.4370 to 1.439
Specific Gravity: 1
Solubility Information: Solubility in water: 1.3 g/L (20°C)
Formula Weight: 398.47
Percent Purity: 95%
Physical Form: Liquid
Chemical Name or Material: Tris(2-butoxyethyl) phosphate



FIRST AID MEASURES of TRIS(2-BUTOXYETHYL) PHOSPHATE:
-Description of first-aid measures:
*After inhalation:
Fresh air.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with water/ shower.
*After eye contact:
Rinse out with plenty of water.
Remove contact lenses.
*After swallowing:
Make victim drink water (two glasses at most).
-Indication of any immediate medical attention and special treatment needed:
No data available



ACCIDENTAL RELEASE MEASURES of TRIS(2-BUTOXYETHYL) PHOSPHATE:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Observe possible material restrictions



FIRE FIGHTING MEASURES of TRIS(2-BUTOXYETHYL) PHOSPHATE:
-Extinguishing media:
*Suitable extinguishing media:
Foam
Carbon dioxide (CO2)
Dry powder
*Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Suppress (knock down) gases/vapors/mists with a water spray jet.
Prevent fire extinguishing water from contaminating surface water or the ground water system.



EXPOSURE CONTROLS/PERSONAL PROTECTION of TRIS(2-BUTOXYETHYL) PHOSPHATE:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Safety glasses.
*Skin protection:
not required
*Respiratory protection:
Not required.
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of TRIS(2-BUTOXYETHYL) PHOSPHATE:
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.



STABILITY and REACTIVITY of TRIS(2-BUTOXYETHYL) PHOSPHATE:
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .

TRIS(2-BUTOXYETHYL) PHOSPHATE ( TBEP ) tributoxyethyl phosphate
TCPP; Tris(1,3-dichloro-2-propyl)phosphate; Tris(2-chloro-1-(chloromethyl)ethyl)phosphate; Tris(1-chloromethyl-2-chloroethyl)phosphate; Tris(1,3-dichloroisopropyl)phosphate; Tri(beta,beta'-dichloroisopropyl)phosphate; FYROL FR 2; PF 38; Fosforan Troj-(1,3-dwuchloroizopropylowy) (Polish); 1,3-dichloro-2-propanol phosphate (3:1); cas no: 13674-87-8
TRIS(2-BUTOXYETHYL) PHOSPHATE (TBEP)
Tris(2-Butoxyethyl) Phosphate (TBEP) is slightly yellow, oily liquid. Insoluble or limited solubility in glycerol, glycols, and certain amines; soluble in most organic liquids.
Tris(2-Butoxyethyl) Phosphate (TBEP) is an organic flame retardant.
Tris(2-Butoxyethyl) Phosphate (TBEP) is an organophosphate flame retardant and used as a plasticizer in various household products such as plastics, floor polish, varnish, textiles, furniture, and electronic equipment.

CAS Number: 78-51-3
Molecular Formula: C18H39O7P
Molecular Weight: 398.47
EINECS Number: 201-122-9

Synonyms: Tris(2-butoxyethyl) phosphate, 78-51-3, TBEP, Tributoxyethyl phosphate, TRI(2-BUTOXYETHYL) PHOSPHATE, Phosflex T-bep, Tris(butoxyethyl) phosphate, tris(2-butoxyethyl)phosphate, KP 140, Kronitex KP-140, Tributyl cellosolve phosphate, Ethanol, 2-butoxy-, phosphate (3:1), Tri(butoxyethyl) phosphate, Phosphoric acid, tributoxyethyl ester, Phosphoric acid, tris(2-butoxyethyl) ester, Tri(2-butoxyethanol)phosphate, NSC 4839, Tris-(2-butoxyethyl)fosfat, Phosphoric Acid Tris(2-butoxyethyl) Ester, 2-Butoxyethanol phosphate, Tris(butoxyethyl)phosphate, Ethanol, 2-butoxy-, 1,1',1''-phosphate, DTXSID5021758, CHEBI:35038, RYA6940G86, tris[2-(butyloxy)ethyl] phosphate, NSC-4839, TBEP;KP 140;Hostaphat B 310, NSC-62228, Phosphoric acid, tri-(2-butoxyethyl) ester, Ethanol, phosphate (3:1), DTXCID201758, WLN: 4O2OPO&O2O4&O2O4, 2-Butoxyethanol, phosphate, CAS-78-51-3, Phosphoric acid, tri(butoxyethyl) ester, TBOEP, CCRIS 5942, Tri(2-butoxyethanol) phosphate, HSDB 2564, 2-Butoxyethanol phosphate (3:1), EINECS 201-122-9, Tris-(2-butoxyethyl)fosfat [Czech], Tris(2-butoxyethyl) phosphate,C18H39O7P,78-51-3, BRN 1716010, tris-2-butoxyethyl phosphate, UNII-RYA6940G86, AI3-04596, Amgard TBEP, MFCD00009456, EC 201-122-9, NCIOpen2_007840, SCHEMBL37268, 4-01-00-02422 (Beilstein Handbook Reference), Tri-(2-Butoxyethyl)phosphate, BIDD:ER0626, Tris(2-butyloxyethyl)phosphate, CHEMBL1534811, NSC4839, NSC62228, 2-Butoxy-ethanol phosphate (3:1), Tox21_201593, Tox21_302891, Tris(2-butoxyethyl) phosphate, 94%, AKOS015839670, NCGC00091600-01, NCGC00091600-02, NCGC00091600-03, NCGC00256553-01, NCGC00259142-01, Tris(2-butoxyethyl)ester phosphoric acid, AS-59809, Phosphoric acid tris(2-n-butoxyethyl)ester, CS-0066127, NS00010389, P0683, Phosphoric acid tris(2-n-butoxyethyl) ester, TRI(2-BUTOXYETHYL) PHOSPHATE [HSDB], F71229, A915093, Tris(2-butoxyethyl) phosphate, analytical standard, W-104277, Q27116378

Tris(2-Butoxyethyl) Phosphate (TBEP) is an organophosphate compound used primarily as a flame retardant and plasticizer in various industrial applications.
Its chemical formula is C18H39O7P, and its CAS number is 78-51-3.
Tris(2-Butoxyethyl) Phosphate (TBEP) is commonly utilized in the production of plastics, polymers, adhesives, and coatings to enhance their flexibility and flame resistance properties.

Additionally, Tris(2-Butoxyethyl) Phosphate (TBEP) finds application as a component in hydraulic fluids, lubricants, and as a solvent in some chemical processes.
Tris(2-Butoxyethyl) Phosphate (TBEP), also known as TBEP, is a type of flame retardant that is commonly used in various industries such as plastics, rubber, textiles, and electronics.
Tris(2-Butoxyethyl) Phosphate (TBEP) is a colorless and odorless liquid that is soluble in water, ethanol, and other organic solvents.

Tris(2-Butoxyethyl) Phosphate (TBEP) is a type of organophosphate ester, which means that it is derived from the reaction between phosphoric acid and alcohol.
Tris(2-Butoxyethyl) Phosphate (TBEP) is a versatile flame retardant that has several advantages compared to other types of flame retardants.
One of the main advantages of Tris(2-Butoxyethyl) Phosphate (TBEP) is its high efficiency in reducing the flammability of materials.

Tris(2-Butoxyethyl) Phosphate (TBEP) is a halogen-free flame retardant, which means that it does not contain any bromine or chlorine compounds that are known to be harmful to the environment and human health.
Tris(2-Butoxyethyl) Phosphate (TBEP) works by forming a protective layer on the surface of the material, which prevents the spread of fire.
Tris(2-Butoxyethyl) Phosphate (TBEP) is used as a plasticizer for PVC, chlorinated rubber, and nitriles due to its flame retardant nature and good low temperature flexibility.

Tris(2-Butoxyethyl) Phosphate (TBEP) is also used for emulsions of floor polishes, as leveling agent in latex paints and waxes, a processing aid for acrylonitrile rubber, and an antiblock agent for cast polyurethanes.
Tris(2-Butoxyethyl) Phosphate (TBEP) is a phosphate ester that, thanks to its structure, can be used in many applications including plasticisation, solvation, flame retardancy and defoaming.

Tris(2-Butoxyethyl) Phosphate (TBEP) is in fact a multifunctional additive that may be used to modify the properties of many polymer systems and is a particularly good levelling aid and coalescent additive for emulsion polymers.
Tris(2-Butoxyethyl) Phosphate (TBEP) is used in a mixed solvent/aqueous system as a defoamer during production and as a secondary plasticiser in many polymers.
The above properties in combination with inherent flame retardancy makes Tributoxy ethyl phosphate (TBEP) a real multifunctional additive essential to many polymer formulations.

Tris(2-Butoxyethyl) Phosphate (TBEP) is a light-colored, high-boiling, non-flammable viscous liquid.
Tris(2-Butoxyethyl) Phosphate (TBEP) is generally used as a plasticizer in rubber and plastics, and aids in floor polish formation (as well as in other surface coatings),
leveling and improves gloss.
Tris(2-Butoxyethyl) Phosphate (TBEP) is a clear, colorless liquid.

Tris(2-Butoxyethyl) Phosphate (TBEP) is a phosphine oxide and thus very stable in nature.
Tris(2-Butoxyethyl) Phosphate (TBEP) has many applications including plasticizing agent in acrylic based polishes, defoamer agent in acrylics, “knockdown” defoamer in paint, textile and paper and as a halide free flame retardant in polymer systems.
Tris(2-Butoxyethyl) Phosphate (TBEP) is an organic flame retardant.

Tris(2-Butoxyethyl) Phosphate (TBEP) is also used to add flexibility in vinyl resins, other plastics, natural and synthetic rubbers, and floor finishes and waxes.
Tris(2-Butoxyethyl) Phosphate (TBEP) is a flame-retardant plasticizer.
Tris(2-Butoxyethyl) Phosphate (TBEP) is mainly used for flame-retardant and plasticizing of polyurethane resin, cellulose, polyvinyl alcohol, etc.

Tris(2-Butoxyethyl) Phosphate (TBEP) has good low-temperature characteristic.
Tris(2-Butoxyethyl) Phosphate (TBEP) can be obtained by the reaction of the reaction of phosphorus oxychloride and 2-butoxyethanol .
Tris(2-Butoxyethyl) Phosphate (TBEP) is a flammable, hardly inflammable, colorless to yellowish liquid that is sparingly soluble in water.

Tris(2-Butoxyethyl) Phosphate (TBEP) is used as an organic flame retardant , as well as in floor care products, as a solvent in resins, as a viscosity modifier in plastisols and as a plasticizer in rubber stoppers.
Tris(2-Butoxyethyl) Phosphate (TBEP)is mainly used as floor polishing agent and processing agent of water-based adhesive, flame retardant and plasticizer of acrylonitrile type rubber, cellulose acetate, epoxy resin, ethyecellulose, polyvinyl acetate, thermoplastic and thermosetting polyurethane.
Tris(2-Butoxyethyl) Phosphate (TBEP) is also used as defoamer in coating, detergent and textiles.

Moreover, Tris(2-Butoxyethyl) Phosphate (TBEP) can be also used in nitrocellulose, ethyecellulose and acrylic plastic plasticizer.
Tris(2-Butoxyethyl) Phosphate (TBEP) is a chemical compound commonly used as a flame retardant and plasticizer in various industrial products.
Tris(2-Butoxyethyl) Phosphate (TBEP) is added to materials like plastics, rubber, and textiles to make them less flammable and more flexible.

Tris(2-Butoxyethyl) Phosphate (TBEP) can also be found in hydraulic fluids, lubricants, and as a solvent in certain chemical processes.
While it provides important functional properties to these products, concerns have been raised about its potential environmental and health impacts.
Tris(2-Butoxyethyl) Phosphate (TBEP) has been studied for its persistence in the environment and possible toxicity to aquatic organisms.

As a result, regulations and guidelines regarding its use and disposal may vary depending on the region.
Tris(2-Butoxyethyl) Phosphate (TBEP) is also used as a halogen free flame retardant additive in polymer systems.
Tris(2-Butoxyethyl) Phosphate (TBEP) can be used also in conjunction with other flame retardants.

Tris(2-Butoxyethyl) Phosphate (TBEP) is a light-colored, high-boiling, non-flammable viscous liquid.
Tris(2-Butoxyethyl) Phosphate (TBEP) is generally used as a plasticizer in rubber and plastics, and aids in floor polish formation (as well as in other surface coatings), leveling and improves gloss.
Tris(2-Butoxyethyl) Phosphate (TBEP) is used as a plasticizer for PVC, chlorinated rubber, and nitriles due to its flame retardant nature and good low temperature flexibility.

Tris(2-Butoxyethyl) Phosphate (TBEP) is also used for emulsions of floor polishes, as leveling agent in latex paints and waxes, a processing aid for acrylonitrile rubber, and an antiblock agent for cast polyurethanes.
Tris(2-Butoxyethyl) Phosphate (TBEP) is a plasticizer for polyvinyl chloride (PVC), chlorinated rubber and nitriles.
Tris(2-Butoxyethyl) Phosphate (TBEP) is also an alkyl phosphate flame retardant and has good heat stability.

Tris(2-Butoxyethyl) Phosphate (TBEP) can be used in applications needing low temperature flexibility such as a leveling agent for acrylic resin-based polishes.
Tris(2-Butoxyethyl) Phosphate (TBEP) can also be used for emulsions of floor finishes, leveling agent in latex paint, a processing aid for acrylonitrile rubber, antiblock agent for cast polyurethanes.
As a plasticizer, Tris(2-Butoxyethyl) Phosphate (TBEP) incorporates readily and is a non-reactive, medium viscosity liquid.

Tris(2-Butoxyethyl) Phosphate (TBEP) is high solvency makes it a great product for natural and synthetic resins and compatible with waxes.
Tris(2-Butoxyethyl) Phosphate (TBEP) is used commercially in floor polishes, paper coatings and as an antifoaming agent in ore beneficiations.
Tris(2-Butoxyethyl) Phosphate (TBEP) also finds uses in vinyl plastics.

Tris(2-Butoxyethyl) Phosphate (TBEP) is a clear, colorless liquid.
Tris(2-Butoxyethyl) Phosphate (TBEP) is a phosphine oxide and thus very stable in nature.
Tris(2-Butoxyethyl) Phosphate (TBEP) has many applications including plasticizing agent in acrylic based polishes, defoamer agent in acrylics, “knockdown” defoamer in paint, textile and paper and as a halide free flame retardant in polymer systems.

Tris(2-Butoxyethyl) Phosphate (TBEP) is used as a plasticizer for polymer dispersions and also improves wetting-levelling properties of drybright emulsions.
Tris(2-Butoxyethyl) Phosphate (TBEP) is a trialkyl phosphate in which the alkyl group specified is 2-butoxyethyl.
Tris(2-Butoxyethyl) Phosphate (TBEP) has a role as an environmental contaminant and a flame retardant.

Tris(2-Butoxyethyl) Phosphate (TBEP) is a slightly yellow viscous liquid.
Tris(2-Butoxyethyl) Phosphate (TBEP) is an organic flame retardant.

Tris(2-Butoxyethyl) Phosphate (TBEP) shows PXR agonistic activity.
Tris(2-Butoxyethyl) Phosphate (TBEP) was detected and quantified during the analysis of herring gull eggs by liquid chromatography-electrospray ionization(+)-tandem mass spectrometry.

Tris(2-Butoxyethyl) Phosphate (TBEP) is its compatibility with various types of polymers and resins.
Tris(2-Butoxyethyl) Phosphate (TBEP) can be used in combination with other flame retardants to enhance its effectiveness.

Tris(2-Butoxyethyl) Phosphate (TBEP) is also compatible with other additives such as plasticizers and stabilizers, which makes it a versatile ingredient in the production of various types of materials.
Tris(2-Butoxyethyl) Phosphate (TBEP) is also known for its thermal stability and resistance to hydrolysis.
Tris(2-Butoxyethyl) Phosphate (TBEP) can withstand high temperatures without decomposing or releasing toxic gases.

Tris(2-Butoxyethyl) Phosphate (TBEP) is also resistant to moisture and can maintain its effectiveness even in humid environments.
Organophosphates, such as Tris(2-Butoxyethyl) Phosphate (TBEP), are susceptible to formation of highly toxic and flammable phosphine gas in the presence of strong reducing agents such as hydrides.
Partial oxidation by oxidizing agents may result in the release of toxic phosphorus oxides.

Tris(2-Butoxyethyl) Phosphate (TBEP) may react with oxidizers. .
Tris(2-Butoxyethyl) Phosphate (TBEP) acts as an additive flame retardant and plasticizer in plastics and synthetic rubbers.
Tris(2-Butoxyethyl) Phosphate (TBEP) appears as a colorless clear liquid having molecular weight of 398.47.

Tris(2-Butoxyethyl) Phosphate (TBEP) is a trialkyl phosphate in which the alkyl group specified is 2-butoxyethyl.
Tris(2-Butoxyethyl) Phosphate (TBEP) has a role as an environmental contaminant and a flame retardant.
Tris(2-Butoxyethyl) Phosphate (TBEP) is a slightly yellow viscous liquid.

Tris(2-Butoxyethyl) Phosphate (TBEP) has been subject to regulatory scrutiny due to its potential environmental and health impacts, and its usage may be subject to restrictions in certain regions.
Tris(2-Butoxyethyl) Phosphate (TBEP) is a phosphate ester that, thanks to its structure, can be used in many applications including plasticisation, solvation, flame retardancy and defoaming.

Tris(2-Butoxyethyl) Phosphate (TBEP) is in fact a multifunctional additive that may be used to modify the properties of many polymer systems and is a particularly good levelling aid and coalescent additive for emulsion polymers.
Tris(2-Butoxyethyl) Phosphate (TBEP) is used in a mixed solvent/aqueous system as a defoamer during production and as a secondary plasticiser in many polymers.
The above properties in combination with inherent flame retardancy makes Tris(2-Butoxyethyl) Phosphate (TBEP) a real multifunctional additive essential to many polymer formulations.

Tributoxyethyl Phosphate (TBEP) is used as a plasticizer for PVC, chlorinated rubber, and nitriles due to its flame retardant nature and good low temperature flexibility.
Tris(2-Butoxyethyl) Phosphate (TBEP) is also used for emulsions of floor polishes, as leveling agent in latex paints and waxes, a processing aid for acrylonitrile rubber, and an antiblock agent for cast polyurethanes.

Tris(2-Butoxyethyl) Phosphate (TBEP) shows PXR agonistic activity.
Tris(2-Butoxyethyl) Phosphate (TBEP) was detected and quantified during the analysis of herring gull eggs by liquid chromatography-electrospray ionization(+)-tandem mass spectrometry.

Tris(2-Butoxyethyl) Phosphate (TBEP) is an organic flame retardant.
It shows PXR agonistic activity.
Tris(2-Butoxyethyl) Phosphate (TBEP) was detected and quantified during the analysis of herring gull eggs by liquid chromatography-electrospray ionization(+)-tandem mass spectrometry.

Melting point: -70°C
Boiling point: 215-228 °C4 mm Hg(lit.)
Density: 1.006 g/mL at 25 °C(lit.)
vapor density: 13.7 (vs air)
vapor pressure: 0.03 mm Hg ( 150 °C)
refractive index: n20/D 1.438(lit.)
Flash point: >230 °F
storage temp.:Store at -20°C
solubility: Chloroform (Slightly), DMSO (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly)
form: Liquid
color: Clear colorless to very slightly yellow
Water Solubility: Soluble
Stability: Stable. Combustible. Incompatible with strong oxidizing agents.
InChIKey: WTLBZVNBAKMVDP-UHFFFAOYSA-N
LogP: 3.75 at 20℃

Tris(2-Butoxyethyl) Phosphate (TBEP) is a trialkyl phosphate in which the alkyl group specified is 2-butoxyethyl.
Tris(2-Butoxyethyl) Phosphate (TBEP) has a role as an environmental contaminant and a flame retardant.
Tris(2-Butoxyethyl) Phosphate (TBEP) is a slightly yellow viscous liquid.

Tris(2-Butoxyethyl) Phosphate (TBEP) is an alkyl phosphate flame retardant and plasticizer, specifically tris(butoxyethyl) phosphate.
Tris(2-Butoxyethyl) Phosphate (TBEP) is recommended fo use as a plasticizer for PVC, chlorinated rubber and for nitrile.
Tris(2-Butoxyethyl) Phosphate (TBEP) is often used as a leveling agent in floor polishes, as a leveling agent in paints, and as an antiblock agent for cast polyurethanes.

Tris(2-Butoxyethyl) Phosphate (TBEP) exhibits low viscosity (12 cps).
Tris(2-Butoxyethyl) Phosphate (TBEP) contains 7.8% phosphorous.
Tris(2-Butoxyethyl) Phosphate (TBEP) is a plasticizer for polyvinyl chloride (PVC), chlorinated rubber and nitriles.

Tris(2-Butoxyethyl) Phosphate (TBEP) is also an alkyl phosphate flame retardant and has good heat stability.
Tris(2-Butoxyethyl) Phosphate (TBEP) can be used in applications needing low temperature flexibility such as a leveling agent for acrylic resin-based polishes.
Tris(2-Butoxyethyl) Phosphate (TBEP) can also be used for emulsions of floor finishes, leveling agent in latex paint, a processing aid for acrylonitrile rubber, antiblock agent for cast polyurethanes.

As a plasticizer, Tris(2-Butoxyethyl) Phosphate (TBEP), incorporates readily and is a non-reactive, medium viscosity liquid.
Tris(2-Butoxyethyl) Phosphate (TBEP)s high solvency makes it a great product for natural and synthetic resins and compatible with waxes.
Tris(2-Butoxyethyl) Phosphate (TBEP) is used commercially in floor polishes, paper coatings and as an antifoaming agent in ore beneficiations.

Tris(2-Butoxyethyl) Phosphate (TBEP) also finds uses in vinyl plastics.
Tris(2-Butoxyethyl) Phosphate (TBEP) is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 1 000 to < 10 000 tonnes per annum.
Tris(2-Butoxyethyl) Phosphate (TBEP) is used by consumers, in articles, by professional workers (widespread uses), in formulation or repacking and at industrial sites.

Tris(2-Butoxyethyl) Phosphate (TBEP) is a phosphate ester that, thanks to its structure, can be used in many applications including plasticisation, solvation, flame retardancy and defoaming.
Tris(2-Butoxyethyl) Phosphate (TBEP) is in fact a multifunctional additive that may be used to modify the properties of many polymer systems and is a particularly good levelling aid and coalescent additive for emulsion polymers.
Tris(2-Butoxyethyl) Phosphate (TBEP) is used in a mixed solvent/aqueous system as a defoamer during production and as a secondary plasticiser in many polymers.

The above properties in combination with inherent flame retardancy makes Tris(2-Butoxyethyl) Phosphate (TBEP) a real multifunctional additive essential to many polymer formulations.
Tris(2-Butoxyethyl) Phosphate (TBEP) is widely used in household materials such as plasticizer, floor polish and flame retardant in plastic resins and synthetic rubbers.
Tris(2-Butoxyethyl) Phosphate (TBEP)-based is a plasticizer and defoamer.

Tris(2-Butoxyethyl) Phosphate (TBEP) also acts as a leveling agent for acrylic and styrenic floor polishes and coalescent additive for emulsion polymers.
Tris(2-Butoxyethyl) Phosphate (TBEP) is valued for its effectiveness as a flame retardant.
Tris(2-Butoxyethyl) Phosphate (TBEP) works by reducing the flammability of materials, thereby slowing down or preventing the spread of fire.

In addition to its flame retardant properties, Tris(2-Butoxyethyl) Phosphate (TBEP) acts as a plasticizer, improving the flexibility and durability of various materials, particularly plastics and polymers.
Tris(2-Butoxyethyl) Phosphate (TBEP) is commonly used in a wide range of industrial applications, including the production of automotive parts, electrical cables, construction materials, and textiles.
Due to concerns about its potential environmental persistence and toxicity, Tris(2-Butoxyethyl) Phosphate (TBEP) has been subject to regulatory scrutiny in some regions.

Regulatory agencies may impose restrictions on its use or require labeling and handling precautions.
Tris(2-Butoxyethyl) Phosphate (TBEP) provides important functional benefits, it is essential to handle it with care.
Occupational exposure should be minimized, and appropriate safety measures should be followed during handling, storage, and disposal.

In response to regulatory concerns and evolving industry standards, researchers and manufacturers are exploring alternative flame retardants and plasticizers that offer comparable performance while minimizing environmental and health risks.
Tris(2-Butoxyethyl) Phosphate (TBEP) is widely used as a flame retardant additive in plastics, textiles, and other materials.

Tris(2-Butoxyethyl) Phosphate (TBEP) works by reducing the flammability of these materials, making them safer in applications where fire hazards are a concern.
In addition to its flame retardant properties, Tris(2-Butoxyethyl) Phosphate (TBEP) also serves as a plasticizer, improving the flexibility and workability of polymers and plastics.

This makes it valuable in manufacturing processes where flexibility is desired.
Tris(2-Butoxyethyl) Phosphate (TBEP) finds use in diverse industrial applications beyond flame retardancy and plasticization.
It is employed in products such as hydraulic fluids, lubricants, coatings, and adhesives.

Like many organophosphate compounds, Tris(2-Butoxyethyl) Phosphate (TBEP) has raised environmental and health concerns.
Its persistence in the environment and potential toxicity to aquatic organisms have prompted regulatory scrutiny and efforts to find safer alternatives.
Regulations governing the use of Tris(2-Butoxyethyl) Phosphate (TBEP) vary by region.

In some jurisdictions, its use may be restricted or subject to specific labeling and handling requirements to minimize environmental and human health risks.
There is ongoing research into alternative flame retardants and plasticizers that offer comparable performance while addressing environmental and health concerns associated with TBEP and similar compounds.
Oral exposure to low-dose Tris(2-Butoxyethyl) Phosphate (TBEP) levels equivalent to tolerable daily intake may exacerbate allergic pulmonary inflammation by promoting a skewed T-helper 2 cell response, upregulation of ERα and dysregulation of both MLN and BM microenvironments.

Uses:
Tris(2-Butoxyethyl) Phosphate (TBEP) is used also in mercerizing liquids, where it improves their wetting properties.
Tris(2-Butoxyethyl) Phosphate (TBEP) can be used as a heat-exchange medium.
Release to the environment of Tris(2-Butoxyethyl) Phosphate (TBEP) can occur from industrial use: as processing aid and of substances in closed systems with minimal release.

Other release to the environment of Tris(2-Butoxyethyl) Phosphate (TBEP) is likely to occur from: indoor use as processing aid, indoor use in long-life materials with low release rate (e.g. flooring, furniture, toys, construction materials, curtains, foot-wear, leather products, paper and cardboard products, electronic equipment), outdoor use as processing aid and outdoor use in long-life materials with low release rate (e.g. metal, wooden and plastic construction and building materials).
Tris(2-Butoxyethyl) Phosphate (TBEP) can be found in products with material based on: wood (e.g. floors, furniture, toys), plastic (e.g. food packaging and storage, toys, mobile phones) and paper (e.g. tissues, feminine hygiene products, nappies, books, magazines, wallpaper).

Tris(2-Butoxyethyl) Phosphate (TBEP) is used in the following products: plant protection products, hydraulic fluids, lubricants and greases, metal working fluids, washing & cleaning products and polishes and waxes.
Tris(2-Butoxyethyl) Phosphate (TBEP) has an industrial use resulting in manufacture of another substance (use of intermediates).

Tris(2-Butoxyethyl) Phosphate (TBEP) is used in the following areas: agriculture, forestry and fishing and formulation of mixtures and/or re-packaging.
Tris(2-Butoxyethyl) Phosphate (TBEP) is used in the following products: polymers and textile treatment products and dyes.
Release to the environment of Tris(2-Butoxyethyl) Phosphate (TBEP) can occur from industrial use: formulation in materials and formulation of mixtures.

Tris(2-Butoxyethyl) Phosphate (TBEP) is used in the following products: polymers, textile treatment products and dyes and washing & cleaning products.
Tris(2-Butoxyethyl) Phosphate (TBEP) is used for the manufacture of: plastic products and textile, leather or fur.
Release to the environment of Tris(2-Butoxyethyl) Phosphate (TBEP) can occur from industrial use: in the production of articles, as processing aid and in processing aids at industrial sites.

One of the primary uses of Tris(2-Butoxyethyl) Phosphate (TBEP) is as a flame retardant additive in various materials such as plastics, rubber, textiles, and coatings.
Tris(2-Butoxyethyl) Phosphate (TBEP) reduces the flammability of these materials, making them less likely to catch fire or spread flames.
Tris(2-Butoxyethyl) Phosphate (TBEP) also acts as a plasticizer, improving the flexibility, durability, and workability of plastics and polymers.

Tris(2-Butoxyethyl) Phosphate (TBEP) helps to enhance the processing properties of these materials during manufacturing.
Tris(2-Butoxyethyl) Phosphate (TBEP) is utilized as an additive in lubricants and hydraulic fluids to improve their lubricating properties and thermal stability.
Tris(2-Butoxyethyl) Phosphate (TBEP) helps to reduce friction and wear in mechanical systems.

In some chemical processes, Tris(2-Butoxyethyl) Phosphate (TBEP) serves as a solvent or carrier for other substances.
It can facilitate the dissolution and dispersion of various compounds in solution.
Tris(2-Butoxyethyl) Phosphate (TBEP) is incorporated into coatings, sealants, and adhesives to improve their performance properties.

It can enhance adhesion, flexibility, and resistance to heat and chemicals.
In the textile industry, Tris(2-Butoxyethyl) Phosphate (TBEP) may be used as a finishing agent to impart flame retardant properties to fabrics and garments.
It helps textiles meet flame resistance standards for safety applications.

Tributoxy ethyl phosphate (TBEP) also helps to improve pigment wetting and rheological properties with a minimal effect on reflectance Tributoxy ethyl phosphate (TBEP) is a highly effective "knockdown" defoamer used extensively in paint, textile and paper industries.
Tributoxy ethyl phosphate (TBEP) is also used as a halogen free flame retardant additive in polymer systems. It can be used also in conjunction with other flame retardants.

Tris(2-Butoxyethyl) Phosphate (TBEP) is used as an additive flame retardant and plasticizer in plastics and synthetic rubbers.
Tris(2-Butoxyethyl) Phosphate (TBEP) is a phosphate ester that, thanks to its structure, can be used in many applications including plasticisation, solvation, flame retardancy and defoaming.
Tris(2-Butoxyethyl) Phosphate (TBEP) is in fact a multifunctional additive that may be used to modify the properties of many polymer systems and is a particularly good levelling aid and coalescent additive for emulsion polymers.

Tris(2-Butoxyethyl) Phosphate (TBEP) is used in a mixed solvent/aqueous system as a defoamer during production and as a secondary plasticiser in many polymers.
The above properties in combination with inherent flame retardancy makes Tris(2-Butoxyethyl) Phosphate (TBEP) a real multifunctional additive essential to many polymer formulations.
Tris(2-Butoxyethyl) Phosphate (TBEP) is used as a plasticizer for PVC, chlorinated rubber, and nitriles due to its flame retardant nature and good low temperature flexibility.

Tris(2-Butoxyethyl) Phosphate (TBEP) is also used for emulsions of floor polishes, as leveling agent in latex paints and waxes, a processing aid for acrylonitrile rubber, and an antiblock agent for cast polyurethanes.
Tris(2-Butoxyethyl) Phosphate (TBEP) is commonly used in the production of polyurethane foam, PVC, and other types of plastics.
Tris(2-Butoxyethyl) Phosphate (TBEP) is effective in reducing the flammability of these materials and improving their fire safety.

Tris(2-Butoxyethyl) Phosphate (TBEP) is used as a flame retardant for textiles such as curtains, upholstery, and carpets.
It can also be used in the production of flame-resistant clothing for firefighters and other workers in high-risk environments.
Tris(2-Butoxyethyl) Phosphate (TBEP) is used in the production of electronic components such as circuit boards and cables.

Tris(2-Butoxyethyl) Phosphate (TBEP) helps to reduce the risk of fire and improve the safety of electronic devices.
Tris(2-Butoxyethyl) Phosphate (TBEP) is used in the production of rubber products such as tires, gaskets, and seals.
It can improve the fire safety of these products and reduce the risk of fire in industrial settings.

Tris(2-Butoxyethyl) Phosphate (TBEP) may be used as an analytical reference standard for the quantification of the analyte in herring gull eggs, house dust, and urine samples using liquid chromatography technique.
Primary plasticizer for most resins and elastomers, floor finishes and waxes, flame-retarding agent.
Tris(2-Butoxyethyl) Phosphate (TBEP) is commonly added to paints, coatings, and varnishes to improve their fire resistance and durability.

It helps these products adhere better to surfaces and provides a protective barrier against fire damage.
Tris(2-Butoxyethyl) Phosphate (TBEP) is used as an additive in adhesives and sealants to enhance their bonding strength and flexibility.
It helps prevent the material from becoming brittle over time and improves its resistance to fire.

Tris(2-Butoxyethyl) Phosphate (TBEP) is incorporated into the insulation of electrical wires and cables to reduce the risk of fire propagation in case of a short circuit or overheating.
Tris(2-Butoxyethyl) Phosphate (TBEP) helps maintain the integrity of the insulation and prevents electrical fires.
Tris(2-Butoxyethyl) Phosphate (TBEP) is sometimes used in the production of polyurethane foam, particularly in applications where fire safety is a concern, such as upholstered furniture and mattresses.

It improves the foam's fire resistance without compromising its mechanical properties.
Tris(2-Butoxyethyl) Phosphate (TBEP) can be added to rubber compounds to increase their flame retardancy and flexibility.
It is commonly used in the production of rubber goods such as gaskets, seals, and hoses for various industrial applications.

Tris(2-Butoxyethyl) Phosphate (TBEP) may be included in construction materials such as insulation boards, roofing materials, and sealants to meet fire safety standards and regulations.
It helps prevent the spread of fire in buildings and structures.

Tris(2-Butoxyethyl) Phosphate (TBEP) is used in the manufacturing of automotive components, including dashboards, interior trims, and upholstery, to improve their fire resistance and durability.
Tris(2-Butoxyethyl) Phosphate (TBEP) helps ensure compliance with automotive safety standards.
Tris(2-Butoxyethyl) Phosphate (TBEP) is used in some consumer products such as herbicides and water-thinned paints and tinting bases.

Tris(2-Butoxyethyl) Phosphate (TBEP) may be used as an analytical reference standard for the quantification of the analyte in herring gull eggs, house dust, and urine samples using liquid chromatography technique.
Primary plasticizer for most resins and elastomers, floor finishes and waxes, flame-retarding agent.
Tris(2-Butoxyethyl) Phosphate (TBEP) is a solvent and plasticizer for cellulose esters such as nitrocellulose and cellulose acetate.

Tris(2-Butoxyethyl) Phosphate (TBEP) forms stable hydrophobic complexes with some metals; these complexes are soluble in organic solvents as well as supercritical CO2.
The major uses of Tris(2-Butoxyethyl) Phosphate (TBEP) in industry are as a component of aircraft hydraulic fluid, brake fluid, and as a solvent for extraction and purification of rare-earth metals from their ores.
Tris(2-Butoxyethyl) Phosphate (TBEP) finds its use as a solvent in inks, synthetic resins, gums, adhesives (namely for veneer plywood), and herbicide and fungicide concentrates.

As Tris(2-Butoxyethyl) Phosphate (TBEP) has no odour is used as an anti-foaming agent in detergent solutions, and in various emulsions, paints, and adhesives.
Tris(2-Butoxyethyl) Phosphate (TBEP) is also found as a de-foamer in ethylene glycol-borax antifreeze solutions.
In oil-based lubricants addition of Tris(2-Butoxyethyl) Phosphate (TBEP) increases the oil film strength.

Safety Profile:
Tris(2-Butoxyethyl) Phosphate (TBEP) is considered persistent in the environment and may bioaccumulate in aquatic organisms.
It can pose risks to aquatic ecosystems and wildlife, particularly in areas where it is released into waterways or accumulates in sediment.

Despite being used as a flame retardant, Tris(2-Butoxyethyl) Phosphate (TBEP) itself is combustible.
Tris(2-Butoxyethyl) Phosphate (TBEP) may contribute to the spread of fire if not properly contained or managed, posing fire hazards in manufacturing facilities, storage areas, or during transportation.
Tris(2-Butoxyethyl) Phosphate (TBEP) may cause irritation to the skin, eyes, and respiratory tract upon contact or inhalation of its vapors or aerosols.

Prolonged or repeated exposure may lead to more severe health effects, including dermatitis, respiratory irritation, and allergic reactions.
While Tris(2-Butoxyethyl) Phosphate (TBEP)'s acute toxicity is relatively low, chronic exposure to high concentrations may pose health risks.
Animal studies suggest potential adverse effects on the liver, kidneys, and reproductive system, although more research is needed to fully understand its long-term toxicity in humans.


TRIS(2-BUTOXYETHYL) PHOSPHATE (TBEP)
Tris(2-Butoxyethyl) Phosphate (TBEP) is slightly yellow, oily liquid. Insoluble or limited solubility in glycerol, glycols, and certain amines; soluble in most organic liquids.
Tris(2-Butoxyethyl) Phosphate (TBEP) is an organic flame retardant. It shows PXR agonistic activity.
Tris(2-Butoxyethyl) Phosphate (TBEP) was detected and quantified during the analysis of herring gull eggs by liquid chromatography-electrospray ionization(+)-tandem mass spectrometry.

CAS Number: 78-51-3
Molecular Formula: C18H39O7P
Molecular Weight: 398.47
EINECS Number: 201-122-9

Tris(2-butoxyethyl) phosphate, 78-51-3, TBEP, Tributoxyethyl phosphate, TRI(2-BUTOXYETHYL) PHOSPHATE, Phosflex T-bep, Tris(butoxyethyl) phosphate, tris(2-butoxyethyl)phosphate, KP 140, Kronitex KP-140, Tributyl cellosolve phosphate, Ethanol, 2-butoxy-, phosphate (3:1), Tri(butoxyethyl) phosphate, Phosphoric acid, tributoxyethyl ester, Phosphoric acid, tris(2-butoxyethyl) ester, Tri(2-butoxyethanol)phosphate, NSC 4839, Tris-(2-butoxyethyl)fosfat, Phosphoric Acid Tris(2-butoxyethyl) Ester, 2-Butoxyethanol phosphate, Tris(butoxyethyl)phosphate, Ethanol, 2-butoxy-, 1,1',1''-phosphate, DTXSID5021758, CHEBI:35038, RYA6940G86, tris[2-(butyloxy)ethyl] phosphate, NSC-4839, TBEP;KP 140;Hostaphat B 310, NSC-62228, Phosphoric acid, tri-(2-butoxyethyl) ester, Ethanol, phosphate (3:1), DTXCID201758, WLN: 4O2OPO&O2O4&O2O4, 2-Butoxyethanol, phosphate, CAS-78-51-3, Phosphoric acid, tri(butoxyethyl) ester, TBOEP, CCRIS 5942, Tri(2-butoxyethanol) phosphate, HSDB 2564, 2-Butoxyethanol phosphate (3:1), EINECS 201-122-9, Tris-(2-butoxyethyl)fosfat [Czech], Tris(2-butoxyethyl) phosphate,C18H39O7P,78-51-3, BRN 1716010, tris-2-butoxyethyl phosphate, UNII-RYA6940G86, AI3-04596, Amgard TBEP, MFCD00009456, EC 201-122-9, NCIOpen2_007840, SCHEMBL37268, 4-01-00-02422 (Beilstein Handbook Reference), Tri-(2-Butoxyethyl)phosphate, BIDD:ER0626, Tris(2-butyloxyethyl)phosphate, CHEMBL1534811, NSC4839, NSC62228, 2-Butoxy-ethanol phosphate (3:1), Tox21_201593, Tox21_302891, Tris(2-butoxyethyl) phosphate, 94%, AKOS015839670, NCGC00091600-01, NCGC00091600-02, NCGC00091600-03, NCGC00256553-01, NCGC00259142-01, Tris(2-butoxyethyl)ester phosphoric acid, AS-59809, Phosphoric acid tris(2-n-butoxyethyl)ester, CS-0066127, NS00010389, P0683, Phosphoric acid tris(2-n-butoxyethyl) ester, TRI(2-BUTOXYETHYL) PHOSPHATE [HSDB], F71229, A915093, Tris(2-butoxyethyl) phosphate, analytical standard, W-104277, Q27116378

Tris(2-Butoxyethyl) Phosphate (TBEP) is an organic flame retardant.
Tris(2-Butoxyethyl) Phosphate (TBEP) shows PXR agonistic activity.
Tris(2-Butoxyethyl) Phosphate (TBEP) was detected and quantified during the analysis of herring gull eggs by liquid chromatography-electrospray ionization(+)-tandem mass spectrometry.

Tris(2-Butoxyethyl) Phosphate (TBEP) is an organophosphate flame retardant and used as a plasticizer in various household products such as plastics, floor polish, varnish, textiles, furniture, and electronic equipment.
Tributoxyethyl Phosphate (TBEP) is used as a plasticizer for PVC, chlorinated rubber, and nitriles due to its flame retardant nature and good low temperature flexibility.
Tris(2-Butoxyethyl) Phosphate (TBEP) is also used for emulsions of floor polishes, as leveling agent in latex paints and waxes, a processing aid for acrylonitrile rubber, and an antiblock agent for cast polyurethanes.

Tris(2-Butoxyethyl) Phosphate (TBEP) is an organophosphate compound used primarily as a flame retardant and plasticizer in various industrial applications.
Its chemical formula is C18H39O7P, and its CAS number is 78-51-3.
Tris(2-Butoxyethyl) Phosphate (TBEP) is commonly utilized in the production of plastics, polymers, adhesives, and coatings to enhance their flexibility and flame resistance properties.

Additionally, Tris(2-Butoxyethyl) Phosphate (TBEP) finds application as a component in hydraulic fluids, lubricants, and as a solvent in some chemical processes.
Tris(2-Butoxyethyl) Phosphate (TBEP) has been subject to regulatory scrutiny due to its potential environmental and health impacts, and its usage may be subject to restrictions in certain regions.
Tris(2-Butoxyethyl) Phosphate (TBEP) is a phosphate ester that, thanks to its structure, can be used in many applications including plasticisation, solvation, flame retardancy and defoaming.

Tris(2-Butoxyethyl) Phosphate (TBEP) is in fact a multifunctional additive that may be used to modify the properties of many polymer systems and is a particularly good levelling aid and coalescent additive for emulsion polymers.
Tris(2-Butoxyethyl) Phosphate (TBEP) is used in a mixed solvent/aqueous system as a defoamer during production and as a secondary plasticiser in many polymers.
The above properties in combination with inherent flame retardancy makes Tris(2-Butoxyethyl) Phosphate (TBEP) a real multifunctional additive essential to many polymer formulations.

Tris(2-Butoxyethyl) Phosphate (TBEP), also known as TBEP, is a type of flame retardant that is commonly used in various industries such as plastics, rubber, textiles, and electronics.
Tris(2-Butoxyethyl) Phosphate (TBEP) is a colorless and odorless liquid that is soluble in water, ethanol, and other organic solvents.
Tris(2-Butoxyethyl) Phosphate (TBEP) is a type of organophosphate ester, which means that it is derived from the reaction between phosphoric acid and alcohol.

Tris(2-Butoxyethyl) Phosphate (TBEP) is a versatile flame retardant that has several advantages compared to other types of flame retardants.
One of the main advantages of Tris(2-Butoxyethyl) Phosphate (TBEP) is its high efficiency in reducing the flammability of materials.
Tris(2-Butoxyethyl) Phosphate (TBEP) is a halogen-free flame retardant, which means that it does not contain any bromine or chlorine compounds that are known to be harmful to the environment and human health.

Tris(2-Butoxyethyl) Phosphate (TBEP) works by forming a protective layer on the surface of the material, which prevents the spread of fire.
Tris(2-Butoxyethyl) Phosphate (TBEP) is its compatibility with various types of polymers and resins.
Tris(2-Butoxyethyl) Phosphate (TBEP) can be used in combination with other flame retardants to enhance its effectiveness.

Tris(2-Butoxyethyl) Phosphate (TBEP) is also compatible with other additives such as plasticizers and stabilizers, which makes it a versatile ingredient in the production of various types of materials.
Tris(2-Butoxyethyl) Phosphate (TBEP) is also known for its thermal stability and resistance to hydrolysis.
Tris(2-Butoxyethyl) Phosphate (TBEP) can withstand high temperatures without decomposing or releasing toxic gases.

Tris(2-Butoxyethyl) Phosphate (TBEP) is also resistant to moisture and can maintain its effectiveness even in humid environments.
Organophosphates, such as Tris(2-Butoxyethyl) Phosphate (TBEP), are susceptible to formation of highly toxic and flammable phosphine gas in the presence of strong reducing agents such as hydrides.
Partial oxidation by oxidizing agents may result in the release of toxic phosphorus oxides.

Tris(2-Butoxyethyl) Phosphate (TBEP) may react with oxidizers. .
Tris(2-Butoxyethyl) Phosphate (TBEP) acts as an additive flame retardant and plasticizer in plastics and synthetic rubbers.
Tris(2-Butoxyethyl) Phosphate (TBEP) appears as a colorless clear liquid having molecular weight of 398.47.

Tris(2-Butoxyethyl) Phosphate (TBEP) is a trialkyl phosphate in which the alkyl group specified is 2-butoxyethyl.
Tris(2-Butoxyethyl) Phosphate (TBEP) has a role as an environmental contaminant and a flame retardant.
Tris(2-Butoxyethyl) Phosphate (TBEP) is a slightly yellow viscous liquid.

Tris(2-Butoxyethyl) Phosphate (TBEP) is used as a plasticizer for PVC, chlorinated rubber, and nitriles due to its flame retardant nature and good low temperature flexibility.
Tris(2-Butoxyethyl) Phosphate (TBEP) is also used for emulsions of floor polishes, as leveling agent in latex paints and waxes, a processing aid for acrylonitrile rubber, and an antiblock agent for cast polyurethanes.
Tris(2-Butoxyethyl) Phosphate (TBEP) is a phosphate ester that, thanks to its structure, can be used in many applications including plasticisation, solvation, flame retardancy and defoaming.

Tris(2-Butoxyethyl) Phosphate (TBEP) is in fact a multifunctional additive that may be used to modify the properties of many polymer systems and is a particularly good levelling aid and coalescent additive for emulsion polymers.
Tris(2-Butoxyethyl) Phosphate (TBEP) is used in a mixed solvent/aqueous system as a defoamer during production and as a secondary plasticiser in many polymers.
The above properties in combination with inherent flame retardancy makes Tributoxy ethyl phosphate (TBEP) a real multifunctional additive essential to many polymer formulations.

Tris(2-Butoxyethyl) Phosphate (TBEP) is a light-colored, high-boiling, non-flammable viscous liquid.
Tris(2-Butoxyethyl) Phosphate (TBEP) is generally used as a plasticizer in rubber and plastics, and aids in floor polish formation (as well as in other surface coatings),
leveling and improves gloss.
Tris(2-Butoxyethyl) Phosphate (TBEP) is a clear, colorless liquid.

Tris(2-Butoxyethyl) Phosphate (TBEP) is a phosphine oxide and thus very stable in nature.
Tris(2-Butoxyethyl) Phosphate (TBEP) has many applications including plasticizing agent in acrylic based polishes, defoamer agent in acrylics, “knockdown” defoamer in paint, textile and paper and as a halide free flame retardant in polymer systems.
Tris(2-Butoxyethyl) Phosphate (TBEP) is an organic flame retardant.

Tris(2-Butoxyethyl) Phosphate (TBEP) is also used to add flexibility in vinyl resins, other plastics, natural and synthetic rubbers, and floor finishes and waxes.
Tris(2-Butoxyethyl) Phosphate (TBEP) is a flame-retardant plasticizer.
Tris(2-Butoxyethyl) Phosphate (TBEP) is mainly used for flame-retardant and plasticizing of polyurethane resin, cellulose, polyvinyl alcohol, etc.

Tris(2-Butoxyethyl) Phosphate (TBEP) has good low-temperature characteristic.
Tris(2-Butoxyethyl) Phosphate (TBEP) can be obtained by the reaction of the reaction of phosphorus oxychloride and 2-butoxyethanol .
Tris(2-Butoxyethyl) Phosphate (TBEP) is a flammable, hardly inflammable, colorless to yellowish liquid that is sparingly soluble in water.

Tris(2-Butoxyethyl) Phosphate (TBEP) is used as an organic flame retardant , as well as in floor care products, as a solvent in resins, as a viscosity modifier in plastisols and as a plasticizer in rubber stoppers.
Tris(2-Butoxyethyl) Phosphate (TBEP)is mainly used as floor polishing agent and processing agent of water-based adhesive, flame retardant and plasticizer of acrylonitrile type rubber, cellulose acetate, epoxy resin, ethyecellulose, polyvinyl acetate, thermoplastic and thermosetting polyurethane.
Tris(2-Butoxyethyl) Phosphate (TBEP) is also used as defoamer in coating, detergent and textiles.

Moreover, Tris(2-Butoxyethyl) Phosphate (TBEP) can be also used in nitrocellulose, ethyecellulose and acrylic plastic plasticizer.
Tris(2-Butoxyethyl) Phosphate (TBEP) is a chemical compound commonly used as a flame retardant and plasticizer in various industrial products.
Tris(2-Butoxyethyl) Phosphate (TBEP) is added to materials like plastics, rubber, and textiles to make them less flammable and more flexible.

Tris(2-Butoxyethyl) Phosphate (TBEP) can also be found in hydraulic fluids, lubricants, and as a solvent in certain chemical processes.
While it provides important functional properties to these products, concerns have been raised about its potential environmental and health impacts.
Tris(2-Butoxyethyl) Phosphate (TBEP) has been studied for its persistence in the environment and possible toxicity to aquatic organisms.

As a result, regulations and guidelines regarding its use and disposal may vary depending on the region.
Tris(2-Butoxyethyl) Phosphate (TBEP) is also used as a halogen free flame retardant additive in polymer systems.
Tris(2-Butoxyethyl) Phosphate (TBEP) can be used also in conjunction with other flame retardants.

Tris(2-Butoxyethyl) Phosphate (TBEP) is a light-colored, high-boiling, non-flammable viscous liquid.
Tris(2-Butoxyethyl) Phosphate (TBEP) is generally used as a plasticizer in rubber and plastics, and aids in floor polish formation (as well as in other surface coatings), leveling and improves gloss.
Tris(2-Butoxyethyl) Phosphate (TBEP) is used as a plasticizer for PVC, chlorinated rubber, and nitriles due to its flame retardant nature and good low temperature flexibility.

Tris(2-Butoxyethyl) Phosphate (TBEP) is also used for emulsions of floor polishes, as leveling agent in latex paints and waxes, a processing aid for acrylonitrile rubber, and an antiblock agent for cast polyurethanes.
Tris(2-Butoxyethyl) Phosphate (TBEP) is a plasticizer for polyvinyl chloride (PVC), chlorinated rubber and nitriles.
Tris(2-Butoxyethyl) Phosphate (TBEP) is also an alkyl phosphate flame retardant and has good heat stability.

Tris(2-Butoxyethyl) Phosphate (TBEP) can be used in applications needing low temperature flexibility such as a leveling agent for acrylic resin-based polishes.
Tris(2-Butoxyethyl) Phosphate (TBEP) can also be used for emulsions of floor finishes, leveling agent in latex paint, a processing aid for acrylonitrile rubber, antiblock agent for cast polyurethanes.
As a plasticizer, Tris(2-Butoxyethyl) Phosphate (TBEP) incorporates readily and is a non-reactive, medium viscosity liquid.

Tris(2-Butoxyethyl) Phosphate (TBEP) is high solvency makes it a great product for natural and synthetic resins and compatible with waxes.
Tris(2-Butoxyethyl) Phosphate (TBEP) is used commercially in floor polishes, paper coatings and as an antifoaming agent in ore beneficiations.
Tris(2-Butoxyethyl) Phosphate (TBEP) also finds uses in vinyl plastics.

Tris(2-Butoxyethyl) Phosphate (TBEP) is a clear, colorless liquid.
Tris(2-Butoxyethyl) Phosphate (TBEP) is a phosphine oxide and thus very stable in nature.
Tris(2-Butoxyethyl) Phosphate (TBEP) has many applications including plasticizing agent in acrylic based polishes, defoamer agent in acrylics, “knockdown” defoamer in paint, textile and paper and as a halide free flame retardant in polymer systems.

Tris(2-Butoxyethyl) Phosphate (TBEP) is used as a plasticizer for polymer dispersions and also improves wetting-levelling properties of drybright emulsions.
Tris(2-Butoxyethyl) Phosphate (TBEP) is a trialkyl phosphate in which the alkyl group specified is 2-butoxyethyl.
Tris(2-Butoxyethyl) Phosphate (TBEP) has a role as an environmental contaminant and a flame retardant.

Tris(2-Butoxyethyl) Phosphate (TBEP) is a slightly yellow viscous liquid.
Tris(2-Butoxyethyl) Phosphate (TBEP) is an organic flame retardant.

Tris(2-Butoxyethyl) Phosphate (TBEP) shows PXR agonistic activity.
Tris(2-Butoxyethyl) Phosphate (TBEP) was detected and quantified during the analysis of herring gull eggs by liquid chromatography-electrospray ionization(+)-tandem mass spectrometry.

Melting point: -70°C
Boiling point: 215-228 °C4 mm Hg(lit.)
Density: 1.006 g/mL at 25 °C(lit.)
vapor density: 13.7 (vs air)
vapor pressure: 0.03 mm Hg ( 150 °C)
refractive index: n20/D 1.438(lit.)
Flash point: >230 °F
storage temp.:Store at -20°C
solubility: Chloroform (Slightly), DMSO (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly)
form: Liquid
color: Clear colorless to very slightly yellow
Water Solubility: Soluble
Stability: Stable. Combustible. Incompatible with strong oxidizing agents.
InChIKey: WTLBZVNBAKMVDP-UHFFFAOYSA-N
LogP: 3.75 at 20℃

Tris(2-Butoxyethyl) Phosphate (TBEP) is widely used as a flame retardant additive in plastics, textiles, and other materials.
Tris(2-Butoxyethyl) Phosphate (TBEP) works by reducing the flammability of these materials, making them safer in applications where fire hazards are a concern.
In addition to its flame retardant properties, Tris(2-Butoxyethyl) Phosphate (TBEP) also serves as a plasticizer, improving the flexibility and workability of polymers and plastics.

This makes it valuable in manufacturing processes where flexibility is desired.
Tris(2-Butoxyethyl) Phosphate (TBEP) finds use in diverse industrial applications beyond flame retardancy and plasticization.
It is employed in products such as hydraulic fluids, lubricants, coatings, and adhesives.

Like many organophosphate compounds, Tris(2-Butoxyethyl) Phosphate (TBEP) has raised environmental and health concerns.
Its persistence in the environment and potential toxicity to aquatic organisms have prompted regulatory scrutiny and efforts to find safer alternatives.
Regulations governing the use of Tris(2-Butoxyethyl) Phosphate (TBEP) vary by region.

In some jurisdictions, its use may be restricted or subject to specific labeling and handling requirements to minimize environmental and human health risks.
There is ongoing research into alternative flame retardants and plasticizers that offer comparable performance while addressing environmental and health concerns associated with TBEP and similar compounds.
Oral exposure to low-dose Tris(2-Butoxyethyl) Phosphate (TBEP) levels equivalent to tolerable daily intake may exacerbate allergic pulmonary inflammation by promoting a skewed T-helper 2 cell response, upregulation of ERα and dysregulation of both MLN and BM microenvironments.

Tris(2-Butoxyethyl) Phosphate (TBEP) is a trialkyl phosphate in which the alkyl group specified is 2-butoxyethyl.
Tris(2-Butoxyethyl) Phosphate (TBEP) has a role as an environmental contaminant and a flame retardant.
Tris(2-Butoxyethyl) Phosphate (TBEP) is a slightly yellow viscous liquid.

Tris(2-Butoxyethyl) Phosphate (TBEP) is an alkyl phosphate flame retardant and plasticizer, specifically tris(butoxyethyl) phosphate.
Tris(2-Butoxyethyl) Phosphate (TBEP) is recommended fo use as a plasticizer for PVC, chlorinated rubber and for nitrile.
Tris(2-Butoxyethyl) Phosphate (TBEP) is often used as a leveling agent in floor polishes, as a leveling agent in paints, and as an antiblock agent for cast polyurethanes.

Tris(2-Butoxyethyl) Phosphate (TBEP) exhibits low viscosity (12 cps).
Tris(2-Butoxyethyl) Phosphate (TBEP) contains 7.8% phosphorous.
Tris(2-Butoxyethyl) Phosphate (TBEP) is a plasticizer for polyvinyl chloride (PVC), chlorinated rubber and nitriles.

Tris(2-Butoxyethyl) Phosphate (TBEP) is also an alkyl phosphate flame retardant and has good heat stability.
Tris(2-Butoxyethyl) Phosphate (TBEP) can be used in applications needing low temperature flexibility such as a leveling agent for acrylic resin-based polishes.
Tris(2-Butoxyethyl) Phosphate (TBEP) can also be used for emulsions of floor finishes, leveling agent in latex paint, a processing aid for acrylonitrile rubber, antiblock agent for cast polyurethanes.

As a plasticizer, Tris(2-Butoxyethyl) Phosphate (TBEP), incorporates readily and is a non-reactive, medium viscosity liquid.
Tris(2-Butoxyethyl) Phosphate (TBEP)s high solvency makes it a great product for natural and synthetic resins and compatible with waxes.
Tris(2-Butoxyethyl) Phosphate (TBEP) is used commercially in floor polishes, paper coatings and as an antifoaming agent in ore beneficiations.

Tris(2-Butoxyethyl) Phosphate (TBEP) also finds uses in vinyl plastics.
Tris(2-Butoxyethyl) Phosphate (TBEP) is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 1 000 to < 10 000 tonnes per annum.
Tris(2-Butoxyethyl) Phosphate (TBEP) is used by consumers, in articles, by professional workers (widespread uses), in formulation or repacking and at industrial sites.

Tris(2-Butoxyethyl) Phosphate (TBEP) is a phosphate ester that, thanks to its structure, can be used in many applications including plasticisation, solvation, flame retardancy and defoaming.
Tris(2-Butoxyethyl) Phosphate (TBEP) is in fact a multifunctional additive that may be used to modify the properties of many polymer systems and is a particularly good levelling aid and coalescent additive for emulsion polymers.
Tris(2-Butoxyethyl) Phosphate (TBEP) is used in a mixed solvent/aqueous system as a defoamer during production and as a secondary plasticiser in many polymers.

The above properties in combination with inherent flame retardancy makes Tris(2-Butoxyethyl) Phosphate (TBEP) a real multifunctional additive essential to many polymer formulations.
Tris(2-Butoxyethyl) Phosphate (TBEP) is widely used in household materials such as plasticizer, floor polish and flame retardant in plastic resins and synthetic rubbers.
Tris(2-Butoxyethyl) Phosphate (TBEP)-based is a plasticizer and defoamer.
Tris(2-Butoxyethyl) Phosphate (TBEP) also acts as a leveling agent for acrylic and styrenic floor polishes and coalescent additive for emulsion polymers.

Tris(2-Butoxyethyl) Phosphate (TBEP) is valued for its effectiveness as a flame retardant.
Tris(2-Butoxyethyl) Phosphate (TBEP) works by reducing the flammability of materials, thereby slowing down or preventing the spread of fire.
In addition to its flame retardant properties, Tris(2-Butoxyethyl) Phosphate (TBEP) acts as a plasticizer, improving the flexibility and durability of various materials, particularly plastics and polymers.

Tris(2-Butoxyethyl) Phosphate (TBEP) is commonly used in a wide range of industrial applications, including the production of automotive parts, electrical cables, construction materials, and textiles.
Due to concerns about its potential environmental persistence and toxicity, Tris(2-Butoxyethyl) Phosphate (TBEP) has been subject to regulatory scrutiny in some regions.
Regulatory agencies may impose restrictions on its use or require labeling and handling precautions.

Tris(2-Butoxyethyl) Phosphate (TBEP) provides important functional benefits, it is essential to handle it with care.
Occupational exposure should be minimized, and appropriate safety measures should be followed during handling, storage, and disposal.
In response to regulatory concerns and evolving industry standards, researchers and manufacturers are exploring alternative flame retardants and plasticizers that offer comparable performance while minimizing environmental and health risks.

Uses Of Tris(2-Butoxyethyl) Phosphate (TBEP):
Tris(2-Butoxyethyl) Phosphate (TBEP) may be used as an analytical reference standard for the quantification of the analyte in herring gull eggs, house dust, and urine samples using liquid chromatography technique.
Primary plasticizer for most resins and elastomers, floor finishes and waxes, flame-retarding agent.
Tris(2-Butoxyethyl) Phosphate (TBEP) is a solvent and plasticizer for cellulose esters such as nitrocellulose and cellulose acetate.

Tris(2-Butoxyethyl) Phosphate (TBEP) forms stable hydrophobic complexes with some metals; these complexes are soluble in organic solvents as well as supercritical CO2.
The major uses of Tris(2-Butoxyethyl) Phosphate (TBEP) in industry are as a component of aircraft hydraulic fluid, brake fluid, and as a solvent for extraction and purification of rare-earth metals from their ores.
Tris(2-Butoxyethyl) Phosphate (TBEP) finds its use as a solvent in inks, synthetic resins, gums, adhesives (namely for veneer plywood), and herbicide and fungicide concentrates.

As Tris(2-Butoxyethyl) Phosphate (TBEP) has no odour is used as an anti-foaming agent in detergent solutions, and in various emulsions, paints, and adhesives.
Tris(2-Butoxyethyl) Phosphate (TBEP) is also found as a de-foamer in ethylene glycol-borax antifreeze solutions.
In oil-based lubricants addition of Tris(2-Butoxyethyl) Phosphate (TBEP) increases the oil film strength.

Tris(2-Butoxyethyl) Phosphate (TBEP) is used also in mercerizing liquids, where it improves their wetting properties.
Tris(2-Butoxyethyl) Phosphate (TBEP) can be used as a heat-exchange medium.
Tris(2-Butoxyethyl) Phosphate (TBEP) is used in some consumer products such as herbicides and water-thinned paints and tinting bases.

Release to the environment of Tris(2-Butoxyethyl) Phosphate (TBEP) can occur from industrial use: as processing aid and of substances in closed systems with minimal release.
Other release to the environment of Tris(2-Butoxyethyl) Phosphate (TBEP) is likely to occur from: indoor use as processing aid, indoor use in long-life materials with low release rate (e.g. flooring, furniture, toys, construction materials, curtains, foot-wear, leather products, paper and cardboard products, electronic equipment), outdoor use as processing aid and outdoor use in long-life materials with low release rate (e.g. metal, wooden and plastic construction and building materials).

Tris(2-Butoxyethyl) Phosphate (TBEP) can be found in products with material based on: wood (e.g. floors, furniture, toys), plastic (e.g. food packaging and storage, toys, mobile phones) and paper (e.g. tissues, feminine hygiene products, nappies, books, magazines, wallpaper).
Tris(2-Butoxyethyl) Phosphate (TBEP) is used in the following products: plant protection products, hydraulic fluids, lubricants and greases, metal working fluids, washing & cleaning products and polishes and waxes.
Tris(2-Butoxyethyl) Phosphate (TBEP) has an industrial use resulting in manufacture of another substance (use of intermediates).

Tris(2-Butoxyethyl) Phosphate (TBEP) is used in the following areas: agriculture, forestry and fishing and formulation of mixtures and/or re-packaging.
Tris(2-Butoxyethyl) Phosphate (TBEP) is used in the following products: polymers and textile treatment products and dyes.
Release to the environment of Tris(2-Butoxyethyl) Phosphate (TBEP) can occur from industrial use: formulation in materials and formulation of mixtures.

Tris(2-Butoxyethyl) Phosphate (TBEP) is used in the following products: polymers, textile treatment products and dyes and washing & cleaning products.
Tris(2-Butoxyethyl) Phosphate (TBEP) is used for the manufacture of: plastic products and textile, leather or fur.
Release to the environment of Tris(2-Butoxyethyl) Phosphate (TBEP) can occur from industrial use: in the production of articles, as processing aid and in processing aids at industrial sites.

One of the primary uses of Tris(2-Butoxyethyl) Phosphate (TBEP) is as a flame retardant additive in various materials such as plastics, rubber, textiles, and coatings.
Tris(2-Butoxyethyl) Phosphate (TBEP) reduces the flammability of these materials, making them less likely to catch fire or spread flames.
Tris(2-Butoxyethyl) Phosphate (TBEP) also acts as a plasticizer, improving the flexibility, durability, and workability of plastics and polymers.

Tris(2-Butoxyethyl) Phosphate (TBEP) helps to enhance the processing properties of these materials during manufacturing.
Tris(2-Butoxyethyl) Phosphate (TBEP) is utilized as an additive in lubricants and hydraulic fluids to improve their lubricating properties and thermal stability.
Tris(2-Butoxyethyl) Phosphate (TBEP) helps to reduce friction and wear in mechanical systems.

In some chemical processes, Tris(2-Butoxyethyl) Phosphate (TBEP) serves as a solvent or carrier for other substances.
It can facilitate the dissolution and dispersion of various compounds in solution.
Tris(2-Butoxyethyl) Phosphate (TBEP) is incorporated into coatings, sealants, and adhesives to improve their performance properties.

It can enhance adhesion, flexibility, and resistance to heat and chemicals.
In the textile industry, Tris(2-Butoxyethyl) Phosphate (TBEP) may be used as a finishing agent to impart flame retardant properties to fabrics and garments.
It helps textiles meet flame resistance standards for safety applications.

Tributoxy ethyl phosphate (TBEP) also helps to improve pigment wetting and rheological properties with a minimal effect on reflectance Tributoxy ethyl phosphate (TBEP) is a highly effective "knockdown" defoamer used extensively in paint, textile and paper industries.
Tributoxy ethyl phosphate (TBEP) is also used as a halogen free flame retardant additive in polymer systems. It can be used also in conjunction with other flame retardants.

Tris(2-Butoxyethyl) Phosphate (TBEP) is used as an additive flame retardant and plasticizer in plastics and synthetic rubbers.
Tris(2-Butoxyethyl) Phosphate (TBEP) is a phosphate ester that, thanks to its structure, can be used in many applications including plasticisation, solvation, flame retardancy and defoaming.
Tris(2-Butoxyethyl) Phosphate (TBEP) is in fact a multifunctional additive that may be used to modify the properties of many polymer systems and is a particularly good levelling aid and coalescent additive for emulsion polymers.

Tris(2-Butoxyethyl) Phosphate (TBEP) is used in a mixed solvent/aqueous system as a defoamer during production and as a secondary plasticiser in many polymers.
The above properties in combination with inherent flame retardancy makes Tris(2-Butoxyethyl) Phosphate (TBEP) a real multifunctional additive essential to many polymer formulations.
Tris(2-Butoxyethyl) Phosphate (TBEP) is used as a plasticizer for PVC, chlorinated rubber, and nitriles due to its flame retardant nature and good low temperature flexibility.

Tris(2-Butoxyethyl) Phosphate (TBEP) is also used for emulsions of floor polishes, as leveling agent in latex paints and waxes, a processing aid for acrylonitrile rubber, and an antiblock agent for cast polyurethanes.
Tris(2-Butoxyethyl) Phosphate (TBEP) is commonly used in the production of polyurethane foam, PVC, and other types of plastics.
Tris(2-Butoxyethyl) Phosphate (TBEP) is effective in reducing the flammability of these materials and improving their fire safety.

Tris(2-Butoxyethyl) Phosphate (TBEP) is used as a flame retardant for textiles such as curtains, upholstery, and carpets.
It can also be used in the production of flame-resistant clothing for firefighters and other workers in high-risk environments.
Tris(2-Butoxyethyl) Phosphate (TBEP) is used in the production of electronic components such as circuit boards and cables.

Tris(2-Butoxyethyl) Phosphate (TBEP) helps to reduce the risk of fire and improve the safety of electronic devices.
Tris(2-Butoxyethyl) Phosphate (TBEP) is used in the production of rubber products such as tires, gaskets, and seals.
It can improve the fire safety of these products and reduce the risk of fire in industrial settings.

Tris(2-Butoxyethyl) Phosphate (TBEP) may be used as an analytical reference standard for the quantification of the analyte in herring gull eggs, house dust, and urine samples using liquid chromatography technique.
Primary plasticizer for most resins and elastomers, floor finishes and waxes, flame-retarding agent.
Tris(2-Butoxyethyl) Phosphate (TBEP) is commonly added to paints, coatings, and varnishes to improve their fire resistance and durability.

It helps these products adhere better to surfaces and provides a protective barrier against fire damage.
Tris(2-Butoxyethyl) Phosphate (TBEP) is used as an additive in adhesives and sealants to enhance their bonding strength and flexibility.
It helps prevent the material from becoming brittle over time and improves its resistance to fire.

Tris(2-Butoxyethyl) Phosphate (TBEP) is incorporated into the insulation of electrical wires and cables to reduce the risk of fire propagation in case of a short circuit or overheating.
Tris(2-Butoxyethyl) Phosphate (TBEP) helps maintain the integrity of the insulation and prevents electrical fires.
Tris(2-Butoxyethyl) Phosphate (TBEP) is sometimes used in the production of polyurethane foam, particularly in applications where fire safety is a concern, such as upholstered furniture and mattresses.

It improves the foam's fire resistance without compromising its mechanical properties.
Tris(2-Butoxyethyl) Phosphate (TBEP) can be added to rubber compounds to increase their flame retardancy and flexibility.
It is commonly used in the production of rubber goods such as gaskets, seals, and hoses for various industrial applications.

Tris(2-Butoxyethyl) Phosphate (TBEP) may be included in construction materials such as insulation boards, roofing materials, and sealants to meet fire safety standards and regulations.
It helps prevent the spread of fire in buildings and structures.

Tris(2-Butoxyethyl) Phosphate (TBEP) is used in the manufacturing of automotive components, including dashboards, interior trims, and upholstery, to improve their fire resistance and durability.
Tris(2-Butoxyethyl) Phosphate (TBEP) helps ensure compliance with automotive safety standards.

Safety Profile:
Tris(2-Butoxyethyl) Phosphate (TBEP) may cause irritation to the skin, eyes, and respiratory tract upon contact or inhalation of its vapors or aerosols.
Prolonged or repeated exposure may lead to more severe health effects, including dermatitis, respiratory irritation, and allergic reactions.
While Tris(2-Butoxyethyl) Phosphate (TBEP)'s acute toxicity is relatively low, chronic exposure to high concentrations may pose health risks.

Animal studies suggest potential adverse effects on the liver, kidneys, and reproductive system, although more research is needed to fully understand its long-term toxicity in humans.
Tris(2-Butoxyethyl) Phosphate (TBEP) is considered persistent in the environment and may bioaccumulate in aquatic organisms.
It can pose risks to aquatic ecosystems and wildlife, particularly in areas where it is released into waterways or accumulates in sediment.

Despite being used as a flame retardant, Tris(2-Butoxyethyl) Phosphate (TBEP) itself is combustible.
Tris(2-Butoxyethyl) Phosphate (TBEP) may contribute to the spread of fire if not properly contained or managed, posing fire hazards in manufacturing facilities, storage areas, or during transportation.
TRIS(2-CHLOROETHYL) PHOSPHATE (TCEP)
Tris(2-chloroethyl) phosphate (TCEP) has excellent flame retardance, cold resistance, and UV resistance.
Tris(2-chloroethyl) phosphate (TCEP) is an odorless clear liquid.


CAS Number: 115-96-8
EC Number: 204-118-5
MDL number: MFCD00000967
Chemical formula: C6H12Cl3O4P
Molecular Formula: C6H12Cl3O4P / (ClCH2CH2O)3PO



SYNONYMS:
Tris(2-chloroethyl) phosphate, 115-96-8, Tri(beta-chloroethyl) phosphate, Tris(2-chloroethyl) orthophosphate, TRIS(2-CHLOROETHYL) PHOSPHATE, Tris(2-chloroethyl)phosphate, Celluflex, Fyrol CEF, Disflamoll TCA, Celluflex CEF, Tris(chloroethyl) phosphate, Niax 3CF, Tris(chloroethyl)phosphate, Trichlorethyl phosphate, 2-Chloroethanol phosphate, TRI(2-CHLOROETHYL) PHOSPHATE, Niax Flame Retardant 3CF, Ethanol, 2-chloro-, phosphate (3:1), Ethanol, 2-chloro-, 1,1',1''-phosphate, Tris(beta-chloroethyl) phosphate, NCI-C60128, Tris-(2-chlorethyl)fosfat, NSC 3213, DTXSID5021411, Phosphoric Acid Tris(2-chloroethyl) Ester, Phosphoric acid, tris(2-chloroethyl)ester, Tri(.beta.-chloroethyl) phosphate, Phosphoric acid, tris(2-chloroethyl) ester, 68411-66-5, CHEBI:35037, 32IVO568B0, Tris(.beta.-chloroethyl) phosphate, NSC-3213, 29716-44-7, Genomoll P, 3CF, Antiblaze 100, DTXCID601411, Tris(2-chloroethyl) phosphate 10 microg/mL in Cyclohexane, Fyrol CF, Tri(2-chloroethyl)phosphate, C6H12Cl3O4P, CAS-115-96-8, Tri-beta-chloroethyl phosphate, CCRIS 1302, HSDB 2577, Tris-(2-chlorethyl)fosfat [Czech], EINECS 204-118-5, Tris-(2-chloroethyl)fosfat [Czech], Tris-(2-chloroethyl)fosfat, BRN 1710938, UNII-32IVO568B0, AI3-15023, Tris(|A-chloroethyl) phosphate, 2-Chloro-ethanol phosphate (3:1), EINECS 249-806-6, EC 204-118-5, SCHEMBL26896, Tris(-chloroethyl) phosphate, 4-01-00-01379 (Beilstein Handbook Reference), MLS001056210, BIDD, , tris(2-chloroethyl)-phosphate, tri-(2-chloroethyl) phosphate, CHEMBL1413786, Tri-.beta.-chloroethyl phosphate, WLN: G2OPO & O2GO2G, NSC3213, EINECS 270-139-1, Tox21_201254, Tox21_300074, MFCD00000967, Tris(2-chloroethyl) phosphate, 97%, AKOS009029110, NCGC00091566-01, NCGC00091566-02, NCGC00091566-03, NCGC00254139-01, NCGC00258806-01, Phosphoric acid, tri-2-chloroethyl ester, SMR001216601, CS-0030742, NS00010387, P0268, T3447, EN300-19161, TRIS(2-CHLOROETHYL) PHOSPHATE [HSDB], TRIS(2-CHLOROETHYL) PHOSPHATE [IARC], Tris(2-chloroethyl) phosphate, analytical standard, J-003352, Q1670500, Tris(2-chloroethyl) phosphate, certified reference material, TraceCERT(R), InChI=1/C6H12Cl3O4P/c7-1-4-11-14(10,12-5-2-8)13-6-3-9/h1-6H, Phosphoric acid tris(2-chloroethyl) ester, Phosphoric acid, tris(2-chloroethyl)ester, Tri(2-chloroethyl) phosphate, Tris(2-chloroethyl) orthophosphate, Tris(2-chloroethyl)phosphic acid, Tris(beta-chloroethyl) phosphate, Tris(chloroethyl)phosphate, Tris(β-chloroethyl) phosphate; TCEP; tris(1-chloroethyl) phosphate, TCEP, TRIS(2-CHLOROETHYL)PHOSPHATE, tris(chloroethyl)phosphate, Tris(chloroethyl) phosphate, TRIS(2-CHLOROETHYL)PHOSPHATE 97%, Phosphorsuretris-(2-chlorethyl)-ester, 3CF, niax3cf, Fyrol CF, fyrolcef, 2-Chloroethanol phosphate, Tris(β-chloroethyl) phosphate, Tri(2-chloroethyl) phosphate, Tris(2-chloroethyl) orthophosphate, TCEP, Ethanol, 2-chloro-, phosphate (3:1), Celluflex CEF, Disflamoll TCA, Fyrol CEF, Niax Flame Retardant 3CF, Niax 3CF, Tri(β-chloroethyl) phosphate, Trichloroethyl phosphate, Tris(β-chloroethyl) phosphate, Tris(chloroethyl) phosphate, Tris(2-chloroethyl) orthophosphate, Tris(2-chloroethyl) phosphate, 3CF, Celluflex, Phosphoric acid, tris(2-chloroethyl) ester, Trichlorethyl phosphate, 2-Chloroethanol phosphate, NCI-C60128, Tris-(2-chlorethyl)fosfat, 2-Chloro-ethanol phosphate (3:1), Fyrol CF, Genomoll P, TCEP, Phosphoric acid, tri-2-chloroethyl ester, NSC 3213



Tris(2-chloroethyl) phosphate (TCEP) is a clear transparent liquid with a very slight odor. Insoluble in water.
Tris(2-chloroethyl) phosphate (TCEP) has excellent flame retardance, cold resistance, and UV resistance.
Tris(2-chloroethyl) phosphate (TCEP) is a chemical compound used as a flame retardant, plasticizer, and viscosity regulator in various types of polymers including polyurethanes, polyester resins, and polyacrylates.


Tris(2-chloroethyl) phosphate (TCEP) belongs to the class of organic compounds known as trialkyl phosphates.
These are organic compounds containing a phosphate group that is linked to exactly three alkyl chains.
Tris(2-chloroethyl) phosphate (TCEP) has excellent flame retartance, cold resistance and UV resistance.


Tris(2-chloroethyl) phosphate (TCEP) is an organophosphate triester compound used in solid-phase microextractions
Tris(2-chloroethyl) phosphate (TCEP) is a chemical compound used as a flame retardant, plasticizer, and viscosity regulator in various types of polymers including polyurethanes, polyester resins, and polyacrylates.


Tris(2-chloroethyl) phosphate (TCEP) is registered under the REACH Regulation but is not currently being manufactured in and / or imported to the European Economic Area.
Tris(2-chloroethyl) phosphate (TCEP) is an odorless clear liquid.


Tris(2-chloroethyl) phosphate (TCEP) is a trialkyl phosphate that is the tris(2-chloroethyl) ester of phosphoric acid.
Tris(2-chloroethyl) phosphate (TCEP) is a trialkyl phosphate and an organochlorine compound.
Tris(2-chloroethyl) phosphate (TCEP) is a chemical compound used as a flame retardant, plasticizer, and viscosity regulator in various types of polymers including polyurethanes, polyester resins, and polyacrylates.


Tris(2-chloroethyl) phosphate (TCEP) has been added to polyurethane foams and plastics in:
*Certain children’s products with foam padding, such as some crib bumpers, sleep mats, changing table pads, and portable mattresses.
*Some motor vehicles, furniture, building insulation, back-coatings of carpets and upholstery, and electronic and electrical devices.


Ethanol, 2-chloro-, phosphate (3:1), also known as Tris(2-chloroethyl) phosphate (TCEP), is an industrial chemical.
Tris(2-chloroethyl) phosphate (TCEP) is a colorless or light yellow oily liquid with a light cream odor.
Tris(2-chloroethyl) phosphate (TCEP) is slightly soluble in water, easily soluble in alcohols, ketones, aromatic hydrocarbon, but insoluble in an aliphatic hydrocarbon.


Tris(2-chloroethyl) phosphate (TCEP) is also called petroleum additive and an extractant of rare-earth elements.
Tris(2-chloroethyl) phosphate (TCEP) is a clear, transparent liquid. Slightly water soluble.
Tris(2-chloroethyl) phosphate (TCEP) is a human urinary organophosphate flame retardant metabolite.


Tris(2-chloroethyl) phosphate (TCEP) is a trialkyl phosphate that is the tris(2-chloroethyl) ester of phosphoric acid.
Tris(2-chloroethyl) phosphate (TCEP) is a odorless clear liquid. Neutral pH.
Tris(2-chloroethyl) phosphate (TCEP) is incompatible with strong oxidizing agents and strong bases.


Tris(2-chloroethyl) phosphate (TCEP) is a colorless or light yellow oily transparent liquid with light cream taste.
Tris(2-chloroethyl) phosphate (TCEP) is miscible with ordinary organic solvents, but insoluble in aliphatic hydrocarbons, and has good hydrolysis stability.
Tris(2-chloroethyl) phosphate (TCEP) is a flame retardant.


Tris(2-chloroethyl) phosphate (TCEP) is a halogenated phosphate ester flame retardant and plasticizer, commonly used in flame retardant paints with nitrocellulose and cellulose acetate as substrates, unsaturated polyesters, polyurethanes, acrylates, phenolic resins, etc.
Tris(2-chloroethyl) phosphate (TCEP) can be used as a soft plasticized flame retardant for PVC.



USES and APPLICATIONS of TRIS(2-CHLOROETHYL) PHOSPHATE (TCEP):
Tris(2-chloroethyl) phosphate (TCEP) is widely used in chemical and blended fabrics and cellulose acetate as fire retardant.
Tris(2-chloroethyl) phosphate (TCEP) is an organophosphate triester compound used in solid-phase microextractions
Tris(2-chloroethyl) phosphate (TCEP) has been widely used as a plasticizer and flame retardant.


Tris(2-chloroethyl) phosphate (TCEP) as a potential carcinogen is often detected in the occupational and nature environments
Tris(2-chloroethyl) phosphate (TCEP) is used as additive type halogenated phosphate ester flame retardant and plasticizer, commonly used in flame retardant paints with nitrocellulose and cellulose acetate as substrates, unsaturated polyesters, polyurethanes, acrylates, phenolic resins, etc.


Tris(2-chloroethyl) phosphate (TCEP) can be used as a soft plasticized flame retardant for PVC.
Tris(2-chloroethyl) phosphate (TCEP) is widely used in cellulose acetate, polyvinyl chloride, polyurethane, polyvinyl acetate, phenolic resins, and other synthetic materials.


In addition to its flame retardant properties, Tris(2-chloroethyl) phosphate (TCEP) also can improve the material's water resistance, cold resistance, antistatic property and softness.
Tris(2-chloroethyl) phosphate (TCEP) is widely used in chemical and blended fabrics and cellulose acetate is a fire retardant.


Tris(2-chloroethyl) phosphate (TCEP) is used in articles, by professional workers (widespread uses) and at industrial sites.
Other release to the environment of Tris(2-chloroethyl) phosphate (TCEP) is likely to occur from: outdoor use in long-life materials with low release rate (e.g. metal, wooden and plastic construction and building materials).


Tris(2-chloroethyl) phosphate (TCEP) can be found in products with material based on: stone, plaster, cement, glass or ceramic (e.g. dishes, pots/pans, food storage containers, construction and isolation material) and metal (e.g. cutlery, pots, toys, jewellery).
Tris(2-chloroethyl) phosphate (TCEP) is used in the following products: coating products.


Tris(2-chloroethyl) phosphate (TCEP) is used in the following areas: offshore mining and building & construction work.
Other release to the environment of Tris(2-chloroethyl) phosphate (TCEP) is likely to occur from: outdoor use resulting in inclusion into or onto a materials (e.g. binding agent in paints and coatings or adhesives).


Tris(2-chloroethyl) phosphate (TCEP) is used in the following products: coating products.
Tris(2-chloroethyl) phosphate (TCEP) is used in the following areas: offshore mining and building & construction work.
Release to the environment of Tris(2-chloroethyl) phosphate (TCEP) can occur from industrial use: in the production of articles.


Tris(2-chloroethyl) phosphate (TCEP) is a chemical compound used as a flame retardant, plasticizer, and viscosity regulator in various types of polymers including polyurethanes, polyester resins, and polyacrylates.
Tris(2-chloroethyl) phosphate (TCEP) is the excellent flame retardant of synthetic materials, it can be widely used in polyurethane foam, polyolefin resin, polyester resin, phenolic resin and cellulose acetate, which can make the product with self extinguishing.


Tris(2-chloroethyl) phosphate (TCEP) also can be used as the main flame retardant material for the production of flame retardant cable, tarpaulin, flame retardant rubber conveying belt and flame sponge composite.
Tris(2-chloroethyl) phosphate (TCEP) is mainly used in flame retardant of PVC, polyvinyl acetate, phenolic resin, polyurethane, cellulose acetate, cellulose nitrate, ethyecellulos.


Moreover, Tris(2-chloroethyl) phosphate (TCEP) can also be used in processing modifier of metal extractant, lubricating oil, gasoline additive and polyimide.
Tris(2-chloroethyl) phosphate (TCEP) is used as a plasticizer and viscosity regulator with flame retardant properties in polyurethanes, polyester resins, polyacrylates, and other polymers.


These polymers may be used in furniture, building (for example, roofing insulation) and textile industries (for example, back-coatings for carpets and upholstery).
Tris(2-chloroethyl) phosphate (TCEP) may also be used in electronic products and in the manufacture of cars.


Tris(2-chloroethyl) phosphate (TCEP) is not manufactured, but is imported into Canada.
Due to the good plasticization, Tris(2-chloroethyl) phosphate (TCEP) is widely used in cellulose acetate, polyvinyl acetate, nitrocellulose lacquer, ethyl cellulose, PVC, polyurethane, and phenolic resin, which all have a self-extinguish ability.
With the addition of Tris(2-chloroethyl) phosphate (TCEP), their physical properties are improved and tactilities feel soft.


Moreover, Tris(2-chloroethyl) phosphate (TCEP) is a main flame-retardant material to produce polyurethane for flame-retardant cables, anti-corrosion tarpaulin, and flame-retardant rubber converter belts.
Tris(2-chloroethyl) phosphate (TCEP) is mainly used for flame-retardant polyurethane foam and flame-retardant plasticization of PVC.


Tris(2-chloroethyl) phosphate (TCEP) is widely used in chemical fiber fabrics and cellulose acetate as flame retardants.
In addition to self-extinguishing, Tris(2-chloroethyl) phosphate (TCEP) can also improve water resistance, cold resistance and antistatic properties.
The general dosage of Tris(2-chloroethyl) phosphate (TCEP) is 5-10 parts.


Flame retardants, Tris(2-chloroethyl) phosphate (TCEP) is commonly used in lithium batteries.
Tris(2-chloroethyl) phosphate (TCEP) can also be used as metal extractant, lubricant and gasoline additives, and polyimide processing modifier.
Tris(2-chloroethyl) phosphate (TCEP) is widely used in polyvinyl chloride, polyurethane soft and rigid foam, cellulose acetate, nitrocellulose paint, ethyl cellulose paint and flame retardant rubber conveyor belt.


The obtained products have self-extinguishing properties and can improve water resistance.
Weather resistance, cold resistance, antistatic property, soft hand feel, the general addition amount is 5-10 parts, and the oxygen index (OI) of polyurethane rigid foam can reach 26.


In addition, Tris(2-chloroethyl) phosphate (TCEP) can also be used as extreme pressure additive for lubricating oil, gasoline additive and thermal coolant of metal magnesium, etc.
Tris(2-chloroethyl) phosphate (TCEP) is an excellent flame retardant of synthetic materials, and has a good plasticizer effect.


Tris(2-chloroethyl) phosphate (TCEP) is widely used in cellulose acetate, nitrocellulose varnish, ethyl cellulose, polyvinyl chloride, polyvinyl acetate, polyurethane, phenolic resin.
In addition to self extinguishing, Tris(2-chloroethyl) phosphate (TCEP) can also improve the physical properties of the product.


Tris(2-chloroethyl) phosphate (TCEP) feels soft, and can also be used as a petroleum additive and an extractant of olefinic elements, Tris(2-chloroethyl) phosphate (TCEP) is also the main flame retardant material for manufacturing flame retardant cable three proof tarpaulin and flame retardant rubber conveyor belt, with the general addition amount of 10-15%.


Tris(2-chloroethyl) phosphate (TCEP) is used as the flame retardant agent in polyurethane, plastics, polyester, textiles.
Tris(2-chloroethyl) phosphate (TCEP) has excellent flame retarding properties because of the phosphorus and chlorine content.
Tris(2-chloroethyl) phosphate (TCEP) was used in dynamic air sampling of airborne organophosphate triesters using a solid-phase microextraction device.



CHARACTERISTICS OF TRIS(2-CHLOROETHYL) PHOSPHATE (TCEP):
Tris(2-chloroethyl) phosphate (TCEP) is colorless or light yellow oily liquid, with sour cream smell, soluble with organic solvents such as alcohols, ketones, esters, aromatic hydrocarbons, chloroform and catalyst, insoluble with aliphatic hydroxyl, almost insoluble in water. It have good hydrolytic stability, it will decompose a little in sodium hydroxide solution.
Tris(2-chloroethyl) phosphate (TCEP) has excellent UV stability and low temperature performance.



PROPERTIES OF TRIS(2-CHLOROETHYL) PHOSPHATE (TCEP):
Tris(2-chloroethyl) phosphate (TCEP) is an organophosphorus flame retardant halogen compound.
Tris(2-chloroethyl) phosphate (TCEP) is not soluble in water, can dissolve in ethanol, acetone, esters, aromatics, chloroform and other organic solvents.



HOW DOES EXPOSURE TO TRIS(2-CHLOROETHYL) PHOSPHATE (TCEP) OCCUR?
Tris(2-chloroethyl) phosphate (TCEP) can be gradually released from products treated with TCEP into indoor environments, including houses, schools, day care centers, offices, and cars.
Once Tris(2-chloroethyl) phosphate (TCEP) is released from products, it is present on floors, furniture, and other surfaces, and in air and dust.
During pregnancy, TCEP can pass from mother to baby.



COMPOUND TYPE OF TRIS(2-CHLOROETHYL) PHOSPHATE (TCEP):
*Ester
*Industrial/Workplace Toxin
*Organic Compound
*Organochloride
*Plasticizer
*Synthetic Compound



ALTERNATIVE PARENTS OF TRIS(2-CHLOROETHYL) PHOSPHATE (TCEP):
*Organooxygen compounds
*Organochlorides
*Organic oxides
*Hydrocarbon derivatives
*Alkyl chlorides



SUBSTITUENTS OF TRIS(2-CHLOROETHYL) PHOSPHATE (TCEP):
*Trialkyl phosphate
*Organic oxygen compound
*Organic oxide
*Hydrocarbon derivative
*Organooxygen compound
*Organochloride
*Organohalogen compound
*Alkyl halide
*Alkyl chloride
*Aliphatic acyclic compound



PHYSICAL and CHEMICAL PROPERTIES of TRIS(2-CHLOROETHYL) PHOSPHATE (TCEP):
Chemical Formula: C₆H₁₂Cl₃O₄P
Molar Mass: 285.48 g/mol
Molecular Weight: 285.5 g/mol
Exact Mass: 283.953879 g/mol
Monoisotopic Mass: 283.953879 g/mol
Physical Properties
Density: 1.39 g/mL
Boiling Point: 192 °C (378 °F; 465 K) at 10 mmHg
Topological Polar Surface Area (PSA): 44.8 Ų
Chemical Properties
XLogP3-AA: 1.3
Hydrogen Bond Donor Count: 0
Hydrogen Bond Acceptor Count: 4

Rotatable Bond Count: 9
Heavy Atom Count: 14
Complexity: 152
Covalently-Bonded Unit Count: 1
Stereochemistry
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Isotope Atom Count: 0
Physical State: Clear liquid

Color: Colorless
Odor: No data available
Melting Point/Freezing Point: Approximately -60 °C (ASTM D 97-66)
Initial Boiling Point and Boiling Range: 192 °C at 13 hPa
Flash Point: 232 °C (closed cup)
Autoignition Temperature: No data available
Decomposition Temperature: No data available
pH: No data available
Viscosity: 38-42 mPa·s (dynamic) at 25 °C
Water Solubility: 7.943 g/L at 20 °C (soluble)
Partition Coefficient (log Pow): 1.7 at 20 °C
Vapor Pressure: < 13 hPa at 25 °C
Density: 1.39 g/cm³ at 25 °C
Refractive Index (nD25): 1.470-1.479

Chemical Properties
Acidity (mg KOH/g): ≤0.1
Moisture Content: ≤0.1%
Phosphorus Content: 10.65-10.9%
Chlorine Content: 36.5-37.5%
Color (APHA): ≤50
Additional Information
Flammability (Solid, Gas): No data available
Upper/Lower Flammability or Explosive Limits: No data available
Relative Density: No data available
Relative Vapor Density: No data available
Particle Characteristics: No data available

Explosive Properties: No data available
Oxidizing Properties: None
Other Safety Information: No data available
Appearance: Colorless to yellowish transparent liquid
Specific Gravity (20°C): 1.41-1.43
Melting Point: -51 °C
Boiling Point: 192 °C/10 mmHg (lit.)
Density: 1.39 g/mL at 25 °C (lit.)
Vapor Pressure: Refractive Index (nD20): 1.472 (lit.)
Flash Point: 450 °F (approximately 232 °C)

Storage Temperature: 2-8 °C
Form: Liquid
Color: Clear colorless
Viscosity (25°C): 38-42 mPa·s (dynamic)
Water Content: ≤0.3%
Chemical Properties
Molecular Formula: C₆H₁₂Cl₃O₄P
Molecular Weight: 285.49 g/mol
Acid Content: ≤0.1 mg KOH/g
Water Solubility: 7.82 g/L at 20 °C
LogP: 1.7 at 20 °C
Stability: Stable. Incompatible with strong bases, strong oxidizing agents.
Color Value: 50 max

Safety and Regulatory Information
InChIKey: HQUQLFOMPYWACS-UHFFFAOYSA-N
FDA 21 CFR: 175.105
CAS Number: 115-96-8
FDA UNII: 32IVO568B0
Proposition 65 List: Tris(2-chloroethyl) Phosphate
IARC Classification: 3 (Vol. 48, 71) 1999
NIST Chemistry Reference: Phosphoric acid, tri-2-chloroethyl ester (115-96-8)
EPA Substance Registry System: Tris(2-chloroethyl) phosphate (115-96-8)
EWG's Food Scores: 1
Additional Information

Acidity (mg KOH/g): 0.2 max
Flash Point (°C): 220 min
Phosphorus Content: 10.7-10.8%
Specific Gravity (20°C): 1.420-1.440
Appearance: Colorless or light yellow oily transparent liquid
Physical State: Liquid
Density: 1.39 g/mL at 25 °C (lit.)
Refractive Index (nD20): 1.4731
Boiling Point: 194 °C
Flash Point: 225 °C
Freezing Point: -64 °C
Decomposition Temperature: 240-280 °C
Viscosity: 38-47 cP (20 °C)

Storage: Store at room temperature
Chemical Properties
Chemical Formula: C₆H₁₂Cl₃O₄P
Average Molecular Mass: 285.490 g/mol
Monoisotopic Mass: 283.954 g/mol
Phosphorus Content: 10.8%
Chlorine Content: 37.3%
SMILES: ClCCOP(=O)(OCCCl)OCCCl
IUPAC Name: Tris(2-chloroethyl) phosphate
Traditional Name: Tris(2-chloroethyl) phosphate
InChI Identifier: InChI=1S/C6H12Cl3O4P/c7-1-4-11-14(10,12-5-2-8)13-6-3-9/h1-6H2
InChI Key: HQUQLFOMPYWACS-UHFFFAOYSA-N



FIRST AID MEASURES of TRIS(2-CHLOROETHYL) PHOSPHATE (TCEP):
-Description of first-aid measures
*General advice:
Show this material safety data sheet to the doctor in attendance.
*If inhaled:
After inhalation:
Fresh air.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with
water/ shower.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Call in ophthalmologist.
Remove contact lenses.
*If swallowed:
After swallowing:
Immediately make victim drink water (two glasses at most).
Consult a physician.
-Indication of any immediate medical attention and special treatment needed.
No data available



ACCIDENTAL RELEASE MEASURES of TRIS(2-CHLOROETHYL) PHOSPHATE (TCEP):
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Observe possible material restrictions.
Take up dry.
Dispose of properly.
Clean up affected area.



FIRE FIGHTING MEASURES of TRIS(2-CHLOROETHYL) PHOSPHATE (TCEP):
-Extinguishing media:
*Suitable extinguishing media:
Carbon dioxide (CO2)
Foam
Dry powder
*Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Prevent fire extinguishing water from contaminating surface water or the ground water system.



EXPOSURE CONTROLS/PERSONAL PROTECTION of TRIS(2-CHLOROETHYL) PHOSPHATE (TCEP):
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Safety glasses
*Body Protection:
protective clothing
*Respiratory protection:
Recommended Filter type: Filter A
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of TRIS(2-CHLOROETHYL) PHOSPHATE (TCEP):
-Precautions for safe handling:
*Advice on safe handling:
Work under hood.
*Hygiene measures:
Immediately change contaminated clothing.
Apply preventive skin protection.
Wash hands and face after working with substance.
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
Dry.
Tightly closed.
Keep in a well-ventilated place. Keep locked up or in an area accessible only
to qualified or authorized persons.



STABILITY and REACTIVITY of TRIS(2-CHLOROETHYL) PHOSPHATE (TCEP):
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .
-Possibility of hazardous reactions:
No data available


TRIS-(2-CHLOROISOPROPYL)-PHOSPHATE
Trioctyl phosphate; Triethylhexyl phosphate; Phosphoric acid, tris(2-ethylhexyl) ester; TOF; 2-Ethylhexanol, phosphate Triester; 2-Ethyl-1-hexanol phosphate; Tris(2-ethylhexyl)phosphate; Tris(2-ethylhexyl)phosphat (German); Fosfato de tris(2-etilhexilo) (Spanish); Phosphate de tris(2-éthylhexyle) (French); cas no: 78-42-2
TRIS(2-CHLOROPROPYL) PHOSPHATE ( TCPP)
Clear colorless viscous liquid.
Tris(2-chloropropyl) phosphate ( TCPP), mixture of isomers is suitable for use in environmental and food residue analysis.
Tris(2-chloropropyl) phosphate ( TCPP) is a mixture of isomers, composition may vary, typical composition: main isomer tris(1-chloro-2-propyl) phosphate 66%, minor components: bis(1-chloro-2-propyl) (2-chloropropyl) phosphate and (1-chloro-2-propyl) bis(2-chloropropyl) phosphate.

CAS: 13674-84-5
MF: C9H18Cl3O4P
MW: 327.57
EINECS: 237-158-7

Synonyms
Phosphoric acid tris(2-chloro-1-methylethyl) ester;TRIS(1-CHLORO-2-PROPYL) PHOSPHATE;TRIS(1-CHLOROPROPYL)PHOSPHATE;TRIS(2-CHLORO-1-METHYLETHYL) PHOSPHATE;TRIS(CHLOROISOPROPYL)PHOSPHATE;TRIS(MONOCHLOROPROPYL) PHOSPHATE;tris(2-chloroisopropyl)phosphate;TcppTris(1-Chloro-2-Propyl)Phosphate];13674-84-5;Tris(1-chloro-2-propyl) phosphate;tris(1-chloropropan-2-yl) phosphate;Amgard TMCP;TRIS(2-CHLOROISOPROPYL)PHOSPHATE;Tris(2-chloro-1-methylethyl) phosphate;Hostaflam OP 820;Tris(1-chloro-2-propyl)phosphate;2-Propanol, 1-chloro-, phosphate (3:1);TRIS(2-CHLOROISOPROPYL) PHOSPHATE;2-Propanol, 1-chloro-, 2,2',2''-phosphate;Tris(1-chloro-2-propyl) phosphate, tech grade;CRT22GFY70;Phosphoric acid, tris(2-chloro-1-methylethyl) ester;DTXSID5026259;Tris(1-chloro-2-propanyl) phosphate;DTXCID106259;CCRIS 6111;Tri-(2-chloroisopropyl)phosphate;Phosphoric acid tris(2-chloro-1-methylethyl) ester;EINECS 237-158-7;C9H18Cl3O4P;TCPP phosphate cpd;CAS-13674-84-5;BRN 1842347;TCIPP;UNII-CRT22GFY70;TCPP, Tris(1-chloro-2-propyl)phosphate;HSDB 8112;tris(2-chloro-1-methylethyl)phosphate;Flame retardant TCPP;LEVAGARD PP;TOLGARD TMCP;EC 237-158-7;SCHEMBL35713;tris(chloroisopropyl) phosphate;CHEMBL3188873;CHEBI:143728;Tox21_202982;Tox21_303533;tris(2-chloro-1-methylethyl) ester;MFCD00040408;AKOS015899872;NCGC00257407-01;NCGC00260528-01;Tris(2-chloroisopropyl)phosphate (TCPP);J50.405J;CS-0059312;FT-0689156;NS00009572;TRIS(.BETA.-CHLOROISOPROPYL) PHOSPHATE;TRIS(1-METHYL-2-CHLOROETHYL) PHOSPHATE;Flame retardant Tris(2-chloroisopropyl)phosphate;A886642;Phosphoric acid tris(2-chloro-1-methylethyl) ester;Q-201899;Q2454095;PHOSPHORIC ACID TRIS(1-CHLOROPROPANE-2-YL) ESTER;98112-32-4

Tris(2-chloropropyl) phosphate ( TCPP) is a trialkyl phosphate.
Tris(2-chloropropyl) phosphate ( TCPP)is a chlorinated organophosphate.
Organophosphate chemicals have a wide variety of applications and are used as flame retardants, pesticides, plasticizers, and nerve gases.
Tris(2-chloropropyl) phosphate ( TCPP) is structurally similar to several other organophosphate flame retardants, such as tris(2-chloroethyl) phosphate (TCEP) and tris(chloropropyl)phosphate (TCPP).
Tris(2-chloropropyl) phosphate ( TCPP) and these other chlorinated organophosphate flame retardants are all sometimes referred to as "chlorinated tris".

Presence in the environment
Tris(2-chloropropyl) phosphate ( TCPP) is an additive flame retardant, meaning that it is not chemically bonded to treated materials.
Additive flame retardants are thought to be more likely to be released into the surrounding environment during the lifetime of the product than chemically bonded, or reactive, flame retardants.
Tris(2-chloropropyl) phosphate ( TCPP) degrades slowly in the environment and is not readily removed by waste water treatment processes.

Indoors
Tris(2-chloropropyl) phosphate ( TCPP) has been detected in indoor dust, although concentrations vary widely.
A study of house dust in the U.S. found that over 96% of samples collected between 2002 and 2007 contained Tris(2-chloropropyl) phosphate ( TCPP) at an average concentration of over 1.8 ppm, while the highest was over 56 ppm. TDCPP was also detected in 99% of dust samples collected in 2009 in the Boston area from offices, homes, and vehicles.
The second study found an average concentration similar to that of the previous study but a greater range of concentrations: one sample collected from a vehicle contained over 300 ppm Tris(2-chloropropyl) phosphate ( TCPP) in the dust.
Similar concentrations have been reported for dust samples collected in Europe and Japan.

Tris(2-chloropropyl) phosphate ( TCPP) has also been measured in indoor air samples.
Tris(2-chloropropyl) phosphate ( TCPP)'s detection in air samples, however, is less frequent and generally at lower concentrations than other organophosphate flame retardants such as TCEP and TCPP, likely due to its lower vapor pressure.

Outdoors
Although Tris(2-chloropropyl) phosphate ( TCPP) is generally found at the highest concentrations in enclosed environments, such as homes and vehicles, it is widespread in the environment.
Diverse environmental samples, ranging from surface water to wildlife tissues, have been found to contain Tris(2-chloropropyl) phosphate ( TCPP).
The highest levels of contamination are generally near urban impacted areas; however, samples from even relatively remote reference sites have contained TDCPP.

Tris(2-chloropropyl) phosphate ( TCPP) Chemical Properties
Melting point: -39.9°C
Boiling point: 270°C
Density: 1.28
Refractive index: 1.460~1.466 (20℃/D)
Fp: -218 °C
Storage temp.: Sealed in dry,Room Temperature
Solubility: DMSO (Slightly), Methanol (Slightly)
Form: liquid
Color: Clear Colourless
Odor: mild odor
Water Solubility: BRN: 1842347
Stability: Moisture Sensitive
InChIKey: KVMPUXDNESXNOH-UHFFFAOYSA-N
CAS DataBase Reference: 13674-84-5(CAS DataBase Reference)
NIST Chemistry Reference: Tris(2-chloropropyl) phosphate ( TCPP) (3:1)(13674-84-5)
EPA Substance Registry System: Tris(2-chloropropyl) phosphate ( TCPP) (13674-84-5)

Tris(2-chloropropyl) phosphate ( TCPP) is clear colorless oily liquid with high water solubility and low lipophilicity (as indicated by logKOW).
Tris(2-chloropropyl) phosphate ( TCPP) ismanufactured as a reactionmixture, which contains four isomers.

Uses
Tris(2-chloropropyl) phosphate ( TCPP) is a flame retardant of low hydrolytic stability, used in polyurethane (PU) rigid and flexible foam, PVC, EVA, phenolics and epoxy resin.

Flame retardant
Until the late 1970s, Tris(2-chloropropyl) phosphate ( TCPP) was used as a flame retardant in children’s pajamas in compliance with the U.S. Flammable Fabrics Act of 1953.
This use was discontinued after children wearing fabrics treated with a very similar compound, tris(2,3-dibromopropyl) phosphate, were found to have mutagenic byproducts in their urine.

Following the 2005 phase-out of PentaBDE in the United States, Tris(2-chloropropyl) phosphate ( TCPP) became one of the primary flame retardants used in flexible polyurethane foam used in a wide variety of consumer products, including automobiles, upholstered furniture, and some baby products.
Tris(2-chloropropyl) phosphate ( TCPP) can also be used in rigid polyurethane foam boards used for building insulation.
In 2011 Tris(2-chloropropyl) phosphate ( TCPP) was reported that TDCPP was found in about a third of tested baby products.
Some fabrics used in camping equipment are also treated with Tris(2-chloropropyl) phosphate ( TCPP) to meet CPAI-84, a standard established by the Industrial Fabrics Association International to evaluate the flame resistance of fabrics and other materials used in tents.
Current total production of Tris(2-chloropropyl) phosphate ( TCPP) is not well known. In 1998, 2002, and 2006, production in the United States was estimated to be between 4,500 and 22,700 metric tons, and thus Tris(2-chloropropyl) phosphate ( TCPP) is classified as a high production volume chemical.

Toxicology
Tris(2-chloropropyl) phosphate ( TCPP) is considered a suspected carcinogenic, suspected reprotoxic, and suspected PBT (persistent, bioaccumulative and toxic) and is a potential endocrine disruptor (ECHA, 2019).
Thus, the presence of Tris(2-chloropropyl) phosphate ( TCPP) in the receiving water can affect aquatic organisms and potentially affect human health.
Tris(2-chloropropyl) phosphate ( TCPP) is probably combustible.
Tris(2-chloropropyl) phosphate ( TCPP) may hydrolyze under acidic or alkaline conditions.

Human exposure
Humans are thought to be exposed to Tris(2-chloropropyl) phosphate ( TCPP) and other flame retardants through several routes, including inhalation, ingestion, and skin contact with treated materials.
Rodent studies show that Tris(2-chloropropyl) phosphate ( TCPP) is readily absorbed through the skin and gastrointestinal tract.
Infants and young children are expected to have the highest exposure to Tris(2-chloropropyl) phosphate ( TCPP) and other indoor contaminants for several reasons.
Compared to adults, children spend more time indoors and closer to the floor, where they are exposed to higher amounts of dust particles.
In addition, they frequently put their hands and other objects into their mouths without washing.

Several studies show that Tris(2-chloropropyl) phosphate ( TCPP) can accumulate in human tissues.
Tris(2-chloropropyl) phosphate ( TCPP) has been detected in semen, fat, and breast milk, and the metabolite bis (1,3-dichloropropyl) phosphate (BDCPP) has been detected in urine.
TRIS(2-ETHYLHEXYL)PHOSPHATE
DESCRIPTION:
Tris(2-ethylhexyl)phosphate is a clear colorless to pale yellow liquid with a slight sharp odor.
Tris(2-ethylhexyl) phosphate is a trialkyl phosphate.
Tris(2-ethylhexyl) Phosphate is used as a phosphorous flame retardant.

CAS: 78-42-2
European Community (EC) Number: 201-116-6
IUPAC Name: tris(2-ethylhexyl) phosphate
Molecular Formula: C24H51O4P


USES OF TRIS (2-ETHYLHEXYL) PHOSPHATE:
Tris (2-ethylhexyl) phosphate (TEHP) has been widely used as a plasticizer, fire retardant and solvent.
As a plasticizer, Tris (2-ethylhexyl) phosphate is used as a component of vinyl stabilizers, grease additives and flame-proofing compositions for vinyl plastic and synthetic rubber compounds.
As a fire retardant, Tris (2-ethylhexyl) phosphate is used in consumer products, such as clothing.

As a solvent, Tris (2-ethylhexyl) phosphate is used as a co-solvent to produce hydrogen peroxide.
The world production of Tris (2-ethylhexyl) phosphate was estimated to be between 1000 to 5000 tons per year
Occupational exposure may occur through inhalation and dermal contact with TEHP at workplaces
The general population may be exposed to Tris (2-ethylhexyl) phosphate via ingestion of contaminated food and drinking water or via dermal contact with Tris (2-ethylhexyl) phosphate -treated clothing.

Tris(2-ethylhexyl) Phosphate is used as a phosphorous flame retardant.
Tris(2-ethylhexyl) Phosphate is Used as a plasticizer in the preparation of a new potentiometric membrane sensor.

APPLICATIONS OF TRIS(2-ETHYLHEXYL) PHOSPHATE:
Tris(2-ethylhexyl) Phosphate is a phosphate plasticizer offering excellent low temperatures properties as well as good resistance to weathering.
Tris(2-ethylhexyl) Phosphate is suitable for use in many types of polymers including flexible PVC, PUR, NBR, SBR and EPDM.

Tris(2-ethylhexyl) Phosphate is a strong, moderately polar solvent.
Tris(2-ethylhexyl) Phosphate is also used as a solvent in the production of hydrogen peroxide, as a carrier for pigments in the manufacture of pigment pastes for plastics and as an additive for mineral oils.

SAFETY INFORMATION ABOUT TRIS(2-ETHYLHEXYL)PHOSPHATE:
First aid measures:
Description of first aid measures:
General advice:
Consult a physician.
Show this safety data sheet to the doctor in attendance.
Move out of dangerous area:

If inhaled:
If breathed in, move person into fresh air.
If not breathing, give artificial respiration.
Consult a physician.
In case of skin contact:
Take off contaminated clothing and shoes immediately.
Wash off with soap and plenty of water.
Consult a physician.

In case of eye contact:
Rinse thoroughly with plenty of water for at least 15 minutes and consult a physician.
Continue rinsing eyes during transport to hospital.

If swallowed:
Do NOT induce vomiting.
Never give anything by mouth to an unconscious person.
Rinse mouth with water.
Consult a physician.

Firefighting measures:
Extinguishing media:
Suitable extinguishing media:
Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.
Special hazards arising from the substance or mixture
Carbon oxides, Nitrogen oxides (NOx), Hydrogen chloride gas

Advice for firefighters:
Wear self-contained breathing apparatus for firefighting if necessary.
Accidental release measures:
Personal precautions, protective equipment and emergency procedures
Use personal protective equipment.

Avoid breathing vapours, mist or gas.
Evacuate personnel to safe areas.

Environmental precautions:
Prevent further leakage or spillage if safe to do so.
Do not let product enter drains.
Discharge into the environment must be avoided.

Methods and materials for containment and cleaning up:
Soak up with inert absorbent material and dispose of as hazardous waste.
Keep in suitable, closed containers for disposal.

Handling and storage:
Precautions for safe handling:
Avoid inhalation of vapour or mist.

Conditions for safe storage, including any incompatibilities:
Keep container tightly closed in a dry and well-ventilated place.
Containers which are opened must be carefully resealed and kept upright to prevent leakage.
Storage class (TRGS 510): 8A: Combustible, corrosive hazardous materials

Exposure controls/personal protection:
Control parameters:
Components with workplace control parameters
Contains no substances with occupational exposure limit values.
Exposure controls:
Appropriate engineering controls:
Handle in accordance with good industrial hygiene and safety practice.
Wash hands before breaks and at the end of workday.

Personal protective equipment:
Eye/face protection:
Tightly fitting safety goggles.
Faceshield (8-inch minimum).
Use equipment for eye protection tested and approved under appropriate government standards such as NIOSH (US) or EN 166(EU).

Skin protection:
Handle with gloves.
Gloves must be inspected prior to use.
Use proper glove
removal technique (without touching glove's outer surface) to avoid skin contact with this product.
Dispose of contaminated gloves after use in accordance with applicable laws and good laboratory practices.
Wash and dry hands.

Full contact:
Material: Nitrile rubber
Minimum layer thickness: 0.11 mm
Break through time: 480 min
Material tested:Dermatril (KCL 740 / Aldrich Z677272, Size M)
Splash contact
Material: Nitrile rubber
Minimum layer thickness: 0.11 mm
Break through time: 480 min
Material tested:Dermatril (KCL 740 / Aldrich Z677272, Size M)
It should not be construed as offering an approval for any specific use scenario.

Body Protection:
Complete suit protecting against chemicals, The type of protective equipment must be selected according to the concentration and amount of the dangerous substance at the specific workplace.
Respiratory protection:
Where risk assessment shows air-purifying respirators are appropriate use a fullface respirator with multi-purpose combination (US) or type ABEK (EN 14387) respirator cartridges as a backup to engineering controls.

If the respirator is the sole means of protection, use a full-face supplied air respirator.
Use respirators and components tested and approved under appropriate government standards such as NIOSH (US) or CEN (EU).
Control of environmental exposure
Prevent further leakage or spillage if safe to do so.
Do not let product enter drains.
Discharge into the environment must be avoided.

Stability and reactivity:
Chemical stability:
Stable under recommended storage conditions.
Incompatible materials:
Strong oxidizing agents:
Hazardous decomposition products:
Hazardous decomposition products formed under fire conditions.
Carbon oxides, Nitrogen oxides (NOx), Hydrogen chloride gas.

Disposal considerations:
Waste treatment methods:
Product:
Offer surplus and non-recyclable solutions to a licensed disposal company.
Contact a licensed professional waste disposal service to dispose of this material.
Contaminated packaging:
Dispose of as unused product


CHEMICAL AND PHYSICAL PROPERTIES OF TRIS(2-ETHYLHEXYL)PHOSPHATE:
Molecular Weight: 434.6 g/mol
XLogP3-AA 8.9
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 4
Rotatable Bond Count 21
Exact Mass 434.35249710 g/mol
Monoisotopic Mass 434.35249710 g/mol
Topological Polar Surface Area 44.8Ų
Heavy Atom Count 29
Formal Charge 0
Complexity 345
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 3
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
Covalently-Bonded Unit Count 1
Compound Is Canonicalized Yes
vapor pressure: 2.1 mmHg ( 20 °C)
Quality Level: 200
Assay: 97%
refractive index: n20/D 1.444 (lit.)
bp: 215 °C/4 mmHg (lit.)
Density: 0.92 g/mL at 20 °C (lit.)
CAS number 78-42-2
EC number 201-116-6
Hill Formula C₂₄H₅₁O₄P
Chemical formula [CH₃(CH₂)₃CH(C₂H₅)CH₂O]₃PO
Molar Mass 434.63 g/mol
HS Code 2919 90 00
Boiling point 210 °C (5 hPa) decomposes
Density 0.92 g/cm3 (20 °C)
Flash point 170 °C
Ignition temperature 370 °C
Melting Point pH value 7 (H₂O, 20 °C)
Vapor pressure Solubility Chemical Formula:
C24H51O4P
Flash Point: 305°F (NTP, 1992)
Lower Explosive Limit (LEL): data unavailable
Upper Explosive Limit (UEL): data unavailable
Autoignition Temperature: 698°F (NTP, 1992)
Melting Point: -94°F (NTP, 1992)
Vapor Pressure: 1.9 mmHg at 392°F (NTP, 1992)
Vapor Density (Relative to Air): 14.95 (NTP, 1992)
Specific Gravity: 0.9262 at 68°F (NTP, 1992)
Boiling Point: 374 to 451°F at 760 mmHg (decomposes) (NTP, 1992)
Molecular Weight: 434.65 (NTP, 1992)
Water Solubility: less than 1 mg/mL at 64°F
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Specific Gravity: 0.92400 @ 25.00 °C.
Flash Point: > 230.00 °F. TCC ( > 110.00 °C. )
Soluble in:
water, 0.6 mg/L @ 24C (exp)
water, 1.461e-005 mg/L @ 25 °C (est)


SYNONYMS OF TRIS(2-ETHYLHEXYL)PHOSPHATE:
2-ethyl-1-hexanol phosphate
tris(2-ethylhexyl)phosphate
Tris(2-ethylhexyl) phosphate
78-42-2
Tris(2-ethylhexyl)phosphate
Disflamoll TOF
Kronitex TOF
Phosphoric acid, tris(2-ethylhexyl) ester
Flexol TOF
Flexol plasticizer TOF
Tri(2-ethylhexyl) phosphate
2-Ethyl-1-hexanol phosphate
Tris(ethylhexyl) phosphate
Tri(2-ethylhexyl)phosphate
1-Hexanol, 2-ethyl-, phosphate
NCI-C54751
TEHP
Phosphoric acid, tris(ethylhexyl) ester
Tri(ethylhexyl) phosphate
2-Ethylhexanol, phosphate triester
Tris-(2-ethylhexyl)fosfat
NSC 407921
BQC0BKB72S
TOF
DTXSID0021414
NSC-407921
Phosphoric Acid Tris(2-ethylhexyl) Ester
DTXCID801414
Triethylhexyl phosphate
Tris(2-ethylhexy)phosphate
CAS-78-42-2
CCRIS 615
HSDB 2562
Tris-(2-ethylhexyl)fosfat [Czech]
EINECS 201-116-6
UNII-BQC0BKB72S
Tris-2(2-ethylhexyl)fosfat [Czech]
BRN 1715839
Tris-2(2-ethylhexyl)fosfat
AI3-07852
Amgard TOF
MFCD00009491
1-Hexanol, phosphate
Phosphoric acid, tris(2-ethylhexyl)ester
Trioctyl Phosphate (TOP)
Tris(2-ethylhexl)phosphate
EC 201-116-6
SCHEMBL35485
tris-(2-ethylhexyl)phosphate
MLS002415769
Phosphoric Acid Trioctyl Ester
CHEMBL1562290
2-Ethylhexanol phosphate (3:1)
CHEBI:181994
HMS3039O17
Phosphoric acid tris(2-ethylhexyl)
Tox21_201369
Tox21_300321
NSC407921
Tris(2-ethylhexyl) phosphate, 97%
AKOS015843194
CS-W009670
NCGC00091821-01
NCGC00091821-02
NCGC00091821-03
NCGC00254160-01
NCGC00258921-01
SMR001370923
P1022
TRIS(2-ETHYLHEXYL) PHOSPHATE [HSDB]
WLN: 4Y2&1OPO&O1Y4&2&O1Y4&2
A865029
Q2454094
Tris(2-ethylhexyl) phosphate, Selectophore(TM), >=99.0%
Tris(2-ethylhexyl) phosphate [ACD/IUPAC Name]
2-Ethylhexyl phosphate [ACD/IUPAC Name]
Phosphate de tris(2-éthylhexyle) [French] [ACD/IUPAC Name]
Phosphoric acid, tris(2-ethylhexyl) ester [ACD/Index Name]
Phosphoric acid, tris(2-ethylhexyl)ester
Tri(2-ethylhexyl) phosphate
Tri(2-ethylhexyl)phosphate
Tris(2-ethylhexyl)phosphat [German] [ACD/IUPAC Name]
UNII:BQC0BKB72S
1-Hexanol, 2-ethyl-, phosphate
201-116-6 [EINECS]
2-ETHYL-1-HEXANOL PHOSPHATE
2-Ethylhexanol phosphate (3:1)
2-Ethylhexanol, phosphate triester
4Y2&1OPO&O1Y4&2&O1Y4&2 [WLN]
78-42-2 [RN]
Amgard TOF
disflamoll tof
Flexol plasticizer TOF
flexol tof
kronitex tof
MFCD00009491 [MDL number]
phosphoric acid tris-(2-ethylhexyl) ester
Phosphoric acid tris(2-ethylhexyl) ester
Phosphoric acid, tris (2-ethylhexyl) ester
Phosphoric acid, tris(ethylhexyl) ester
TOF
tri-(2-ethylhexyl) phosphate
Tri(ethylhexyl) phosphate
triethylhexyl phosphate
trioctyl phosphate [ACD/IUPAC Name]
Tris(2-ethylhexy)phosphate
Tris-(2-ethylhexyl)fosfat [Czech]
Tris-(2-ethylhexyl)phosphate
TRIS(2-ETHYLHEXYL)PHOSPHATE
Tris(ethylhexyl) phosphate
Tris-2(2-ethylhexyl)fosfat



TRIS(2-ETHYLHEXYL)PHOSPHATE
SYNONYMS 1,3,5-Triazine, 2,4,6-tris[1,1'-biphenyl]-4-yl-;Tinosorb A2B;Tris-biphenyl triazine [INCI];2,4,6-Tris(p-biphenylyl)-s-triazine;S-Triazine, 2,4,6-tri-4-biphenylyl CAS NO:31274-51-8
TRIS-BIPHENYL TRIAZINE
SYNONYMS Sodium Citrate Dihydrate; 2-Hydroxy-1,2,3-propanetricarboxylic acid, trisodium salt, dihydrate;CAS NO. 6132-04-3
TRISILOXANE

Trisiloxane is a colorless and odorless liquid.
Trisiloxane is a type of siloxane compound with three silicon atoms and six oxygen atoms.
Trisiloxane is soluble in both water and many organic solvents.

CAS Number: 540-97-6



APPLICATIONS


Trisiloxane is used as an emulsifier in the production of personal care products like shampoo, conditioner, and lotions.
Trisiloxane is used as a surfactant in agricultural formulations to improve the spread of pesticides and herbicides.

Trisiloxane is used as an antifoaming agent in industrial processes such as paper production and wastewater treatment.
Trisiloxane is used as a mold release agent in the manufacturing of rubber and plastics.

Trisiloxane is used as an ingredient in automotive care products like car wax and polish.
Trisiloxane is used as a lubricant in metalworking processes to reduce friction and improve tool life.

Trisiloxane is used as a solvent in the chemical industry for the synthesis of various compounds.
Trisiloxane is used as a processing aid in the food industry for the production of baked goods, confectionery, and frozen desserts.
Trisiloxane is used in the production of polyurethane foam to improve cell structure and foam quality.

Trisiloxane is used as a defoamer in oil and gas drilling operations to prevent the buildup of foam.
Trisiloxane is used in the production of adhesives to improve bonding and reduce curing time.

Trisiloxane is used in the textile industry as a softening agent for fabrics and fibers.
Trisiloxane is used as a cleaning agent in household and industrial applications.

Trisiloxane is used as a drying agent in coatings and paints to improve drying time and reduce surface defects.
Trisiloxane is used as an additive in the production of silicone rubber to improve the processing and handling properties.
Trisiloxane is used as a conditioning agent in hair care products to improve combability and manageability.

Trisiloxane is used as a dispersant in the pigment and ink industry to improve color intensity and stability.
Trisiloxane is used as a foaming agent in the production of foam insulation and packaging materials.

Trisiloxane is used as a wetting agent in the production of emulsions and suspensions.
Trisiloxane is used in the production of high-performance coatings and sealants.

Trisiloxane is used as an anti-blocking agent in plastic films and sheets to prevent sticking.
Trisiloxane is used as a processing aid in the rubber industry to improve mixing and reduce viscosity.
Trisiloxane is used as an anti-corrosion agent in the metalworking industry.

Trisiloxane is used in the production of industrial detergents and cleaning agents.
Trisiloxane is used as a conditioning agent in fabric softeners to improve softness and reduce static cling.


Trisiloxane has a variety of applications across different industries. Some of its major applications include:


Agriculture:
Trisiloxane is used as a surfactant and wetting agent in agricultural formulations to increase the effectiveness of pesticides and herbicides.

Cosmetics:
Trisiloxane is used as an emollient, conditioning agent, and lubricant in cosmetic products such as hair conditioners, skin creams, and lotions.

Textile:
Trisiloxane is used in the textile industry as a hydrophobic finishing agent to impart water and stain resistance to fabrics.

Personal care:
Trisiloxane is used in personal care products such as deodorants and antiperspirants to increase the effectiveness of active ingredients.

Industrial:
Trisiloxane is used as an industrial defoamer to control foam in various processes such as pulp and paper production.

Adhesives and sealants:
Trisiloxane is used as a wetting agent and dispersant in the production of adhesives and sealants to improve their flow and adhesion properties.

Construction:
Trisiloxane is used as a water repellent in construction materials such as concrete, masonry, and stucco.

Automotive:
Trisiloxane is used as an anti-foaming agent in automotive fluids such as engine oil, transmission fluid, and brake fluid.

Agriculture:
Trisiloxane is also used in the agriculture industry as a spray adjuvant to improve the efficacy of agrochemicals.

Food and beverage:
Trisiloxane is used as a defoaming agent in the production of food and beverage products such as beer, soft drinks, and fruit juices.

Paints and coatings:
Trisiloxane is used as a leveling agent and defoaming agent in the production of paints and coatings to improve their performance.

Paper and pulp:
Trisiloxane is used as a defoamer in the production of paper and pulp to reduce foam formation during processing.

Plastics:
Trisiloxane is used as a processing aid in the production of plastics to improve their flow properties.

Rubber:
Trisiloxane is used as a lubricant and processing aid in the production of rubber products.

Fuel and lubricant:
Trisiloxane is used as an anti-foaming agent and viscosity improver in fuel and lubricant formulations.

Metalworking:
Trisiloxane is used as a lubricant and anti-foaming agent in metalworking fluids.

Water treatment:
Trisiloxane is used as a coagulant aid and flocculant in water treatment processes to improve the efficiency of the treatment.

Textile auxiliaries:
Trisiloxane is used as a textile auxiliary in the production of dyeing and finishing agents.

Petroleum industry:
Trisiloxane is used as a flow improver in crude oil transportation.

Surface coatings:
Trisiloxane is used as a surface coating agent to provide water repellency to various substrates.

Firefighting:
Trisiloxane is used as a foam suppressant in firefighting foams.

Metal cleaning:
Trisiloxane is used as a surfactant in metal cleaning formulations.

Industrial cleaning:
Trisiloxane is used as a cleaning agent in industrial cleaning formulations.

Pharmaceuticals:
Trisiloxane is used as an ingredient in some pharmaceutical formulations.

Polymer processing:
Trisiloxane is used as a processing aid in the polymer processing industry to improve the flow and molding properties of the polymers.


Trisiloxane is commonly used as a surfactant in a variety of personal care and cleaning products.
Trisiloxane can be found in shampoos, conditioners, and other hair care products to improve wetting and conditioning properties.
In skincare products, trisiloxane can help improve the texture and feel of creams and lotions.

Trisiloxane is often used as a lubricant in industrial applications, such as metalworking and textile manufacturing.
Trisiloxane can also be used as a foam control agent in the production of polyurethane foam.

Trisiloxane is used as a spreading agent in agricultural applications to help improve the effectiveness of herbicides and pesticides.
In the construction industry, trisiloxane is used as a water repellent and to improve the durability of building materials.

Trisiloxane can also be used as a mold release agent in the production of concrete and other construction materials.
Trisiloxane is used in the automotive industry as an additive to improve the performance of engine oils and other lubricants.

Trisiloxane can also be found in windshield washer fluids as a de-icing agent.
In the electronics industry, trisiloxane is used as a component in electronic adhesives and coatings.
Trisiloxane is used in the production of silicone elastomers, which are used in a variety of applications, including medical devices and automotive parts.

Trisiloxane can be used as a water-repellent coating on fabrics, such as outdoor clothing and tents.
Trisiloxane is used as a foam control agent in the production of polyurethane foam for furniture and bedding.

Trisiloxane can also be found in spray foam insulation products.
In the oil and gas industry, trisiloxane is used as a defoamer and lubricant in drilling fluids.

Trisiloxane can be used as a solvent in the production of silicone resins and other silicone-based materials.
Trisiloxane can be used as a heat transfer fluid in high-temperature applications.
Trisiloxane is used as a coating on contact lenses to improve comfort and clarity.

In the food industry, trisiloxane is used as a lubricant in food processing equipment.
Trisiloxane can also be used as a coating on food packaging to improve moisture resistance.

Trisiloxane is used in the production of silicone-based inks and coatings for printing and graphic arts applications.
Trisiloxane can be used as a component in sealants and adhesives used in the construction industry.

Trisiloxane is used as a component in some personal care products, such as anti-aging creams and hair serums.
Trisiloxane can also be found in some industrial cleaners and degreasers as a surfactant and solvent.

Trisiloxane is used in the manufacture of personal care products such as hair conditioners and skin moisturizers.
Trisiloxane is used in the production of surfactants and emulsifiers that are used in various industries.
Trisiloxane is used as an antifoaming agent in the food industry.

Trisiloxane is used in the production of high-performance coatings and adhesives.
Trisiloxane is used as a water-repellent coating for glass, ceramic, and other surfaces.

Trisiloxane is used in the production of silicone rubbers and resins.
Trisiloxane is used in the manufacturing of electronic components and semiconductors.

Trisiloxane is used in the production of lubricants and greases for machinery and equipment.
Trisiloxane is used as a mold release agent in the manufacturing of plastic and rubber products.
Trisiloxane is used as a conditioning agent in the textile industry.

Trisiloxane is used in the production of flame retardants for various applications.
Trisiloxane is used as a dispersing agent in the formulation of agricultural chemicals.

Trisiloxane is used as a foam control agent in the production of paper and pulp.
Trisiloxane is used in the formulation of cosmetics such as foundations and lipsticks.
Trisiloxane is used in the production of ceramics and glass fibers.

Trisiloxane is used as a lubricant in the textile industry.
Trisiloxane is used in the formulation of polishes and cleaners for various surfaces.

Trisiloxane is used in the production of polyurethane foams and elastomers.
Trisiloxane is used as a solvent for various chemical reactions.
Trisiloxane is used as a wetting agent in the formulation of paints and coatings.

Trisiloxane is used in the manufacturing of plastic films and sheets.
Trisiloxane is used in the formulation of printing inks and toners.

Trisiloxane is used as a heat transfer fluid in industrial processes.
Trisiloxane is used in the production of automotive parts such as gaskets and seals.
Trisiloxane is used as a binder in the formulation of concrete and construction materials.



DESCRIPTION


Trisiloxane is a chemical compound with the molecular formula Si3H8O2.
Trisiloxane is a type of siloxane, which is a class of organosilicon compounds.

Trisiloxane is a clear, colorless liquid with a mild, pleasant odor.
Trisiloxane is highly soluble in water and is nonflammable.

Trisiloxane is primarily used as a surfactant, which is a substance that helps to reduce the surface tension of a liquid.
Trisiloxane is commonly used in the production of personal care products, such as shampoos, conditioners, and lotions, to improve their wetting ability and to help the products spread more evenly over the skin or hair.

Trisiloxane is also used as a foam control agent in various industrial processes, including in the production of paints and coatings, pulp and paper manufacturing, and metalworking.
Its ability to reduce surface tension makes it useful for preventing the formation of foam during these processes, which can interfere with the quality and efficiency of the end product.

Additionally, trisiloxane is used as a wetting agent in agricultural formulations to help improve the absorption and spreading of pesticides, herbicides, and other agricultural chemicals.
Trisiloxane can also be used as an additive in the production of silicone-based polymers and resins.

Other applications of trisiloxane include its use as a lubricant and as an ingredient in the production of adhesives and sealants.
Trisiloxane is also used in the formulation of household cleaning products, such as laundry detergents and dish soaps, to improve their cleaning performance and reduce streaking.

Overall, trisiloxane is a versatile chemical with a wide range of applications, primarily due to its ability to reduce surface tension and improve wetting and spreading properties of liquids.


Trisiloxane is a colorless and odorless liquid.
Trisiloxane is a type of siloxane compound with three silicon atoms and six oxygen atoms.
Trisiloxane is soluble in both water and many organic solvents.

Trisiloxane has a relatively low boiling point and is therefore easily vaporized.
Trisiloxane has good wetting and spreading properties.

Trisiloxane is commonly used as a surfactant in a variety of applications.
Trisiloxane can lower surface tension, making it useful in emulsification and foam stabilization.

Trisiloxane can also be used as a lubricant and release agent due to its low surface tension.
Trisiloxane is commonly used in personal care products such as shampoos and conditioners.
Trisiloxane can help to improve the wetting ability of these products on hair and skin.

Trisiloxane is also used as a defoaming agent in the production of polyurethane foam.
Trisiloxane can reduce the formation of bubbles during the manufacturing process.

Trisiloxane is used as an ingredient in agricultural products such as herbicides and insecticides.
Trisiloxane can help these products to spread more evenly across plant surfaces.

Trisiloxane is used in the formulation of inkjet printer inks as a solvent and wetting agent.
Trisiloxane can help to improve the printing quality and speed.
Trisiloxane is used in the manufacturing of silicone rubber.

Trisiloxane can improve the flow and mold release properties of the rubber.
Trisiloxane can be used as a mold release agent in the production of plastic parts.

Trisiloxane can help to prevent sticking and improve part release.
Trisiloxane is used as a lubricant and release agent in the production of molded glass products.
Trisiloxane can help to prevent sticking and improve the surface finish of the glass.

Trisiloxane is used in the textile industry as a wetting agent and to improve dye penetration.
Trisiloxane can help to reduce the amount of dye needed and improve color fastness.
Trisiloxane is a versatile compound with many applications in a range of industries.



PROPERTIES


Chemical formula: C3H10O2Si3
Molecular weight: 222.48 g/mol
Appearance: Colorless to light yellow liquid
Density: 0.891 g/cm3 at 20°C
Boiling point: 130-131°C
Melting point: -70°C
Flash point: 35-37°C
Solubility: Insoluble in water; soluble in many organic solvents
Vapor pressure: 10 mm Hg at 25°C
Refractive index: 1.422 at 25°C
Viscosity: 1.6 cSt at 25°C
Surface tension: 19.5 mN/m at 25°C
Dielectric constant: 2.90 at 25°C
pH: Neutral
Odor: Mild, characteristic
Flammability: Flammable liquid, with a flash point below 60°C
Autoignition temperature: 260°C
Explosive limits: 1.1-14% (volume)
Corrosivity: Corrosive to metals
Oxidizing properties: Not classified as oxidizing agent
Stability: Stable under normal conditions of use and storage
Hazardous decomposition products: Carbon monoxide, carbon dioxide, silicon dioxide
Hazardous polymerization: Will not occur
Environmental hazards: Not considered to be an environmental hazard
Health hazards: May cause irritation to skin, eyes, and respiratory system upon prolonged exposure. May be harmful if ingested.
Reactivity: Reacts with strong oxidizing agents and acids, and can undergo hydrolysis in the presence of moisture.



FIRST AID


Inhalation:

If inhaled, remove the person to fresh air immediately.
If the person is not breathing, provide artificial respiration.
Seek immediate medical attention if the person has difficulty breathing or shows other signs of respiratory distress.


Skin Contact:

Remove any contaminated clothing and rinse the affected skin with plenty of water for at least 15 minutes.
If skin irritation or redness develops, seek medical attention.


Eye Contact:

Immediately flush the affected eye(s) with plenty of water for at least 15 minutes, while holding the eyelid(s) open.
Seek immediate medical attention if irritation or pain persists.


Ingestion:

Rinse the mouth with water, but do not induce vomiting.
Seek immediate medical attention if a large amount of the chemical is swallowed, or if the person shows signs of vomiting or convulsions.



HANDLING AND STORAGE


Handling:

Trisiloxane should be handled with care to prevent skin and eye contact, inhalation, and ingestion.
Operators should wear personal protective equipment (PPE) such as gloves, goggles, and respiratory protection when handling Trisiloxane.
In case of skin contact, wash the affected area thoroughly with soap and water.

In case of eye contact, flush the eyes with plenty of water for at least 15 minutes and seek medical attention.
If Trisiloxane is inhaled, move the affected person to fresh air and seek medical attention immediately.
If swallowed, do not induce vomiting and seek medical attention immediately.


Storage:

Trisiloxane should be stored in a cool, dry, and well-ventilated area, away from heat, sparks, and flames.
It should be stored in a tightly sealed container, away from incompatible materials such as strong acids, strong bases, and oxidizers.
Containers of Trisiloxane should be properly labeled with the product name, composition, and hazard warnings.

Do not store Trisiloxane near food, beverages, or animal feed.
Keep Trisiloxane out of the reach of children and unauthorized personnel.
Check the container regularly for leaks and damage.


Transportation:

Trisiloxane should be transported in a properly labeled, sealed, and secured container to prevent spills or leakage.
The container should be placed in a well-ventilated area, away from heat sources and incompatible materials.

Transportation of Trisiloxane should comply with local, state, and federal regulations.
Drivers transporting Trisiloxane should be trained and certified to handle hazardous materials.
In case of a spill or leak during transportation, follow the emergency response procedures and contact the appropriate authorities immediately.


Disposal:

Trisiloxane should be disposed of in accordance with local, state, and federal regulations.
Do not dispose of Trisiloxane in household or municipal waste streams.
Consult with a licensed waste disposal company for safe disposal options.
Containers that previously held Trisiloxane should be properly cleaned and recycled or disposed of according to the manufacturer's instructions.



SYNONYMS


Triethylsiloxane
1,1,1-Tris(dimethylsilyloxy)silane
Tri(trimethylsilyloxy)silane
Tris(trimethylsiloxy)silane
Trialkylsiloxy silane
TES
TMSO3
TTS
1,1,1-Tris(trimethylsilyloxy)silane
Silane, tris(trimethylsilyloxy)-
Tris(trimethylsilyl) orthosilicate
Tri(trimethylsilyl) silicate
Silicic acid, tri(trimethylsilyl) ester
Tris(trimethylsilyloxy)silicon
Silicon tris(trimethylsiloxy)
TMSOT
Tris(trimethylsilyl)silanol
Tris(trimethylsilyl) silicate
Tri(trimethylsilyl) orthosilicate
Tri(trimethylsilyl) silicic acid
Triethylsilyloxysilane
Trialkylsilyloxy silane
Tris(trimethylsilyloxy) silicium
Triethoxysilane trimethylsilyl derivative
Silicon tris(trimethylsilyloxy)
Triethylsilanol
1,1,1-Trisiloxane
Trisilicon tetrahydride
Triethylsiloxane
Siloxane, tris(triethylsiloxy)-
Tris(triethylsilyl)oxide
Triethylsilyl ether
TTSO
Silanetriol, triethyl-
Triethylsilyl alcohol
Tris(triethylsilyl)silanol
Trisiloxane, [(triethylsilyl)oxy]-
Triethylsiloxysilane
Triethoxytrisilane
Tris(triethoxysilyl)amine
Tris(triethoxysilyl)phosphate
Triethylsilyltrifluoroacetate
Triethylsilylethynylbenzene
Tris(2,2,6,6-tetramethyl-3,5-heptanedionato)europium(III)
Tris(trifluoroacetylacetonato)samarium(III)
Tris(acetylacetonato)iron(III)
Tris(ethylenediamine)cobalt(III)chloride
Tris(trimethylsilyl)phosphine
Tris(trimethylsilyl)silane
Tris(trimethylsilyl)amine
TRISILOXANE POLYETHER
Trisiloxane Polyether is a type of surfactant that contains a silicone-based (trisiloxane) backbone and polyether side chains.
Trisiloxane Polyether is a clear liquid that is soluble in both water and organic solvents.



APPLICATIONS


Trisiloxane Polyether has several applications in various industries, including:

Coatings:
Trisiloxane Polyether is used as a surfactant in coatings to improve wetting and leveling properties.


Personal care products:
Trisiloxane Polyether is used as a surfactant and emulsifier in personal care products, such as shampoos and body washes, to improve their texture and stability.


Agriculture:
Trisiloxane Polyether is used as a spray adjuvant in agriculture to improve the performance of pesticides and herbicides.


Textiles:
Trisiloxane Polyether is used as a softener and lubricant in textile manufacturing to improve the hand-feel and processing of fabrics.


Foam control:
Trisiloxane Polyether is used as a foam control agent in industrial processes to reduce foam formation and improve process efficiency.


Automotive:
Trisiloxane Polyether is used as an additive in automotive fluids, such as brake fluids and engine oils, to improve their lubricity and anti-wear properties.


Construction:
Trisiloxane Polyether is used as a water repellent in construction materials, such as concrete and masonry, to improve their durability and resistance to moisture.


Electronics:
Trisiloxane Polyether is used as a surface treatment in electronics manufacturing to improve the adhesion and performance of coatings and adhesives.


Food processing:
Trisiloxane Polyether is used as a processing aid in food manufacturing to improve the efficiency and quality of production processes.


Pharmaceuticals:
Trisiloxane Polyether is used as an emulsifier and solubilizer in pharmaceutical formulations to improve their stability and bioavailability.


Trisiloxane Polyether is commonly used as a surfactant in coatings to improve their wetting and leveling properties.
Trisiloxane Polyether is often used as an emulsifier and surfactant in personal care products such as shampoos, conditioners, and body washes.
In the agriculture industry, Trisiloxane Polyether is used as a spray adjuvant to improve the performance of pesticides and herbicides.

Trisiloxane Polyether is often used as a softener and lubricant in textile manufacturing to improve the feel and processing of fabrics.
Trisiloxane Polyether is used as a foam control agent in industrial processes to reduce foam formation and improve process efficiency.

In automotive fluids such as brake fluids and engine oils, Trisiloxane Polyether is added to improve lubricity and anti-wear properties.
Trisiloxane Polyether is used as a water repellent in construction materials such as concrete and masonry to improve their durability and resistance to moisture.

Trisiloxane Polyether is used as a surface treatment in electronics manufacturing to improve the adhesion and performance of coatings and adhesives.
In food manufacturing, Trisiloxane Polyether is used as a processing aid to improve the efficiency and quality of production processes.

Trisiloxane Polyether is used as an emulsifier and solubilizer in pharmaceutical formulations to improve their stability and bioavailability.
Trisiloxane Polyether is used in the manufacture of surfactants and detergents.
Trisiloxane Polyether is used as a wetting agent in the production of polyurethane foam.

In the petroleum industry, Trisiloxane Polyether is used as a lubricant and anti-foaming agent.
Trisiloxane Polyether is used as a defoaming agent in the pulp and paper industry.

Trisiloxane Polyether is used as a leveling agent in printing inks and coatings.
In metalworking fluids, Trisiloxane Polyether is used as a lubricant and corrosion inhibitor.

Trisiloxane Polyether is used as a wetting agent in the production of silicone rubber.
Trisiloxane Polyether is used as an emulsifier in the production of food additives and flavors.

Trisiloxane Polyether is used as a surfactant in the production of detergents and cleaners.
In the textile industry, Trisiloxane Polyether is used as a lubricant and dyeing aid.
Trisiloxane Polyether is used as a processing aid in the production of paper and cardboard.

Trisiloxane Polyether is used as a surfactant and defoamer in the production of latex paints.
Trisiloxane Polyether is used as a foam control agent in the production of polyurethane foam.

In the water treatment industry, Trisiloxane Polyether is used as a coagulant aid and scale inhibitor.
Trisiloxane Polyether is used as a wetting agent and emulsifier in the production of agrochemicals.

Trisiloxane Polyether is used as a dispersant in the production of pigments and dyes.
Trisiloxane Polyether is used as a plasticizer in the production of plastics and resins.
Trisiloxane Polyether is used as a release agent in the production of molded rubber and plastic parts.

In the cosmetics industry, Trisiloxane Polyether is used as a humectant and skin conditioning agent.
Trisiloxane Polyether is used as a surfactant and emulsifier in the production of petroleum products such as lubricating oils and fuel additives.


Trisiloxane Polyether is used as a surfactant in personal care products such as shampoos and conditioners.
Trisiloxane Polyether acts as a wetting agent in printing inks, coatings, and adhesives.
Trisiloxane Polyether enhances the water resistance of textiles and leather goods.

Trisiloxane Polyether improves the slip properties of packaging films and coatings.
Trisiloxane Polyether aids in the dispersion of pigments and other additives in coatings.

Trisiloxane Polyether is used in the production of anti-foaming agents for industrial processes.
Trisiloxane Polyether acts as a dispersant in ceramic and glass manufacturing.

Trisiloxane Polyether is used as a release agent in the production of molded rubber and plastic products.
Trisiloxane Polyether enhances the spreading and wetting properties of agricultural sprays and formulations.

Trisiloxane Polyether improves the flow properties of cementitious materials and concrete.
Trisiloxane Polyether acts as a leveling agent in coatings and adhesives.
Trisiloxane Polyether is used as a foam stabilizer in the production of polyurethane foams.

Trisiloxane Polyether improves the gloss and clarity of coatings and films.
Trisiloxane Polyether is used as a wetting agent and anti-static agent in the production of electronic components.

Trisiloxane Polyether enhances the release properties of mold releases and casting agents.
Trisiloxane Polyether is used in the production of defoamers and emulsifiers for industrial processes.

Trisiloxane Polyether acts as a lubricant and anti-wear agent in metalworking fluids.
Trisiloxane Polyether enhances the water-repellency of coatings and textiles.

Trisiloxane Polyether is used as a release agent in the production of food packaging and processing equipment.
Trisiloxane Polyether improves the wetting and dispersing properties of inks and pigments in printing applications.
Trisiloxane Polyether acts as a solvent in cleaning and degreasing formulations.

Trisiloxane Polyether is used in the production of optical coatings for lenses and displays.
Trisiloxane Polyether enhances the stain resistance of textiles and carpets.

Trisiloxane Polyether is used as a coupling agent in polymer processing and compounding.
Trisiloxane Polyether improves the adhesion of coatings and adhesives to difficult substrates.

Trisiloxane Polyether acts as a defoaming agent in oil and gas production.
Trisiloxane Polyether enhances the surface smoothness of plastics and films.

Trisiloxane Polyether is used as a leveling and anti-cratering agent in coatings.
Trisiloxane Polyether improves the hydrophobicity of building materials such as stone and concrete.
Trisiloxane Polyether acts as a lubricant and corrosion inhibitor in metalworking and industrial fluids.


Some applications of Trisiloxane Polyether:

Water repellent coatings for textile fibers
Anti-fouling coatings for marine vessels
Wood coatings to enhance water resistance
Release agents for molding processes
Lubricants for moving mechanical parts
Surfactants for foam control in various industries
Adhesives for difficult-to-bond surfaces
Ink and paint additives to improve flow and leveling
Coatings for electronic components to improve water resistance
Soil-repellent treatments for carpets and upholstery
Anti-corrosion coatings for metals
Hydrophobic coatings for optical lenses
Oil and gas recovery
Personal care products such as hair conditioners and skin lotions
Laundry detergents and fabric softeners
Agriculture as an adjuvant in pesticide formulations
Construction as a water repellent for concrete and masonry
Cleaning products as a surfactant and wetting agent
Food packaging to prevent moisture absorption
Paper coatings to improve water resistance and printability



DESCRIPTION


Trisiloxane Polyether is a type of surfactant that contains a silicone-based (trisiloxane) backbone and polyether side chains.
Trisiloxane Polyether is a clear liquid that is soluble in both water and organic solvents.

Trisiloxane Polyether is commonly used as a wetting agent, emulsifier, and dispersant in a wide range of applications, including personal care products, agricultural formulations, and industrial cleaning agents.
Its unique chemical structure allows it to reduce surface tension and enhance spreading and wetting properties, making it a highly effective and versatile surfactant.

Trisiloxane Polyether is a highly efficient surfactant due to its unique chemical structure.
The silicone-based backbone of Trisiloxane Polyether provides excellent stability and durability.
Trisiloxane Polyether is used in a variety of industries, including agriculture, cosmetics, and industrial cleaning.

The polyether side chains in Trisiloxane Polyether allow it to be highly soluble in both water and organic solvents.
Trisiloxane Polyether is known for its excellent wetting and dispersing properties, making it a highly effective emulsifier.

Due to its low surface tension, Trisiloxane Polyether is often used as a wetting agent in agricultural formulations to improve spray coverage.
Trisiloxane Polyether can be used as a foam control agent in industrial processes due to its ability to reduce surface tension and foam generation.

The combination of hydrophobic and hydrophilic properties in Trisiloxane Polyether makes it highly effective at reducing interfacial tension between different phases.
Trisiloxane Polyether is biodegradable and has a low toxicity profile, making it an environmentally friendly option for many applications.
The unique properties of Trisiloxane Polyether allow it to provide enhanced performance and efficiency compared to traditional surfactants.



PROPERTIES


Molecular weight: 1000-5000 g/mol
Density: 1.00-1.10 g/mL
Boiling point: >200°C
Flash point: >100°C
Solubility: soluble in water and most organic solvents
Viscosity: low to moderate
Surface tension: low
Hydrophilicity: high
Thermal stability: good
Chemical stability: good
Biocompatibility: good
Emulsifying ability: good
Foaming ability: good
Lubricating ability: good
Wetting ability: good



FIRST AID


The first aid measures for Trisiloxane Polyether are as follows:

In case of inhalation:

Move the affected person to a well-ventilated area and provide fresh air.
If symptoms persist, seek medical attention.


In case of skin contact:

Remove contaminated clothing and wash the affected area thoroughly with soap and water.
If skin irritation or rash develops, seek medical attention.


In case of eye contact:

Rinse the affected eye(s) with water for several minutes, while holding the eyelid(s) open.
Seek medical attention if irritation persists.


In case of ingestion:

Do not induce vomiting.
Rinse mouth with water and drink plenty of water.
Seek medical attention immediately.
Note: It is important to seek medical attention if any symptoms persist or in case of doubt.



HANDLING AND STORAGE


The handling and storage conditions for Trisiloxane Polyether are as follows:

Storage:

Store in a cool, dry, and well-ventilated area away from direct sunlight, heat, sparks, and flame.


Handling:

Handle with appropriate protective equipment, such as gloves, safety glasses, and respiratory protection if required.
Avoid inhalation of vapors and contact with skin and eyes.
Use in a well-ventilated area or with local exhaust ventilation.


Storage containers:

Use appropriate containers made of compatible materials, such as stainless steel or high-density polyethylene (HDPE).


Shelf life:

The shelf life of Trisiloxane Polyether can vary depending on the storage conditions and the manufacturer's recommendations.
It is recommended to use it within the expiry date mentioned on the label or as specified by the supplier.


Note: Follow the manufacturer's instructions and local regulations regarding handling, storage, and disposal of the product.



SYNONYMS


Poly(oxyethylene)-tris(trimethylsiloxy)silane
Silicone polyether
Trisiloxane ethylene oxide copolymer
Trialkoxy polyether silane
Ethylene oxide terminated polydimethylsiloxane
Siloxane polyalkyleneoxide copolymer
Trialkoxy silane polyether
Ethoxylated trisiloxane
Trialkoxy silane ethylene oxide copolymer
Poly(ethylene oxide)-terminated trimethylsiloxy siloxane
Siloxane-polyalkylene oxide block copolymer
Triethoxysilyl poly(ethylene oxide) copolymer
Polyethylene oxide-terminated polydimethylsiloxane
Poly(dimethylsiloxane)-poly(ethylene oxide) block copolymer
Trisiloxane-polyethylene oxide copolymer
Trimethylsiloxy-terminated polyethylene oxide
Trialkoxy silane-terminated polyethylene oxide
Siloxane-polyether copolymer
Trisiloxane-poly(oxyethylene) copolymer
Polydimethylsiloxane-poly(oxyethylene) copolymer
TRISODIUM CITRATE
DESCRIPTION:
Trisodium citrate has the chemical formula of Na3C6H5O7.
Trisodium citrate is sometimes referred to simply as "sodium citrate", though sodium citrate can refer to any of the three sodium salts of citric acid.
Trisodium citrate possesses a saline, mildly tart flavor, and is a mild alkali.

CAS Number: 68-04-2
Molecular Formula: C6H5Na3O7

Trisodium Citrate is one of the sodium salts of citric acid which is found in every living organism, part of the key metabolic pathways in all body cells.
Trisodium Citrate is found in sour fruits such as kiwi, strawberries and many other fruits which has high concentration.
Trisodium Citrate is commercially prepared by fermenting molasses of Aspergillus niger mould.

Citrate is a conjugate base of a weak acid, can function as a buffering agent or acidity regulator by resisting the change in pH.
Trisodium Citrate, also referred to as Sodium Citrate, Trisodium Salt or food additive E331, is the tribasic salt of citric acid.

Trisodium Citrate appears as a white crystalline powder or granular crystals and, given it is a salt, possesses a salty / saline taste with no real detectable odour.
Trisodium Citrate has the CAS number 6132-04-3 and formula Na3C6H5O7.
Trisodium citrate is water-soluble, non-toxic and fully biodegradable.


USES OF TRISODIUM CITRATE:
Trisodium citrate is used in similar applications to citric acid .
These uses include as an acidity regulator in food and drink, as a sequestering agent to prevent limescale inference with soaps and detergents and as an emulsifying agent to aid chemical mixing processes where two separate elements are incapable of mixing (for example oil and water) and helps to keep these mixtures stable once formulated.

Trisodium Citrate in Food:
Trisodium Citrate is a food additive with the E number E331.
Trisodium Citrate is used in a variety of processed food and drink primarily as a flavour enhancer and a preservative.


As an emulsifying agent it is also used in cheesemaking to allow cheese to melt without the separation of oils and fats.
Trisodium citrate in food buffers pH levels to help regulate acidity in a variety of foods to balance taste and is also able to impart a tart / sour flavour in a wide variety of drink products.






APPLICATIONS OF TRISODIUM CITRATE:
Foods:
Sodium citrate is chiefly used as a food additive, usually for flavor or as a preservative.
Its E number is E331.
Sodium citrate is employed as a flavoring agent in certain varieties of club soda.

Trisodium citrate is common as an ingredient in bratwurst, and is also used in commercial ready-to-drink beverages and drink mixes, contributing a tart flavor.
Trisodium citrate is found in gelatin mix, ice cream, yogurt, jams, sweets, milk powder, processed cheeses, carbonated beverages, and wine, amongst others.

Trisodium citrate can be used as an emulsifying stabilizer when making cheese.
Trisodium citrate allows the cheese to melt without becoming greasy by stopping the fats from separating.

Buffering:
Speciation diagram for a 10-millimolar solution of citric acid.
The violet curve corresponds to the trisodium citrate.
As a conjugate base of a weak acid, citrate can perform as a buffering agent or acidity regulator, resisting changes in pH.

Trisodium citrate is used to control acidity in some substances, such as gelatin desserts.
Trisodium citrate can be found in the milk minicontainers used with coffee machines.
The compound is the product of antacids, such as Alka-Seltzer, when they are dissolved in water.

The pH of a solution of 5 g/100 ml water at 25 °C is 7.5 – 9.0.
Trisodium citrate is added to many commercially packaged dairy products to control the pH impact of the gastrointestinal system of humans, mainly in processed products such as cheese and yogurt, although it also has beneficial effects on the physical gel microstructure.

Chemistry:
Trisodium citrate is a component in Benedict's qualitative solution, often used in organic analysis to detect the presence of reducing sugars such as glucose.

Medicine:
In 1914, the Belgian doctor Albert Hustin and the Argentine physician and researcher Luis Agote successfully used sodium citrate as an anticoagulant in blood transfusions, with Richard Lewisohn determining its correct concentration in 1915.
It continues to be used today in blood-collection tubes and for the preservation of blood in blood banks.

The citrate ion chelates calcium ions in the blood by forming calcium citrate complexes, disrupting the blood clotting mechanism.
Recently, trisodium citrate has also been used as a locking agent in vascath and haemodialysis lines instead of heparin due to its lower risk of systemic anticoagulation.

In 2003, Ööpik et al. showed the use of sodium citrate (0.5 g/kg body weight) improved running performance over 5 km by 30 seconds.
Sodium citrate is used to relieve discomfort in urinary-tract infections, such as cystitis, to reduce the acidosis seen in distal renal tubular acidosis, and can also be used as an osmotic laxative.
It is a major component of the WHO oral rehydration solution.

Trisodium citrate is used as an antacid, especially prior to anaesthesia, for caesarian section procedures to reduce the risks associated with the aspiration of gastric contents.

Boiler descaling:
Trisodium citrate is a particularly effective agent for removal of carbonate scale from boilers without removing them from operation and for cleaning automobile radiators


CHEMICAL AND PHYSICAL PROPERTIES OF TRISODIUM CITRATE:
Chemical formula Na3C6H5O7
Molar mass 258.06 g/mol (anhydrous), 294.10 g/mol (dihydrate)
Appearance White crystalline powder
Density 1.7 g/cm3
Melting point > 300 °C (572 °F; 573 K) (hydrates lose water ca. 150 °C)
Boiling point Decomposes
Solubility in water Pentahydrate form: 92 g/100 g H2O (25 °C)



SAFETY INFORMATION ABOUT TRISODIUM CITRATE:
First aid measures:
Description of first aid measures:
General advice:
Consult a physician.
Show this safety data sheet to the doctor in attendance.
Move out of dangerous area:

If inhaled:
If breathed in, move person into fresh air.
If not breathing, give artificial respiration.
Consult a physician.
In case of skin contact:
Take off contaminated clothing and shoes immediately.
Wash off with soap and plenty of water.
Consult a physician.

In case of eye contact:
Rinse thoroughly with plenty of water for at least 15 minutes and consult a physician.
Continue rinsing eyes during transport to hospital.

If swallowed:
Do NOT induce vomiting.
Never give anything by mouth to an unconscious person.
Rinse mouth with water.
Consult a physician.

Firefighting measures:
Extinguishing media:
Suitable extinguishing media:
Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.
Special hazards arising from the substance or mixture
Carbon oxides, Nitrogen oxides (NOx), Hydrogen chloride gas

Advice for firefighters:
Wear self-contained breathing apparatus for firefighting if necessary.
Accidental release measures:
Personal precautions, protective equipment and emergency procedures
Use personal protective equipment.

Avoid breathing vapours, mist or gas.
Evacuate personnel to safe areas.

Environmental precautions:
Prevent further leakage or spillage if safe to do so.
Do not let product enter drains.
Discharge into the environment must be avoided.

Methods and materials for containment and cleaning up:
Soak up with inert absorbent material and dispose of as hazardous waste.
Keep in suitable, closed containers for disposal.

Handling and storage:
Precautions for safe handling:
Avoid inhalation of vapour or mist.

Conditions for safe storage, including any incompatibilities:
Keep container tightly closed in a dry and well-ventilated place.
Containers which are opened must be carefully resealed and kept upright to prevent leakage.
Storage class (TRGS 510): 8A: Combustible, corrosive hazardous materials

Exposure controls/personal protection:
Control parameters:
Components with workplace control parameters
Contains no substances with occupational exposure limit values.
Exposure controls:
Appropriate engineering controls:
Handle in accordance with good industrial hygiene and safety practice.
Wash hands before breaks and at the end of workday.

Personal protective equipment:
Eye/face protection:
Tightly fitting safety goggles.
Faceshield (8-inch minimum).
Use equipment for eye protection tested and approved under appropriate government standards such as NIOSH (US) or EN 166(EU).

Skin protection:
Handle with gloves.
Gloves must be inspected prior to use.
Use proper glove
removal technique (without touching glove's outer surface) to avoid skin contact with this product.
Dispose of contaminated gloves after use in accordance with applicable laws and good laboratory practices.
Wash and dry hands.

Full contact:
Material: Nitrile rubber
Minimum layer thickness: 0.11 mm
Break through time: 480 min
Material tested:Dermatril (KCL 740 / Aldrich Z677272, Size M)
Splash contact
Material: Nitrile rubber
Minimum layer thickness: 0.11 mm
Break through time: 480 min
Material tested:Dermatril (KCL 740 / Aldrich Z677272, Size M)
It should not be construed as offering an approval for any specific use scenario.

Body Protection:
Complete suit protecting against chemicals, The type of protective equipment must be selected according to the concentration and amount of the dangerous substance at the specific workplace.
Respiratory protection:
Where risk assessment shows air-purifying respirators are appropriate use a fullface respirator with multi-purpose combination (US) or type ABEK (EN 14387) respirator cartridges as a backup to engineering controls.

If the respirator is the sole means of protection, use a full-face supplied air respirator.
Use respirators and components tested and approved under appropriate government standards such as NIOSH (US) or CEN (EU).
Control of environmental exposure
Prevent further leakage or spillage if safe to do so.
Do not let product enter drains.
Discharge into the environment must be avoided.

Stability and reactivity:
Chemical stability:
Stable under recommended storage conditions.
Incompatible materials:
Strong oxidizing agents:
Hazardous decomposition products:
Hazardous decomposition products formed under fire conditions.
Carbon oxides, Nitrogen oxides (NOx), Hydrogen chloride gas.

Disposal considerations:
Waste treatment methods:
Product:
Offer surplus and non-recyclable solutions to a licensed disposal company.
Contact a licensed professional waste disposal service to dispose of this material.
Contaminated packaging:
Dispose of as unused product



SYNONYMS OF TRISODIUM CITRATE:
Trisodium citrate [ACD/IUPAC Name] [Wiki]
1,2,3-Propanetricarboxylic acid, 2-hydroxy-, sodium salt (1:3) [ACD/Index Name]
200-675-3 [EINECS]
68-04-2 [RN]
994-36-5 [RN]
Citrate de trisodium [French] [ACD/IUPAC Name]
Citric Acid Trisodium Salt
MFCD00012462 [MDL number]
RS7A450LGA
Sodium 2-hydroxy-1,2,3-propanetricarboxylate
Sodium Citrate [JAN] [USAN] [Wiki]
Sodium citrate anhydrous
Trinatriumcitrat [German] [ACD/IUPAC Name]
Tris sodium citrate
trisodium 2-hydroxypropane-1,2,3-tricarboxylate
1,2,3-Propanetricarboxylic acid, 2-hydroxy-, trisodium salt
114456-61-0 [RN]
205-623-3 [EINECS]
2-Hydroxy-1,2,3-propanenetricarboxylic acid trisodium salt
2-Hydroxy-1,2,3-propanetricarboxylic acid trisodium salt
2-Hydroxy-1,2,3-propanetricarboxylic acid, trisodium salt
Citnatin
Citrate Concentratedmissing
citrate sodium
citrate trisodium
Citratemissing
Citreme
Citric acid sodium salt anhydrous
Citric acid trisodium salt, anhydrous
Citric acid, trisodium salt
Citrosodina
Citrosodine
Citrosodna
Isolyte E
Natrocitral
Sodium 2-hydroxypropane-1,2,3-tricarboxylate
Sodium citrate (USP)
Sodium citrate buffer
SODIUM CITRATE TRIBASIC
Sodium citrate, anhydrous
Synthesis on demand
tri-sodium citrate
Trisodium citrate anhydrous
tris-sodium citrate
UNII-RS7A450LGA


TRISODIUM CITRATE
Sodium Citrate Dihydrate; 2-Hydroxy-1,2,3-propanetricarboxylic acid, trisodium salt, dihydrate;TRISODIUM CITRATE 5,5-HYDRATE; TRISODIUM CITRATE DIHYDRATE; TRISODIUM PHOSPHATE (12HYDRATE) ; TRISODIUM PHOSPHATE ANHYDRATE cas no: 6132-04-3
TRISODIUM CITRATE (TSC)
Trisodium citrate (TSC) is a versatile chemical substance used in a variety of applications in different industries.
In the food industry, Trisodium citrate (TSC) is used as a flavor enhancer, acidity regulator, and emulsifier.
In the medical field, Trisodium citrate (TSC) is used as an anticoagulant but it is also an ingredient in many personal care products.

CAS: 6132-04-3
MF: C6H9Na3O9
MW: 294.1
EINECS: 612-118-5

Synonyms
ANTI-BABOON IGM, BIOTIN;BETA-HYDROXY-TRICARBOXYLIC ACID MONOHYDRATE;HYDROXYTRICARBALLYLIC ACID MONOHYDRATE;CITRIC ACID NA3-SALT 2H2O;CITRIC ACID H2O;CITRIC ACID TRISODIUM SALT DIHYDRATE;CITRIC ACID, 3NA, DIHYDRATE;CITRIC ACID-1-HYDRATE;Trisodium citrate dihydrate;Sodium citrate dihydrate;6132-04-3;Sodium citrate tribasic dihydrate;1,2,3-Propanetricarboxylic acid, 2-hydroxy-, trisodium salt, dihydrate;Sodium citrate hydrate;Citric acid trisodium salt dihydrate;MFCD00150031;B22547B95K;Nauzene;trisodium 2-hydroxypropane-1,2,3-tricarboxylate dihydrate;trisodium;2-hydroxypropane-1,2,3-tricarboxylate;dihydrate;DTXSID1049437;SODIUM CITRATE, DIHYDRATE;Citric acid, trisodium salt, dihydrate;N-1560;Sodium citrate hydrous;Natrii citras, dehydrate;Trisodium citrate dihydrate;Citric acid trisodium salt dihydrate;MFCD00130806;tri-sodium citrate dihydrate;TRISODIUM CITRATE DIHYDRATE (II);TRISODIUM CITRATE DIHYDRATE [II];TRISODIUM CITRATE DIHYDRATE (USP MONOGRAPH);TRISODIUM CITRATE DIHYDRATE [USP MONOGRAPH];sodium 2-hydroxypropane-1,2,3-tricarboxylate dihydrate;Tricitrasol;Natrum citricum;Emetrol Chewables;Tricitrasol (TN);Sodium citrate; Trisodium 2-hydroxypropane-1,2,3-tricarboxylatedihydrate; Sodium Citrate ;Dihydrate;Sodium citrate (TN);CVS HealthNausea Relief;Emetrol Chewables Orange;Sodium citrate [USP:JAN];Sodiumcitratetribasicdihydrate;EmetrolChewables Mixed Berry;SODIUM CITRATE [FHFI];DTXCID0029397;Sodium citrate hydrate (JP17);UNII-B22547B95K;CHEBI:32142;Trisodium citrate dihydrate, ACS;SODIUM CITRATE HYDROUS [II];SODIUM CITRATE HYDRATE [JAN];SODIUM CITRATE [EP MONOGRAPH];SODIUM CITRATE DIHYDRATE [MI];AKOS025293920;Citronensaeure,Trinatrium-Salz-Dihydrat
;Sodium citrate dihydrate, >=99%, FG;SODIUM CITRATE DIHYDRATE [VANDF];BP-31019;SODIUM CITRATE DIHYDRATE [WHO-DD];Sodium citrate tribasic dihydrate, >=98%;Sodium citrate dihydrate, ACS reagent grade;SODIUM CITRATE, DIHYDRATE [WHO-IP];NS00074299;D01781;F82065;Sodium citrate tribasic dihydrate, AR, >=99%;Sodium citrate tribasic dihydrate, LR, >=99%;Citric acid trisodium salt dihydrate ACS reagent;NATRII CITRAS, DEHYDRATE [WHO-IP LATIN];A833161;A835986;Q22075862;Sodium citrate dihydrate Biochemical grade, Fine Granular;Sodium citrate tribasic dihydrate, USP, 99.0-100.5%;Sodium Citrate Tribasic Dihydrate (Molecular Biology Grade);Sodium citrate tribasic dihydrate, ACS reagent, >=99.0%;trisodium 2-oxidanylpropane-1,2,3-tricarboxylate dihydrate;Sodium citrate tribasic dihydrate, BioUltra, >=99.0% (NT);Sodium citrate tribasic dihydrate, insect cell culture tested;Sodium citrate tribasic dihydrate, JIS special grade, >=99.0%;Sodium citrate tribasic dihydrate, p.a., ACS reagent, 99.0%;Sodium citrate tribasic dihydrate, purum p.a., >=99.0% (NT);Sodium citrate tribasic dihydrate, SAJ first grade, >=99.0%;Sodium citrate tribasic dihydrate, tested according to Ph.Eur.;trisodium 2-hydroxypropane-1,2,3-tricarboxylate--water (1/2);Trisodium citrate dihydrate, meets USP testing specifications;2-hydroxy-1,2,3-propanetricarboxylic acid trisodium salt dihydrate;Sodium citrate tribasic dihydrate, BioXtra, >=99.0% (titration);Sodium citrate tribasic dihydrate, for molecular biology, >=99%;Sodium citrate tribasic dihydrate, Vetec(TM) reagent grade, 98%;Sodium citrate, United States Pharmacopeia (USP) Reference Standard;1,2,3-Propanetricarboxylic acid, 2-hydroxy-, sodium salt, dihydrate;Sodium citrate tribasic dihydrate, p.a., ACS reagent, reag. ISO, 99-101%;1,2,3-Propanetricarboxylic acid, 2-hydroxy-, sodium salt, hydrate (1:3:2);Sodium citrate tribasic dihydrate, BioUltra, for molecular biology, >=99.5% (NT);Sodium citrate tribasic dihydrate, puriss. p.a., ACS reagent, >=99.0% (NT);Sodium citrate tribasic dihydrate, suitable for amino acid analysis, >=99.0%;Sodium Citrate, Pharmaceutical Secondary Standard; Certified Reference Material;Sodium citrate tribasicdihydrate, puriss. p.a., ACS reagent, reag. ISO, reag. Ph. Eur., >=99.5%;Sodium citrate tribasic dihydrate, suitable for amino acid analysis, >=98% (titration), powder

Trisodium citrate (TSC) is the sodium salt of citric acid.
Trisodium citrate (TSC) is widely used as a preservative or for flavour.
Trisodium citrate (TSC) is also used in dietary supplements.
Trisodium citrate (TSC) is also an essential ingredient in dishwasher tablets, industrial cleaners, detergents, etc.
Trisodium citrate (TSC) has molecular weight of 294.1, is a colorless crystal or white crystalline powder product; it is odorless, salty taste, and cool.
Trisodium citrate (TSC) will lose its crystal water at 150 °C and will be decomposed at even higher temperature.
Trisodium citrate (TSC) also has slight deliquescence in wet air and has weathering property upon hot air.
Trisodium citrate (TSC) is soluble in water and glycerol, but insoluble in alcohol and some other organic solvents.
Trisodium citrate (TSC) has no toxic effect, and has pH adjusting capability as well as having a good stability, and therefore can be used in the food industry.

Trisodium citrate (TSC) has the greatest demand when being used as a food additive; As food additives, it is mainly used as flavoring agents, buffers, emulsifiers, bulking agents, stabilizers and preservatives; in addition, combination between sodium citrate and citric acid can be used in a variety of jams, jelly, juice, drinks, cold drinks, dairy products and pastries gelling agents, flavoring agents and nutritional supplements.
The dihydrate of Trisodium citrate (TSC).
Trisodium citrate (TSC) is the tribasic dihydrate sodium salt of citric acid.
Trisodium citrate (TSC) has the molecular formula Na3C6H5O7.
Trisodium citrate (TSC) is sometimes referred to simply as "sodium citrate", though sodium citrate can refer to any of the three sodium salts of citric acid.
Trisodium citrate (TSC) possesses a saline, mildly tart flavor, and is a mild alkali.

Trisodium citrate (TSC) is a tribasic salt of citric acid.
Trisodium citrate (TSC) is produced by complete neutralisation of citric acid with high purity sodium hydroxide or carbonate and subsequent crystallisation.
Trisodium citrate (TSC) is widely used in foods, beverages and various technical applications mainly as buffering, sequestering or emulsifying agent.
Trisodium citrate (TSC) occurs as white, granular crystals or as white, crystalline powder with a pleasant, salty taste.
Trisodium citrate (TSC) is slightly deliquescent in moist air, freely soluble in water and practically insoluble in ethanol (96 %).
Trisodium citrate (TSC) is a non-toxic, neutral salt with low reactivity.
Trisodium citrate (TSC) is chemically stable if stored at ambient temperatures.
Trisodium citrate (TSC) is fully biodegradable and can be disposed of with regular waste or sewage.

Trisodium citrate (TSC) Chemical Properties
Melting point: >300 °C(lit.)
Density: 1.76
FEMA: 3026 | SODIUM CITRATE
Fp: 173.9 °C
Storage temp.: Store at +5°C to +30°C.
Solubility H2O: 100 mg/mL
Form: powder
Color: white
PH: 7.0-9.0 (25℃, 50mg/mL in H2O)
Odor: Odorless
PH Range: 7.5 - 9 at 29.4 g/l at 25 °C
Water Solubility: 720 g/L (25 ºC)
λmax λ: 260 nm Amax: 0.01
λ: 280 nm Amax: 0.01
Merck: 14,8602
BRN: 6104939
Stability: Stable. Incompatible with bases, reducing agents, oxidizing agents.
InChIKey: NLJMYIDDQXHKNR-UHFFFAOYSA-K
LogP: -1.72
CAS DataBase Reference: 6132-04-3(CAS DataBase Reference)
EPA Substance Registry System: Trisodium citrate (TSC) (6132-04-3)

Trisodium citrate (TSC) is colorless crystals or white crystalline powder, and is odorless, cool and salty.
Trisodium citrate (TSC) has no melting point with a relative density of 1.857.
Trisodium citrate (TSC) is stable in air at room temperature with loss of crystal water when being heated to 150 °C loss of crystal water; further heating will cause its decomposition.
Trisodium citrate (TSC) is insoluble in ethanol but highly soluble in water. 5% aqueous solution has a pH value of 7.6 to 8.6.
Trisodium citrate (TSC) consists of odorless, colorless, monoclinic crystals, or a white crystalline powder with a cooling, saline taste.
Trisodium citrate (TSC) is slightly deliquescent in moist air, and in warm dry air it is efflorescent.
Although most pharmacopeias specify that Trisodium citrate (TSC) is the dihydrate, the USP 32 states that sodium citrate may be either the dihydrate or anhydrous material.

Uses
Trisodium citrate (TSC) can be used as Ph adjusting agents and emulsifying enhancers applied to jam, candy, jelly and ice cream; its combination with citric acid has an effect of alleviating tour; Trisodium citrate (TSC) also has effects on forming complex with metal ions.
China rules that Trisodium citrate (TSC) can be applied to various types of food with appropriate usage according to the absolute necessity.
Trisodium citrate (TSC) can be used as a food additive, as complex agent and buffering agent in electroplating industry; at the field of pharmaceutical industry, it is used for the manufacturing of anti-clotting drugs; and used as the detergent additives in light industry.
Trisodium citrate (TSC) is used as the analysis agents used for chromatography analysis and can also used for preparing bacterial culture medium; moreover, it can also be applied into pharmaceutical industry.

Trisodium citrate (TSC) can be used for the flavoring processing of food, as stabilizers, buffers and deputy complex-forming agents in non-toxic electroplating industry; at pharmaceutical industry, it is used as anti-clotting agent, phlegm drugs and diuretics drugs.
Trisodium citrate (TSC) can also be used in brewing, injection, newspaper and movies medicines.
Anticoagulant for collection of blood.
In photography; as sequestering agent to remove trace metals; as emulsifier, acidulant and sequestrant in foods.
An anticoagulant also used as a biological buffer
Trisodium citrate (TSC), is widely applied in food, beverages and fillers as a buffering, sequestering or an emulsifying agent.
Trisodium citrate (TSC) used as an anticoagulant in blood transfusions, osmotic laxative, functional fluids, solvents cleaning, furnishing care products, laundry dishwashing products and cleaning automobile radiators.
Trisodium citrate (TSC) is chiefly used as a food additive, usually for flavor or as a preservative.

Foods
Trisodium citrate (TSC) is chiefly used as a food additive, usually for flavor or as a preservative.
Trisodium citrate (TSC) 2s E number is E331.
Trisodium citrate (TSC) is employed as a flavoring agent in certain varieties of club soda.
Trisodium citrate (TSC) is common as an ingredient in bratwurst, and is also used in commercial ready-to-drink beverages and drink mixes, contributing a tart flavor.
Trisodium citrate (TSC) is found in gelatin mix, ice cream, yogurt, jams, sweets, milk powder, processed cheeses, carbonated beverages, and wine, amongst others.
Trisodium citrate (TSC) can be used as an emulsifying stabilizer when making cheese.
Trisodium citrate (TSC) allows the cheese to melt without becoming greasy by stopping the fats from separating.

Buffering
As a conjugate base of a weak acid, citrate can perform as a buffering agent or acidity regulator, resisting changes in pH.
Trisodium citrate (TSC) is used to control acidity in some substances, such as gelatin desserts.
Trisodium citrate (TSC) can be found in the milk minicontainers used with coffee machines.
Trisodium citrate (TSC) is the product of antacids, such as Alka-Seltzer, when they are dissolved in water.
The pH range of a solution of 5 g/100 ml water at 25 °C is 7.5 to 9.0.
Trisodium citrate (TSC) is added to many commercially packaged dairy products to control the pH impact of the gastrointestinal system of humans, mainly in processed products such as cheese and yogurt, although Trisodium citrate (TSC) also has beneficial effects on the physical gel microstructure.

Chemistry
Trisodium citrate (TSC) is a component in Benedict's qualitative solution, often used in organic analysis to detect the presence of reducing sugars such as glucose.

Medicine
In 1914, the Belgian doctor Albert Hustin and the Argentine physician and researcher Luis Agote successfully used sodium citrate as an anticoagulant in blood transfusions, with Richard Lewisohn determining its correct concentration in 1915.
Trisodium citrate (TSC) continues to be used today in blood-collection tubes and for the preservation of blood in blood banks.
The citrate ion chelates calcium ions in the blood by forming calcium citrate complexes, disrupting the blood clotting mechanism.
Recently, Trisodium citrate (TSC) has also been used as a locking agent in vascath and haemodialysis lines instead of heparin due to its lower risk of systemic anticoagulation.

In 2003, Ööpik et al. showed the use of Trisodium citrate (TSC) improved running performance over 5 km by 30 seconds.
Trisodium citrate (TSC) is used to relieve discomfort in urinary-tract infections, such as cystitis, to reduce the acidosis seen in distal renal tubular acidosis, and can also be used as an osmotic laxative.
Trisodium citrate (TSC) is a major component of the WHO oral rehydration solution.
Trisodium citrate (TSC) is used as an antacid, especially prior to anaesthesia, for caesarian section procedures to reduce the risks associated with the aspiration of gastric contents.

Boiler descaling
Trisodium citrate (TSC) is a particularly effective agent for removal of carbonate scale from boilers without removing them from operation and for cleaning automobile radiators.

Pharmaceutical Applications
Trisodium citrate (TSC), as either the dihydrate or anhydrous material, is widely used in pharmaceutical formulations.
Trisodium citrate (TSC) is used in food products, primarily to adjust the pH of solutions.
Trisodium citrate (TSC) is also used as a sequestering agent.
The anhydrous material is used in effervescent tablet formulations.
Trisodium citrate (TSC) is additionally used as a blood anticoagulant either alone or in combination with other citrates such as disodium hydrogen citrate.
Therapeutically, Trisodium citrate (TSC) is used to relieve the painful irritation caused by cystitis, and also to treat dehydration and acidosis due to diarrhea.

Excellent performance
Trisodium citrate (TSC) is currently the most important citrate.
Trisodium citrate (TSC) is produced by two steps: first starch food is fermented to generate citric acid; secondly, citric acid is neutralized by alkali to generate the final products.
Sodium citrate has the following excellent performance:
Safe and nontoxic properties; Since the basic raw material for the preparation of sodium citrate mainly comes from the food, Trisodium citrate (TSC) is absolutely safe and reliable without causing harm to human health.
The United Nations Food and Agriculture and the World Health Organization has no restriction in its daily intake, which means that this product can be considered as non-toxic food.
Trisodium citrate (TSC) is biodegradable.
After subjecting to the dilution of a large amount of water, sodium citrate is partially converted into citrate, which coexists with sodium citrate in the same system.
Trisodium citrate (TSC) is easy to subject to biological degradation at water by the action of oxygen, heat, light, bacteria and microbes.

Trisodium citrate (TSC)'s decomposition pathways are generally going through aconitic acid, itaconic acid, citraconic acid anhydride to be further converted to carbon dioxide and water.
The ability of forming complex with metal ions.
Trisodium citrate (TSC) has a good capability of forming complex with some metal ions such as Ca2+, Mg2+; for other ions such as Fe2+, Trisodium citrate (TSC) also has a good complex-forming ability.
Excellent solubility, and the solubility increases with increasing temperature of water.
Trisodium citrate (TSC) has a good capability for pH adjustment and a good buffering property.
Sodium citrate is a weak acid-strong alkali salt; When combined with citrate, they can form a pH buffer with strong compatibility; therefore, this is very useful for some cases in which it is not suitable to have large change of pH value.
In addition, Trisodium citrate (TSC) also has excellent retardation performance and stability.

Effect and application
During the process of clinically taking fresh blood, adding some amount of sterile Trisodium citrate (TSC) can play a role in prevent blood clotting; this is exactly taking advantage of the features that calcium citrate can form soluble complexes with calcium ion; In the field of medicine, Trisodium citrate (TSC) is used for the in vitro anti-clotting drugs and anticoagulants drugs, phlegm drugs, and diuretics drugs during blood transfusions; it can also used for cyanide-free electroplating industry; also used as developer for photographic industry.
Trisodium citrate (TSC) can be used as flavoring agents, buffering materials, emulsifiers, and stabilizer in the food industry.
Moreover, Trisodium citrate (TSC) is also widely used in chemical, metallurgical industry, the absorption of sulfur dioxide exhaust with the absorption rate of 99% and regenerate liquid sulfur dioxide citrate for recycle application.
Trisodium citrate (TSC) has a good water solubility and a excellent cheating capability with Ca2 +, Mg2 + and other metal ions; it is biodegradable and has a strong dispersing ability and anti-redeposition ability; Daily-applied chemical detergents use it as alternative to trimer sodium phosphate for production of non-phosphorus detergent and phosphate-free liquid detergent.
Adding a certain amount Trisodium citrate (TSC) to the detergent can significantly increase the cleaning ability of detergent cleaning.
The large scale of application of Trisodium citrate (TSC) as a builder in detergents is an important discovery in synthetic detergent industry.
Trisodium citrate (TSC) is non-toxic without environmental pollution; it can also be acted as a buffer for the production of cosmetics.

Production methods
Trisodium citrate (TSC) is produced by the neutralization of citric acid by sodium hydroxide or sodium bicarbonate.
Dissolve sodium bicarbonate in water upon stirring and heating; add citric acid, continue to heat up to 85-90 °C; adjust the pH to 6.8; adjust active carbon for bleaching.
Filter when the mixture is still hot; condense the filtrate under reduced pressure; cool and the crystal comes out; filter, wash, dry to obtain the final products of sodium citrate.
C6H8O7 + 3NaHCO3 → C6H5Na3O7 • 2H2O + 3CO2 ↑ + H2O

Production Methods
Trisodium citrate (TSC) is prepared by adding sodium carbonate to a solution of citric acid until effervescence ceases.
The resulting solution is filtered and evaporated to dryness.

Biochem/physiol Actions
Trisodium citrate (TSC) can act as a buffering agent, resisting changes in pH.
Used in blood collection tubes, the citrate chelates calcium ions in blood and thereby disrupts blood clotting.
Citrate is a intermediate in the TCA cycle and fatty acid synthesis.
Trisodium citrate (TSC) is an allosteric modulator of acetyl-CoA carboxylase, the enzyme that regulates the conversion of acetyl-CoA to malonyl-CoA.
TRISODIUM CITRATE DIHYDRATE
Trisodium Citrate Dihydrate is a white, crystalline powder with a slightly salty, sour taste.
Trisodium Citrate Dihydrate is a tribasic salt of citric acid.


CAS Number: 6132-04-3
EC Number: 200-675-3
MDL number: MFCD00150031
Molecular Formula: C6H9Na3O9


Trisodium Citrate Dihydrate is the trisodium salt of citric acid.
Trisodium Citrate Dihydrate is a crystalline white powder that is slightly deliquescent in moist air, freely soluble in water, and practically insoluble in alcohol.


Trisodium Citrate Dihydrate is a non-toxic, neutral salt with low reactivity.
Trisodium Citrate Dihydrate is a versatile chemical substance used in a variety of applications in different industries.
Trisodium Citrate Dihydrate is a white, crystalline powder with a slightly salty, sour taste.


Trisodium Citrate Dihydrate is a white odorless chemical used as a food additive.
Trisodium Citrate Dihydrate occurs as white, granular crystals or as white, crystalline powder with a pleasant, salty taste.
Trisodium Citrate Dihydrate is slightly deliquescent in moist air, freely soluble in water and practically insoluble in ethanol (96 %).


Trisodium Citrate Dihydrate is a non-toxic, neutral salt with low reactivity.
Trisodium Citrate Dihydrate is chemically stable if stored at ambient temperatures.
Trisodium Citrate Dihydrate is fully biodegradable and can be disposed of with regular waste or sewage.


Trisodium Citrate Dihydrate is a tribasic salt of citric acid.
Trisodium Citrate Dihydrate is produced by complete neutralisation of citric acid with high purity sodium hydroxide or carbonate and subsequent crystallisation.


Citric acid is the product of a microbial fermentation using carbohydrate substrates.
Trisodium Citrate Dihydrate is widely used as an excellent pH regulator and odourless buffering agent for bath and shower gels, creams, styling or decorative products.


Trisodium Citrate Dihydrate is both ECOCERT and COSMOS approved.
Trisodium Citrate Dihydrate is for the preparation of total ribosomal RNA from E. coli
Trisodium Citrate Dihydrate is a tribasic salt of citric acid.


Trisodium Citrate Dihydrate is produced by complete neutralization of citric acid with high purity sodium source and subsequent crystallization.
Trisodium Citrate Dihydrate is a tribasic salt of citric acid.
Trisodium Citrate Dihydrate is produced by complete neutralisation of citric acid with high purity sodium hydroxide or carbonate and subsequent crystallisation.


Trisodium Citrate Dihydrate has a sour taste similar to citric acid, and is salty as well.
Trisodium Citrate Dihydrate, (molecular formula: Na3C6H5O7 • 2H2O) has molecular weight of 294.1, is a colorless crystal or white crystalline powder product; it is odorless, salty taste, and cool.


Trisodium Citrate Dihydrate will lose its crystal water at 150 °C and will be decomposed at even higher temperature.
Trisodium Citrate Dihydrate also has slight deliquescence in wet air and has weathering property upon hot air.
Trisodium Citrate Dihydrate is soluble in water and glycerol, but insoluble in alcohol and some other organic solvents.


Trisodium Citrate Dihydrate is manufactured by neutralizing citric acid derived from a submerged fermentation process.
Trisodium Citrate Dihydrate is produced in accordance with current Good Manufacturing Practices (GMP’s) under a comprehensive HACCP (Hazard Analysis and Critical Control Points) program.


Trisodium Citrate Dihydrate is considered “GRAS” (Generally
Recognized As Safe) by the United States Food and Drug Administration without restriction as to the quantity of use within good manufacturing practice.
Trisodium Citrate Dihydrate is also considered by the Experts Committee of the FAO/WHO to be a safe food additive without limitation according to good manufacturing practice.


Trisodium Citrate Dihydrate is a stable material.
Trisodium Citrate Dihydrate is manufactured to meet the monograph specifications of major world codex and pharmacopoeia standards including the USP, FCC, BP, EP, FAO/WHO and is certified Kosher Pareve, Kosher for Passover, and Halal.


Trisodium Citrate Dihydrate is available as translucent white crystals and has a slight saline taste.
Water of crystallization constitutes approximately twelve percent by weight of the dihydrate form.
Trisodium Citrate Dihydrate is a white powder or colourless crystals.


Trisodium Citrate Dihydrate is the dihydrate of trisodium citrate.
Trisodium Citrate Dihydrate is the tribasic dihydrate sodium salt of citric acid.
Trisodium Citrate Dihydrate (C6H5Na3O7.2H2O) is a tribasic salt of citric acid.


Trisodium Citrate Dihydrate is a urine alkalinizing agent.
After absorption Trisodium Citrate Dihydrate is metabolized to produce bicarbonate.
Trisodium Citrate Dihydrate is a white crystalline powder that is composed of sodium salt of citric acid.


Trisodium Citrate Dihydrate is highly soluble in water and has a sour taste.
Trisodium Citrate Dihydrate (E331) is the sodium salt of citric acid.
Like citric acid, Trisodium Citrate Dihydrate has a sour taste.


Like other salts, Trisodium Citrate Dihydrate also has a salty taste.
Trisodium Citrate Dihydrate gives club soda both its sour and salty flavors.
Trisodium Citrate Dihydrate reduces the acidity of foods, so it allows spherification with strongly acidic ingredients.


Trisodium Citrate Dihydrate is also used as an antioxidant in food as well as a sequestrant.
Trisodium Citrate Dihydrate dissolves easily and acts instantaneously.
Trisodium Citrate Dihydrate is odorless with a slightly saline taste.


Trisodium Citrate Dihydrate is sodium salt of citrate which has an alkalinizing activity with the chemical name Trisodium Citrate Dihydrate.
Trisodium Citrate Dihydrate is also called TriTrisodium Citrate Dihydrate or Citrosodine or Natrocitral.
Trisodium Citrate Dihydrate (C6H5Na3O7•2H2O, CAS Reg. No. 68–0904–092) is the sodium salt of citric acid.


Trisodium Citrate Dihydrate is prepared by neutralizing citric acid with sodium hydroxide or sodium carbonate.
Trisodium Citrate Dihydrate occurs as colorless crystals or a white crystalline powder.
Trisodium Citrate Dihydrate may be prepared in an anhydrous state or may contain two moles of water per mole of Trisodium Citrate Dihydrate.


Trisodium Citrate Dihydrate is the sodium salt of Citric Acid.
Like Citric acid, Trisodium Citrate Dihydrate has a sour taste.
Like other salts, Trisodium Citrate Dihydrate also has a salty taste.


Trisodium Citrate Dihydrate is commonly known as sour salt and is mainly used as a food additive, usually for flavor or as a preservative.
Trisodium Citrate Dihydrate gives club soda both its salty and sour flavors.
Trisodium Citrate Dihydrate reduces the acidity of foods, so it allows spherification with strongly acidic ingredients.


Trisodium Citrate Dihydrate is also used as an antioxidant in food as well as a sequestrant.
Trisodium Citrate Dihydrate dissolves easily and acts instantaneously.
Trisodium Citrate Dihydrate and citric acid combine in an oral solution to prevent kidney stones and metabolic acidosis.


This solution works by making your blood and pee less acidic.
You can mix this solution with 6 ounces of water before drinking it as directed.


Trisodium Citrate Dihydrate may refer to any of the sodium salts of citric acid (though most commonly the third):
*MonoTrisodium Citrate Dihydrate
*DiTrisodium Citrate Dihydrate
*TriTrisodium Citrate Dihydrate


The three forms of salt are collectively known by the E number E331.
Trisodium Citrate Dihydrate is the trisodium salt of citric acid.
Trisodium Citrate Dihydrate has a role as a flavouring agent and an anticoagulant.


Trisodium Citrate Dihydrate contains a citrate(3-).
Trisodium Citrate Dihydrate is the sodium salt of citric acid.
Trisodium Citrate Dihydrate is white, crystalline powder or white, granular crystals, slightly deliquescent in moist air, freely soluble in water, practically insoluble in alcohol.


Like citric acid, Trisodium Citrate Dihydrate has a sour taste.
From the medical point of view, Trisodium Citrate Dihydrate is used as alkalinizing agent.
Trisodium Citrate Dihydrate works by neutralizing excess acid in the blood and urine.


Upon absorption, Trisodium Citrate Dihydrate dissociates into sodium cations and citrate anions; organic citrate ions are metabolized to bicarbonate ions, resulting in an increase in the plasma bicarbonate concentration, the buffering of excess hydrogen ion, the raising of blood pH, and potentially the reversal of acidosis.


In addition, increases in free sodium load due to Trisodium Citrate Dihydrate administration may increase intravascular blood volume, facilitating the excretion of bicarbonate compounds and an anti-urolithic effect.
Sodium salts of citric acid are used as buffers and food preservatives.


They are used medically as anticoagulants in stored blood, and for urine alkalization in the prevention of KIDNEY STONES.
Trisodium Citrate Dihydrate increases the strong ion differenceSID=(Na++K++Ca2++Mg2+)−(Cl−+lactate−)provided that citrate is metabolized (Stewart concept).
TriTrisodium Citrate Dihydrate is often referred to as Trisodium Citrate Dihydrate, though Trisodium Citrate Dihydrate can refer to any of the three sodium salts of citric acid.


Trisodium Citrate Dihydrate has a saline, mildly tart flavor.
The Cosmetics Ingredient Review panel has deemed Trisodium Citrate Dihydrate safe as used in skin care products.
Trisodium Citrate Dihydrate serves as a preservative to ensure safe and durable products by inhibiting microbial growth.


Trisodium Citrate Dihydrate also assists in the regulation of pH of cosmetic formulations.
Trisodium Citrate Dihydrate refers to sodium salts of citric acid.
MonoTrisodium Citrate Dihydrate, diTrisodium Citrate Dihydrate, and triTrisodium Citrate Dihydrate are the three types of sodium salts of citric acid.


The three types of salts get collectively known as E number E 331.
However, Trisodium Citrate Dihydrate mostly refers to the third type, that is, triTrisodium Citrate Dihydrate.
Trisodium Citrate Dihydrate is a compound obtained after the alkalizing activity, and it’s a sodium salt of citrate.


Trisodium Citrate Dihydrate's chemical formula is Na3C6H5O7.
Trisodium Citrate Dihydrate is a sodium salt of citrate, and it has an alkalinizing activity.
Trisodium Citrate Dihydrate is also Known as TriTrisodium Citrate Dihydrate.


The sodium salts of citric acid are known as Trisodium Citrate Dihydrates.
There are three sodium salts of citric acid types: monoTrisodium Citrate Dihydrate, diTrisodium Citrate Dihydrate, and triTrisodium Citrate Dihydrate.
E number 331 (E331) refers to all three types of salts combined.


Trisodium Citrate Dihydrate has the chemical formula Na3C6H5O7.
Trisodium Citrate Dihydrate possesses a saline, mildly tart flavor, and is a mild alkali.
Trisodium Citrate Dihydrate has been indicated for the treatment of metabolic acidosis.


Trisodium Citrate Dihydrate is the sodium salt of citrate with alkalinizing activity.
Trisodium Citrate Dihydrate is a sodium salt of citrate obtained after the alkalizing activity, and its chemical formula is Na3C6H507.
On the other hand, Trisodium Citrate Dihydrate refers to a third type: triTrisodium Citrate Dihydrate.



USES and APPLICATIONS of TRISODIUM CITRATE DIHYDRATE:
In the cleaning industry Trisodium Citrate Dihydrate is commonly used because of its excellent cleaning characteristics and its unusual property of being almost neutral yet portraying the characteristics of an acid as in descalers and an alkali as in degreasers.
Cleaning products include laundry powders and detergents, toilet cleaners, hard surface cleaners, carpet cleaners, dish washing liquids, powder and liquid degreasers and pre-soaks.


Trisodium Citrate Dihydrate is becoming more and more popular now as it is considered environmentally friendly, it substitutes phosphates and is readily biodegradable.
In industry Trisodium Citrate Dihydrate finds many uses including alkaline degreaser baths, electroplating chemicals for copper and nickel etc, photo chemicals.


Trisodium Citrate Dihydrate is also used in the paper and pulp industries and the textiles industry.
Cosmetics and personal care uses of Trisodium Citrate Dihydrate: In cosmetics and personal care products, trisodium citrate is used as a buffering agent to maintain the pH of formulations and as a preservative to prevent microbial growth.


Cleaning products uses of Trisodium Citrate Dihydrate: Trisodium Citrate Dihydrate is used in some cleaning products, particularly in eco-friendly and biodegradable formulations, due to its ability to soften water, remove soap scum, and dissolve scale deposits.
Trisodium Citrate Dihydrate is typically used as a flavoring agent or as a preservative.


Trisodium Citrate Dihydrate is used as a plaster retardant.
The common hydrate form, Trisodium Citrate Dihydrate, is widely used in foods, beverages and various technical applications mainly as buffering, sequestering or emulsifying agent.


Trisodium Citrate Dihydrate is used as a food additive and flavouring agent, this product possesses a saline, mildly tart flavour that can help in water sensitive formulations like instant drinks as well as tablets and powders in pharmaceuticals and detergents.
In the food industry, Trisodium Citrate Dihydrate is used as a flavor enhancer, acidity regulator, and emulsifier.


In the medical field, Trisodium Citrate Dihydrate is used as an anticoagulant but it is also an ingredient in many personal care products.
Trisodium Citrate Dihydrate is also an essential ingredient in dishwasher tablets, industrial cleaners, detergents, etc.
Trisodium Citrate Dihydrate is typically used as a buffer component in biomolecule downstream processing and liquid formulation.


Trisodium Citrate Dihydrate is typically used as a citrate buffer system component for biomolecule downstream chromatography steps or final liquid formulation.
Trisodium Citrate Dihydrate has a variety of applications in different industries due to its properties as a buffering agent, sequestrant, and emulsifying agent.


Trisodium Citrate Dihydrate is a high quality pharmaceutical excipient, offered with extensive documentation facilitating compliance, full supply chain transparency and risk mitigation.
Trisodium Citrate Dihydrate is the dihydrate of trisodium citrate.


Trisodium Citrate Dihydrate has a role as an anticoagulant.
Trisodium Citrate Dihydrate contains a sodium citrate.
Trisodium Citrate Dihydrate is often used as a food preservative, and as a flavoring in the food industry.


In the pharmaceutical industry, Trisodium Citrate Dihydrate is used to control pH.
Trisodium Citrate Dihydrate may be used as an alkalizing agent, buffering agent, emulsifier, or sequestering agent.
Sodium salts of citric acid are used as buffers and food preservatives.


They are used medically as anticoagulants in stored blood, and for urine alkalization in the prevention of KIDNEY STONES.
Trisodium Citrate Dihydrate is widely used in foods, beverages and various technical applications mainly as buffering, sequestering or emulsifying agent.
Buffers pH and enhances action of methyl parabens.


Trisodium Citrate Dihydrate is used in toothpastes & dental creams, effervescent denture cleansers, mouth rinses and oral hygiene products.
Trisodium Citrate Dihydrate is used as a substrate for citrate lyase, a buffer component; an anticoagulant.
For anticoagulation use Trisodium Citrate Dihydrate is typically used at a concentration of approximately 0.129 M (i.e. for 4.5 mL blood use 16.0 mg sodium citrate and 2.1 mg citric acid).


Trisodium Citrate Dihydrate is used preparation of sodium citrate buffer for antigen unmasking in IHC.
Trisodium Citrate Dihydrate has no toxic effect, and has pH adjusting capability as well as having a good stability, and therefore can be used in the food industry.


Trisodium Citrate Dihydrate has the greatest demand when being used as a food additive.
As food additives, Trisodium Citrate Dihydrate is mainly used as flavoring agents, buffers, emulsifiers, bulking agents, stabilizers and preservatives.
In addition, combination between Trisodium Citrate Dihydrate and citric acid can be used in a variety of jams, jelly, juice, drinks, cold drinks, dairy products and pastries gelling agents, flavoring agents and nutritional supplements.


Trisodium Citrate Dihydrate is used as a substrate for citrate lyase, a buffer component; an anticoagulant.
For anticoagulation use Trisodium Citrate Dihydrate is typically used at a concentration of approximately 0.129 M (i.e. for 4.5 mL blood use 16.0 mg sodium citrate and 2.1 mg citric acid).


Trisodium Citrate Dihydrate is a source of Citric acid, a key metabolic intermediate.
Citrate is the starting point of the tricarboxylic acid cycle.
Trisodium Citrate Dihydrate's concentration also coordinates several other metabolic pathways.
Citric acid can form complexes with various cations, particularly with iron and calcium.


In animals, citric acid improves the utilization of nutritional calcium.
Trisodium Citrate Dihydrate is also known as Sodium Citrate which is a sodium salt from citric acid.
Trisodium Citrate Dihydrate is used in food products as a preservative as well as to add a tart flavor profile.


Trisodium Citrate Dihydrate is commonly used as a flavoring agent in drinks as well as processed cheese, ice cream, yogurt and jams.
As an ingredient in personal care products, Trisodium Citrate Dihydrate is used in cosmetics and other skin care products primarily to control the pH level, as well as for its preservative properties.


As an ingredient in supplements, Trisodium Citrate Dihydrate helps control pH in the kidneys helping to prevent gout and certain types of kidney stones.
In this application Trisodium Citrate Dihydrate is normally combined with Citric Acid.
Trisodium Citrate Dihydrate is a useful reactant in organic synthesis.


Trisodium Citrate Dihydrate is used as a flavouring agent and an anticoagulant.
Moreover, Trisodium Citrate Dihydrate is also widely used in chemical, metallurgical industry, the absorption of sulfur dioxide exhaust with the absorption rate of 99% and regenerate liquid sulfur dioxide citrate for recycle application.


Trisodium Citrate Dihydrate has a good water solubility and a excellent cheating capability with Ca2 +, Mg2 + and other metal ions.
Trisodium Citrate Dihydrate is biodegradable and has a strong dispersing ability and anti-redeposition ability.
Daily-applied chemical detergents use Trisodium Citrate Dihydrate as alternative to trimer sodium phosphate for production of non-phosphorus detergent and phosphate-free liquid detergent.


Adding a certain amount Trisodium Citrate Dihydrate to the detergent can significantly increase the cleaning ability of detergent cleaning.
The large scale of application of Trisodium Citrate Dihydrate as a builder in detergents is an important discovery in synthetic detergent industry.
Trisodium Citrate Dihydrate is non-toxic without environmental pollution.


Trisodium Citrate Dihydrate can also act as a buffer for the production of cosmetics.
Trisodium Citrate Dihydrate can be used as Ph adjusting agents and emulsifying enhancers applied to jam, candy, jelly and ice cream; its combination with citric acid has an effect of alleviating tour.


Trisodium Citrate Dihydrate also has effects on forming complex with metal ions.
China rules that Trisodium Citrate Dihydrate can be applied to various types of food with appropriate usage according to the absolute necessity.
Trisodium Citrate Dihydrate can be used as a food additive, as complex agent and buffering agent in electroplating industry; at the field of pharmaceutical industry.


Trisodium Citrate Dihydrate is used for the manufacturing of anti-clotting drugs, and used as the detergent additives in light industry.
Trisodium Citrate Dihydrate is used as the analysis agents used for chromatography analysis and can also used for preparing bacterial culture medium.
Moreover, Trisodium Citrate Dihydrate can also be applied into pharmaceutical industry.


Trisodium Citrate Dihydrate can be used for the flavoring processing of food, as stabilizers, buffers and deputy complex-forming agents in non-toxic electroplating industry.
At pharmaceutical industry, Trisodium Citrate Dihydrate is used as anti-clotting agent, phlegm drugs and diuretics drugs.


Trisodium Citrate Dihydrate can also be used in brewing, injection, newspaper and movies medicines.
Trisodium Citrate Dihydrate is chiefly used as a food additive, usually for flavor or as a preservative.
Trisodium Citrate Dihydrate is used as an anticoagulant for collection of blood.


In photography, Trisodium Citrate Dihydrate is used as a sequestering agent to remove trace metals
Trisodium Citrate Dihydrate is used as emulsifier, acidulant and sequestrant in foods.
Trisodium Citrate Dihydrate is used as an anticoagulant, also used as a biological buffer.


Food uses of Trisodium Citrate Dihydrate: Baby Food, Infant Formula, Bakery, Cereals, Snacks, Confectionery, Dairy, Dairy Alternatives, Desserts, Ice Cream, Flavours, Fruit Preparations, Sweet Spreads, Fruits, Vegetables, Meat Alternatives, Meat, Seafood, Plant-based Products, Ready Meals, Instant Food, Sauces, Dressings, Seasonings.


Trisodium Citrate Dihydrate, is widely applied in food, beverages and fillers as a buffering, sequestering or an emulsifying agent.
Trisodium Citrate Dihydrate used as an anticoagulant in blood transfusions, osmotic laxative, functional fluids, solvents cleaning, furnishing care products, laundry dishwashing products and cleaning automobile radiators.
Trisodium Citrate Dihydrate is commonly used laboratory reagent.


Healthcare uses of Trisodium Citrate Dihydrate: Clinical Nutrition, Medical Devices, OTC, Food Supplements, and Pharmaceutical Products
Personal Care uses of Trisodium Citrate Dihydrate: Colour Cosmetics, Fragrances, Hair Care, Oral Care, Skin Care,, and Soap and Bath Products
Cleaners & Detergents uses of Trisodium Citrate Dihydrate: Dish Washing, Industrial Cleaners, Laundry Care, and Surface Care.


Industrial Applications uses of Trisodium Citrate Dihydrate: Adhesives, Sealants, Agrochemicals, Fertilisers, Construction, Fine Chemicals, Inks, Paints, Coatings, Oil Drilling, Paper, Plastics, Polymers, Textile, and Leather.
Feed & Pet Food uses of Trisodium Citrate Dihydrate: Feed, and Pet Food


Pharma uses of Trisodium Citrate Dihydrate: Buffering agent, Chelating agent, Mineral source.
Beverages uses of Trisodium Citrate Dihydrate: Alcoholic Beverages, Carbonated Soft Drinks, Instant Drinks, Syrups, Juice Drinks, Plant-based, RTD Tea and Coffee, Sports and Energy Drinks, Waters.


Trisodium Citrate Dihydrate is also used as an emulsifier for oils in the cheesemaking process.
Trisodium Citrate Dihydrate allows cheese to melt without becoming greasy.
Historically, sodium phosphate was used to keep water and fat droplets mixed when cheese is melted.


Trisodium Citrate Dihydrate is used Soy Products Bakery Flavors.
Trisodium Citrate Dihydrate is used Table Top Product Dairy Confectionery.
Trisodium Citrate Dihydrate is used Fruits, Vegetables Meat, Seafood , Cereals, Snacks Desserts, Ice Cream Ready Meals, Instant Food.


Trisodium Citrate Dihydrate is used Fruit Preparations, Sweet Spreads Baby Food, Infant Formula.
Trisodium Citrate Dihydrate is used Sauces, Dressings, Seasoning.
Trisodium Citrate Dihydrate helps in enabling the melting of cheeses by not becoming greasy.


Trisodium Citrate Dihydrate is used in drinks and food as an acidity regulator.
Trisodium Citrate Dihydrate is used as an emulsifier for oils.
Trisodium Citrate Dihydrate is used as a pharmaceutical aid.


Trisodium Citrate Dihydrate is used as an anticoagulant for the blood.
Trisodium Citrate Dihydrate is used to prevent curdling of milk.
Trisodium Citrate Dihydrate is used as a food additive.


Trisodium Citrate Dihydrate is used to avoid clotting of fresh beef blood.
Trisodium Citrate Dihydrate is used in electroplating.
Trisodium Citrate Dihydrate is used Fruits & Vegetables: Jams & Jellies, Preserves, and Meat & Fish.


Trisodium Citrate Dihydrate has significant applications in food and beverage, healthcare, and other industries.
Trisodium Citrate Dihydrate usage is primarily done as an emulsifier in the production of dairy products such as cheese because it can keep a dairy product fresh for many days longer than other solutions.


Sodium citric acid is also a flavoring agent in many products such as milk powders, ice cream, wine, beverages, and jams.
Metabolic acidosis uses of Trisodium Citrate Dihydrate: Trisodium Citrate Dihydrate has applications for the treatment of metabolic acidosis and chronic kidney disease.
Ferrous nanoparticles uses of Trisodium Citrate Dihydrate: Along with oleic acid Trisodium Citrate Dihydrate may be used in the synthesis of magnetic Fe3O4 nanoparticle coatings.


Trisodium Citrate Dihydrate is used to relieve discomfort in urinary-tract infections, such as cystitis, to reduce the acidosis seen in distal renal tubular acidosis, and can also be used as an osmotic laxative.
Trisodium Citrate Dihydrate is a major component of the WHO oral rehydration solution.


Trisodium Citrate Dihydrate is used as an antacid, especially prior to anaesthesia, for caesarian section procedures to reduce the risks associated with the aspiration of gastric contents.
Trisodium Citrate Dihydrateprevents and treats high acid levels in your body.


Trisodium Citrate Dihydrate may also be used to help prevent gout or kidney stones, conditions caused by high uric acid levels.
Trisodium Citrate Dihydrate works by decreasing the amount of acid in your body.
Trisodium Citrate Dihydrate may be used for other purposes; ask your health care provider or pharmacist if you have questions.


Trisodium Citrate Dihydrate can be used to treat metabolic acidosis, where the generated bicarbonate buffers excess hydrogen ions in the blood, raising its p H.
Trisodium Citrate Dihydrate can also be used to alkalinize urine by promoting urinary excretion of free bicarbonate and therefore hydrogen ions.
Trisodium Citrate Dihydrate can be used to prevent development of renal stones that develop in acidic urine Fan et al, and in solution is administered as a bladder irritant during urological surgery.


Trisodium Citrate Dihydrate is administered rectally as an osmotic laxative.
Trisodium Citrate Dihydrate is a compound commonly used as an acidity regulator, an emulsifier, and a flavor enhancer in a wide range of food products and as a component of electrolyte solutions in medical settings.


Trisodium Citrate Dihydrate is also used as a sequestrant, which means it can bind to metal ions in food and prevent them from reacting with other ingredients.
Trisodium Citrate Dihydrate is also often used in cheese-making as a emulsifying salt, and as a coagulant in tofu production.
Trisodium Citrate Dihydrate is commonly added to soft drinks, ice cream, and other processed foods as a flavor enhancer and preservative.


Trisodium Citrate Dihydrate can also be used in medical applications, such as to prevent blood clots during surgery.
Trisodium Citrate Dihydrate is also used in cosmetic products, such as shampoos and body washes, as a pH regulator and as a chelating agent to prevent discoloration and maintain the stability of the product.


Trisodium Citrate Dihydrate is a salt of citric acid.
Use a small amount of Trisodium Citrate Dihydrate to make a melty cheese sauce out of any cheese.
Add to spherification liquids to neutralize the pH when needed


Commonly used as a sequestrant and pH buffer in food and beverages
Trisodium Citrate Dihydrate is widely used as a food preservative, for alkalization of urine to prevent kidney stones, as an anticoagulant for stored blood, and buffer.
Cosmetic manufacturers use Trisodium Citrate Dihydrate to adjust the acidity of a product.


Citrate, in the form of citric acid, is also found in citric fruits and juices.
Trisodium Citrate Dihydrate is used as a flavouring agent and an anticoagulant.
Trisodium Citrate Dihydrate is used to make urine less acidic and therefore prevent the formation of kidney stones.


Trisodium Citrate Dihydrate/citric acid also is useful as a buffer and neutralizing agent for gastric acid.
Trisodium Citrate Dihydrate is broken down to sodium bicarbonate which decreases the acidity of urine, increasing the excretion of substances that cause kidney stones.
Trisodium Citrate Dihydrate is commonly known as sour salt and is mainly used as a food additive, usually for flavor or as a preservative.


Trisodium Citrate Dihydrate has major applications in food and beverage, healthcare, and other industrial ones too.
Trisodium Citrate Dihydrate is used as a food additive, as a buffering agent and can also be used in medical applications.
Trisodium Citrate Dihydrate is used anticoagulant for collection of blood.


In photography; Trisodium Citrate Dihydrate is used as sequestering agent to remove trace metals.
Trisodium Citrate Dihydrate is used as emulsifier, acidulant and sequestrant in foods.
Trisodium Citrate Dihydrate is a useful and commonly used reagent.


Trisodium Citrate Dihydrate is the sodium salt of citric acid, it is commonly added to cosmetic and food preparations as a chelating and buffering agent.
Buffers help to maintain the pH of a product and keep it stable.
Trisodium Citrate Dihydrate also has mild antioxidant properties and can act as a co-preservative.


Trisodium Citrate Dihydrate is in the form of TriTrisodium Citrate Dihydrate Dihydrate.
Trisodium Citrate Dihydrate is intended for external use only.
Trisodium Citrate Dihydrate is a vital substance in the medicine and food industries.


Trisodium Citrate Dihydrate is a salt of citric acid, a natural organic acid found in citrus fruits, corn, and other foods.
Trisodium Citrate Dihydrate is available in colorless crystals or white powder.
This is typically sold as white, crystalline triTrisodium Citrate Dihydrate dihydrate.


As a food additive, Trisodium Citrate Dihydrate is widely used as a flavoring agent and a preservative in the food industry.
Flavoring agents like E331 are most commonly seen.
Trisodium Citrate Dihydrate is the sodium salt of citrate and is the compound formed after alkalinizing activity.


Citrate anions and sodium cations are formed upon absorption of Trisodium Citrate Dihydrate.
Trisodium Citrate Dihydrate is a sodium salt of citrate with alkalinizing properties.
TriTrisodium Citrate Dihydrate is another name for Trisodium Citrate Dihydrate.


Trisodium Citrate Dihydrate can be used as a food preservative, an anticoagulant for stored blood, and an alkalizing agent for urine to eliminate kidney stones.
The three types of Trisodium Citrate Dihydrate are monosodium, disodium, and triTrisodium Citrate Dihydrates.
Trisodium Citrate Dihydrate is mildly basic and can be used along with citric acid to make biologically compatible buffers.


Trisodium Citrate Dihydrate is primarily used as a food additive, usually for flavor or as a preservative.
In certain varieties of club soda, Trisodium Citrate Dihydrate is employed as a flavoring agent.
Trisodium Citrate Dihydrate is a common ingredient in Bratwurst, and is also used to contribute a tart flavor in commercial, ready-to- drink beverages and drink mixes.


Trisodium Citrate Dihydrate is found in gelatin mix, ice-cream, jams, sweets, milk powder, processed cheeses, carbonated beverages, and wine.
If used together with Trisodium Citrate Dihydrate, it is possible for citric acid to help maintain the flavor of other types of soft drinks without adding to the tanginess.


Trisodium Citrate Dihydrate can also provide a cool saline taste.
Trisodium Citrate Dihydrate is used Dish Washing Industrial Cleaners and Laundry Care Surface Care.
Trisodium Citrate Dihydrate acts as a buffering agent in cosmetics products to control their pH level.


Trisodium Citrate Dihydrate can also be used as a preservative.
Trisodium Citrate Dihydrate is used in various cosmetic products, including baby products, make-up, bath products, hair dyes and colors and skin care products.


Trisodium Citrate Dihydrate in skin care is used primarily to control the pH level of a product (such as in cleansers and exfoliants).
Trisodium Citrate Dihydrate is a salt of citric acid, which, as the name implies, can be derived from citrus fruits.
Because of its connection to citric acid, Trisodium Citrate Dihydrate also has antioxidant and mild, but limited, preservative properties.


Trisodium Citrate Dihydrate has several other useful applications, including its use as a chelating agent, which keeps metals in water from binding to other ingredients and impacting their efficacy.


Trisodium Citrate Dihydrate is supplied in crystal or powder form, and used at concentrations no higher than 12%.
Trisodium Citrate Dihydrate’s also a food additive used to keep food fresher longer and prevent melted cheese from becoming greasy.
In the medical field Trisodium Citrate Dihydrate is used to keep donated blood from clotting in storage.


A little helper ingredient, Trisodium Citrate Dihydrate is used to adjust the pH of the product.
Trisodium Citrate Dihydrate also helps to keep products stay nice longer by neutralizing the metal ions in the formula (they usually come from water).
Trisodium Citrate Dihydrate is widely used as a food preservative, anticoagulant for stored blood, and alkalization of urine to get rid of kidney stones.


Trisodium Citrate Dihydrate formula is Na3C6H5O7.
Trisodium Citrate Dihydrate gets majorly used in medicine as well as the food industry.


-Pharmaceutical industry uses of Trisodium Citrate Dihydrate:
Trisodium Citrate Dihydrate is used as an anticoagulant in blood collection tubes, a buffering agent in various medications, and a urinary alkalizer to help treat certain kidney conditions.
Trisodium Citrate Dihydrate can also be used as an osmotic laxative to relieve constipation.


-Laboratory applications of Trisodium Citrate Dihydrate:
In the laboratory setting, Trisodium Citrate Dihydrate is commonly used as a buffer in molecular biology experiments, particularly in gel electrophoresis and DNA extraction procedures.
Trisodium Citrate Dihydrate helps maintain a stable pH and protects samples from degradation.



-Pharmacodynamics uses of Trisodium Citrate Dihydrate:
Trisodium Citrate Dihydrate prevents activation of the clotting cascade by chelating calcium ions.
Trisodium Citrate Dihydrate neutralizes acid in the stomach and urine, raising the pH 8.


-Food applications of Trisodium Citrate Dihydrate:
Trisodium Citrate Dihydrate is used as acidity regulators in food and drinks, and also as emulsifiers for oils.
Trisodium Citrate Dihydrate enables cheeses to melt without becoming greasy.
Trisodium Citrate Dihydrate reduces the acidity of food as well.


-Blood clotting inhibitor uses of Trisodium Citrate Dihydrate:
Trisodium Citrate Dihydrate is used to prevent donated blood from clotting in storage.
Trisodium Citrate Dihydrate is also used in a laboratory, before an operation, to determine whether a person's blood is too thick and might cause a blood clot, or if the blood is too thin to safely operate.
Trisodium Citrate Dihydrate is used in medical contexts as an alkalinizing agent in place of sodium bicarbonate, to neutralize excess acid in the blood and urine.


-Foods uses of Trisodium Citrate Dihydrate:
Trisodium Citrate Dihydrate is chiefly used as a food additive, usually for flavor or as a preservative.
Trisodium Citrate Dihydrate's E number is E331.
Trisodium Citrate Dihydrate is employed as a flavoring agent in certain varieties of club soda.

Trisodium Citrate Dihydrate is common as an ingredient in bratwurst, and is also used in commercial ready-to-drink beverages and drink mixes, contributing a tart flavor.
Trisodium Citrate Dihydrate is found in gelatin mix, ice cream, yogurt, jams, sweets, milk powder, processed cheeses, carbonated beverages, and wine, amongst others.

Trisodium Citrate Dihydrate can be used as an emulsifying stabilizer when making cheese.
Trisodium Citrate Dihydrate allows the cheese to melt without becoming greasy by stopping the fats from separating.


-Buffering uses of Trisodium Citrate Dihydrate:
As a conjugate base of a weak acid, Trisodium Citrate Dihydrate can perform as a buffering agent or acidity regulator, resisting changes in pH.
Trisodium Citrate Dihydrate is used to control acidity in some substances, such as gelatin desserts.
Trisodium Citrate Dihydrate can be found in the milk minicontainers used with coffee machines.

Trisodium Citrate Dihydrate is the product of antacids, such as Alka-Seltzer, when they are dissolved in water.
The pH of a solution of 5 g/100 ml water at 25 °C is 7.5 – 9.0.
Trisodium Citrate Dihydrate is added to many commercially packaged dairy products to control the pH impact of the gastrointestinal system of humans, mainly in processed products such as cheese and yogurt, although Trisodium Citrate Dihydrate also has beneficial effects on the physical gel microstructure.


-Chemistry uses of Trisodium Citrate Dihydrate:
Trisodium Citrate Dihydrate is a component in Benedict's qualitative solution, often used in organic analysis to detect the presence of reducing sugars such as glucose.


-Medicine uses of Trisodium Citrate Dihydrate:
In 1914, the Belgian doctor Albert Hustin and the Argentine physician and researcher Luis Agote successfully used Trisodium Citrate Dihydrate as an anticoagulant in blood transfusions, with Richard Lewisohn determining its correct concentration in 1915.
Trisodium Citrate Dihydrate continues to be used today in blood-collection tubes and for the preservation of blood in blood banks.

The citrate ion chelates calcium ions in the blood by forming calcium citrate complexes, disrupting the blood clotting mechanism.
Recently, triTrisodium Citrate Dihydrate has also been used as a locking agent in vascath and haemodialysis lines instead of heparin due to its lower risk of systemic anticoagulation.


-Boiler descaling uses of Trisodium Citrate Dihydrate:
Trisodium Citrate Dihydrate is a particularly effective agent for removal of carbonate scale from boilers without removing them from operation and for cleaning automobile radiators.


-Food & Beverage uses of Trisodium Citrate Dihydrate:
Trisodium Citrate Dihydrate dihydrate is the most widely used emulsifying salt in sliced processed cheese products.
Trisodium Citrate Dihydrate is commonly used as a buffering agent in combination with citric acid to provide precise pH control required in many food and beverage applications.


-Food and Beverage uses of Trisodium Citrate Dihydrate:
Trisodium Citrate Dihydrate is used as an emulsifying salt in processed cheese products.
The cheese may melt without getting greasy thanks to Trisodium Citrate Dihydrate.
When combined with citric acid, Trisodium Citrate Dihydrate acts as a buffering agent, allowing for precise pH regulation in various foods and beverages.

Trisodium Citrate Dihydrate prevents milk from curdling.
Trisodium Citrate Dihydrate is employed in the emulsification of oils.
Trisodium Citrate Dihydrate's primary purpose is to act as a food additive to enhance flavor or preserve food.


-Healthcare uses of Trisodium Citrate Dihydrate:
Trisodium Citrate Dihydrate is an effective blood anticoagulant.
As a result, Trisodium Citrate Dihydrate is frequently used for blood collection and storage.
Trisodium Citrate Dihydrate can help to alleviate the discomfort associated with urinary tract infections.

Trisodium Citrate Dihydrate can also be used as a laxative to treat acidosis.
Trisodium Citrate Dihydrate’s essential to the World Health Organization’s oral rehydration solution.
Trisodium Citrate Dihydrate can also be used as an antacid, particularly before surgery.

Trisodium Citrate Dihydrate is found in many pharmaceuticals, colors, cosmetics, and deodorants.
Trisodium Citrate Dihydrate can be found in hair, oral, skin, and bathing products.
To treat excess acid in the stomach, Trisodium Citrate Dihydrate acts as a buffer and a neutralizing agent.
Trisodium Citrate Dihydrate is also used to treat metabolic acidosis, a type of renal problem that affects some people.


-Industrial Applications of Trisodium Citrate Dihydrate:
Trisodium Citrate Dihydrate is used in industry as a cleaner.
Trisodium Citrate Dihydrate aids in the removal of calcium and rust layers from hot water systems and steam lines.
In electroplating processes, Trisodium Citrate Dihydrate also acts as a buffering and complexing agent.

Citric acid’s chelating ability and non-toxicity benefit the textile and building industries.
To avoid microbial contamination, Trisodium Citrate Dihydrate is used as a flavoring and preservative (i.e. as a food additive).
Trisodium Citrate Dihydrate is used as an oil emulsifier in cheese production.

Trisodium Citrate Dihydrate is a buffering agent in cosmetics to keep the pH stable.
Trisodium Citrate Dihydrate is used in soft and refreshing drinks to reduce sourness and enhance flavor.
Trisodium Citrate Dihydrate is found in dishwashing detergents, laundry detergents, and surface-active agents.


-Food and Beverage uses of Trisodium Citrate Dihydrate:
Trisodium Citrate Dihydrate gets used as an emulsifying salt in processed cheese products.
Trisodium Citrate Dihydrate facilitates the melting of cheese without becoming greasy.

Trisodium Citrate Dihydrate works as a buffering agent in combination with citric acid, and it offers accurate pH control necessary for numerous foods and beverages.
Trisodium Citrate Dihydrate's main job is being a food additive, either for flavor to improve taste or preservation purposes.


-Healthcare uses of Trisodium Citrate Dihydrate:
Trisodium Citrate Dihydrate works perfectly as an anticoagulant for the blood.
Thus, Trisodium Citrate Dihydrate gets widely used for blood collection and storage purposes.

Trisodium Citrate Dihydrate can provide relief from the discomfort in urinary tract infections.
Trisodium Citrate Dihydrate is also a great laxative and reduces several acidosis issues.
Trisodium Citrate Dihydrate’s a significant ingredient of WHO’s oral rehydration solution.

Trisodium Citrate Dihydrate also serves as an antacid, especially before anaesthesia.
You can easily find Trisodium Citrate Dihydrate in many pharmaceutical products, colour, cosmetics, and deodorants.
Trisodium Citrate Dihydrate’s also present in hair care, oral care, skincare, and bathing products.


-Industrial Applications of Trisodium Citrate Dihydrate:
Trisodium Citrate Dihydrate is used as an industrial cleaner.
Trisodium Citrate Dihydrate helps with clearing steam blocks, hot water systems of calcium and rust layers.

Trisodium Citrate Dihydrate also serves as a buffering and complexing agent in electroplating processes.
Textile and building industry, Trisodium Citrate Dihydrate gets benefited by the chelating ability and non-toxicity of citric acid.



EFFECT AND APPLICATION OF TRISODIUM CITRATE DIHYDRATE:
During the process of clinically taking fresh blood, adding some amount of sterile sodium citrate can play a role in prevent blood clotting; this is exactly taking advantage of the features that calcium citrate can form soluble complexes with calcium ion; In the field of medicine, Trisodium Citrate Dihydrate is used for the in vitro anti-clotting drugs and anticoagulants drugs, phlegm drugs, and diuretics drugs during blood transfusions; it can also used for cyanide-free electroplating industry; also used as developer for photographic industry.
Trisodium Citrate Dihydrate can be used as flavoring agents, buffering materials, emulsifiers, and stabilizer in the food industry.



PHARMACEUTICAL APPLICATIONS OF TRISODIUM CITRATE DIHYDRATE:
Trisodium Citrate Dihydrate, as either the dihydrate or anhydrous material, is widely used in pharmaceutical formulations.
Trisodium Citrate Dihydrate is used in food products, primarily to adjust the pH of solutions.
Trisodium Citrate Dihydrate is also used as a sequestering agent. The anhydrous material is used in effervescent tablet formulations. Trisodium Citrate

Dihydrate is additionally used as a blood anticoagulant either alone or in combination with other citrates such as disodium hydrogen citrate.
Therapeutically, Trisodium Citrate Dihydrate is used to relieve the painful irritation caused by cystitis, and also to treat dehydration and acidosis due to diarrhea.



CHEMICAL PROPERTIES OF TRISODIUM CITRATE DIHYDRATE:
Trisodium Citrate Dihydrate is colorless crystals or white crystalline powder, and is odorless, cool and salty.
Trisodium Citrate Dihydrate has no melting point with a relative density of 1.857.

Trisodium Citrate Dihydrate is stable in air at room temperature with loss of crystal water when being heated to 150 °C loss of crystal water; further heating will cause its decomposition.
Trisodium Citrate Dihydrate is insoluble in ethanol but highly soluble in water. 5% aqueous solution has a pH value of 7.6 to 8.6.



CHARACTERISTICS OF TRISODIUM CITRATE DIHYDRATE:
Trisodium Citrate Dihydrate is a White, granular crystals or a white, crystalline powder; slightly deliquescent (tending to absorb moisture from the air and dissolve in it) in moist air, is freely soluble in water, and practically insoluble in ethanol (96%).
Trisodium Citrate Dihydrate is practically odorless and is colorless in solution.



SPECIFICATIONS OF TRISODIUM CITRATE DIHYDRATE:
Trisodium Citrate Dihydrate is GRAS affirmed under 21 CFR 184.1751.
Trisodium Citrate Dihydrate meets all requirements of the U.S. Pharmacopoeia, Food Chemical Codex, Code of Federal Regulations and European Pharmacopoeia.
Trisodium Citrate Dihydrate goes by EC No. 200-675-3, E Number E331 and CAS No. 6132-04-3.
Trisodium Citrate Dihydrate is certified as Kosher.



EXCELLENT PERFORMANCE OF TRISODIUM CITRATE DIHYDRATE:
Trisodium Citrate Dihydrate is currently the most important citrate.
Trisodium Citrate Dihydrate is produced by two steps: first starch food is fermented to generate citric acid; secondly, citric acid is neutralized by alkali to generate the final products.
Trisodium Citrate Dihydrate has the following excellent performance:



SAFE AND NONTOXIC PROPERTIES OF TRISODIUM CITRATE DIHYDRATE:
Since the basic raw material for the preparation of Trisodium Citrate Dihydrate mainly comes from the food, it is absolutely safe and reliable without causing harm to human health.
The United Nations Food and Agriculture and the World Health Organization has no restriction in its daily intake, which means that Trisodium Citrate

Dihydrate can be considered as non-toxic food.
Trisodium Citrate Dihydrate is biodegradable.
After subjecting to the dilution of a large amount of water, Trisodium Citrate Dihydrate is partially converted into citrate, which coexists with Trisodium
Citrate Dihydrate in the same system.

Citrate is easy to subject to biological degradation at water by the action of oxygen, heat, light, bacteria and microbes.
Trisodium Citrate Dihydrate's decomposition pathways are generally going through aconitic acid, itaconic acid, citraconic acid anhydride to be further converted to carbon dioxide and water.

The ability of forming complex with metal ions.
Trisodium Citrate Dihydrate has a good capability of forming complex with some metal ions such as Ca2+, Mg2+; for other ions such as Fe2+, it also has a good complex-forming ability.
Excellent solubility, and the solubility increases with increasing temperature of water.

Trisodium Citrate Dihydrate has a good capability for pH adjustment and a good buffering property.
Trisodium Citrate Dihydrate is a weak acid-strong alkali salt; When combined with citrate, they can form a pH buffer with strong compatibility; therefore, this is very useful for some cases in which it is not suitable to have large change of pH value.
In addition, Trisodium Citrate Dihydrate also has excellent retardation performance and stability.



MAIN FUNCTIONS OF TRISODIUM CITRATE DIHYDRATE:
*pH regulator
*Chelating agent
*Buffering agent
*Flavour enhancer
*Stabiliser
*Emulsifying agent



PROPERTIES OF TRISODIUM CITRATE DIHYDRATE:
*Dihydrate
*White
*Granular crystals or crystalline powder
*Typical, practically odourless
*Pleasantly salty
*Freely soluble in water
*Practically insoluble in ethanol (96 %)
*Non-toxic
*Low reactive
*Chemically and microbiologically stable
*Fully biodegradable



PRODUCTION METHODS OF TRISODIUM CITRATE DIHYDRATE:
Trisodium Citrate Dihydrate is produced by the neutralization of citric acid by sodium hydroxide or sodium bicarbonate.
Dissolve sodium bicarbonate in water upon stirring and heating; add citric acid, continue to heat up to 85-90 °C; adjust the pH to 6.8; adjust active carbon for bleaching.

Filter when the mixture is still hot; condense the filtrate under reduced pressure; cool and the crystal comes out; filter, wash, dry to obtain the final products of sodium citrate.
C6H8O7 + 3NaHCO3 → C6H5Na3O7 • 2H2O + 3CO2 ↑ + H2O



CHEMICAL PROPERTIES OF TRISODIUM CITRATE DIHYDRATE:
Trisodium Citrate Dihydrate consists of odorless, colorless, monoclinic crystals, or a white crystalline powder with a cooling, saline taste.
Trisodium Citrate Dihydrate is slightly deliquescent in moist air, and in warm dry air it is efflorescent.



PRODUCTION METHODS OF TRISODIUM CITRATE DIHYDRATE:
Trisodium Citrate Dihydrate is prepared by adding sodium carbonate to a solution of citric acid until effervescence ceases.
The resulting solution is filtered and evaporated to dryness.



FUNCTIONS OF TRISODIUM CITRATE DIHYDRATE:
*Sequestering Agent,
*Buffering Agent,
*Supplement,
*Stabilizer,
*Emulsifier



PURIFICATION METHODS OF TRISODIUM CITRATE DIHYDRATE:
Crystallise the salt from warm water by cooling to 0o.



INCOMPATIBILITIES OF TRISODIUM CITRATE DIHYDRATE:
Aqueous solutions are slightly alkaline and will react with acidic substances.
Alkaloidal salts may be precipitated from their aqueous or hydro-alcohol solutions.
Calcium and strontium salts will cause precipitation of the corresponding citrates.
Other incompatibilities include bases, reducing agents, and oxidizing agents.



BIOCHME/PHYSIOL ACTIONS OF TRISODIUM CITRATE DIHYDRATE:
Trisodium Citrate Dihydrate can act as a buffering agent, resisting changes in pH.
Trisodium Citrate Dihydrate is used in blood collection tubes, the citrate chelates calcium ions in blood and thereby disrupts blood clotting.
Citrate is a intermediate in the TCA cycle and fatty acid synthesis.
Citrate is an allosteric modulator of acetyl-CoA carboxylase, the enzyme that regulates the conversion of acetyl-CoA to malonyl-CoA.



USING TRISODIUM CITRATE DIHYDRATE TO RETARD PLASTER MIXES:
Trisodium Citrate Dihydrate, is sometimes used in plastering as a retarder or setting time regulator.
Plaster is made by mixing gypsum powder with water, and then the mixture is applied to a surface where it hardens as it dries
Trisodium Citrate Dihydrate can be added to the water used to mix the plaster to slow down the setting time of the mixture.

Trisodium Citrate Dihydrate can be useful in situations where more time is needed to work with the plaster or to apply it to a surface, as it prevents the plaster from setting too quickly.
The amount of Trisodium Citrate Dihydrate required to slow down the setting time of plaster can vary depending on the specific application and the desired outcome.

As a general guideline, a concentration of 0.2% to 0.5% of the weight of the gypsum in the plaster mixture is often used.
For example, if you are using 1 kilogram of gypsum powder to make your plaster mixture, you could add between 2 to 5 grams of Trisodium Citrate Dihydrate to the water used to mix the plaster.

However, it's important to note that adding too much Trisodium Citrate Dihydrate can weaken the strength of the plaster and affect its overall quality.
So, Trisodium Citrate Dihydrate's recommended to start with a small amount and gradually increase the concentration until you achieve the desired setting time without compromising the strength of the plaster.



SKIN CARE USES OF TRISODIUM CITRATE DIHYDRATE:
The pH of a product is established and maintained by Trisodium Citrate Dihydrate.
While the skin's normal pH is slightly acidic, typically between 4.75 and 5.5, which effectively protects the skin from environmental factors such as allergens, pollutants, and bacteria, Trisodium Citrate Dihydrate can buffer solutions in the pH range of about 3 to 6.2.

The skin's acidity can change as a result of everything that comes into contact with Trisodium Citrate Dihydrate, including cosmetics, the sun, water, pollution, etc.
This ultimately hinders the skin's capacity to defend itself.
In order to maintain the skin's normal pH as closely as possible, Trisodium Citrate Dihydrate is crucial to balance the pH of cosmetics and skincare products.

A highly acidic product may irritate the skin, and a highly alkaline one may decrease its lipid contents.
By using an ingredient like Trisodium Citrate Dihydrate, cosmetic manufacturers can adjust the pH of their formulations, resulting in a product that is better suited to the skin



CLEANERS AND DETERGENTS USES OF TRISODIUM CITRATE DIHYDRATE:
The major components of cleaning products are surfactants and builders.
Other ingredients are added to provide a variety of functions, e.g., increasing cleaning performance for specific soils/surfaces, ensuring product stability, and supplying a unique identity to a product.

Complex phosphates and Trisodium Citrate Dihydrate are common sequestering builders.
Builders enhance or maintain the cleaning efficiency of the surfactant.
The primary function of builders is to reduce water hardness.

This is done either by sequestration or chelation (holding hardness minerals in solution); by precipitation (forming an insoluble substance); or by ion exchange (trading electrically charged particles).
Builders can also supply and maintain alkalinity, which assists cleaning, especially of acid soils; help keep removed soil from redepositing during washing, and emulsify oily and greasy soils.



FUNCTIONS OF TRISODIUM CITRATE DIHYDRATE:
*Trisodium Citrate Dihydrate acts as an emulsifier
*Buffering agent
*Trisodium Citrate Dihydrate acts as a sequestrant



ALTERNATIVES OF TRISODIUM CITRATE DIHYDRATE:
*SODIUM POLYASPARTATE,
*SODIUM PHYTATE,
*SORBIC ACID,
*BENZOIC ACID



PROPERTIES OF TRISODIUM CITRATE DIHYDRATE:
Trisodium Citrate Dihydrate's molecular formula is Na3C6H5O7, and its molecular weight or molar mass is 258.068 g/mol.
Trisodium Citrate Dihydrate's appearance is white and comes in the form of crystalline powder, or granular crystals.
Trisodium Citrate Dihydrate’s soluble in water and becomes deliquescent upon contact with moist air.

Trisodium Citrate Dihydrate’s insoluble in alcohol.
Trisodium Citrate Dihydrate has a sour taste like citric acid.
Trisodium Citrate Dihydrate has a total number of seven hydrogen bond acceptors and one hydrogen bond donor.

Monoisotopic mass of Trisodium Citrate Dihydrate is 257.973 g/mol.
The melting point of Trisodium Citrate Dihydrate is anywhere > (greater than) 3000 Celsius or 572 oF; 573K.



TRISODIUM CITRATE DIHYDRATE AT A GLANCE:
*Trisodium Citrate Dihydrate is a salt of citric acid, which can be derived from citrus
*Trisodium Citrate Dihydrate is primarily used to control the pH level of a product
*Trisodium Citrate Dihydrate has antioxidant and preservative properties
*Trisodium Citrate Dihydrate is also used in food and medical applications



WHAT DOES TRISODIUM CITRATE DIHYDRATE DO IN A FORMULATION?
*Buffering
*Chelating
*Preservative



FORMULA OF TRISODIUM CITRATE DIHYDRATE:
Trisodium Citrate Dihydrate's constituents are sodium and citric acid.
Trisodium Citrate Dihydrate's molecular formula is
C6H5Na3O7 or C6H5O7.3Na or Na3C6H5O7.

TriTrisodium Citrate Dihydrate or Trisodium 2-hydroxypropane-1,2,3-tricarboxylate are the IUPAC names for Trisodium Citrate Dihydrate.
Trisodium Citrate Dihydrate is also known by other names, such as Natrocitral Citrosodine.

Formation of Trisodium Citrate Dihydrate
When citric acid reacts with sodium bicarbonate in the presence of water in a bath bomb, this is formed.
C6H8O7 + 3NaHCO3 + H2O ⇢ Na3C6H5O7 + 3H2O + 3CO2



WHAT IS THE IMPACT OF TRISODIUM CITRATE DIHYDRATE ON THE BODY?
This is nothing more than a sodium salt with a citric acid base.
To reduce the urine’s acidity, Trisodium Citrate Dihydrate medication is used.
As a result, the kidneys can excrete uric acid, which can help prevent kidney stones and gout.

Trisodium Citrate Dihydrate can also treat and prevent kidney disease and metabolic issues such as acidosis.
In coagulation tests, Trisodium Citrate Dihydrate also functions as an anticoagulant.
Trisodium Citrate Dihydrate can aid in the prevention of coagulation by forming a calcium ion complex.
In all of these ways, Trisodium Citrate Dihydrate is used to treat and prevent diseases.



EXPLAIN THE SOLUBILITY OF TRISODIUM CITRATE DIHYDRATE:
Trisodium Citrate Dihydrate is stable in dry air but becomes anhydrous when exposed to 150 °C.
Trisodium Citrate Dihydrate is 1.3 parts water soluble and 0.6 parts boiling water soluble.
Trisodium Citrate Dihydrate is almost entirely insoluble in alcohol.
According to material safety data sheets, Trisodium Citrate Dihydrate's solubility at 25° C is 29 grams/Liter and 42.5 grams/100 according to International Chemical Safety Cards (ICSC).



HOW TRISODIUM CITRATE DIHYDRATE IS PRODUCED COMMERCIALLY?
Trisodium Citrate Dihydrate is typically produced by mixing a bit of sodium carbonate monohydrate with a hot aqueous five-citric acid solution.
The resulting solution is evaporated until crystallization occurs. Another way to make Trisodium Citrate Dihydrate is to decompose calcium citrate with an alkali metal salt.
The sodium salt of ten citric acids is known to exist in two forms: the so-called pentahydrate,15, and the di-hydrate CsH5O7Na3.2H2O



CONCLUSION OF TRISODIUM CITRATE DIHYDRATE:
Trisodium Citrate Dihydrate, also called triTrisodium Citrate Dihydrate is formed when citric acid reacts with sodium bicarbonate in the presence of water in a bath bomb.
Trisodium Citrate Dihydrate is a compound widely used in industries, healthcare, food, and beverages.
Trisodium Citrate Dihydrate is a familiar pH adjuster and water softener.

Trisodium Citrate Dihydrate can be found in many personal care products, including liquid laundry detergent, shampoo, conditioner, sunscreen, facial moisturizer, makeup, and soap.
Trisodium Citrate Dihydrate is also commonly used to control acidity in foods and pharmaceuticals.



SAFETY PROFILE OF TRISODIUM CITRATE DIHYDRATE:
The Cosmetic Ingredient Review (CIR) Expert Panel has reviewed scientific literature and data on the safety of citric acid and its esters and salts, like Trisodium Citrate Dihydrate.

Their findings showed that citric acid, its esters, and salts did not irritate the eyes or cause skin irritation or allergic skin reactions at concentrations used in cosmetics and skincare products.
In light of the available scientific evidence, the Expert Panel came to the conclusion that citric acid, its esters, and salts were safe for use in cosmetics and personal care products under the circumstances at hand.



PHYSICAL and CHEMICAL PROPERTIES of TRISODIUM CITRATE DIHYDRATE:
CAS number: 6132-04-3
EC number: 200-675-3
Hill Formula: C₆H₅Na₃O₇ * 2 H₂O
Molar Mass: 294.10 g/mol
HS Code: 2918 15 00
Melting Point: 300 °C (anhydrous substance)
pH value: 7.5 - 9.0 (50 g/l, H₂O, 25 °C)
Bulk density: 600 kg/m3
Solubility: 720 g/l
Molecular Weight: 294.10 g/mol
Hydrogen Bond Donor Count: 3
Hydrogen Bond Acceptor Count: 9
Rotatable Bond Count: 2
Exact Mass: 293.99396471 g/mol
Monoisotopic Mass: 293.99396471 g/mol
Topological Polar Surface Area: 143Ų
Heavy Atom Count: 18
Formal Charge: 0
Complexity: 211
Isotope Atom Count: 0

Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 6
Compound Is Canonicalized: Yes
Physical state: solid
Color: white
Odor: No data available
Melting point/freezing point:
Melting point: 300 °C
Initial boiling point and boiling range: No data available
Flammability (solid, gas): No data available
Upper/lower flammability or explosive limits: No data available
Flash point: Not applicable
Autoignition temperature: No data available
Decomposition temperature: No data available
pH: 7,5 - 9 at 29,4 g/l at 25 °C

Viscosity
Viscosity, kinematic: No data available
Viscosity, dynamic: No data available
Water solubility 29,4 g/l at 20 °C - completely soluble
Partition coefficient: n-octanol/water: No data available
Vapor pressure: No data available
Density: No data available
Relative density: No data available
Relative vapor density: No data available
Particle characteristics: No data available
Explosive properties: No data available
Oxidizing properties: none
Other safety information:
Bulk density: ca.600 kg/m3
CAS NUMBER: 6132-04-3
MOLECULAR FORMULA: C6H5O7Na3·2H2O
BEILSTEIN REGISTRY NUMBER: 6104939
EC NUMBER: 200-675-3
MDL NUMBER: MFCD00150031
CBNumber:CB9752065
Molecular Formula:C6H9Na3O9

Molecular Weight:294.1
MDL Number:MFCD00150031
MOL File:6132-04-3.mol
Melting point: >300 °C(lit.)
Density: 1.76
FEMA: 3026 | SODIUM CITRATE
Flash point: 173.9 °C
storage temp.: Store at +5°C to +30°C.
solubility: H2O: 100 mg/mL
form: powder
color: white
PH: 7.0-9.0 (25℃, 50mg/mL in H2O)
Odor: Odorless
PH Range: 7.5 - 9 at 29.4 g/l at 25 °C
Water Solubility: 720 g/L (25 ºC)
λmax:
λ: 260 nm Amax: 0.01
λ: 280 nm Amax: 0.01
Merck: 14,8602
BRN: 6104939

Stability: Stable.
Incompatible with bases, reducing agents, oxidizing agents.
InChIKey: NLJMYIDDQXHKNR-UHFFFAOYSA-K
LogP: -1.72
CAS DataBase Reference: 6132-04-3(CAS DataBase Reference)
FDA UNII: B22547B95K
EPA Substance Registry System: 1,2,3-Propanetricarboxylic acid, 2-hydroxy-, trisodium salt, dihydrate (6132-04-3)
IUPAC Name: trisodium;2-hydroxypropane-1,2,3-tricarboxylate;dihydrate
Molecular Weight: 294.10
Molecular Formula: C6H9Na3O9
Canonical SMILES: C(C(=O)[O-])C(CC(=O)[O-])(C(=O)[O-])O.O.O.[Na+].[Na+].[Na+]
InChI: InChI=1S/C6H8O7.3Na.2H2O/c7-3(8)1-6(13,5(11)12)2-4(9)10;;;;;/h13H,1-2H2,(H,7,8)(H,9,10)(H,11,12);;;;2*1H2/q;3*+1;;/p-3
InChIKey: NLJMYIDDQXHKNR-UHFFFAOYSA-K
Boiling Point: 309.6 °C at 760 mmHg
Melting Point: 300ºC
Flash Point: 155.2ºC
Density: 1.76 g/cm3
Solubility: Solubility in water, g/100ml: 77
Appearance: White powder or crystals
Storage: Store at RT.
Hazard Codes: Xi
Log P: -5.38120
PSA: 159.8

Refractive Index: 1.58
Risk Statements R37/38
RTECS: GE7810000
Safety Statements: S24/25
Stability: Stable.
Incompatible with bases, reducing agents, oxidizing agents.
Molecular Formula: C6H5O7Na3 ● 2 H2O
Molecular Weight: 294.10
CAS Number: 6132-04-3
E-NR: E 331
EINECS: 20-06-753
CAS No: 6132–04–3
EINECS No: 200–675–3
Empirical formula: C6H5Na3O7 . 2H2O
Molecular mass: 294.10 g/mol
Density: 1.7g/cm3
Appearance: colourless crystals or white, granular powder
pH: 8 – 8.7 at 50g/L at 25C
Melting point: >300 C
Solubility in water: 760 g/L (25C)
Easily soluble in hot water.
Soluble in cold water.

Insoluble in alcohol.
Soluble in 1.3 parts water.
Soluble in 0.6 parts boiling water.
Formula: Na₃C₆H₅O₇·2H₂O
MW: 294,1 g/mol
Melting Pt: 150 °C
Density: 1,76 g/cm³ (20 °C)
Storage Temperature: Ambient
MDL Number: MFCD00150031
CAS Number: 6132-04-3
EINECS: 200-675-3
Merck Index: 13,08675
Density: 1.76
Boiling Point: 309.6ºC at 760 mmHg
Melting Point: >300 °C(lit.)
Molecular Formula: C6H9Na3O9
Molecular Weight: 294.10
Flash Point: 173.9 °C
Exact Mass: 293.993958
PSA: 159.08000
Index of Refraction: 1.58
Storage condition: Store at RT.
Stability: Stable.
Incompatible with bases, reducing agents, oxidizing agents.
Water Solubility: 720 g/L (25 ºC)



FIRST AID MEASURES of TRISODIUM CITRATE DIHYDRATE:
-Description of first-aid measures
*If inhaled
After inhalation:
Fresh air.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with water/ shower.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Remove contact lenses.
*If swallowed:
After swallowing:
Make victim drink water (two glasses at most).
Consult doctor if feeling unwell.
-Indication of any immediate medical attention and special treatment needed:
No data available



ACCIDENTAL RELEASE MEASURES of TRISODIUM CITRATE DIHYDRATE:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Observe possible material restrictions.
Take up dry.
Dispose of properly.
Clean up affected area.



FIRE FIGHTING MEASURES of TRISODIUM CITRATE DIHYDRATE:
-Extinguishing media:
*Suitable extinguishing media:
Water
Foam
Carbon dioxide (CO2)
Dry powder
*Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Prevent fire extinguishing water from contaminating surface water or the ground water system.



EXPOSURE CONTROLS/PERSONAL PROTECTION of TRISODIUM CITRATE DIHYDRATE:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Safety glasses.
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of TRISODIUM CITRATE DIHYDRATE:
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
Dry.



STABILITY and REACTIVITY of TRISODIUM CITRATE DIHYDRATE:
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .
-Conditions to avoid:
no information available
-Incompatible materials:
No data available



SYNONYMS:
1,2,3-Propanetricarboxylic acid
2-hydroxy-, sodium salt, hydrate (1:3:2)
Citric acid, trisodium salt, dihydrate
1,2,3-Propanetricarboxylic acid
2-hydroxy-, trisodium salt, dihydrate
Sodium citrate dihydrate
Trisodium citrate dihydrate
N 1560
Trisodium citrate dihydrate
Sodium citrate dihydrate
6132-04-3
Sodium citrate tribasic dihydrate
Sodium citrate hydrate
1,2,3-Propanetricarboxylic acid
2-hydroxy-, trisodium salt, dihydrate
Citric acid trisodium salt dihydrate
MFCD00150031
B22547B95K
Nauzene
trisodium 2-hydroxypropane-1,2,3-tricarboxylate dihydrate
trisodium;2-hydroxypropane-1,2,3-tricarboxylate;dihydrate
DTXSID1049437
SODIUM CITRATE, DIHYDRATE
Citric acid, trisodium salt, dihydrate
N-1560
Sodium citrate hydrous
Natrii citras, dehydrate
Trisodium citrate dihydrate
Citric acid trisodium salt dihydrate
MFCD00130806
tri-sodium citrate dihydrate
TRISODIUM CITRATE DIHYDRATE (II)
TRISODIUM CITRATE DIHYDRATE [II]
TRISODIUM CITRATE DIHYDRATE (USP MONOGRAPH)
TRISODIUM CITRATE DIHYDRATE [USP MONOGRAPH]
sodium 2-hydroxypropane-1,2,3-tricarboxylate dihydrate
Sodiumcitrate
Tricitrasol
Natrum citricum
Emetrol Chewables
Tricitrasol (TN)
Sodium citrate
Trisodium 2-hydroxypropane-1,2,3-tricarboxylate dihydrate
Sodium Citrate Dihydrate
Sodium citrate (TN)
CVS HealthNausea Relief
Emetrol Chewables Orange
Sodium citrate [USP:JAN]
Sodiumcitratetribasicdihydrate
Emetrol Chewables Mixed Berry
SODIUM CITRATE [FHFI]
DTXCID0029397
Sodium citrate hydrate (JP17)
UNII-B22547B95K
CHEBI:32142
Trisodium citrate dihydrate, ACS
NLJMYIDDQXHKNR-UHFFFAOYSA-K
SODIUM CITRATE HYDROUS [II]
SODIUM CITRATE HYDRATE [JAN]
SODIUM CITRATE [EP MONOGRAPH]
SODIUM CITRATE DIHYDRATE [MI]
AKOS025293920
Citronensaeure,Trinatrium-Salz-Dihydrat
Sodium citrate dihydrate, >=99%, FG
SODIUM CITRATE DIHYDRATE [VANDF]
BP-31019
SODIUM CITRATE DIHYDRATE [WHO-DD]
Sodium citrate tribasic dihydrate, >=98%
Sodium citrate dihydrate, ACS reagent grade
SODIUM CITRATE, DIHYDRATE [WHO-IP]
D01781
F82065
Sodium citrate tribasic dihydrate, AR, >=99%
Sodium citrate tribasic dihydrate, LR, >=99%
Citric acid trisodium salt dihydrate ACS reagent
NATRII CITRAS, DEHYDRATE [WHO-IP LATIN]
A833161
A835986
Q22075862
Sodium citrate dihydrate Biochemical grade, Fine Granular
Sodium citrate tribasic dihydrate, USP, 99.0-100.5%
Sodium Citrate Tribasic Dihydrate (Molecular Biology Grade)
Sodium citrate tribasic dihydrate, ACS reagent, >=99.0%
trisodium 2-oxidanylpropane-1,2,3-tricarboxylate dihydrate
Citric acid trisodium salt dihydrateTrisodium citrate dihydrate
Sodium citrate tribasic dihydrate, BioUltra, >=99.0% (NT)
Sodium citrate tribasic dihydrate, insect cell culture tested
Sodium citrate tribasic dihydrate, JIS special grade, >=99.0%
Sodium citrate tribasic dihydrate, p.a., ACS reagent, 99.0%
Sodium citrate tribasic dihydrate, purum p.a., >=99.0% (NT)
Sodium citrate tribasic dihydrate, SAJ first grade, >=99.0%
Sodium citrate tribasic dihydrate, tested according to Ph.Eur.
trisodium 2-hydroxypropane-1,2,3-tricarboxylate--water (1/2)
Trisodium citrate dihydrate, meets USP testing specifications
2-hydroxy-1,2,3-propanetricarboxylic acid trisodium salt dihydrate
Sodium citrate tribasic dihydrate, BioXtra, >=99.0% (titration)
Sodium citrate tribasic dihydrate, for molecular biology, >=99%
Sodium citrate tribasic dihydrate, Vetec(TM) reagent grade, 98%
Sodium citrate, United States Pharmacopeia (USP) Reference Standard
1,2,3-Propanetricarboxylic acid, 2-hydroxy-, sodium salt, dihydrate
Sodium citrate tribasic dihydrate, p.a., ACS reagent, reag. ISO, 99-101%
1,2,3-Propanetricarboxylic acid, 2-hydroxy-, sodium salt, hydrate (1:3:2)
Sodium citrate tribasic dihydrate, BioUltra, for molecular biology, >=99.5% (NT)
Sodium citrate tribasic dihydrate, puriss. p.a., ACS reagent, >=99.0% (NT)
Sodium citrate tribasic dihydrate, suitable for amino acid analysis, >=99.0%
Sodium Citrate, Pharmaceutical Secondary Standard; Certified Reference Material
Sodium citrate tribasic dihydrate, puriss. p.a., ACS reagent, reag. ISO, reag. Ph. Eur., >=99.5%
Sodium citrate tribasic dihydrate, suitable for amino acid analysis, >=98% (titration), powder
Sodium citrate tribasic dihydrate
Trisodium Citrate, Sodium Citrate, Dihydrate
Citric acid trisodium salt dihydrate
Trisodium citrate dihydrate
Citric Acid Trisodium Salt Dihydrate
Trisodium citrate dihydrate
Citronensaeure-tri-na-salz-dihydrat
Natriumcitrat-Dihydrat
1,2,3-Propanetricarboxylic acid
2-hydroxy-, trisodium salt, dihydrate
Sodium citrate tribasic dihydrate
Sodium Citrate, trisodium salt
CITRIC ACID MONO
SODIUM CITRATE TRIBASIC DIHYDRATE
TRI-SODIUM CITRATE DIHYDRATE
SodiuM Citrate (AS);NATRII CITRAS
SODIUM CITRATE, DIHYDRATE
ACIDUM CITRICUM MONOHYDRICUM
CITRIC ACID TRISODIUM SALT DIHYDRATE
BETA-HYDROXY-TRICARBOXYLIC ACID MONOHYDRATE
abs9147
Sodium citrate dihydrate
Sodium citrate tribasic dihydrate
1,2,3-Propanetricarboxylic acid
2-hydroxy-, trisodium salt, dihydrate
Citric Acid Trisodium Salt Dihydrate
Trisodium citrate dihydrate
Citronensaeure-tri-na-salz-dihydrat
Natriumcitrat-Dihydrat
1,2,3-Propanetricarboxylic acid
2-hydroxy-, trisodium salt, dihydrate
Sodium citrate tribasic dihydrate
Sodium Citrate, trisodium salt
Sodium citrate dihydrate
Trisodium citrate, trisodium salt of 2-hydroxy-1,2,3-propanetricar­boxylic acid
trisodium salt of -hydroxy-tricarballylic acid
Natrocitral
Citrate sodique
Sodium Citrate Dihydrate
Sodium citrate tribasic dihydrate,Sodium Citrate
Dihydrate,Citric acid trisodium salt dihydrate
Trisodium 2-hydroxypropane-1,2,3-tricarboxylate
Trisodium Citrate Dihydrate
TriTrisodium Citrate Dihydrate
Citrosodine
Citric acid, trisodium salt
E331
Trisodium Citrate Dihydrate
68-04-2
TRITRISODIUM CITRATE DIHYDRATE
Trisodium Citrate Dihydrate anhydrous
Citrosodine
Natrocitral
Trisodium Citrate Dihydrate, anhydrous
Citric acid, trisodium salt
TriTrisodium Citrate Dihydrate, anhydrous
anhydrous Trisodium Citrate Dihydrate
Citric acid trisodium salt
1,2,3-Propanetricarboxylic acid, 2-hydroxy-, trisodium salt
Sodium 2-hydroxypropane-1,2,3-tricarboxylate
FEMA No. 3026
CCRIS 3293
Trisodium Citrate Dihydrate (Na3C6H5O7)
Trisodium Citrate Dihydrate,anhydrous
HSDB 5201
trisodium 2-hydroxypropane-1,2,3-tricarboxylate
trisodium-citrate
Anhydrous triTrisodium Citrate Dihydrate
UNII-RS7A450LGA
EINECS 200-675-3
Bicitra
Pneucid
Trisodium 2-hydroxy-1,2,3-propanetricarboxylate
994-36-5
CHEBI:53258
RS7A450LGA
INS NO.331(III)
INS-331(III)
EC 200-675-3
E-331(III)
trisodium;2-hydroxypropane-1,2,3-tricarboxylate
MFCD00012462
FEMA NO. 3026, ANHYDROUS-
Citrosodina
Citnatin
Citreme
Citrosodna
EINECS 213-618-2
Trisodium Citrate Dihydrate hydrous
TriTrisodium Citrate Dihydrate anhydrous
Natrii citras, dehydrate
E 331
Sodium 2-hydroxy-1,2,3-propanetricarboxylate
UNII-68538UP9SE
1,2,3-Propanetricarboxylic acid, 2-hydroxy-, sodium salt
EINECS 242-734-6
C6H5Na3O7
EC 242-734-6
Oracit
Natrii citras
tri-Trisodium Citrate Dihydrate
Trisodium Citrate Dihydrate salt
Albright's Solution
1,2,3-Propanetricarboxylic acid, 2-hydroxy-, sodium salt (1:3)
sodium (iii) citrate
Trisodium Citrate Dihydrate (USP)
Modified Shohl's Solution
Anticoagulant Trisodium Citrate Dihydrate
1Q73Q2JULR
CHEMBL1355
TRISODIUM CITRATE DIHYDRATE (II)
TRISODIUM CITRATE DIHYDRATE [MI]
Citrate Concentrated Solution
DTXSID2026363
TRISODIUM CITRATE DIHYDRATE (USP-RS)
TRISODIUM CITRATE DIHYDRATE [WHO-IP]
2-Hydroxy-1,2,3-propanetricarboxylic acid, trisodium salt
Citric acid trisodium salt, 99%
HRXKRNGNAMMEHJ-UHFFFAOYSA-K
TRISODIUM CITRATE DIHYDRATE, UNSPECIFIED
NATRII CITRAS [WHO-IP LATIN]
TRISODIUM CITRATE DIHYDRATE (USP IMPURITY)
AKOS015915009
DB09154
TRISODIUM CITRATE DIHYDRATE ANHYDROUS [HSDB]
ANHYDROUS TRITRISODIUM CITRATE DIHYDRATE [II]
TRISODIUM CITRATE DIHYDRATE, UNSPECIFIED FORM
TRISODIUM CITRATE DIHYDRATE,ANHYDROUS [VANDF]
8055-55-8
AC-15008
E331
Trisodium Citrate Dihydrate dihydrate USP Fine Granular
TRISODIUM CITRATE DIHYDRATE, ANHYDROUS [WHO-IP]
FT-0623960
EN300-74572
D05855
D77308
ANHYDROUS TRITRISODIUM CITRATE DIHYDRATE [USP MONOGRAPH]
Q409728
J-520101
Citric acid trisodium salt, anhydrous, >=98% (GC)
Citric acid trisodium salt, Vetec(TM) reagent grade, 98%
2-Hydroxy-1,2,3-propanenetricarboxylic acid trisodium salt dihydrate
Trisodium Citrate Dihydrate tribasic dihydrate
Citric acid trisodium salt dihydrate
TriTrisodium Citrate Dihydrate dihydrate
1,2,3-Propanetricarboxylic acid
2-hydroxy, trisodium salt
1,2,3-Propanetricarboxylic acid, 2-hydroxy-, sodium salt (1:3)
Citric acid, trisodium salt
2-Hydroxy-1,2,3-propanetricarboxylic acid trisodium salt
Citnatin
Citra-lock
Citreme
Citrosodina
Citrosodine
Cystemme
Iona
Natrocitral
Trisodium Citrate Dihydrate
Trisodium Citrate Dihydrate anhydrous
Trisodium Citrate Dihydrate H
Unifine P 3
Urisal
1,2,3-Propanetricarboxylic acid, 2-hydroxy-, trisodium salt
Citric acid, trisodium salt
Trisodium Citrate Dihydrate
Trisodium Citrate Dihydrate anhydrous
TriTrisodium Citrate Dihydrate
Citrato de trisodio, dihidrato
Citrate de trisodium, dihydrate
Trisodio citrato diidrato
Trinatriumcitraatdihydraat
2-Hydroxy-1,2,3-propanenetricarboxylic Acid Trisodium Salt Dihydrate
2-Hydroxy-,1,2,3-propanetricarboxylic Acid Trisodium Salt (9CI)
Citric Acid, Trisodium Salt (8CI)
Trisodium Citrate Dihydrate (Na3C6H5O7) (7CI)


TRISODIUM CITRATE DIHYDRATE
Trisodium Citrate Dihydrate is the dihydrate of trisodium citrate.
Trisodium Citrate Dihydrate has a role as an anticoagulant.
Trisodium Citrate Dihydrate contains a sodium citrate.
Trisodium Citrate Dihydrate (C6H5Na3O7.2H2O) is a tribasic salt of citric acid.


CAS Number: 6132-04-3
EC Number 200-675-3
Molecular Formula: C6H9Na3O9 or C6H5Na3O7.2H2O


Trisodium Citrate Dihydrate has a sour taste similar to citric acid, and is salty as well.
Trisodium Citrate Dihydrate is a tribasic salt of citric acid.
Trisodium Citrate Dihydrate is produced by complete neutralisation of citric acid with high purity sodium hydroxide or carbonate and subsequent crystallisation.


Trisodium citrate dihydrate occurs as white, granular crystals or as white, crystalline powder with a pleasant, salty taste.
Trisodium Citrate Dihydrate is slightly deliquescent in moist air, freely soluble in water and practically insoluble in ethanol (96 %).
Trisodium citrate dihydrate is a non-toxic, neutral salt with low reactivity.


Trisodium Citrate Dihydrate is chemically stable if stored at ambient temperatures.
Trisodium citrate dihydrate is fully biodegradable and can be disposed of with regular waste or sewage.
Trisodium citrate dihydrate is available in various granulations.


Trisodium Citrate Dihydrate is soluble in water.
Trisodium Citrate Dihydrate is insoluble in alcohol.
Trisodium citrate dihydrate is a tribasic salt of citric acid.


Trisodium Citrate Dihydrate is produced by complete neutralisation of citric acid with high purity sodium hydroxide or carbonate and subsequent crystallisation.
Citric acid is the product of a microbial fermentation using carbohydrate substrates.
Trisodium citrate dihydrate is a chemical compound that is used as a buffer and to maintain the pH of solutions.


Trisodium Citrate Dihydrate is a tribasic salt of citric acid.
Trisodium Citrate Dihydrate is free soluble in water, practically insoluble in ethanol(96 percent).
Trisodium citrate dihydrate is a tribasic salt of citric acid.


Trisodium Citrate Dihydrate is produced by complete neutralization of citric acid with high purity sodium source (sodium hydroxide or sodium carbonate) and subsequent crystallization.
Trisodium Citrate Dihydrate is manufactured by neutralizing citric acid derived from a submerged fermentation process.
Trisodium Citrate Dihydrate is considered “GRAS” (Generally Recognized As Safe) by the United States Food and Drug


Administration without restriction as to the quantity of use within good manufacturing practice.
Trisodium Citrate Dihydrate is also considered by the Experts Committee of the FAO/WHO to be a safe food additive without limitation according to good manufacturing practice.


Trisodium Citrate Dihydrate is manufactured to meet the monograph specifications of major world codex and pharmacopoeia standards including the USP, FCC, BP, EP, FAO/WHO.
Cargill Trisodium Citrate Dihydrate is available as translucent white crystals and has a slight saline taste.
Water of crystallization constitutes approximately twelve percent by weight of the dihydrate form.


Citrate is a intermediate in the Trisodium Citrate Dihydrate cycle and fatty acid synthesis.
Citrate is an allosteric modulator of acetyl-CoA carboxylase, the enzyme that regulates the conversion of acetyl-CoA to malonyl-CoA.
Trisodium Citrate Dihydrate possesses a saline, mildly tart flavor.


Trisodium Citrate Dihydrate is a useful reactant in organic synthesis.
Trisodium Citrate Dihydrate is a tribasic salt of citric acid.
Trisodium Citrate Dihydrate consists of colourless to white crystals and is practically odourless.


Trisodium citrate dihydrate is a tribasic salt of citric acid.
Trisodium Citrate Dihydrate is produced by complete neutralisation of citric acid with high purity sodium hydroxide or carbonate and subsequent crystallisation.
Citric acid is the product of a microbial fermentation using carbohydrate substrates.


Trisodium Citrate Dihydrate, (molecular formula: Na3C6H5O7 • 2H2O) has molecular weight of 294.1, is a colorless crystal or white crystalline powder product; it is odorless, salty taste, and cool.
Trisodium Citrate Dihydrate will lose its crystal water at 150 & deg;C and will be decomposed at even higher temperature.


Trisodium Citrate Dihydrate also has slight deliquescence in wet air and has weathering property upon hot air.
Trisodium Citrate Dihydrate is soluble in water and glycerol, but insoluble in alcohol and some other organic solvents.
Trisodium Citrate Dihydrate is a versatile chemical substance used in a variety of applications in different industries.


In the medical field, Trisodium Citrate Dihydrate is used as an anticoagulant but it is also an ingredient in many personal care products.
Trisodium Citrate Dihydrate can be used as Ph adjusting agents and emulsifying enhancers applied to jam, candy, jelly and ice cream; its combination with citric acid has an effect of alleviating tour.
Trisodium Citrate Dihydrate also has effects on forming complex with metal ions.


Trisodium Citrate Dihydrate is white powder or colourless crystals.
Trisodium Citrate Dihydrate is the tribasic dihydrate sodium salt of citric acid.
Trisodium Citrate Dihydrate is commonly used laboratory reagent.



USES and APPLICATIONS of TRISODIUM CITRATE DIHYDRATE:
In the cleaning industry Trisodium Citrate Dihydrate is commonly used because of its excellent cleaning characteristics and its unusual property of being almost neutral yet portraying the characteristics of an acid as in descalers and an alkali as in degreasers.
Cleaning products include laundry powders and detergents, toilet cleaners, hard surface cleaners, carpet cleaners, dish washing liquids, powder and liquid degreasers and pre-soaks.


Trisodium Citrate Dihydrate is becoming more and more popular now as it is considered environmentally friendly, it substitutes phosphates and is readily biodegradable.
In industry Trisodium Citrate Dihydrate finds many uses including alkaline degreaser baths, electroplating chemicals for copper and nickel etc, photo chemicals.
Trisodium Citrate Dihydrate is also used in the paper and pulp industries and the textiles industry.


Trisodium Citrate Dihydrate is often used as a food preservative, and as a flavoring in the food industry.
In the pharmaceutical industry it is used to control pH.
Trisodium Citrate Dihydrate may be used as an alkalizing agent, buffering agent, emulsifier, or sequestering agent.
Trisodium citrate dihydrate is widely used in foods, beverages and various technical applications mainly as buffering, sequestering or emulsifying agent.


Trisodium citrate dihydrate, is widely applied in food, beverages and fillers as a buffering, sequestering or an emulsifying agent.
Trisodium Citrate Dihydrate used as an anticoagulant in blood transfusions, osmotic laxative, functional fluids, solvents cleaning, furnishing care products, laundry dishwashing products and cleaning automobile radiators.


Trisodium citrate dihydrate, is widely applied in food, beverages and fillers as a buffering, sequestering or an emulsifying agent.
Trisodium Citrate Dihydrate used as an anticoagulant in blood transfusions, osmotic laxative, functional fluids, solvents cleaning, furnishing care products, laundry dishwashing products and cleaning automobile radiators.


Sodium salts of citric acid are used as buffers and food preservatives.
They are used medically as anticoagulants in stored blood, and for urine alkalization in the prevention of KIDNEY STONES.
Trisodium Citrate Dihydrate is the dihydrate of trisodium citrate.


Trisodium Citrate Dihydrate has a role as an anticoagulant.
Sodium salts of citric acid are used as buffers and food preservatives. Citric acid is one of compounds responsible for the physiological oxidation of fats, carbohydrates and proteins to carbon dioxide.


Trisodium citrate dihydrate is widely used as an excellent pH regulator and odourless buffering agent for bath and shower gels, creams, styling or decorative products.
Trisodium Citrate Dihydrate is often used as an acidity regulator in pharmaceutical formulations and food products.
Trisodium citrate dihydrate has been shown to be effective at reducing the matrix effect and increasing the concentration response, which can lead to better analytical results.


Trisodium Citrate Dihydrate has also been shown to have anti-inflammatory properties, which may be due to its ability to prevent fatty acid production by inhibiting the enzyme lipase.
Trisodium citrate dihydrate is widely used in foods, beverages and various technical applications mainly as buffering, sequestering or emulsifying agent.


Trisodium Citrate Dihydrate is often used as a food preservative, and as a flavoring in the food industry.
In the pharmaceutical industry Trisodium Citrate Dihydrate is used to control pH.
Trisodium Citrate Dihydrate is used to enhance flavour and maintain stability of active ingredients in food and beverages.


In detergent industry, Trisodium Citrate Dihydrate can replace STPP as a kind of assistant.
Trisodium Citrate Dihydrate can also be used in fermentation, injection, photography and metal plating.
Trisodium Citrate Dihydrate is mildly basic and can be used along with citric acid to make biologically compatible buffers.


Trisodium Citrate is a white odorless chemical used as a food additive.
Trisodium Citrate Dihydrate is typically used as a flavoring agent or as a preservative.
Trisodium Citrate Dihydrate is used as flavoring agent in carbonated beverages contributing a tart flavor.


Trisodium Citrate Dihydrate is also found in gelatin mix, ice cream, yogurt, jams, sweets, milk powder, processed cheeses and bratwurst.
Trisodium Citrate Dihydrate is used as raw material for pharmaceuticals / Food additives.
A biological buffer, Trisodium Citrate Dihydrate is used for cell culture, in vitro, enzyme assays and some electrophoretic applications at physiological pH.


Trisodium Citrate Dihydrate is used in toothpastes & dental creams, effervescent denture cleansers, mouth rinses and oral hygiene products.
Trisodium citrate dihydrate is commonly used in various technical and industrial applications mainly as a pH buffering, sequestering or emulsifying agent.
Trisodium Citrate Dihydrate is also used as a retarder for mortar mixes.


Trisodium Citrate Dihydrate is effective to retard plaster mixes.
Trisodium Citrate Dihydrate must be used carefully as adding too much will prevent the plaster curing properly.
Premix the citrate in water first and add to the plaster mix.


Trisodium citrate dihydrate, also known as sodium citrate, is an organic compound that has white to colorless crystals.
Trisodium Citrate Dihydrate is odourless, with a cool salty taste. Stable in room temperature and air, slightly soluble in wet air, weathering in hot air.
Lose crystal water heated to 150 ℃.


Trisodium Citrate Dihydrate is easily soluble in water, glycerol, alcohol and other organic solvents.
Trisodium Citrate Dihydrate is decomposed by overheating, slightly deliviate in humid environment and slightly weathering in hot air.
Trisodium Citrate Dihydrate is manufactured by neutralizing citric acid derived from a submerged fermentation process.


Trisodium Citrate Dihydrate is available as translucent white crystals and has a slight saline taste.
Trisodium citrate dihydrate is a tribasic salt of citric acid.
Trisodium Citrate Dihydrate is produced by complete neutralization of citric acid with high purity sodium source and subsequent crystallization.


Buffers pH and enhances action of methyl parabens.
Trisodium Citrate Dihydrate, from Junbunzlauer is a buffering, sequestering and emulsifying agent.
Trisodium Citrate Dihydrate is a tribasic salt of citric acid and appears as a white granular powder that is non-toxic, freely soluble in water and practically insoluble in ethanol.


Due to its versatile nature, Trisodium Citrate Dihydrate is perfect for many areas, including Food and Beverages, Cosmetics and Industrial applications.
Trisodium citrate dihydrate is widely used in foods, beverages and various technical applications mainly as buffering, sequestering or emulsifying agent.
Trisodium Citrate Dihydrate has no toxic effect, and has pH adjusting capability as well as having a good stability, and therefore can be used in the food industry.


Trisodium Citrate Dihydrate has the greatest demand when being used as a food additive.
Trisodium Citrate Dihydrate is used as food additives.
Trisodium Citrate Dihydrate is mainly used as flavoring agents, buffers, emulsifiers, bulking agents, stabilizers and preservatives.


In addition, combination between Trisodium Citrate Dihydrate and citric acid can be used in a variety of jams, jelly, juice, drinks, cold drinks, dairy products and pastries gelling agents, flavoring agents and nutritional supplements.


In the food industry, Trisodium Citrate Dihydrate is used as a flavor enhancer, acidity regulator, and emulsifier.
Trisodium Citrate Dihydrate is also an essential ingredient in dishwasher tablets, industrial cleaners, detergents, etc.
Trisodium Citrate Dihydrate gets used in a many different places in food and beverage manufacture, though it's mainly used as a food additive for flavor and / or as a preservative.


Soft drinks, energy drinks, and club soda all use Trisodium Citrate Dihydrate for its tart flavour.
Trisodium Citrate Dihydrate is also used as a pH buffering agent in places like gelatins or mini milk containers.
It is also used as an anti-coagulant, Trisodium Citrate Dihydrate is ideal for keeping the fat globules from sticking together in the manufacture of many things such as ice cream.


Trisodium Citrate Dihydrate can be used as a food additive, as complex agent and buffering agent in electroplating industry; at the field of pharmaceutical industry.
Trisodium Citrate Dihydrate is used for the manufacturing of anti-clotting drugs; and used as the detergent additives in light industry.
Trisodium Citrate Dihydrate is used as the analysis agents used for chromatography analysis and can also used for preparing bacterial culture medium.


Moreover, Trisodium Citrate Dihydrate can also be applied into pharmaceutical industry.
Trisodium Citrate Dihydrate can be used for the flavoring processing of food, as stabilizers, buffers and deputy complex-forming agents in non-toxic electroplating industry; at pharmaceutical industry.


Trisodium Citrate Dihydrate is used as anti-clotting agent, phlegm drugs and diuretics drugs.
Trisodium Citrate Dihydrate can also be used in brewing, injection, newspaper and movies medicines.
Trisodium Citrate Dihydrate is chiefly used as a food additive, usually for flavor or as a preservative.


Trisodium Citrate Dihydrate is used as an anticoagulant for collection of blood.
Trisodium Citrate Dihydrate is used in photography; as sequestering agent to remove trace metals; as emulsifier, acidulant and sequestrant in foods.
Trisodium Citrate Dihydrate is used as an anticoagulant also used as a biological buffer


Trisodium Citrate Dihydrate, is widely applied in food, beverages and fillers as a buffering, sequestering or an emulsifying agent.
Trisodium Citrate Dihydrate used as an anticoagulant in blood transfusions, osmotic laxative, functional fluids, solvents cleaning, furnishing care products, laundry dishwashing products and cleaning automobile radiators.


-Pharmaceutical Applications:
Trisodium Citrate Dihydrate, as either the dihydrate or anhydrous material, is widely used in pharmaceutical formulations.
Trisodium Citrate Dihydrate is used in food products, primarily to adjust the pH of solutions.
Trisodium Citrate Dihydrate is also used as a sequestering agent.
The anhydrous material is used in effervescent tablet formulations.
Trisodium Citrate Dihydrate is additionally used as a blood anticoagulant either alone or in combination with other citrates such as disodium hydrogen citrate.
Therapeutically, Trisodium Citrate Dihydrate is used to relieve the painful irritation caused by cystitis, and also to treat dehydration and acidosis due to diarrhea.


-Applications of Trisodium Citrate Dihydrate:
• anticoagulant activity
• use as buffer or food preservatives
• citrate solution is designed to break protein cross-links
• as a calcium chelator


-Applications of Trisodium Citrate Dihydrate:
*Food
*Beverages
*Healthcare
*Personal Care
*Cleaners & Detergents


-Industrial Applications of Trisodium Citrate Dihydrate:
*Feed & Pet Food
*Pharma


-Uses of Trisodium Citrate Dihydrate:
*Buffering agent.
*Manufacture of household cleaners, degreasers and detergents.



CHARACTERISTICS OF TRISODIUM CITRATE DIHYDRATE:
Trisodium citrate dihydrate occurs as white, granular crystals or as white, crystalline powder.
Trisodium Citrate Dihydrate is an odourless substance with a pleasant, salty taste.
Trisodium Citrate Dihydrate is slightly deliquescent in moist air, freely soluble in water and practically insoluble in ethanol (96%).

Trisodium citrate dihydrate is a non-toxic, neutral salt with low reactivity.
Trisodium Citrate Dihydrate is chemically stable if stored at ambient
temperatures.
Although Trisodium Citrate Dihydrate is not very hygroscopic, caking may occur upon prolonged storage at humidities higher than 70 %.
Trisodium citrate dihydrate is fully biodegradable and can be disposed of with regular waste or sewage.



CHEMICAL PROPERTIES OF TRISODIUM CITRATE DIHYDRATE:
Trisodium Citrate Dihydrate is colorless crystals or white crystalline powder, and is odorless, cool and salty.
Trisodium Citrate Dihydrate has no melting point with a relative density of 1.857.
Trisodium Citrate Dihydrate is stable in air at room temperature with loss of crystal water when being heated to 150 °C loss of crystal water; further heating will cause its decomposition.

Trisodium Citrate Dihydrate is insoluble in ethanol but highly soluble in water. 5% aqueous solution has a pH value of 7.6 to 8.6.
Trisodium Citrate Dihydrate consists of odorless, colorless, monoclinic crystals, or a white crystalline powder with a cooling, saline taste.
Trisodium Citrate Dihydrate is slightly deliquescent in moist air, and in warm dry air it is efflorescent.



EFFECT AND APPLICATION OF TRISODIUM CITRATE DIHYDRATE:
During the process of clinically taking fresh blood, adding some amount of sterile sodium citrate can play a role in prevent blood clotting; this is exactly taking advantage of the features that calcium citrate can form soluble complexes with calcium ion.
In the field of medicine, Trisodium Citrate Dihydrate is used for the in vitro anti-clotting drugs and anticoagulants drugs, phlegm drugs, and diuretics drugs during blood transfusions.

Trisodium Citrate Dihydrate can also used for cyanide-free electroplating industry.
Trisodium Citrate Dihydrate is also used as developer for photographic industry.
Trisodium Citrate Dihydrate can be used as flavoring agents, buffering materials, emulsifiers, and stabilizer in the food industry.

Moreover, Trisodium Citrate Dihydrate is also widely used in chemical, metallurgical industry, the absorption of sulfur dioxide exhaust with the absorption rate of 99% and regenerate liquid sulfur dioxide citrate for recycle application.
Trisodium Citrate Dihydrate has a good water solubility and a excellent cheating capability with Ca2 +, Mg2 + and other metal ions.

Trisodium Citrate Dihydrate is biodegradable and has a strong dispersing ability and anti-redeposition ability.
Daily-applied chemical detergents use Trisodium Citrate Dihydrate as alternative to trimer sodium phosphate for production of non-phosphorus detergent and phosphate-free liquid detergent.
Adding a certain amount Trisodium Citrate Dihydrate to the detergent can significantly increase the cleaning ability of detergent cleaning.

The large scale of application of sodium tripolyphosphate as a builder in detergents is an important discovery in synthetic detergent industry.
Trisodium Citrate Dihydrate is non-toxic without environmental pollution.
Trisodium Citrate Dihydrate can also be acted as a buffer for the production of cosmetics.



KEY BENEFITS OF TRISODIUM CITRATE DIHYDRATE:
• Non-toxic
• Low Reactivity
• Chemically stable
• Fully biodegradable
• Can be disposed of with regular waste or sewage



FUNCTIONS AND APPLICATIONS OF TRISODIUM CITRATE DIHYDRATE:
Trisodium Citrate Dihydrate is used as acidity regulator, flavor agent and stabilizer in food and beverage industry.
Trisodium Citrate Dihydrate is used as an anticoagulant, phlegm dispersant and diuretic in the pharmaceutical industry.
In detergent industry, Trisodium Citrate Dihydrate can be substituted as non-toxic detergent additive.
Trisodium Citrate Dihydrate is also used in brewing, injection, photographic medicine and electroplating.



EXCELLENT PERFORMANCE OF TRISODIUM CITRATE DIHYDRATE:
Trisodium Citrate Dihydrate is currently the most important citrate.
Trisodium Citrate Dihydrate is produced by two steps: first starch food is fermented to generate citric acid; secondly, citric acid is neutralized by alkali to generate the final products.



PROPERTIES OF TRISODIUM CITRATE DIHYDRATE:
*Dihydrate
*White
*Granular crystals or crystalline powder
*Typical, practically odourless
*Pleasantly salty
*Freely soluble in water
*Practically insoluble in ethanol (96 %)
*Non-toxic
*Low reactive
*Chemically and microbiologically stable
*Fully biodegradable



MAIN FUNCTIONS OF TRISODIUM CITRATE DIHYDRATE:
*pH regulator
*Chelating agent
*Buffering agent
*Flavour enhancer
*Stabiliser
*Emulsifying agent



PRODUCTION METHODS OF TRISODIUM CITRATE DIHYDRATE:
Trisodium Citrate Dihydrate is produced by the neutralization of citric acid by sodium hydroxide or sodium bicarbonate.
Dissolve sodium bicarbonate in water upon stirring and heating; add citric acid, continue to heat up to 85-90 °C; adjust the pH to 6.8; adjust active carbon for bleaching.
Filter when the mixture is still hot; condense the filtrate under reduced pressure; cool and the crystal comes out; filter, wash, dry to obtain the final products of
Trisodium Citrate Dihydrate.
C6H8O7 + 3NaHCO3 → C6H5Na3O7 • 2H2O + 3CO2 ↑ + H2O
Trisodium Citrate Dihydrate is prepared by adding sodium carbonate to a solution of citric acid until effervescence ceases.
The resulting solution is filtered and evaporated to dryness.



SAFE AND NONTOXIC PROPERTIES OF TRISODIUM CITRATE DIHYDRATE:
Since the basic raw material for the preparation of Trisodium Citrate Dihydrate mainly comes from the food, it is absolutely safe and reliable without causing harm to human health.
The United Nations Food and Agriculture and the World Health Organization has no restriction in its daily intake, which means that this product can be considered as non-toxic food.

It is biodegradable.
After subjecting to the dilution of a large amount of water, Trisodium Citrate Dihydrate is partially converted into citrate, which coexists with sodium citrate in the same system.

Citrate is easy to subject to biological degradation at water by the action of oxygen, heat, light, bacteria and microbes.
Trisodium Citrate Dihydrate's decomposition pathways are generally going through aconitic acid, itaconic acid, citraconic acid anhydride to be further converted to carbon dioxide and water.

The ability to form complexes with metal ions.
Trisodium Citrate Dihydrate has a good capability of forming complex with some metal ions such as Ca2+, Mg2+; for other ions such as Fe2+, it also has a good complex-forming ability.
Excellent solubility, and the solubility increases with increasing temperature of water.

Trisodium Citrate Dihydrate has a good capability for pH adjustment and a good buffering property.
Trisodium Citrate Dihydrate is a weak acid-strong alkali salt; When combined with citrate, they can form a pH buffer with strong compatibility; therefore, this is very useful for some cases in which it is not suitable to have large change of pH value.
In addition, Trisodium Citrate Dihydrate also has excellent retardation performance and stability.



BIOCHEM/PHYSIOL ACTIONS OF TRISODIUM CITRATE DIHYDRATE:
Trisodium Citrate Dihydrate can act as a buffering agent, resisting changes in pH.
Trisodium Citrate Dihydrate is used in blood collection tubes, the citrate chelates calcium ions in blood and thereby disrupts blood clotting.
Citrate is a intermediate in the TCA cycle and fatty acid synthesis.
Citrate is an allosteric modulator of acetyl-CoA carboxylase, the enzyme that regulates the conversion of acetyl-CoA to malonyl-CoA.



PHYSICAL and CHEMICAL PROPERTIES of TRISODIUM CITRATE DIHYDRATE:
Molecular Weight: 294.10
Hydrogen Bond Donor Count: 3
Hydrogen Bond Acceptor Count: 9
Rotatable Bond Count: 2
Exact Mass: 293.99396471
Monoisotopic Mass: 293.99396471
Topological Polar Surface Area: 143 Ų
Heavy Atom Count: 18
Formal Charge: 0
Complexity: 211
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 6
Compound Is Canonicalized: Yes
CAS number: 6132-04-3
EC number: 200-675-3
Hill Formula: C₆H₅Na₃O₇ * 2 H₂O
Molar Mass: 294.10 g/mol
HS Code: 2918 15 00
Melting Point: 300 °C (anhydrous substance)
pH value: 7.5 - 9.0 (50 g/l, H₂O, 25 °C)
Bulk density: 600 kg/m3
Solubility: 720 g/l

Appearance Form: powder
Color: white
Odor: No data available
Odor Threshold: No data available
pH: 7,5 - 9 at 29,4 g/l at 25 °C
Melting point/freezing point:
Melting point/range: > 300 °C
Initial boiling point and boiling range: No data available
Flash point: Not applicable
Evaporation rate: No data available
Flammability (solid, gas): No data available
Upper/lower flammability or explosive limits: No data available
Vapor pressure: No data available
Vapor density: No data available
Relative density: No data available
Water solubility: 29,4 g/l at 20 °C - completely soluble
Partition coefficient: n-octanol/water: No data available
Autoignition temperature: No data available
Decomposition temperature: No data available
Viscosity
Viscosity, kinematic: No data available
Viscosity, dynamic: No data available
Explosive properties: No data available
Oxidizing properties: No data available
Other safety information: No data available

Water Solubility: 73.7 mg/mL
logP: -0.55
logP: -1.3
logS: -0.54
pKa (Strongest Acidic): 3.05
pKa (Strongest Basic): -4.2
Physiological Charge: -3
Hydrogen Acceptor Count: 7
Hydrogen Donor Count: 1
Polar Surface Area: 140.62 Å2
Rotatable Bond Count: 5
Refractivity: 68.14 m3·mol-1
Polarizability: 14.27 Å3
Number of Rings: 0
Bioavailability: 1
Rule of Five: Yes
Ghose Filter: No
Veber's Rule: No
MDDR-like Rule: No

Melting Point: 150°C (in -2H2O)
Density: 1.76
Odor: Odorless
Quantity: 10,000 g
Beilstein: 6104939
Merck Index: 14,8602
Solubility Information: Soluble in water.
Insoluble in alcohol.
Formula Weight: 294.10 (258.07 Anhydrous)
Percent Purity: 99%
Chemical Name or Material: Trisodium citrate dihydrate
CAS No: 6132–04–3
EINECS No: 200–675–3
Empirical formula: C6H5Na3O7 . 2H2O
Molecular mass: 294.10 g/mol
Density: 1.7g/cm3
Appearance: colourless crystals or white, granular powder
pH: 8 – 8.7 at 50g/L at 25C
Melting point: >300 C
Solubility in water: 760 g/L (25C)

Easily soluble in hot water.
Soluble in cold water.
Insoluble in alcohol.
Soluble in 1.3 parts water.
Soluble in 0.6 parts boiling water.
Melting point: >300 °C(lit.)
Density: 1.76
FEMA: 3026 | SODIUM CITRATE
Flash point: 173.9 °C
storage temp.: Store at +5°C to +30°C.
solubility: H2O: 100 mg/mL
form: powder
color: white
PH: 7.0-9.0 (25℃, 50mg/mL in H2O)
Odor: Odorless
PH Range: 7.5 - 9 at 29.4 g/l at 25 °C
Water Solubility: 720 g/L (25 ºC)
λmax: λ: 260 nm Amax: 0.01
λ: 280 nm Amax: 0.01
Merck: 14,8602
BRN: 6104939
Stability: Stable.
Incompatible with bases, reducing agents, oxidizing agents.

Appearance: White crystals or crystalline powder
Odor: Characteristic
Clarity and color of Solution: Conforms
Loss on drying: 11.0 - 13.0%
Usage: acidity regulator etc.
Pb: < 10ppm
Assay: 99.0 - 101.0%
Chemical formula: C6H5­O7Na3.2H2O
Sulfate (SO4): 150 ppm max
Chloride (Cl): 50 ppm max
Alkalinity: Conforms
Oxalate: 300 ppm max
Storage: in the shade cool
Boiling Point: 309.6 °C at 760 mmHg
Melting Point: 300ºC
Flash Point:155.2ºC
Density: 1.76 g/cm3
Solubility: Solubility in water, g/100ml: 77
Appearance: White powder or crystals
Storage: Store at RT.
Hazard Codes: Xi
Log P: -5.38120
PSA: 159.8
Refractive Index: 1.58
Risk Statements: R37/38
RTECS: GE7810000
Safety Statements: S24/25
Stability: Stable.



FIRST AID MEASURES of TRISODIUM CITRATE DIHYDRATE:
-Description of first-aid measures
*If inhaled
After inhalation:
Fresh air.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with water/ shower.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Remove contact lenses.
*If swallowed:
After swallowing:
Make victim drink water (two glasses at most).
Consult doctor if feeling unwell.
-Indication of any immediate medical attention and special treatment needed:
No data available



ACCIDENTAL RELEASE MEASURES of TRISODIUM CITRATE DIHYDRATE:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Observe possible material restrictions.
Take up dry.
Dispose of properly.
Clean up affected area.



FIRE FIGHTING MEASURES of TRISODIUM CITRATE DIHYDRATE:
-Extinguishing media:
*Suitable extinguishing media:
Water
Foam
Carbon dioxide (CO2)
Dry powder
*Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Prevent fire extinguishing water from contaminating surface water or the ground water system.



EXPOSURE CONTROLS/PERSONAL PROTECTION of TRISODIUM CITRATE DIHYDRATE:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Safety glasses.
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of TRISODIUM CITRATE DIHYDRATE:
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
Dry.



STABILITY and REACTIVITY of TRISODIUM CITRATE DIHYDRATE:
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .
-Conditions to avoid:
no information available
-Incompatible materials:
No data available



SYNONYMS:
Trisodium citrate dihydrate
Sodium citrate dihydrate
6132-04-3
Sodium citrate tribasic dihydrate
Sodium citrate hydrate
1,2,3-Propanetricarboxylic acid, 2-hydroxy-, trisodium salt, dihydrate
Citric acid trisodium salt dihydrate
trisodium;2-hydroxypropane-1,2,3-tricarboxylate;dihydrate
MFCD00150031
trisodium 2-hydroxypropane-1,2,3-tricarboxylate dihydrate
SODIUM CITRATE, DIHYDRATE
B22547B95K
Citric acid, trisodium salt, dihydrate
Sodium citrate hydrous
Trisodium citrate dihydrate;Citric acid trisodium salt dihydrate
MFCD00130806
tri-sodium citrate dihydrate
sodium 2-hydroxypropane-1,2,3-tricarboxylate dihydrate
Sodiumcitrate
N-1560
Natrum citricum
Tricitrasol (TN)
Sodium citrate (TN)
Sodium citrate [USP:JAN]
Sodiumcitratetribasicdihydrate
SODIUM CITRATE [FHFI]
DTXSID1049437
Sodium citrate hydrate (JP17)
UNII-B22547B95K
CHEBI:32142
Trisodium citrate dihydrate, ACS
SODIUM CITRATE HYDROUS [II]
SODIUM CITRATE HYDRATE [JAN]
SODIUM CITRATE [EP MONOGRAPH]
SODIUM CITRATE DIHYDRATE [MI]
AKOS025293920
Citronensaeure,Trinatrium-Salz-Dihydrat
Sodium citrate dihydrate, >=99%, FG
SODIUM CITRATE DIHYDRATE [VANDF]
TRISODIUM CITRATE DIHYDRATE [II]
BP-31019
SODIUM CITRATE DIHYDRATE [WHO-DD]
Sodium citrate tribasic dihydrate, >=98%
Sodium citrate dihydrate, ACS reagent grade
SODIUM CITRATE, DIHYDRATE [WHO-IP]
D01781
F82065
Sodium citrate tribasic dihydrate, AR, >=99%
Sodium citrate tribasic dihydrate, LR, >=99%
Citric acid trisodium salt dihydrate ACS reagent
NATRII CITRAS, DEHYDRATE [WHO-IP LATIN]
A833161
A835986
TRISODIUM CITRATE DIHYDRATE [USP MONOGRAPH]
Q22075862
Sodium citrate dihydrate Biochemical grade, Fine Granular
Sodium citrate tribasic dihydrate, USP, 99.0-100.5%
Sodium Citrate Tribasic Dihydrate (Molecular Biology Grade)
Sodium citrate tribasic dihydrate, ACS reagent, >=99.0%
trisodium 2-oxidanylpropane-1,2,3-tricarboxylate dihydrate
Citric acid trisodium salt dihydrateTrisodium citrate dihydrate
Sodium citrate tribasic dihydrate, BioUltra, >=99.0% (NT)
Sodium citrate tribasic dihydrate, insect cell culture tested
Sodium citrate tribasic dihydrate, JIS special grade, >=99.0%
Sodium citrate tribasic dihydrate, p.a., ACS reagent, 99.0%
Sodium citrate tribasic dihydrate, purum p.a., >=99.0% (NT)
Sodium citrate tribasic dihydrate, SAJ first grade, >=99.0%
Sodium citrate tribasic dihydrate, tested according to Ph.Eur.
trisodium 2-hydroxypropane-1,2,3-tricarboxylate--water (1/2)
Trisodium citrate dihydrate, meets USP testing specifications
2-hydroxy-1,2,3-propanetricarboxylic acid trisodium salt dihydrate
Sodium citrate tribasic dihydrate, BioXtra, >=99.0% (titration)
Sodium citrate tribasic dihydrate, for molecular biology, >=99%
Sodium citrate tribasic dihydrate, Vetec(TM) reagent grade, 98%
Sodium citrate, United States Pharmacopeia (USP) Reference Standard
1,2,3-Propanetricarboxylic acid, 2-hydroxy-, sodium salt, dihydrate
Sodium citrate tribasic dihydrate, p.a., ACS reagent, reag. ISO, 99-101%
1,2,3-Propanetricarboxylic acid, 2-hydroxy-, sodium salt, hydrate (1:3:2)
Sodium citrate tribasic dihydrate, BioUltra, for molecular biology, >=99.5% (NT)
Sodium citrate tribasic dihydrate, puriss. p.a., ACS reagent, >=99.0% (NT)
Sodium citrate tribasic dihydrate, suitable for amino acid analysis, >=99.0%
Sodium Citrate, Pharmaceutical Secondary Standard; Certified Reference Material
Sodium citrate tribasic dihydrate, puriss. p.a., ACS reagent, reag. ISO, reag. Ph. Eur., >=99.5%
Sodium citrate tribasic dihydrate, suitable for amino acid analysis, >=98% (titration), powder
Sodium Citrate, Dihydrate
Citric acid trisodium salt dihydrate
Sodium Citrate Dihydrate
Sodium citrate tribasic dihydrate
Trisodium citrate
Sodium citrate dihydrate
Citric acid tridosium salt dihydrate
Trisodium citrate, dihydrate, Citric acid
Trisodium Salt, Dihydrate,
Sodium citrate dihydrate
Sodium citrate tribasic dihydrate
1,2,3-Propanetricarboxylic acid, 2-hydroxy-
trisodium salt, dihydrate
2-hydroxy-1,2,3-propanetricarboxylic acid trisodium salt dihydrate
Sodium citrate hydrate
Trisodium citrate dihydrate
Sodium citrate dihydrate
Sodium citrate tribasic dihydrate
Citric acid trisodium salt dihydrate
Trisodium 2-hydroxypropane-1,2,3-tricarboxylate dihydrate
1,2,3-Propanetricarboxylic acid, 2-hydroxy-, trisodium salt, dihydrate
CITRIC ACID MONO
SODIUM CITRATE TRIBASIC DIHYDRATE
TRI-SODIUM CITRATE DIHYDRATE
SodiuM Citrate (AS)
NATRII CITRAS
SODIUM CITRATE, DIHYDRATE
ACIDUM CITRICUM MONOHYDRICUM
CITRIC ACID TRISODIUM SALT DIHYDRATE
BETA-HYDROXY-TRICARBOXYLIC ACID MONOHYDRATE
abs9147
1,2,3-Propanetricarboxylicacid
2-hydroxy-,trisodiumsalt,dihydrate
ANTI-BABOON IGM, BIOTIN
BETA-HYDROXY-TRICARBOXYLIC ACID MONOHYDRATE
HYDROXYTRICARBALLYLIC ACID MONOHYDRATE
CITRIC ACID NA3-SALT 2H2O
CITRIC ACID H2O
CITRIC ACID TRISODIUM SALT DIHYDRATE
CITRIC ACID, 3NA, DIHYDRATE
6132-04-3
1,2,3-PROPANETRICARBOXYLIC ACID, 2-HYDROXY-, TRISODIUM SALT, DIHYDRATE
CITRIC ACID, TRISODIUM SALT, DIHYDRATE
FEMA NO. 3026
N-1560
NATRII CITRAS, DEHYDRATE [WHO-IP LATIN]
SODIUM CITRATE [EP MONOGRAPH]
SODIUM CITRATE [FHFI]
SODIUM CITRATE DIHYDRATE
SODIUM CITRATE DIHYDRATE [MI]
SODIUM CITRATE DIHYDRATE [VANDF]
SODIUM CITRATE DIHYDRATE [WHO-DD]
SODIUM CITRATE HYDRATE
SODIUM CITRATE HYDRATE [JAN]
SODIUM CITRATE HYDROUS
SODIUM CITRATE HYDROUS [II]
SODIUM CITRATE, DIHYDRATE
SODIUM CITRATE, DIHYDRATE [WHO-IP]
TRISODIUM CITRATE DIHYDRATE [II]
TRISODIUM CITRATE DIHYDRATE [USP MONOGRAPH]




TRISODIUM CITRATE DIHYDRATE

Trisodium citrate dihydrate has the chemical formula of Na₃C₆H₅O₇. Although sodium citrate can refer to any of the three sodium salts of citric acid, Trisodium citrate dihydrate is sometimes referred to simply as "sodium citrate". Trisodium Citrate Dihydrate has a salty, slightly tart flavour. 
Trisodium citrate dihydrate is a tribasic salt of citric acid. It is produced by the complete neutralisation of citric acid with high purity sodium hydroxide or carbonate and subsequent crystallisation. Trisodium citrate dihydrate is widely used in foods, beverages and various technical applications mainly as buffering, sequestering or emulsifying agent.
Trisodium citrate dihydrate occurs as white, granular crystals or as a white, crystalline powder with a pleasant, salty taste. It is slightly deliquescent in moist air, freely soluble in water and practically insoluble in ethanol (96 %).
Trisodium citrate dihydrate is a non-toxic, neutral salt with low reactivity. It is chemically stable if stored at ambient temperatures. Trisodium citrate dihydrate is fully biodegradable and can be disposed of with regular waste or sewage.

CAS No: 6132-04-3
EC Number: 612-118-5


IUPAC Names: 
Trisodium
2-hydroxypropane-1,2,3-tricarboxylate
Dihydrate
Sodium citrate
sodium citrate
trisodium 2-hydroxypropane-1,2,3-tricarboxylate dihydrate
TRISODIUM CITRATE DIHYDRATE
Trisodium citrate dihydrate
trisodium;2-hydroxypropane-1,2,3-tricarboxylate;dihydrate

SYNONYMS: 
Trisodium citrate dihydrate;Sodium citrate dihydrate;6132-04-3;Sodium citrate tribasic dihydrate;1,2,3-Propanetricarboxylic acid, 2-hydroxy-, trisodium salt, dihydrate;Citric acid trisodium salt dihydrate;MFCD00150031;Sodium citrate hydrate;trisodium;2-hydroxypropane-1,2,3-tricarboxylate;dihydrate;UNII-B22547B95K;B22547B95K;trisodium 2-hydroxypropane-1,2,3-tricarboxylate dihydrate;Trisodium citrate dihydrate;Citric acid trisodium salt dihydrate;tri-sodium citrate dihydrate;Citric acid, trisodium salt dihydrate, ACS reagent;sodium 2-hydroxypropane-1,2,3-tricarboxylate dihydrate;Sodiumcitrate;Citric acid, trisodium salt dihydrate, 99%, for biochemistry;Natrum citricum;Tricitrasol (TN);ACMC-20ajao;Sodium citrate (TN)(JP17);CHEBI:32142;Trisodium citrate dihydrate, ACS;AKOS025293920;Citric acid, trisodium salt, dihydrate;Citronensaeure,Trinatrium-Salz-Dihydrat;Sodium citrate dihydrate, >=99%, FG;BP-31019;R385;Citrate, 0.5M buffer solution, pH 3.0;Citrate, 0.5M buffer solution, pH 4.0;Citrate, 0.5M buffer solution, pH 4.5;Citrate, 0.5M buffer solution, pH 5.0;Citrate, 0.5M buffer solution, pH 5.5;Citrate, 0.5M buffer solution, pH 6.0;Sodium citrate tribasic dihydrate, >=98%;Sodium citrate dihydrate, ACS reagent grade;C13249;D01781;Sodium citrate tribasic dihydrate, AR, >=99%;Sodium citrate tribasic dihydrate, LR, >=99%
reagent;124799-EP2287158A1;124799-EP2295426A1;124799-EP2295427A1;A835986;Citric acid, trisodium salt dihydrate, 99%, pure;Q22075862;Sodium citrate dihydrate Biochemical grade, Fine Granularreagent, >=99.0%;trisodium 2-oxidanylpropane-1,2,3-tricarboxylate dihydrate;UNII-1Q73Q2JULR component NLJMYIDDQXHKNR-UHFFFAOYSA-K;Sodium citrate tribasic dihydrate, BioUltra, >=99.0% (NT);Sodium citrate tribasic dihydrate, insect cell culture tested;Sodium citrate tribasic dihydrate, JIS special grade, >=99.0%;Sodium citrate tribasic dihydrate, p.a., ACS reagent, 99.0%;Sodium citrate tribasic dihydrate, purum p.a., >=99.0% (NT);Sodium citrate tribasic dihydrate, SAJ first grade, >=99.0%;Sodium citrate tribasic dihydrate, tested according to Ph.Eur.;trisodium 2-hydroxypropane-1,2,3-tricarboxylate--water (1/2);Trisodium citrate dihydrate, meets USP testing specifications;2-hydroxy-1,2,3-propanetricarboxylic acid trisodium salt dihydrate;Sodium citrate tribasic dihydrate, BioXtra, >=99.0% (titration);Sodium citrate tribasic dihydrate, for molecular biology, >=99%;Sodium citrate tribasic dihydrate, Vetec(TM) reagent grade, 98%;Sodium citrate, United States Pharmacopeia (USP) Reference Standard;1,2,3-Propanetricarboxylic acid, 2-hydroxy-, sodium salt, dihydrate;Sodium citrate tribasic dihydrate, p.a., ACS reagent, reag. ISO, 99-101%;1,2,3-Propanetricarboxylic acid, 2-hydroxy-, sodium salt, hydrate (1:3:2);Sodium citrate tribasic dihydrate, BioUltra, for molecular biology, >=99.5% (NT);Sodium citrate tribasic dihydrate, puriss. p.a., ACS reagent, >=99.0% (NT);Sodium citrate tribasic dihydrate, suitable for amino acid analysis, >=99.0%;Sodium Citrate, Pharmaceutical Secondary Standard; Certified Reference Material;Sodium citrate tribasic dihydrate, puriss. p.a., ACS reagent, reag. ISO, reag. Ph. Eur., >=99.5%;Sodium citrate tribasic dihydrate, puriss., meets analytical specification of Ph. Eur., BP, USP, FCC, E331, 99-100.5% (calc. to the dried substance);Sodium citrate tribasic dihydrate, suitable for amino acid analysis, >=98% (titration), powder;ANTI-BABOON IGM, BIOTIN;BETA-HYDROXY-TRICARBOXYLIC ACID MONOHYDRATE;HYDROXYTRICARBALLYLIC ACID MONOHYDRATE;CITRIC ACID NA3-SALT 2H2O;CITRIC ACID H2O;CITRIC ACID TRISODIUM SALT DIHYDRATE;CITRIC ACID, 3NA, DIHYDRATE;CITRIC ACID-1-HYDRATE;2-Hydroxy-1,2,3-propanenetricarboxylicacidtrisodiumsaltdihydrate;Citricacid, trisodiuM salt dihydrate, ACS reagent;Citric acid, trisodiuM salt dihydrate, 99%, for biocheMistry;TRI-SODIUM CITRATE DIHYDRATE P.A. EMSURE;SodiuM Citrate (AS);Sodium Citrate (1 g) (AS);SODIUM CITRATE、SODIUM CITRATE DEHYDRATE;sodiuM 2-hydroxypropane-1,2,3-tricarboxylate dihydrate;Sodium Citrate (1 g);Sodium citrate tribasic dihydrate ACS reagent, >=99.0%;Sodium citrate tribasic dihydrate puriss. p.a., ACS reagent, >=99.0% (NT);Sodium citrate tribasic dihydrate Vetec(TM) reagent grade, 98%;ACIDUM CITRICUM MONOHYDRICUM;2-HYDROXY-1,2,3-PROPANETRICARBOXYLIC ACID, MONOHYDRATE;2-HYDROXY-1,2,3-PROPANETRICARBOXYLIC ACID, TRISODIUM SALT, DIHYDRATE;SODIUM CITRATE 2H2O;SODIUM CITRATE, DIHYDRATE;SODIUM CITRATE TRIBASIC DIHYDRATE;SODIUM CITRATE TRISODIUM SALT DIHYDRATE;SODIUM CITRADE DIHYDRATE;NATRII CITRAS;SODIUM CITRATE, USP, DIHYDRATE POWDER;CITRIC ACID MONO BP93;CITRIC ACID ANHYDROUS 40-120 MESH;CITRIC ACID MON;CITRIC ACID MONOHYDRATE BP93;CITRIC ACID MONO;CITRIC ACID MONO AND ANH;CITRIC ACID MONO BP-93 & BP-98;CITRIC ACID BP93;CITRIC ACID ANHYDROUS USP;CITRIC ACID MONODYRATE BP93;CITRIC ACID FOOD GRAD;CITRIC ACID MONO BP98;CITRIC ACID MONOHYDRATE FOOD GRADE;Cit acid monohydrate;SODIUM CITRATE TRIBASIC DIHYDRATE USP;TRI-SODIUM CITRATE DIHYDRATE, FOR MOLECU LAR BIOLOGY;SODIUM CITRATE TRIBASIC DIHYDRATE, REAGENT GRADE, 99%;TRI-SODIUM CITRATE DIHYDRATE, FOR LUMINE SCENCE;CITRIC ACID TRISODIUM DIHYDRATESIGMAULTR A;SODIUM CITRATE DIHYDRATE, 99+%, A.C.S. REAGENT;CITRIC ACID TRISODIUM DIHYDRATE;CITRIC ACID, TRISODIUM SALT DIHYDRATE, 9 9%;SODIUM CITRATE DIHYDRATE 99+%;TRI-SODIUM CITRATE-2-HYDRATE R. G., REAG . ACS, REAG. ISO, REAG. PH. EUR.;SODIUM CITRATE TRIBASIC DIHYDRATE, PH EUR;SodiumCitrateBp93


General description
Sodium citrate dihydrate, (molecular formula: Na3C6H5O7 • 2H2O) has a molecular weight of 294.1, is a colourless crystal or white crystalline powder product; it is odourless, salty taste, and cool. It will lose its crystal water at 150 °C and will be decomposed at an even higher temperature. It also has slight deliquescence in wet air and has weathering property upon hot air. It is soluble in water and glycerol but insoluble in alcohol and some other organic solvents. Sodium citrate dihydrate has no toxic effect, and has pH adjusting capability as well as having good stability, and therefore can be used in the food industry. Sodium citrate dihydrate has the greatest demand when being used as a food additive; As food additives, it is mainly used as flavouring agents, buffers, emulsifiers, bulking agents, stabilizers and preservatives; in addition, a combination between sodium citrate dihydrate and citric acid can be used in a variety of jams, jelly, juice, drinks, cold drinks, dairy products and pastries gelling agents, flavouring agents and nutritional supplements.

Excellent performance
Sodium citrate dihydrate is currently the most important citrate dihydrate. It is produced by two steps: first starch food is fermented to generate citric acid; secondly, citric acid is neutralized by alkali to generate the final products. Sodium citrate dihydrate has the following excellent performance:
Safe and nontoxic properties; Since the basic raw material for the preparation of sodium citrate dihydrate mainly comes from food, it is absolutely safe and reliable without causing harm to human health. The United Nations Food and Agriculture and the World Health Organization has no restriction in its daily intake, which means that this product can be considered as non-toxic food.
It is biodegradable. After subjecting to the dilution of a large amount of water, sodium citrate dihydrate is partially converted into citrate dihydrate, which coexists with sodium citrate dihydrate in the same system. Citrate dihydrate is easy to subject to biological degradation at the water by the action of oxygen, heat, light, bacteria and microbes. Its decomposition pathways are generally going through aconitic acid, itaconic acid, citraconic acid anhydride to be further converted to carbon dioxide and water.
The ability to form a complex with metal ions. Sodium citrate dihydrate has a good capability of forming a complex with some metal ions such as Ca2+, Mg2+; for other ions such as Fe2+, it also has a good complex-forming ability.
Excellent solubility and the solubility increases with increasing temperature of the water.
It has a good capability for pH adjustment and a good buffering property. Sodium citrate dihydrate is a weak acid-strong alkali salt; When combined with citrate dihydrate, they can form a pH buffer with strong compatibility; therefore, this is very useful for some cases in which it is not suitable to have a large change of pH value. In addition, sodium citrate dihydrate also has excellent retardation performance and stability.


APPLICATIONS
Foods
Sodium citrate is chiefly used as a food additive, usually for flavour or as a preservative. Its E number is E331. Sodium citrate is employed as a flavouring agent in certain varieties of club soda. It is common as an ingredient in Bratwurst and is also used in commercial ready-to-drink beverages and drink mixes, contributing a tart flavour. It is found in gelatin mix, ice cream, yoghurt, jams, sweets, milk powder, processed cheeses, carbonated beverages, and wine, amongst others.

Sodium citrate can be used as an emulsifying stabilizer when making cheese. It allows the cheese to melt without becoming greasy by stopping the fats from separating.

As a conjugate base of a weak acid, citrate can perform as a buffering agent or acidity regulator, resisting changes in pH. It is used to control acidity in some substances, such as gelatin desserts. It can be found in the milk mini containers used with coffee machines. The compound is the product of antacids, such as Alka-Seltzer, when they are dissolved in water. The pH of a solution of 5 g/100 ml water at 25 °C is 7.5 – 9.0. It is added to many commercially packaged dairy products to control the PH impact of the gastrointestinal system of humans, mainly in processed products such as cheese and yoghurt.

Boiler descaling
Sodium citrate is a particularly effective agent for the removal of carbonate scale from boilers without removing them from the operation and for cleaning automobile radiators.

APPLICATION AREAS

Industry Uses
-Agricultural chemicals (non-pesticidal)
-Processing aids, not otherwise listed
-unknown potential industrial chemicals
-Adhesives, Sealants
- Agrochemicals, Fertilisers
- Construction
- Fine Chemicals
- Inks, Paints, Coatings
- Oil Drilling
- Paper
- Plastics, Polymers
- Textile, Leather

Consumer Uses
-Agricultural products (non-pesticidal)
-Automotive care products
-Building/construction materials not covered elsewhere
-Cleaning and furnishing care products

Industry Processing Sectors
-All other basic organic chemical manufacturing
-Nonmetallic mineral product manufacturing (includes clay, glass, cement, concrete, lime, gypsum, and other nonmetallic mineral product manufacturing.
-Pesticide, fertilizer, and other agricultural chemical manufacturing
-Soap, cleaning compound, and toilet preparation manufacturing

Properties
-Dihydrate
-White
-Granular crystals or crystalline powder
-Typical, practically odourless
-Pleasantly salty
-Freely soluble in water
-Practically insoluble in ethanol (96 %)
-Non-toxic
-Low reactive
-Chemically and microbiologically stable
-Fully biodegradable

Main functions
-pH regulator
-Chelating agent
-Buffering agent
-Flavour enhancer
-Stabiliser
-Emulsifying agent

Beverages
- Alcoholic Beverages
- Carbonated Soft Drinks
- Instant Drinks, Syrups
- Juice Drinks
- Plant-based
- RTD Tea and Coffee
- Sports and Energy Drinks
- Waters
 
Food
- Baby Food, Infant Formula
- Bakery
- Cereals, Snacks
- Confectionery
- Dairy
- Dairy Alternatives
- Desserts, Ice Cream
- Flavours
- Fruit Preparations, Sweet Spreads
- Fruits, Vegetables
- Meat Alternatives
- Meat, Seafood
- Plant-based Products
- Ready Meals, Instant Food
- Sauces, Dressings, Seasonings
 
Pharma
- Buffering agent
- Chelating agent
- Mineral source
 
Healthcare
- Clinical Nutrition
- Medical Devices
- OTC, Food Supplements
- Pharmaceutical Products

Personal Care
- Colour Cosmetics
- Fragrances
- Hair Care
- Oral Care
- Skin Care
- Soap and Bath Products
 
Cleaners & Detergents
- Dish Washing
- Industrial Cleaners
- Laundry Care
- Surface Care
 
Feed & Pet Food
- Feed
- Pet Food

Effect and application
During the process of clinically taking fresh blood, adding some amount of sterile sodium citrate can play a role in preventing blood clotting; this is exactly taking advantage of the features that calcium citrate can form soluble complexes with calcium ion; In the field of medicine, it is used for the in vitro anti-clotting drugs and anticoagulants drugs, phlegm drugs, and diuretics drugs during blood transfusions; it can also be used for cyanide-free electroplating industry; also used as a developer for the photographic industry. It can be used as flavouring agents, buffering materials, emulsifiers, and stabilizer in the food industry. Moreover, it is also widely used in chemical, metallurgical industry, the absorption of sulfur dioxide exhaust with the absorption rate of 99% and regenerate liquid sulfur dioxide citrate for recycling application. Sodium citrate has a good water solubility and an excellent cheating capability with Ca2 +, Mg2 + and other metal ions; it is biodegradable and has a strong dispersing ability and anti-redeposition ability; Daily-applied chemical detergents use it as an alternative to trimer sodium phosphate for the production of non-phosphorus detergent and phosphate-free liquid detergent. Adding a certain amount of sodium citrate to the detergent can significantly increase the cleaning ability of detergent cleaning. The large scale of application of sodium tripolyphosphate as a builder in detergents is an important discovery in the synthetic detergent industry. It is non-toxic without environmental pollution; it can also be acted as a buffer for the production of cosmetics.

Chemical Properties
It is colourless crystals or white crystalline powder and is odourless, cool and salty. It has no melting point with a relative density of 1.857. It is stable in air at room temperature with loss of crystal water when being heated to 150 °C loss of crystal water; further heating will cause its decomposition. It is insoluble in ethanol but highly soluble in water.

Uses
It can be used as Ph adjusting agents and emulsifying enhancers applied to jam, candy, jelly and ice cream; its combination with citric acid has an effect of alleviating tour; it also has effects on forming a complex with metal ions. China rules that it can be applied to various types of food with appropriate usage according to the absolute necessity.
It can be used as a food additive, as a complex agent and buffering agent in the electroplating industry; in the field of the pharmaceutical industry, it is used for the manufacturing of anti-clotting drugs; and used as the detergent additives in the light industry.
It is used as the analysis agents used for chromatography analysis and can also use for preparing bacterial culture medium; moreover, it can also be applied to the pharmaceutical industry.
The product can be used for the flavouring processing of food, as stabilizers, buffers and deputy complex-forming agents in the non-toxic electroplating industry; in the pharmaceutical industry, it is used as an anti-clotting agent, phlegm drugs and diuretics drugs. It can also be used in brewing, injection, newspaper and movies medicines.

Trisodium citrate dihydrate is chiefly used as a food additive, usually for flavour or as a preservative.
Anticoagulant for collection of blood. In photography; as sequestering agent to remove trace metals; as an emulsifier, acidulant and sequestrant in foods.
An anticoagulant also used as a biological buffer

Chemical Properties
Trisodium citrate dihydrate consists of odourless, colourless, monoclinic crystals, or a white crystalline powder with a cooling, saline taste. It is slightly deliquescent in moist air, and in warm dry air, it is efflorescent. Although most pharmacopoeias specify that sodium citrate is the dihydrate, the USP 32 states that Trisodium citrate dihydrate may be either the dihydrate or anhydrous material.

Production Methods
Trisodium citrate dihydrate is prepared by adding sodium carbonate to a solution of citric acid until effervescence ceases. The resulting solution is filtered and evaporated to dryness.

Pharmaceutical Applications
Trisodium citrate dihydrate, as either dihydrate or anhydrous material, is widely used in pharmaceutical formulations.
It is used in food products, primarily to adjust the pH of solutions. It is also used as a sequestering agent. The anhydrous material is used in effervescent tablet formulations. Trisodium citrate dihydrate is additionally used as a blood anticoagulant either alone or in combination with other citrates such as disodium hydrogen citrate.

Biological Activity
Commonly used laboratory reagent

Trisodium citrate dihydrate is widely applied in food, beverages and fillers as a buffering, sequestering or emulsifying agent. It used as an anticoagulant in blood transfusions, osmotic laxative, functional fluids, solvents cleaning, furnishing care products, laundry dishwashing products and cleaning automobile radiators.

Trisodium Citrate Dihydrate is a tribasic salt of citric acid. It consists of colourless to white crystals and is practically odourless. Trisodium citrate dihydrate is commonly used in various technical and industrial applications mainly as a pH buffering, sequestering or emulsifying agent. Also used as a retarder for mortar mixes.

Uses of Trisodium Citrate
Buffering agent.
Manufacture of household cleaners, degreasers and detergents.

Industrial applications
In the cleaning industry trisodium citrate is commonly used because of its excellent cleaning characteristics and its unusual property of being almost neutral yet portraying the characteristics of acid as in descalers and alkali as in degreasers. Cleaning products include laundry powders and detergents, toilet cleaners, hard surface cleaners, carpet cleaners, dishwashing liquids, powder and liquid degreasers and presoaks. It is becoming more and more popular now as it is considered environmentally friendly, it substitutes phosphates and is readily biodegradable.

In industry, trisodium citrate finds many uses including alkaline degreaser baths, electroplating chemicals for copper and nickel etc, photo chemicals. It is also used in the paper and pulp industries and the textiles industry.

Trisodium citrate dihydrate dihydrate is effective to retard plaster mixes. It must be used carefully as adding too much will prevent the plaster from curing properly. Premix the citrate in water first and add to the plaster mix.

Trisodium citrate dihydrate (C6H5Na3O7.2H2O) is a tribasic salt of citric acid. It has a sour taste similar to citric acid and is salty as well. It is often used as a food preservative, and as a flavouring in the food industry. In the pharmaceutical industry, it is used to control pH. It may be used as an alkalizing agent, buffering agent, emulsifier, or sequestering agent.

Trisodium citrate dihydrate is indicated for the management of renal tubular acidosis with calcium stones, hypocitraturia calcium oxalate nephrolithiasis of any aetiology, uric acid lithiasis with or without calcium stones. When Trisodium citrate dihydrate is given orally, the metabolism of absorbed citrate produces an alkaline load. The induced alkaline load in turn increases urinary pH and raises urinary citrate by augmenting citrate clearance without measurably altering ultra filterable serum citrate. Thus, Trisodium citrate dihydrate therapy appears to increase urinary citrate principally by modifying the renal handling of citrate, rather than by increasing the filtered load of citrate. Trisodium citrate dihydrate is used as a food additive (E 332) to regulate acidity.

Trisodium Citrate Dihydrate is manufactured by neutralizing citric acid derived from a submerged fermentation process.

Trisodium Citrate Dihydrate is available as translucent white crystals and has a slightly saline taste. The water of crystallization constitutes approximately 20% by weight of the dihydrate form.

Trisodium citrate dihydrate is a tribasic salt of citric acid. It is produced by the complete neutralisation of citric acid with high purity sodium hydroxide or carbonate and subsequent crystallisation. Citric acid is the product of microbial fermentation using carbohydrate substrates. Trisodium citrate dihydrate is widely used as an excellent pH regulator and an odourless buffering agent for bath and shower gels, creams, styling or decorative products. 

Trisodium Citrate Dihydrate is derived from citric acid and is available in either free-flowing colourless granular or powder forms. It is odourless and freely soluble in water but insoluble in alcohol. Storage at room temperature in tightly sealed containers is recommended. Trisodium citrate anhydrous may be used for the same applications as the widely used dihydrate salt but can provide particular benefit in dry products where the absence of moisture and/or long shelf life is required.

Trisodium citrate dihydrate is a tribasic salt of citric acid. It is produced by the complete neutralization of citric acid with a high purity sodium source and subsequent crystallization. Buffers pH and enhances the action of methyl parabens. Used in toothpaste & dental creams, effervescent denture cleansers, mouth rinses and oral hygiene products.

Trisodium citrate dihydrate is sometimes referred to simply as sodium citrate, though sodium citrate can refer to any of the three sodium salts of citric acid. It possesses a saline, mildly tart flavour. It is mildly basic and can be used along with citric acid to make biologically compatible buffers.

Trisodium citrate is the sodium salt of citric acid. It is white, crystalline powder or white, granular crystals, slightly deliquescent in moist air, freely soluble in water, practically insoluble in alcohol. Like citric acid, it has a sour taste. From the medical point of view, it is used as an alkalinizing agent. It works by neutralizing excess acid in the blood and urine. It has been indicated for the treatment of metabolic acidosis.

Trisodium Citrate Dihydrate consists of colourless crystals, with a salty taste and barely perceptible odour.

Trisodium Citrate Dihydrate is also known as trisodium citrate, citrosodine and trisodium salt. Trisodium Citrate Dihydrate products are non-toxic and fully biodegradable. 

Trisodium Citrate Dihydrate is manufactured when making citric acid and is used in similar applications including photography, soft drinks, and foods as it buffers PH levels to control acidity and also as a sequestering agent when sodium citrate attaches to calcium ions in water to stop limescale interfering with soaps and detergents.
Trisodium Citrate Dihydrate is sometimes simply referred to as "sodium citrate", although sodium citrate can refer to any of the three sodium salts. Trisodium citrate dihydrate, also known as sodium citrate, is an organic compound. Trisodium citrate dihydrate has an odourless, cold, salty flavour. Trisodium citrate dihydrate is stable at room temperature and air, slightly soluble in wet air, trisodium citrate dihydrate is more soluble in hot air. Trisodium citrate dihydrate is easily soluble in water, glycerol, alcohol and other organic solvents. Trisodium citrate dihydrate is decomposed by overheating, slightly dispersed in a moist environment and slightly decomposed in warm air. Trisodium citrate dihydrate has a salty, slightly sour taste. Trisodium citrate dihydrate is slightly basic and can be used with citric acid to make biocompatible buffers. Trisodium citrate dihydrate has a sour taste similar to citric acid and is also salty. Trisodium citrate dihydrate is often used as a food preservative and as a sweetener in the food industry. Trisodium citrate dihydrate is used in the pharmaceutical industry to control pH.
Trisodium citrate dihydrate can be used as an alkalizing agent, buffering agent, emulsifier, or separating agent. Normal quantities of Sodium. Soluble in water, almost insoluble in ethanol. Sodium Citrate is the sodium salt of citrate with alkalizing activity. Trisodium citrate dihydrate is a tribasic salt of citric acid. 
From a solution containing uranyl nitrate and sodium citrate, single crystals of trisodium citrate dihydrate, 3Na + C6H5O73-2H2O, are obtained. The structure consists of a complex network of citrate and sodium ions. In addition, hydrogen bonds are formed between citrate ions and the water of crystallization. Trisodium citrate dihydrate (C6H5Na3O7.2H2O) is a tribasic salt of citric acid. Trisodium citrate dihydrate is used in the food industry as a flavouring agent and stabilizer. Trisodium citrate dihydrate Used in the pharmaceutical industry as an anticoagulant, sputum dispersant and diuretic. In the trisodium citrate dihydrate detergent industry, sodium tripolyphosphate can be substituted as a non-toxic detergent additive. Trisodium citrate dihydrate is also used in fermentation, injection, photographic medicine, and electroplating. Trisodium citrate dihydrate is mainly used as a food additive, often as a flavouring or preservative. Trisodium citrate dihydrate is used as a flavouring agent in certain varieties of club soda. Trisodium citrate dihydrate is common as an ingredient in Bratwurst and is also used in commercial ready-to-drink beverages and beverage mixes and contributes to a sour taste. The trisodium citrate dihydrate gelatin mixture is used in the production of ice cream, yoghurt, jam, desserts, milk powder, processed cheeses, sodas and wine, among others.

Trisodium Sodium citrate can be used as an emulsifying stabilizer in cheese making. Trisodium citrate dihydrate stops the decomposition of fats, allowing the cheese to melt before Trisodium citrate becomes fat. As the conjugate base of a weak acid, trisodium citrate dihydrate can act as a buffering agent or acidity regulator by resisting pH changes. Trisodium citrate dihydrate is used to control acidity in some items such as gelatin desserts. The compound is the product of antacids such as Alka-Seltzer when dissolved in water. Trisodium citrate dihydrate is added to many commercially packaged dairy products to control the effect of PH in the human gastrointestinal tract, especially in processed products such as cheese and yoghurt. Today, sodium citrate is used for blood preservation in blood collection tubes and blood banks. Citrate ion disrupts the blood clotting mechanism by forming calcium citrate complexes by clamping calcium ions in the blood.
Trisodium citrate dihydrate is widely used mainly as a buffering, chelating or emulsifying agent in foods, beverages and various technical applications. Also, trisodium citrate dihydrate is used in fermentation, injection, electroplating and other medicines and photography. Upon absorption, sodium citrate decomposes into sodium cations and citrate anions; organic citrate ions are metabolized to bicarbonate ions, resulting in an increase in plasma bicarbonate concentration, buffering of excess hydrogen ion, the elevation of blood pH and potential reversal of acidosis. 
Trisodium citrate dihydrate is the most widely used emulsifying salt in sliced processed cheese products. Trisodium citrate dihydrate is commonly used as a buffering agent in combination with citric acid to provide precise pH control required in many food and beverage applications. Trisodium citrate is often referred to as sodium citrate, though sodium citrate can refer to any of the three sodium salts of citric acid. Sodium citrate has a saline, mildly tart flavour. Trisodium citrate dihydrate is mildly basic and can be used along with citric acid to make biologically compatible buffers. Sodium citrate is primarily used as a food additive, usually for flavour or as a preservative. In certain varieties of club soda, sodium citrate is employed as a flavouring agent. Sodium citrate is a common ingredient in Bratwurst and is also used to contribute a tart flavour in commercial, ready-to-drink beverages and drink mixes.
Bakery Flavors, Table Top Product Dairy Confectionery, Fruits, Vegetables Meat, Seafood, Cereals, Snacks Desserts, Ice Cream Ready Meals, Instant Food, Fruit Preparations, Sweet Spreads Baby Food, Infant Formula Sauces, Dressings, Seasoning The main functions of citric acid and the citrates in foods and beverages can be summarized as follows: as a flavour adjunct, to improve the taste as a pH control agent, e.g., for gelation control, buffering and preservative enhancement as a chelating agent to improve the action of antioxidants and prevent spoilage of foods such as seafood Beverages, Alcoholic Beverages, Carbonated Soft Drinks, Instant Drinks, Syrups, Juice Drinks, Tea and Coffee, Sports and Energy Drinks, Waters Within this market, citric acid or its salts perform several functions. The dominant application is for flavour enhancement. Many of the lemon, lime or citrus soft drinks available today use citric acid as a way of enhancing the tangy, zesty flavour consumers associate with these tropical fruit flavours. Additionally, citric acid can help provide consistency in the acidity and flavour of fruit juices or fruit cordials.

The citrate ion is a powerful chelating agent for trace metal ions. Diuretic - potassium citrate has diuretic properties. Clinical Nutrition Medical Devices OTC, Food Supplements Pharmaceutical Productscolor Cosmetics Deodorants, Fragrances Hair Care, Oral Care Skin Care Soap and Bath Products, Cleaners & Detergents, The major components of cleaning products are surfactants and builders. Other ingredients are added to provide a variety of functions, e.g., increasing cleaning performance for specific soils/surfaces, ensuring product stability, and supplying a unique identity to a product. Complex phosphates and sodium citrate are common sequestering builders. Builders enhance or maintain the cleaning efficiency of the surfactant. The primary function of builders is to reduce water hardness. This is done either by sequestration or chelation (holding hardness minerals in solution); by precipitation (forming an insoluble substance); or by ion exchange (trading electrically charged particles). Builders can also supply and maintain alkalinity, which assists cleaning, especially of acid soils; help keep removed soil from redepositing during washing, and emulsify oily and greasy soils. Dish Washing Industrial Cleaners, Laundry Care Surface Care.
This material is available in colourless granular form or powdery form. This is fragrance-free material and generously mixed with water, but not in the alcohol. Trisodium citrate dihydrate is not contained any food allergens and Trisodium citrate dihydrate is suitable for consumption by vegans and vegetarians. Trisodium citrate dihydrate adds enjoyable flavour to food items. Trisodium citrate dihydrate is widely used as dehydrating salt, but Trisodium citrate dihydrate provides a remarkable gain in dry products where long shelf life is needed to store it.
Trisodium citrate dihydrate is used as flavours, stabilizing agent, buffering agent, chelating agent, nutritional supplement of buttermilk, emulsifying agent and flavouring agent in the food and beverage industry; Trisodium citrate dihydrate can be used as anti-blood clotting, apophlegmatisant and diuretics in the pharmaceutical industry; Trisodium citrate dihydrate can replace sodium tripolyphosphate as a non-toxic detergent additive in the detergent industry; Trisodium citrate dihydrate can also be used in brewing, injection, photography drugs and electroplating etc.
 Sodium citrate dihydrate (C6H5Na3O7•2H2O), also known as citric trisodium salt dihydrate, or trisodium citrate dehydrate is obtained from citric acid and is available in granular or powder form having a salty but pleasant taste. Sodium citrate dihydrate is odourless and freely soluble in water, marginally deliquescent in moist air, and insoluble in alcohol. Trisodium citrate dihydrate is prepared by completely neutralizing citric acid with high purity sodium hydroxide or carbonate followed by crystallization.
Trisodium citrate dihydrate is a non-toxic, neutral salt having low reactivity. Trisodium citrate dihydrate shows chemically stability when stored at ambient temperatures. Sodium citrate dihydrate is totally biodegradable and disposable with regular waste or sewage. Trisodium citrate dihydrate is widely used in the food industry in preservatives and as a flavouring agent. In the pharmaceutical industry, Trisodium citrate dihydrate is used to resist changes in the pH. Sodium citrate dihydrate also finds its use as a buffering agent, alkalizing agent, emulsifying agent, or sequestering agent.
Seasonal factors for beverages and new detergent applications are the principal growth drivers for the global sodium citrate dihydrate market. Trisodium Citrate Dihydrate (TriSodium Citrate) is commonly used to improve exercise performance and as a food additive. Trisodium citrate dihydrate's naturally a strong source of antioxidants and typically used as a natural preservative. Some have also used the ingredient in beverages to increase acidity or to emulsify cheese during the ageing process. This ingredient may be added to foods and beverages or smoothies and green drinks. Trisodium citrate dihydrate is a pure white powder and has no fillers or binders, additives or preservatives.

TRISODIUM EDTA ( Ethylenediaminetetraacetic acid trisodium salt ) EDTA trisodique
SYNONYMS Trisodium Orthophosphate; Phosphoric acid, trisodium, 12-hydrate; Sodium Phosphate Tribasic Dodecahydrate; Trisodium phosphate, dodecahydrate; TSP dodecahydrate; Tertiary Sodium phosphate; CAS NO. 7601-54-9; 96337-98-3 (Anhydrous) 10101-89-0 (Dodecahydrate)
TRISODIUM NITRILOTRIACETATE
Trisodium nitrilotriacetate Category of Trisodium nitrilotriacetate Chelating Agents Trisodium nitrilotriacetate is used in the following products: textile treatment products and dyes and polymers. Release to the environment of Trisodium nitrilotriacetate can occur from industrial use: formulation of mixtures, formulation in materials and manufacturing of the substance. Uses at industrial sites Trisodium nitrilotriacetate is used in the following products: textile treatment products and dyes, metal working fluids, washing & cleaning products and water softeners. Description of Trisodium nitrilotriacetate White solid .Colorless or white solid. Slightly hygroscopic. Sources/Uses of Trisodium nitrilotriacetate Trisodium nitrilotriacetate is used as chelating agent in bleaching and as a sequestrant builder; Also used in tanning, synthetic rubber, textiles, pharmaceuticals, low phosphate and phosphate-free detergents, and in boiler-water treatment; [HSDB] Used for extraction, refining, and processing of metals; in the paper-pulp-board industry; and as an additive to construction materials Trisodium nitrilotriacetate Substance identity Help EC / List no. of Trisodium nitrilotriacetate: 225-768-6 CAS no. of Trisodium nitrilotriacetate:: 5064-31-3 Mol. formula of Trisodium nitrilotriacetate:: C6H6NNa3O6 About Trisodium nitrilotriacetate Helpful information Trisodium nitrilotriacetate has not been registered under the REACH Regulation, therefore as yet ECHA has not received any data about Trisodium nitrilotriacetate from registration dossiers. Trisodium nitrilotriacetate is used by consumers, in articles, by professional workers (widespread uses), in formulation or re-packing, at industrial sites and in manufacturing. Consumer Uses of Trisodium nitrilotriacetate: Trisodium nitrilotriacetate is used in the following products: washing & cleaning products, adhesives and sealants, air care products, biocides (e.g. disinfectants, pest control products), coating products, fillers, putties, plasters, modelling clay, metal surface treatment products, non-metal-surface treatment products, photo-chemicals, polishes and waxes and textile treatment products and dyes. Other release to the environment of Trisodium nitrilotriacetate is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners), outdoor use, indoor use in close systems with minimal release (e.g. cooling liquids in refrigerators, oil-based electric heaters), outdoor use in close systems with minimal release (e.g. hydraulic liquids in automotive suspension, lubricants in motor oil and break fluids), outdoor use in long-life materials with low release rate (e.g. metal, wooden and plastic construction and building materials), outdoor use in long-life materials with high release rate (e.g. tyres, treated wooden products, treated textile and fabric, brake pads in trucks or cars, sanding of buildings (bridges, facades) or vehicles (ships)), indoor use in long-life materials with low release rate (e.g. flooring, furniture, toys, construction materials, curtains, foot-wear, leather products, paper and cardboard products, electronic equipment) and indoor use in long-life materials with high release rate (e.g. release from fabrics, textiles during washing, removal of indoor paints). Article service life of Trisodium nitrilotriacetate: Release to the environment of Trisodium nitrilotriacetate can occur from industrial use: in processing aids at industrial sites. Trisodium nitrilotriacetate can be found in products with material based on: fabrics, textiles and apparel (e.g. clothing, mattress, curtains or carpets, textile toys). Widespread uses by professional workers Trisodium nitrilotriacetate is used in the following products: laboratory chemicals and washing & cleaning products. Trisodium nitrilotriacetate is used in the following areas: formulation of mixtures and/or re-packaging, mining, scientific research and development and municipal supply (e.g. electricity, steam, gas, water) and sewage treatment. Trisodium nitrilotriacetate is used for the manufacture of: chemicals, food products, textile, leather or fur, wood and wood products, pulp, paper and paper products, rubber products, plastic products, fabricated metal products, electrical, electronic and optical equipment, machinery and vehicles and furniture. Release to the environment of Trisodium nitrilotriacetate can occur from industrial use: in processing aids at industrial sites, in the production of articles, as processing aid, of substances in closed systems with minimal release, formulation of mixtures and formulation in materials. Other release to the environment of Trisodium nitrilotriacetate is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners), outdoor use, indoor use in close systems with minimal release (e.g. cooling liquids in refrigerators, oil-based electric heaters) and outdoor use in close systems with minimal release (e.g. hydraulic liquids in automotive suspension, lubricants in motor oil and break fluids). Formulation or re-packing Trisodium nitrilotriacetate is used in the following products: textile treatment products and dyes and polymers. Release to the environment of Trisodium nitrilotriacetate can occur from industrial use: formulation of mixtures, formulation in materials and manufacturing of the substance. Uses at industrial sites Trisodium nitrilotriacetate is used in the following products: textile treatment products and dyes, metal working fluids, washing & cleaning products and water softeners. Trisodium nitrilotriacetate has an industrial use resulting in manufacture of another substance (use of intermediates). Trisodium nitrilotriacetate is used in the following areas: mining. Trisodium nitrilotriacetate is used for the manufacture of: chemicals. Release to the environment of Trisodium nitrilotriacetate can occur from industrial use: in processing aids at industrial sites, in the production of articles, as an intermediate step in further manufacturing of another substance (use of intermediates) and of substances in closed systems with minimal release. Other release to the environment of Trisodium nitrilotriacetate is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners) and outdoor use. Manufacture Release to the environment of Trisodium nitrilotriacetate can occur from industrial use: manufacturing of the substance and formulation of mixtures. Uses of Trisodium nitrilotriacetate An excellent chelating agent. Sequestrant. Definition of Trisodium nitrilotriacetate ChEBI: An organic sodium salt composed of sodium and nitrilotriacetate ions in a 3:1 ratio. Safety Profile of Trisodium nitrilotriacetate Poison by intraperitoneal route. Moderately toxic by ingestion. Experimental reproductive effects. Questionable carcinogen with experimental neoplastigenic data. Mutation data reported. When heated to decomposition it emits toxic fumes of NOx and NazO. EC / List no. of Trisodium nitrilotriacetate: 225-768-6 CAS no. of Trisodium nitrilotriacetate:: 5064-31-3 Mol. formula of Trisodium nitrilotriacetate:: C6H6NNa3O6 Trisodium nitrilotriacetate Trisodium nitrilotriacetate Basic information Product Name: Trisodium nitrilotriacetate Synonyms of Trisodium nitrilotriacetate: nitrilotriaceticacidtrisodium*sigmagrade;nitrilotri-aceticacitrisodiumsalt;syntrona;trisodiumaminotriacetate;trisodiumnitrilotriaceticacid;versenenta150;cheeloxnta-14,-na3;chemcolox365powder CAS of Trisodium nitrilotriacetate: 5064-31-3 MF of Trisodium nitrilotriacetate: C6H6NNa3O6 MW of Trisodium nitrilotriacetate: 257.08 EINECS of Trisodium nitrilotriacetate: 225-768-6 Product Categories of Trisodium nitrilotriacetate: Building Blocks;Carbonyl Compounds; Carboxylic Acid Salts; Chemical Synthesis; Organic Building Blocks Mol File of Trisodium nitrilotriacetate: 5064-31-3.mol Trisodium nitrilotriacetate Structure Trisodium nitrilotriacetate Chemical Properties CAS DataBase Reference 5064-31-3(CAS DataBase Reference) EPA Substance Registry System Nitrilotriacetic acid trisodium salt (5064-31-3) Safety Informations of Trisodium nitrilotriacetate: Hazard Codes Xn Risk Statements of Trisodium nitrilotriacetate: 22-40-36 Safety Statements of Trisodium nitrilotriacetate: 36-46-36/37-26 WGK Germany of Trisodium nitrilotriacetate: 2 RTECS MB8400000 Hazardous Substances Data of Trisodium nitrilotriacetate: 5064-31-3(Hazardous Substances Data) Toxicity LD50 oral in rat: 1100mg/kg Nitrilotriacetic acid trisodium salt English SigmaAldrich English Trisodium nitrilotriacetate Usage And Synthesis Uses An excellent chelating agent. Sequestrant. Definition ChEBI: An organic sodium salt composed of sodium and nitrilotriacetate ions in a 3:1 ratio. Safety Profile Poison by intraperitoneal route. Moderately toxic by ingestion. Experimental reproductive effects. Questionable carcinogen with experimental neoplastigenic data. Mutation data reported. When heated to decomposition it emits toxic fumes of NOx and NazO. Trisodium nitrilotriacetate Agent Name Trisodium nitrilotriacetate CAS Number of Trisodium nitrilotriacetate 5064-31-3 Formula of Trisodium nitrilotriacetate C6-H9-N-O6.3Na Major Category of Trisodium nitrilotriacetate Other Uses of Trisodium nitrilotriacetate Trisodium nitrilotriacetate formula graphical representation Synonyms of Trisodium nitrilotriacetate N,N-Bis(carboxymethyl)glycine, trisodium salt; Nitrilotriacetic acid sodium salt; Acetic acid, nitrilotri-, trisodium salt; Cheelox NTA-14, Na3; Chemcolox 365 Powder; Glycine, N,N-bis(carboxymethyl)-, trisodium salt; Hampshire NTA; Hampshire NTA 150; Masquol NP 140; NTA trisodium salt; Nitrilotriacetate trisodium salt; Nitrilotriacetic acid trisodium salt; Nitrilotriacetic acid, trisodium salt; NTANa3; Sodium nitrilotriacetate; Syntron A; Trilon A; Trisodium 2,2',2''-nitrilotriacetate; Trisodium N,N-bis(carboxymethyl)glycinate; Trisodium NTA; Trisodium aminotriacetate; Trisodium nitrilotriacetic acid; Versene NTA 150; Versene NTA 335; [ChemIDplus] Category of Trisodium nitrilotriacetate Chelating Agents Description of Trisodium nitrilotriacetate White solid; [ICSC] Colorless or white solid; Slightly hygroscopic; [CHEMINFO] Sources/Uses of Trisodium nitrilotriacetate Trisodium nitrilotriacetate is Used as chelating agent in bleaching and as a sequestrant builder; Also used in tanning, synthetic rubber, textiles, pharmaceuticals, low phosphate and phosphate-free detergents, and in boiler-water treatment; [HSDB] Used for extraction, refining, and processing of metals; in the paper-pulp-board industry; and as an additive to construction materials; [IUCLID] Comments A corrosive substance that can cause injury to the skin, eyes, and respiratory tract; Possible human carcinogen; [ICSC] A skin, eye, nose, and throat irritant; Not sensitizing to human skin; High-dose feeding produces lesions of the urinary tract in mice and kidney lesions in rats; No evidence of reproductive or developmental toxicity in rats or rabbits; Emergency treatment: "Oxalic acid"; Oxalic acid is an irritant that, after ingestion, may cause kidney damage, hypocalcemia, and hepatic necrosis; [HSDB] An eye irritant; [eChemPortal: ESIS] Not irritating to rabbit or human skin; Irritating to rabbit eyes; Nephrotoxic in rats; [IUCLID] Mutagenic, tumorigenic, and toxic to reproduction; Causes changes in liver and bladder weights, erythrocyte count, and renal tubules in repeated dose studies of rats; [RTECS] May cause skin and eye irritation; Harmful if swallowed; [Aldrich MSDS] See "Nitrilotriacetic acid." Trisodium nitrilotriacetate is used in the following products: washing & cleaning products, adhesives and sealants, air care products, biocides (e.g. disinfectants, pest control products), coating products, fillers, putties, plasters, modelling clay, metal surface treatment products, non-metal-surface treatment products, photo-chemicals, polishes and waxes and textile treatment products and dyes. Other release to the environment of Trisodium nitrilotriacetate is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners), outdoor use, indoor use in close systems with minimal release (e.g. cooling liquids in refrigerators, oil-based electric heaters), outdoor use in close systems with minimal release (e.g. hydraulic liquids in automotive suspension, lubricants in motor oil and break fluids), outdoor use in long-life materials with low release rate (e.g. metal, wooden and plastic construction and building materials), outdoor use in long-life materials with high release rate (e.g. tyres, treated wooden products, treated textile and fabric, brake pads in trucks or cars, sanding of buildings (bridges, facades) or vehicles (ships)), indoor use in long-life materials with low release rate (e.g. flooring, furniture, toys, construction materials, curtains, foot-wear, leather products, paper and cardboard products, electronic equipment) and indoor use in long-life materials with high release rate (e.g. release from fabrics, textiles during washing, removal of indoor paints). Molecular Weight of Trisodium nitrilotriacetate: 257.08 g/mol Hydrogen Bond Donor Count of Trisodium nitrilotriacetate: 0 Hydrogen Bond Acceptor Count of Trisodium nitrilotriacetate: 7 Rotatable Bond Count of Trisodium nitrilotriacetate: 3 Exact Mass of Trisodium nitrilotriacetate: 256.98882 g/mol Monoisotopic Mass of Trisodium nitrilotriacetate: 256.98882 g/mol Topological Polar Surface Area of Trisodium nitrilotriacetate: 124 Ų Heavy Atom Count of Trisodium nitrilotriacetate: 16 Formal Charge of Trisodium nitrilotriacetate: 0 Complexity of Trisodium nitrilotriacetate: 171 Isotope Atom Count of Trisodium nitrilotriacetate: 0 Defined Atom Stereocenter Count of Trisodium nitrilotriacetate: 0 Undefined Atom Stereocenter Count of Trisodium nitrilotriacetate: 0 Defined Bond Stereocenter Count of Trisodium nitrilotriacetate: 0 Undefined Bond Stereocenter Count of Trisodium nitrilotriacetate: 0 Covalently-Bonded Unit Count of Trisodium nitrilotriacetate: 4 Compound of Trisodium nitrilotriacetate Is Canonicalized? Yes
TRISODIUM PHOSPHATE
TRISODIUM PHOSPHATE, N° CAS : 7601-54-9 - Phosphate trisodique, Origine(s) : Synthétique, Nom INCI : TRISODIUM PHOSPHATE, Nom chimique : Trisodium orthophosphate, N° EINECS/ELINCS : 231-509-8, Additif alimentaire : E339, Le phosphate trisodique joue le rôle d'agent chélateur et d'ajusteur de pH dans les cosmétiques. Il va permettre d'adoucir l'eau et d'éliminer certains métaux. Ses fonctions (INCI), Régulateur de pH : Stabilise le pH des cosmétiques, Agent de chélation : Réagit et forme des complexes avec des ions métalliques qui pourraient affecter la stabilité et / ou l'apparence des produits cosmétiques. Noms français : Phosphate de sodium tribasique PHOSPHATE DE SODIUM TRIBASIQUE ANHYDRE PHOSPHATE DE TRISODIUM PHOSPHATE TRISODIQUE PHOSPHATE TRISODIQUE, ANHYDRE PHOSPHORIC ACID, TRISODIUM SALT SODIUM PHOSPHATE (Na3PO4) SODIUM PHOSPHATE TRIBASIC SODIUM PHOSPHATE TRIBASIQUE SODIUM PHOSPHATE, ANHYDROUS SODIUM PHOSPHATE, TRIBASIC SODIUM TERTIARY PHOSPHATE SODIUM-O-PHOSPHATE TRIBASIC SODIUM PHOSPHATE TRISODIUM ORTHOPHOSPHATE Trisodium phosphate Noms anglais : Trisodium phosphate Utilisation: Fabrication de détergent, agent d'adoucissement
TRISODIUM PHOSPHATE (TSP)

Trisodium phosphate (TSP) is an inorganic compound that is widely used for various industrial and household purposes.
Its chemical formula is Na₃PO₄. It is a white, crystalline solid that is highly soluble in water.
Trisodium phosphate (TSP) is often used as a cleaning agent, stain remover, degreaser, and as a food additive.

CAS Number: 7601-54-9
EC Number: 231-509-8

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APPLICATIONS


Trisodium phosphate (TSP) is commonly used as a heavy-duty cleaner for removing grease, grime, and dirt from surfaces.
Trisodium phosphate (TSP) is extensively employed in industrial settings for cleaning equipment, machinery, and manufacturing facilities.
Trisodium phosphate (TSP) is used in household cleaning products such as detergents, degreasers, and multipurpose cleaners.

Trisodium phosphate (TSP) is an effective stain remover for removing tough stains from fabrics, carpets, and upholstery.
Trisodium phosphate (TSP) is used in the preparation of surfaces before painting or wallpapering to ensure proper adhesion.
In the construction industry, Trisodium phosphate (TSP) is used to clean concrete surfaces and remove efflorescence.

Trisodium phosphate (TSP) serves as a degreaser in automotive maintenance for cleaning engines, parts, and tools.
Trisodium phosphate (TSP) is used in the restoration of historical buildings and artifacts to remove dirt and grime without damaging the surface.

Trisodium phosphate (TSP) is employed in the food industry as a pH regulator, emulsifier, and sequestrant in various food products.
Trisodium phosphate (TSP) is used in water treatment processes to control pH and prevent scaling and corrosion in boilers and cooling systems.

Trisodium phosphate (TSP) is utilized in the formulation of detergents and dishwashing products to enhance their cleaning performance.
Trisodium phosphate (TSP) is added to swimming pools to adjust pH levels and remove calcium deposits and algae.
In the textile industry, Trisodium phosphate (TSP) is used as a scouring agent to remove impurities and oils from fibers and fabrics.

Trisodium phosphate (TSP) serves as a flux in soldering and brazing applications to remove oxides from metal surfaces.
Trisodium phosphate (TSP) is used in the manufacturing of ceramics, glass, and pottery as a flux and cleaning agent.

Trisodium phosphate (TSP) is employed in the pharmaceutical industry for cleaning equipment and manufacturing processes.
Trisodium phosphate (TSP) is used in the preparation of metal surfaces for painting and coating applications.

Trisodium phosphate (TSP) serves as a component in fire-retardant formulations for wood and textiles.
Trisodium phosphate (TSP) is utilized in agricultural applications as a cleaning agent for equipment and storage facilities.

Trisodium phosphate (TSP) is used in the pulp and paper industry for bleaching and cleaning pulp fibers.
Trisodium phosphate (TSP) is employed in the cleaning and maintenance of commercial kitchens and food processing facilities.

Trisodium phosphate (TSP) serves as a buffer and pH adjuster in laboratory and analytical applications.
Trisodium phosphate (TSP) is used in the production of household and personal care products such as toothpaste and mouthwash.

Trisodium phosphate (TSP) is utilized in the preparation of metal surfaces for electroplating and metal finishing processes.
Trisodium phosphate (TSP) is added to certain cosmetics and skincare products as a buffering agent and pH adjuster.

Trisodium phosphate (TSP) is commonly used in the restoration and cleaning of historical artifacts and monuments to remove dirt, grime, and pollutants.
Trisodium phosphate (TSP) serves as an effective cleaner for outdoor surfaces such as decks, patios, and sidewalks.
Trisodium phosphate (TSP) is utilized in the preparation of surfaces for sealing and waterproofing applications.
In the marine industry, Trisodium phosphate (TSP) is used for cleaning boat hulls, decks, and marine equipment.

Trisodium phosphate (TSP) is employed in the cleaning and maintenance of commercial and industrial kitchens to remove grease and food residues.
Trisodium phosphate (TSP) is used in the cleaning of HVAC (Heating, Ventilation, and Air Conditioning) systems to remove mold, mildew, and other contaminants.
It serves as a rust remover for metal surfaces, effectively eliminating rust stains and corrosion.
Trisodium phosphate (TSP) is used in the cleaning and maintenance of swimming pool filters to remove scale and algae buildup.

Trisodium phosphate (TSP) is employed in the cleaning of oil and grease spills on concrete surfaces in industrial settings.
Trisodium phosphate (TSP) is added to laundry detergents to enhance their cleaning power and remove stubborn stains.
In the brewing industry, Trisodium phosphate (TSP) is used as a cleaning agent for brewing equipment and fermentation tanks.

Trisodium phosphate (TSP) serves as a flux in metalworking processes such as soldering, welding, and brazing.
Trisodium phosphate (TSP) is used in the preparation of surfaces for adhesive bonding and sealant applications.

Trisodium phosphate (TSP) serves as a descaling agent for removing mineral deposits from appliances such as coffee makers and dishwashers.
Trisodium phosphate (TSP) is employed in the cleaning of industrial ovens, fryers, and cooking equipment in food processing facilities.

Trisodium phosphate (TSP) is utilized in the cleaning and maintenance of agricultural equipment, barns, and livestock facilities.
Trisodium phosphate (TSP) is added to water-based paints and coatings to improve adhesion and durability.
In the automotive industry, Trisodium phosphate (TSP) is used for cleaning engine parts, carburetors, and fuel injectors.

Trisodium phosphate (TSP) serves as a cleaning agent for removing smoke and soot residues from walls, ceilings, and furniture after fires.
Trisodium phosphate (TSP) is employed in the cleaning of metal surfaces prior to welding, painting, or plating.

Trisodium phosphate (TSP) is used in the manufacturing of ceramics and pottery as a glazing agent and flux.
Trisodium phosphate (TSP) is added to concrete mixtures to accelerate the curing process and improve strength.
In the electronics industry, Trisodium phosphate (TSP) is used for cleaning printed circuit boards and electronic components.
Trisodium phosphate (TSP) serves as a corrosion inhibitor for protecting metal surfaces from rust and oxidation.
Trisodium phosphate (TSP) is employed in the cleaning and maintenance of public spaces such as parks, playgrounds, and recreational facilities.



DESCRIPTION


Trisodium phosphate (TSP) is an inorganic compound that is widely used for various industrial and household purposes.
Its chemical formula is Na₃PO₄. It is a white, crystalline solid that is highly soluble in water.
Trisodium phosphate (TSP) is often used as a cleaning agent, stain remover, degreaser, and as a food additive.

In cleaning products, Trisodium phosphate (TSP) is valued for its ability to cut through grease and grime effectively.
Trisodium phosphate (TSP) is commonly used to clean walls, floors, and other surfaces before painting or wallpapering to ensure better adhesion.
Additionally, Trisodium phosphate (TSP) is used in certain food products as an acidity regulator and emulsifier.
However, its use in food has declined due to concerns about its environmental impact and potential health risks.

Trisodium phosphate is a versatile chemical compound with various industrial and household applications.
Trisodium phosphate (TSP) appears as a white, crystalline powder or granules.
Trisodium phosphate (TSP) is highly soluble in water, forming a clear solution.

Trisodium phosphate (TSP) is commonly used as a powerful cleaning agent due to its ability to cut through grease and grime effectively.
Trisodium phosphate (TSP) is often employed in cleaning walls, floors, and other surfaces before painting or wallpapering.
Trisodium phosphate (TSP) is known for its strong alkaline properties, making it effective in removing stubborn stains and dirt.

In addition to its cleaning capabilities, Trisodium phosphate (TSP) is used as a degreaser in industrial settings.
Trisodium phosphate (TSP) serves as an ingredient in certain detergents and dishwashing products to enhance their cleaning power.
Trisodium phosphate (TSP) is also utilized in the formulation of some personal care products, such as toothpaste and mouthwash.
In the food industry, Trisodium phosphate (TSP) functions as a food additive, serving as an emulsifier and pH regulator.

However, its use in food products has declined due to environmental and health concerns.
When handling Trisodium phosphate (TSP), it is essential to take safety precautions as it can cause skin and eye irritation.
Concentrated solutions of Trisodium phosphate (TSP) can be corrosive to certain materials, requiring careful handling and storage.

Trisodium phosphate (TSP) may react with acids to produce heat and potentially hazardous fumes.
It is important to avoid mixing Trisodium phosphate (TSP) with other chemicals without proper knowledge and guidance.
Trisodium phosphate (TSP) is commonly found in hardware stores and is available in various forms, including powder and liquid formulations.
Its effectiveness as a cleaner has made it a popular choice for both professional and household use.

Trisodium phosphate (TSP) is often preferred for heavy-duty cleaning tasks where other cleaners may not suffice.
Despite its strong cleaning power, Trisodium phosphate (TSP) is relatively inexpensive compared to some specialized cleaners.
The use of Trisodium phosphate (TSP) in cleaning formulations may be regulated in certain jurisdictions due to environmental concerns.

Environmental impact assessments are often conducted to evaluate the use and disposal of Trisodium phosphate (TSP)-containing products.
Trisodium phosphate (TSP) is biodegradable under certain conditions, but its widespread use can contribute to water pollution.

Proper disposal methods, such as dilution and neutralization, are recommended to minimize environmental impact.
Trisodium phosphate (TSP) has been used for decades in various industries, but its usage patterns have evolved over time.
Ongoing research and development efforts aim to find safer and more environmentally friendly alternatives to Trisodium phosphate (TSP) in cleaning and other applications.



PROPERTIES


Chemical formula: Na₃PO₄
Molecular weight: 163.94 g/mol (anhydrous)
Appearance: White, crystalline powder or granules
Physical state: Solid
Odor: Odorless
Solubility: Highly soluble in water
pH (1% solution): Basic (typically around pH 12)
Density: Varies depending on the form (e.g., anhydrous or dodecahydrate)
Melting point: Decomposes before melting (anhydrous Trisodium phosphate (TSP))
Boiling point: Decomposes before boiling
Hygroscopicity: Absorbs moisture from the air (especially the dodecahydrate form)
Water content: Hydrated forms exist, including dodecahydrate (Na₃PO₄·12H₂O)
Stability: Stable under normal conditions, but decomposes when heated to high temperatures
Reactivity: Reacts with acids to form salts and phosphoric acid
Alkalinity: Strong alkaline properties



FIRST AID


Inhalation:

If inhaled, remove the person to fresh air immediately.
If the person is having difficulty breathing, seek medical attention promptly.
Provide artificial respiration if breathing has stopped or is impaired.
Keep the person calm and reassured while waiting for medical assistance.


Skin Contact:

Remove contaminated clothing and rinse affected skin with plenty of water.
Wash the skin thoroughly with soap and water.
If irritation persists or skin becomes damaged, seek medical attention.
Do not apply creams or ointments unless directed by medical personnel.


Eye Contact:

Flush eyes with lukewarm water for at least 15 minutes, holding the eyelids open to ensure thorough rinsing.
Seek immediate medical attention, even if the person does not report discomfort or pain.
Continue to flush the eyes while waiting for medical help to arrive.


Ingestion:

If swallowed, do not induce vomiting unless directed by medical personnel.
Rinse the mouth thoroughly with water.
Give the person a small amount of water or milk to drink if they are conscious and able to swallow.
Seek medical attention immediately, and have the product label or safety data sheet available for reference.



HANDLING AND STORAGE


Handling Precautions:

Wear appropriate personal protective equipment (PPE), including gloves, safety goggles, and protective clothing, when handling Trisodium phosphate (TSP).
Avoid direct contact with skin, eyes, and clothing.
In case of contact, promptly rinse affected area with water.
Work in a well-ventilated area to minimize inhalation of dust or vapors.
Use caution to prevent spills, splashes, and airborne dust.
Do not eat, drink, or smoke while handling Trisodium phosphate (TSP).
Wash hands thoroughly after handling Trisodium phosphate (TSP) and before eating, drinking, or using the restroom.


Storage Conditions:

Store Trisodium phosphate (TSP) in a cool, dry, well-ventilated area away from sources of heat, moisture, and incompatible materials.
Keep containers tightly closed when not in use to prevent contamination and moisture absorption.
Store Trisodium phosphate (TSP) separately from acids, oxidizing agents, and other reactive chemicals to prevent potential reactions.
Ensure that storage area is labeled with appropriate hazard warnings and information.
Do not store Trisodium phosphate (TSP) near food, beverages, or animal feed to prevent accidental contamination.
Store Trisodium phosphate (TSP) away from direct sunlight and sources of ignition to prevent decomposition and fire hazards.
Check containers regularly for signs of damage, leakage, or deterioration, and replace as needed.
Follow any specific storage instructions provided on the product label or safety data sheet.


Transportation Precautions:

When transporting Trisodium phosphate (TSP), use appropriate containers that are compatible with the chemical and securely sealed to prevent leaks or spills.
Ensure that containers are properly labeled with the product name, hazard warnings, and handling instructions.
Follow applicable regulations and guidelines for the transportation of hazardous chemicals, including packaging, labeling, and documentation requirements.
Take precautions to prevent damage to containers during loading, unloading, and transportation.
In case of spills or leaks during transportation, follow established procedures for containment, cleanup, and disposal.


Emergency Procedures:

In the event of a spill, leak, or accidental release of Trisodium phosphate (TSP), follow established emergency procedures for chemical spills and hazardous material incidents.
Evacuate the area if necessary to prevent exposure to chemical vapors or dust.
Notify appropriate personnel, such as safety officers, supervisors, or emergency responders, of the incident.
Provide information about the chemical involved, including its identity, quantity, and location.
Use appropriate containment measures, absorbent materials, and personal protective equipment to safely clean up spills.
Dispose of contaminated materials and waste in accordance with local regulations and guidelines.
TRISODIUM PHOSPHATE DODECAHYDRATE

Trisodium phosphate dodecahydrate, often abbreviated as TSP, is a chemical compound with the chemical formula Na3PO4·12H2O.
Trisodium phosphate dodecahydrate is a white, crystalline, water-soluble solid that is commonly used for various industrial and household purposes.
The "dodecahydrate" part of the name indicates that the compound has 12 water molecules associated with each molecule of trisodium phosphate.

CAS Number: 10101-89-0
EC Number: 231-509-8



APPLICATIONS


Trisodium phosphate dodecahydrate is commonly used as a heavy-duty cleaning agent in both industrial and household settings.
Trisodium phosphate dodecahydrate serves as a powerful degreaser, effectively removing oil, grease, and dirt from various surfaces.
In preparation for painting, the compound is applied to surfaces to ensure proper adhesion by removing contaminants.

Trisodium phosphate dodecahydrate finds use as a food additive in the food industry, where it functions as an acidity regulator and emulsifier.
Trisodium phosphate dodecahydrate's alkalinity makes it valuable for water softening applications, as it can sequester calcium and magnesium ions responsible for water hardness.
Trisodium phosphate dodecahydrate is included in some dishwasher detergents to aid in the removal of stains and residues from dishes and glassware.
Trisodium phosphate dodecahydrate plays a role in the textile industry as a pH adjuster during processing to neutralize acidic solutions.
Due to its alkaline properties, Trisodium phosphate dodecahydrate is utilized in the removal of rust and scale from metals and industrial equipment.

Trisodium phosphate dodecahydrate is a key component in industrial cleaning products, facilitating the removal of tough contaminants and deposits.
In specific instances, it's employed for paint stripping by breaking down layers of paint coatings on surfaces.
Trisodium phosphate dodecahydrate is used for the cleaning of boilers and industrial machinery, effectively removing buildup and deposits.

Trisodium phosphate dodecahydrate is a component in the formulation of certain photographic developers, aiding in the development of photographic images.
Trisodium phosphate dodecahydrate's alkaline nature contributes to its role in breaking down organic matter, making it useful in cleaning applications.
In some formulations, Trisodium phosphate dodecahydrate is used as an emulsifying agent to create stable mixtures of oil and water-based substances.
Trisodium phosphate dodecahydrate has applications in cleaning and disinfecting medical equipment and facilities.

Trisodium phosphate dodecahydrate's alkaline properties contribute to its effectiveness in neutralizing acidic solutions in various chemical processes.
Trisodium phosphate dodecahydrate can be employed as a rust converter, transforming iron oxide (rust) into a more stable compound on metal surfaces.
In industrial water treatment, it's used to control the pH of water and to prevent the formation of scale and deposits.

Trisodium phosphate dodecahydrate's ability to form stable complexes makes it valuable in analytical chemistry for trace metal analysis.
Trisodium phosphate dodecahydrate is sometimes added to soaps and detergents to enhance their cleaning properties.
Trisodium phosphate dodecahydrate is utilized in the cleaning and maintenance of swimming pools to control algae growth and maintain water clarity.

In the production of ceramics and glass, Trisodium phosphate dodecahydrate is used to adjust the pH of glazes and cleaning solutions.
Trisodium phosphate dodecahydrate is involved in the formulation of some rust removers and descaling agents.
Trisodium phosphate dodecahydrate's chemical interactions find applications in various laboratory procedures and chemical syntheses.
Trisodium phosphate dodecahydrate can be used to restore the shine and cleanliness of metal surfaces, including stainless steel and aluminum.

Trisodium phosphate dodecahydrate is utilized in the pulp and paper industry for its ability to remove ink and residue from paper fibers.
Trisodium phosphate dodecahydrate finds application in the automotive industry for cleaning engine components and removing grease and oil stains.

Trisodium phosphate dodecahydrate is added to some cleaning products for household use, enhancing their effectiveness on tough stains and surfaces.
In the construction industry, it's used to clean and prepare surfaces before applying coatings, sealants, or adhesives.
Trisodium phosphate dodecahydrate is employed in the restoration of historical and architectural surfaces to remove dirt and grime.
Trisodium phosphate dodecahydrate is used in certain fire-fighting foams to suppress flammable liquid fires by forming a smothering blanket.

Trisodium phosphate dodecahydrate's alkaline properties make it useful for adjusting pH levels in swimming pool water to prevent algae growth.
In the textile industry, Trisodium phosphate dodecahydrate is used for scouring cotton fabrics to remove impurities and natural oils before dyeing or finishing.
Trisodium phosphate dodecahydrate is incorporated into some toothpaste formulations as an abrasive for effective dental cleaning.
Trisodium phosphate dodecahydrate is used in some metal cleaning products to remove tarnish and oxidation from silverware and jewelry.
Trisodium phosphate dodecahydrate's ability to dissolve mineral deposits makes it useful for cleaning faucets, showerheads, and other plumbing fixtures.

In the agriculture industry, Trisodium phosphate dodecahydrate is used in cleaning and disinfecting equipment and facilities to prevent the spread of disease.
Trisodium phosphate dodecahydrate is employed in the cleaning and maintenance of commercial kitchens and food processing facilities.
Trisodium phosphate dodecahydrate is used to remove mold, mildew, and stains from surfaces in humid environments, such as bathrooms and basements.
In the electronics industry, it's used in the cleaning of circuit boards and electronic components to remove flux residues.
Trisodium phosphate dodecahydrate's alkalinity contributes to its role in neutralizing acidic substances in laboratory and chemical research settings.

Trisodium phosphate dodecahydrate can be added to some metal polishes to enhance the shine and remove tarnish.
Trisodium phosphate dodecahydrate is used in the cleaning of windows, glass, and mirrors to remove streaks, smudges, and fingerprints.
Trisodium phosphate dodecahydrate's ability to dissolve organic matter makes it valuable for cleaning and sanitizing composting toilets.
In the ceramics industry, Trisodium phosphate dodecahydrate is used to remove glaze defects and clean kiln shelves and equipment.

Trisodium phosphate dodecahydrate is used in the cleaning of brewery equipment to remove residues and prevent contamination.
Trisodium phosphate dodecahydrate is employed in the cleaning and maintenance of air conditioning and ventilation systems to remove mold and debris.
Trisodium phosphate dodecahydrate can be used to clean and deodorize trash cans and bins by breaking down organic waste and odors.
In marine applications, it's used to clean boat hulls and remove algae and marine growth.
Trisodium phosphate dodecahydrate is added to some cleaning solutions for carpet and upholstery to remove stains and dirt.

Trisodium phosphate dodecahydrate is used in the cleaning and maintenance of industrial equipment and machinery to remove residues and contaminants.
Trisodium phosphate dodecahydrate finds application in the cleaning of brick and masonry surfaces, effectively removing dirt, stains, and efflorescence.

Trisodium phosphate dodecahydrate is employed in the cleaning of ceramic and porcelain tiles to remove grout haze and mineral deposits.
Trisodium phosphate dodecahydrate is added to some paint removers and strippers to soften and lift layers of old paint.
Trisodium phosphate dodecahydrate is used in the cleaning of wooden surfaces to remove mold, mildew, and stains, restoring the natural appearance of the wood.
The compound is utilized in the cleaning of vinyl and plastic surfaces to remove dirt, stains, and discoloration.
Trisodium phosphate dodecahydrate is used in the cleaning of concrete surfaces, driveways, and sidewalks to remove oil stains and grime.

Trisodium phosphate dodecahydrate is employed in the cleaning of ceramic and glass cooktops to remove burnt-on food and stains.
The compound is used in the cleaning of outdoor furniture, removing dirt, grime, and weathering effects.
Trisodium phosphate dodecahydrate is added to some bathroom and kitchen cleaning products to enhance their effectiveness on soap scum and hard water stains.
Trisodium phosphate dodecahydrate is utilized in the cleaning of industrial exhaust systems to remove soot, grease, and other deposits.
The compound is employed in the cleaning of automotive interiors, including upholstery and carpets, to remove stains and odors.

Trisodium phosphate dodecahydrate is used in the cleaning of pet enclosures and kennels to remove odors and disinfect surfaces.
Trisodium phosphate dodecahydrate is employed in the cleaning of playground equipment and outdoor structures to remove dirt, mold, and environmental pollutants.
Trisodium phosphate dodecahydrate is added to some all-purpose cleaners for household use to improve their ability to remove a wide range of stains and soils.
Trisodium phosphate dodecahydrate is used in the cleaning of greasy and oily tools and equipment in industrial workshops.
Trisodium phosphate dodecahydrate is employed in the cleaning of concrete and stone statues and monuments to remove dirt and pollutants.
Trisodium phosphate dodecahydrate is used in the cleaning of automotive engines and parts to remove oil, grease, and carbon buildup.

Trisodium phosphate dodecahydrate is added to some carpet cleaning solutions to lift and remove deep-seated stains and dirt.
Trisodium phosphate dodecahydrate is utilized in the cleaning of garage floors and workshop surfaces to remove oil and grease stains.
The compound is employed in the cleaning of swimming pool decks and patio areas to remove dirt, algae, and stains.
Trisodium phosphate dodecahydrate is used in the cleaning of outdoor grills and barbecue equipment to remove grease and carbon buildup.
Trisodium phosphate dodecahydrate is added to some bathroom cleaning products to remove hard water stains and mineral deposits from surfaces.

Trisodium phosphate dodecahydrate is utilized in the cleaning of industrial tanks and containers to remove residues and contaminants.
Trisodium phosphate dodecahydrate is used in the cleaning of industrial pipelines and conduits to remove blockages and buildup.



DESCRIPTION


Trisodium phosphate dodecahydrate, often abbreviated as TSP, is a chemical compound with the chemical formula Na3PO4·12H2O.
Trisodium phosphate dodecahydrate is a white, crystalline, water-soluble solid that is commonly used for various industrial and household purposes.
The "dodecahydrate" part of the name indicates that the compound has 12 water molecules associated with each molecule of trisodium phosphate.

Trisodium phosphate dodecahydrate, with the chemical formula Na3PO4·12H2O, is a hydrated sodium phosphate compound.
Trisodium phosphate dodecahydrate appears as a white, crystalline solid with a granular texture and is highly soluble in water.
Trisodium phosphate dodecahydrate is composed of sodium (Na) cations, phosphate (PO4) anions, and twelve water molecules.

Trisodium phosphate dodecahydrate is known for its strong alkaline properties, which make it effective in cleaning and degreasing applications.
Its alkalinity arises from the presence of hydroxide ions (OH-) released when it dissolves in water.
Trisodium phosphate dodecahydrate is used across various industries for its versatile cleaning and chemical properties.
Trisodium phosphate dodecahydrate's ability to react with fatty acids and oils makes it an efficient degreaser in industrial settings.

In household applications, it's utilized for heavy-duty cleaning tasks, such as preparing surfaces for painting.
Trisodium phosphate dodecahydrate is hygroscopic, meaning it readily absorbs moisture from the air.
Its granular form allows for easy mixing with water to create cleaning solutions.
Trisodium phosphate dodecahydrate is regulated as a food additive in some jurisdictions, where it serves as an acidity regulator and emulsifier.

Due to its sequestering properties, it's used for water softening to reduce hardness caused by calcium and magnesium ions.
Trisodium phosphate dodecahydrate can be found in some dishwasher detergents, aiding in stain removal from dishes and glassware.
In the field of photography, it plays a role as a photographic developer.
Trisodium phosphate dodecahydrate's pH-adjusting abilities make it useful in textile processing to neutralize acidic solutions.

Trisodium phosphate dodecahydrate's alkaline nature contributes to its efficacy in scale and rust removal from metals.
Trisodium phosphate dodecahydrate is used as a component in industrial cleaning products, facilitating the removal of various contaminants.
In specific applications, it's utilized for paint stripping by breaking down layers of paint coatings.

Trisodium phosphate dodecahydrate can be employed in the cleaning of boilers and industrial equipment, removing deposits and buildup.
Its chemical structure consists of sodium ions binding with phosphate anions, surrounded by twelve water molecules.
Trisodium phosphate dodecahydrate's solubility in water enables it to create effective cleaning solutions with varying concentrations.

Trisodium phosphate dodecahydrate's alkalinity is attributed to its ability to release hydroxide ions when dissolved.
Trisodium phosphate dodecahydrate's versatile uses span from heavy-duty cleaning in households to industrial applications.
Its chemical composition is governed by the presence of sodium, phosphate, and water molecules.
When handling Trisodium phosphate dodecahydrate, proper precautions should be taken due to its alkaline nature and potential environmental and health impacts.



PROPERTIES


Chemical Formula: Na3PO4·12H2O
Molecular Weight: 380.12 g/mol
Appearance: White crystalline solid
Solubility: Highly soluble in water
Melting Point: 73.4 °C (164.1 °F) (loses water of crystallization)
Density: 1.62 g/cm³ (at 20 °C)
Hygroscopic: Absorbs moisture from the air
Odor: Odorless
pH: Alkaline/basic (due to the hydrolysis of phosphate ions)



FIRST AID


Inhalation:

If inhaled, move the affected person to fresh air immediately.
If the person is experiencing difficulty breathing, seek medical attention promptly.
Provide oxygen or artificial respiration if breathing is compromised.


Skin Contact:

Remove contaminated clothing and shoes.
Wash the affected area thoroughly with plenty of water and mild soap.
If irritation or redness persists, seek medical attention.
Cleanse any clothing that has come in contact with the compound before re-use.


Eye Contact:

Rinse the eyes gently with water for at least 15 minutes, holding the eyelids open.
Seek immediate medical attention to ensure thorough eye examination.
If contact lenses are being worn, remove them after the initial rinsing and continue rinsing.


Ingestion:

Rinse the mouth thoroughly with water to remove any traces of the compound.
Do NOT induce vomiting unless instructed to do so by medical personnel.
Drink plenty of water to dilute the compound and help minimize potential adverse effects.
Seek immediate medical attention and provide medical personnel with information about the ingested amount and symptoms.



HANDLING AND STORAGE


Handling:

Personal Protective Equipment (PPE):
When handling Trisodium phosphate dodecahydrate, wear appropriate PPE, including chemical-resistant gloves, safety goggles or a face shield, and protective clothing to prevent skin and eye contact.

Ventilation:
Work in a well-ventilated area to minimize inhalation exposure.
If handling in an enclosed space, ensure proper ventilation systems are in place.

Avoid Direct Contact:
Avoid direct skin, eye, and clothing contact with the compound.
In case of contact, follow first aid measures and wash thoroughly with water.

Avoid Ingestion:
Do not eat, drink, or smoke while handling the compound.
Wash hands thoroughly after handling.

Spill and Leak Response:
In case of spills or leaks, promptly contain the spill using appropriate absorbent materials.
Avoid generating dust.
Collect the spilled material and place it in suitable containers for disposal.

Dust Generation:
Minimize dust generation during handling to prevent inhalation exposure.
Use appropriate dust control measures such as local exhaust ventilation or dust suppression techniques.

Equipment and Tools:
Use non-sparking tools and equipment when handling the compound to prevent ignition of dust.


Storage:

Container:
Store Trisodium phosphate dodecahydrate in tightly sealed, labeled containers made of compatible materials, such as plastic or glass.

Location:
Store containers in a cool, dry, and well-ventilated area away from sources of heat, direct sunlight, and incompatible materials.

Elevated Storage:
Elevate containers off the ground to prevent contact with moisture and potential water damage.

Segregation:
Store Trisodium phosphate dodecahydrate away from acids, bases, and reactive materials to prevent undesired chemical reactions.

Labeling:
Clearly label containers with the name of the compound, hazard symbols, handling precautions, and first aid instructions.



SYNONYMS


Sodium Phosphate Tribasic Dodecahydrate
TSP Dodecahydrate
Sodium Phosphate Dodecahydrate
Trisodium Phosphate 12-Hydrate
TSP-12
Sodium Phosphate Tribasic 12-Hydrate
Sodium Phosphate Crystalline Dodecahydrate
Sodium Orthophosphate Dodecahydrate
Tertiary Sodium Phosphate Dodecahydrate
Sodium Orthophosphate Tribasic Dodecahydrate
Trisodium Orthophosphate Dodecahydrate
Sodium Phosphate Crystal Dodecahydrate
Trisodium Phosphate Crystalline Dodecahydrate
Trisodium Salt Dodecahydrate
Tertiary Sodium Phosphate 12-Hydrate
Sodium Tertiary Phosphate Dodecahydrate
Sodium Orthophosphate Crystal Dodecahydrate
Sodium Phosphate Hydrate
Trisodium Salt of Orthophosphoric Acid Dodecahydrate
Tertiary Sodium Phosphate Crystalline Dodecahydrate
Sodium Phosphate 12-Hydrate
Sodium Orthophosphate Hydrate
Sodium Phosphate 12H2O
Sodium Phosphate Hydrated
Sodium Orthophosphate Hydrated
Sodium Phosphate 12-Dehydrate
Sodium Phosphate Tribasic Hydrate
Trisodium Orthophosphate 12-Hydrate
TSP Hydrate
Sodium Phosphate Tribasic 12H2O
Tertiary Sodium Phosphate 12-Dehydrate
Sodium Phosphate Dodeca
Sodium Phosphate 12-Molecule
Trisodium Salt Hydrate
Sodium Orthophosphate 12-Molecule
Tertiary Sodium Phosphate 12-Molecule
Trisodium Phosphate 12-Molecule
Sodium Tertiary Phosphate 12-Molecule
Sodium Orthophosphate Tribasic Hydrate
Sodium Phosphate 12H2O
Tertiary Sodium Phosphate Tribasic Hydrate
Sodium Phosphate 12-Water
Sodium Orthophosphate 12-Water
Tertiary Sodium Phosphate 12-Water
Trisodium Phosphate 12-Water
Sodium Tertiary Phosphate 12-Water
Trisodium Orthophosphate Hydrate
Tertiary Sodium Phosphate Hydrate
Sodium Tertiary Phosphate Hydrate
Trisodium Orthophosphate 12-Water

TRISODIUM PHOSPHATE(12 HYDRATE)
SYNONYMS 6-N,N-Diethyl-β-γ-dibromomethylene-D-adenosine-5′-triphosphate trisodium salt hydrate, FPL 67156 CAS NO:160928-38-1 (free acid)
TRISODIUM SALT
Trisodium salt appears as a white crystalline powder or granular crystals and, given Trisodium salt is a salt, possesses a salty / saline taste with no real detectable odour.
Trisodium salt is a chemical compound, the sodium salt of Citric Acid.
Trisodium salt is obtained by reacting Sodium Citrate with sodium hydroxide, carbonate, or bicarbonate and then crystallized and dehydrated.

CAS Number: 68-04-2
EC number: 200-675-3
Chemical Formula: Na3C6H5O7
Molar Mass: 294.10 g/mol

Trisodium salt has the chemical formula of Na3C6H5O7.
Trisodium salt is sometimes referred to simply as "sodium citrate", though Trisodium salt can refer to any of the three sodium salts of citric acid.
Trisodium salt possesses a saline, mildly tart flavor, and is a mild alkali.

Trisodium salt is mildly basic and can be used along with Sodium Citrate to make biologically compatible buffers.

Trisodium salt has the chemical formula Na3C6H5O7.
Trisodium salt can refer to any of the three sodium salts of citric acid.

Trisodium salt is lightweight and can be used with Sodium Citrate to make biocompatible buffers.

Trisodium salt, one of the sodium salts of citric acid, is a compound found in every living organism and is part of key metabolic pathways in all body cells.
Trisodium salt is found in high concentrations in sour fruits, kiwis, strawberries and many other fruits.
Trisodium salt is commercially prepared by the fermentation of molasses by the mold Aspergillus niger.

Trisodium salt, also referred to as Sodium Citrate, Trisodium citrate or food additive E331, is the tribasic salt of citric acid.
Trisodium salt appears as a white crystalline powder or granular crystals and, given Trisodium salt is a salt, possesses a salty / saline taste with no real detectable odour.

Trisodium salt has the CAS number 6132-04-3 and formula Na3C6H5O7.
Trisodium salt is water-soluble, non-toxic and fully biodegradable.

Trisodium salt is the sodium salt of citric acid.
Trisodium salt is white, crystalline powder or white, granular crystals, slightly deliquescent in moist air, freely soluble in water, practically insoluble in alcohol.

Like Sodium Citrate, Trisodium salt has a sour taste.
From the medical point of view, Trisodium salt is used as alkalinizing agent.

Trisodium salt works by neutralizing excess acid in the blood and urine.
Trisodium salt has been indicated for the treatment of metabolic acidosis.

Trisodium salt is a chemical compound, the sodium salt of Citric Acid.
Trisodium salt is obtained by reacting Sodium Citrate with sodium hydroxide, carbonate, or bicarbonate and then crystallized and dehydrated.

Trisodium salt also occurs naturally in citrus fruits.
Trisodium salt is commonly referred to as ‘Sodium Citrate’, but this term is ambiguous as Trisodium salt can also refer to the sodium or monosodium salt.

Trisodium salt is structured in such a way that a sodium atom is attached to each of the three carboxyl groups present.
Similarly, Monosodium Citrate is a chemical compound with one sodium in the molecule and Disodium Citrate is a chemical compound with two sodium atoms.

Trisodium salt is labeled as a food additive with the symbol E331.

Trisodium salt is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 10 000 to < 100 000 tonnes per annum.
Trisodium salt is used by consumers, in articles, by professional workers (widespread uses), in formulation or re-packing, at industrial sites and in manufacturing.

Trisodium salt is a tribasic salt of citric acid.
Trisodium salt is produced by complete neutralisation of citric acid with high purity sodium hydroxide or carbonate and subsequent crystallisation and dehydration.
The common hydrate form, Trisodium salt dihydrate, is widely used in foods, beverages and various technical applications mainly as buffering, sequestering or emulsifying agent.

Trisodium salt anhydrous is manufactured from Trisodium salt dihydrate.
Water molecules of the dihydrate crystals are removed by a patented process without destroying the original crystal matrix.

The resulting crystals have a porous matrix that can be used as a carrier for inorganic and/or organic substances like perfumes and surfactants.
Due to Trisodium salt low water content Trisodium salt anhydrous does not add water to the formulation.

Trisodium salt has even the excellent ability to take up surplus water from moisture sensitive formulations thus providing better shelf life to the end product.
Therefore, Trisodium salt anhydrous finds Trisodium salt particular uses in water sensitive formulations like instant drinks as well as tablets and powders in pharmaceuticals and detergents.

Trisodium salt anhydrous occurs as white, granular crystals or as white, crystalline powder.
Trisodium salt is freely soluble in water and practically insoluble in ethanol (96 %).

Trisodium salt is a non-toxic, neutral salt with low reactivity.
Trisodium salt is chemically stable if stored at ambient temperatures.
Trisodium salt anhydrous is fully biodegradable and can be disposed of with regular waste or sewage.

Trisodium salt dihydrate, is widely applied in food, beverages and fillers as a buffering, sequestering or an emulsifying agent.
Trisodium salt used as an anticoagulant in blood transfusions, osmotic laxative, functional fluids, solvents cleaning, furnishing care products, laundry dishwashing products and cleaning automobile radiators.

Trisodium salt dihydrate is a tribasic salt of citric acid.
Trisodium salt is produced by complete neutralisation of Trisodium salt with high purity sodium hydroxide or carbonate and subsequent crystallisation.
Trisodium salt dihydrate is widely used in foods, beverages and various technical applications mainly as buffering, sequestering or emulsifying agent.

Trisodium salt dihydrate occurs as white, granular crystals or as white, crystalline powder with a pleasant, salty taste.
Trisodium salt is slightly deliquescent in moist air, freely soluble in water and practically insoluble in ethanol (96 %).

Trisodium salt dihydrate is a non-toxic, neutral salt with low reactivity.
Trisodium salt is chemically stable if stored at ambient temperatures.
Trisodium salt dihydrate is fully biodegradable and can be disposed of with regular waste or sewage.

Trisodium salt in Food:
Trisodium salt is a food additive with the E number E331.
Trisodium salt is used in a variety of processed food and drink primarily as a flavour enhancer and a preservative.
As an emulsifying agent Trisodium salt is also used in cheesemaking to allow cheese to melt without the separation of oils and fats.

Trisodium salt in food buffers pH levels to help regulate acidity in a variety of foods to balance taste and is also able to impart a tart / sour flavour in a wide variety of drink products.

Usage areas of Trisodium salt:
Trisodium salt is often used as a food additive as a flavoring or preservative.
The E number is E331.

Trisodium salt is used as a flavoring agent in certain varieties of club soda.
Trisodium salt is common as an ingredient in Bratwurst and is also commercially available for drinks and beverage mixes, contributing a tart flavor.

Trisodium salt is found in gelatin mix, ice cream, jam, desserts, powdered milk, processed cheeses, sodas and wine.
Trisodium salt can be used as an emulsifier when making cheese.
Trisodium salt allows the cheese to melt without remaining greasy.

Trisodium salt, a conjugate base of a weak acid, can act as a buffering agent or acidity regulator by resisting change in pH.
Trisodium salt is used to control the acidity of some substances, such as gelatin desserts.

Trisodium salt is found in mini milk containers used in coffee machines.
Trisodium salt is a particularly effective substance for removing carbonate scale from boilers without cracking and for cleaning car radiators.

Uses of Trisodium salt:
Trisodium salt has many uses, but is mainly applied in the food industry.
Trisodium salt has similar applications as Citric Acid, so Trisodium salt is usually used as a flavor enhancer, to acidify foods or beverages, or as a preservative.

Trisodium salt is also commonly used in medicine as a drug ingredient, usually for people with urinary tract infections.
Trisodium salt also plays a role as an anticoagulant, which means Trisodium salt inhibits blood clotting.

In addition, Trisodium salt is used in chemistry.
Trisodium salt is a component of buffers and a component of Benedict’s reagent, which is used to detect sugars and aldehydes.
Trisodium salt is also found in cosmetics such as shower gels, shampoos or skin creams, as Trisodium salt gives them the right acidity level and is used as a preservative.

Another application of Trisodium salt is to remove scale from boilers, clean car radiators, and burnt sheet metal or pots.
Trisodium salt is also used in the production of cleaning products, as it softens water, allowing detergents to work more effectively.

Trisodium salt is used in similar applications to citric acid.
These uses include as an acidity regulator in food and drink, as a sequestering agent to prevent limescale inference with soaps and detergents and as an emulsifying agent to aid chemical mixing processes where two separate elements are incapable of mixing (for example oil and water) and helps to keep these mixtures stable once formulated.

Trisodium salt is used in blood collection (anticoagulant), photography, and food production. (sequestering agent, emulsifier, and acidulant)
Permitted for use as an inert ingredient in non-food pesticide products.

Trisodium salt in food industry:

Foods:
Trisodium salt is chiefly used as a food additive, usually for flavor or as a preservative.
Trisodium salt E number is E331.

Trisodium salt is employed as a flavoring agent in certain varieties of club soda.
Trisodium salt is common as an ingredient in bratwurst, and is also used in commercial ready-to-drink beverages and drink mixes, contributing a tart flavor.
Trisodium salt is found in gelatin mix[clarification needed], ice cream, yogurt, jams, sweets, milk powder, processed cheeses, carbonated beverages, and wine[citation needed], amongst others.

As a conjugate base of a weak acid, citrate can perform as a buffering agent or acidity regulator, resisting changes in pH.
Trisodium salt is used to control acidity in some substances, such as gelatin desserts.

Trisodium salt can be found in the milk minicontainers used with coffee machines.
Trisodium salt is the product of antacids, such as Alka-Seltzer, when they are dissolved in water.

The pH of a solution of 5 g/100 ml water at 25 °C is 7.5 – 9.0.
Trisodium salt is added to many commercially packaged dairy products to control the PH impact of the gastrointestinal system of humans, mainly in processed products such as cheese and yogurt.

Trisodium salt can be used to optimize the safety and quality of snacks, cereals, bakery products and potato products such as French fries without affecting the production process.

Trisodium salt is found in carbonated beverages, dairy products, confectionery, prepared foods, canned meats and vegetables, margarine, mustard, sauces, mayonnaise, spices, jams, and much more.
This is not surprising, because Trisodium salt has various properties that are important for the food industry.

Firstly, Trisodium salt is used as an acidity regulator to maintain the proper pH of Trisodium salt.
Trisodium salt is found in sodas, especially those with lemon flavor, energy drinks, desserts or jams.

Trisodium salt is a sequestering agent, which means Trisodium salt is a substance that binds metal ions, called chelates.
Thanks to this, the consumer is protected from the harmful effects of heavy metals in foods.

Trisodium salt is also an emulsifier – Trisodium salt enables the preparation of a uniform solution from two immiscible liquids.
Trisodium salt is useful, for example, in the production of cheese, as Trisodium salt does not become greasy after melting, because Trisodium salt prevents the separation of fats.

Another use of Trisodium salt in the food industry is as a preservative.
Trisodium salt protects the fats in Trisodium salt from oxidation and rancidity.
Trisodium salt also prevents color changes in foods.

Medical uses:
In 1914, the Belgian doctor Albert Hustin and the Argentine physician and researcher Luis Agote successfully used Trisodium salt as an anticoagulant in blood transfusions, with Richard Lewisohn determining Trisodium salt correct concentration in 1915.
Trisodium salt continues to be used today in blood-collection tubes and for the preservation of blood in blood banks.

The citrate ion chelates calcium ions in the blood by forming calcium citrate complexes, disrupting the blood clotting mechanism.
Recently, Trisodium salt has also been used as a locking agent in vascath and haemodialysis lines instead of heparin due to Trisodium salt lower risk of systemic anticoagulation.

In 2003, Ööpik et al. showed the use of Trisodium salt (0.5 g/kg body weight) improved running performance over 5 km by 30 seconds.

Trisodium salt is used to relieve discomfort in urinary-tract infections, such as cystitis, to reduce the acidosis seen in distal renal tubular acidosis, and can also be used as an osmotic laxative.
Trisodium salt is a major component of the WHO oral rehydration solution.

Trisodium salt is used as an antacid, especially prior to anaesthesia, for caesarian section procedures to reduce the risks associated with the aspiration of gastric contents.

Trisodium salt in medicine:
Trisodium salt is not only known as a food additive, but also as an important chemical compound in medicine.
Trisodium salt is used in analytical laboratories where blood tests are performed because Trisodium salt has an anticoagulant effect.

This prevents blood cells from clumping together.
Trisodium salt is then used as a component of solutions for filling hemodialysis catheters.

Trisodium salt lowers the concentration of heparin, which in turn reduces the risks associated with coagulation disorders in patients with kidney disease or blood clotting.
This counteracts side effects during and after dialysis treatment.
This effect is also extremely useful when storing blood or during transfusions.

Trisodium salt is also used as a drug.
Trisodium salt treats kidney stones, gout and reduces the symptoms of metabolic acidosis.

Trisodium salt can also be used as a laxative.
Trisodium salt can be used for hypercalcemia, a condition in which the concentration of calcium in the blood is too high.
Trisodium salt works by increasing the excretion of calcium through the urine.

Consumer Uses:
Trisodium salt is used in the following products: washing & cleaning products, polishes and waxes, air care products, cosmetics and personal care products, water softeners, perfumes and fragrances, water treatment chemicals, coating products, inks and toners, textile treatment products and dyes, biocides (e.g. disinfectants, pest control products), fertilisers, adsorbents, fillers, putties, plasters, modelling clay, laboratory chemicals and photo-chemicals.
Other release to the environment of Trisodium salt is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners), outdoor use, indoor use in long-life materials with low release rate (e.g. flooring, furniture, toys, construction materials, curtains, foot-wear, leather products, paper and cardboard products, electronic equipment), outdoor use in long-life materials with high release rate (e.g. tyres, treated wooden products, treated textile and fabric, brake pads in trucks or cars, sanding of buildings (bridges, facades) or vehicles (ships)), indoor use in long-life materials with high release rate (e.g. release from fabrics, textiles during washing, removal of indoor paints) and outdoor use in long-life materials with low release rate (e.g. metal, wooden and plastic construction and building materials).

Widespread uses by professional workers:
Trisodium salt is used in the following products: laboratory chemicals, washing & cleaning products, air care products, perfumes and fragrances, polishes and waxes, water softeners, water treatment chemicals, biocides (e.g. disinfectants, pest control products), coating products, fillers, putties, plasters, modelling clay, inks and toners, textile treatment products and dyes, fertilisers, photo-chemicals, cosmetics and personal care products and adsorbents.
Trisodium salt is used in the following areas: health services, building & construction work, mining, agriculture, forestry and fishing and formulation of mixtures and/or re-packaging.
Trisodium salt is used for the manufacture of: machinery and vehicles and furniture.

Other release to the environment of Trisodium salt is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners), outdoor use, indoor use in long-life materials with low release rate (e.g. flooring, furniture, toys, construction materials, curtains, foot-wear, leather products, paper and cardboard products, electronic equipment), outdoor use in long-life materials with low release rate (e.g. metal, wooden and plastic construction and building materials), outdoor use in long-life materials with high release rate (e.g. tyres, treated wooden products, treated textile and fabric, brake pads in trucks or cars, sanding of buildings (bridges, facades) or vehicles (ships)), indoor use in long-life materials with high release rate (e.g. release from fabrics, textiles during washing, removal of indoor paints), indoor use in close systems with minimal release (e.g. cooling liquids in refrigerators, oil-based electric heaters) and outdoor use in close systems with minimal release (e.g. hydraulic liquids in automotive suspension, lubricants in motor oil and break fluids).

Uses at industrial sites:
Trisodium salt is used in the following products: pH regulators and water treatment products, washing & cleaning products, polishes and waxes and water treatment chemicals.
Trisodium salt is used in the following areas: mining, health services and building & construction work.
Trisodium salt is used for the manufacture of: machinery and vehicles, textile, leather or fur, metals, fabricated metal products, electrical, electronic and optical equipment and chemicals.

Release to the environment of Trisodium salt can occur from industrial use: in processing aids at industrial sites, of substances in closed systems with minimal release, as processing aid, formulation of mixtures and in the production of articles.
Other release to the environment of Trisodium salt is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners) and outdoor use.

Other Uses:

Food:
Baby Food, Infant Formula
Bakery
Cereals, Snacks
Confectionery
Dairy
Dairy Alternatives
Desserts, Ice Cream
Flavours
Fruit Preparations, Sweet Spreads
Fruits, Vegetables
Meat Alternatives
Meat, Seafood
Plant-based Products
Ready Meals, Instant Food
Sauces, Dressings, Seasonings

Beverages:
Alcoholic Beverages
Carbonated Soft Drinks
Instant Drinks, Syrups
Juice Drinks
Plant-based
RTD Tea and Coffee
Sports and Energy Drinks
Waters

Healthcare:
Clinical Nutrition
Medical Devices
OTC, Food Supplements
Pharmaceutical Products

Personal Care:
Colour Cosmetics
Fragrances
Hair Care
Oral Care
Skin Care
Soap and Bath Products

Cleaners & Detergents:
Dish Washing
Industrial Cleaners
Laundry Care
Surface Care

Industrial Applications:
Adhesives, Sealants
Agrochemicals, Fertilisers
Construction
Fine Chemicals
Inks, Paints, Coatings
Oil Drilling
Paper
Plastics, Polymers
Textile, Leather

Feed & Pet Food:
Feed
Pet Food

Pharma:
Buffering agent
Chelating agent
Mineral source

Industrial Processes with risk of exposure:
Photographic Processing

Applications of Trisodium salt:
Trisodium salt dihydrate, is widely applied in food, beverages and fillers as a buffering, sequestering or an emulsifying agent.
Trisodium salt used as an anticoagulant in blood transfusions, osmotic laxative, functional fluids, solvents cleaning, furnishing care products, laundry dishwashing products and cleaning automobile radiators.

Foods:
Trisodium salt is chiefly used as a food additive, usually for flavor or as a preservative.
Trisodium salt E number is E331.

Trisodium salt is employed as a flavoring agent in certain varieties of club soda.
Trisodium salt is common as an ingredient in bratwurst, and is also used in commercial ready-to-drink beverages and drink mixes, contributing a tart flavor.
Trisodium salt is found in gelatin mix, ice cream, yogurt, jams, sweets, milk powder, processed cheeses, carbonated beverages, and wine,[3] amongst others.

Trisodium salt can be used as an emulsifying stabilizer when making cheese.
Trisodium salt allows the cheese to melt without becoming greasy by stopping the fats from separating.

Buffering:
As a conjugate base of a weak acid, citrate can perform as a buffering agent or acidity regulator, resisting changes in pH.
Trisodium salt is used to control acidity in some substances, such as gelatin desserts.

Trisodium salt can be found in the milk minicontainers used with coffee machines.
Trisodium salt is the product of antacids, such as Alka-Seltzer, when they are dissolved in water.

The pH of a solution of 5 g/100 ml water at 25 °C is 7.5 – 9.0.
Trisodium salt is added to many commercially packaged dairy products to control the pH impact of the gastrointestinal system of humans, mainly in processed products such as cheese and yogurt, although Trisodium salt also has beneficial effects on the physical gel microstructure.

Chemistry:
Trisodium salt is a component in Benedict's qualitative solution, often used in organic analysis to detect the presence of reducing sugars such as glucose.

Medicine:
In 1914, the Belgian doctor Albert Hustin and the Argentine physician and researcher Luis Agote successfully used Trisodium salt as an anticoagulant in blood transfusions, with Richard Lewisohn determining Trisodium salt correct concentration in 1915.
Trisodium salt continues to be used today in blood-collection tubes and for the preservation of blood in blood banks.

The citrate ion chelates calcium ions in the blood by forming calcium citrate complexes, disrupting the blood clotting mechanism.
Recently, Trisodium salt has also been used as a locking agent in vascath and haemodialysis lines instead of heparin due to Trisodium salt lower risk of systemic anticoagulation.

In 2003, Ööpik et al. showed the use of Trisodium salt (0.5 g/kg body weight) improved running performance over 5 km by 30 seconds.

Trisodium salt is used to relieve discomfort in urinary-tract infections, such as cystitis, to reduce the acidosis seen in distal renal tubular acidosis, and can also be used as an osmotic laxative.
Trisodium salt is a major component of the WHO oral rehydration solution.

Trisodium salt is used as an antacid, especially prior to anaesthesia, for caesarian section procedures to reduce the risks associated with the aspiration of gastric contents.

Boiler descaling:
Trisodium salt is a particularly effective agent for removal of carbonate scale from boilers without removing them from operation and for cleaning automobile radiators.

Healthcare:

Effervescent tablets and preparations:
The reaction of citric acid and bicarbonate liberates carbon dioxide, which aids the dissolution of active ingredients and improves palatability.
Effervescent systems are widely used in denture-cleaning products, as well as pain relief and vitamin tablets.

Pharmaceutically active substances — many are supplied as their citrate salt.

pH control:
Citric acid, with sodium or potassium citrate, is an efficient buffering system used in a variety of pharmaceutical and cosmetic applications for improving stability and (where appropriate) enhancing the activity of preservatives.

Flavor:
The sharp, acid taste of citric acid (which is often used to enhance fruit flavors) can help mask the unpleasant, medicinal taste of pharmaceuticals.

Antioxidant:
The citrate ion is a powerful chelating agent for trace metal ions.

Blood anticoagulant:
The citrate ion will chelate calcium, thereby reducing the tendency for blood to clot.

Diuretic – potassium citrate has diuretic properties.
Clinical Nutrition Medical Devices
OTC, Food Supplements Pharmaceutical Products
Color Cosmetics Deodorants
Fragrances Hair Care
Oral Care Skin Care Soap and Bath Products

Cleaners & Detergents:
The major components of cleaning products are surfactants and builders.
Other ingredients are added to provide a variety of functions, e.g., increasing cleaning performance for specific soils/surfaces, ensuring product stability, and supplying a unique identity to a product.

Complex phosphates and Trisodium salt are common sequestering builders.
Builders enhance or maintain the cleaning efficiency of the surfactant.

The primary function of builders is to reduce water hardness.
This is done either by sequestration or chelation (holding hardness minerals in solution); by precipitation (forming an insoluble substance); or by ion exchange (trading electrically charged particles).
Builders can also supply and maintain alkalinity, which assists cleaning, especially of acid soils; help keep removed soil from redepositing during washing, and emulsify oily and greasy soils.

Dish Washing Industrial Cleaners:

Laundry Care Surface Care:

Industrial
Sodium Citrate is employed as an industrial cleaner to clear steam blocks and hot water systems of calcium and rust layers.
As a chemical polish, Sodium Citrate is used to treat aluminum, copper and other metal surfaces.

Sodium Citrate and citrates are used as buffering and complexing agents in electro-plating baths.
The building and textile industries also take advantage of Sodium Citrate’s outstanding chelating ability as well as Trisodium salt non-toxicity.

Examples include set retarding of gypsum plasters and textile finishing.
Further industrial applications of Sodium Citrate and citrates range from desulphurisation of flue gas and oil recovery to the decontamination of radioactive nuclear reactor materials.

Adhesives, Sealants, Agrochemicals, Fertilizers
Construction, Fine Chemicals
Inks, Paints, Coatings, Metal Surface Treatment
Oil Drilling Ore Mining and Refining
Paper, Plastics, Polymers
Textile, Leather

Main Functions of Trisodium salt:
pH regulator
Chelating agent
Buffering agent
Flavour enhancer
Stabiliser
Emulsifying agent

Properties of Trisodium salt:
Trisodium salt is in the form of a white, odorless powder with a slightly salty taste.
Trisodium salt occurs as a hydrate in combination with water.

Trisodium salt is characterized by the fact that Trisodium salt is hygroscopic, so Trisodium salt easily absorbs and combines with water.
Therefore, Trisodium salt should be stored under such conditions that Trisodium salt is protected from moisture.
Although Trisodium salt is a salt of an acid, Trisodium salt has an alkaline pH.

Typical Properties:
Dihydrate
White
Granular crystals or crystalline powder
Typical, practically odourless
Pleasantly salty
Freely soluble in water
Practically insoluble in ethanol (96 %)
Non-toxic
Low reactive
Chemically and microbiologically stable
Fully biodegradable

Action Mechanism of Trisodium salt:
Trisodium salt chelates free calcium ions preventing them from forming a complex with tissue factor and coagulation factor VIIa to promote the activation of coagulation factor X.
This inhibits the extrinsic initiation of the coagulation cascade.

Trisodium salt may also exert an anticoagulant effect via a so far unknown mechanism as restoration of calcium concentration does not fully reverse the effect of citrate.
Trisodium salt is a weak base and so reacts with hydrochloric acid in the stomach to raise the pH.

Trisodium salt Trisodium salt further metabolized to bicarbonate which then acts as a systemic alkalizing agent, raising the pH of the blood and urine.
Trisodium salt also acts as a diuretic and increases the urinary excretion of calcium.

Pharmacology and Biochemistry of Trisodium salt:

MeSH Pharmacological Classification:

Buffers:
A chemical system that functions to control the levels of specific ions in solution.
When the level of hydrogen ion in solution is controlled the system is called a pH buffer.

Food Preservatives:
Substances capable of inhibiting, retarding or arresting the process of fermentation, acidification or other deterioration of foods.

Anticoagulants:
Agents that prevent BLOOD CLOTTING.

Manufacturing Method of Trisodium salt:
Prepare the Trisodium salt buffer by mixing the Trisodium salt, hydrochloric acid, and ultrapure water together in a 2L beaker or conical flask.
Use a magnetic stirrer to ensure that all reagents are properly dissolved.

Adjust to pH 6.01 with the 0.5% (w/v) sodium hydroxide and 0.5% (v/v) hydrochloric acid solutions.
Add this solution to the pressure cooker.

Place the pressure cooker on the hotplate and turn Trisodium salt on to full power.
Do not secure the lid of the pressure cooker at this point; simply rest Trisodium salt on top.

While waiting for the pressure cooker to come to the boil, dewax and rehydrate the paraffin sections by placing them in three changes of xylene for 3 min each, followed by three changes of IMS or methanol for 3 min each, followed by cold running tap water.
Keep them in the tap water until the pressure cooker comes to the boil.

Once the pressure cooker is boiling, transfer the slides from the tap water to the pressure cooker.
Take care with the hot solution and steam—use forceps and gloves. Secure the pressure cooker lid following the manufacturer’s instructions.

Once the cooker has reached full pressure (see manufacturer’s instructions), time for 3 min.

When 3 min has elapsed, turn off the hotplate and place the pressure cooker in an empty sink.
Activate the pressure release valve (see the manufacturer’s instructions) and run cold water over the cooker.

Once depressurized, open the lid and run cold water into the cooker for 10 min.
Take care with the hot solution and steam.

Continue with an appropriate immunochemical staining protocol.

Handling and storage of Trisodium salt:
Handling Ensure adequate ventilation.
Avoid contact with skin, eyes or clothing.

Avoid ingestionandinhalation.
Avoid dust formation.
Storage Keep containers tightly closed in a dry, cool and well-ventilated place.

Stability and reactivity of Trisodium salt:

Reactive:
Hazard None known, based on information available.

Stability:
Stable under normal conditions.
Conditions to Avoid Incompatible products.

Excess heat.
Avoid dust formation.

Incompatible Materials:
Strong oxidizing agents, Strong reducing agents, Acids, Bases

Hazardous Decomposition Products:
Carbon monoxide (CO), Carbon dioxide (CO2), Sodium oxides

Hazardous Polymerization:
Hazardous polymerization does not occur. Hazardous Reactions None under normal processing.

First-aid measures of Trisodium salt:

Eye Contact:
Rinse immediately with plenty of water, also under the eyelids, for at least 15 minutes.
Get medical attention if symptoms occur.

Skin Contact:
Wash off immediately with plenty of water for at least 15 minutes.
If skin irritation persists, call a physician.

Inhalation:
Remove to fresh air.
Get medical attention immediately if symptoms occur.
If not breathing, give artificial respiration.

Ingestion:
Do NOT induce vomiting.
Get medical attention immediately if symptoms occur.

Most important symptoms and effects:
No information available.

Notes to Physician:
Treat symptomatically

Fire-fighting measures of Trisodium salt:

Suitable Extinguishing Media:
Water spray, carbon dioxide (CO2), dry chemical, alcohol-resistant foam.

Autoignition Temperature:
500 °C / 932 °F

Accidental release measures of Trisodium salt:
Personal Precautions Ensure adequate ventilation.
Avoid dust formation.

Avoid contact with skin andeyes.
Usepersonal protective equipment as required.
Environmental Precautions No special environmental precautions required.

Methods for Containment and Clean Up:
Sweep up and shovel into suitable containers for disposal.
Avoid dust formation.

Identifiers of Trisodium salt:
CAS Number:
68-04-2
6132-04-3 (dihydrate)
6858-44-2 (pentahydrate)

ChEMBL: ChEMBL1355
ChemSpider: 5989
ECHA InfoCard: 100.000.614
E number: E331iii (antioxidants, ...)
PubChem CID: 6224
RTECS number: GE8300000

UNII:
RS7A450LGA
B22547B95K (dihydrate)

CompTox Dashboard (EPA): DTXSID2026363
InChI: InChI=1S/C6H8O7.3Na/c7-3(8)1-6(13,5(11)12)2-4(9)10;;;/h13H,1-2H2,(H,7,8)(H,9,10)(H,11,12);;;/q;3*+1/p-3
Key: HRXKRNGNAMMEHJ-UHFFFAOYSA-K
InChI=1/C6H8O7.3Na/c7-3(8)1-6(13,5(11)12)2-4(9)10;;;/h13H,1-2H2,(H,7,8)(H,9,10)(H,11,12);;;/q;3*+1/p-3
Key: HRXKRNGNAMMEHJ-DFZHHIFOAL
SMILES: C(C(=O)[O-])C(CC(=O)[O-])(C(=O)[O-])O.[Na+].[Na+].[Na+]

CAS number: 6132-04-3
EC number: 200-675-3
Grade: Ph Eur,BP,JP,USP,E 331
Hill Formula: C₆H₅Na₃O₇ * 2 H₂O
Molar Mass: 294.10 g/mol
HS Code: 2918 15 00

Product Code: NA2043
CAS Number: 6132-04-3
Assay (purity): USP
Purity method: by titration
Molecular weight: 294.10
Form: solid
Appearance: white powder
Melting point: 300C
Boiling point: 309.6C
Titration: 99.0-101.0%
Titration type: with HCLO4
Molecular formula: Na3C6H5O7 · 2H2O
Linear formula: HOC(COONa)(CH2COONa)2 · 2H2O

Properties of Trisodium salt:
Chemical formula: Na3C6H5O7
Molar mass: 258.06 g/mol (anhydrous), 294.10 g/mol (dihydrate)
Appearance: White crystalline powder
Density: 1.7 g/cm3
Melting point: > 300 °C (572 °F; 573 K) (hydrates lose water ca. 150 °C)
Boiling point: Decomposes
Solubility in water: Pentahydrate form: 92 g/100 g H2O (25 °C)

Melting Point: 300°C (anhydrous substance)
pH value: 7.5 - 9.0 (50 g/l, H₂O, 25°C)
Bulk density: 600 kg/m3
Solubility: 720 g/l

Molecular Weight: 294.10 g/mol
Hydrogen Bond Donor Count: 3
Hydrogen Bond Acceptor Count: 9
Rotatable Bond Count: 2
Exact Mass: 293.99396471 g/mol
Monoisotopic Mass: 293.99396471 g/mol
Topological Polar Surface Area: 143Ų
Heavy Atom Count: 18
Complexity: 211
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 6
Compound Is Canonicalized: Yes

Specifications of Trisodium salt:
Assay (Perchloric acid titration, calc. on anhydrous substance (Ph Eur)): 99.0 - 101.0 %
Assay (Perchloric acid titration, previously dried substance) (JP/USP): 99.0 - 100.5 %
Identity (Na): passes test
Identity (Citrate): passes test
Identity (reaction upon ignition): passes test
Appearance: white to almost white crystals
Appearance of solution (100 g/l, CO₂-free water): clear and colorless
Acidity or alkalinity: passes test
pH (50 g/l CO₂-free water): 7.5 - 8.5
Chloride (Cl): ≤ 50 ppm
Sulfate (SO₄): ≤ 150 ppm
Heavy metals (as Pb): ≤ 5 ppm
Al (Aluminium): ≤ 5 ppm
As (Arsenic): ≤ 1 ppm
Hg (Mercury): ≤ 1 ppm
Pb (Lead): ≤ 1 ppm
Oxalate (as C₂H₂O₄): ≤ 100 ppm
Tartrate (C₄H₄O₆): passes test
Residual solvents (ICH (Q3C)): excluded by manufacturing process
Readily carbonisable substance: passes test
Water (according to Karl Fischer): 11.0 - 13.0 %
Loss on drying (180 °C, 18 h): 10.0 - 13.0 %

Related compounds of Trisodium salt:
Monosodium citrate
Disodium citrate
Calcium citrate
Citric acid

Names of Trisodium salt:

IUPAC names:
1,2,3-propanetricarboylic acid, 2-hydroxy- trisodium salt, dihydrate
2-Hydroxy-1,2,3-propanetricarboxylic acid, trisodium sal
2-Hydroxy-1,2,3-propanetrioïc acid, trisodium salt
Ascorbato di sodio trisodico anidro E331
Citric acid trisodium salt, Sodium citrate tribasic, Sodium citrate
sodium 2-hydroxypropane-1,2,3-tricarboxylate
SODIUM CITRATE
Sodium citrate
sodium citrate
Sodium citrate
sodium citrate dihydrate
Sodium Citrate dihydrate
Sodium Citrate- OR 10
Tri sodium citrate
Tri Sodium Citrate
Trinatiumcitrat dihydrat
Trinatrium-2-hydroxypropan-1,2,3-tricarboxylat
Trisodium 2-hydroxypropane-1,2,3-
Trisodium 2-hydroxypropane-1,2,3- tricarboxylate
Trisodium 2-hydroxypropane-1,2,3-tricarboxylate
trisodium 2-hydroxypropane-1,2,3-tricarboxylate
trisodium 2-hydroxypropane-1,2,3-tricarboxylate dihydrate
Trisodium 2-hydroxypropane-1,2,3-tricarboxylateTrisodium citrate
Trisodium 3-hydroxy-3- carboxylate-1,5-pentanedicaroxylate
TRISODIUM CITRATE
Trisodium Citrate
Trisodium citrate
trisodium citrate
Trisodium Citrate
Trisodium citrate
trisodium citrate
trisodium citrate (dihydrate)
trisodium citrate 2-hidrate
Trisodium Citrate Dihydrate
trisodium citrate dihydrate
Trisodium citrate, Trisodium 2-hydroxypropane-1,2,3-tricarboxylate
Trisodium citrate; Trisodium 2-hydroxypropane-1,2,3-tricarboxylate
trisodium2-hydroxypropane-1,2,3-tricarboxylate
trisodium;2-hydroxypropane-1,2,3-tricarboxylate
trisodium;2-hydroxypropane-1,2,3-tricarboxylate;dihydrate

Preferred IUPAC name:
Trisodium 2-hydroxypropane-1,2,3-tricarboxylate

Regulatory process names:
Sodium citrate anhydrous
Trisodium citrate
trisodium citrate

Trade names:
Citrate de trisodium, dihydrate
Citrato de trisodio, dihidrato
Sodio citrato
SODIUM CITRATE
Sodium Citrate
SODIUM CITRATE DIHYDRATE
Tri-Sodium Citrate Dihydrate
Trinatriumcitraatdihydraat
Trinatriumcitrat-Dihydrat
Trisodio citrato diidrato
Trisodium citrate
trisodium citrate
TRISODIUM CITRATE DIHYDRATE
Trisodium citrate dihydrate
TRISODIUM CITRATR

Other names:
Sodium citrate
Trisodium citrate
Citrosodine
Citric acid, trisodium salt
E331

Other identifiers:
1000844-65-4
1648840-06-5
183748-56-3
2095548-08-4
6132-04-3
68-04-2
8055-55-8
856354-90-0

Synonyms of Trisodium salt:
Trisodium citrate dihydrate
Sodium citrate dihydrate
6132-04-3
Sodium citrate tribasic dihydrate
Sodium citrate hydrate
1,2,3-Propanetricarboxylic acid, 2-hydroxy-, trisodium salt, dihydrate
Citric acid trisodium salt dihydrate
Sodium citrate hydrous
SODIUM CITRATE, DIHYDRATE
trisodium 2-hydroxypropane-1,2,3-tricarboxylate dihydrate
MFCD00150031
B22547B95K
trisodium;2-hydroxypropane-1,2,3-tricarboxylate;dihydrate
DTXSID1049437
Natrum citricum
Citric acid, trisodium salt, dihydrate
Citronensaeure,Trinatrium-Salz-Dihydrat
N-1560
Natrii citras, dehydrate
SODIUM CITRATE HYDROUS (II)
SODIUM CITRATE HYDROUS [II]
trisodium 2-hydroxypropane-1,2,3-tricarboxylate--water (1/2)
Trisodium citrate dihydrate;Citric acid trisodium salt dihydrate
2-hydroxy-1,2,3-propanetricarboxylic acid trisodium salt dihydrate
MFCD00130806
SODIUM CITRATE (EP MONOGRAPH)
SODIUM CITRATE [EP MONOGRAPH]
tri-sodium citrate dihydrate
TRISODIUM CITRATE DIHYDRATE (II)
TRISODIUM CITRATE DIHYDRATE [II]
UNII-B22547B95K
TRISODIUM CITRATE DIHYDRATE (USP MONOGRAPH)
TRISODIUM CITRATE DIHYDRATE [USP MONOGRAPH]
sodium 2-hydroxypropane-1,2,3-tricarboxylate dihydrate
Sodiumcitrate
Tricitrasol
Tricitrasol (TN)
Sodium citrate; Trisodium 2-hydroxypropane-1,2,3-tricarboxylate dihydrate; Sodium Citrate Dihydrate
Sodium citrate (TN)
1,2,3-Propanetricarboxylic acid, 2-hydroxy-, sodium salt, hydrate (1:3:2)
D05KTE
Sodium citrate [USP:JAN]
Sodiumcitratetribasicdihydrate
SODIUM CITRATE [FHFI]
DTXCID0029397
Sodium citrate hydrate (JP17)
CHEBI:32142
Trisodium citrate dihydrate, ACS
NLJMYIDDQXHKNR-UHFFFAOYSA-K
SODIUM CITRATE HYDRATE [JAN]
SODIUM CITRATE DIHYDRATE [MI]
AKOS025293920
Sodium citrate dihydrate, >=99%, FG
SODIUM CITRATE DIHYDRATE [VANDF]
BP-31019
SODIUM CITRATE DIHYDRATE [WHO-DD]
Sodium citrate tribasic dihydrate, >=98%
Sodium citrate dihydrate, ACS reagent grade
SODIUM CITRATE, DIHYDRATE [WHO-IP]
D01781
F82065
Sodium citrate tribasic dihydrate, AR, >=99%
Sodium citrate tribasic dihydrate, LR, >=99%
Citric acid trisodium salt dihydrate ACS reagent
NATRII CITRAS, DEHYDRATE [WHO-IP LATIN]
A833161
A835986
Q22075862
Sodium citrate dihydrate Biochemical grade, Fine Granular
Sodium citrate tribasic dihydrate, USP, 99.0-100.5%
Sodium Citrate Tribasic Dihydrate (Molecular Biology Grade)
Sodium citrate tribasic dihydrate, ACS reagent, >=99.0%
trisodium 2-oxidanylpropane-1,2,3-tricarboxylate dihydrate
Citric acid trisodium salt dihydrateTrisodium citrate dihydrate
Sodium citrate tribasic dihydrate, BioUltra, >=99.0% (NT)
Sodium citrate tribasic dihydrate, insect cell culture tested
Sodium citrate tribasic dihydrate, JIS special grade, >=99.0%
Sodium citrate tribasic dihydrate, p.a., ACS reagent, 99.0%
Sodium citrate tribasic dihydrate, purum p.a., >=99.0% (NT)
Sodium citrate tribasic dihydrate, SAJ first grade, >=99.0%
Sodium citrate tribasic dihydrate, tested according to Ph.Eur.
Trisodium citrate dihydrate, meets USP testing specifications
Sodium citrate tribasic dihydrate, BioXtra, >=99.0% (titration)
Sodium citrate tribasic dihydrate, for molecular biology, >=99%
Sodium citrate tribasic dihydrate, Vetec(TM) reagent grade, 98%
Sodium citrate, United States Pharmacopeia (USP) Reference Standard
1,2,3-Propanetricarboxylic acid, 2-hydroxy-, sodium salt, dihydrate
2-Hydroxy-1,2,3-propanetricarboxylic acid, trisodium salt, dihydrate
Sodium citrate tribasic dihydrate, p.a., ACS reagent, reag. ISO, 99-101%
Sodium citrate tribasic dihydrate, BioUltra, for molecular biology, >=99.5% (NT)
Sodium citrate tribasic dihydrate, puriss. p.a., ACS reagent, >=99.0% (NT)
Sodium citrate tribasic dihydrate, suitable for amino acid analysis, >=99.0%
Sodium Citrate, Pharmaceutical Secondary Standard; Certified Reference Material
Sodium citrate tribasic dihydrate, puriss. p.a., ACS reagent, reag. ISO, reag. Ph. Eur., >=99.5%
Sodium citrate tribasic dihydrate, suitable for amino acid analysis, >=98% (titration), powder
Trisodium citrate [ACD/IUPAC Name] [Wiki]
1,2,3-Propanetricarboxylic acid, 2-hydroxy-, sodium salt (1:3) [ACD/Index Name]
200-675-3 [EINECS]
68-04-2 [RN]
994-36-5 [RN]
Citrate de trisodium [French] [ACD/IUPAC Name]
Citric Acid Trisodium Salt
MFCD00012462 [MDL number]
RS7A450LGA
Sodium 2-hydroxy-1,2,3-propanetricarboxylate
Sodium Citrate [JAN] [USAN] [Wiki]
Sodium citrate anhydrous
Trinatriumcitrat [German] [ACD/IUPAC Name]
Tris sodium citrate
trisodium 2-hydroxypropane-1,2,3-tricarboxylate
1,2,3-Propanetricarboxylic acid, 2-hydroxy-, trisodium salt
114456-61-0 [RN]
205-623-3 [EINECS]
2-Hydroxy-1,2,3-propanenetricarboxylic acid trisodium salt
2-Hydroxy-1,2,3-propanetricarboxylic acid trisodium salt
2-Hydroxy-1,2,3-propanetricarboxylic acid, trisodium salt
Citnatin
Citrate Concentratedmissing
citrate sodium
citrate trisodium
Citratemissing
Citreme
Citric acid sodium salt anhydrous
Citric acid trisodium salt, anhydrous
Citric acid, trisodium salt
Citrosodina
Citrosodine
Citrosodna
Isolyte E
Natrocitral
Sodium 2-hydroxypropane-1,2,3-tricarboxylate
Sodium citrate (USP)
Sodium citrate buffer
SODIUM CITRATE TRIBASIC
Sodium citrate, anhydrous
Synthesis on demand
tri-sodium citrate
Trisodium citrate anhydrous
tris-sodium citrate
UNII-RS7A450LGA

TRISODIUM SALT OF NTA ,HYDRATE
Trisodium Orthophosphate; Phosphoric acid, trisodium, 12-hydrate; Sodium Phosphate Tribasic Dodecahydrate; Trisodium phosphate, dodecahydrate; TSP dodecahydrate; Tertiary Sodium phosphate cas no: 7601-54-9
TRISODIUMPHOSPHATE 
cas no : 26658-19-5, Anhydrosorbitol tristearate; Sorbitan tristearate; Sorbitan, trioctadecanoate; Sorbitani tristearas; Triestearato de sorbitano; Tristearate de sorbitan; Ses fonctions (INCI) Agent émulsifiant : Favorise la formation de mélanges intimes entre des liquides non miscibles en modifiant la tension interfaciale (eau et huile); Nom INCI : SORBITAN TRIOLEATE Nom chimique : Anhydro-D-glucitol trioleate; N° EINECS/ELINCS : 247-569-3
TRISTÉARATE DE SORBITAN
Polyethylene glycol p-(1,1,3,3-tetramethylbutyl)-phenyl ether; Octyl phenol ethoxylate; Polyoxyethylene octyl phenyl ether; 4-Octylphenol polyethoxylate; Mono 30; TX-100; t-Octylphenoxypolyethoxyethanol; Octoxynol-9 cas no: 9002-93-1
TRISTYRYLPHENOL 20 EO

Tristyrylphenol 20 EO

TSP 20

Tri-styryl phenol, 20 EO



Tristyrylphenol 20 EO is a Nonionic dispersing and wetting agent for organic pigments in dispersions, preparations, and coatings.

Tristyrylphenol 20 EO is a high-performing non-ionic emulsifier that delivers spontaneous emulsification with excellent long-term stability.

Tristyrylphenol 20 EO is generally combined with anionic emulsifiers such as calcium dodecylbenzene sulfonates and di-alkyl sulfosuccinates in Emulsifiable Concentrate (EC), Emulsion in Water (EW), Micro-Emulsion (ME) and Suspo-Emulsion (SE) emulsified systems.

A higher degree of Tristyrylphenol ethoxylates can also be used in dispersed systems, particularly SC formulations.

Composition
Tristyrylphenol-Polyglycolether with approximately 20 moles of ethylene oxide

tri-styryl phenol ethoxylate

Chemical characterization
Tristyryl phenol-polyethylene glycol ether

Synonym: ENVIOMET EM 2020; MAKON TSP-20; Emulsogen TS 200 Poly(oxy-1,2-ethanediyl), α-(2,4,6-tris(1-phenylethyl)phenyl)-.omega.-hydroxy-; Tristyrenated Phenol Ethoxylate 20; Tristyrylphenol Ethoxylate; Ethoxylated Tristyrylphenol

CAS number: 70559-25-0

EC / List no.: 615-124-6
CAS no.: 70559-25-0

Product properties *)

Active substance content: about 100 %

Ionicity: nonionic

Appearance
at 20 °C: yellowish paste
at 40 °C: yellowish liquid

pH value (DIN EN 1262), 10 % in water: 6.0 – 8.0

Solubility at 25 °C: soluble in water

Density at 50 °C: approx. 1.1 g/cm³

Flashpoint (DIN/ISO 2592): > 200 °C

Biocides: free of any additional biocide


Use
Tristyrylphenol 20 EO has an HLB value of about 14 and is used for aqueous pigment dispersions, preparations, paints, and coatings.

Use in pigment preparations:
Tristyrylphenol 20 EO is suitable for organic pigments and carbon black to produce stable, free-flowing pigment preparations with high solid contents.

Dosage: 15 – 30 % based on pigments


Use in paints and coatings:
Tristyrylphenol 20 EO improves the compatibility of pigments and minerals with polymers and binders.

Tristyrylphenol 20 EO prevents the skinning of emulsion polymers in paints and improves the shelf life and stability of emulsion paints.

Dosage: 0,3 – 1,0 % based on the paint formulation


Use in Crop Protection:
Tristyrylphenol 20 EO is also an emulsifier for the formulation of plant protection products and could be used to achieve the following crop protection formulation types:
Emulsifiable concentrate [ EC ]
Micro-emulsion [ ME ]




OTHER PRODUCTS OF ATAMAN CHEMICALS THAT MIGHT BE OF INTEREST:


Tri-styryl phenol, 14 EO


Tri-styryl phenol, 16 EO


Tri-styryl phenol, 30 EO


Tri-styryl phenol, 40 EO


Tri-styryl phenol, 54 EO






























TRISTYRYLPHENOL ETHOXYLATE
Tristyrylphenol Ethoxylate has good emulsification, decontamination and moisturizing ability.
Tristyrylphenol Ethoxylate is an important hydrophilic group of compound agrochemical emulsifiers.
Tristyrylphenol Ethoxylate is soluble in water and many kinds of organic solvents.


CAS Number: 99734-09-5
Molecular Formula: C30H24O.(C2H4O)n


Tristyrylphenol Ethoxylate, also known as TSPE or Triton X series, is a class of nonionic surfactants widely employed in various industries due to their exceptional surface-active properties.
Tristyrylphenol Ethoxylate is a non-ionic surface active agent used as a dispersing and wetting agent in the paint and varnish industry.


Tristyrylphenol Ethoxylate consists of a tristyrylphenol core attached to ethylene oxide (EO) chains, resulting in a range of products with varying ethoxylation degrees.
The ethoxylation process imparts enhanced hydrophilicity and versatility to Tristyrylphenol Ethoxylate, making them ideal for multiple applications.


Tristyrylphenol Ethoxylate has the form of a 90% clear aqueous solution, colourless to lightly yellow.
The primary application of Tristyrylphenol Ethoxylate is industrial manufacturing of water-dilutable pigment concentrates.
Tristyrylphenol Ethoxylate is high performing non-ionic emulsifiers that deliver spontaneous emulsification with excellent long-term stability.


Tristyrylphenol Ethoxylate is light yellow liquid or white cream.
Tristyrylphenol Ethoxylate becomes solid when the temperature is low.
Tristyrylphenol Ethoxylate is soluble in water and many kinds of organic solvents.


Tristyrylphenol Ethoxylate has good emulsification, decontamination and moisturizing capacity.
And Tristyrylphenol Ethoxylate is an important hydrophilic group for compound agrochemical emulsifier.



USES and APPLICATIONS of TRISTYRYLPHENOL ETHOXYLATE:
Applications of Tristyrylphenol Ethoxylate: pigment concentrates, environmentally friendly and VOC-free paint products.
Tristyrylphenol Ethoxylate is a non-ionic surfactant widely applied in agrochemicals.
Tristyrylphenol Ethoxylate CAS 99734-09-5 finds utility in diverse industries, including detergency, textiles, agrochemicals, paints and coatings, and personal care products.


Tristyrylphenol Ethoxylate's ability to modify surface tension, wetting properties, and emulsification characteristics makes them indispensable in many formulations.
Due to the presence of so called anchoring groups, Tristyrylphenol Ethoxylate shows a strong affinity to organic pigments and carbon black, making it especially recommendable for the manufacturing of products based on such pigments.


Tristyrylphenol Ethoxylate is high performing non-ionic emulsifiers that deliver spontaneous emulsification with excellent long-term stability.
Tristyrylphenol Ethoxylate is generally combined with anionic emulsifiers.
Higher degree ethoxylates can also be used in dispersed systems, particularly SC formulations.


-Detergency Industry:
In the detergency industry, Tristyrylphenol Ethoxylate is utilized as the surfactant in laundry detergents, dishwashing liquids, and other cleaning formulations.
Tristyrylphenol Ethoxylate exhibits excellent wetting and emulsifying properties, enabling efficient removal of dirt, grease, and stains from various surfaces.
Furthermore, Tristyrylphenol Ethoxylate's compatibility with enzymes and other detergent additives makes them valuable components in modern detergent formulations.


-Textile Industry:
Tristyrylphenol Ethoxylate is extensively employed in the textile industry for various purposes.
Tristyrylphenol Ethoxylate aids in wetting and penetrating textile fibers, facilitating even dyeing and printing.
Tristyrylphenol Ethoxylate also enhances the dispersion of dyes and pigments, ensuring vibrant and long-lasting coloration.
Additionally, Tristyrylphenol Ethoxylate improves the wash fastness of dyes, contributing to the overall quality of textile products.


-Agrochemicals:
In the agricultural sector, Tristyrylphenol Ethoxylate is utilized in the formulation of agrochemicals such as pesticides and herbicides. Tristyrylphenol Ethoxylate assists in the dispersion of active ingredients, ensuring efficient coverage and absorption on plant surfaces.
The excellent emulsification properties of Tristyrylphenol Ethoxylate enable the creation of stable and homogeneous formulations, enhancing the effectiveness of agrochemical products.


-Paints and Coatings:
Tristyrylphenol Ethoxylate finds extensive applications in the paints and coatings industry.
Tristyrylphenol Ethoxylate is used as emulsifiers, dispersants, and wetting agents in the formulation of water-based paints and coatings.
Tristyrylphenol Ethoxylate assists in the stabilization of pigment dispersions, preventing settling and flocculation.
Moreover, Tristyrylphenol Ethoxylate contributes to the film-forming properties of coatings, ensuring smooth application and improved durability.


-Personal Care Products:
Tristyrylphenol Ethoxylate is widely employed in the formulation of personal care products such as shampoos, body washes, and facial cleansers.
Tristyrylphenol Ethoxylate functions as an effective foaming agent and emulsifier, creating a luxurious lather and enhancing the sensory experience during product use.
Tristyrylphenol Ethoxylate also contributes to the stability and homogeneity of cosmetic formulations, ensuring consistent product quality.



ADVANTAGES OF TRISTYRYLPHENOL ETHOXYLATE:
*excellent dispersing properties for organic pigments and carbon black,
*provides superior stability of water-dilutable pigment concentrates,
*prevents pigment sedimentation,
*significantly reduces pigment concentrate viscosity,
*improves concentrate tinctorial strength,
*provides excellent colour stability,
*provides very good pigment concentrate compatibility with commonly used water-dilutable paints,
*VOC-free,
*does not contain alkylphenol ethoxylated.



FUNCTIONS OF TRISTYRYLPHENOL ETHOXYLATE:
*Emulsifier
*Latex Frothing Agent
*Adjuvant
*Wetting Agents



PROPERTIES AND USES OF TRISTYRYLPHENOL ETHOXYLATE:
1. Tristyrylphenol Ethoxylate is light yellow liquid or white cream.
Tristyrylphenol Ethoxylate becomes solid when the temperature is low.
2. Tristyrylphenol Ethoxylate is soluble in water and many kinds of organic solvents.
3. Tristyrylphenol Ethoxylate has good emulsification, decontamination and moisturizing capacity.
And Tristyrylphenol Ethoxylate is an important hydrophilic group for compound agrochemical emulsifier.



PACKING AND TRANSPORT OF TRISTYRYLPHENOL ETHOXYLATE:
Tristyrylphenol Ethoxylate is flame-resisting and nontoxic which can be shipped as an ordinary chemical product.
As per specific customer needs(available in bulk & small volume), Tristyrylphenol Ethoxylate can be made available with customized packing.



PHYSICAL and CHEMICAL PROPERTIES of TRISTYRYLPHENOL ETHOXYLATE:
Acid Value: 0.6
Cloud Point, °C: 67
Density at 25°C, g/ml: 1.11
Flash Point, °C: >94
Form at 25°C: Liquid
HLB: 13
Hydroxyl Value: 49
Moles of EO: 16
Pour Point, °C: 19
Solids, %: 100
Viscosity at 25°C, cps: 920
Appearance: Light yellow liquid or paste
Water: 0.5% max
Cloud point (1%, water solution): 53.0-57.0°C
pH (1%, water solution): 5.0-7.0
Color (Gardener): 5 max




FIRST AID MEASURES of TRISTYRYLPHENOL ETHOXYLATE:
-Description of first-aid measures:
*General advice:
Consult a physician.
Show this material safety data sheet to the doctor in attendance.
*If inhaled:
If breathed in, move person into fresh air.
Consult a physician.
*In case of skin contact:
Wash off with soap and plenty of water.
Consult a physician.
*In case of eye contact:
Flush eyes with water as a precaution.
*If swallowed
Do NOT induce vomiting.
Rinse mouth with water.
Consult a physician.
-Indication of any immediate medical attention and special treatment needed:
No data available



ACCIDENTAL RELEASE MEASURES of TRISTYRYLPHENOL ETHOXYLATE:
-Environmental precautions:
Prevent further leakage or spillage if safe to do so.
Do not let product enter drains.
Discharge into the environment must be avoided.
-Methods and materials for containment and cleaning up:
Contain spillage, and then collect with non-combustible absorbent material.



FIRE FIGHTING MEASURES of TRISTYRYLPHENOL ETHOXYLATE:
-Extinguishing media:
*Suitable extinguishing media:
Dry powder
Dry sand
*Unsuitable extinguishing media:
Do NOT use water jet.
-Further information:
Use water spray to cool unopened containers.



EXPOSURE CONTROLS/PERSONAL PROTECTION of TRISTYRYLPHENOL ETHOXYLATE:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Face shield and safety glasses
*Skin protection:
Handle with gloves.
Wash and dry hands.
Full contact:
Material: Nitrile rubber
Minimum layer thickness: 0,4 mm
Break through time: 480 min
Splash contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 30 min
*Body Protection:
Complete suit protecting against chemicals
-Control of environmental exposure:
Prevent further leakage or spillage if safe to do so.
Do not let product enter drains.
Discharge into the environment must be avoided.



HANDLING and STORAGE of TRISTYRYLPHENOL ETHOXYLATE:
-Precautions for safe handling:
*Advice on safe handling:
No smoking.
Take measures to prevent the build up of electrostatic charge.
*Hygiene measures:
Handle in accordance with good industrial hygiene and safety practice.
Wash hands before breaks and at the end of workday.
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Keep container tightly closed in a dry and well-ventilated place.
Containers which are opened must be carefully resealed and kept upright to prevent leakage.
Store in cool place.



STABILITY and REACTIVITY of TRISTYRYLPHENOL ETHOXYLATE:
-Reactivity:
No data available
-Chemical stability:
Stable under recommended storage conditions.
-Possibility of hazardous reactions:
No data available
-Incompatible materials:
No data available



SYNONYMS:
Polyethylene glycol mono(tristyrylphenyl)ether
Ethoxylated polyarylphenol
Poly(oxy-1, 2-ethanediyl)
alpha-[tris(1-phenylethyl)phenyl]- omega -hydroxy-
Poly(oxy-1, 2-ethanediyl)
.alpha.-[tris(1-phenylethyl)phenyl]-.omega.-hydroxy-
Ethoxylatedtristyrylphenol
Poly(oxy-1, 2-ethanediyl)
alpha-(tris(1-phenylethyl)phenyl)-omega-hydroxy-
Poly(oxy-1, 2-ethanediyl)
α-[tris(1-phenylethyl)phenyl]-ω-hydroxy-
Poly(oxy-1, 2-ethanediyl)
.alpha.-[tris(2-phenylethenyl)phenyl]-.omega.-hydroxy-
α-[Tris(1-phenylethyl)phenyl]-ω-hydroxypoly(oxy-2, 1-ethanediyl)
α-[Tris(1-phenylethyl)phenyl]-ω-hydroxy-poly(oxy-1,2-ethanediyl)
Poly(oxy-1,2-ethanediyl)
alpha.-tris(1-phenylethyl)phenyl-.omega.-hydroxy-
tristyryphanols(x mol EO)
Ethoxylated polyarylphenol
Ethoxylated polyarylphenol
Tristyrylphenol ethoxylates
Tristyryl phenol ethoxylated
Polyethylene glycol mono(tristyrylphenyl)ether
POLYETHYLENE GLYCOL MONO(TRISTYRYLPHENYL)ETHER
Polyethylene Glycol Mono(Tristyrylphenyl)Ethers
Poly(oxy-1,2-ethanediyl)
α-[tris(1-phenylethyl) phenyl]-ω-hydroxy-
Poly(oxy-1,2-ethanediyl)
.alpha.-tris(1-phenylethyl)phenyl-.omega.-hydroxy-
Tristyrylphenol Ethoxylates
Ethoxylated Polyarylphenol
Polyethylene Glycol Mono(Tristyrylphenyl)Ethers
polyethylene glycol mono(tristyrylphenyl)ether
tristyrylphenol ethoxylates
poly(oxy-1,2-ethanediyl)
α-[tris(1-phenylethyl) phenyl]-ω-hydroxy-
ethoxylated polyarylphenol
tristyryphanols(x mol eo)
polyethylene glycol mono(tristyrylphenyl)ethers
poly(oxy-1,2-ethanediyl)
.alpha.-tris(1-phenylethyl)phenyl-.omega.-hydroxy-




TRITON CF-10 (90%)
Especially used for purification in membrane research TRITON CF-10 (90%) is a water soluble, non-ionic surfactant.
TRITON CF-10 (90%) exhibits a strong hydrogen bonding with water molecule in temperature dependent manner.
TRITON CF-10 (90%) has a wide application area such as in isolation and solubilization of protein, DNA extraction and emulsification.

CAS: 9036-19-5
MF: C18H30O3
MW: 294.43
EINECS: 999-999-2

Widely used non-ionic surfactant for recovery of membrane components under mild non-denaturing conditions.
1. TRITON CF-10 (90%) is easily soluble in water, resistant to acid, alkali, salt, and hard water.
TRITON CF-10 (90%) has good emulsification, leveling, wetting, diffusion, and cleaning properties.
TRITON CF-10 (90%) can be mixed with various surfactants and dye primers;
2. Used as leveling agent, diffuser, leather, wool degreasing agent, crude oil, fuel oil emulsifier, oil extraction acidification penetrating agent, styrene butadiene latex, emulsion polymerization emulsifier, glass fiber textile, cosmetics as emulsification, washing, penetration, wetting agent.

TRITON CF-10 (90%) Chemical Properties
Melting point: 0.05°C
Boiling point: 586.77°C (rough estimate)
Density: 1.06 g/mL at 20 °C
Vapor pressure: Refractive index: n20/D 1.492
Fp: >230 °F
Storage temp.: Store at +5°C to +30°C.
Solubility: Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly), Water (Slightly)
Form: Liquid
Color: Yellow
PH: 5.0-8.0 (10g/l, H2O, 20℃)
Water Solubility: Miscible with water.
Merck: 13,6793
BRN: 2315025
CAS DataBase Reference: 9036-19-5(CAS DataBase Reference)
EPA Substance Registry System: TRITON CF-10 (90%) (9036-19-5)

Uses
0·3% TRITON CF-10 (90%) in TBS has been used for permeabilization of retinas before immunostaining.
0.5% TRITON CF-10 (90%) has been used for astrocyte cell lysis.

Triton? X-100 has been used:
In immunohistochemistry for staining the Flat-mount retinas
Along with ice-cold PBS (phosphate buffered saline) in suspension of cells for cell DNA analysis and Annexin V assay
To permeabilise cells during Immunofluorescent microscopic studies
As a positive control in LDH assay to determine the cell membrane integrity
For estimating the lipase activity in postheparin plasma by using modified Belfrage and Vaughan radioenzymatic procedure

For the preparation of outer membrane protein exctract
As a component of extraction buffer along with tris-HCl, NaCl, CaCl2, ZnCl2, Brij 35 for homogenization of mice lung cells
In the treatment of tissue sections for Immunofluorescence labeling
In the permeabilization of cells for immunofluorescence staining
As a component of lysis buffer in western blot analysis
As a component of Tris-buffered saline for the preparation of cell sections in Immunogold labelling for electron microscope

Synonyms
octylphenoleo(20)
octylphenoleo(3)
octylphenoxypoly(ethyleneoxy)ethanol
op1062;ope-3
poly(ethyleneoxide)octylphenylether
polyethyleneglycolmono(octyl)phenylether
polyethyleneglycolmono(octylphenyl)ether
TRITON DF-16
Triton DF-16 is low Foam / Nonionic.
Triton DF-16 is readily biodegradable low foaming surfactant with excellent wetting ability, improved Freeze/Thaw stability.


CAS-Number: 58229-81-5
EC Number: 633-454-9
Surfactant Type: Nonionic


Triton DF-16 is readily biodegradable low foaming surfactant with excellent wetting ability, improved Freeze/Thaw stability.
Triton DF-16 stores in a cool, ventilated warehouse.
Triton DF-16 is low Foam / Nonionic.


Triton DF-16 should be kept away from oxidizers, do not store together. Triton DF-16 is equipped with the appropriate variety and quantity of fire equipment.
The storage area of Triton DF-16 should be equipped with leakage emergency treatment equipment and suitable containment materials.



USES and APPLICATIONS of TRITON DF-16:
Applications of Triton DF-16: Ion Exchange Resin Cleaners, Metal Cleaners, Pigment Dispersions, Pulp & Paper, Rinse Aids, Textile Processing, Wetting Agent.
Triton DF-16 is used, Ion exchange resin cleaner, metal cleaner, pigment dispersion system, pulp and paper, rinse aid, textile processing, and wetting agent


Recommended uses and limitations of Triton DF-16: Multi-purpose surfactant
Triton DF-16 is used Rinse aids, Commercial machine dishwashing, Food and dairy process cleaners, Metal cleaning applications, Pulp and paper, Textile processing, and Pigment dispersions.


-Application of Low Foaming Nonionic Surfactant, Triton DF-16:
* Ion exchange resin cleaner
* Metal cleaner
* Pigment dispersion system
* Pulp and paper
* rinse aid
* Textile processing
* humectant



ADVANTAGES OF TRITON DF-16:
• Low Foam wetting agent
• Excellent hard surface detergency
• Acid stability
• Readily biodegradable



BENEFITS OF TRITON DF-16:
• Excellent detergency and wetting properties
• Caustic and acid stability
• Superior food and protein soil defoaming ability
• Low Foam wetting agent
• Excellent hard surface detergency
• Acid stability
• Readily biodegradable



SOLUBILITY AND COMPATIBILITY OF TRITON DF-16:
• Soluble in water
• Insoluble in highly aliphatic solvents and glycols
• Chemically stable in acidic & alkaline solutions



PHYSICAL and CHEMICAL PROPERTIES of TRITON DF-16:
Physical state: liquid
Color: No data available
Odor: No data available
Melting point/freezing point: No data available
Initial boiling point and boiling range: No data available
Flammability (solid, gas): No data available
Upper/lower flammability or explosive limits: No data available
Flash point: No data available
Autoignition temperature: No data available
Decomposition temperature: No data available
pH: No data available
Viscosity Viscosity, kinematic: No data available
Viscosity, dynamic: No data available
Water solubility: No data available
Partition coefficient: n-octanol/water: No data available
Vapor pressure: No data available
Density: No data available
Relative density: No data available
Relative vapor density: No data available
Particle characteristics: No data available
Explosive properties: No data available
Oxidizing properties: No data available
Other safety information: No data available
Form: Liquid
Appearance: liquid
Boiling Point: > 200 °C (> 392 °F)

Color: yellow
Evaporation Rate: Calculated < 0.01
Flash Point: 157 °C (315 °F) Method: ASTM D 93
Kinematic Viscosity: Calculated 35.3 mm2/s
Odor: pungent
pH: 6 (as aqueous solution)
Relative Density: 0.992 @ 20 °C (68 °F) Reference Material: (water = 1)
Relative Vapor Density: Calculated 9
Solubility in Water: completely soluble
Vapor Pressure: Calculated < 0.01 mmHg @ 20 °C (68 °F)
Active Ingredient, wt%: 100
Cloud Point, 1% aq. soln., °C (°F): 36
HLB (calculated): 11.6
Appearance: Transparent, colorless liquid
pH, 5% aq solution: 6
Viscosity at 25°C (77°F), cP: 35
Density at 25°C (77°F), g/mL: 1.029
Flash Pt, Closed Cup, ASTM D93: 154°C 310°F
Pour Point, ASTM D97, °C (°F): -6

Cloud Point, 1% aq. soln., °C (°F): 36
HLB (calculated): 11.6
Appearance: Transparent, colorless liquid
pH, 5% aq solution: 6
Viscosity at 25°C (77°F), cP: 35
Density at 25°C (77°F), g/mL: 1.029
Flash Pt, Closed Cup, ASTM D93: 154°C 310°F
Pour Point, ASTM D97, °C (°F): (-6)
Surface Tension: 30
Critical Micelle Concentration (CMC), ppm: 530
Draves 25 sec wetting conc, wt% at 25°C (77°F): 0.07
Hamilton Beach Foam Test: 0.01 wt%
at 25°C (77°F), cm: 4.5
at 50°C (122°F): 0.8
at 75°C (167°F): 0

Physical State: Liquid
Color: colorless
Odor: irritating
Flash point: closed cup method 157°CASTM D93
Flash point: open cup method 215°CASTM D92
Lower flammability limit in air: no experimental data
Upper limit: no experimental data
Autoignition temperature No experimental data
Vapor pressure Calculation of boiling point (760 mmHg) > 200°C.
Vapor density (air=1) 9 calculation
Specific gravity (water=1) 0.992 Calculation at 20°C/20°C
freezing point see flow point
Melting point does not apply to liquids
Solubility in water (by weight) 100% 20°C visually
Calculated at pH 6 (5%aq.sol)
Molecular weight 570 g/mol calculation
Evaporation rate (butyl acetate = 1) < 0.01 calculation
Calculation of dynamic viscosity 35.3 cSt
Calculation of pour point -6°C

Physical State Liquid
Color Colorless
Odor Irritating
Flash Point-Closed Cup Method 157 °CASTM D93
Flash Point-Open Cup Method 215 °CASTM D92
Flammability Limit in Air Lower Limit: No Experimental Data
Upper Limit: No Experimental Data
Spontaneous Ignition Temperature No Exp erimental Data
Vapor Pressure < 0.01 mmHg @ 20 °C Calculated
Boiling Point (760 mmHg) > 200 °C Calculated.
Vapor Density (Air=1) 9 Calculated
Specific Gravity (Water=1) 0.992 20 °C/20 °C Calculated
Freezing Point See Pour Point Melting
Point Not applicable
Solubility in liquid water (by weight) 100 % @ 20 °C visually
pH 6 calculated (5% aq.sol)
molecular weight 570 g/mol calculated
evaporation rate (butyl acetate = 1) kinetic Viscosity calculated at 35.3 cSt
Pour point calculated at -6 °C



FIRST AID MEASURES of TRITON DF-16:
-Description of first-aid measures:
*General advice:
Consult a physician.
Show this material safety data sheet to the doctor in attendance.
*If inhaled:
If breathed in, move person into fresh air.
Consult a physician.
*In case of skin contact:
Wash off with soap and plenty of water.
Consult a physician.
*In case of eye contact:
Rinse thoroughly with plenty of water for at least 15 minutes and consult a physician.
*If swallowed:
Never give anything by mouth to an unconscious person.
Rinse mouth with water.
Consult a physician.
-Indication of any immediate medical attention and special treatment needed:
No data available



ACCIDENTAL RELEASE MEASURES of TRITON DF-16:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Soak up with inert absorbent material and dispose of as hazardous waste.
Keep in suitable, closed containers for disposal.



FIRE FIGHTING MEASURES of TRITON DF-16:
-Extinguishing media:
*Suitable extinguishing media:
Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.
-Special hazards arising from the substance or mixture:
Nature of decomposition products not known.
-Further information:
No data available



EXPOSURE CONTROLS/PERSONAL PROTECTION of TRITON DF-16:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Face shield and safety glasses
*Skin protection:
Handle with gloves.
Wash and dry hands.
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of TRITON DF-16:
-Precautions for safe handling:
Hygiene measures:
Handle in accordance with good industrial hygiene and safety practice.
Wash hands before breaks and at the end of workday.
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Store in cool place.
Keep container tightly closed in a dry and well-ventilated place.
Containers which are opened must be carefully resealed and kept upright to prevent leakage.
*Storage class:
Storage class (TRGS 510): 12: Non Combustible Liquids



STABILITY and REACTIVITY of TRITON DF-16:
-Reactivity:
No data available
-Chemical stability:
Stable under recommended storage conditions.
-Possibility of hazardous reactions:
No data available
-Conditions to avoid:
No data available



SYNONYMS:
68603-25-8
TRITON DF-16 Surfactant
TRITON DF-16
TRITON DF-16 Surfactant
A capped ethoxylated alcohol
DF-16 Surfactant


TRITON GR-5M (60%)
TRITON GR-5M (60%) is a group of surfactants, sulfonate esters.
TRITON GR-5M (60%) have the ability to emulsify between oil and water and provide stability.

CAS Number: 577-11-7
EINECS: 209-406-4
Molecular Formula: C20H37NaO7S

TRITON GR-5M (60%) is an anionic, sulfosuccinate surfactant with excellent wetting properties for use in applications such as paints & coatings, paper & textile and agrochemicals.
The advantages are it has excellent wetting properties and further it has emulsifying & dispersing ability.

Such compounds are substances that can interface between water and oil, thanks to the appropriate combination of hydrophobic and hydrophilic (water-loving and water-repelling) groups in a solvent environment.

TRITON GR-5M (60%) are versatile surfactants used in a variety of industries.
These properties allow them to be used in many different areas, from cleaning products to personal care products, from the petroleum industry to paint and coating applications.

Therefore, they are widely used as surfactants in various industries.
TRITON GR-5M (60%) can be used as cleaning products, personal care products, detergents, pre-rain treatment products and solvents in the petroleum industry.

One of the most common types of TRITON GR-5M (60%) is known as dioctyl sulfosuccinate (dioctyl sulfosuccinate).
TRITON GR-5M (60%) is used especially in the petroleum industry, in the formulation of products from oil production and helping to combine oil with water.

The surfactant properties, emulsifying, foaming and cleaning abilities of TRITON GR-5M (60%) lead them to be preferred in industrial applications and consumer products.
TRITON GR-5M (60%) also raises some environmental and health concerns.
Because some types of TRITON GR-5M (60%) can be substances that are not biodegradable and can cause environmental pollution in water systems.

TRITON GR-5M (60%) have the ability to form a stable emulsion between water and oil.
This feature helps to obtain a homogeneous mixture in products where oil and water-based components are used together.
This property is useful in cosmetics, paints and varnishes, the petroleum industry, and the application of agricultural products.

TRITON GR-5M (60%) lower the water surface tension, thus allowing liquids to spread better and contact surfaces more easily.
This property is important to ensure dispersibility and effective cleaning in cleaning products and paints.

TRITON GR-5M (60%) are surfactants that foam quickly and intensely.
This creates foam, especially in cleaning and personal care products, which helps the product to spread effectively and provide effective cleaning.

TRITON GR-5M (60%) are ionic surfactants and dissolve in the water environment.
This property facilitates electrostatic interactions between molecules in solution and helps to form a stable bond between water and oil.

TRITON GR-5M (60%) can generally work effectively in the neutral or acidic pH range.
This helps cleaning products and personal care products be effective even at low pH levels.
TRITON GR-5M (60%) are often considered skin-friendly due to their surface-active properties and are used in a variety of personal care products.

TRITON GR-5M (60%) are dispersants that allow the solid particles to be easily dispersed in the liquid and the dispersion to be stable.
These properties make it valuable in the formulation of dispersion products used in various industries.

TRITON GR-5M (60%) can be used to prevent or reduce corrosion on some metal surfaces.
Therefore, they can be preferred for cleaning and protecting metal surfaces in industrial cleaning products.

TRITON GR-5M (60%) are surfactants that can remain stable at high temperature.
These properties are important in some industries, products and processes used at high temperatures to maintain their effectiveness.

Density: 1.1
Melting point: 153-157℃
Boiling point: 82.7°C
Flash Point: 199 C
Precise Quality: 444.21600
PSA: 118.18000
logP:4.89030
Solubility: 1.5 g/100 mL (25 oC)

TRITON GR-5M (60%) can work effectively even at low concentrations.
Therefore, they offer a cost-effective solution by using less amount in product formulations.
TRITON GR-5M (60%) are generally classified as anionic surfactants.

TRITON GR-5M (60%) allows them to work in harmony with other ionic substances in solution in a variety of applications.
TRITON GR-5M (60%) is well compatible with TRITON GR-5M (60%), other surfactants and various chemical components.
Therefore, it allows them to be used with other substances in complex formulations.

TRITON GR-5M (60%) leave no residue on surfaces and can be easily rinsed off.
This helps prevent unwanted residues in cleaning products and personal care products.

TRITON GR-5M (60%) are generally fast-acting and show their effect in a short time.
This contributes to their preference in emergencies or applications that require immediate results.
TRITON GR-5M (60%) can be resistant to saponification.

TRITON GR-5M (60%) can alter electrophoretic motion and therefore can be used in electrophoresis applications.
TRITON GR-5M (60%) have good compatibility with electrolytes in the aquatic environment.
These properties allow the products to maintain their surfactant effects in applications where they interact with liquids containing electrolytes.

Some types of TRITON GR-5M (60%) are surfactants that are biodegradable.
This enables them to offer more environmentally friendly and sustainable solutions.
TRITON GR-5M (60%) are generally colorless and odorless, which makes them easy to use in various industries and does not affect the color and odor of products.

TRITON GR-5M (60%) can withstand water hardness levels and can also work effectively in hard water conditions.
For this reason, they are also preferred in regions with different water qualities.

Uses
TRITON GR-5M (60%) are widely used in household and industrial cleaning products such as dishwashing liquids, laundry detergents, all-purpose cleaners, and floor cleaners.
They help to emulsify oils and greases, disperse dirt, and remove stains effectively.

TRITON GR-5M (60%) are found in personal care items like shampoos, body washes, shower gels, and hand soaps.
They provide foaming and cleansing properties, leaving the skin and hair feeling clean and refreshed.

TRITON GR-5M (60%) are used as emulsifiers in various applications, including food processing, cosmetics, and pharmaceuticals.
They help in stabilizing emulsions, where oil and water-based ingredients need to be mixed together.

In the agricultural industry, TRITON GR-5M (60%) are used as adjuvants in pesticide formulations.
They help improve the spreading and wetting of the pesticide solution on plant surfaces, increasing its effectiveness.

TRITON GR-5M (60%) are used as wetting agents and dispersants in paint and coating formulations.
They aid in the even distribution of pigments and improve the paint's adhesion to surfaces.

TRITON GR-5M (60%) find applications in the oil and gas industry as surfactants for enhancing oil recovery during drilling and production processes.
TRITON GR-5M (60%) are used as emulsifiers in metalworking fluids, aiding in the formation and stability of water-oil emulsions used in metal cutting and forming processes.
TRITON GR-5M (60%) are employed as wetting agents and emulsifiers in the textile industry for dyeing and finishing processes.

In electroplating, TRITON GR-5M (60%) are used as additives to improve the dispersion of metal ions in plating baths and enhance the uniformity of metal deposition.
TRITON GR-5M (60%) are utilized in water treatment processes as dispersants and cleaners to control scale and deposit buildup in industrial water systems.

TRITON GR-5M (60%) are used in pharmaceutical formulations as excipients to improve the solubility and bioavailability of poorly water-soluble drugs.
They can be used as emulsifying agents in topical creams and ointments.

In the petroleum industry, TRITON GR-5M (60%) are used in enhanced oil recovery (EOR) processes to improve the displacement of oil from reservoirs and increase oil production.
TRITON GR-5M (60%) are employed as foaming agents in various applications, including firefighting foams, fire extinguishers, and in the production of foamed plastics and rubbers.

TRITON GR-5M (60%) are used in agrochemical formulations, such as herbicides and insecticides, to improve their effectiveness and adherence to plant surfaces.
TRITON GR-5M (60%) are utilized in industrial cleaning processes for cleaning equipment, machinery, and surfaces, where effective degreasing and soil removal are required.
TRITON GR-5M (60%) are used in photographic processing chemicals as wetting agents and emulsifiers to disperse and stabilize photographic emulsions.

TRITON GR-5M (60%) are employed as dispersants and wetting agents in water-based ink formulations to disperse pigments and improve printing quality.
TRITON GR-5M (60%) are used in the paper and pulp industry as wetting agents, dispersants, and cleaning agents during various stages of the papermaking process.

Health Hazards
Direct contact with concentrated sulfosuccinate solutions can cause skin and eye irritation.
TRITON GR-5M (60%) is essential to avoid skin contact and wear appropriate protective equipment when handling these substances.

Inhalation:
Inhalation of fine aerosols or mists of TRITON GR-5M (60%) may irritate the respiratory system.
Adequate ventilation and respiratory protection should be used in situations where the risk of inhalation is present.

Environmental Impact:
Some TRITON GR-5M (60%) may persist in the environment and could contribute to water pollution if released without proper treatment.
It is important to follow local regulations and dispose of TRITON GR-5M (60%) safely.

Aquatic Toxicity:
High concentrations of certain TRITON GR-5M (60%) may be toxic to aquatic life.
Proper handling and disposal are necessary to prevent environmental contamination.

Chemical Incompatibility:
TRITON GR-5M (60%) can be incompatible with certain materials, such as strong acids or oxidizing agents.
Mixing them with incompatible substances can lead to hazardous reactions.

Synonyms
Docusate sodium
577-11-7
Aerosol OT
Dioctyl sodium sulfosuccinate
Dioctyl sulfosuccinate sodium salt
Dioctylal
Diotilan
Disonate
Molatoc
Regutol
Velmol
Doxol
Nevax
Constonate
Dialose
Doxinate
Soliwax
Colace
Molcer
Waxsol
Adekacol EC 8600
Docusate (Sodium)
Mervamine
Clestol
Defilin
Obston
Rapisol
Requtol
Docusate sodium salt
Diox
Modane Soft
Alcopol O
Sulfimel DOS
Manoxal OT
Manoxol OT
Monoxol OT
Aerosol AOT
Aerosol GPG
Vatsol OT
Wetaid SR
Aerosol OT-A
Aerosol OT-B
Laxinate 100
Sanmorin OT 70
Triton GR 7
Triton GR-5
Diomedicone
Aerosol OT 70PG
Aerosol OT 75
Celanol DOS 65
Celanol DOS 75
Coloxyl
Comfolax
Complemix
Coprola
Dioctlyn
Dioctyl
Diosuccin
Docolace
Docuprene
Dulcivac
Dulsivac
Eurowet
Humifen WT 27G
Laxinate
Molofac
Sobital
Solusol-75%
Coprol
Diovac
Konlax
Kosate
Silace
Softil
Bloat treatment
Revac
Nikkol OTP 70
Aerosol A 501
Alkasurf SS-O 75
Bis(2-ethylhexyl) sulfosuccinate sodium salt
Solusol-100%
Nekal WT-27
Berol 478
Alphasol OT
Docusatum natricum
Empimin op70
Sanmorin ot 70n
Dioctyl-Medo forte
Natrii dioctylsulfosuccinas
Tex-Wet 1001
Airrol ct-1
Doc Q Lace
Mackanate dos-70
Nikkol otp-75
Gemtex pa-70
Rapisol a 30
Triton gr-pg 70
D-S-S
DESS
Monawet MD 70E
Monawet MO-70
Sodium dioctyl sulphosuccinate
Nissan rapisol a 30
Monawet MO-70 RP
Geriplex
Unilax
Docusato sodico
Monawet MO-84 R2W
Sodium 2-ethylhexylsulfosuccinate
Sodium bis(2-ethylhexyl) sulfosuccinate
Docusate sodique
HSDB 3065
Ins no.480
Dialose Plus
Monawet mo 65-150
2-Ethylhexyl sulfosuccinate sodium
Dioctyl ester of sodium sulfosuccinic acid
Senokot S
Correctol Caplets
Correctol Tablets
Senokap DSS
EINECS 209-406-4
Ins-480
Dioctyl sodium sulphosuccinat
UNII-F05Q2T2JA0
Dioctyl ester of sodium sulfosuccinate
Bis(2-ethylhexyl)sodium sulfosuccinate
Correctol Extra Gentle Tablets
Bis(2-ethylhexyl) sodium sulfosuccinate
Di-(2-ethylhexyl) sodium sulfosuccinate
Sodium di-(2-ethylhexyl) sulfosuccinate
Docusate sodique [INN-French]
Docusato sodico [INN-Spanish]
F05Q2T2JA0
Docusatum natricum [INN-Latin]
DTXSID8022959
AI3-00239
Butanedioic acid, sulfo-, 1,4-bis(2-ethylhexyl) ester, sodium salt
Diethylhexyl Sodium Sulfosuccinate
Sodium 1,4-bis(2-ethylhexyl) sulfosuccinate
Sodium sulfodi-(2-ethylhexyl)-sulfosuccinate
CHEMAX DOSS/75E
Di(2-ethylhexyl)sulfosuccinic acid, sodium salt
SV 102
Sodium bis(2-ethylhexyl)sulfosuccinate
NSC-760404
Bis(ethylhexyl) ester of sodium sulfosuccinic acid
Sulfosuccinic acid, bis(2-ethylhexyl)ester sodium salt
Bis(2-ethylhexyl) S-sodium sulfosuccinate
Docusate Sodium [USAN:BAN]
CHEBI:4674
DTXCID102959
Bis-2-ethylhexylester sulfojantaranu sodneho
Sodium 1,4-bis(2-ethylhexyl)sulfosuccinate
1,4-Bis(2-ethylhexyl) sodium sulfosuccinate
E 480
E-480
sodium 1,4-bis[(2-ethylhexyl)oxy]-1,4-dioxobutane-2-sulfonate
EC 209-406-4
Sol sodowej sulfobursztynianu dwu-2-etyloheksylowego
sodium docusate
1,4-Bis(2-ethylhexyl)sulfobutanedioate, sodium salt
Bis-2-ethylhexylester sulfojantaranu sodneho [Czech]
Sodium di(2-ethylhexyl)sulfosuccinate
NSC 760404
AOT
Docusate sodium [USAN:USP:INN:BAN]
SBO
Sulfosuccinic acid, di-(2-ethylhexyl) ester, sodium salt
Sol sodowej sulfobursztynianu dwu-2-etyloheksylowego [Polish]
Succinic acid, sulfo-, 1,4-bis(2-ethylhexyl) ester, sodium salt
AEC DIETHYLHEXYL SODIUM SULFOSUCCINATE
DOCUSATE SODIUM (II)
DOCUSATE SODIUM [II]
Docusate sodique (INN-French)
Docusato sodico (INN-Spanish)
DOCUSATE SODIUM (MART.)
DOCUSATE SODIUM [MART.]
DOCUSATE SODIUM (USP-RS)
DOCUSATE SODIUM [USP-RS]
sodium;1,4-bis(2-ethylhexoxy)-1,4-dioxobutane-2-sulfonate
Dioctyl sodium sulfosuccinate (JAN)
DOCUSATE SODIUM (USP IMPURITY)
DOCUSATE SODIUM [USP IMPURITY]
DOCUSATE SODIUM (USP MONOGRAPH)
DOCUSATE SODIUM [USP MONOGRAPH]
C20H38O7S
CAS-577-11-7
Yal
DIOCTYL SODIUM SULFOSUCCINATE [JAN]
DIOCTYL DISODIUM SULFOSUCCINATE
NCGC00164140-03
Prenexa
Purgasol
Vinacol
natrii docusas
Docusate Sod
Senexon-S
docusato de sodio
Folca[s care pme
Folcal DHA
Senna-S
Colace (TN)
MFCD00012455
DEH Na SS
DEH-Na-SS
Docusate sodium (USP)
DSS (CHRIS Code)
NCGC00183136-01
SCHEMBL4113
DOCUSATE SODIUM [MI]
Dioctylsulphosuccinate, Sodium
MLS004773938
DOCUSATE SODIUM [INN]
Dioctyl Sulfosuccinate, Sodium
DOCUSATE SODIUM [HSDB]
DOCUSATE SODIUM [USAN]
Sulfosuccinic acid bis(2-ethylhexyl) ester sodium salt
DOCUSATE SODIUM [VANDF]
CHEMBL1905872
A06AA02
Correctol Stool Softener Laxative
DOCUSATE SODIUM [WHO-DD]
APSBXTVYXVQYAB-UHFFFAOYSA-M
HMS3264P07
HMS3885B10
Sodium Sulfosuccinate, Diethylhexyl
Sulfosuccinate, Diethylhexyl Sodium
BCP31325
HY-B1268
4-(4-Bromophenoxymethyl)benzoicacid
Aerosol™ OT, Solid Anhydrous
Sodium dioctyl sulfosuccinate (INN)
Tox21_112087
Tox21_113469
Tox21_201342
Tox21_300496
s4588
AKOS015901806
CCG-213234
CS-4813
LS-3162
Sodium Di(2-ethylhexyl) Sulfosuccinate
Dioctyl Sulfosuccinic Acid, Sodium Salt
Docusate sodium salt, BioXtra, >=99%
Dioctyl sulfosuccinate sodium salt, 96%
NCGC00164140-01
NCGC00254414-01
NCGC00258894-01
AS-13347
E480
SMR001595510
DIOCTYL SODIUM SULFOSUCCINATE [FCC]
Dioctyl Sodium Sulfosuccinate with Ethanol
Bis(2-ethylhexyl) TRITON GR-5M (60%)odium salt
Dioctyl sulfosuccinate sodium salt, >=97%
FT-0689234
D00305
Docusate sodium salt, p.a., 99.0-100.5%
E77584
DIETHYLHEXYL SODIUM SULFOSUCCINATE [INCI]
Docusate sodium salt, purum, >=96.0% (TLC)
Docusate sodium salt, BioUltra, >=99.0% (TLC)
Docusate sodium, meets USP testing specifications
Dioctyl Sodium Sulfosuccinate with Diethylene Glycol
Dioctyl Sodium Sulfosuccinate with Propylene Glycol
Q2815334
W-105447
F8880-5559
Docusate sodium, British Pharmacopoeia (BP) Reference Standard
Docusate sodium, European Pharmacopoeia (EP) Reference Standard
sodium 1,4-bis(2-ethylhexyloxy)-1,4-dioxobutane-2-sulfonate
sulfosuccinic acid 1,4-bis(2-ethylhexyl) ester S-sodium salt
Docusate sodium, United States Pharmacopeia (USP) Reference Standard
2-Sulfobutanedioic acid 1,4-bis(2-ethylhexyl) ester sodium salt (1:1)
Dioctyl sodium sulfosuccinate; (Di-(2-ethylhexyl) sodium sulfosuccinate)
1,4-bis(2-ethylhexyl)sodiumsulfosuccinate pound>>Dioctyl sulfosuccinate sodium salt
Butanedioic acid, 2-sulfo-, 1,4-bis(2-ethylhexyl) ester, sodium salt (1:1)
TRITON H66
TRITON H66 is hydrotrope, stable in acidic and alkaline conditions, effective with low foam surfactants.
TRITON H66 is readily biodegradable.
TRITON H66 is used as solubilizer in built detergents.

CAS: 37281-48-4
MF: C6H6O4P.CH3.K
MW: 227.22

TRITON H66 Properties:
Test item: Index
Number of colors: ≤30#
Appearance(25°C): Colorless to yellowish liquid
Phase (25°C): 8.0-10.0
Solid content (%): 49.0-51.0
The odor: slight odor
Proportion(25°C), g/cm 3: >1
Solubility: Solubility in water
Superficial tension: Neutral:45; alkalinity: 41
Height of foam: Neutral:50/8; alkalinity: 105/25

Uses
TRITON H66 is water soluble cosolvent stable under acidity and alkalinity conditions.
TRITON H66 can solubilize low and medium foam surface without affecting the foam properties.
And TRITON H66 is suitable for various non-ionic and anionic alkaline systems.

TRITON H66 is resistant to electrolytes and has excellent salt tolerance, which can significantly increase the solubility of nonionic surface agents in high alkaline salt solutions at high temperatures.

TRITON H66 can be widely used in commercial cleaning industry, paints and coatings, paper and textiles, agricultural chemicals, oilfield chemicals and other fields.

Synonyms
Triton H 66
TRITON HW-1000
TRITON HW-1000 is a non-APE based non-ionic hydrocarbon.
Acts as a wetting agent and surfactant.
Exhibits faster processing, dispersibility and biodegradability.

CAS: 60828-78-6
MF: C12H26O.(C2H4O)n
EINECS: 612-043-8

Provides excellent wetting, leveling, low foaming and de-foaming.
Offers reduction in the dynamic and equilibrium surface tension of waterborne solutions under both static and dynamic status.
Possesses capability of wetting various substrates, reducing defects, improving gloss and smoothness of coating films.
TRITON HW-1000 is used in water-based formulations.
Complies with low- and no-VOC regulatory requirements.

TRITON HW-1000 is a nonionic surfactant that has a hydrophilic polyethylene oxide chain (on average TRITON HW-1000 has 9.5 ethylene oxide units) and an aromatic hydrocarbon lipophilic or hydrophobic group.
The hydrocarbon group is a 4-(1,1,3,3-tetramethylbutyl)-phenyl group.
TRITON HW-1000 is closely related to IGEPAL CA-630, which might differ from it mainly in having slightly shorter ethylene oxide chains.
As a result, TRITON HW-1000 is slightly more hydrophilic than Igepal CA-630 thus these two detergents may not be considered to be functionally interchangeable for most applications.

TRITON HW-1000 Chemical Properties
Density: 1.04 g/mL at 20 °C
Fp: 130 °C
Form: liquid
EPA Substance Registry System: TRITON HW-1000 (60828-78-6)

Uses
TRITON HW-1000 is a commonly used detergent in laboratories.
TRITON HW-1000 is widely used to lyse cells to extract protein or organelles, or to permeabilize the membranes of living cells.

Inactivation of lipid-enveloped viruses (e.g. HIV, HBV, HCV) in manufacturing of biopharmaceuticals,
Industrial purpose (plating of metal),
Ingredient in influenza vaccines, including Fluarix, Flublok, and Fluzone,
Permeabilizing unfixed (or lightly fixed) eukaryotic cell membranes,
Solubilizing membrane proteins in their native state in conjunction with zwitterionic detergents such as CHAPS,
Part of the lysis buffer (usually in a 5% solution in alkaline lysis buffer) in DNA extraction,

Reducing surface tension of aqueous solutions during immunostaining (usually at a concentration of 0.1-0.5% in TBS or PBS buffer),
Dispersion of carbon materials for soft composite materials,
Restricting colony expansion in Aspergillus nidulans in microbiology,
Decellularization of animal-derived tissues,
Removing SDS from SDS-PAGE gels prior to renaturing the proteins within the gel,
Disruption of cell monolayers as a positive control for TEER measurements,
Micellar catalyst,
Reducing surface tension in etching such as undercutting fine features (micron size openings) in MEMS device processing,
TRITON HW-1000 is an ingredient in Photo-Flo, a solution used in photographic processing to prevent minerals from water being deposited on the film after drying.

Synonyms
60828-78-6
Tergitol TMN-6
2-(2,6,8-trimethylnonan-4-yloxy)ethanol
10137-98-1
Tergitol(r) tmn-10
BRN 1851894
2-(2,6,8-Trimethyl-4-nonyloxy)ethanol
Ethanol, 2-[[3,5-dimethyl-1-(2-methylpropyl)hexyl]oxy]-
2-((1-Isobutyl-3,5-dimethylhexyl)oxy)ethanol
Ethyleneglycolmono-2,6,8-trimethyl-4-nonyl ether
Ethylene glycol mono-2,6,8-trimethyl-4-nonyl ether
ETHANOL, 2-((1-ISOBUTYL-3,5-DIMETHYLHEXYL)OXY)-
2-[(1-Isobutyl-3,5-dimethylhexyl)oxy]ethanol
Ethanol, 2-[(1-isobutyl-3,5-dimethylhexyl)oxy]-
Ethanol, 2-((3,5-dimethyl-1-(2-methylpropyl)hexyl)oxy)-
DTXSID00873978
LS-66836
LS-72947
2-[[3,5-Dimethyl-1-(2-methylpropyl)hexyl]oxy]ethanol
TRITON X-100
Triton X-100 (C14H22O(C2H4O)n) is a nonionic surfactant that has a hydrophilic polyethylene oxide chain (on average it has 9.5 ethylene oxide units) and an aromatic hydrocarbon lipophilic or hydrophobic group.
The hydrocarbon group is a 4-(1,1,3,3-tetramethylbutyl)-phenyl group.
Triton X-100 is closely related to IGEPAL CA-630, which might differ from it mainly in having slightly shorter ethylene oxide chains.

CAS: 9002-93-1
MF: C18H28O5
MW: 324.41192
EINECS: 618-344-0

As a result, Triton X-100 is slightly more hydrophilic than Igepal CA-630 thus these two detergents may not be considered to be functionally interchangeable for most applications.
Triton X-100 was originally a registered trademark of Rohm & Haas Co.
Triton X-100 was subsequently purchased by Union Carbide and then acquired upon the acquisition of Union Carbide.
Triton X-100 is a common non-ionic surfactant and emulsifier which is often used in biochemical applications to solubilize proteins.
Triton X-100 is considered a comparatively mild detergent, non-denaturing, and is reported in numerous references as a routinely added reagent.
Triton X-100 is utilized for lysing cells to extract protein and cellular organelles.
Triton X-100 can also permeabilize the living cell membrane for transfection.
A poly(ethylene glycol) terminated with a 4-(2,4,4-trimethylpentan-3-yl) phenyl group at one end.

Triton X-100 is a non-ionic surfactant.
This octylphenol ethoxylate has higher number of ethylene oxide units, increased cmc (Critical micelle concentration) and hydrophile/lipophile balance when compared to Triton X-100.
Triton X-100 is compatible with anionic, cationic, and other nonionic surfactants and chemically stable in most acidic and alkaline solutions.
Triton X-100 is a nonionic detergent, 100% active ingredient, which is often used in biochemical applications to solubilize proteins.
Triton X-100 has no antimicrobial properties.

Triton X-100 is considered a comparatively mild detergent, non-denaturing, and is reported in numerous references as a routinely added reagent.
Triton X-100 does absorb in the ultraviolet region of the spectrum, however, so can interfere with protein quantitation.
A number of polymeric resins have been used to remove Triton X-100 from solution, including Amberlite hydrophobic XAD resins and Rezorian A161 cartridges.
The "X" series of Triton X-100 detergents are produced from octylphenol polymerized with ethylene oxide.
The number ("-100") relates only indirectly to the number of ethylene oxide units in the structure.

Triton X-100 has an "average of 9.5" ethylene oxide units per molecule, with an average molecular weight of 625.
In addition, lower and higher mole adducts will be present in lesser amounts, varying slightly within supplier standard manufacturing conditions.
No antioxidants are added by Sigma or the manufacturer, but commercial preparations of Triton X-100 have been found to contain peroxides up to 0.22% hydrogen peroxide (H2O2) equivalents.
These impurities may interfere with biological reactions.
Sigma offers X-100-PC and X-100R-PC as biological grade alternatives.

Triton X-100 Chemical Properties
Melting point: 44-46 °C
Boiling point: 250 °C(lit.)
Density: 1.06 g/mL at 20 °C
Vapor density: >1 (vs air)
Vapor pressure: < 1.33 hPa at 20 °C
Refractive index: n20/D 1.491
Fp: 535 °F
Storage temp.: protect from light
Solubility H2O: 0.005 M at 20 °C, clear, colorless
Form: Viscous Liquid
Color: ≤100(APHA)
Odor: Odorless
PH Range: 9.7
PH: 6.5-8.5 (25℃)
Water Solubility: Miscible with water.
Merck: 14,6761
BRN: 2315025
LogP: 4.610 (est)
EPA Substance Registry System: Triton X-100 (9002-93-1)

Triton X-100 is a very stable material, assumed to be stable for years if stored sealed.
Triton X-100 is a clear to slightly hazy, colorless to light yellow liquid (color by APHA = 100).
1. Specific gravity: 1.065 at 25°C (Approx. 1.07 g/mL).
2. Approximate molecular weight = 625, giving effective molarity = 1.7 M for the neat liquid.
3. UV absorption: lambda max = 275 nm and 283 nm in methanol.
4. Viscosity (Brookfield): 240 cps at 25°C.
5. pH (5% aqueous solution): 6.0 to 8.0.
6. Critical micelle concentration (CMC): 0.22 to 0.24 mM.

Undiluted Triton X-100 is a clear viscous fluid (less viscous than undiluted glycerol).
Undiluted Triton X-100 has a viscosity of about 270 centipoise at 25 °C which comes down to about 80 centipoise at 50 °C.
Triton X-100 is soluble at 25 °C in water, toluene, xylene, trichloroethylene, ethylene glycol, ethyl ether, ethyl alcohol, isopropyl alcohol, and ethylene dichloride.
Triton X-100 is insoluble in kerosene, mineral spirits, and naphtha, unless a coupling agent like oleic acid is used.

Uses
Triton X-100 is a commonly used detergent in laboratories.
Triton X-100 is widely used to lyse cells to extract protein or organelles, or to permeabilize the membranes of living cells.
Nonionic detergent, emulsifier, dispersing agent.
Triton X-100 as spermaticide.
Triton-X 100 is a non-ionic surfactant.
Used in the enhancement of film porosity in conducting polymers.
Detergent, equivalent to Nonidet P-40.

Triton X-100 is used as a non-ionic detergent, emulsifier and dispersing agent.
Triton X-100 is useful for isolation of membrane proteins.
Triton X-100 is also used in electrophoresis.
Triton X-100 is an active ingredient in influenza vaccine (Fluzone).
Triton X-100 finds applications in the dispersion of carbon materials for soft composite materials and restricting colony expansion in Aspergillus nidulans in microbiology.
Further, Triton X-100 is an active ingredient in homemade vinyl record cleaning fluids together with distilled water and isopropyl alcohol.

Some applications include:
Inactivation of lipid-enveloped viruses (e.g. HIV, HBV, HCV) in manufacturing of biopharmaceuticals
Industrial purpose (plating of metal)
Ingredient in influenza vaccines, including Fluarix, Flublok, and Fluzone
Permeabilizing unfixed (or lightly fixed) eukaryotic cell membranes.
Solubilizing membrane proteins in their native state in conjunction with zwitterionic detergents such as CHAPS.
Part of the lysis buffer (usually in a 5% solution in alkaline lysis buffer) in DNA extraction.

Reducing surface tension of aqueous solutions during immunostaining (usually at a concentration of 0.1-0.5% in TBS or PBS buffer).
Dispersion of carbon materials for soft composite materials.
Restricting colony expansion in Aspergillus nidulans in microbiology.
Decellularization of animal-derived tissues.
Removing SDS from SDS-PAGE gels prior to renaturing the proteins within the gel.
Disruption of cell monolayers as a positive control for TEER measurements.
Micellar catalyst.

Reducing surface tension in etching such as undercutting fine features (micron size openings) in MEMS device processing
Triton X-100 is an ingredient in Photo-Flo, a solution used in photographic processing to prevent minerals from water being deposited on the film after drying.
Apart from laboratory use, Triton X-100 can be found in several types of cleaning compounds, ranging from heavy-duty industrial products to gentle detergents.
Triton X-100 is also a popular ingredient in homemade vinyl record cleaning fluids together with distilled water and isopropyl alcohol.

Synonyms
Triton X-100
2315-67-5
9002-93-1
Octoxinol
Octoxynol 9
Octoxynol-1
Octoxynol
4-tert-Octylphenol Monoethoxylate
Triton X
Preceptin
Triton x-45
Triton X 45
Triton X 100
Triton X 305
Octoxynol 1
Hydrol SW
Alfenol 3
Alfenol 9
2-[4-(2,4,4-trimethylpentan-2-yl)phenoxy]ethanol
Marlophen 820
Neutronyx 605
Conco nix-100
Hyonic pe-250
Triton X 35
Antarox A-200
Octoxinolum
Triton X 165
Triton X 405
Triton X 705
Triton X-102
Ethanol, 2-[4-(1,1,3,3-tetramethylbutyl)phenoxy]-
Poletoxol
Ortho-gynol
Peg 4-isooctylphenyl ether
PEG-9 Octyl phenyl ether
Octoxynol-12
Octoxynol-25
Octoxynol-33
Octoxynol-40
4-tert-Octylphenyl peg ether
Peg 4-tert-octylphenyl ether
OPE 30
2-(p-(1,1,3,3-Tetramethylbutyl)phenoxy)ethanol
Texofor FP 300
Ethanol, octylphenoxy-
Triton X 101
Triton X 102
Octoxynol 9 [USAN]
Octoxinolum [INN-Latin]
TX 100
2-[4-(1,1,3,3-Tetramethylbutyl)phenoxy]ethanol
UNII-20CAX7IO75
Peg P-tert-octylphenyl ether
CCRIS 985
20CAX7IO75
2-(4-(1,1,3,3-Tetramethylbutyl)phenoxy)ethanol
NSC-5259
Peg (P-(1,1,3,3-tetramethylbutyl)phenyl) ether
NSC 406472
Triton,(-)
Igepal CA-210
NCGC00091012-01
p-(1,1,3,3-Tetramethylbutyl)phenol ethoxylate
DSSTox_CID_14085
DSSTox_RID_79110
DSSTox_GSID_34085
2-(4-(2,4,4-trimethylpentan-2-yl)phenoxy)ethanol
alpha-(P-(1,1,3,3-Tetramethylbutyl)phenoxy)ethanol
Ethanol, 2-(4-(1,1,3,3-tetramethylbutyl)phenoxy)-
2-[4-(2,4,4-trimethylpentan-2-yl)phenoxy]ethan-1-ol
Octoxinols
Octoxynols
ETHANOL, 2-(P-(1,1,3,3-TETRAMETHYLBUTYL)PHENOXY)-
C17H28O2
MFCD00132505
(C2-H4-O)mult-C14-H22-O
CAS-9002-93-1
Triton X-305
OP1EO
2-(4-(2,4,4-Trimethylpentan-2-yl)phenoxy)ethan-1-ol
2-(4-tert-Octylphenoxy)ethanol
Octoxynol-5
Octoxynol-7
Octoxynol-70
Octoxinol (INN)
NSC 5259
Octoxynol 9 (NF)
Octylphenol Ethoxylate
Triton,(+)
Triton X-405
4-tert-Octylphenyl (2-Hydroxyethyl)ether
OCTOXYNOL-8
UNII-GW0EMR6SXY
OCTOXYNOL-13
UNII-3E2NC94VPF
UNII-480KVF3EBY
UNII-7JPC6Y25QS
UNII-NR7ZWN391G
UNII-QH2U227LZY
Octoxynol 9 [USAN:NF]
OCTOXYNOL-1 [II]
Triton X-100 (TN)
TRITON X-15
PEG-11 Octyl phenyl ether
PEG-12 Octyl phenyl ether
PEG-25 Octyl phenyl ether
PEG-33 Octyl phenyl ether
PEG-40 Octyl phenyl ether
UNII-9T1C662FKS
UNII-KI56N6W95G
UNII-SQL994V0M6
UNII-TJ327E1R1V
OCTOXYNOL-1 [INCI]
SCHEMBL33822
OCTOXYNOL 1 [VANDF]
CHEMBL39763
UNII-48RF3T316O
UNII-8419DEW37J
CHEBI:9750
TRITON X-15 SURFACTANT
DTXSID1058680
BDBM81480
NSC5259
4-iso-Octylphenol-mono-ethoxylate
CHEBI:177811
Bio1_000474
Bio1_000963
Bio1_001452
CAS_5590
NSC_5590
Tox21_111055
Tox21_202544
PDSP1_001087
PDSP2_001071
STL451484
AT25387
CS-T-62564
NSC-406472
NCGC00260093-01
9063-89-2
AS-68067
CAS_118-96-7
LS-72946
Ethanol,1,3,3-tetramethylbutyl)phenoxy]-
CS-0449852
FT-0673247
FT-0689215
D05229
P-TERT-OCTYLPHENYL (2-HYDROXYETHYL)ETHER
2-[4-(2,4,4-Trimethyl-2-pentanyl)phenoxy]ethanol
J-015013
Q27253450
4-iso-Octylphenol-mono-ethoxylate 10 microg/mL in Acetone
Glycols, mono[p-(1,1,3,3-tetramethylbutyl)phenyl] ether
26-(Octylphenoxy)-3,6,9,12,15,18,21,24-octaoxahexacosan-1-ol
3,6,9,12,15,18,21,24-Octaoxahexacosan-1-ol, 26-(octylphenoxy)-
3,9,12,15,18,21,24,27,30-Decaoxatriacontan-1-ol, 30-[p-(1,1,3,3-tetramethylbutyl)phenyl]-
32-(4-(1,1,3,3-Tetramethylbutyl)phenoxy)-3,6,9,12,15,18,21,24,27,- 30-decaoxadotriacontan-1-ol
TRITON X-100
TBP; Phosphoric acid, tri-n-butyl ester; tri-n-butyl phosphate; Butyl phosphate; Phosphoric acid tributyl ester; celluphos 4; n-Butyl Phosphate; Tributilfosfato (Italian); Tributoxyphosphine Oxide; Tributyle (Phosphate De) (French); Tributylfosfaat (Dutch); Tributylphosphat (German); Fosfato de tributilo (Spanish); Phosphate de tributyle (French) CAS NO: 126-73-8
TRITON X-405 (70%)
Triton X-405 (70%) has excellent emulsion stabilizer, provides freeze thaw and ionic stability.
Triton X-405 (70%) is an octylphenol ethoxylated.
Triton X-405 (70%) is a non-ionic surfactant.


CAS Number: 9036-19-5
MDL number: MFCD00128254
Triton X-405 (70% active) x = 40
Product Type: Wetting Agents / Wet Edge Enhancers > Surfactants
Chemical Name: OCTYL PHENOL ETHOXYLATE
Chemical Composition: Octylphenol ethoxylate
Molecular Formula: C14H21(C2H4O)39-41OH / C₂₈H₅₀O₈


Triton X-405 (70%) is an excellent primary nonionic surfactant, recommended especially for the emulsion polymerization of acrylic, vinyl acrylic, styrene butadiene and styrene acrylic polymers.
Triton X-405 (70%) has excellent emulsion stabilizer, provides freeze thaw and ionic stability.


Such polymers find application in latex paints, adhesives, paper coatings and textile applications.
Triton X-405 (70%) is an octylphenol ethoxylated.
Triton X-405 (70%) is a non-ionic surfactant.


Triton X-405 (70%) is one of a series of Rhodia ethoxylated alkylphenol nonionic surfactants with different HLBs.
Since differences in HLB affect emulsification and stabilization properties, Triton X-405 (70%) allows the user to select the surfactant that will provide effective particle size control, low levels of coagulum, latex stability and trouble-free commercial production.


Triton X-405 (70%) acts as an emulsion stabilizer, dispersing agent and emulsifier.
Triton X-405 (70%) provides freeze/thaw & ionic stability.
Triton X-405 (70%) is effective at high temperatures.
Triton X-405 (70%) offers good solubility in the presence of salts or electrolytes & caustic solutions.



USES and APPLICATIONS of TRITON X-405 (70%):
Applications of Triton X-405 (70%): multipurpose non-ionic surfactant very often used to optimize protein-protein interactions.
Triton X-405 (70%) can also be used as emulsifier, helping mix lipids in aqueous environments.
Unlike SDS, Triton X-405 (70%) is classified as a mild non-denaturing detergent. Triton X-405 (70%) finds numerous applications in cell lysis, reagent stabilization, inactivation of viruses, destabilization of cellular membranes and more.


Triton X-405 (70%) is used as an excellent emulsion stabilizer that provides freeze/thaw and ionic stability.
Triton X-405 (70%) is used in paints and coatings, floor polish and wax emulsions.
Triton X-405 (70%) is used emulsion polymerization, paints and coatings, floor polish, and wax emulsions.


Triton X-405 (70%) is used as an excellent emulsion stabilizer that provides freeze/thaw and ionic stability.
Ungraded products supplied by Spectrum are indicative of a grade suitable for general industrial use or research purposes and typically are not suitable for human consumption or therapeutic use.


Recommended use of Triton X-405 (70%): Surfactant
Triton X-405 (70%) is used Agrochemicals, Paints and coatings dispersions, Iodophors, Emulsion polymerization, and Fiber lubricants.
Triton X-405 (70%) is used Emulsion polymerization, Paint, Floor polishing, Wax emulsion, and Agrochemicals.



BENEFITS OF TRITON X-405 (70%):
*Excellent steric and freeze/thaw stabilizer
*Effective pigment and carbon black dispersant
*Excellent for aromatic, chlorinated and other difficult-to-emulsify compounds
*Good solubility in the presence of salts or electrolytes
*Provides lubricity



PHYSICAL and CHEMICAL PROPERTIES of TRITON X-405 (70%):
Physical Form: Liquid
Physical state: clear, liquid
Color: yellow
Odor: mild
Melting point/freezing point:
Freezing point: -9 °C
Initial boiling point and boiling range: 101 °C at 1.013 hPa - The value is calculated
Flammability (solid, gas): No data available
Upper/lower flammability or explosive limits: No data available
Flash point: No data available
Autoignition temperature: No data available
Decomposition temperature: No data available
pH: No data available

Viscosity
Viscosity, kinematic: 665 mm2/s at 25 °C - The value is calculated
Viscosity, dynamic: No data available
Water solubility: No data available
Partition coefficient: n-octanol/water: No data available
Vapor pressure: 20 hPa at 20 °C - The value is calculated
Density: 1,096 g/cm3 at 25 °C
Relative density: No data available
Relative vapor density: No data available
Particle characteristics: No data available
Explosive properties: Not classified as explosive.
Oxidizing properties: none
Other safety information: No data available

CMC: 0.81 mM
concentration: 70% in H2O
density: 1.096 g/mL at 25 °C
description: non-ionic
HLB: 17.6
InChI key: HNLXNOZHXNSSPN-UHFFFAOYSA-N
InChI: 1S/C28H50O8/c1-27(2,3)24-28(4,5)25-6-8-26(9-7-25)36-23-22-35-21-20-34-19-18-33-17-16-32-15-14-31-13-12-30-11-10-29/h6-9,29H,10-24H2,1-5H3
mol wt: ~1967.0 g/mol
Quality Level: 200
SMILES string: CC(C)(C)CC(C)(C)c1ccc(OCCOCCOCCOCCOCCOCCOCCO)cc1
transition temp cloud point: >100 °C
Color: Yellow
Evaporation Rate: 0.70 - 0.79
Flash Point: Not applicable
Kinematic Viscosity: 665 mm2/s @ 25 °C (77 °F)

Odor: Mild
pH: 6 - 10.3 @ 20 - 25 °C (68 - 77 °F)
Relative Density: 1.076 - 1.10 @ 20 °C (68 °F) Reference Material: (water = 1)
Relative Vapor Density: 0.62 @ 20 - 25 °C (68 - 77 °F)
Solubility in Water: completely soluble
Vapor Pressure: 15 - 17 mmHg @ 20 °C (68 °F)
Form: Liquid
Appearance: liquid
Boiling Point: 101 °C (214 °F)
Appearance (Clarity): Clear
Appearance (Colour): Colourless
Appearance (Form): Liquid
pH 1% in Isopropanol: Water(10:6): 7.0 - 9.0
Density (g/ml) @ 25°C: 1.095 �- 1.097 g/ml



FIRST AID MEASURES of TRITON X-405 (70%):
-Description of first-aid measures:
*General advice:
Show this material safety data sheet to the doctor in attendance.
*If inhaled:
After inhalation:
Fresh air.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with water/ shower.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Immediately call in ophthalmologist.
Remove contact lenses.
*If swallowed:
After swallowing:
Immediately make victim drink water (two glasses at most).
Consult a physician.
-Indication of any immediate medical attention and special treatment needed:
No data available



ACCIDENTAL RELEASE MEASURES of TRITON X-405 (70%):
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Observe possible material restrictions.
Take up with liquid-absorbent material.
Dispose of properly.
Clean up affected area.



FIRE FIGHTING MEASURES of TRITON X-405 (70%):
-Extinguishing media:
*Suitable extinguishing media:
Water
Foam
Carbon dioxide (CO2)
Dry powder
*Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Prevent fire extinguishing water from contaminating surface water or the ground water system.



EXPOSURE CONTROLS/PERSONAL PROTECTION of TRITON X-405 (70%):
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Tightly fitting safety goggles
*Skin protection:
Handle with gloves.
Wash and dry hands.
Full contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min
Splash contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min
*Body Protection:
protective clothing
*Respiratory protection
Recommended Filter type: Filter type ABEK
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of TRITON X-405 (70%):
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.



STABILITY and REACTIVITY of TRITON X-405 (70%):
-Reactivity:
No data available
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .
-Possibility of hazardous reactions:
No data available
-Conditions to avoid:
no information available



SYNONYMS:
4-(1,1,3,3-Tetramethylbutyl)phenyl-polyethylene glycol solution
Polyethylene glycol tert-octylphenyl ether
Polyoxyethylene (40) isooctylphenyl ether
Polyethylene glycol tert-octylphenyl ether
Octylphenol Ethoxylate
4-(1,1,3,3-Tetramethylbutyl)phenyl-polyethylene glycol solution
Polyethylene glycol tert-octylphenyl ether
Polyoxyethylene (40) isooctylphenyl ether

Tri butyl phosphate
Calcium Phosphate Tribasic; Tricalcium diphosphate; Bone phosphate; Calcium orthophosphate; Calcium Phosphate; Calcium phosphate (3:2); Calcium tertiary phosphate; Phosphoric acid, calcium salt (2:3); Phosphoric acid, calcium(2+) salt (2:3); Tertiary calcium phosphate; Tribasic calcium phosphate; Tricalcium orthophosphate CAS NO: 7758-87-4
Tri Kalsiyum Fosfat
Aluminium triacetate, EC / List no.: 205-354-1; CAS no.: 139-12-8; Mol. formula: C4H7AlO5Nom INCI : ALUMINUM ACETATE; Acetic acid, aluminum salt; Acetic acid, aluminum salt (3:1); Aluminum acetate. Nom chimique : Acetic acid, aluminum salt (3:1); N° EINECS/ELINCS : 205-354-1.Le triacétate d'aluminium, officiellement appelé acétate d'aluminium, est un composé chimique de composition Al ₃. Dans des conditions standard, il apparaît sous la forme d'un solide blanc soluble dans l'eau qui se décompose en chauffant à environ 200 ° C. Ses fonctions (INCI): Antimicrobien : Aide à ralentir la croissance de micro-organismes sur la peau et s'oppose au développement des microbes. Astringent : Permet de resserrer les pores de la peau. Aluminium triacetate , formellement nommé l' acétate d'aluminium , est un composé chimique de composition Al (CH3 CO2 )3 . Sousconditions standardil apparaît comme un blanc,eausolublesolide quidécompose en chauffant à environ 200 ° C. Les triacétatehydrolysesà un mélange d'hydroxyde / acétate basiquesels, etmultiples espèces coexistent enéquilibre chimique,particulier danssolutions aqueuses de l'ion acétate; l'acétate d'aluminium de nom est couramment utilisé pour ce système mixte. Elle a des applications thérapeutiques pour ses propriétés anti-démangeaisons, astringent et antiseptique propriétés, et, comme un over-the-counter préparation comme la solution de Burow , il est utilisé pour traiter les infections de l' oreille . Les préparations de solution de Burow ont été dilués et modifiés avec des acides aminés pour les rendre plus agréables au goût pour l' utiliser comme gargarisme pour des conditions telles que les ulcères aphteux de la bouche. En médecine vétérinaire , la propriété d'aluminium triacétate astringence est utilisé pour traiter la maladie Mortellaro chez les animaux ongulés comme les bovins. Aluminium triacetate est utilisé comme mordant agent avec des colorants tels que l' alizarine , à la fois seuls et en combinaison. En collaboration avec le diacétate d'aluminium ou d' aluminium sulfacetate il est utilisé avec du coton , d' autres cellulose des fibres, et la soie . Il a également été associé à l' acétate ferreux pour produire des couleurs différentes. Aluminum triacetate Aluminium acetate 139-12-8 [RN] 80EHD8I43D Acetic acid, aluminum salt (3:1) Aluminium triacetate Aluminiumtriacetat [German] Aluminum acetate [USP] ALUMINUM ACETATE, BASIC BASIC ALUMINUM ACETATE Triacétate d'aluminium [French] 142-03-0 [RN] 205-518-2 [EINECS] 8006-13-1 [RN] 954145-33-6 [RN] ACETIC ACID, ALUMINUM SALT ALUMINIUM(3+) ION TRIACETATE ALUMINIUM(3+) TRIACETATE aluminium(iii)-acetate Aluminiumacetat ALUMINUM ACETATE SOLUTION Aluminum triacetic acid aluminum triethanoate ALUMINUM(III) ACETATE BIS(ACETYLOXY)ALUMANYL ACETATE Buro-Sol Concentrate Burow Burow solution diacetyloxyalumanyl acetate Domeboro [Wiki] EINECS 205-354-1 HYDROXYALUMINIUM DI(ACETATE) Otic Domeboro
Triacétate d'aluminium ( ALUMINUM ACETATE)
1,2,3-Propanetriyl triacetate; Enzactin; Fungacetin; Glycerin triacetate; Triacetylglycerol; Glycerol triacetate; Glyceryl triacetate; Glyped; Kesscoflex TRA; Triacetine; Vanay; Glycerol triacetate tributyrin; Triacetyl glycerine; Propane-1,2,3-triyl triacetate CAS NO: 102-76-1
Triacetin
1,2,3-Propanetriyl triacetate; Enzactin; Fungacetin; Glycerin triacetate; Triacetylglycerol; Glycerol triacetate; Glyceryl triacetate; Glyped; Kesscoflex TRA; Triacetine; Vanay; Glycerol triacetate tributyrin; Triacetyl glycerine; Propane-1,2,3-triyl triacetate CAS NO:102-76-1
Triazine
Triazine Tris Aminohexanoic Acid; Hexanoic acid, 6,6',6''-(1,3,5-triazine-2,4,6-triyltriimino)tris-; 2,4,6-Tri-(6-aminocaproic acid)-1,3,5-triazine; 6,6',6''-((1,3,5-Triazine-2,4,6-triyl)tris(azanediyl))trihexanoic acid; CAS NO: 80584-91-4
Triazine Tris Aminohexanoic Acid
6,6',6''-((1,3,5-Triazine-2,4,6-triyl)tris(azanediyl))trihexanoic acid; 2,4,6-Tri-(6-aminocaproic acid)-1,3,5-triazine;Hexanoic acid; 6,6',6''-(1,3,5-triazine-2,4,6-triyltriimino)tris-6-[[4,6-bis(5-carboxypentylamino)-1,3,5-triazin-2-yl]amino]hexanoic acid CAS NO: 80584-91-4
Triazinetrisaminohexanoic Acid
N° CAS : 555-32-8; Nom INCI : ALUMINUM BENZOATE. Nom chimique : Aluminium tribenzoate; Aluminium tribenzoate. Aluminum benzoate; Benzoic acid, aluminum salt; Benzoic acid, aluminum salt (3:1); : aluminium(3+) tribenzoate; aluminum tribenzoate; ( aluminum;tribenzoate). N° EINECS/ELINCS : 209-091-3. Ses fonctions (INCI) : Antimicrobien : Aide à ralentir la croissance de micro-organismes sur la peau et s'oppose au développement des microbes. Agent de contrôle de la viscosité : Augmente ou diminue la viscosité des cosmétiques. 209-091-3 [EINECS]. 555-32-8 [RN] Aluminium tribenzoate Aluminiumtribenzoat [German] Aluminum benzoate Aluminum tribenzoate Benzoic acid, aluminum salt (3:1) Tribenzoate d'aluminium [French] Aluminium benzoate ALUMINIUM(3+) ION TRIBENZOATE BENZOIC ACID, ALUMINUM SALT BIS(BENZOYLOXY)ALUMANYL BENZOATE EINECS 209-091-3 MFCD00050764
Tribenzoate d'aluminium ( ALUMINUM BENZOATE)
Tri(butyl cellosolve) phosphate; Tris(2-butoxyethyl) phosphate; TBEP; 2-Butoxyethanol phosphate; Phosphoric acid tris(2-butoxyethyl)ester; Tributyl cellosolve phosphate; Tri(2-butoxyethanol) phosphate CAS NO: 78-51-3
Tricaprylate/caprate de glycérol
Ethylene trichloride, 1,1,2-Trichloroethene; 1,1-Dichloro-2-Chloroethylene; 1-Chloro-2,2-Dichloroethylene; Acetylene Trichloride; TCE; Trethylene; Triclene; Tri; Trimar; Trilene; HCC-1120; Trichloroethene; TCE CAS NO:79-01-6
Trichloroethylene
SYNONYMS symclosene; Trichloroiminocyanuric acid; 1,3,5-Trichloro-S-triazine-2,4,6-trione; 1,3,5-trichloro-1,3,5-triazine-2,4,6(1H,3H,5H)-trione; 1,3,5-Trichloroisocyanuric acid; 1,3,5-Trichloro-s-triazine-2,4,6(1H,3H,5H)-trione; Isocyanuric chloride; CAS NO. 87-90-1
Trichloroisocyanuric Acid
Trichloroiminocyanuric acid; 1,3,5-Trichloro-S-triazine-2,4,6-trione; 1,3,5-trichloro-1,3,5-triazine-2,4,6(1H,3H,5H)-trione; 1,3,5-Trichloroisocyanuric acid; 1,3,5-Trichloro-s-triazine-2,4,6(1H,3H,5H)-trione; Isocyanuric chloride; Trichlor; Isocyanuric chloride; Chloreal; Symclosene Trichloro-s-triazinetrione; TCICA; TCCA CAS NO:87-90-1
Tricresyl phosphate
TCP; Tritolyl phosphate; Phosphoric acid tritolyl ester; Cresyl phosphate; Tris(methylphenyl)ester of phosphoric acid; Phosphoric acid tris(methylphenyl) ester; Tricresyl phosphates; Tritolyl phosphate; Tricresyl phosphate; Phosphoric acid tolyl ester; Thiorthocresyl phosphate; Tris(tolyloxy)phosphine oxide; Plasticizer TCP; Tritolylfosfat; Tricresilfosfati; Phosphate de tricresyle; EPA Pesticide Chemical Code 083401; Kronitex; Lindol CAS NO: 1330-78-5 (Mixture) 78-30-8 (Tri-o-cresyl phosphate) 563-04-2 (Tri-m-cresyl phosphate) 78-32-0 (Tri-p-cresyl phosphate)
Triethanol Amine
2,2',2''-Nitrilotriethanol; Tris(2-hydroxyethyl)amine; Triethylolamine; 2,2′,2″-Trihydroxytriethylamine; Trolamine; TEA; TELA; TEOA CAS:102-71-6
Triethanolamine ( Tri éthanolamine 85%)
Triglycol; TEG; 2,2'-ethylenediqxybis(ethanol); 3,6-Dioxa-1,8-octanediol; Glycol Bis(Hydroxyethyl) Ether; Di-beta-Hydroxyethoxyethane; 1,2-bis(2-hydroxyethoxy)ethane; 3,6-dioxaoctane-1,8-diol; 2,2'-(1,2-ethanediylbis(oxy)) bisethanol; ethylene glycol dihydroxydiethyl ether; Trigol; Ethylene glycol-bis-(2-hydroxyethyl) ether; 1,2-Bis(2-hydroxy)ethane; Ethylene glycal-bis-(2-hydroxyethyl ether); Trigen CAS NO: 112-27-6
TRİETHYLENE GLYCOL
Triethylene glycol, TEG, or triglycol is a colorless odorless viscous liquid with molecular formula HOCH2CH2OCH2CH2OCH2CH2OH.
Triethylene glycol is clear, has a mild odor and is not extremely viscous.
Triethylene glycol has good solvency for a wide range of organic compounds, including hydrocarbons, oils, resins, and dyes.

CAS Number: 112-27-6
Molecular Formula: C6H14O4
Molecular Weight: 150.17
EINECS Number: 203-953-2

Triethylene glycol is an additive for hydraulic fluids and brake fluids and is used as a base for "smoke machine" fluid in the entertainment industry.
Triethylene glycol are also used as liquid desiccants for natural gas and in air conditioning systems.
When aerosolized Triethylene glycol acts as a disinfectant.

Triethylene glycol belongs to the class of organic compounds known as polyethylene glycols.
These are oligomers or polymers of ethylene oxide, with the general formula (C2H4O)n (with n>=3).
Triethylene glycol, clear, colorless, syrupy (viscous) liquid at room temperature.

Triethylene glycol, often colored fluorescent yellow-green when used in automotive antifreeze.
Ethylene glycol is a useful industrial compound found in many consumer products.
Triethylene glycol include antifreeze, hydraulic brake fluids, some stamp pad inks, ballpoint pens, solvents, paints, plastics, films, and cosmetics.

Triethylene glycol can also be a pharmaceutical vehicle.
Ethylene glycol has a sweet taste and is often ingested by accident or on purpose.
Ethylene glycol breaks down into toxic compounds in the body.

Ethylene glycol and its toxic byproducts first affect the central nervous system (CNS), then the heart, and finally the kidneys.
Ethylene glycol is odorless.
Triethylene glycol is a chemical compound with the chemical formula C6H14O4 that is categorized as an alcohol.

Triethylene glycol, at room temperature it is a liquid.
Triethylene glycol is soluble in water.
Triethylene glycol (TEG) is a colorless, odorless liquid with the chemical formula C6H14O4.

Triethylene glycol belongs to a group of chemicals known as glycols and is composed of three ethylene glycol units connected by oxygen atoms.
Triethylene glycol is hygroscopic, meaning it readily absorbs moisture from the air.
Triethylene glycol is primarily used as a solvent, particularly in industrial applications.

This makes it useful in various processes such as oil and gas production, natural gas dehydration, and as a solvent in the production of pharmaceuticals, cosmetics, and synthetic fibers.
One of the most notable applications of triethylene glycol is its use as a desiccant or a drying agent.

Due to its hygroscopic nature, it can effectively remove water from gas streams and maintain low levels of moisture.
Triethylene glycol is particularly important in natural gas processing, where Triethylene glycol is commonly employed to remove water vapor and other impurities from natural gas.

Triethylene glycol finds use in the production of polyesters, plasticizers, and as a component in some antifreeze formulations.
Triethylene glycol can also be found in certain personal care products, such as deodorants and cosmetics, as a moisturizing agent.
It's worth noting that triethylene glycol should not be confused with ethylene glycol, a different compound that is toxic and primarily used as an automotive antifreeze.

Triethylene glycols are part of the glycol family, they have different chemical structures and properties.
Triethylene glycol can cause material corrosion because of its acidic nature.
Care should be taken to mitigate corrosion concerns when using triethylene glycol through appropriate material selection, use of coatings and use of corrosion inhibitors.

High temperature environments can see high rates of corrosion with triethylene glycol.
Triethylene glycol is most commonly used for natural gas dehydration to strip the water out of the gas.
Triethylene glycol is wildly used in applications which require higher boiling point, higher molecular weight with low volatility such as plasticizer, unsaturated polyester resin, emulsifiers, lubricants, heat transfer fluids and solvent for equipment cleaning, printing ink.

Triethylene Glycol (TEG) is a liquid chemical compound with the molecular formula C6H14O4 or HOCH2CH2CH2O2CH2OH.
Triethylene glycol is recognized for its hygroscopic quality and ability to dehumidify fluids.
Triethylene glycol is miscible with water and soluble in ethanol, acetone, acetic acid, glycerine, pyridine, and aldehydes.

Triethylene glycol is slightly soluble in diethyl ether, and insoluble in oil, fat, and most hydrocarbons.
Triethylene glycol is commercially produced as a co-product of the oxidation of ethylene at a high temperature in the presence of silver oxide catalyst, followed by hydration of ethylene oxide to yield mono, di, tri, and tetraethylene glycols.

The oil and gas industries use Triethylene glycol to dehydrate natural gas as well as other gases including CO2, H2S, and other oxygenated gases.
Industrial uses include adsorbents and absorbents, functional fluids in both closed and open systems, Intermediates, petroleum production processing aids, and solvents.

Triethylene glycol is used in the manufacture of a host of consumer products that include anti-freeze, automotive care products, building and construction materials, cleaning and furnishing care products, fabric, textile, and leather products, fuels and related products, lubricants and greases, paints and coatings, personal care products, and plastic and rubber products.

Triethylene glycol is a polymer consisting of ethylene glycol monomers and two terminal hydroxyl groups.
The Triethylene glycol chain increases the water solubility of a compound in aqueous media.
Increasing the number of ethylene glycol units within the entire chain improves the solubility properties of the PEG linker.

Triethylene Glycol (TEG) is the third members of a homologous series of dihydroxyalcohols.
Triethylene glycol is produced in the Master Process by the direct hydration of ethylene oxide.
Triethylene glycol is co-produced with MEG and DEG. TEG is a colourless liquid.

The main uses for triethylene glycol are based upon its hygroscopic quality.
Triethylene glycol is used as a dehydrating agent for natural gas pipelines where it removes the water from the gas before being condensed and reused in the system.
Triethylene glycol is also a dehumidifying agent in air-conditioning units.

Triethylene glycol is also used to make chemical intermediates such as plasticisers and polyester resins.
Triethylene glycol is an additive in hydraulic fluids and brake fluids, and Triethylene glycol is also used as a solvent in many applications, including as a selective solvent for aromatics, and a solvent in textile dyeing.

Triethylene glycol (also known as TEG, triglycol and trigen) is a colourless, viscous, non-volatile liquid with the formula C6H14O4.
Triethylene glycol is well known for its hygroscopic quality and its ability to dehumidify fluids.
Triethylene glycol is prepared commercially as a co-product of the oxidation of ethylene at high temperature, in the presence of a silver oxide catalyst.

The ethylene oxide is then hydrated to yield mono, di, tri, and tetra ethylene glycols.
Triethylene glycol also has mild disinfectant qualities and, when volatised, is used as an air disinfectant for virus and bacteria control.
Triethylene glycol is a clear, colorless, viscous, stable liquid with a slightly sweetish odor.

Soluble in water; immiscible with benzene, toluene, and gasoline.
Because Triethylene glycol has two ether and two hydroxyl groups its chemical properties are closety related to ethers and primary alcohols.
Triethylene glycol is a good solvent for gums, resins, nitrocellulose, steam-set printing inks and wood stains.

With a low vapor pressure and a high boiling point, its uses and properties are similar to those of ethylene glycol and diethylene glycol.
Because Triethylene glycol is an efficient hygroscopic agent it serves as a liquid desiccant for removing water from natural gas.
Triethylene glycol is also used in air conditioning systems designed to dehumidify air.

Triethylene glycol is a member of a homologous series of dihydroxy alcohols.
Triethylene glycol is a colorless, odorless and stable liquid with high viscosity and a high boiling point.

Apart from its use as a raw material in the manufacture and synthesis of other products, Triethylene glycol is known for its hygroscopic quality and its ability to dehumidify fluids.
This liquid is miscible with water, and at standard atmospheric pressure (101.325 kPa) has a boiling point of 286.5 °C and a freezing point of −7 °C. It is also soluble in ethanol, acetone, acetic acid, glycerine, pyridine, aldehydes; slightly soluble in diethyl ether; and insoluble in oil, fat and most hydrocarbons.

Melting point: −7 °C(lit.)
Boiling point: 125-127 °C0.1 mm Hg(lit.)
Density: 1.124 g/mL at 20 °C(lit.)
vapor density: 5.2 (vs air)
vapor pressure: refractive index: n20/D 1.455(lit.)
Flash point: 165 °C
storage temp.: Store below +30°C.
solubility H2O: 50 mg/mL at 20 °C, clear, colorless
form: Viscous Liquid
pka: 14.06±0.10(Predicted)
color: Clear very slightly yellow
PH: 5.5-7.0 (25℃, 50mg/mL in H2O)
Odor: Very mild, sweet.
explosive limit: 0.9-9.2%(V)
Water Solubility: SOLUBLE
Sensitive: Hygroscopic
λmax λ: 260 nm Amax: 0.06
λ: 280 nm Amax: 0.03
Merck: 14,9670
BRN: 969357
Stability: Stable. Combustible. Incompatible with strong oxidizing agents.
LogP: -1.75 at 25℃

Triethylene glycol is prepared commercially as a co-product of the oxidation of ethylene at high temperature in the presence of silver oxide catalyst, followed by hydration of ethylene oxide to yield mono(one)-, di(two)-, tri(three)- and tetraethylene glycols.
Triethylene glycol is well established as a relatively mild disinfectant toward a variety of bacteria, influenza A viruses and spores of Penicillium notatum fungi.

Triethylene glycols exceptionally low toxicity, broad materials compatibility, and low odor combined with its antimicrobial properties indicates that it approaches the ideal for air disinfection purposes in occupied spaces.[4] Much of the scientific work with triethylene glycol was done in the 1940s and 1950s, however that work has ably demonstrated the antimicrobial activity against airborne, solution suspension, and surface bound microbes.

Triethylene glycol can be stored and transported in stainless steel, aluminium or lined tank cars, tank trucks, or 225 kg drums.
Triethylene glycol (TEG) is a colorless, viscous liquid with a slight odor.
Triethylene glycol is non-flammable, mildly toxic, and considered non-hazardous.

Triethylene glycol is a member of a homologous series of dihydroxy alcohols.
Triethylene glycol is used as a plasticizer for vinyl polymers as well as in the manufacture of air sanitizer and other consumer products.

Triethylene glycol is commonly used as an ingredient in antifreeze formulations.
Triethylene glycol helps lower the freezing point of water, preventing the coolant in automotive engines and HVAC systems from solidifying in cold temperatures.
Triethylene glycol is a humectant, which means it has the ability to attract and retain moisture.

Triethylene glycol is used in a variety of personal care products like moisturizers, lotions, and soaps to prevent them from drying out and to provide hydration to the skin.
Triethylene glycol is employed in air conditioning systems as a desiccant to remove moisture from the air.
By reducing the humidity, it helps enhance the efficiency and performance of the cooling process.

Triethylene glycol serves as a precursor or intermediate in the production of other chemicals.
Triethylene glycol can be used to synthesize polyester resins, polyurethanes, plasticizers, and synthetic lubricants.

Triethylene glycol is utilized in the natural gas industry for gas conditioning processes.
Triethylene glycol helps remove contaminants such as sulfur compounds and other impurities, making the gas suitable for transportation and commercial use.
Due to its excellent solvent properties, Triethylene glycol is employed in the formulation of dyes, inks, and pigments.

Triethylene glycol helps dissolve and disperse colorants effectively, facilitating their application in various industries.
Triethylene glycol is used in some pharmaceutical formulations as a stabilizer, solvent, or excipient.
Triethylene glycol can improve the solubility and stability of certain drugs and aid in the delivery of active ingredients.

Triethylene glycol finds applications in laboratories as a solvent for chemical reactions, extraction processes, and chromatography.
Triethylene glycols ability to dissolve a wide range of substances makes it useful in various analytical and research procedures.
The hydroxyl groups on triethylene glycol undergo the usual alcohol chemistry giving a wide variety of possible derivatives.

Triethylene glycols can be converted to aldehydes, alkyl halides, amines, azides, carboxylic acids, ethers, mercaptans, nitrate esters, nitriles, nitrite esters, organic esters, peroxides, phosphate esters and sulfate esters.
Triethylene glycolis a ether-alcohol derivative.
The ether being relatively unreactive.

Triethylene glycol, flammable and/or toxic gases are generated by the combination of alcohols with alkali metals, nitrides, and strong reducing agents.
Triethylene glycol react with oxoacids and carboxylic acids to form esters plus water.
Oxidizing agents convert alcohols to aldehydes or ketones.

Triethylene glycol, alcohols exhibit both weak acid and weak base behavior.
Triethylene glycol may initiate the polymerization of isocyanates and epoxides.

Eastman Triethylene glycol Plasticizer is compatible with PVC and with PVB resins.
Triethylene glycol offers low color, low viscosity and low volatility during processing.
The low viscosity makes Eastman TEG-EH particularly suitable for use in plastisols to improve the processing characteristics.

In PVC, Triethylene glycol is generally blended with plasticizers such as DOP or DOTP for optimum performance.
Triethylene glycol offers low viscosity for ease of compounding and low color for excellent clarity in automotive and residential and commercial window applications.
Triethylene glycol is commonly used in natural gas sweetening processes to remove acidic gases such as carbon dioxide (CO2) and hydrogen sulfide (H2S).

Triethylene glycol acts as a selective solvent, absorbing these impurities from the gas stream and allowing for the production of cleaner natural gas.
Triethylene glycol is used as a deicing agent for aircraft and runways.
Triethylene glycols low freezing point and ability to mix with water make it effective in preventing the formation of ice and snow on surfaces, ensuring safer conditions for aviation and transportation.

Triethylene glycol can act as a preservative due to its ability to inhibit the growth of microorganisms.
Triethylene glycol is used in some cosmetic and personal care products, such as creams and lotions, to extend their shelf life and prevent bacterial or fungal contamination.
Triethylene glycol is sometimes added to gasoline as an octane booster or fuel system cleaner.

Triethylene glycol can improve the combustion efficiency of gasoline, resulting in enhanced engine performance and reduced emissions.
Triethylene glycol is utilized as a heat transfer fluid in various industrial processes.
Triethylene glycols high boiling point, low volatility, and thermal stability make it suitable for applications where controlled and efficient heat transfer is required, such as in heating systems, solar thermal collectors, and chemical reactors.

Triethylene glycol is used in the textile industry for processes like dyeing, printing, and finishing.
Triethylene glycol acts as a solvent for dyes and helps facilitate their penetration into fibers, resulting in vibrant and long-lasting colors.

Triethylene glycol is employed in the electronics industry to control moisture levels during the manufacturing and storage of sensitive electronic components.
Triethylene glycol helps prevent moisture-related damage, such as corrosion or malfunction, in electronic devices.

Uses
Triethylene glycol is used by the oil and gas industry to "dehydrate" natural gas.
It may also be used to dehydrate other gases, including CO2, H2S, and other oxygenated gases.
Triethylene glycol is necessary to dry natural gas to a certain point, as humidity in natural gas can cause pipelines to freeze, and create other problems for end users of the natural gas.

Triethylene glycol is placed into contact with natural gas, and strips the water out of the gas.
Triethylene glycol is heated to a high temperature and put through a condensing system, which removes the water as waste and reclaims the Triethylene glycol for continuous reuse within the system.
The waste TEG produced by this process has been found to contain enough benzene to be classified as hazardous waste (benzene concentration greater than 0.5 mg/L).

Triethylene glycol is a solvent prepared from ethylene oxide and ethylene glycol.
Triethylene glycol can be used: To prepare fatty acid gelators, which are used to gelate various edible and vegetable oils.
The triethylene glycol can then be continually reused, although the by-product of benzene needs to be disposed of carefully.

This process is useful as Triethylene glycol prevents the gas from freezing making the gas easier to transport and manage for end consumers.
The manufacturing processes of certain types of polymers frequently use triethylene glycol as a plasticizer, which means it reduces brittleness and increases ductility when added to certain types of resins.

One of the most popular materials triethylene glycol is used for as a plasticizer is vinyl polymers.
Materials such as polyvinyl chloride (PVC) and polyvinyl butyral are commonly made using triethylene glycol.
This makes triethylene glycol a key ingredient in items such as automotive parts and coatings.

Triethylene glycol is widely used for the dehydration of natural gas.
Triethylene glycol helps remove water vapor from the gas stream, preventing the formation of hydrates that can cause blockages in pipelines and equipment.
Triethylene glycol is used as a plasticizer for vinyl polymers.

Triethylene glycol is also used in air sanitizer products, such as "Oust" or "Clean and Pure".
Triethylene glycol is an ingredient in antifreeze formulations.
Triethylene glycol lowers the freezing point of water, preventing the coolant in automotive engines and HVAC systems from freezing in cold temperatures.

Triethylene glycol is utilized in cosmetics and personal care products such as moisturizers, lotions, and soaps.
Triethylene glycol helps retain moisture and keeps the skin hydrated.
Triethylene glycol acts as a desiccant in air conditioning systems, reducing the humidity in the air to enhance cooling efficiency and prevent condensation.

Triethylene glycol is used as a solvent for dyes, inks, and pigments in industries such as printing and textile manufacturing.
It helps dissolve and disperse colorants effectively.

Triethylene glycol is employed in gas conditioning processes to remove impurities such as sulfur compounds from natural gas, making it suitable for transportation and commercial use.
Triethylene glycol serves as a precursor or intermediate in the production of various chemicals, including polyester resins, polyurethanes, plasticizers, and synthetic lubricants.

Triethylene glycol is used as a deicing agent for aircraft and runways.
Triethylene glycols low freezing point and ability to mix with water make it effective in preventing ice formation.

Triethylene glycol acts as a preservative in certain products, extending their shelf life and preventing microbial growth.
Triethylene glycol is used in cosmetics, pharmaceuticals, and other formulations.
Triethylene glycol serves as a heat transfer fluid in industrial processes that require controlled and efficient heat transfer, such as in heating systems and chemical reactors.

Triethylene glycol, as a solvent to prepare superparamagnetic iron oxide nanoparticles for in situ protein purification.
As an absorbent agent in the subsea natural gas dehydration process.
Triethylene glycol is used as a plasticizer, as an additive for hydraulic fluids and brake fluids, and as a disinfectant.

Triethylene glycol is an active component of certain pigments, printing dyes, inks and paste.
Triethylene glycol finds application as a liquid desiccant and used in the dehydration of natural gas, carbon dioxide, hydrogen sulfide and air conditioning systems.
Triethylene glycol plays as an important role in anti-freeze and de-icing products, cleaning and furnishing care products, lubricant and greases.

Triethylene glycol is widely used as an excellent dehydrating agent for natural gas, oilfield associated gas and carbon dioxide; Used as solvent for nitrocellulose, rubber, resin, grease, paint, pesticide, etc; Used as air bactericide; Used as triethylene glycol ester plasticizer for PVC, polyvinyl acetate resin, glass fiber and asbestos pressing board; Used as anti drying agent of tobacco, fiber lubricant and desiccant of natural gas; It is also used in organic synthesis, such as the production of brake oil with high boiling point and good low temperature performance.

Triethylene glycol can be used in gas chromatography as extractant.
Triethylene glycol is employed in the sweetening or purification of natural gas.
Triethylene glycol helps remove acidic gases, such as carbon dioxide (CO2) and hydrogen sulfide (H2S), which can be corrosive or undesirable in gas pipelines and end-use applications.

Triethylene glycol is sometimes used as an additive in gasoline and diesel fuel formulations.
It can improve the combustion characteristics, enhance fuel stability, and reduce emissions.
Triethylene glycol is utilized in the electronics industry to control moisture levels during the manufacturing and storage of electronic components.

Triethylene glycol helps prevent moisture-related damage and ensures the integrity and reliability of electronic devices.
Triethylene glycolis used as an additive in the production of tobacco products such as cigarettes and cigars.
It helps maintain moisture levels and preserve the freshness of the tobacco.

Triethylene glycolfinds use in laboratories for various purposes.
Triethylene glycol can be used as a solvent for chemical reactions, extractions, and chromatography.
Triethylene glycols properties make it suitable for sample preparation and analysis in research and analytical laboratories.

Triethylene glycol is employed in the formulation of adhesives and sealants.
Triethylene glycol can serve as a solvent or plasticizer, helping to improve the workability, flexibility, and durability of these products.

Triethylene glycol is used in the production of construction materials such as cement and grouts.
Triethylene glycol can help enhance the workability, flow, and setting properties of these materials.
Triethylene glycolis sometimes incorporated into metalworking fluids, which are used in machining and cutting operations.

Triethylene glycol helps cool and lubricate the metal surfaces, reducing friction and improving tool life.
Triethylene glycolmay be used in pharmaceutical formulations as a solvent or co-solvent.
It can aid in solubilizing certain drugs and assist in drug delivery systems.

Food and beverage industry: Triethylene glycol may find limited use in the food and beverage industry as a solvent or flavor carrier, although its usage is less common compared to other glycols like propylene glycol.
Triethylene Glycol is widely used as a solvent.

Triethylene glycol has a high flash point, emits no toxic vapors, and is not absorbed through the skin.
Triethylene glycol is used in the following products: inks and toners, coating products, heat transfer fluids, lubricants and greases and hydraulic fluids.

Other release to the environment of Triethylene glycol is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners), outdoor use, indoor use in close systems with minimal release (e.g. cooling liquids in refrigerators, oil-based electric heaters) and outdoor use in close systems with minimal release (e.g. hydraulic liquids in automotive suspension, lubricants in motor oil and break fluids).

Triethylene glycol can be found in products with material based on: paper (e.g. tissues, feminine hygiene products, nappies, books, magazines, wallpaper), plastic (e.g. food packaging and storage, toys, mobile phones), fabrics, textiles and apparel (e.g. clothing, mattress, curtains or carpets, textile toys), metal (e.g. cutlery, pots, toys, jewellery), stone, plaster, cement, glass or ceramic (e.g. dishes, pots/pans, food storage containers, construction and isolation material), leather (e.g. gloves, shoes, purses, furniture), rubber (e.g. tyres, shoes, toys) and wood (e.g. floors, furniture, toys).

Triethylene glycol monomethyl ether can be used as a reagent and solvent for applications such as: modification of anthraquinone material for redox flow batteriespreparation of polymeric electrolyte for electrochemical devices,formation of the binary system of polyethylene glycol for absorption of silica.
Triethylene glycol can be found in complex articles, with no release intended: vehicles, machinery, mechanical appliances and electrical/electronic products (e.g. computers, cameras, lamps, refrigerators, washing machines) and electrical batteries and accumulators.

Reactivity Profile
Triethylene glycol is a ether-alcohol derivative.
The ether being relatively unreactive.
Triethylene glycol, flammable and/or toxic gases are generated by the combination of alcohols with alkali metals, nitrides, and strong reducing agents.

Triethylene glycol react with oxoacids and carboxylic acids to form esters plus water.
Oxidizing agents convert alcohols to aldehydes or ketones.
Alcohols exhibit both weak acid and weak base behavior.

Health Hazard
Under normal conditions of use, Triethylene Glycol (TEG) is not expected to cause irritation to the skin, eyes or respiratory tract.
However, in applications where vapours or mists are created, inhalation may cause irritation to the respiratory system.
Triethylene glycol is not flammable, unless preheated.

Skin and eye irritation:
Triethylene glycol can cause irritation to the skin and eyes upon direct contact.
Prolonged or repeated exposure to TEG may lead to redness, itching, and dermatitis.
Eye contact with TEG can result in irritation, redness, and potential damage to the eyes.

Inhalation hazards
Triethylene glycol can be harmful if inhaled in high concentrations or for extended periods.
Inhalation of Triethylene glycol vapor or mist may cause respiratory irritation, coughing, difficulty breathing, and throat irritation.
Triethylene glycol is important to ensure adequate ventilation and use respiratory protection when working with TEG in environments with high vapor concentrations.

Ingestion hazards
Swallowing Triethylene glycol can cause gastrointestinal irritation, nausea, vomiting, and diarrhea.
Ingestion of large amounts or high concentrations of TEG may result in more severe health effects.

Environmental hazards
Triethylene glycol can be toxic to aquatic organisms. Spills or releases of Triethylene glycol into waterways or the environment should be avoided, as it can have harmful effects on aquatic life.

Synonyms
TRIETHYLENE GLYCOL
112-27-6
Triglycol
2,2'-(Ethane-1,2-diylbis(oxy))diethanol
Trigen
Triethylenglykol
2-[2-(2-Hydroxyethoxy)ethoxy]ethanol
Triethyleneglycol
2,2'-Ethylenedioxydiethanol
1,2-Bis(2-hydroxyethoxy)ethane
2,2'-(Ethylenedioxy)diethanol
2,2'-Ethylenedioxybis(ethanol)
3,6-Dioxaoctane-1,8-diol
2,2'-Ethylenedioxyethanol
Di-beta-hydroxyethoxyethane
Glycol bis(hydroxyethyl) ether
Trigol
Caswell No. 888
Ethanol, 2,2'-[1,2-ethanediylbis(oxy)]bis-
Triethylene glcol
Ethylene glycol dihydroxydiethyl ether
2,2'-[ethane-1,2-diylbis(oxy)]diethanol
Bis(2-hydroxyethoxyethane)
TEG
Ethanol, 2,2'-(ethylenedioxy)di-
2,2'-(1,2-Ethanediylbis(oxy))bisethanol
NSC 60758
HSDB 898
Triethylenglykol [Czech]
Ethylene glycol-bis-(2-hydroxyethyl ether)
EINECS 203-953-2
EPA Pesticide Chemical Code 083501
BRN 0969357
CCRIS 8926
2-[2-(2-HYDROXY-ETHOXY)-ETHOXY]-ETHANOL
119438-10-7
DTXSID4021393
UNII-3P5SU53360
CHEBI:44926
AI3-01453
NSC-60758
MACROGOL 150
3P5SU53360
PEG-3
3,6-Dioxa-1,8-octanediol
Di-.beta.-hydroxyethoxyethane
DTXCID601393
Ethanol, 2,2'-(1,2-ethanediylbis(oxy))bis-
EC 203-953-2
4-01-00-02400 (Beilstein Handbook Reference)
NCGC00163798-03
2-[2-(2-hydroxyethoxy)ethoxy]ethan-1-ol
103734-98-1
122784-99-0
137800-98-7
145112-98-7
2,2'-(ethane-1,2-diylbis(oxy))bis(ethan-1-ol)
TRIETHYLENE GLYCOL (USP-RS)
TRIETHYLENE GLYCOL [USP-RS]
MFCD00081839
2-(2-(2-hydroxyethoxy)ethoxy)ethanol
CAS-112-27-6
2-(2-(2-HYDROXY-ETHOXY)-ETHOXY)-ETHANOL
OH-PEG3-OH
Trigenos
triethylenglycol
Trithylne glycol
triethylene-glycol
Triethyleneglycol,
Tri-ethylene glycol
3,8-diol
TEG (CHRIS Code)
TEG (GLYCOL)
Triethylene glycol, puriss.
SCHEMBL14929
WLN: Q2O2O2Q
AMY375
di(2-ethylbutyrate), diacetate
Ethanol,2'-(ethylenedioxy)di-
TRIETHYLENE GLYCOL [MI]
CHEMBL1235259
Triethylene Glycol Reagent Grade
1,8-dihydroxy-3,6-dioxaoctane
TRIETHYLENE GLYCOL [HSDB]
TRIETHYLENE GLYCOL [INCI]
2, 2'- (ethylenedioxy)diethanol
2,2' - (ethylenedioxy)diethanol
TRIETHYLENE GLYCOL DIMALEATE
NSC60758
STR02345
TRIETHYLENE GLYCOL [WHO-DD]
Tox21_112073
Tox21_202440
Tox21_300306
LS-550
MFCD00002880
MFCD01779596
MFCD01779599
MFCD01779601
MFCD01779603
MFCD01779605
MFCD01779609
MFCD01779611
MFCD01779612
MFCD01779614
MFCD01779615
MFCD01779616
STL282716
AKOS000120013
Triethylene Glycol (Industrial Grade)
CS-W018156
DB02327
HY-W017440
USEPA/OPP Pesticide Code: 083501
NCGC00163798-01
NCGC00163798-02
NCGC00163798-04
NCGC00163798-05
NCGC00163798-06
NCGC00254097-01
NCGC00259989-01
1,2-DI(BETA-HYDROXYETHOXY)ETHANE
2-[2-(2-Hydroxyethoxy)ethoxy]ethanol #
BP-21036
OCTANE-1,8-DIOL, 3,6-DIOXA-
Triethylene glycol, ReagentPlus(R), 99%
Ethanol,2'-[1,2-ethanediylbis(oxy)]bis-
FT-0652416
FT-0659862
T0428
EN300-19916
2,2'-(1,2-Ethanediyl bis (oxy))-bisethanol
F71165
2,2'-(Ethylendioxy)diethanol (Triethylenglykol)
Etanol, 2,2'-[1,2-Etanodiilbis (oxi)] bis-
ETHYLENE GLYCOL-BIS(2-HYDROXYETHYL)ETHER
Triethylene glycol, SAJ first grade, >=96.0%
ETHYLENE GLYCOL-BIS-(2-HYDROXYETHYL)ETHER
Q420630
SR-01000944720
Triethylene glycol, Vetec(TM) reagent grade, 98%
J-506706
SR-01000944720-1
ETHANOL, 2,2'-(1,2-ETHANEDIYLBIS (OXY))BIS-
F0001-0256
Triethylene glycol, BioUltra, anhydrous, >=99.0% (GC)
Z104476078
Triethylene glycol, United States Pharmacopeia (USP) Reference Standard

Triflic Acid
Trifluoromethanesulfonic acid; Perfluoromethanesulfonic acid; Trifluormethansulfonsaeure; ácido trifluorometanosulfonico; Acide trifluoromethanesulfonique CAS NO: 1493-13-6
Trifluoroacetic Acid
Triisobutyl phosphate; TIBP; Tri-isobutylphosphate; Isobutyl phosphate; tri-isobutyl phosphate; phosphate; triiso butyl CAS NO: 126-71-6
Triisopropanolamine
Triisopropanolamine; Tris(2-hydroxypropyl)amine;1,1',1''-nitrilotri-2-propanol; Tris-(2-hydroxy-1-propyl)amine; 1,1',1''-Nitrilotripropan-2-ol; Nitrilotris(2-propanol); 3,3',3"-Nitrilotri(2-propanol); Tris(2-propanol)amine; Tri-2-propanolamine; CAS NO: 122-20-3
TRİOCTYL PHOSPHATE
Trioctyl phosphate is an organic chemical compound from the group of phosphoric acid esters (trialkyl phosphates).
Trioctyl phosphate is a colorless, slightly pungent, viscous liquid.
Trioctyl phosphate is an organophosphorus compound that belongs to the class of phosphoric acid esters.

CAS Number: 1806-54-8
Molecular Formula: C25H56NO4P
Molecular Weight: 465.690201
EINECS Number: 217-305-1

Trioctyl phosphate is derived from phosphoric acid and octanol, which is an alcohol with eight carbon atoms.
Trioctyl phosphate is commonly used as a plasticizer, flame retardant, and lubricant in various industrial applications.
Trioctyl phosphate has a viscosity of 15 mPas at 20 °C.

Trioctyl Phosphate is a plasticizer compatible with many types of polymers such as PVC, PUR, NBR and SBR.
Trioctyl phosphate have to low temperatures.
Trioctyl Phosphate resists very well and has excellent weather conditions.
Trioctyl phosphate can also be used as a carrier for pigments.

Trioctyl phosphate finds application as a fire-retardant, plasticizer for polyvinyl chloride and cellulose nitrate.
Trioctyl phosphate is used as a stimulant for the chemical warfare nerve agent VX.
Further, Trioctyl phosphate used as an alkylation agent for nitrogen heterocyclic compounds and as a catalyst to produce phenolic and urea resins.

In addition to this, Trioctyl phosphate is used as an antifoaming agent and a co-solvent in hydrogen peroxide production.
Trioctyl phosphate, a clear, viscous liquid, is a component of vinyl stabilizers, oil additives and flame resistant used as; it is mainly used as a plasticizer for vinyl plastic and synthetic rubber construction.
Trioctyl phosphate is a special flame retardant, for example in military tarpaulins, for vinyl composts where low temperature efficiency is critical.

Trioctyl phosphate uses a plasticizer.
Trioctyl phosphate is included in blends with general purpose plasticizers such as phthalate esters to improve low temperature formations.
Trioctyl Phosphate is a viscous, clear to pale yellow plasticizer with a slight pungent odor.

Trioctyl phosphate can also be used as a fire retardant and solvent.
As a plasticizer, Trioctyl phosphate is compatible with many types of polymers such as PVC, PUR, NBR, and SBR.
Trioctyl phosphate can be used as a component of vinyl stabilizers, grease additives, and flame-proofing compositions for vinyl plastic and synthetic rubber compounds.

Trioctyl phosphate has the chemical formula C25H56NO4P.
Trioctyl phosphate consists of three octyl (8-carbon) groups attached to a central phosphoric acid molecule.
The octyl groups provide the compound with its unique properties, such as plasticizing and lubricating effects.

Trioctyl phosphate is a clear colorless to pale yellow liquid with a slightly pungent odour.
Insoluble in water; Trioctyl Phosphate is soluble in alcohol, acetone and ether.
Trioctyl phosphate is widely used as a flame retardant, plasticizer and extractant in the production of chemical enterprises.

Trioctyl Phosphates most important use is the production of hydrogen peroxide.
As the solvent of hydrogen anthraquinone, trioctyl phosphate, high solubility of hydrogen anthron, between water and solvent.
Trioctyl Phosphate has high hydrogen peroxide distribution coefficient, high boiling point and high flash point conditions.

As a plasticizer, Trioctyl Phosphate is added to polymers and plastics to increase their flexibility and ease of processing.
Trioctyl Phosphate helps to lower the glass transition temperature of the material, making it more pliable and less brittle.
This is particularly important for materials that need to be molded, extruded, or shaped.

Trioctyl phosphate is a carrier material for pigments and dyes to color polymers.
Trioctyl phosphate is used as a component of cutting oils.
Trioctyl phosphate finds application as a component of release agent preparations used in the metal industry.

Trioctyl phosphate is a solvent for hydrogen peroxide synthesis.
Trioctyl phosphate finds application as a fire retardant, plasticizer for polyvinyl chloride and cellulose nitrate.
Trioctyl phosphate is used as a stimulant for the chemical warfare nerve agent VX.

Also, as an alkylating agent for Trioctyl Phosphate and as a catalyst to produce phenolic and urea resins.
In addition, Trioctyl Phosphate is used as an anti-foaming agent and co-solvent in the production of hydrogen peroxide.
In flame-retardant applications, when exposed to heat or flames, Trioctyl Phosphate undergoes pyrolysis and releases phosphoric acid.

Trioctyl Phosphate reacts with the combustion process, forming a char layer that acts as a barrier, preventing the spread of flames and reducing the overall flammability of the material.
Trioctyl Phosphate's lubricating properties are especially useful in situations where high temperatures and pressures are involved, such as in metalworking processes.
It can reduce friction and wear between moving parts, enhancing the efficiency and lifespan of mechanical systems.

Form: Liquid
Appearance (Color): Colorless
Assay from Supplier's CofA: ≥95.0%
Density at 20°C g/cm3: 0.924 +/- 0.003
Refractive Index at 20°C: 1.441 +/- 0.001
Viscosity at 25°C Centipoises: 14
Surface Tension nN/m: 18
Acidity mgKOH/g: 0.10
2-Ethyl Hexanol Content %: 0.10
Bis (2-Ethylhexyl) Phosphate Content %: 0.10
Water Content %: 0.15
Flash Point °C: 192
Boiling point: 210 °C (5 hPa) decomposes
Ignition temperature: 370 °C
Melting Point: pH value: 7 (H₂O, 20 °C)
Vapor pressure: Solubility:
Trioctyl Phosphate finds applications in industries such as plastics, textiles, rubber, electronics, and manufacturing.
Its ability to impart flexibility to plastics and act as a flame retardant makes it valuable in these industries.
Trioctyl phosphate has faced some scrutiny due to potential environmental and health concerns.

Trioctyl Phosphate's important to handle and use this chemical with proper precautions.
Toxicity and exposure risks are factors that should be considered, especially in industrial settings.
Regulations and guidelines vary by region regarding the use and handling of chemicals like trioctyl phosphate.

Trioctyl Phosphate has been subject to scrutiny due to potential health and environmental concerns.
Exposure to high concentrations of Trioctyl Phosphate may lead to adverse health effects, including irritation to the skin, eyes, and respiratory system.
Long-term exposure could potentially have more serious health consequences.

Environmental concerns stem from Trioctyl Phosphates persistence in the environment and potential bioaccumulation in aquatic organisms.
Trioctyl Phosphate vary by country and region.
Regulatory authorities often set limits on its use in certain applications and establish guidelines for safe handling, storage, and disposal.

As with Trioctyl Phosphate, it's important to follow safety data sheets and guidelines provided by manufacturers and regulatory bodies.
Due to concerns about the health and environmental impact of Trioctyl Phosphate, there has been growing interest in finding alternative flame retardants, plasticizers, and lubricants that offer similar benefits without the associated risks.
These alternatives are often evaluated based on their performance, safety profile, and environmental impact.

Uses
As a fire retardant Trioctyl Phosphate is used in various consumer products such as clothing.
As a solvent Trioctyl Phosphate is used in the production of hydrogen peroxide.
It is soluble in alcohol, acetone, and ether however, Trioctyl Phosphate is insoluble in water.

Trioctyl Phosphate uses include as a carrier in the manufacture of pigments for plastics and as an additive for mineral oils, vinyl, and synthetic rubbers.
Trioctyl Phosphate also has weather resistant properties and a good resistance to low temperatures

Trioctyl Phosphate used as a flame-retardant plasticizer for polyvinyl chloride and cellulose nitrate, an antifoaming agent, and a co-solvent in hydrogen peroxide production.
Trioctyl Phosphate has been widely used as a plasticizer, fire retardant and solvent.
As a plasticizer, Trioctyl Phosphate is used as a component of vinyl stabilizers, grease additives and flame-proofing compositions for vinyl plastic and synthetic rubber compounds.

As a fire retardant, Trioctyl Phosphate is used in consumer products, such as clothing.
As a solvent, Trioctyl Phosphate is used as a co-solvent to produce hydrogen peroxide.
Trioctyl phosphate, to impart or improve light stability, weather resistance and flame retardant properties.

Trioctyl Phosphate is primarily used as an additive in vinyls and synthetic rubbers.
Trioctyl phosphate is also used as a solvent in the production of hydrogen peroxide, as a carrier in the manufacture of pigments for plastics, and as a mineral mineral.
Trioctyl Phosphate used as additive for oils.

Trioctyl phosphate is a kind of practical good fire retardant and is suitable for Vinylite, cellulosic resin, resol, urethane, synthetic rubber, solvent, foam cutter etc.
Trioctyl phosphate finds application as a fire retardant, plasticizer for polyvinyl chloride and cellulose nitrate.
Trioctyl phosphate is used as a warning for the chemical warfare nerve agent VX.

Trioctyl phosphate has been used as an extractant in hydrometallurgical processes to extract metals from ores and solutions.
Trioctyl Phosphate forms stable complexes with metal ions, allowing for selective separation and recovery of specific metals.
Trioctyl phosphate is often used as a plasticizer, a substance added to plastics and other materials to increase their flexibility, durability, and workability.

When added to plastics, Trioctyl Phosphate helps to reduce brittleness and improve their processing properties.
Trioctyl Phosphate is also used as a flame retardant additive in plastics, textiles, and other materials.
Trioctyl Phosphate works by releasing phosphoric acid when exposed to heat, which forms a protective layer that inhibits the spread of flames.

Due to its chemical properties, trioctyl phosphate can act as a lubricant, especially in situations involving high temperatures and pressures.
Trioctyl Phosphate's used in metalworking fluids, hydraulic fluids, and other lubrication applications.

Trioctyl Phosphate is used as a plasticizer in the polymer and plastics industry.
Trioctyl Phosphate enhances the flexibility and workability of polymers, making them easier to mold, shape, and process.
However, its use as a plasticizer has decreased over time due to the availability of safer alternatives.

Trioctyl Phosphate serves as a flame retardant additive in plastics, textiles, and other materials.
When exposed to heat or flames, it releases phosphoric acid, which forms a protective char layer that inhibits the spread of flames.
Flame retardant applications have raised environmental concerns due to Trioctyl Phosphate's potential persistence in the environment.

Its lubricating properties make Trioctyl Phosphate useful in metalworking fluids, hydraulic fluids, and lubrication applications where high temperatures and pressures are involved.
Trioctyl Phosphate can reduce friction and wear between moving parts, extending the life of machinery.
In the extraction and metallurgical industries, Trioctyl Phosphate has been used as an extraction agent to recover metals from ores and solutions.

Trioctyl Phosphate forms stable complexes with metal ions, aiding in selective metal separation.
Trioctyl Phosphate is used as a solvent in laboratory settings for certain chemical reactions, particularly in research involving polymers, materials science, and analytical chemistry.
Trioctyl Phosphate has been utilized in gas chromatography as a nonpolar solvent or diluent to aid in the separation and analysis of different compounds.

Trioctyl Phosphate has been employed in the mining industry as a flotation agent to aid in the separation of minerals from ores by creating hydrophobic surfaces on mineral particles.
In the coatings industry, Trioctyl Phosphate has been used to improve the flexibility, adhesion, and overall performance of surface coatings.
Trioctyl phosphate can be used as a solvent and extraction agent in various chemical processes, including the extraction of metals from ores.

In addition to its industrial applications, Trioctyl Phosphate is also used in laboratory settings for various purposes.
Trioctyl Phosphate can be used as a solvent for certain chemical reactions and as a component in research experiments, especially those involving polymers, materials science, and analytical chemistry.

Trioctyl Phosphate has been used in analytical techniques, particularly in gas chromatography.
Trioctyl Phosphate can serve as a nonpolar solvent or diluent in sample preparation processes, aiding in the separation and analysis of different compounds.
In the mining industry, Trioctyl Phosphate has been used as a flotation agent to assist in separating minerals from ores.

Trioctyl Phosphate can enhance the separation process by helping to create a hydrophobic surface on the mineral particles.
Trioctyl Phosphate's plasticizing properties make it useful in polymer processing, including the production of flexible plastics, films, and coatings.
It helps to improve the flow of the polymer during processing and enhances the final product's flexibility.

Toxicity and Health Effects:
Trioctyl Phosphate is considered toxic and exposure to high concentrations can have adverse health effects.
Inhalation, skin contact, and ingestion can lead to irritation of the respiratory tract, skin, and eyes.
Chronic exposure may cause more serious health issues, including potential effects on the nervous system, liver, and reproductive system.

Given its toxicity, proper protective measures should be taken when working with or around Trioctyl Phosphate.
Trioctyl Phosphate is considered toxic and has the potential to cause adverse health effects if absorbed through the skin, ingested, or inhaled.
Long-term or repeated exposure to high concentrations may lead to more serious health issues, including effects on the nervous system, liver, and reproductive system.

Environmental Impact:
Trioctyl Phosphate has the potential to persist in the environment, and there is concern about its potential to bioaccumulate in aquatic organisms.
Trioctyl Phosphates use has raised environmental issues, and many regulatory agencies have taken steps to limit its use or encourage its replacement with less hazardous alternatives.
Trioctyl Phosphate can persist in the environment, potentially leading to bioaccumulation in organisms and affecting ecosystems over time.

Synonyms
TRIOCTYL PHOSPHATE
1806-54-8
Phosphoric acid, trioctyl ester
Tri-N-octyl phosphate
EINECS 217-305-1
CCRIS 4886
0LV8VW3YJZ
AI3-05904
Tri Octyl Phosphate
tri-n-Octylphosphate
Phosphoric acid trioctyl
Tris(n-octyl) phosphate
UNII-0LV8VW3YJZ
SCHEMBL37521
DTXSID6026246
LS-949
AKOS015899269
Trioléate de glycérol
Numéro CAS : 7758-29-4; Noms français :PENTASODIUM SALT, PENTASODIUM TRIPHOSPHATE, PENTASODIUM TRIPOLYPHOSPHATE, SODIUM PHOSPHATE (Na5P3O10), SODIUM TRIPHOSPHATE, Sodium tripolyphosphate; SODIUM TRIPOLYPHOSPHATE (NA5P3O10); SODIUM, TRIPOLYPHOSPHATE DE; Triphosphate pentasodique; TRIPHOSPHORIC ACID, PENTASODIUM SALT TRIPOLYPHOSPHATE; Tripolyphosphate de sodium. Noms anglais : Sodium tripolyphosphate. Utilisation et sources d'émission. Agent d'adoucissement, agent de préservation alimentaireSTPP, Le Triphosphate de sodium (STP), également tripolyphosphate de sodium (STPP), ou le tripolyphosphate (TPP), est un composé inorganique. Il est produit à grande échelle en tant que composant de nombreux produits domestiques et industriels, en particulier les poudres détergentes. Numéro CAS : 7758-29-4. TRIPHOSPHATE PENTASODIQUE; Tripolyphosphate de sodium; Triphosphate de sodium. Sodium triphosphate (STP), also sodium tripolyphosphate (STPP), or tripolyphosphate (TPP),[1]) is an inorganic compound with formula Na5P3O10. It is the sodium salt of the polyphosphate penta-anion, which is the conjugate base of triphosphoric acid. It is produced on a large scale as a component of many domestic and industrial products, especially detergents. Environmental problems associated with eutrophication are attributed to its widespread use. sodium tripolyphosphate, polygon, STPP. IUPAC name: Pentasodium triphosphate. The majority of STPP is consumed as a component of commercial detergents. It serves as a "builder," industrial jargon for a water softener.Food applications STPP is a preservative for seafood, meats, poultry, and animal feeds. It is common in food production as E number E451. In foods, STPP is used as an emulsifier and to retain moisture. Many governments regulate the quantities allowed in foods, as it can substantially increase the sale weight of seafood in particular. uses (hundreds of thousands of tons/year) include ceramics (decrease the viscosity of glazes up to a certain limit), leather tanning (as masking agent and synthetic tanning agent - SYNTAN), anticaking, setting retarders, flame retardants, paper, anticorrosion pigments, textiles, rubber manufacture, fermentation, antifreeze
Triphosphate de sodium (STP)
3-(3-(3-methoxypropoxy)propoxy)-Propanol; Methoxy Methyl Ethoxy; Methyl Ethoxy Propanol; ARCOSOLV® TPM; (2-(2-Methoxymethylethoxy)methylethoxy)propanol; TPG Methyl Ether; 1-(2-(2-Methoxy-1-methylethoxy)-1-methylethoxy)-2-propanol; 2-(2-(2-Methoxy propoxy)propoxy)-1-propanol; Dowanol TPM; O-Methyltripropylene glycol; [Metil-2-(metil-2-metoxietoxi)etoxi] propanol CAS NO:25498-49-1
Tripropylene Glycol Monomethyl Ether
1,3,5-Tris(2-hydroxyethyl)-1,3,5-triazine-2,4,6-trione; THEIC; Tris(hydroxyethyl) isocyanurate; Tris(beta-hydroxyethyl) isocyanurate; N,N',N''-Tris(2-hydroxyethyl) isocyanurate; 1,3,5-Tris(2-hydroxyethyl) isocyanurate; 1,3,5-Tris(2-hydroxyethyl) isocyanuric acid; 1,3,5-Tris(2-hydroxyethyl) cyanurate; Tris(hydroxyethyl) cyanurate; Tris(2-hydroxyethyl) cyanurate; Tris(2-hydroxyethyl)-1,3,5- triazinetrione; 1,3,5-Tris(2'-hydroxyethyl)isocyanuric acid CAS NO: 839-90-7
Tris (2-Hydroxyethyl) isocyanurate (THEIC)
1,3,5-Tris(2-hydroxyethyl)-1,3,5-triazine-2,4,6-trione; THEIC; Tris(hydroxyethyl) isocyanurate; Tris(beta-hydroxyethyl) isocyanurate; N,N',N''-Tris(2-hydroxyethyl) isocyanurate; 1,3,5-Tris(2-hydroxyethyl) isocyanurate; 1,3,5-Tris(2-hydroxyethyl) isocyanuric acid; 1,3,5-Tris(2-hydroxyethyl) cyanurate; Tris(hydroxyethyl) cyanurate; Tris(2-hydroxyethyl) cyanurate; Tris(2-hydroxyethyl)-1,3,5- triazinetrione; 1,3,5-Tris(2'-hydroxyethyl)isocyanuric acid CAS NO: 839-90-7
TRİS(2-BUTOXYETHYL) PHOSPHATE (TBEP)

Tris(2-butoxyethyl) phosphate, commonly abbreviated as Tris(2-butoxyethyl) phosphate (TBEP), is a chemical compound belonging to the family of organophosphates.
Its chemical formula is C18H39O7P, and its molecular structure consists of three 2-butoxyethyl groups attached to a phosphate (phosphoric acid) molecule.
Tris(2-butoxyethyl) phosphate (TBEP) is also known by other names, including tri(butoxyethyl) phosphate.

CAS Number: 78-51-3
EC Number: 201-122-9



APPLICATIONS


Tris(2-butoxyethyl) phosphate (TBEP) is widely utilized as a plasticizer in the production of flexible polymeric materials, such as PVC (polyvinyl chloride), enhancing their pliability.
In the manufacturing of coatings, Tris(2-butoxyethyl) phosphate (TBEP) serves as a crucial additive, contributing to the film-forming properties and flexibility of the coating.
The flame-retardant properties of Tris(2-butoxyethyl) phosphate (TBEP) make it a valuable component in the formulation of fire-resistant coatings and paints.

As a plasticizer in PVC formulations, Tris(2-butoxyethyl) phosphate (TBEP) aids in reducing brittleness and improving the overall workability of the material.
Tris(2-butoxyethyl) phosphate (TBEP) finds applications in the production of automotive interiors, where it contributes to the flexibility of materials used in dashboards and upholstery.
In the construction industry, Tris(2-butoxyethyl) phosphate (TBEP) is incorporated into coatings and sealants to enhance their resistance to fire and improve their application properties.
Tris(2-butoxyethyl) phosphate (TBEP) is used in the formulation of adhesives, providing improved flexibility and bond strength in adhesive materials.

Tris(2-butoxyethyl) phosphate (TBEP) is employed in the production of wire and cable insulation to enhance their flexibility and flame retardancy.
In the textile industry, Tris(2-butoxyethyl) phosphate (TBEP) is utilized as a plasticizer in the production of flame-resistant fabrics used in protective clothing.
Tris(2-butoxyethyl) phosphate (TBEP) plays a role in the formulation of flexible foam materials, such as those used in upholstery and mattresses.

Tris(2-butoxyethyl) phosphate (TBEP) is utilized in the manufacturing of flexible films and sheets, where its plasticizing properties contribute to the material's malleability.
Tris(2-butoxyethyl) phosphate (TBEP) is added to certain polymers used in medical devices to improve their flexibility and processing characteristics.
Tris(2-butoxyethyl) phosphate (TBEP) is employed in the formulation of printing inks, contributing to their adhesion and durability on various surfaces.
Tris(2-butoxyethyl) phosphate (TBEP) is used in the production of flexible hoses and tubing, where it enhances the material's flexibility and flame resistance.

Tris(2-butoxyethyl) phosphate (TBEP) finds application in the production of floor coverings, ensuring that materials remain flexible and resistant to ignition.
In the aerospace industry, Tris(2-butoxyethyl) phosphate (TBEP) is used in the formulation of coatings for aircraft interiors to meet fire safety standards.
Tris(2-butoxyethyl) phosphate (TBEP) is added to certain types of synthetic leather to improve their flexibility and resistance to flame.

Tris(2-butoxyethyl) phosphate (TBEP) serves as a plasticizer in the production of resilient flooring materials, contributing to their durability and flexibility.
Tris(2-butoxyethyl) phosphate (TBEP) is utilized in the manufacturing of protective films for electronic devices, where flexibility and fire resistance are essential.
Tris(2-butoxyethyl) phosphate (TBEP) is incorporated into certain formulations for rubber products, such as gaskets and seals, to enhance their flexibility and fire performance.
In the production of artificial leather and upholstery fabrics, Tris(2-butoxyethyl) phosphate (TBEP) contributes to the material's softness and flame retardancy.

Tris(2-butoxyethyl) phosphate (TBEP) is employed in the formulation of sealants used in the automotive and construction industries, providing flexibility and fire resistance.
Tris(2-butoxyethyl) phosphate (TBEP) finds applications in the production of flexible molded goods, including shoe soles and cushions.
Tris(2-butoxyethyl) phosphate (TBEP) is used in the formulation of certain types of caulks, ensuring their flexibility and resistance to fire.
Tris(2-butoxyethyl) phosphate (TBEP) is applied in the production of flexible packaging materials, contributing to their pliability and flame retardancy.

Tris(2-butoxyethyl) phosphate (TBEP) is a key ingredient in the formulation of flame-retardant coatings for electronic components and devices, ensuring fire safety in electronic applications.
In the production of automotive upholstery, Tris(2-butoxyethyl) phosphate (TBEP) is added to materials to provide a balance of flexibility and resistance to ignition.
Tris(2-butoxyethyl) phosphate (TBEP) is employed in the manufacturing of flexible hoses used in various industries, including automotive and industrial applications.

Tris(2-butoxyethyl) phosphate (TBEP) is utilized in the formulation of resilient flooring adhesives, contributing to the adhesive's strength and flexibility.
In the construction industry, Tris(2-butoxyethyl) phosphate (TBEP) finds applications in the production of fire-resistant sealants for joints and gaps in structures.

Tris(2-butoxyethyl) phosphate (TBEP) is used in the formulation of flame-retardant conveyor belts for industries where fire hazards are a concern.
Tris(2-butoxyethyl) phosphate (TBEP) plays a role in the production of flame-resistant conveyor belts for mining and industrial applications, enhancing safety measures.
Tris(2-butoxyethyl) phosphate (TBEP) is applied in the production of flame-resistant fabrics used in military uniforms and protective gear.
Tris(2-butoxyethyl) phosphate (TBEP) is used in the manufacturing of flexible PVC cables, providing both flexibility and flame-retardant properties.

In the formulation of flexible membranes for roofing materials, Tris(2-butoxyethyl) phosphate (TBEP) contributes to the material's durability and fire resistance.
Tris(2-butoxyethyl) phosphate (TBEP) is employed in the production of flame-resistant hydraulic fluids used in industrial machinery.
Tris(2-butoxyethyl) phosphate (TBEP) is utilized in the formulation of flexible foam insulation materials for use in construction and HVAC applications.

Tris(2-butoxyethyl) phosphate (TBEP) finds application in the production of flame-resistant conveyor belts for material handling in industries such as mining and manufacturing.
Tris(2-butoxyethyl) phosphate (TBEP) is used in the formulation of flame-retardant adhesives for bonding materials in high-temperature environments.
In the production of flame-resistant synthetic leather for upholstery, Tris(2-butoxyethyl) phosphate (TBEP) ensures both flexibility and fire safety.
Tris(2-butoxyethyl) phosphate (TBEP) is applied in the formulation of fire-resistant conveyor belts for the transportation of materials in various industries.

Tris(2-butoxyethyl) phosphate (TBEP) is used in the production of flame-resistant coatings for textiles used in curtains and upholstery in public spaces.
Tris(2-butoxyethyl) phosphate (TBEP) plays a role in the formulation of flame-resistant gaskets and seals for use in industrial machinery.
Tris(2-butoxyethyl) phosphate (TBEP) is applied in the production of flame-resistant insulation materials for wiring and electrical components.

In the formulation of flame-resistant hydraulic fluids for aircraft, Tris(2-butoxyethyl) phosphate (TBEP) enhances the fluid's fire safety properties.
Tris(2-butoxyethyl) phosphate (TBEP) is utilized in the production of flame-retardant coatings for flexible ducts used in HVAC systems.

Tris(2-butoxyethyl) phosphate (TBEP) is added to the formulation of flame-resistant conveyor belts for use in airport luggage handling systems.
In the production of flame-resistant coatings for industrial textiles, Tris(2-butoxyethyl) phosphate (TBEP) contributes to the textiles' fire safety features.
Tris(2-butoxyethyl) phosphate (TBEP) is used in the formulation of flame-resistant coatings for flexible packaging materials in the food and pharmaceutical industries.
Tris(2-butoxyethyl) phosphate (TBEP) finds application in the production of flame-resistant gaskets and seals for use in marine and offshore applications, ensuring safety in challenging environments.

Tris(2-butoxyethyl) phosphate (TBEP) is used in the formulation of flame-retardant coatings for industrial textiles, providing an additional layer of fire protection.
In the aerospace industry, Tris(2-butoxyethyl) phosphate (TBEP) is incorporated into the production of flame-resistant insulation materials for aircraft components.
Tris(2-butoxyethyl) phosphate (TBEP) finds application in the production of flame-resistant hydraulic fluids for machinery operating in potentially hazardous environments.

Tris(2-butoxyethyl) phosphate (TBEP) is added to the formulation of flame-retardant adhesives used in the bonding of materials for aerospace and automotive applications.
In the production of flame-resistant conveyor belts for mining operations, Tris(2-butoxyethyl) phosphate (TBEP) enhances safety measures in material handling.

Tris(2-butoxyethyl) phosphate (TBEP) is employed in the manufacturing of flame-resistant coatings for flexible ductwork used in ventilation and air conditioning systems.
Tris(2-butoxyethyl) phosphate (TBEP) is utilized in the formulation of flame-retardant materials for protective covers used in the transportation of goods.
In the textile industry, Tris(2-butoxyethyl) phosphate (TBEP) contributes to the production of flame-resistant fabrics used in curtains, upholstery, and home furnishings.

Tris(2-butoxyethyl) phosphate (TBEP) finds application in the production of flame-resistant paints for structural steel in buildings and infrastructure.
Tris(2-butoxyethyl) phosphate (TBEP) is used in the formulation of flame-resistant coatings for industrial curtains, providing fire safety in manufacturing settings.
Tris(2-butoxyethyl) phosphate (TBEP) is added to the formulation of flame-retardant adhesives for bonding materials in the construction of fire doors and partitions.
In the automotive sector, Tris(2-butoxyethyl) phosphate (TBEP) is incorporated into the production of flame-resistant materials for interior components such as dashboards and panels.

Tris(2-butoxyethyl) phosphate (TBEP) plays a role in the formulation of flame-resistant hydraulic fluids used in heavy machinery and equipment in construction and mining.
Tris(2-butoxyethyl) phosphate (TBEP) is utilized in the production of flame-resistant coatings for flexible conduits used in electrical installations.

Tris(2-butoxyethyl) phosphate (TBEP) contributes to the fire safety of flexible pipes used in various industries, preventing the spread of flames in case of a fire incident.
In the production of flame-resistant insulation materials for electrical wiring, Tris(2-butoxyethyl) phosphate (TBEP) enhances safety in electrical systems.
Tris(2-butoxyethyl) phosphate (TBEP) is added to the formulation of flame-retardant adhesives for bonding materials in the construction of fire-resistant building structures.

Tris(2-butoxyethyl) phosphate (TBEP) is used in the formulation of flame-resistant coatings for flexible packaging materials in the pharmaceutical and food industries.
Tris(2-butoxyethyl) phosphate (TBEP) finds application in the production of flame-resistant gaskets and seals for use in high-temperature and high-pressure environments.
In the manufacturing of flame-resistant conveyor belts for industrial ovens and furnaces, Tris(2-butoxyethyl) phosphate (TBEP) contributes to fire safety.
Tris(2-butoxyethyl) phosphate (TBEP) is incorporated into the production of flame-resistant coatings for flexible expansion joints used in construction and infrastructure.

Tris(2-butoxyethyl) phosphate (TBEP) is utilized in the formulation of flame-retardant adhesives for bonding materials in the construction of fire-resistant flooring.
Tris(2-butoxyethyl) phosphate (TBEP) plays a role in the production of flame-resistant insulation materials for pipes and ducts in industrial settings.
Tris(2-butoxyethyl) phosphate (TBEP) is added to the formulation of flame-resistant coatings for flexible connectors used in chemical processing plants.
In the marine industry, Tris(2-butoxyethyl) phosphate (TBEP) contributes to the production of flame-resistant materials for interior components of ships, ensuring safety at sea.

Tris(2-butoxyethyl) phosphate (TBEP) is employed in the formulation of flame-resistant coatings for industrial curtains used in manufacturing facilities, providing fire safety in enclosed spaces.
In the production of flame-resistant hydraulic fluids for marine vessels, Tris(2-butoxyethyl) phosphate (TBEP) enhances safety measures in the operation of critical equipment.
Tris(2-butoxyethyl) phosphate (TBEP) is used in the manufacturing of flame-resistant insulation materials for pipes and vessels in chemical processing plants.
Tris(2-butoxyethyl) phosphate (TBEP) finds application in the formulation of flame-retardant adhesives for bonding materials in the construction of fire-resistant walls and barriers.

In the aerospace industry, Tris(2-butoxyethyl) phosphate (TBEP) is incorporated into the production of flame-resistant materials for aircraft interiors, meeting stringent safety standards.
Tris(2-butoxyethyl) phosphate (TBEP) contributes to the formulation of flame-resistant coatings for flexible hoses used in fuel and chemical transfer applications, minimizing fire risks.
Tris(2-butoxyethyl) phosphate (TBEP) is utilized in the production of flame-resistant conveyor belts for material handling in recycling and waste management facilities.

Tris(2-butoxyethyl) phosphate (TBEP) is added to the formulation of flame-retardant adhesives for bonding materials in the construction of fire-resistant ceilings and partitions.
In the automotive sector, Tris(2-butoxyethyl) phosphate (TBEP) is applied to the production of flame-resistant materials for engine compartments, enhancing overall vehicle safety.
Tris(2-butoxyethyl) phosphate (TBEP) plays a role in the formulation of flame-resistant hydraulic fluids used in mining equipment, ensuring fire safety in mining operations.

Tris(2-butoxyethyl) phosphate (TBEP) is used in the manufacturing of flame-resistant coatings for flexible joints used in chemical and petrochemical processing.
Tris(2-butoxyethyl) phosphate (TBEP) is incorporated into the production of flame-resistant insulation materials for electrical cables and wiring in industrial settings.
Tris(2-butoxyethyl) phosphate (TBEP) contributes to the formulation of flame-resistant coatings for flexible connectors used in fuel and gas distribution systems.
Tris(2-butoxyethyl) phosphate (TBEP) is utilized in the production of flame-resistant paints for structural components in oil and gas facilities, preventing fire hazards.

Tris(2-butoxyethyl) phosphate (TBEP) is added to the formulation of flame-retardant adhesives for bonding materials in the construction of fire-resistant columns and beams.
In the textile industry, Tris(2-butoxyethyl) phosphate (TBEP) is applied in the production of flame-resistant fabrics used in protective clothing for industrial workers.
Tris(2-butoxyethyl) phosphate (TBEP) plays a role in the formulation of flame-resistant hydraulic fluids used in agricultural machinery, ensuring fire safety in farming operations.
Tris(2-butoxyethyl) phosphate (TBEP) is used in the manufacturing of flame-resistant coatings for flexible seals and gaskets in high-temperature applications.
Tris(2-butoxyethyl) phosphate (TBEP) contributes to the formulation of flame-resistant adhesives for bonding materials in the construction of fire-resistant roofing materials.

In the production of flame-resistant insulation materials for HVAC ducts, Tris(2-butoxyethyl) phosphate (TBEP) enhances safety in heating, ventilation, and air conditioning systems.
Tris(2-butoxyethyl) phosphate (TBEP) is incorporated into the production of flame-resistant coatings for flexible expansion joints used in power plants and energy facilities.

Tris(2-butoxyethyl) phosphate (TBEP) is utilized in the formulation of flame-resistant hydraulic fluids for construction equipment, ensuring safety on job sites.
Tris(2-butoxyethyl) phosphate (TBEP) plays a role in the production of flame-resistant materials for electrical cabinets and enclosures, preventing fire incidents in electrical systems.
Tris(2-butoxyethyl) phosphate (TBEP) is added to the formulation of flame-retardant adhesives for bonding materials in the construction of fire-resistant flooring for public spaces.
In the marine industry, Tris(2-butoxyethyl) phosphate (TBEP) contributes to the production of flame-resistant materials for ship interiors, meeting safety requirements for maritime applications.



DESCRIPTION


Tris(2-butoxyethyl) phosphate, commonly abbreviated as Tris(2-butoxyethyl) phosphate (TBEP), is a chemical compound belonging to the family of organophosphates.
Its chemical formula is C18H39O7P, and its molecular structure consists of three 2-butoxyethyl groups attached to a phosphate (phosphoric acid) molecule.
Tris(2-butoxyethyl) phosphate (TBEP) is also known by other names, including tri(butoxyethyl) phosphate.

Tris(2-butoxyethyl) phosphate, commonly known as Tris(2-butoxyethyl) phosphate (TBEP), is an organophosphate compound.
Tris(2-butoxyethyl) phosphate (TBEP) has the molecular formula C18H39O7P, indicating its composition of carbon, hydrogen, oxygen, and phosphorus.

Tris(2-butoxyethyl) phosphate (TBEP) is a colorless to pale yellow liquid with a molecular weight of approximately 430.47 g/mol.
The chemical structure of Tris(2-butoxyethyl) phosphate (TBEP) features three 2-butoxyethyl groups attached to a central phosphate molecule.
Tris(2-butoxyethyl) phosphate (TBEP) exhibits solubility in various organic solvents, contributing to its versatility in industrial applications.

Tris(2-butoxyethyl) phosphate (TBEP) is known for its use as a plasticizer, enhancing the flexibility and workability of polymers and resins.
As a flame retardant, Tris(2-butoxyethyl) phosphate (TBEP) is employed to improve the fire resistance of materials in the manufacturing of coatings and plastics.
Tris(2-butoxyethyl) phosphate (TBEP) plays a crucial role in the modification of physical properties, making it valuable in the formulation of flexible and fire-resistant materials.
Its slight odor and flammability necessitate careful handling and adherence to safety protocols.
Tris(2-butoxyethyl) phosphate (TBEP) is often utilized in the production of coatings where both flexibility and flame retardancy are desired.

Tris(2-butoxyethyl) phosphate (TBEP) acts as a key ingredient in certain types of polymers, contributing to their processing characteristics.
Due to its effectiveness as a flame retardant, Tris(2-butoxyethyl) phosphate (TBEP) finds applications in materials requiring compliance with fire safety standards.
Tris(2-butoxyethyl) phosphate (TBEP)'s compatibility with various industrial processes makes it a versatile additive in the manufacturing sector.
Tris(2-butoxyethyl) phosphate (TBEP) has gained recognition for its role in improving the durability and safety features of products in the construction and automotive industries.
As a plasticizer, it aids in reducing the stiffness of materials, enhancing their moldability during processing.

Tris(2-butoxyethyl) phosphate (TBEP) is subject to regulatory considerations, and its use is guided by safety guidelines to minimize environmental and health risks.
Tris(2-butoxyethyl) phosphate (TBEP) has been studied for its thermal stability, an important factor in its application as a flame retardant.
Tris(2-butoxyethyl) phosphate (TBEP)'s effectiveness in retarding flames makes it a preferred choice in applications where fire safety is a primary concern.

Tris(2-butoxyethyl) phosphate (TBEP)'s ability to reduce the ignition and flame spread rates contributes to its significance in fire-resistant formulations.
In the realm of materials science, Tris(2-butoxyethyl) phosphate (TBEP) is recognized for its impact on the physical and mechanical properties of finished products.
Its inclusion in certain resins and adhesives enhances the overall performance and safety features of these materials.

Tris(2-butoxyethyl) phosphate (TBEP) undergoes rigorous testing to ensure that products containing it meet relevant safety standards and regulations.
As an organophosphate, Tris(2-butoxyethyl) phosphate (TBEP)'s chemical structure makes it suitable for specific applications in the field of polymer chemistry.
Tris(2-butoxyethyl) phosphate (TBEP)'s role in enhancing the thermal stability of materials is particularly valuable in environments where fire hazards are prevalent.
Tris(2-butoxyethyl) phosphate (TBEP)'s widespread use underscores its importance in modern industries seeking to balance flexibility, durability, and fire resistance in their products.



PROPERTIES


Physical Properties:

State: Tris(2-butoxyethyl) phosphate (TBEP) is typically a liquid at room temperature.
Color: It is often colorless to pale yellow.
Odor: Tris(2-butoxyethyl) phosphate (TBEP) may have a slight odor.
Density: The density of Tris(2-butoxyethyl) phosphate (TBEP) is approximately [insert value] g/cm³.
Melting Point: Tris(2-butoxyethyl) phosphate (TBEP) does not have a distinct melting point; it may undergo phase transitions based on temperature.
Boiling Point: Tris(2-butoxyethyl) phosphate (TBEP) has a boiling point in the range of [insert range] °C.
Solubility: It is soluble in organic solvents but has limited solubility in water.


Chemical Properties:

Chemical Formula: C18H39O7P
Molecular Weight: Approximately 430.47 g/mol.
Structural Formula: Tris(2-butoxyethyl) phosphate (TBEP) features three 2-butoxyethyl groups attached to a central phosphate molecule.



FIRST AID


Inhalation:

Move to Fresh Air:
If Tris(2-butoxyethyl) phosphate (TBEP) is inhaled and respiratory irritation occurs, promptly move the affected person to an area with fresh air.

Seek Medical Attention:
If breathing difficulties persist or if significant inhalation has occurred, seek immediate medical attention.

Artificial Respiration:
If the person is not breathing and trained to do so, provide artificial respiration.


Skin Contact:

Remove Contaminated Clothing:
In case of skin contact, remove contaminated clothing promptly.

Wash Skin:
Wash the affected area with plenty of soap and water.

Seek Medical Advice:
If irritation or redness persists after washing, seek medical advice.


Eye Contact:

Flush Eyes:
In case of eye contact, immediately flush the eyes with gently flowing lukewarm water for at least 15 minutes, holding the eyelids open.

Remove Contact Lenses:
If present and easy to do, remove contact lenses during the eye-rinsing process.

Seek Medical Attention:
Seek immediate medical attention if irritation, redness, or other symptoms persist.


Ingestion:

Do Not Induce Vomiting:
If Tris(2-butoxyethyl) phosphate (TBEP) is swallowed and the person is conscious, do not induce vomiting unless instructed to do so by medical personnel.

Rinse Mouth:
Rinse the mouth with water.

Seek Medical Attention:
Seek immediate medical attention.


General Advice:

Keep Person Calm:
Keep the affected person calm.

Do Not Leave Unattended:
Do not leave the person unattended.

Provide Information to Medical Personnel:
If first aid measures are administered, provide medical personnel with information about the substance involved.



HANDLING AND STORAGE


Handling:

Personal Protective Equipment (PPE):
Wear appropriate PPE, including chemical-resistant gloves, safety goggles, and, if necessary, respiratory protection, when handling Tris(2-butoxyethyl) phosphate (TBEP).

Ventilation:
Use in a well-ventilated area to minimize inhalation exposure.
If ventilation is inadequate, use local exhaust systems.

Avoid Skin Contact:
Avoid skin contact by wearing protective clothing, such as long sleeves and pants, along with chemical-resistant gloves.

Avoid Eye Contact:
Wear safety goggles or a face shield to protect against potential eye contact.

Avoid Inhalation:
Use respiratory protection if airborne concentrations exceed recommended exposure limits.

Do Not Eat, Drink, or Smoke During Handling:
Refrain from eating, drinking, or smoking while handling Tris(2-butoxyethyl) phosphate (TBEP) to prevent accidental ingestion.

Handling Equipment:
Use handling equipment, such as pumps or dispensers, to minimize direct contact with the substance.

Static Electricity:
Take precautions to avoid the build-up of static electricity.
Grounding and bonding equipment may be necessary.

Spill Response:
Implement proper spill response procedures, including using absorbent materials to contain and clean up spills.

Storage Containers:
Use appropriate containers made of compatible materials to store and transport Tris(2-butoxyethyl) phosphate (TBEP).


Storage:

Storage Temperature:
Store Tris(2-butoxyethyl) phosphate (TBEP) in a cool, well-ventilated area. Avoid exposure to direct sunlight and heat sources.

Temperature Limits:
Store within the recommended temperature limits specified by the manufacturer.

Keep Containers Closed:
Keep containers tightly closed when not in use to prevent contamination and evaporation.

Separate from Incompatible Materials:
Store Tris(2-butoxyethyl) phosphate (TBEP) away from incompatible materials, including strong acids, bases, and oxidizing agents.

Avoid Contamination:
Avoid cross-contamination by storing Tris(2-butoxyethyl) phosphate (TBEP) away from other chemicals and substances.

Use Proper Storage Facilities:
Use dedicated storage facilities that comply with local regulations and are equipped with appropriate safety features.

Storage Area Design:
Design the storage area to minimize the risk of spills and facilitate easy clean-up.

Prevent Leaks:
Inspect containers regularly for leaks and replace damaged containers promptly.

Labeling:
Clearly label storage containers with the product name, hazard information, and any other relevant details.

Control Access:
Restrict access to the storage area to authorized personnel only.


Emergency Response:

Emergency Procedures:
Establish and communicate emergency procedures, including spill response and evacuation plans.

Emergency Equipment:
Keep emergency equipment, such as spill control materials and first aid supplies, readily available.

Emergency Contacts:
Maintain a list of emergency contacts, including local emergency services and poison control centers.



SYNONYMS


Tri(butoxyethyl) phosphate
Phosphoric acid tris(2-butoxyethyl) ester
Tris(2-butoxyethyl) phosphate (TBEP)
Ethanol, 2-butoxy-, phosphate (3:1)
2-Butoxyethyl phosphate
Butyl Cellosolve phosphate
Tris(2-butoxyethyl)phosphate
Tris(butoxyethyl) phosphate
Phosphate tris(2-butoxyethyl) ester
Ethylene glycol monobutyl ether phosphate
Tris(butoxyethyl)phosphate
Phosphoric acid tris(2-butoxyethyl) ester
Triethylene glycol monobutyl ether phosphate
Ethanol, 2-butoxy-, phosphate (3:1)
Tris(2-butoxyethyl) phosphate (TBEP)
Phosphate tris(2-butoxyethyl) ester
Ethylene glycol monobutyl ether phosphate
Tris(2-butoxyethyl) phosphate
Phosphoric acid tris(2-butoxyethyl) ester
Triethylene glycol monobutyl ether phosphate
Ethanol, 2-butoxy-, phosphate (3:1)
Tris(2-butoxyethyl) phosphate (TBEP)
Phosphate tris(2-butoxyethyl) ester
Ethylene glycol monobutyl ether phosphate
Tris(2-butoxyethyl) phosphate
Butyl Oxyethyl Phosphate
Phosphoric Acid Tris(2-butoxyethyl) Ester
Ethylene Glycol Monobutyl Ether Phosphate
Tris(2-butoxyethyl) Orthophosphate
Butyl Cellosolve Phosphate
Triethylene Glycol Monobutyl Ether Phosphate
Tris(2-butoxyethyl) Phosphonate
Phosphate, Tris(butoxyethyl) Ester
Phosphoric Acid Tri(butoxyethyl) Ester
Butyl Oxyethyl Phosphate
Tris(butoxyethyl) Phosphoric Acid Ester
Phosphoric Acid Tri(2-butoxyethyl) Ester
Tri(2-butoxyethyl) Phosphate
2-Butoxyethyl Phosphate
Tris(butoxyethyl) Orthophosphate
Tris(2-butoxyethyl) phosphate (TBEP)
Phosphate, Triethylene Glycol Monobutyl Ether Ester
Ethanol, 2-butoxy-, phosphate (3:1)
Triethylene Glycol Monobutyl Ether Phosphate
Butyl Oxyethyl Phosphate
Phosphoric Acid Tris(2-butoxyethyl) Ester
Ethylene Glycol Monobutyl Ether Phosphate
Tris(2-butoxyethyl) Orthophosphate
Butyl Cellosolve Phosphate
Phosphoric Acid Tri(butoxyethyl) Ester
Trisodium Phosphate Dodecahydrate
Trisodium salt of methylglycinediacetic acid (MGDA-Na3) in solid form CAS No. 164462-16-2
Trisodium salt of Methylglycinediacetic acid
dry film preservative cas no: 330-54-1; 10605-21-7; 1332-58-7
TROYKYD D762
Troykyd D762 is an air release additive for aqueous systems - Troykyd D762 is an emulsion of mineral oil, surfactants and silica.Troykyd D762 It provides excellent foam control for aqueous systems and can be used in low to high PVC systems.Troykyd D762 The product is effective over a wide range of pH and temperatures. Troykyd D726 is a robust defoamer containing multi-hydrophobes.Troykyd D762 It provides long term defoaming efficacy in flat to semi gloss architectural coatings. Troykyd D726 can often be used as a single defoaming material in formulations where multiple defoamers have been required previously for adequate defoaming function.Troykyd D762 Its strong performance provides excellent cost-in-use. Troykyd D762 is an air release additive for aqueous systems - Troykyd D762 is an emulsion of mineral oil, surfactants and silica.Troykyd D762 It provides excellent foam control for aqueous systems and can be used in low to high PVC systems.Troykyd D762 The product is effective over a wide range of pH and temperatures.Troykyd D762 General purpose, Aqueous Excellent foam control for low to high PVC systems.Troykyd D762 Defoaming, Anti-Foaming High Efficiency Defoamer and Antifoam for Flat to Gloss Formulations for Aqueous Formulations.Troykyd D762 High Efficiency Defoamer and Antifoam for Flat to Gloss Formulations for Aqueous Formulations Polymer Systems: acrylic, vinyl-acrylic, styrene acrylic, vinyl acetate-ethylene, köpük giderici köpük önleyici Troykyd D762.Troykyd D762 First Aid Measures.Ingestion.Never give anything by mouth to an unconscious person. Get medical aid. Do NOT induce vomiting.Troykyd D762 If conscious and alert, rinse mouth and drink 2-4 cupfuls of milk or water.Troykyd D762 Inhalation.Remove from exposure to fresh air immediately.Troykyd D762 If not breathing, give artificial respiration.Troykyd D762 If breathing is difficult, give oxygen.Troykyd D762 Get medical aid.Skin.Get medical aid.Troykyd D762 Flush skin with plenty of soap and water for at least 15 minutes while removing contaminated clothing and shoes.Troykyd D762 Wash clothing before reuse.Eyes.Troykyd D762 Immediately flush eyes with plenty of water for at least 15 minutes, occasionally lifting the upper and lower eyelids. Get medical aid.Troykyd D762 Stability.Stable under normal temperatures and pressures.Troykyd D762 Incompatibilities.Strong oxidizing agents, strong bases.Troykyd D762 Decomposition.Carbon monoxide, irritating and toxic fumes and gases, carbon dioxide.Troykyd D762 Acrylic elastomer is a general term for a type of synthetic rubber whose main component is acrylic acid alkylester (ethyl or butyl ester).Troykyd D762 Acrylic elastomer has characteristics of heat and oil resistance.Troykyd D762 It is divided into old type and new type: Old types include ACM (copolymer of acrylic acid ester and 2-chloroethyl vinyl ether) containing chlorine and ANM (copolymer of acrylic acid ester and acrylonitrile) without chloride.Troykyd D762 Other than the slightly better water resistance of ANM, there are no physical differences; even processability is poor for both types.Troykyd D762 Since prices are also high, demand is not so high vis-à-vis the characteristics.Troykyd D762 On the other hand, the new type of acrylic rubber does not contain any chlorine despite its unclear chemical composition.Troykyd D762 Processability has been improved; most of the tackiness to rolls, as well as staining problems related to mold have been solved. Major characteristics of acrylic rubber include heat resistance and oil resistance; it can endure a temperature of 170-180 ℃ under dry heat or in oil.Troykyd D762 Since it does not have a double bond, acrylic rubber also boasts of good weatherability and ozone resistance.Troykyd D762 Its cold resistance is not that good, however.Troykyd D762 The saturation point is -15 ℃ for the old type and -28...-30 ℃ for the new type.Troykyd D762 In terms of vulcanization, the standard method for the old type is amine vulcanization.Troykyd D762 To minimize permanent deformation, the old type requires curing for 24 hours at a temperature of 150 ℃. On the other hand, for the new type, the press curing time and follow-up vulcanization time are significantly reduced by combining metal soap and sulfur.Troykyd D762 It has no special characteristics.Troykyd D762 The rebound resilience and abrasion resistance of the new type are poor, and even its electrical characteristics are considerably poor compared with acrylonitrile-butadiene rubber and butyl rubber.Troykyd D762 The materials are used mainly for oil seals and packagings related to automobiles.Troykyd D762 Other acrylic polymers:Polymethyl methacrylate, is the clear break-resistant sheeting sold as acrylic glass (or simply acrylic sheet) or under the trade name Plexiglas, Perspex, etc.Troykyd D762 Polyacrylate emulsion, water-borne coating, are used as binder for outdoor and indoor "latex" house paints.Troykyd D762 Acrylic paints as artist paints, Acrylic fibre, Sodium polyacrylate water-soluble thickeners, a polymer for the production of the Superabsorbent polymer (SAP) used in disposable diapers due to its high absorbency per unit mass , Acrylic resin as pressure-sensitive adhesive, "Super glue" is a formulation of cyanoacrylate.Troykyd D762 PVAc copolymer emulsion adhesive of vinyl acetate (VAM) and acrylic acid (VAA), Polyacrylamide copolymer used as flocculation agent in water treatment ,Mineral oil is any of various colorless, odorless, light mixtures of higher alkanes from a mineral source, particularly a distillate of petroleum, as distinct from usually edible vegetable oils.The name mineral oil by itself is imprecise, having been used for many specific oils over the past few centuries. Other names, similarly imprecise, include white oil, paraffin oil, liquid paraffin (a highly refined medical grade), paraffinum liquidum (Latin), and liquid petroleum. Baby oil is a perfumed mineral oil.Most often, mineral oil is a liquid by-product of refining crude oil to make gasoline and other petroleum products. This type of mineral oil is a transparent, colorless oil, composed mainly of alkanes and cycloalkanes, related to petroleum jelly. It has a density of around 0.8–0.87 g/cm3.Some of the imprecision in the definition of the names (e.g., "mineral oil", "white oil") reflects usage by buyers and sellers who did not know, and usually did not need to care about, the precise chemical makeup. Merriam-Webster states the first use of the term “mineral oil” was 1771. Prior to the late 19th century, the chemical science to determine such makeup was unavailable in any case. A similar lexical situation occurred with the term "white metal"."Mineral oil", sold widely and cheaply in the US, is not sold as such in Britain. Instead British pharmacologists use the terms "paraffinum perliquidum" for light mineral oil and "paraffinum liquidum" or "paraffinum subliquidum" for somewhat thicker (more viscous) varieties. The term "paraffinum liquidum" is often seen on the ingredient lists of baby oil and cosmetics. British aromatherapists commonly use the term "white mineral oil". In lubricating oils, mineral oil is termed from groups 1 to 2 worldwide and group 3 in certain regions. This is because the high end of group 3 mineral lubricating oils are so pure that they exhibit properties similar to polyalphaolefin – PAO oils (group 4 synthetics). Troykyd D762 The World Health Organization classifies untreated or mildly treated mineral oils as group 1 carcinogens to humans; highly refined oils are classified as group 3, meaning that they are not suspected to be carcinogenic, but available information is not sufficient to classify them as harmless. Troykyd D762 The UK Food Standards Agency (FSA) carried out a risk assessment on the findings of a survey made in 2011 on risks due to migration of components from printing inks used on carton-board packaging, including mineral oils, into food. Troykyd D762 The FSA did not identify any specific food safety concerns due to inks. Troykyd D762 People can be exposed to mineral oil mist in the workplace by breathing it in, skin contact, or eye contact. Troykyd D762 In the United States, the Occupational Safety and Health Administration has set the legal limit for mineral oil mist exposure in the workplace as 5 mg/m3 over an 8-hour workday, the National Institute for Occupational Safety and Health has set a recommended exposure limit of 5 mg/m3 over an 8-hour workday, and 10 mg/m3 short-term exposure has been rescinded according to the 2019 Guide to Occupational Exposure Values compiled by the ACGIH. Troykyd D762 Levels of 2500 mg/m3 and higher are indicated as immediately dangerous to life and health. Troykyd D762 However, current toxicological data does not contain any evidence of irreversible health effects due to short-term exposure at any level; the current value of 2500 mg/m3 is indicated as being arbitrary. Troykyd D762 Comestics containing mineral oil shouldn't be used for lip care because of their toxicity. Troykyd D762 Mineral oil is used as a laxative to alleviate constipation by retaining water in stool and the intestines. Troykyd D762 Although generally considered safe, as noted above, there is a concern of mist inhalation leading to serious health conditions such as pneumonia. Troykyd D762 Mineral oil can be administered either orally or as an enema. Troykyd D762 Also, it is sometimes used as a lubricant in enema preparations, because most of the ingested material is excreted in the stool rather than being absorbed by the body. Troykyd D762Mineral oil of special purity is often used as an overlay covering microdrops of culture medium in petri dishes, during the culture of oocytes and embryos in IVF and related procedures. Troykyd D762 The use of oil presents several advantages over the open culture system: it allows for several oocytes and embryos to be cultured simultaneously, but observed separately, in the same dish; it minimizes concentration and pH changes by preventing evaporation of the medium; it allows for a significant reduction of the medium volume used (as few as 20 microlitres per oocyte instead of several millilitres for the batch culture); and it serves as a temperature buffer minimizing thermal shock to the cells while the dish is taken out of the incubator for observation. Troykyd D762Over-the-counter veterinarian-use mineral oil is intended as a mild laxative for pets and livestock. Troykyd D762 Certain mineral oils are used in livestock vaccines, as an adjuvant to stimulate a cell-mediated immune response to the vaccinating agent. Troykyd D762[citation needed] In the poultry industry, plain mineral oil can also be swabbed onto the feet of chickens infected with scaly mites on the shank, toes, and webs. Troykyd D762 Mineral oil suffocates these tiny parasites. Troykyd D762 In beekeeping, food grade mineral oil-saturated paper napkins placed in hives are used as a treatment for tracheal and other mites. Troykyd D762[citation needed] It is also used along with a cotton swab to remove un-shed skin (ashes) on reptiles such as lizards and snakes. Troykyd D762Mineral oil is a common ingredient in baby lotions, cold creams, ointments, and cosmetics. Troykyd D762 It is a lightweight inexpensive oil that is odorless and tasteless. Troykyd D762 It can be used on eyelashes to prevent brittleness and breaking and, in cold cream, is also used to remove creme make-up and temporary tattoos. Troykyd D762 One of the common concerns regarding the use of mineral oil is its presence on several lists of comedogenic substances. Troykyd D762 These lists of comedogenic substances were developed many years ago and are frequently quoted in the dermatological literature. Troykyd D762The type of highly refined and purified mineral oil found in cosmetic and skincare products is noncomedogenic (does not clog pores). Troykyd D762Mineral oil is used in a variety of industrial/mechanical capacities as a non-conductive coolant or thermal fluid in electric components as it does not conduct electricity and functions to displace air and water. Troykyd D762 Some examples are in transformers, where it is known as transformer oil, and in high-voltage switchgear, where mineral oil is used as an insulator and as a coolant to disperse switching arcs. Troykyd D762 The dielectric constant of mineral oil ranges from 2. Troykyd D7623 at 50 °C (122 °F) to 2. Troykyd D7621 at 200 °C (392 °F). Troykyd D762 Mineral oil is used as a lubricant, a cutting fluid, and a jute batching oil. Troykyd D762[clarification needed] Spindle oils are light mineral oils used as lubricants in textile industries. Troykyd D762 Electric space heaters sometimes use mineral oil as a heat transfer oil. Troykyd D762 Because it is noncompressible, mineral oil is used as a hydraulic fluid in hydraulic machinery and vehicles. Troykyd D762An often cited limitation of mineral oil is that it is poorly biodegradable; in some applications, vegetable oils such as cottonseed oil or rapeseed oil may be used instead. Troykyd D762Food grade mineral oil has an E number of E905a, although it has not been approved in food products in the European Union, and incidental amounts in foods are carefully regulated. Troykyd D762[citation needed][dubious – discuss] Because of its properties that prevent water absorption, combined with its lack of flavor and odor, food grade mineral oil is a popular preservative for wooden cutting boards, salad bowls, and utensils. Troykyd D762 Rubbing a small amount of mineral oil into a wooden kitchen item periodically, will impede absorption of food liquids, and thereby food odors, and ease cleaning. Troykyd D762 By impeding water absorption, wetting and drying cycles, which can cause cracks or splits in wood, are reduced although some of the mineral oil is picked up by the food and ingested. Troykyd D762 Outside of the European Union, it is occasionally used in the food industry, particularly for confectionery. Troykyd D762 In this application, it is typically used for the glossy effect it produces, and to prevent the candy pieces from adhering to each other. Troykyd D762 It has been discouraged for use in children's foods, though it is still found in many confectioneries, including Swedish Fish. Troykyd D762 The use of food grade mineral oil is self-limiting because of its laxative effect. Troykyd D762 The maximum daily intake is calculated to be about 100 mg, of which some 80 mg are contributed from its use on machines in the baking industry. Troykyd D762Mineral oil's ubiquity has led to its use in some niche applications as well. Troykyd D762 It is used for treating and preserving wooden butcher block counter tops. Troykyd D762 It is recommended by the American Society for Reproductive Medicine for use as a fertility-preserving vaginal lubrication. Troykyd D762 However, it is known that oils degrade latex condoms. Troykyd D762 Mineral oil is commonly used to create a "wear" effect on new clay poker chips, which can otherwise be accomplished only through prolonged use. Troykyd D762 Either the chips are placed in mineral oil for a short time, or the oil is applied to each chip then rubbed off. Troykyd D762 This removes any chalky residue left over from manufacture, and also improve the look and "feel"[clarification needed] of the chips. Troykyd D762It is used as the principal fuel in some types of gel-type scented candles. Troykyd D762 It is used for cooling, for example liquid submersion cooling of components in some custom-built computers. Troykyd D762 Veterinarian-grade mineral oil is inexpensive, and is frequently used by amateur radio operators as coolant in RF dummy loads, as mineral oil is typically used as the insulating and cooling fluid in large electrical equipment such as transformers, see more above. Troykyd D762Mineral oil is used as a brake fluid in some cars, such as Citroën models with hydrodynamic suspension, and bicycle disc brakes. Troykyd D762Mineral oil is burned in specialized “machines” (both manufactured and home-made) to produce a thick white smoke that is then blown into automotive evaporative emissions (EVAP) systems to find leaks. Troykyd D762It is used for polishing alabaster in stonework and lubricating and cleaning pocket knives or food handling tools that use an open bearing, thus needing periodic lubrication. Troykyd D762 Light mineral oil (paraffinum perliquidum) is used as a honing oil when sharpening edge tools (such as chisels) on abrasive oil stones. Troykyd D762 Mineral oil USP or light mineral oil can be used as an anti-rust agent for blades. Troykyd D762It is an inexpensive alternative for storing reactive metals (lithium, sodium, etc. Troykyd D762). Troykyd D762Horticultural oil is often made of a combination of mineral oil and detergent. Troykyd D762 It is sprayed on plants to control scale, aphid, and other pest populations by suffocation. Troykyd D762It is used to overlay polymerase chain reactions in biotechnology to prevent loss of water during heating cycles. Troykyd D762 It is often used to suspend crystals for use in X-ray crystallography. Troykyd D762It is used as a transparent collision material for reactions in particle physics, as in the MiniBooNE neutrino oscillation experiment. Troykyd D762 As a relatively low heat combustible with no flavor or odor, mineral oil can be used in fire breathing and firedancing for entertainment, but there is a risk of injury. Troykyd D762 Paraffin oil is commonly used to fill Galileo thermometers. Troykyd D762 Due to paraffin oil's freezing temp being lower than water (approx. Troykyd D762 24 °F or −4 °C), this makes them less susceptible to freezing during shipment or when stored in a cold environment. Troykyd D762 Hydrophobic silica is a form of silicon dioxide (commonly known as silica) that has hydrophobic groups chemically bonded to the surface. Troykyd D762 The hydrophobic groups are normally alkyl or polydimethylsiloxane chains. Troykyd D762 Hydrophobic silica can be processed in different ways; such as fumed silica, precipitated silica, and aerosol assisted self assembly, all existing in the form of nanoparticles. Troykyd D762Hydrophobic silica displays water resistant properties because of its nanostructure and chemical properties. Troykyd D762 When applied to a surface of a material, the nanoparticles adhere to the host material and prevent liquids from permeating the rough texture. Troykyd D762 The water only comes into contact with the tips of the nanoparticles coating the outside of the material. Troykyd D762 Due to lack of attraction, the water is repelled from the hydrophobic silica. Troykyd D762Initially, silica is hydrophilic due to the presence of the silanol (Si-OH) groups on the surface of the particle. Troykyd D762 These silanol groups can chemically react with various reagents to render the silica hydrophobic. Troykyd D762 There are many different methods of processing silica to become hydrophobic, mainly by adding hydrocarbon groups. Troykyd D762Silica particles can become hydrophobic through plasma polymerization. Troykyd D762 In this process, plasma polymerized 1,7-octadiene (ppOD) (related to the diene hydrocarbons) is used to deposit polymer films onto the silica particles. Troykyd D762 The ppOD films are deposited through the use of radio frequencies, along with a reactor containing a rotating chamber. Troykyd D762 Using low specific energy plasma conditions, the ppOD films chemically render the silica particles hydrophobic. Troykyd D762 By using the ppOD films, the hydrophilic polar Si-OH groups in the polymer itself are concealed by non-polar CxHy hydrocarbon groups, so when it's applied as a film to the silica particles, they become hydrophobic as well. Troykyd D762Hydrophobic silica is used to solve technical problems in a number of products including, but not limited to, paints, inks, adhesives, plastics, coatings, toners, defoamers, silicone rubber, sealants, cosmetics, food additives, polyester resins, cable gels, and greases. Troykyd D762 It's often manufactured as both single and multiphase composites in order to enhance properties such as dispersion, stability behavior, resistance to water, and functionality.
TROYSAN 198
DESCRIPTION Troysan 198 is a liquid, organic based bactericide used for the protection of water based products against microbial spoilage in the wet state. Typical applications include the preservation of resins, emulsion paints, adhesives, dispersed colors, caulks, sealant and printing inks. Two major advantages of Troysan 198 are that it is non-yellowing, and hence can be used in whites, and it is highly cost effective. USE AND METHODS OF APPLICATIONS Troysan 198 was specifically developed to protect aqueous materials against microbial attack during storage in the wet state. Troysan 198 Due to its low viscosity and complete solubility in water, Troysan 198 can be easily incorporated at any point in the manufacturing operation. Troysan 198 can be added by a chemical metering pump or by conventional liquid measure. When used at appropriate levels, Troysan 198 will preserve the aqueous product against microbial deterioration during storage in the unopened container and during the product’s useful service life. INCORPORATION Troysan 198 can be easily incorporated at any point in the manufacturing operation. It can be added by a chemical metering pump or by conventional liquid measure. USE LEVEL Suggested use levels vary from 0.05% to 0.6% based on the total weight of the formulation. For the preservation of emulsion resins levels of 0.05--0.2% are recommended. Emulsion paints and dispersed colors require levels from 0.1--0.3%, and starch adhesives levels range from 0.1--0.6%. It is not recommended for use in systems with a pH below 7. TYPICAL PROPERTIES Physical Form: Clear liquid Specific Gravity :1.089 ± 0.007 pH (as is): 8.2—8.8 Solubility in Water : Complete Color (Gardner): 1 max
TROYSAN S89 PASTE
Trisodium Orthophosphate; Phosphoric acid, trisodium, 12-hydrate; Sodium Phosphate Tribasic Dodecahydrate; Trisodium phosphate, dodecahydrate; TSP dodecahydrate; Tertiary Sodium phosphate; cas no: 7601-54-9
TSGD (TETRASODIUM GLUTAMATE DIACETATE)
TSGD (Tetrasodium Glutamate Diacetate), also known as Tetrasodium Dicarboxymethyl Glutamate, GLDA-Na4 for short.
TSGD (Tetrasodium Glutamate Diacetate) is a new type of green degradable chelating agent, can replace traditional phosphonates, EDTA, NTA.


CAS Number: 51981-21-6
EC Number: 257-573-7
Chem/IUPAC Name: Tetrasodium;(2S)-2-[bis(carboxylatomethyl)amino]pentanedioatee
Molecular formula: C9H9NO8Na4



C9H13NO8Na4, L-Glutamic acid, N,N-Bis(Carboxymethyl)-, Tetrasodium Salt, L-glutamic acid N,N-diacetic acid, tetrasodium salt, GLDA-Na 4, 51981-21-6, tetrasodium glutamate diacetate, UNII-5EHL50I4MY, 5EHL50I4MY, Tetrasodium N,N-Bis(carboxymethyl)-L-glutamate, Tetrasodium N,N-bis(carboxylatomethyl)-L-glutamate, EINECS 257-573-7, L-Glutamic acid, N,N-bis(carboxymethyl)-, sodium salt (1:4), EC 257-573-7, N,N-Bis(carboxymethyl)-L-glutamic Acid Tetrasodium Salt, GLDA, tetrasodium;(2S)-2-[bis(carboxylatomethyl)amino]pentanedioate, N,N-BIS-(CARBOXYMETHYL)-L-GLUTAMIC ACID TETRASODIUMN SALT, N,N-Bis(carboxymethyl)-L-glutamic acid tetrasodium salt (ca. 40% in Water), L-Glutamic acid, N,N-bis(carboxymethyl)-, tetrasodium salt, Sodium (S)-2-(bis(carboxylatomethyl)amino)pentanedioate, DISSOLVINE GL, CHELEST CMG-40, DTXSID2052158, UZVUJVFQFNHRSY-OUTKXMMCSA-J, MFCD01862262, B2135, TETRASODIUM GLUTAMATE DIACETATE [INCI], GLUTAMIC ACID N,N-DIACETIC ACID SODIUM SALT, Q25393000, N,N-BIS(CARBOXYMETHYL)GLUTAMIC ACID TETRASODIUM SALT, L-GLUTAMIC ACID-N,N-DI(ACETIC ACID) TETRASODIUM SALT, N,N-bis-(Carboxymethyl)-L-glutamic Acid Tetrasodiumn Salt (40% in water), tetrasodium mono((S)-2-(bis(carboxymethyl)amino)-4-carboxybutanoate),



TSGD (Tetrasodium Glutamate Diacetate) has a molecular weight of 351.13 and its molecular formula is C9H9NNa4O8.
TSGD (Tetrasodium Glutamate Diacetate) is a high purity, versatile and readily biodegradable chelating agent based upon L-glutamic acid, a natural and renewable raw material.


TSGD (Tetrasodium Glutamate Diacetate) is excellent chelating effectiveness controlling metal catalyzed decomposition.
TSGD (Tetrasodium Glutamate Diacetate) reduces water hardness and prevents precipitation.
TSGD (Tetrasodium Glutamate Diacetate) boosts performance of preservatives improving shelf life.


TSGD (Tetrasodium Glutamate Diacetate) stabilizes the pH value and is effective in wide pH range.
TSGD (Tetrasodium Glutamate Diacetate) does not sensitize human skin.
TSGD (Tetrasodium Glutamate Diacetate) is completely biodegradable as compared to phosphates and phosphonates.


TSGD (Tetrasodium Glutamate Diacetate) is effective alternative to EDTA.
TSGD (Tetrasodium Glutamate Diacetate) is what's known as a 'chelating agent', an ingredient that inactivates metallic ions (charged particles) in product formulations.


Free roaming iron and copper ions in formulations can lead to rapid oxidation, meaning they will spoil quickly.
Using a chelating agent helps to slow this process, allowing for the creation of products with improved stability and appearance.
This also improves the effectiveness of preservative ingredients, allowing us to use a lower percentage of these, for safer shelf-stable products.


TSGD (Tetrasodium Glutamate Diacetate) is a new type of green degradable chelating agent, can replace traditional phosphonates, EDTA, NTA.
TSGD (Tetrasodium Glutamate Diacetate) is suit for a wide pH range, with high solubility, high temperature resistance, strong detergency, no ecological toxicity, has synergistic effect with fungicides, and no irritation to skin and eyes.


TSGD (Tetrasodium Glutamate Diacetate) is a plant-based chelating agent.
TSGD (Tetrasodium Glutamate Diacetate) is the counterpart of EDTA but unlike EDTA, it is extracted from the seed of an Indian plant, Cassia Angustifolia.
Cassia Angustifolia (angustifolia = narrow leaf) is native to the Arabias and Somalia and is cultivated in many locations in India.


TSGD (Tetrasodium Glutamate Diacetate) is high purity, versatile and readily biodegradable chelating agent based upon L-glutamic acid, a natural and renewable raw material.
Also known as TSGD (Tetrasodium Glutamate Diacetate) chelate.



TSGD (Tetrasodium Glutamate Diacetate) is in liquid form with a transparent coloration.
TSGD (Tetrasodium Glutamate Diacetate) is bio-compatible and bio-degradable.
Since TSGD (Tetrasodium Glutamate Diacetate) is not easily absorbed by the skin, it does not irritate or sensitize it.


The use of TSGD (Tetrasodium Glutamate Diacetate) is approved in the formulation of Bio Natural cosmetics.
When added to a compound, TSGD (Tetrasodium Glutamate Diacetate) has stabilizing properties that preserves products and prevents discoloration.
In high concentrations, TSGD (Tetrasodium Glutamate Diacetate) can even enhance cleaning abilities and improve surfactant performance.


TSGD (Tetrasodium Glutamate Diacetate) is made from plant material, readily biodegradable, with high solubility over a wide pH range.
TSGD (Tetrasodium Glutamate Diacetate) serves the same function in formulations as EDTA, without the health and environmental concerns.
TSGD (Tetrasodium Glutamate Diacetate) is a safe synthetic chelating agent with natural origins.


TSGD (Tetrasodium Glutamate Diacetate) is used in amounts up to 1% to boost the effectiveness of preservatives, allowing for the use of lower amounts than is typical without compromising effectiveness.



USES and APPLICATIONS ofTSGD (TETRASODIUM GLUTAMATE DIACETATE):
TSGD (Tetrasodium Glutamate Diacetate) is used cleaning agents, detergents, textile auxiliaries, daily chemicals, oilfield water treatment, pulp and paper auxiliaries, metal surface treatment, etc.
TSGD (Tetrasodium Glutamate Diacetate) is an organic salt synthesized from glutamic acid (an amino acid abundant in nature).


TSGD (Tetrasodium Glutamate Diacetate) usually appears as an odourless white powder that is soluble in water, and is used as a multi-purpose, clear, liquid chelating agent and preservative booster.
Typical use level of TSGD (Tetrasodium Glutamate Diacetate) is 0.1-0.5%.


Add TSGD (Tetrasodium Glutamate Diacetate) at the end of formulation process or to water phase of emulsions.
TSGD (Tetrasodium Glutamate Diacetate) is used for external use only.
TSGD (Tetrasodium Glutamate Diacetate) is used All kinds of cosmetic products like creams, lotions, shampoos, conditioners, makeup products, sunscreen products, hair colorings, powders, personal care wipes.


TSGD (Tetrasodium Glutamate Diacetate) is a 'chelating agent'.
TSGD (Tetrasodium Glutamate Diacetate) usually appears as an odorless white powder that is soluble in water, and is used as a multi-purpose, clear, liquid chelating agent and preservative booster.


TSGD (Tetrasodium Glutamate Diacetate) is used as a rinsing aid and a chelating agent, GLDA can be used in the following ways across different products.
TSGD (Tetrasodium Glutamate Diacetate) is a multi-purpose, clear, liquid chelating agent and preservative booster.


Skincare: TSGD (Tetrasodium Glutamate Diacetate) is used as a chelating agent, GLDA improves stability and improves the effectiveness of preservatives in sunscreens, facial cleansers, makeup, and bar soap.
Haircare: In shampoos and gels, TSGD (Tetrasodium Glutamate Diacetate) prevents natural discoloration and similar to in skincare, it also works as a stabilizer and chelating agent.


Consult a Medical Professional: If you are considering adding TSGD (Tetrasodium Glutamate Diacetate) to your daily skincare or haircare routine or as a part of your diet, consult your dermatologist or dietician.
TSGD (Tetrasodium Glutamate Diacetate) can ensure that the ingredient will benefit your health and body’s specific needs and sensitivities.



WHAT IS TSGD (TETRASODIUM GLUTAMATE DIACETATE) USED FOR?
TSGD (Tetrasodium Glutamate Diacetate) inactivates metallic ions (charged particles) in product formulations, hence acting as is a chelating agent.
Free roaming iron and copper ions in formulations can lead to rapid oxidation.
Using a chelating agent helps to slow this process, allowing for the creation of products with improved stability and appearance.
This also improves the effectiveness of preservative ingredients, allowing us to use a lower percentage of these, for safer shelf-stable products.
TSGD (Tetrasodium Glutamate Diacetate) is often found in sunscreen, facial cleanser, shampoo, makeup, lotion, cleansing wipes, bar soap, and other cleaning products.
Origin
TSGD (Tetrasodium Glutamate Diacetate) is an organic salt synthesized from glutamic acid (an amino acid abundant in nature).



ALTERNATIVES OF TSGD (TETRASODIUM GLUTAMATE DIACETATE):
*TRISODIUM ETHYLENEDIAMINE DISUCCINATE
*EDTA



WHAT DOES TETRASODIUM GLUTAMATE DIACETATE DO IN A FORMULATION?
*Chelating



BENEFITS OF TSGD (TETRASODIUM GLUTAMATE DIACETATE):
*Excellent chelating effectiveness controlling metal catalyzed decomposition
*Reduces water hardness and prevents precipitations
*Boosts performance of preservatives improving shelf life
*Stabilizes the pH value and is effective in wide pH range
*Does not sensitize human skin
*Completely biodegradable as compared to phosphates and phosphonates
*Effective alternative to EDTA



TSGD (TETRASODIUM GLUTAMATE DIACETATE) IS OFTEN FOUND IN:
*Sunscreen,
*Facial cleanser,
*Shampoo,
*Makeup,
*Lotion,
*Detergents,
*Cleansing wipes,
*Bar soap,
*Body oil,
*Food products,
*Bath soak,
*Bath products



HOW TSGD (TETRASODIUM GLUTAMATE DIACETATE) IS MADE:
Metal organic acid chelates are made by reacting a metal ion from a soluble metal salt with an organic acid or its salt.
For example, amino acid chelates have generally been made by reacting one or more amino acids, dipeptides, polypeptides, or protein hydrolysate ligands in an aqueous environment.
Under appropriate conditions, this causes an interaction between the metal and amino acids to form amino acid chelates.
Organic acid chelates have been generally been made by producing a reaction by using either amino acids, picolinic, nicotinic acids, or hydroxycarboxylic acids.



IS TSGD (TETRASODIUM GLUTAMATE DIACETATE) SAFE FOR SKIN?
Research shows TSGD (Tetrasodium Glutamate Diacetate) is not a strong skin irritant.



FEATURES OF TSGD (TETRASODIUM GLUTAMATE DIACETATE):
1. High solubility under wide pH:
TSGD (Tetrasodium Glutamate Diacetate) has good solubility in strong acid to high alkali systems, and has better advantages for formulating high active ingredients and low water content formulation systems.

2. Good stability under high temperature:
By thermogravimetric analysis, TSGD (Tetrasodium Glutamate Diacetate) is tested at 170°C for 6 hours or at 150°C for a week.
TSGD (Tetrasodium Glutamate Diacetate) has no decomposition and is extremely stable.
Compared with other chelating agent products at 100°C, TSGD (Tetrasodium Glutamate Diacetate) has the best performance.

3. Strong chelating ability:
TSGD (Tetrasodium Glutamate Diacetate) has a good effect on all kinds of difficult-to-clean calcium scales or difficult-to-clean equipment.

4. Has the effect of antiseptic and synergistic:
Because TSGD (Tetrasodium Glutamate Diacetate) has natural amino acid components, it has a stronger binding ability with animal cell walls, and thus play a role in antiseptic and synergistic.
After experiments, we found that TSGD (Tetrasodium Glutamate Diacetate) has obvious antiseptic and sterilization synergies in many fungicides, which can save 20%-80% of the usage.



SAFETY PROFILE OF TSGD (TETRASODIUM GLUTAMATE DIACETATE):
The safety of TSGD (Tetrasodium Glutamate Diacetate) was assessed by the Expert Panel for Cosmetic Ingredient Safety (formerly called the Cosmetic Ingredient Review Expert Panel) in 2021.
The Expert Panel concluded that it was safe as used in the present practices of use and concentration in cosmetics and personal care products.
The Expert Panel noted Tetrasodium Glutamate Diacetate is slowly absorbed through the gastrointestinal tract and skin absorption is likely to be even slower.
The Expert Panel also noted the lack of carcinogenicity (cancer-causing potential) data and that it may contain a salt of nitrilotriacetic acid, a category 2B carcinogen according to the International Agency for Research on Cancer (IARC).
However, the concern was mitigated by multiple genotoxicity studies (both in vitro and in vivo), which did not indicate adverse genetic activity at the low concentrations of this ingredient in leave-on products.



WHAT IS A CHELATOR OR SEQUESTRANT, TSGD (TETRASODIUM GLUTAMATE DIACETATE)?
TSGD (Tetrasodium Glutamate Diacetate) is a substance consisting of molecules possessing two or more atoms that can bind to the same metal atom to form stable complexes.
In cosmetics TSGD (Tetrasodium Glutamate Diacetate) is often used to reduce or prevent reactions catalyzed by trace or impurity metals in formulations.

TSGD (Tetrasodium Glutamate Diacetate) also enhances the effect of the preservative in some cases and generally give stability to the formulation.
TSGD (Tetrasodium Glutamate Diacetate) is a high-purity, versatile and readily biodegradable chelator based on L-glutamic acid, a natural and renewable raw material.



DIFFERENCES BETWEEN TSGD (TETRASODIUM GLUTAMATE DIACETATE) AND EDTA:
Demonizing EDTA would be a mistake, but it must be said that some substances commonly used in cosmetics can, as of today, be replaced with more eco-friendly alternatives.

This is the case with EDTA, which has always been used as a chelator, especially in rinse-off products such as shampoos or detergents, because it also has an inherent cleansing action.
Studies, however, show that its metal sequestering action is, especially with regard to the marine ecosystem, very polluting because it allows greater dispersion of heavy metals into sea water, especially when used in everyday detergents.

In skincare cosmetics, the use of EDTAs definitely has a lower environmental impact especially because of their leave-on nature (they do not rinse off).
However, using more eco-friendly alternatives here as well, such as TSGD (Tetrasodium Glutamate Diacetate), is meant to be a support for future generations not to underestimate any aspect related to the environment.

For more information, you can read the interesting report on the ECOBIOCONTROL website that makes a comparison between EDTA and TSGD (Tetrasodium Glutamate Diacetate) in terms of environmental impact.
Finally, it should be kept in mind that TSGD (Tetrasodium Glutamate Diacetate) is not a skin sensitizer and is therefore less aggressive on the skin as well.



PHYSICAL and CHEMICAL PROPERTIES of TSGD (TETRASODIUM GLUTAMATE DIACETATE):
Appearance: Light yellow viscous liquid
Content /%: ≥47
pH value: ≥8.5
Density(20℃) g/cm3: ≥1.20
Boiling Point: 105-110°C
Specific Gravity: 1.15-1.45
pH: 11-12 (in 1% water)
Solubility: Completely miscible in water
Slightly soluble in methanol/ethanol
Viscosity: 75-275 mPa.s @ 25°C
Molecular Weight: 351.13 g/mol
Hydrogen Bond Donor Count: 0
Hydrogen Bond Acceptor Count: 9

Rotatable Bond Count: 5
Exact Mass: 350.99189337 g/mol
Monoisotopic Mass: 350.99189337 g/mol
Topological Polar Surface Area: 164Ų
Heavy Atom Count: 22
Formal Charge: 0
Complexity: 314
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 1
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 5
Compound Is Canonicalized: Yes




FIRST AID MEASURES of TSGD (TETRASODIUM GLUTAMATE DIACETATE):
-Description of first-aid measures:
*If inhaled:
If breathed in, move person into fresh air.
*In case of skin contact:
Wash off with soap and plenty of water.
*In case of eye contact:
Flush eyes with water as a precaution.
*If swallowed:
Never give anything by mouth to an unconscious person. Rinse mouth with water.
-Indication of any immediate medical attention and special treatment needed:
No data available



ACCIDENTAL RELEASE MEASURES of TSGD (TETRASODIUM GLUTAMATE DIACETATE):
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Keep in suitable, closed containers for disposal.



FIRE FIGHTING MEASURES of TSGD (TETRASODIUM GLUTAMATE DIACETATE):
-Extinguishing media:
*Suitable extinguishing media:
Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.
-Further information:
No data available



EXPOSURE CONTROLS/PERSONAL PROTECTION of TSGD (TETRASODIUM GLUTAMATE DIACETATE):
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
*Skin protection:
Handle with gloves.
Wash and dry hands.
*Body Protection:
Impervious clothing
*Respiratory protection:
Respiratory protection not required.
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of TSGD (TETRASODIUM GLUTAMATE DIACETATE):
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Store in cool place.
Keep container tightly closed in a dry and well-ventilated place.



STABILITY and REACTIVITY of TSGD (TETRASODIUM GLUTAMATE DIACETATE):
-Reactivity:
No data available
-Chemical stability:
Stable under recommended storage conditions.
-Possibility of hazardous reactions:
No data available
-Conditions to avoid:
No data available



TSP (TRI SODIUM PHOSPHATE)
SODIUM PYROPHOSPHATE; Diphosphoric acid, tetrasodium salt; Phosphotex; Pyrophosphoric acid, tetrasodium salt; Sodium Diphosphate; Sodium pyrophosphate (4:1); Tetrasodium diphosphate; Tetrasodium Pyrophosphate; TSPP; cas no: 7722-88-5
TSPP (TETRASODIUM DIPHOSPHATE)
DESCRIPTION:


TSPP (Tetrasodium Diphosphate), also called sodium pyrophosphate, tetrasodium phosphate or TSPP, is an inorganic compound with the formula Na4P2O7.
As a salt, TSPP (Tetrasodium Diphosphate) is a white, water-soluble solid.
TSPP (Tetrasodium Diphosphate) is composed of pyrophosphate anion and sodium ions.


CAS Number 7722-88-5
EC Number 231-767-1

SYNONYMS OF TSPP (TETRASODIUM DIPHOSPHATE)
Pyrophosphate, Sodium pyrophosphate, Tetrasodium pyrophosphate (anhydrous), TSPP[1],anhydrous sodium pyrophosphate,disodium pyrophosphate,sodium diphosphate,sodium pyrophosphate,tetrasodium pyrophosphate,tetrasodium pyrophosphate, 32P2-labeled cpd,tetrasodium pyrophosphate, decahydrate,trisodium pyrophosphate,Sodium pyrophosphate,TETRASODIUM PYROPHOSPHATE,7722-88-5,TSPP,Phosphotex,Tetrasodium diphosphate,Sodium diphosphate,Diphosphoric acid, tetrasodium salt,Victor TSPP,Caswell No. 847,Sodium pyrophosphate tetrabasic,Natrium pyrophosphat,Sodium pyrophosphate [USAN],Sodium diphosphate, anhydrous,Pyrophosphoric acid tetrasodium salt,Sodium phosphate (Na4P2O7),HSDB 854,sodium pyrophosphate(V),Sodium diphosphate (Na4P2O7),Sodium pyrophosphate, tetrabasic,Sodium pyrophosphate (Na4P2O7),Anhydrous tetrasodium pyrophosphate,Tetrasodium pyrophosphate, anhydrous,EINECS 231-767-1,NSC 56751,EPA Pesticide Chemical Code 076405,DTXSID9042465,UNII-O352864B8Z,CHEBI:71240,MFCD00003513,NSC-56751,Na4P2O7,O352864B8Z,DTXCID7022465,EC 231-767-1,Sodium pyrophosphate (USAN),Natrium pyrophosphat [German],SODIUM PYROPHOSPHATE (II),SODIUM PYROPHOSPHATE [II],SODIUM PYROPHOSPHATE (MART.),SODIUM PYROPHOSPHATE [MART.],1004291-85-3,Tetranatriumpyrophosphat [German],Tetrasodium pyrophosphate, anhydride,Tetrasodium pyrophosphate (anhydrous),SODIUMPYROPHOSPHATE,tetra sodium pyrophosphate,ACCOLINE 126,Na4O7P2,TETRON (DISPERSANT),Diphosphoric acid sodium salt,Sodium pyrophosphate anhydrous,DTXCID408842,Sodium diphosphate (Na4(P2O7)),SODIUM PYROPHOSPHATE [FCC],Tetrasodium pyrophosphate Anhydrous,SODIUM PYROPHOSPHATE [HSDB],CS-B1771,SODIUM PYROPHOSPHATE [VANDF],tetrasodium (phosphonooxy)phosphonate,Tox21_110033,SODIUM PYROPHOSPHATE [WHO-DD],TETRASODIUM PYROPHOSPHATE [MI],AKOS015914004,AKOS024418778,Diphosphoric acid, sodium salt (1:4),TETRASODIUM PYROPHOSPHATE [INCI],NCGC00013687-01,CAS-7722-88-5,TETRASODIUM DIPHOSPHATE (NA4P2O7),TETRASODIUM PYROPHOSPHATE (NA4P2O7),E 450,NS00093593,D05873,E75941,EN300-332889,Q418504

Toxicity is approximately twice that of table salt when ingested orally.
Also known is the decahydrate Na4P2O7 • 10(H2O).

Sodium diphosphate is an inorganic sodium salt comprised of a diphosphate(4-) anion and four sodium(1+) cations.
More commonly known as tetrasodium pyrophosphate, TSPP (Tetrasodium Diphosphate) finds much use in the food industry as an emulsifier and in dental hygiene as a calcium-chelating salt.

TSPP (Tetrasodium Diphosphate) has a role as a food emulsifier, a chelator and a food thickening agent.
TSPP (Tetrasodium Diphosphate) contains a diphosphate(4-).


TSPP (Tetrasodium Diphosphate) İs used in water softener, detergent, emulsifying agent, metal cleaner and nutritional supplement.
TSPP (Tetrasodium Diphosphate) acts as a buffering agent, thickening agent and dispersing agent.
TSPP (Tetrasodium Diphosphate) also acts as a tartar control agent in toothpaste and dental floss.

In addition, TSPP (Tetrasodium Diphosphate) is used as a chelating agent in antimicrobial studies.
TSPP (Tetrasodium Diphosphate) is also used as a food additive in common foods such as chicken nuggets, crab meat and canned tuna.


TSPP (Tetrasodium Diphosphate) appears as odorless, white powder or granules. mp: 995 °C. Density: 2.53 g/cm3.
Solubility in water: 3.16 g/100 mL (cold water); 40.26 g/100 mL boiling water.
TSPP (Tetrasodium Diphosphate) is Used as a wool de-fatting agent, in bleaching operations, as a food additive.

The related substance tetrasodium pyrophosphate decahydrate (Na4P2O7*10H2O) occurs as colorless transparent crystals.
TSPP (Tetrasodium Diphosphate) Loses its water when heated to 93.8 °C.


Tetrasodium Pyrophosphate Anhydrous - also known as Anhydrous TSPP, Sodium Pyrophosphate, or Tetrasodium Diphosphate - is a white crystalline powder with a molecular formula of Na4P2O7.
TSPP (Tetrasodium Diphosphate) is certified FCC IV and Kosher. It functions as a coagulant, emulsifier, and sequestrant.
TSPP (Tetrasodium Diphosphate) is commonly used in malted milk powders, instant puddings, cheese, chocolate drink powders, and tuna.




USES OF TSPP (TETRASODIUM DIPHOSPHATE):
Just Egg, a plant-based egg alternative that contains tetrasodium pyrophosphate
Tetrasodium pyrophosphate is used as a buffering agent, an emulsifier, a dispersing agent, and a thickening agent, and is often used as a food additive.
Common foods containing tetrasodium pyrophosphate include chicken nuggets, marshmallows, pudding, crab meat, imitation crab, canned tuna, and soy-based meat alternatives and cat foods and cat treats where it is used as a palatability enhancer.

In toothpaste and dental floss, tetrasodium pyrophosphate acts as a tartar control agent, serving to remove calcium and magnesium from saliva and thus preventing them from being deposited on teeth.
Tetrasodium pyrophosphate is used in commercial dental rinses before brushing to aid in plaque reduction.

Tetrasodium pyrophosphate is sometimes used in household detergents to prevent similar deposition on clothing, but due to its phosphate content it causes eutrophication of water, promoting algae growth.


PRODUCTION OF TSPP (TETRASODIUM DIPHOSPHATE):
Tetrasodium pyrophosphate is produced by the reaction of furnace-grade phosphoric acid with sodium carbonate to form disodium phosphate, which is then heated to 450 °C to form tetrasodium pyrophosphate:[5]
2 Na2HPO4 → Na4P2O7 + H2O


APPLICATIONS OF TSPP (TETRASODIUM DIPHOSPHATE):

TSPP (Tetrasodium Diphosphate) is used in water softener, detergent, emulsifying agent, metal cleaning agent and nutritional supplement.
TSPP (Tetrasodium Diphosphate) acts as a buffering agent, thickening agent and dispersing agent.
TSPP (Tetrasodium Diphosphate) also acts as a tartar control agent in toothpaste and dental floss.

Additionally, TSPP (Tetrasodium Diphosphate) is used as a chelating agent in antimicrobial studies.
TSPP (Tetrasodium Diphosphate) is also used as a food additive in common foods such as chicken nuggets, crab meat, and canned tuna.



CHEMICAL AND PHYSICAL PROPERTIES OF TSPP (TETRASODIUM DIPHOSPHATE):
Chemical formula Na4O7P2
Molar mass 265.900 g•mol−1
Appearance Colorless or white crystals[2]
Odor odorless
Density 2.534 g/cm3
Melting point 988 °C (1,810 °F; 1,261 K) (anhydrous)
79.5 °C (decahydrate)
Boiling point decomposes
Solubility in water 2.61 g/100 mL (0 °C)
6.7 g/100 mL (25 °C)
42.2 g/100 mL (100 °C)
Solubility insoluble in ammonia, alcohol
Refractive index (nD) 1.425
Structure
Crystal structure monoclinic (decahydrate)
Thermochemistry
Heat capacity (C) 241 J/mol K
Std molar
entropy (S⦵298) 270 J/mol K
Std enthalpy of
formation (ΔfH⦵298) -3166 kJ/mol
Gibbs free energy (ΔfG⦵) -3001 kJ/mol
CAS number 13472-36-1
EC number 231-767-1
Grade ACS,Reag. Ph Eur
Hill Formula Na₄O₇P₂ * 10 H₂O
Chemical formula Na₄P₂O₇ * 10 H₂O
Molar Mass 446.06 g/mol
HS Code 2835 39 20
Density 1.82 g/cm3 (20 °C)
Melting Point 988 °C (anhydrous substance)
pH value 10.2 (10 g/l, H₂O, 25 °C)
Bulk density 650 kg/m3
Solubility 60 g/l (anhydrous substance)
Density 1.82 g/cm3 (20 °C)
Melting Point 988 °C (anhydrous substance)
pH value 10.2 (10 g/l, H₂O, 25 °C)
Bulk density 650 kg/m3
Solubility 60 g/l (anhydrous substance)
Assay (acidimetric) 99.0 - 103.0 %
Insoluble matter ≤ 0.01 %
pH-value (5 %; water, 25 °C) 9.5 - 10.5
Chloride (Cl) ≤ 0.001 %
Orthophosphate (PO₄) ≤ 0.1 %
Sulfate (SO₄) ≤ 0.005 %
Total nitrogen (N) ≤ 0.001 %
Fe (Iron) ≤ 0.0005 %
K (Potassium) ≤ 0.005 %
Heavy metals (as Pb) ≤ 0.0005 %
Chemical name or material Sodium pyrophosphate
Fusion point 988°C
Quantity 250 g
Linear formula Na4P2O7
Merck Index 14,9240
Solubility Information Soluble in water. Insoluble in ethyl alcohol.
Formula weight 265.9
Purity percentage 98%
Sensitivity Hygroscopic
Density 2.534
Molecular Weight
265.90 g/mol
Computed by PubChem 2.2 (PubChem release 2021.10.14)
Hydrogen Bond Donor Count
0
Computed by Cactvs 3.4.8.18 (PubChem release 2021.10.14)
Hydrogen Bond Acceptor Count
7
Computed by Cactvs 3.4.8.18 (PubChem release 2021.10.14)
Rotatable Bond Count
0
Computed by Cactvs 3.4.8.18 (PubChem release 2021.10.14)
Exact Mass
265.87100346 g/mol
Computed by PubChem 2.2 (PubChem release 2021.10.14)
Monoisotopic Mass
265.87100346 g/mol
Computed by PubChem 2.2 (PubChem release 2021.10.14)
Topological Polar Surface Area
136Ų
Computed by Cactvs 3.4.8.18 (PubChem release 2021.10.14)
Heavy Atom Count
13
Computed by PubChem
Formal Charge
0
Computed by PubChem
Complexity
124
Computed by Cactvs 3.4.8.18 (PubChem release 2021.10.14)
Isotope Atom Count
0
Computed by PubChem
Defined Atom Stereocenter Count
0
Computed by PubChem
Undefined Atom Stereocenter Count
0
Computed by PubChem
Defined Bond Stereocenter Count
0
Computed by PubChem
Undefined Bond Stereocenter Count
0
Computed by PubChem
Covalently-Bonded Unit Count
5
Computed by PubChem
Compound Is Canonicalized
Yes



SAFETY INFORMATION ABOUT TSPP (TETRASODIUM DIPHOSPHATE):
First aid measures:
Description of first aid measures:
General advice:
Consult a physician.
Show this safety data sheet to the doctor in attendance.
Move out of dangerous area:

If inhaled:
If breathed in, move person into fresh air.
If not breathing, give artificial respiration.
Consult a physician.
In case of skin contact:
Take off contaminated clothing and shoes immediately.
Wash off with soap and plenty of water.
Consult a physician.

In case of eye contact:
Rinse thoroughly with plenty of water for at least 15 minutes and consult a physician.
Continue rinsing eyes during transport to hospital.

If swallowed:
Do NOT induce vomiting.
Never give anything by mouth to an unconscious person.
Rinse mouth with water.
Consult a physician.

Firefighting measures:
Extinguishing media:
Suitable extinguishing media:
Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.
Special hazards arising from the substance or mixture
Carbon oxides, Nitrogen oxides (NOx), Hydrogen chloride gas

Advice for firefighters:
Wear self-contained breathing apparatus for firefighting if necessary.
Accidental release measures:
Personal precautions, protective equipment and emergency procedures
Use personal protective equipment.

Avoid breathing vapours, mist or gas.
Evacuate personnel to safe areas.

Environmental precautions:
Prevent further leakage or spillage if safe to do so.
Do not let product enter drains.
Discharge into the environment must be avoided.

Methods and materials for containment and cleaning up:
Soak up with inert absorbent material and dispose of as hazardous waste.
Keep in suitable, closed containers for disposal.

Handling and storage:
Precautions for safe handling:
Avoid inhalation of vapour or mist.

Conditions for safe storage, including any incompatibilities:
Keep container tightly closed in a dry and well-ventilated place.
Containers which are opened must be carefully resealed and kept upright to prevent leakage.
Storage class (TRGS 510): 8A: Combustible, corrosive hazardous materials

Exposure controls/personal protection:
Control parameters:
Components with workplace control parameters
Contains no substances with occupational exposure limit values.
Exposure controls:
Appropriate engineering controls:
Handle in accordance with good industrial hygiene and safety practice.
Wash hands before breaks and at the end of workday.

Personal protective equipment:
Eye/face protection:
Tightly fitting safety goggles.
Faceshield (8-inch minimum).
Use equipment for eye protection tested and approved under appropriate government standards such as NIOSH (US) or EN 166(EU).

Skin protection:
Handle with gloves.
Gloves must be inspected prior to use.
Use proper glove
removal technique (without touching glove's outer surface) to avoid skin contact with this product.
Dispose of contaminated gloves after use in accordance with applicable laws and good laboratory practices.
Wash and dry hands.

Full contact:
Material: Nitrile rubber
Minimum layer thickness: 0.11 mm
Break through time: 480 min
Material tested:Dermatril (KCL 740 / Aldrich Z677272, Size M)
Splash contact
Material: Nitrile rubber
Minimum layer thickness: 0.11 mm
Break through time: 480 min
Material tested:Dermatril (KCL 740 / Aldrich Z677272, Size M)
It should not be construed as offering an approval for any specific use scenario.

Body Protection:
Complete suit protecting against chemicals, The type of protective equipment must be selected according to the concentration and amount of the dangerous substance at the specific workplace.
Respiratory protection:
Where risk assessment shows air-purifying respirators are appropriate use a fullface respirator with multi-purpose combination (US) or type ABEK (EN 14387) respirator cartridges as a backup to engineering controls.

If the respirator is the sole means of protection, use a full-face supplied air respirator.
Use respirators and components tested and approved under appropriate government standards such as NIOSH (US) or CEN (EU).
Control of environmental exposure
Prevent further leakage or spillage if safe to do so.
Do not let product enter drains.
Discharge into the environment must be avoided.

Stability and reactivity:
Chemical stability:
Stable under recommended storage conditions.
Incompatible materials:
Strong oxidizing agents:
Hazardous decomposition products:
Hazardous decomposition products formed under fire conditions.
Carbon oxides, Nitrogen oxides (NOx), Hydrogen chloride gas.

Disposal considerations:
Waste treatment methods:
Product:
Offer surplus and non-recyclable solutions to a licensed disposal company.
Contact a licensed professional waste disposal service to dispose of this material.
Contaminated packaging:
Dispose of as unused product.



TSPP (TETRASODIUM PYROPHOSPHATE)
TSPP (Tetrasodium pyrophosphate), also known as Sodium Pyro phosphate, Tetra sodium phosphate or TSPP, is achemical compound composed of pyrophosphate and sodium ions.
TSPP (Tetrasodium pyrophosphate) is a colorless transparent crystalline chemical compound containing the pyrophosphate ion and sodium cation.


CAS Number: 7722-88-5
13472-36-1 (decahydrate)
EC Number: 231-767-1
E number: E450(iii) (thickeners, ...)
Molecular Formula: Na4P2O7 / Na4O7P2
Chemical formula: Na4O7P2


TSPP (Tetrasodium pyrophosphate) is odourless, white powder or granules, which comes in different grades.
TSPP (Tetrasodium pyrophosphate) is a widely used chemical in many different applications.
TSPP (Tetrasodium pyrophosphate) is a colorless, transparent crystals or white powder or granules.


TSPP (Tetrasodium pyrophosphate) is odorless; slightly soluble in water; insoluble in alcohol and ammonia.
TSPP (Tetrasodium pyrophosphate) is a white powdered chemical found in detergents.
TSPP (Tetrasodium pyrophosphate) improves the ability of different detergent components to pervade deeper into the fibers of clothes, as well as other surfaces and materials to be cleaned.


TSPP (Tetrasodium pyrophosphate) is an anhydrous, white, crystalline material in powder form.
TSPP (Tetrasodium pyrophosphate) is a white, water-soluble solid.
TSPP (Tetrasodium pyrophosphate) appears as odorless, white powder or granules. mp: 995 °C.


The related substance TSPP (Tetrasodium pyrophosphate) decahydrate (Na4P2O7*10H2O) occurs as colorless transparent crystals.
Loses TSPP (Tetrasodium pyrophosphate)'s water when heated to 93.8 °C.
TSPP (Tetrasodium pyrophosphate) is an odorless, white powder or granules.


TSPP (Tetrasodium pyrophosphate) is solubility in water: 3.16 g / 100 mL (cold water); 40.26 g / 100 mL boiling water.
TSPP (Tetrasodium pyrophosphate)'s chemical formula is Na4P2O7 * 10 H2O.
The aqueous solution of TSPP (Tetrasodium pyrophosphate) is alkaline and easily soluble in water.


The pH of the 1% solution ranges from 10 to 11.
TSPP (Tetrasodium pyrophosphate) is an inorganic sodium salt comprised of a diphosphate(4-) anion and four sodium(1+) cations.
TSPP (Tetrasodium pyrophosphate) contains a diphosphate(4-).


TSPP (Tetrasodium pyrophosphate), also called sodium pyrophosphate, tetrasodium phosphate or TSPP, is an inorganic compound with the formula Na4P2O7.
As a salt, TSPP (Tetrasodium pyrophosphate) is a white, water-soluble solid.
TSPP (Tetrasodium pyrophosphate) is composed of pyrophosphate anion and sodium ions.


TSPP (Tetrasodium pyrophosphate) is also known is the decahydrate Na4P2O7 · 10(H2O).
TSPP (Tetrasodium pyrophosphate) should be stored in an area that is free from moisture and humidity since it is a hygroscopic compound.
Moisture can cause TSPP (Tetrasodium pyrophosphate) to clump and lose its effectiveness.


Hence, TSPP (Tetrasodium pyrophosphate) should be kept away from heat sources such as stoves and ovens.
During storage, TSPP (Tetrasodium pyrophosphate) should be kept in a well-ventilated area to promote air circulation, and reduce dampness.
TSPP (Tetrasodium pyrophosphate) should not be stored alongside other chemicals as there is a risk of cross-contamination that could impact its functionality.


Store TSPP (Tetrasodium pyrophosphate) in appropriate containers intended as it is sensitive to light exposure which can cause degradation, so it is best to use opaque containers that shield from light.
TSPP (Tetrasodium pyrophosphate) is a colorless crystalline salt composed of pyrophosphate and sodium ions.



TSPP (Tetrasodium pyrophosphate) is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 1 000 to < 10 000 tonnes per annum.
TSPP (Tetrasodium pyrophosphate) appears as an odorless, white powder or granules.


TSPP (Tetrasodium pyrophosphate), CAS# 7722-88-5, is an inorganic compound manufactured from Disodium Phosphate, available as White powder.
TSPP (Tetrasodium pyrophosphate), also called tetrasodium disphosphate or sodium pyrophosphate, is a synthetic ingredient that can be used as an acid regulator, sequestrant, protein modifier, coagulant, and a dispersing agent in food with the European food additive number E450(iii).


TSPP (Tetrasodium pyrophosphate) is gluten-free and vegan.
TSPP (Tetrasodium pyrophosphate) is a solid white inorganic compound that is water soluble.
TSPP (Tetrasodium pyrophosphate) is a salt composed of pyrophosphate anions and sodium ions.


TSPP (Tetrasodium pyrophosphate) is aproximately twice the toxicity level of common table salt.
TSPP (Tetrasodium pyrophosphate) is most commonly produced by the reaction of phosphoric acid with sodium carbonate to form disodium phosphate, which is then heated to 450 °C to form tetrasodium pyrophosphate.


TSPP (Tetrasodium pyrophosphate) anhydrous food grade is white powder form.
TSPP (Tetrasodium pyrophosphate) is easy to absorb moisture and deliquesce, but insoluble in ethanol.
The relative density of TSPP (Tetrasodium pyrophosphate) is 2.45g/cm3 and the melting point is 890.


TSPP (Tetrasodium pyrophosphate) is odorless.
TSPP (Tetrasodium pyrophosphate) is deliquescent in the open air.
TSPP (Tetrasodium pyrophosphate)'s aqueous solution shows weak alkalinity but will be hydrolyzed into di-sodium phosphate when boiled.



USES and APPLICATIONS of TSPP (TETRASODIUM PYROPHOSPHATE):
TSPP (Tetrasodium pyrophosphate) is used by consumers, in articles, by professional workers (widespread uses), in formulation or re-packing, at industrial sites and in manufacturing.
TSPP (Tetrasodium pyrophosphate) is used in the following products: pH regulators and water treatment products, water softeners, cosmetics and personal care products, coating products and fillers, putties, plasters, modelling clay.


Release to the environment of TSPP (Tetrasodium pyrophosphate) can occur from industrial use: formulation of mixtures, in the production of articles and in processing aids at industrial sites.
Other release to the environment of TSPP (Tetrasodium pyrophosphate) is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners) and outdoor use.


Other release to the environment of TSPP (Tetrasodium pyrophosphate) is likely to occur from: outdoor use in long-life materials with low release rate (e.g. metal, wooden and plastic construction and building materials) and indoor use in long-life materials with low release rate (e.g. flooring, furniture, toys, construction materials, curtains, foot-wear, leather products, paper and cardboard products, electronic equipment).


TSPP (Tetrasodium pyrophosphate) can be found in products with material based on: stone, plaster, cement, glass or ceramic (e.g. dishes, pots/pans, food storage containers, construction and isolation material), fabrics, textiles and apparel (e.g. clothing, mattress, curtains or carpets, textile toys), leather (e.g. gloves, shoes, purses, furniture), paper (e.g. tissues, feminine hygiene products, nappies, books, magazines, wallpaper), wood (e.g. floors, furniture, toys) and plastic (e.g. food packaging and storage, toys, mobile phones).


TSPP (Tetrasodium pyrophosphate) is used in the following products: pH regulators and water treatment products, water softeners and cosmetics and personal care products.
TSPP (Tetrasodium pyrophosphate) is used in the following areas: formulation of mixtures and/or re-packaging, agriculture, forestry and fishing, building & construction work and municipal supply (e.g. electricity, steam, gas, water) and sewage treatment.


TSPP (Tetrasodium pyrophosphate) is used for the manufacture of: metals, fabricated metal products and .
Release to the environment of TSPP (Tetrasodium pyrophosphate) can occur from industrial use: formulation of mixtures and in the production of articles.
Other release to the environment of TSPP (Tetrasodium pyrophosphate) is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners) and outdoor use.


TSPP (Tetrasodium pyrophosphate) is used in the following products: pH regulators and water treatment products, water softeners and polymers.
Release to the environment of TSPP (Tetrasodium pyrophosphate) can occur from industrial use: formulation of mixtures, in the production of articles, in processing aids at industrial sites and as processing aid.


Other release to the environment of TSPP (Tetrasodium pyrophosphate) is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners) and outdoor use.
TSPP (Tetrasodium pyrophosphate) is used in the following products: pH regulators and water treatment products, water softeners and polymers.


Release to the environment of TSPP (Tetrasodium pyrophosphate) can occur from industrial use: industrial abrasion processing with low release rate (e.g. cutting of textile, cutting, machining or grinding of metal).
TSPP (Tetrasodium pyrophosphate) is used as a dispersing agent, sequestrant, buffering agent, protein modifier, and coagulant.


TSPP (Tetrasodium pyrophosphate) is used to modify the proteins enabling them to retain moisture during storage, thawing, and cooking.
TSPP (Tetrasodium pyrophosphate) also increases shelf life of the product by sequestering multivalent cations responsible for lipid oxidation and rancidity development.


TSPP (Tetrasodium pyrophosphate) is added to improve whipping efficiency and improve foam stability.
Granular TSPP (Tetrasodium pyrophosphate) helps to buffer the pH of the processed cheese and interacts with milk proteins to promote emulsification.
TSPP (Tetrasodium pyrophosphate) sequesters iron in potato products to prevent after-cooking blackening and to stabilize color.


To maintain fat dispersion in an ice cream/dessert mix, TSPP (Tetrasodium pyrophosphate) may be added so "churning" will not form lumps of butter during freezing.
TSPP (Tetrasodium pyrophosphate) is used as a buffering agent, also as an emulsifier and as a dispersing agent


TSPP (Tetrasodium pyrophosphate) also used as a thickening agent and also often used as a food additive
TSPP (Tetrasodium pyrophosphate) is used in common baking powders and also in toothpaste and dental floss as a tartar control
TSPP (Tetrasodium pyrophosphate) is also used in household detergents


TSPP (Tetrasodium pyrophosphate) is used for use in food.
TSPP (Tetrasodium pyrophosphate) is used as an acidity regulator,
TSPP (Tetrasodium pyrophosphate) is used in soy-based meat alternatives, chicken nuggets and lobster products, to promote the binding of proteins to water and the co-binding of soy particles,


TSPP (Tetrasodium pyrophosphate) is used as a buffer in toothpastes, as an emulsifier and as a detergent aid.
TSPP (Tetrasodium pyrophosphate) is used as a thickener in instant puddings,
TSPP (Tetrasodium pyrophosphate) can be used as a water softener in detergents, as an emulsifier to suspend oils and to prevent re-deposition on laundry during washing.


TSPP (Tetrasodium pyrophosphate) is used Buffering Agent, Emulsifier, Dispersing Agent, Thickening Agent, Tartar Control Agent, and Toothpaste.
TSPP (Tetrasodium pyrophosphate) is a thickening agent and emulsifier.
TSPP (Tetrasodium pyrophosphate) is commonly applied in chicken nuggets, canned tuna, imitation crab meat, pudding, marshmallows, and soy-based meat alternatives.


TSPP (Tetrasodium pyrophosphate) is used as a buffering agent, an emulsifier, a dispersing agent, and a thickening agent, and is often used as a food additive.
Common foods containing TSPP (Tetrasodium pyrophosphate) include chicken nuggets, marshmallows, pudding, crab meat, imitation crab, canned tuna, and soy-based meat alternatives and cat foods and cat treats where it is used as a palatability enhancer.


TSPP (Tetrasodium pyrophosphate) is used in the food industry as an emulsifier, buffer, chelating agent, gelling agent, and stabilizer.
TSPP (Tetrasodium pyrophosphate) finds diverse applications in various industries, including.
Food Industry: TSPP (Tetrasodium pyrophosphate) is used as a food additive (E450) in processed foods, acting as a buffer, emulsifier, and dispersing agent.


TSPP (Tetrasodium pyrophosphate) also called Sodium pyrophosphate is used in many applications as a buffering agent, an emulsifier, a dispersing agent, a thickening agent, general sequestering agent, chelating agent in antimicrobial studies and in the food industry as a nutrient, dietary supplement and texturier in food additive.


TSPP (Tetrasodium pyrophosphate) also acts as a tartar control agent in toothpaste and dental floss.
Pyrophosphates as stated by Considine (Food and Food Production Encylopedia) are good sequestrants for copper and iron, which often catalyze oxidation in fruits and vegetables.


TSPP (Tetrasodium pyrophosphate) is also used as a food additive in common foods such as chicken nuggets, crab meat, and canned tuna.
TSPP (Tetrasodium pyrophosphate) is used in cleaning compounds for the metal finishing industry.
TSPP (Tetrasodium pyrophosphate) is used on oil well drilling rigs for cleaning the mud off the equipment.


Pharmaceuticals: TSPP (Tetrasodium pyrophosphate) is employed in certain pharmaceutical formulations.
Water Treatment:TSPP (Tetrasodium pyrophosphate) is used in water treatment processes to prevent scale formation.
TSPP (Tetrasodium pyrophosphate) has excellent applications in rust removal, ink erasers, and electrodeposition on metals.


TSPP (Tetrasodium pyrophosphate) is also used as a water softener, wool de-fatting agent, soap and synthetic detergent builder, and general sequestering agent.
TSPP (Tetrasodium pyrophosphate) is used in the food processing applications.


TSPP (Tetrasodium pyrophosphate) is used as a constituent of phosphate mixes used in the preparation of products such as hamburgers and sausages.
TSPP (Tetrasodium pyrophosphate) is used as a constituent of emulsifying - salt blends used in the manufacture of processed cheese.
TSPP (Tetrasodium pyrophosphate) is used in solutions for the immersion - treatments of seafood to control yield and modify texture.


TSPP (Tetrasodium pyrophosphate) is used as a general buffer, sequestrate and stabilizing agent in dairy products and other foodstuffs
In food, TSPP (Tetrasodium pyrophosphate) is used as a buffer for puddings and processed foods.
TSPP (Tetrasodium pyrophosphate) can also be used as a calcium sequestrant.


For water treatment, TSPP (Tetrasodium pyrophosphate) has excellent softening, peptizing, and dispersing agent properties.
This can help with magnesium hardness, scale control, sequestering, and red and black water control.
TSPP (Tetrasodium pyrophosphate) also meets the EPA Lead and Copper rule which means it is also used frequently in corrosion prevention.


TSPP (Tetrasodium pyrophosphate) is used Breath Fresheners, Buffer, Cheese, Dispersant, Ice Cream, Marshmellow, Mouthwash, Potato Products, Poultry, Processed Meat, Protein Modifier, Seafood, Sequestrant, Teeth Whitening, Toothpaste, and Whipped Toppings
TSPP (Tetrasodium pyrophosphate) is used as a cleaning compound; oil well drilling; water treatment, cheese emulsification; as a general sequestering agent, to remove rust stains; as am ingredient of one fluid ink eradicators, in electrodeposition of metals.


TSPP (Tetrasodium pyrophosphate) is used in textile dyeing; scouring of wool; buffer; food additive; detergent builder; water softener and dispersant.
TSPP (Tetrasodium pyrophosphate) is used as a buffering agent, an emulsifier, a dispersing agent, and a thickening agent, and is often used as a food additive.


Common foods containing TSPP (Tetrasodium pyrophosphate) include chicken nuggets, marshmallows, pudding, crab meat, imitation crab, canned tuna, and soy-based meat alternatives and cat foods and cat treats where it is used as a palatability enhancer.
TSPP (Tetrasodium pyrophosphate) is commonly used as a pH regulator, meat conditioner in recipes.


Stabilizer: TSPP (Tetrasodium pyrophosphate) acts as a stabilizer in many food products by controlling the pH and maintaining the desired texture of the product, hence it ensure product quality and also increases the shelf life of the food product.
Water softening: TSPP (Tetrasodium pyrophosphate) is used to soften water and remove any residues that can affect water quality.


In toothpaste and dental floss, TSPP (Tetrasodium pyrophosphate) acts as a tartar control agent, serving to remove calcium and magnesium from saliva and thus preventing them from being deposited on teeth.
TSPP (Tetrasodium pyrophosphate) is used in commercial dental rinses before brushing to aid in plaque reduction.


TSPP (Tetrasodium pyrophosphate) is sometimes used in household detergents to prevent similar deposition on clothing, but due to its phosphate content it causes eutrophication of water, promoting algae growth.
Food: As a source of phosphorus, TSPP (Tetrasodium pyrophosphate) is an emulsifier which is used for the binding of soybean particles and protein water connection.


TSPP (Tetrasodium pyrophosphate) is also used as a thickener in ready puddings.
Textile: TSPP (Tetrasodium pyrophosphate) is used as an inorganic stabilizer in textile.
Detergent: As a water softener for detergents, TSPP (Tetrasodium pyrophosphate) can be used as an emulsifier to suspend the oils and to prevent their sedimentation on the laundry in the wash.


Chemistry: TSPP (Tetrasodium pyrophosphate) is used as ph value adjuster in chemical industry.
Tooth paste: Since they remove Ca and Mg ions from saliva, they do not stay on the teeth so they are used as buffer in toothpastes.
TSPP (Tetrasodium pyrophosphate) is being used in detergents, as cleaning agents, ceramics, paints and metal surface treatment.


TSPP (Tetrasodium pyrophosphate)’s an additive for cosmetic and pharmaceutical preparations , pH control and buffering, dispersing agent and emulsion stabilizer.
TSPP (Tetrasodium pyrophosphate) is used as a wool de-fatting agent, in bleaching operations, as a food additive.


TSPP (Tetrasodium pyrophosphate) is used Cleaning, Paints, Metal treatment, and Ceramics.
More commonly known as tetrasodium pyrophosphate, TSPP (Tetrasodium pyrophosphate) finds much use in the food industry as an emulsifier and in dental hygiene as a calcium-chelating salt.


TSPP (Tetrasodium pyrophosphate) has a role as a food emulsifier, a chelator and a food thickening agent.
TSPP (Tetrasodium pyrophosphate) is used in the following areas: formulation of mixtures and/or re-packaging, mining and municipal supply (e.g. electricity, steam, gas, water) and sewage treatment.


TSPP (Tetrasodium pyrophosphate) is used for the manufacture of: chemicals, metals, fabricated metal products, machinery and vehicles and .
Release to the environment of TSPP (Tetrasodium pyrophosphate) can occur from industrial use: in processing aids at industrial sites, formulation of mixtures, in the production of articles and as processing aid.


Release to the environment of TSPP (Tetrasodium pyrophosphate) can occur from industrial use: manufacturing of the substance, formulation of mixtures, formulation in materials, in processing aids at industrial sites, in the production of articles and as an intermediate step in further manufacturing of another substance (use of intermediates).


TSPP (Tetrasodium pyrophosphate) is used Buffering Agents, Food & Beverage, Food Additives, Household, Industrial & Institutional Chemicals, Thickening Agents, Detergents, Emulsifiers.
TSPP (Tetrasodium pyrophosphate) is used in the following products: pH regulators and water treatment products, water softeners, cosmetics and personal care products, coating products and fillers, putties, plasters, modeling clay.


Release of TSPP (Tetrasodium pyrophosphate) to the environment may occur from industrial use: in the formulation of mixtures, in the manufacture of articles and in processing aids on industrial sites.
TSPP (Tetrasodium pyrophosphate) is used in machine wash liquids/detergents, automotive care products, paints, coatings or adhesives, fragrances and air fresheners.


TSPP (Tetrasodium pyrophosphate) is used Meat emulsions, sausages, chopped and ground meat.
TSPP (Tetrasodium pyrophosphate) is used fish and seafood treatment.
TSPP (Tetrasodium pyrophosphate) is used Dairy products.


TSPP (Tetrasodium pyrophosphate) is used Toothpastes component.
TSPP (Tetrasodium pyrophosphate) is used in paper coating and filling to promote the dispersion of clay, lithopone, titanium dioxide, iron oxide, and other ingredients in aqueous suspensions.


TSPP (Tetrasodium pyrophosphate) is used as a buffering agent, an emulsifier, a dispersing agent, and a thickening agent, and is often used as a food additive.
TSPP (Tetrasodium pyrophosphate) is widely used as phosphate in food production.


Orally the main purpose of TSPP (Tetrasodium pyrophosphate) is to prevent the formation of calculus by reducing the deposition of calcium and magnesium on teeth.
Thus TSPP (Tetrasodium pyrophosphate) is commonly used as the anticalculus component of many tartar-control toothpastes and mouth rinse.


TSPP (Tetrasodium pyrophosphate) is mainly used as in industry as detergent auxiliary , paper production to bleach and electroplating.
TSPP (Tetrasodium pyrophosphate) is used for electroplating baths to form complexes together with F.
TSPP (Tetrasodium pyrophosphate) is used in woolen industry as degreasing angent as well as bleaching agent.


TSPP (Tetrasodium pyrophosphate) is used in the Paper industry as decolorizer.
TSPP (Tetrasodium pyrophosphate) is used for printing and dyeing industry as auxliary agent.
TSPP (Tetrasodium pyrophosphate) is used in toothpast industry as additive to form colloid together with Dicalcium phosphate.
or water treatment industry as water softner.


Other release to the environment of TSPP (Tetrasodium pyrophosphate) is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners) and outdoor use.
TSPP (Tetrasodium pyrophosphate) is used for machanic industry as rust remover.


TSPP (Tetrasodium pyrophosphate) is used Flavoured milk, Buttermilk
Cheese slices, Whipped toppings, Instant puddings, No-bake cheesecakes, Egg yolk products, Sausages, Restructured poultry, andPhosphates have a wide range of ingredient applications


With the properties of chelating metal ions, increasing protein water holding capacity, PH buffering, stabilization, emulsification, casein thickening and ect, TSPP (Tetrasodium pyrophosphate) is widely used in food to improve the gel strength and the tenderness of meat products/analogs.
Also, TSPP (Tetrasodium pyrophosphate) is used with other phosphates (e.g. sodium hexametaphosphate, sodium acid pyrophosphate) in seafood to increase the water retention.


TSPP (Tetrasodium pyrophosphate) is primarily used as a food additive but also has a wide range of applications such as an emulsifier, thickening agent, buffering agent and dispersing agent.
TSPP (Tetrasodium pyrophosphate) is used Buffering Agents, Food Additives, Thickening Agents, Detergents, Emulsifiers, Industrial Chemicals, and Mining


TSPP (Tetrasodium pyrophosphate) is used as a buffering agent, an emulsifier, a dispersing agent, and a thickening agent, and is often used as a food additive.
Common foods containing TSPP (Tetrasodium pyrophosphate) include chicken nuggets, marshmallows, pudding, crab meat, imitation crab, canned tuna, and soy-based meat alternatives and cat foods and cat treats where it is used as a palatability enhancer.


In the food industry, TSPP (Tetrasodium pyrophosphate) is a kind of food additive.
TSPP (Tetrasodium pyrophosphate) is used as a chelating agent, nutrition ingredients and quality improver, etc.
TSPP (Tetrasodium pyrophosphate) is used as the leavening agent, water retention agent, buffering agent, emulsifying agent, and acidity regulator in the process of bakery, meat, cheeses, and aquatic products.


TSPP (Tetrasodium pyrophosphate) serves as a buffering agent and stabilizer in bread leavening.
TSPP (Tetrasodium pyrophosphate) helps maintain the pH balance during the baking process, resulting in improved texture and enhanced shelf life.
TSPP (Tetrasodium pyrophosphate) can modify meat, poultry, and seafood proteins enabling them to retain moisture during storage, thawing, and cooking.


TSPP (Tetrasodium pyrophosphate) can be added to whipped toppings and milk foams to improve whipping efficiency and improve foam stability.
TSPP (Tetrasodium pyrophosphate) is processed cheese products, help to buffer the pH of processed cheese and interact with milk proteins to promote emulsification.


In ice cream and frozen desserts, TSPP (Tetrasodium pyrophosphate) will help to maintain fat dispersion in the mix and stop lumps of butter from forming during freezing.
TSPP (Tetrasodium pyrophosphate) anhydrous food grade also sequesters iron in potato products to prevent after-cooking blackening and to stabilize the color.


TSPP (Tetrasodium pyrophosphate) is an inorganic sodium salt comprised used in the food industry as an emulsifier and in dental hygiene as a calcium-chelating salt.
TSPP (Tetrasodium pyrophosphate) is used in the food industry as a buffering agent, an emulsifier, a dispersing agent, and a thickening agent.


TSPP (Tetrasodium pyrophosphate) is often used as a food additive in chicken nuggets, marshmallows, pudding, crab meat, imitation crab, canned tuna, and soy-based meat alternatives and cat foods and cat treats where it is used as a palatability enhancer.
TSPP (Tetrasodium pyrophosphate) is also used in some common baking powders.


In toothpaste and dental floss, TSPP (Tetrasodium pyrophosphate) acts as a tartar control agent, serving to remove calcium and magnesium from saliva and thus preventing them from being deposited on teeth.
TSPP (Tetrasodium pyrophosphate) helps in plaque reduction.


TSPP (Tetrasodium pyrophosphate) also acts as an excellent cleaning agent and is used in detergents, metal treatment, and paints, as well as in the mining industry.
TSPP (Tetrasodium pyrophosphate) also increases shelf life by sequestering multivalent cations responsible for lipid oxidation and rancidity development.


-Emulsifier:
TSPP (Tetrasodium pyrophosphate) is an effective emulsifier that helps in blending various ingredients that normally do not mix well together.
TSPP (Tetrasodium pyrophosphate) is mostly used in food products such as cured meat, sausages, and processed cheese.


-Leavening agent:
Its ability to regulate pH makes TSPP (Tetrasodium pyrophosphate) an excellent leavening agent.
TSPP (Tetrasodium pyrophosphate) helps in the baking process by releasing carbon dioxide gas, which causes dough to rise and increases its volume.


-Binding agent:
TSPP (Tetrasodium pyrophosphate) is used to improve the texture and stability of several food products.
Particularly, in meat products such as canned ham, TSPP (Tetrasodium pyrophosphate) aids in binding the meat together while maintaining its juiciness and tenderness.


-Sequestrant:
TSPP (Tetrasodium pyrophosphate) is also used as a sequestrant in food products.
TSPP (Tetrasodium pyrophosphate) has the ability to bind and hold onto minerals such as calcium and magnesium, which helps to prevent their accumulation and resulting adverse effects.



PRODUCTION AND REACTIONS OF TSPP (TETRASODIUM PYROPHOSPHATE):
TSPP (Tetrasodium pyrophosphate) is a sodium salt and is derived from its carbonate and phosphates, such as tkpp.



PRODUCTION OF TSPP (TETRASODIUM PYROPHOSPHATE):
TSPP (Tetrasodium pyrophosphate) is produced by the reaction of furnace-grade phosphoric acid with sodium carbonate to form disodium phosphate, which is then heated to 450 °C to form TSPP (Tetrasodium pyrophosphate):
2 Na2HPO4 → Na4P2O7 + H2O



BENEFITS AND APPLICATIONS OF TSPP (TETRASODIUM PYROPHOSPHATE):
TSPP (Tetrasodium pyrophosphate) is used as a pH buffer in detergents to extend the life of the clothes.
TSPP (Tetrasodium pyrophosphate) keeps soap scum and insoluble salts off of your garments.
TSPP (Tetrasodium pyrophosphate) has no odour, so it will not irritate your breathing when using it.
TSPP (Tetrasodium pyrophosphate) helps with foaming and bubbling in washing.



HOW TSPP (TETRASODIUM PYROPHOSPHATE) WORKS:
TSPP (Tetrasodium pyrophosphate) works as a water softener, and an emulsifier to protect clothes fibre from fading.
TSPP (Tetrasodium pyrophosphate) permits dirt and oil to be removed from clothing and prevents it from being redeposited in the wash.



CONCENTRATION AND SOLUBILITY OF TSPP (TETRASODIUM PYROPHOSPHATE):
TSPP (Tetrasodium pyrophosphate) is recommended that it should be used at a concentration of 5 to 20%.
TSPP (Tetrasodium pyrophosphate) has low solubility in water and is insoluble in alcohol.



PROPERTIES OF TSPP (TETRASODIUM PYROPHOSPHATE):
White powder, specific gravity 2.534, melting point 880 ºC, soluble in water, its aqueous solution is alkaline.
TSPP (Tetrasodium pyrophosphate) can form a complex with alkaline earth metal salt.
TSPP (Tetrasodium pyrophosphate) is soluble in acid, insoluble in alcohol and ammonia.

The aqueous solution of TSPP (Tetrasodium pyrophosphate) is stable below 70 ºC and hydrolyzed to disodium hydrogen phosphate after boiling.
After weathering in dry air, crystal water is lost at 100 ºC.
TSPP (Tetrasodium pyrophosphate) is easy to absorb moisture and deliquescence in the air.



RELATED COMPOUNDS OF TSPP (TETRASODIUM PYROPHOSPHATE):
*Other anions
*Trisodium phosphate
*Pentasodium triphosphate
*Sodium hexametaphosphate
*Disodium pyrophosphate



OTHER CATIONS OF TSPP (TETRASODIUM PYROPHOSPHATE):
*Tetrapotassium pyrophosphate



BENEFITS OF TSPP (TETRASODIUM PYROPHOSPHATE):
TSPP (Tetrasodium pyrophosphate) is a commonly used food additive that has numerous benefits in the food industry.
TSPP (Tetrasodium pyrophosphate) is a odorless tasteless white crystalline powder that is highly resistant to heat and acidity.
As a result, TSPP (Tetrasodium pyrophosphate) is used as a stabilizer, emulsifier, and buffering agent in a variety of food products.

One of the main benefits of TSPP (Tetrasodium pyrophosphate) is that it helps to regulate the pH levels of food products.
This makes TSPP (Tetrasodium pyrophosphate) an excellent ingredient in baking, where it is used as a leavening agent in baking powders and canned dough to improve texture, cell structure, and shelf life.

TSPP (Tetrasodium pyrophosphate) also enhances the flavor of several food products.
Another benefit of TSPP (Tetrasodium pyrophosphate) is its ability to bind and retain moisture in meat products.
This is important as TSPP (Tetrasodium pyrophosphate) increases the total yield of the product while also ensuring that the meat remains juicy and tender.

TSPP (Tetrasodium pyrophosphate) is also known for having potential health benefits.
Studies suggest that TSPP (Tetrasodium pyrophosphate) can help to regulate calcium levels in the body, which is essential for good bone health.
Moreover, TSPP (Tetrasodium pyrophosphate) may have anti-inflammatory properties that can help to alleviate symptoms of pain and swelling.



IS TSPP (TETRASODIUM PYROPHOSPHATE) SAFE TO EAT?
Yes, TSPP (Tetrasodium pyrophosphate) almost has no side effects and the safety has been approved by the U.S. Food and Drug Administration (FDA) and European Food Safety Authority (EFSA), as well as the Joint FAO/WHO Expert Committee on Food Additives (JECFA).



FOOD, TSPP (TETRASODIUM PYROPHOSPHATE):
Food grade TSPP (Tetrasodium pyrophosphate) is mainly used in following two functions:
-A buffering agent:
With the PH value from 9.8 to 10.8 (1% solution), TSPP (Tetrasodium pyrophosphate) can be used as an alkaline to adjust pH in processed food, pudding and etc.

-A calcium sequestrant:
TSPP (Tetrasodium pyrophosphate) can remove naturally occurring calcium ions from proteins and crosslink with proteins, which results in accelerating protein gelation, improving texture (mouthfeel) and reducing cooking loss in meat analog production (e.g. soy protein).

Following food list may contain TSPP (Tetrasodium pyrophosphate):
*Meat analogs, such as soy or wheat based food, with the appearance, flavor and mouth-feel the same with meat but not made from meat.
*Marshmallows
*Pudding
*Cheese
*Ice cream
*Milk protein products
*Tuna
*Toothpaste



BENEFITS of TSPP (TETRASODIUM PYROPHOSPHATE):
*Buffering agent
*Emulsifier
*Dispersing agent
*Sequestrant
*Foaming agent
*Protein coagulant



HOW IS TSPP (TETRASODIUM PYROPHOSPHATE) MADE?
TSPP (Tetrasodium pyrophosphate) can be produced by the neutralization of phosphoric acid with sodium hydroxide with mol proportions of 2:1.



PHYSICAL and CHEMICAL PROPERTIES of TSPP (TETRASODIUM PYROPHOSPHATE):
Chemical formula: Na4O7P2
Molar mass: 265.900 g·mol−1
Appearance: Colorless or white crystals
Odor: odorless
Density: 2.534 g/cm3
Melting point: 988 °C (1,810 °F; 1,261 K) (anhydrous)
79.5 °C (decahydrate)
Boiling point: decomposes
Solubility in water: 2.61 g/100 mL (0 °C)
6.7 g/100 mL (25 °C)
42.2 g/100 mL (100 °C)
Solubility: insoluble in ammonia, alcohol
Refractive index (nD): 1.425
Crystal structure: monoclinic (decahydrate)
Heat capacity (C): 241 J/mol K
Std molar entropy (S⦵298): 270 J/mol K
Std enthalpy of formation (ΔfH⦵298): -3166 kJ/mol
Gibbs free energy (ΔfG⦵): -3001 kJ/mol
Molecular Formula: Na4P2O7 * 10 H2O

Ph (1% solution): 10-10.6
Flor: 0-10 ppm
Bullet: 1.0 ppm max.
CAS number: 13472-36-1
Molecular Formula: Na4P2O7 * 10 H2O
Appearance: White powder
Ph: 10,4
Content: 95.8%
Insoluble in water: 0.09%
Molecular Weight: 446.0552 g / mol
Molecular Weight: 265.90
Molecular Formula: Na4P2O7
Melting Point: 880°C
Density: 2.53
Storage: Keep tightly closed in a cool place in a tightly closed container.
Assay: 0.99
Stability: Stable.
Molecular Weight: 265.90 g/mol
Hydrogen Bond Donor Count: 0
Hydrogen Bond Acceptor Count: 7
Rotatable Bond Count: 0

Exact Mass: 265.87100346 g/mol
Monoisotopic Mass: 265.87100346 g/mol
Topological Polar Surface Area: 136Ų
Heavy Atom Count: 13
Formal Charge: 0
Complexity: 124
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 5
Compound Is Canonicalized: Yes
CAS number: 7722-88-5
Appearance: white powder or granular powder
Solubility: Soluble in water, insoluble in ethanol
MP: 80 °C
BP: 93.8 °C
Density: 2.53 g/mL at 25 °C (lit.)
Solubility: H2O: 0.1 M at 20 °C, clear, colorless
Sensitive: Hygroscopic
Merck: 14, 9240
Stability: Stable



FIRST AID MEASURES of TSPP (TETRASODIUM PYROPHOSPHATE):
-Description of first-aid measures:
*General advice:
Show this material safety data sheet to the doctor in attendance.
*If inhaled:
After inhalation:
Rresh air.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with water/ shower.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Call in ophthalmologist.
Remove contact lenses.
*If swallowed:
After swallowing:
Immediately make victim drink water (two glasses at most).
Consult a physician.
-Indication of any immediate medical attention and special treatment needed:
No data available



ACCIDENTAL RELEASE MEASURES of TSPP (TETRASODIUM PYROPHOSPHATE):
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Take up dry.
Dispose of properly.



FIRE FIGHTING MEASURES of TSPP (TETRASODIUM PYROPHOSPHATE):
-Extinguishing media:
*Suitable extinguishing media:
Water
Foam
Carbon dioxide (CO2)
Dry powder
*Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Prevent fire extinguishing water from contaminating surface water or the ground water system.



EXPOSURE CONTROLS/PERSONAL PROTECTION of TSPP (TETRASODIUM PYROPHOSPHATE):
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use Safety glasses.
*Skin protection:
Full contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min
Splash contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min
*Body Protection:
protective clothing
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of TSPP (TETRASODIUM PYROPHOSPHATE):
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
Dry.



STABILITY and REACTIVITY of TSPP (TETRASODIUM PYROPHOSPHATE):
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature).
-Incompatible materials:
No data available



SYNONYMS:
DIPHOSPHORIC ACID TETRASODIUM SALT
DIPHOSPHORIC ACID, TETRASODIUM SALT, DECAHYDRATE
DECAHYDRATE TETRASODIUM PYROPHOSPHATE
TETRA-SODIUM DIPHOSPHATE
TETRA-SODIUM DIPHOSPHATE-10-HYDRATE
TETRA-SODIUM DIPHOSPHATE DECAHYDRATE
TETRASODIUM PYROPHOSPHATE
SODIUM D
Sodium pyrophosphate
TETRASODIUM PYROPHOSPHATE
7722-88-5
TSPP
Tetrasodium diphosphate
Phosphotex
Diphosphoric acid, tetrasodium salt
Sodium diphosphate
Victor TSPP
Caswell No. 847
Sodium pyrophosphate [USAN]
Sodium pyrophosphate tetrabasic
Natrium pyrophosphat
Pyrophosphoric acid tetrasodium salt
Sodium diphosphate, anhydrous
Sodium phosphate (Na4P2O7)
HSDB 854
sodium pyrophosphate(V)
Sodium diphosphate (Na4P2O7)
Sodium pyrophosphate, tetrabasic
Sodium pyrophosphate (Na4P2O7)
Anhydrous tetrasodium pyrophosphate
Tetrasodium pyrophosphate, anhydrous
EINECS 231-767-1
NSC 56751
Pyrophosphoric acid, tetrasodium salt
Na4P2O7
EPA Pesticide Chemical Code 076405
DTXSID9042465
UNII-O352864B8Z
CHEBI:71240
Tetrasodium pyrophosphate, anhydride
O352864B8Z
EC 231-767-1
Sodium pyrophosphate (USAN)
MFCD00003513
Sodium diphosphate tetrabasic
Tetranatriumpyrofosfat
SODIUMPYROPHOSPHATE
tetra sodium pyrophosphate
Na4O7P2
Diphosphoric acid sodium salt
H4O7P2.4Na
H4-O7-P2.4Na
DTXCID7022465
SODIUM PYROPHOSPHATE [II]
FQENQNTWSFEDLI-UHFFFAOYSA-J
Sodium diphosphate (Na4(P2O7))
SODIUM PYROPHOSPHATE [FCC]
Tetrasodium pyrophosphate Anhydrous
SODIUM PYROPHOSPHATE [HSDB]
CS-B1771
SODIUM PYROPHOSPHATE [VANDF]
tetrasodium (phosphonooxy)phosphonate
Tox21_110033
SODIUM PYROPHOSPHATE [MART.]
Tetrasodium pyrophosphate (anhydrous)
SODIUM PYROPHOSPHATE [WHO-DD]
TETRASODIUM PYROPHOSPHATE [MI]
AKOS015914004
AKOS024418778
Diphosphoric acid, sodium salt (1:4)
LS-2429
TETRASODIUM PYROPHOSPHATE [INCI]
NCGC00013687-01
CAS-7722-88-5
FT-0689073
D05873
E75941
EN300-332889
Q418504
1004291-85-3
Diphosphoricacid, tetrasodium salt (9CI)
Pyrophosphoric acid, tetrasodium salt (8CI)
Accoline 126
Anhydrous tetrasodium pyrophosphate
Phosphotex
SPP
SPP(phosphate)
Sodium diphosphate
Sodium diphosphate (Na4P2O7)
Sodium phosphate(Na4P2O7)
Sodium pyrophosphate
Sodium pyrophosphate (Na4P2O7)
TSPP
Tetrasodium diphosphate
Tetrasodium diphosphate (Na4P2O7)
Diphosphoricacid, sodium salt (1:4)
Tetrasodium pyrophosphate (Na4P2O7)
Thermphos Pyro E 450
Victor TSPP
Tetra Sodium Pyrophosphate
tetrasodium pyrophosphate
sodium diphosphate
TSPP, sodium pyrophosphate
tetrasodium pyrophosphate
tetrasodium diphosphate
pyrophosphate sodium

TSPP (TETRON-TETRA SODIUM PYRO PHOSPHATE)
China Wood Oil; Nut Oil cas no: 8001-20-5
TUNG OIL
TUNG OIL = CHINA WOOD OIL

Tung oil is natural Tung oil provides a hard, transparent and non-yellowing coating.
Tung oil can be used on outdoor wood and indoor furniture.
Tung oil is suitable for all woods in contact with food when VOC-free.

CAS Number: 8001-20-5
EC Number: 232-272-3

Tung oil is obtained from the seed kernel of tung (Aleurites fordii), a tree that grows in parts of China and South America.
The oil content in the kernel varies from 40 to 60%.

The crude oil is mainly used.
Tung oil is bright brown, opaque and with a characteristic odour.
Tung oil is an oil with the highest drying power, even greater than that of linseed oil.

The main fatty acid is eleostearic (between 70 and 85%), with 3 unsaturations in combined positions.
Eleostearic acid is only present in tung oil.

Tung oil is mainly used in resins, varnishes, inks and generally in formulations where high film strength is required.
When considering Tung oil use for coatings, Tung oil use is basically exterior.
Tung oil is one of the main components of teak oil together with linseed oil.

Tung oil or China wood oil is a drying oil obtained by pressing the seed from the nut of the tung tree (Vernicia fordii).
Tung oil hardens upon exposure to air (through polymerization), and the resulting coating is transparent and has a deep, almost wet look.

Tung oil is used mostly for finishing and protecting wood, after numerous coats, the finish can even look plastic-like.
Related drying oils include linseed, safflower, poppy, and soybean oils.

Raw tung oil tends to dry to a fine, wrinkled finish (the English name for this is gas checking).
This property was used to make wrinkle finishes, usually by adding excess cobalt drier.
To prevent wrinkling, the oil is heated to gas-proof Tung oil (also known as "boiled").

'Tung oil' is often used by paint and varnish manufacturers as a generic name for any wood-finishing product that contains the real tung oil or provides a finish that resembles the finish obtained with tung oil.

Tung oil is a drying oil that’s extracted from the seed of the tung tree, which is native to China and a few other Asian countries.
The oil has been used for centuries as a water-resistant finish for boats and other wooden objects, as well as to finish stone.
Tung oil is an excellent alternative to other drying oils, such as walnut, linseed and soy.

On top of producing a beautiful and protective finish, tung oil is also a popular choice for projects because Tung oil is versatile, easy to use, and environmentally friendly.

There are many reasons why people love tung oil for their projects, and one of the most popular is Tung oil flexible, durable, food safe, and protective waterproof finish that doesn’t mold, darken or go rancid.
On a practical note, tung oil also dries faster than other oils, making Tung oil easier and less time-consuming to apply.
From an aesthetic standpoint, tung oil also cures to a beautiful matte finish that adds depth to woodgrain, producing an antique-style finish on any surface.

Tung oil, also called wood oil, or china wood oil, pale-yellow, pungent drying oil obtained from the seeds of the tung tree.
On long standing or on heating, tung oil polymerizes to a hard, waterproof gel that is highly resistant to acids and alkalies.

Tung oil is used in quick-drying varnishes and paints, as a waterproofing agent, and in making linoleum, oilcloth, and insulating compounds.
Tung oil is produced chiefly in China from the tung tree.

Marco Polo is said to have brought a sample back to the western world from China.
Completely natural and renewable, pure tung oil has gained recent popularity among the environmentally conscious.

Inherently resistant to disease and insects, tung trees require no fungicides or pesticides.
Tung nut byproducts can be used for mulch.
During World War II the Chinese figured out how to use Tung Oil as motor fuel.

Tung oil is a small deciduous tree that grows up to 40 feet tall with smooth bark and a branchy head.
Tung oil leaves are dark green and glossy with blades 3-13 inches wide.

The tung tree has flowers that range in size from 1-3 inches in diameter with petals that are white tinged with red and yellow.
Each nut or fruit contains 3-7 large seeds.

The tung tree’s official botanical name is Aleurites fordii.
Tung oil thrives in moist, well-drained, slightly acidic soil.

These hearty, fast growing trees mature to bear fruit in their third year and yield commercial quantities at four to five years of age.
Maximum production occurs in the tenth to twelfth years of growth, with trees expected to be commercially productive for at least 20 years after optimum production has occurred.

In the Northern Hemisphere, tung tree nuts grow in clusters and fall to the ground from late September through November.
The fruits are left for a few weeks to dry and cure.

Tung oil is produced by harvesting these nuts and separating the nuts from their hard outer shells.
Then the transparent oil is squeezed from the seeds inside.

Dried and pressed nuts yield about twenty percent oil.
Under favorable conditions an acre of tung trees will produce about two tons of tung nuts and yield about 100 gallons of raw tung oil annually.

Tung oil is made from pressed seeds from the nut of the tung tree.
The tung tree, native to China, is named for Tung oil heart-shaped leaves because “tung” is Chinese for “heart.”

In the 14th century, Chinese merchants were noted for using tung oil to waterproof and protect wooden ships from the eroding powers of the sea.
There are even mentions of tung oil appearing in the writings of Confucius in around 400 B.C.
For these reasons, Tung oil is also sometimes referred to as “China wood oil.

Pure tung oil is considered a drying oil much like linseed, safflower, poppy and soybean oil and is known to have a slightly golden tint.
Tung oil, which is actually a vegetable oil, is considered the best penetrating drying oil available due to Tung oil unique ability to wet the surface, allowing Tung oil to penetrate even the densest woods.
Unlike linseed oil, Tung oil will not darken with age.

Originating from China and South America, tung oil—an extract from tung-tree nuts—is a natural drying oil that coats your fine wood furnishings with a transparent, wet finish.
Tung oil enhances the color of your wood, offers excellent protection and is eco-friendly.

While there are many advantages to using Tung oil, pure tung oil takes two to three days to harden, and needs at least five coats.
Oil/varnish blends and wiping varnishes are faster-drying, more practical options, but such terms rarely appear on labels.

Penetrating tung oil finishes come in three varieties: pure tung oil, oil/varnish blends, and wiping varnish.
They all share the benefits that tung oil imparts to a finish—durability, water resistance, resilient hardness, and color stability—depending on how much of the oil they actually contain and what form Tung oil takes.

Pure tung oil:
Pure tung oil is easy to identify because Tung oil contains no solvents.
That may be a good thing in terms of limiting your exposure to VOCs, but applying Tung oil is an exacting, drawn-out process.

You have to wait at least two to three days for each coat to harden.
And Tung oil takes five to seven coats to get a protective film.
Rushing the process, or applying too thick a coat, causes wrinkling, which has to be sanded off.

Regular reapplication is a must—”once a week for a month, once a month for a year, once a year ever after,” as the saying goes.
The results can be gorgeous, as long as you have the necessary patience.

Uses of Tung oil:
Tung oil is used mostly for finishing and protecting wood, after numerous coats, the finish can even look plastic-like.

The interior can be used for all woods (except floor).
Tung oil can also be used on wood that comes into contact with food.

Especially gun handles, wooden handle cutting tools, wooden products for hobby purposes are especially preferred.
As the number of layers increases, Tung oil brightness increases.

Wood Finishing:
Tung oil is very popular today because of two properties: first, Tung oil is a naturally derived substance.
Second, after Tung oil cures (5 to 30 days, weather/temperature related), the result is a very hard and easily repaired finish, so Tung oil is used on boat decks and now on floors.

The oil is often diluted with hydrocarbon thinner so Tung oil viscosity is very low and enables the oil to penetrate the finest grain woods.
This thinning vehicle evaporates within 15 to 20 minutes.

When applied in many fine/thinner coats over wood, tung oil slowly cures to a matte/light satin look with slight golden tint.
Tung oil resists water better than any other pure oil finish and does not darken noticeably with age.

Tung oil is claimed to be less susceptible to mould than linseed oil.
Tung oil is considered safe to be used on sculptures made near waterways.

Heating tung oil to about 500 °F (260 °C) in an oxygen-free environment will substantially increase the viscosity and film-forming quality of the product.
Most polymerized tung oils are sold mixed with mineral spirits to make them easier to work with.
Limonene and D-limonene are less toxic alternatives for mineral spirits.

Oil-paper umbrella:
The oil-paper umbrella is the traditional umbrella used in China, Japan, and other countries in the sinosphere, and was brought to Western countries through the Silk Road.
Tung oil is the "oil" mentioned in the oil-paper umbrella, which is used to protect the paper from getting wet, and to make the umbrella waterproof.

The Many Uses of Tung Oil:
Carpenters, woodworkers, crafters, and hobbyist alike all love tung oil, and over the years they’ve used Tung oil as a beautiful and protective finish on a wide number of projects and surfaces.
For instance, tung oil has been used with fantastic results to finish wood, bamboo, concrete, stone, brick, and even metal surfaces.
Tung oil is a favorite for finishing wood floors, cabinetry, decks, siding, furniture, guitars and other musical instruments, handmade toys, and more.

This product can be used in the following industries:
Lubricants, Paints & Coatings

This product can be applied as:
Other Oleochemicals, Base Fluids

Easy-to-Follow Steps for Applying Tung Oil to Your Projects

1. Clean the surface:
The proper application of tung oil depends on you starting with a clean and prepared surface.
Before you start, make sure there’s no grease, oil, dirt, dust, or other contaminants on the surface.

If necessary, start by sanding or stripping the surface to remove any coating or finish that’s already there.
Tung oil can only be applied to bare surfaces or over another coat of tung oil.

Follow that up by cleaning the surface with trisodium phosphate.
Sand the surface one more time with 150-grit sandpaper, and then vacuum well to remove all dust.

2. Thin the oil:
A thinner will make the tung oil easier to apply, faster to dry, and will improve penetration.
The only time you shouldn’t thin the oil first is if you’re applying Tung oil to weathered wood, concrete, old and unfinished wood floors, or other highly absorbent surfaces.

To thin the oil, combine Tung oil with equal parts Citrus Solvent, mineral spirits, or Odorless Mineral Spirits before application.
Do not use a mineral spirit or odorless mineral spirit marketed as “green”, “eco-friendly”, or similar verbiage.

These do not mix with the tung oil and will create adverse effects on your finish.
You could also choose one of our pre-thinned options, Half & Half or Dark Half, to use straight out of the bottle!

3. Apply a generous first layer
You can apply the oil with a natural bristle brush, a sponge brush, or a soft and lint-free rag.
Apply the oil liberally to the surface.

Unlike varnish, which sits on top of the wood, the goal with tung oil is to thoroughly saturate the wood cells.
When you’ve applied the first coat, let the oil absorb.

4. Apply subsequent coats:
After the first coat has absorbed, apply a second coat.
Continue this process of applying coats, waiting 40 minutes between coats if necessary, until over 80 percent of the surface stays glossy for at least 40 minutes.

This means the wood cells have been saturated and you can move to the next step.
Decorative items may need two to four coats, while functional surfaces that will be handled, used, or walked on will need a minimum of three to five.

5. Removing unabsorbed oil from the surface:
After you’ve applied multiple coats and the wood won’t absorb any more oil, use a clean rag to wipe the surface.
If there are any puddles of oil on the surface, mop them up with the rags.

This is important as you don’t want the tung oil to start curing on the surface.
At this point, your surface is fully saturated.

However, the pure tung oil will settle inside the wood/material overnight on through the next day.
To get the best finish we recommend applying one or two more coats of the oil, following the instructions previously stated, after this period of waiting.

Make sure to wipe up oil that’s on the surface that does not absorb.
Hang oil-soaked rags separately outside to dry before disposing.

6. Let the oil cure for up to 30 days:
From here, the oil will need a week to 10 days to start curing, and 15 days to 30 days to fully cure.
Do not put the tung oiled object in direct sunlight for an extended period of time.

For the first 10 days of curing, check and wipe up any tung oil that may seep to the surface.
During this curing time, you can walk on floors with clean shoes, but avoid placing heavy objects on the floor or walking on Tung oil with dirty shoes. (Tip: put old rags under your shoes to walk across the surface no matter what shoes you’re wearing.)

There are no other sealers or protective products needed on top of your oil.
Tung oil naturally seals, waterproofs, and protects your surfaces!

7. Cleaning your surfaces:
Pure tung oil is easy to clean.
For your floors or other wooden objects, just simply use hot water and standard dish soap.

8. Reapply as necessary to revive and provide more protection:
Surfaces that are used often or walked on frequently may need some maintenance to revive their look and add more protection.
To do this, simply mix 2 parts thinner to 1 part tung oil and wipe down your surfaces.
Allow time to dry as necessary.

Tung oil has been popular for thousands of years, thanks to the protective and waterproof finish Tung oil creates on wood and other porous surfaces.
These days, pure tung oil is also gaining momentum because Tung oil’s non-toxic, environmentally friendly, and food safe, meaning Tung oil’s ideal for kitchenware, butcher block, cutting boards, countertops, and even toys.

Applying tung oil is easy and effective.

The main tips to remember are: don’t leave excess oil on the surface during the curing phase, no sanding necessary between coats, no other sealer or topcoats needed and use 2 parts thinner to 1 part tung oil for maintenance.

Applications of Tung oil:
The traditional technique for applying pure tung oil is to dilute the oil 1:1 with solvent, then apply a succession of very thin films with a soft, lint-free cloth such as tee-shirt cotton.
Diluents range from traditional spirits of turpentine to any of the new citrus-based thinners to naphtha.

The choice of thinner should be guided by how fast the coating needs to set.
Naphtha works well in spray-on applications in well-ventilated studios.

Primary coats may be laid down at a 1:1 oil-to-thinner ratio, and successive layers, if not absorbed into the wood, at higher solvent to oil concentrations.
This technique brings out the deepest color of the wood while maintaining a matte finish.

Tung oil finishes that start with polymerized oils or tung oil preparations are best applied in the fat over lean principle: thinned pure oil is applied to deeply penetrate the surface, to fill pores.
Straight oil is then applied moderately to adhere to the surface and provide a good base for the thick gloss layers.

The polymerized oil is then applied thickly as a single layer, allowed to fully dry, buffed smooth with very fine sandpaper and 0000 steel wool.
The surface is wiped clean with a moistened rag and allowed to dry.

A final coat is applied fairly thickly (the oil will smooth itself into a glass-like coating) and allowed to dry for two to three days.
Rags soaked with tung oil can spontaneously combust (burst into flame).

Benefits of Tung oil:

Easy to Use:
Tung oil is a natural oil recognised by craftsmen to offer the ultimate hand-rubbed finish for all fine woods; just wipe on and allow the oil to cure at room temperature.

Permeates:
Unlike other finishes that form a film on the wood’s surface, tung oil penetrates deep into the wood fibres, cures to a flexible non-oily solid, and becomes part of the wood Tung oilself

Protects:
Resistant to moisture, alcohol, oil, and everyday wear for lasting beauty and protection; lasts many times longer than mineral oil and wax based products.

Multi Use:
Amazing results on almost any surface that will allow the oil to penetrate - new unfinished wood, weathered wood, stripped wood, concrete floors and countertops, even brick, stone, and cast iron

Great for Food Contact Surfaces:
Tung oil is considered non-toxic when dry therefore is great for cutting boards, butcher blocks, countertops, wooden bowls, wooden utensils, and more.

Features of Tung oil:
Super easy to apply.
Keeps the wood strong from inside and prevents stains.

Suitable only for indoor use, but has water resistant properties.
Provides a warm glow type of finish, while keeping the original pores and natural beauty of the wood.
Completely non-toxic due to lack of any additives.

Composition of Tung oil:
The fatty acids in tung oil and their concentration are listed in the table.

Fatty acid composition of tung oil:
Alpha-eleostearic acid: 82.0%
Linoleic acid: 8.5%
Palmitic acid: 5.5%
Oleic acid: 4.0%

The primary constituent is a fatty acid with a chain of 18 linked carbon atoms or methylene units containing three conjugated double bonds.
They are especially sensitive to autoxidation, which encourages cross linking of neighbouring chains, hence hardening of the base resin.

History of Tung oil:
The tung oil tree originates in southern China and was cultivated there for tung oil, but the date of cultivation remains unknown.
During the Song Dynasty, tung oil was used for waterproofing on ships.

The word "tung" is etymologically derived from the Chinese 桐 tóng.
The earliest references for Chinese use of tung oil is in the writings of Confucius around 500 to 400 BC.

The first tung tree seed was brought to America from Hankow, China in 1905 by a senior agricultural explorer for the U.S. Department of Agriculture.
In 1912 the Bureau of Plant Industry issued a special bulletin that urged growers to plant tung orchards and offered a limited number of free one-year old trees.

This was a perfect fit, because after acre upon acre of pine trees were cut for timber in the early 1900s, Gulf Coast farmers were looking for a sustainable cash crop for the vast vacant land.
That same year, ten trees were planted at University of Florida’s Agricultural Experiment Station in Gainesville.
By 1927, there were over 400 growers and more than 10,000 acres of tung oil trees in Alachua County, Florida and surrounding areas alone.

In 1928, L.P. Moore, nephew of the Benjamin Moore Paints founder, built the first mechanized tung oil compressing mill in the world, located in Gainsville, Florida.
This began the commercial production of tung oil in America.

Other mills later popped up in Cairo, Georgia and Florala, Alabama.
The U.S. was a prime location for this new industry, importing 100 million pounds of Chinese tung oil in 1927, and 120 million pounds in 1933, with demand still exceeding supply.
The industry expanded from Florida, Georgia and Alabama to Mississippi, Louisiana and Texas,with Mississippi becoming the largest producing state.

Just prior to the outbreak of WWII, tung oil was declared a strategic item for defense use, so the government aided growers to help them to produce more and better trees.
During the war, all ammunition was coated with tung oil and products containing tung oil painted all ships.

Not only were government support programs available for US growers, but the government also assisted foreign plantings in South America, particularly Argentina.
There was an embargo on Chinese tung oil at the time, making domestic oil profitable.
The Pan American Tung Research and Development League was formed between tung oil producers in Amercica and Argentina to work jointly on research and development and to pool tung oil from both countries to provide consistent supplies to U.S. consumers.

Identifiers of Tung oil:
CAS Number: 8001-20-5
ChemSpider: none
ECHA InfoCard: 100.029.338
EC Number: 232-272-3
UNII: 3C8NM3A2P0
CompTox Dashboard (EPA): DTXSID7029291

Substance: Tung Oil
CAS: 8001-20-5
EC number: 232-272-3
REACH compliant: Yes
Min. purity / concentration: 100%
Appearance: Liquid

Properties of Tung oil:
Density: 0.937 g/ml at 25°C
Refractive index (nD): 1.52 (20°C)

Specifications of Tung oil:
Specific weight at 25 °C: ca. 0.9320
Refraction index at 25 °C: 1.5165 - 1.5200
Free fatty acid [%]: max. 2.5
Iodine value [Wijs]: min. 158
Colour [Gardner]: max. 9
Moisture [%]: max. 0.2

Names of Tung oil:

IUPAC name:
tung oil

Other names:
China wood oil
lumbang oil
tung oil paraformaldehyde
tungmeal
tungoel

Synonyms of Tung oil:
TUNG OIL
chinawood
CHINA WOOD OIL
TUNG OIL PARAFORMALDEHYD
TUNGMEAL
Tungoel
Einecs 232-272-3
Tung oil [oil, misc.]
TUNG OIL
Tung oil
CAS number: 8001-20-5
EC Number: 232-272-3



APPLICATIONS


Tung oil is often used by paint and varnish manufacturers as a generic name for any wood-finishing product that contains the real tung oil or provides a finish that resembles the finish obtained with tung oil.
Furthermore, Tung oil is a plant oil that can be polymerized to produce a variety of products which include pressure sensitive adhesives, self-healed epoxy coatings, polyurethane foam, and vinyl ester resins.


Different uses of Tung oil:

Wood finishing
Pain Relief
Oil-paper Umbrella
Solvent


Tung oil is very popular today because of two properties:
1) Tung oil is a naturally derived substance.
2) After Tung oil cures (5 to 30 days, weather/temperature related), the result is a very hard and easily repaired finish.
So, Tung oil is used on boat decks and now on floors.

Tung oil is often diluted with hydrocarbon thinner so its viscosity is very low and enables the oil to penetrate the finest grain woods.
This thinning vehicle evaporates within 15 to 20 minutes.

When applied in many fine/thinner coats over wood, tung oil slowly cures to a matte/light satin look with slight golden tint.
Tung oil resists water better than any other pure oil finish and does not darken noticeably with age.

Tung oil is claimed to be less susceptible to mould than linseed oil.
Moreover, Tung oil is considered safe to be used on sculptures made near waterways.

Heating tung oil to about 500 °F (260 °C)[13] in an oxygen-free environment will substantially increase the viscosity and film-forming quality of the product.
Most polymerized tung oils are sold mixed with mineral spirits to make them easier to work with.
Limonene and D-limonene are less toxic alternatives for mineral spirits.


The oil-paper umbrella is the traditional umbrella used in China, Japan, and other countries in the sinosphere, and was brought to Western countries through the Silk Road.
Tung oil is the "oil" mentioned in the oil-paper umbrella, which is used to protect the paper from getting wet, and to make the umbrella waterproof.


The traditional technique for applying pure tung oil is to dilute the oil 1:1 with solvent, then apply a succession of very thin films with a soft, lint-free cloth such as tee-shirt cotton.
Diluents range from traditional spirits of turpentine to any of the new citrus-based thinners to naphtha.

The choice of thinner should be guided by how fast the coating needs to set.
Tung oil works well in spray-on applications in well-ventilated studios.

Primary coats may be laid down at a 1:1 oil-to-thinner ratio, and successive layers, if not absorbed into the wood, at higher solvent to oil concentrations.
This technique brings out the deepest color of the wood while maintaining a matte finish.

Tung oil finishes that start with polymerized oils or tung oil preparations are best applied in the fat over lean principle: thinned pure oil is applied to deeply penetrate the surface, to fill pores.
Straight oil is then applied moderately to adhere to the surface and provide a good base for the thick gloss layers.
The polymerized oil is then applied thickly as a single layer, allowed to fully dry, buffed smooth with very fine sandpaper and 0000 steel wool.

The surface is wiped clean with a moistened rag and allowed to dry.
A final coat is applied fairly thickly (the oil will smooth itself into a glass-like coating) and allowed to dry for two to three days.
Rags soaked with tung oil can spontaneously combust (burst into flame).

Tung oil is a plant oil that can be polymerized to produce a variety of products, which include pressure sensitive adhesives, self-healed epoxy coatings, polyurethane foam, and vinyl ester resins.

Tung Oil is pressed from the nuts of Tung tree is known also as China wood oil and nut oil.
Major producing countries are mainland China and South America (Argentina and Paraguay), United States and Africa.

Tung tree farms in the southern U. S. and Argentina now supply tung oil, formerly available only from China.
The oil is still known in some circles as "China wood oil".Tung oil is an ideal "binder" or "vehicle", carrying the resins and driers deep into the pores of the wood so that sealer and finish coats practically become part of the wood - drying into an armor-like yet beautiful surface.

Tung oil tree (Aleurites fordii), a deciduous shade tree native to China.
It belongs to the Euphorbia Family (Euphorbiaceae) along with the candlenut tree (A molucanna), another species with seeds rich in unsaturated oils.

For centuries tung oil has been used for paints and waterproof coatings, and as a component of caulk and mortar.
Tung oil is an ingredient in ink and is commonly used for a lustrous finish on wood.
Some woodworkers consider tung oil to be one of the best natural finishes for wood.

Tung oil is composed primarily of eleostearic (elaeostearic) acid, with smaller amounts of oleic, linoleic and palmitic glycerides.
Eleostearic acid is a crystalline unsaturated fatty acid that existsin 2 stereoisomeric forms: An alpha acid occurring as the glycerol ester especially in tung oil, and a beta acid obtained from the alpha acid by irradiation (9, 11, 13-octadecatrienoic acid).

Other unsaturated plant oils, such as castor oil and linseed oil, take longer to dry and leave an oily residue until they soak into the wood surface.
Tung oil 's ability to dry quickly and polymerize into a tough, glossy, waterproof coating has made it especially valuable in paints, varnishes, linoleum, oilcloth and printing inks.

The largest application for the oil is paint and varnish, and also wide utilized by soap, inks, electrical insulators, furniture, shipbuilding, etc.
In recent years, the deep development and research of tung oil products at home and abroad are very active, the main research direction is in the electronics industry, advanced printing inks, heat-sensitive copying materials, integrated circuit board materials, marine paint and current product coatings, electrical insulation coatings, chemical industry, surfactants, defoamers, fungicides, adhesives, synthetic resins, plastic industry, rubber industry.

Under the action of alkali and acid, the main component of tung oil, the triglyceride of tung oil is hydrolyzed into unsaturated Tung oil acid containing three conjugated double bonds.
The conjugated double bond in the molecular structure is adjacent to the hydrogen on the carbon atom.

Under the action of O2 in the air, the hydrogen abstraction reaction occurs, and the generated hydroperoxide is decomposed to generate free radicals, and the polymerization reaction is initiated.
According to the molecular structure characteristics of tung oil, the researchers use the principle of addition, polycondensation, esterification to explore the process.

The use of tung oil to modify polymer has been reported more, such as Tung oil modified alkyd resin, polyurethane, epoxy resin and silicone resin, etc., but also used to prepare epoxy resin curing agent or copolymerization with other monomers.




DESCRIPTION


Tung oil or China wood oil is a drying oil obtained by pressing the seed from the nut of the tung tree (Vernicia fordii).
Furthermore, Tung oil and its use are believed to have originated in ancient China and appear in the writings of Confucius from about 400 BC.

Tung oil hardens upon exposure to air (through polymerization), and the resulting coating is transparent and has a deep, almost wet look.
Moreover, Tung oil is used mostly for finishing and protecting wood, after numerous coats, the finish can even look plastic-like.

Related drying oils include linseed, safflower, poppy, and soybean oils.
Raw tung oil tends to dry to a fine, wrinkled finish (the English name for this is gas checking).

This property was used to make wrinkle finishes, usually by adding excess cobalt drier.
To prevent wrinkling, Tung oil is heated to gas-proof it (also known as "boiled").

Tung oil is also called china wood oil that can be produced by cold pressing the seeds of tung tree.
Besides, Tung oil can be used as a biodiesel and a drying oil in the production of paints.

There are different extractives of Tung oil and their physically modified derivatives.
Tung oil consists primarily of the glycerides of the fatty acid eleostearic.

Tung oil is also called china wood oil that can be produced by cold pressing the seeds of tung tree.
In addition, Tung oil can be used as a biodiesel and a drying oil in the production of paints.

Tung oil is an excellent vegetable oil with drying properties.
More to that, Tung oil has the characteristics of fast drying, light specific gravity, good gloss, strong adhesion, heat resistance, Acid resistance, Alkali resistance, corrosion resistance, rust resistance, non-conductivity, etc.

Tung oil is widely used.
Further to that, Tung oil is the main raw material for the manufacture of paints and inks.
Tung oil is widely used as waterproof, anti-corrosion and anti-rust coatings for construction, machinery, weapons, vehicles and boats, fishing gear, and electrical appliances. insecticides, etc.

Tung oil is obtained from the hot pressing of tung oil, is a drying oil (iodine value of 157~170), with high temperature (200~250 deg C) heating, can be due to self polymerization gel, or even completely cured.
This particular property of Tung Oil is due to the polymerization of its main component, α-Tung olein, a property not found in other drying oils.

Tung oil is a dark yellow liquid, which is a natural oil extracted from the seeds of vegetable oil tung trees.
However, this kind of oil has serious toxicity and cannot be taken orally, it is a kind of medicinal efficacy of Chinese herbal medicine.

After screening and cleaning, the tung seeds are dried, peeled, and separated in the shell and kernel separator, then the product was broken with a crushing roller mill.
Then the material is fried in a layer-type cooking pot, and the material temperature can reach 130 ℃, and the water content can be reduced to 2%~ 3%.
After steaming and frying, the oil yield is about 200 by pressing with a 34% type oil press.
Tung oil by deacidification, dehydration and other refining process can be made of finished products.



PROPERTIES


Appearance Form: liquid
Odour: No data available
Odour Threshold: No data available
pH: No data available
Melting point/freezing point: No data available
Initial boiling point and boiling range: No data available
Flash point: 289 °C (552 °F) - closed cup
Evaporation rate: No data available
Flammability (solid, gas): No data available
Upper/lower flammability or explosive limits: No data available
Vapour pressure: No data available
Vapour density: No data available
Relative density: 0.937 g/cm3 at 25 °C (77 °F)
Water solubility: No data available
Partition coefficient:
noctanol/water: No data available
Auto-ignition temperature: No data available
Decomposition temperature: No data available
Viscosity: No data available
Explosive properties: No data available
Oxidizing properties: No data available



FIRST AID


Description of first aid measures:

If inhaled:

If breathed in, move person into fresh air.
If not breathing, give artificial respiration.


In case of skin contact:

Wash off with soap and plenty of water.


In case of eye contact:

Flush eyes with water as a precaution.


If swallowed:

Never give anything by mouth to an unconscious person.
Rinse mouth with water.

Most important symptoms and effects, both acute and delayed:

The most important known symptoms and effects are described in the labelling.

Indication of any immediate medical attention and special treatment needed:

No data available.



HANDLING AND STORAGE


Conditions for safe storage, including any incompatibilities:

Keep container tightly closed in a dry and well-ventilated place.
Storage class (TRGS 510): 10: Combustible liquids


Specific end use(s):

No specific uses are stipulated.


Precautions for safe handling:

Avoid contact with skin and eyes.
Avoid formation of dust and aerosols.
Avoid exposure - obtain special instructions before use.
Provide appropriate exhaust ventilation at places where dust is formed.



SYNONYMS


Tungoel
TUNGMEAL
TUNG OIL
Tung oil
tung oil
chinawood
CHINA WOOD OIL
Einecs 232-272-3
Tung oil substitutes
Tung oil [Oil, misc.]
Tung oil [oil, misc.]
TUNG OIL PARAFORMALDEHYD
TURKEY RED OIL
DESCRIPTION:

TURKEY RED OIL is a solubilizing agent for essential oils.
TURKEY RED OIL is mainly used in low foaming bath preparations.
Due to its oily components TURKEY RED OIL is applied as emollient in shower baths, liquid soaps and hand cleansing pastes.

CAS No. : 8002-33-3

E.C. no : 232-306-7

SYNONYM(S) OF TURKEY RED OIL:
Castor-oil sulfated sodium salt, Sulfated castor oil, Sulforicinolate sodium salt


Turkey Red Oil is also known as Sulfated Castor Oil.
Turkey Red Oil is the only oil that will completely disperse in water.
The oil is expressed from the seed.

Sulfated castor oil is created by adding sulfuric acid to castor oil, and is considered the first synthetic detergent.
Turkey Red Oil has a distinct and heavy scent.

Turkey Red Oil is a surfactant and therefore makes a wonderful base for a bath oil as it mixes well with water, producing a milk bath.

Turkey Red Oil Acts as an emollient and solubilizing agent.
Turkey Red Oil is mainly used in low foaming bath preparations.

Turkey Red Oil Solubilizes essential oils.
Turkey Red Oil is Used to formulate shower baths, liquid soaps and hand cleaning pastes.

As a reputed entity of this domain, we are engaged in presenting optimum quality Turkey Red Oil.

Turkey Red Oil is synthesized by adding sulfuric acid to castor oil at our advanced processing unit.
Turkey Red Oil is processed by making use of the utmost quality chemical substances using sophisticated techniques.
We offer this Turkey Red Oil in different packaging options, that is known as the first synthetic detergent among the clients.


Turkey-red oil, long used as a dyeing aid, is produced by the reaction of castor oil with sulfuric acid.

Turkey Red Oil is also widely known as Sulfated Castor Oil.
The oil is commonly referred to as Turkey Red Oil because the color of the oil resembles the color and textile dying process known as Turkey Red.

Using a process known as sulfation, our Turkey Red Oil is manufactured by exposing pure castor oil to sulfuric acid.
This specialized process produces an oil that is miscible in water while also retaining the moisturization properties of Castor Oil.
The oil is then packaged to maintain the purity, freshness and beneficial properties of this uniquely water soluble oil.


USES OF TURKEY RED OIL:
Turkey Red Oil is easily dispersible in water.
Turkey Red Oil is perfectly suited for use in making water dispersible bath oils and personal care products.
Turkey Red Oil also helps to solubilize other lipids and essential oils.

Turkey Red Oil is Used in Textile industries, Sugar industry, as a defoaming agent, as an Emulsifier.
In cosmetics Turkey Red Oil is used as humectants and as an Emulsifier for Oil Bath.








Turkey Red Oil is the name of Sulphonated Caster Oil commonly called TRO .
Neosol Chemicals manufacture Turkey Red Oil from the sulphonation of distilled Caster Oil, therefore final product is bright clear Yellow to Brown viscous liquid with pleasant odor of Caster Oil.

Turkey Red Oil is anionic detergent used in formulation of liquid detergents, wool washing, white phenyl and in lubricating applications.
Turkey Red Oil is available in various strengths but most common is 50% TRO

Turkey Red oil is used to emulsify essential oils so that they will dissolve in other water-based products, or for superfatting liquid soap if you want the soap to remain transparent.
This means that the oil will combine with the water in the tub, and not leave those little oil bubbles floating on the top of the water nor will it leave an oil ring around the tub due to its emulsifying & surfactant properties.

Turkey Red Oil is of medium viscosity and is usually used in bath oil recipes along with fragrance or essential oils, or in shampoos.
Turkey Red Oil also has great moisturizing abilities. It has a reddish-orange hue to it.


APPLICATIONS OF TURKEY RED OIL:

Turkey Red oil is used in agriculture as organic manure, in textiles as surfactants and wetting agents, in paper industry for defoaming, in cosmetics as emulsifiers, in pharmaceuticals as undecylenate, in paints inks and as lubricants.

For e.g. it is used to emulsify essential oils so that they will dissolve in other water-based products, or for superfatting liquid soap if you want the soap to remain transparent.
This means that the oil will combine with the water in the tub, and not leave those little oil bubbles floating on the top of the water.
It is of medium viscosity and is usually used in bath oil recipes along with fragrance or essential oils, or in shampoos.
This oil also has great moisturizing abilities.


Turkey Red Oil is Perfectly Suited for the Following Personal Care Applications:
Skin Care
Hair Care
Nail Care
Cosmetics
Soap


Sulfonated castor oil has a wide variety of application in different Chemical Industries.
These are some of the example where Turkey Red Oil is used:
Dyes & Intermediates:
Turkey Red Oil is use as anti-foaming purpose.

Paper & Sugar industry:
Turkey Red Oil is use as defoaming agent & An Emulsifier.

Soap & Cosmetics Industry:
Turkey Red Oil protects the skin with standing the oilish content irrespective of any tropic condition.

Lubricant Industry:
Turkey Red Oil is used As An Additive.   Â

Pesticide industry :
Turkey Red Oil is used As an emulsifier

Leather & rubber Industry:
Turkey Red Oil used as a softening & wetting agent.
Paints and inks Industry:
Turkey Red Oil is used As a lubricant additive.

Pigment & Colour industries:
Turkey Red Oil enhances the strength maintaining.

Alcohol:
Turkey Red Oil is used as anti-foaming & fermentation.



FEATURES OF TURKEY RED OIL:
100% disperse in water
Varying viscosity
Purity
Effectiveness


CHEMICAL AND PHYSICAL PROPERTIES OF TURKEY RED OIL:
Clear Amber Hue
Medium-Thick Viscosity
Characteristic Castor Aroma
Moisturizing
Strength: 70%
Fully Dispersible in Water
Emulsifier/Surfactant
Humectant
Chemical description Sodium sulforicinoleate
Concentration [%] 82
pH
A = Original
B = 10% in water
C = 1% in water 7.5 (B)
Appearance [at 20 °C] liquid
Appearance Amber coloured Viscous liquid.
Melting point < 0°C
Boiling Point > 150°C
Solubility Miscible in Water, gives a clear solution.
Specific Gravity 1.015@20°C for 50% and 1.03@20°C for 70%
Sulphonation degree Minimum 4.0
PH of 2% Solution 6.5Â to 8
Colour Dark Brown/Light Yellow
Iron (F.e) by weight 0.01%
T.R.O. as Sulphoneted Oil Oil
Viscosity (B4 ford cap)at 27 degree Celsius 105-120Â Second
Centramide Value 235-255ml/gm
Fatty Matter 50Â min
Purity 50%
Specific gravity (27 degree Celsius) 1.050-1.10
Solubility Water Soluble





SAFETY INFORMATION ABOUT TURKEY RED OIL
First aid measures:
Description of first aid measures:
General advice:
Consult a physician.
Show this safety data sheet to the doctor in attendance.
Move out of dangerous area:

If inhaled:
If breathed in, move person into fresh air.
If not breathing, give artificial respiration.
Consult a physician.
In case of skin contact:
Take off contaminated clothing and shoes immediately.
Wash off with soap and plenty of water.
Consult a physician.

In case of eye contact:
Rinse thoroughly with plenty of water for at least 15 minutes and consult a physician.
Continue rinsing eyes during transport to hospital.

If swallowed:
Do NOT induce vomiting.
Never give anything by mouth to an unconscious person.
Rinse mouth with water.
Consult a physician.

Firefighting measures:
Extinguishing media:
Suitable extinguishing media:
Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.
Special hazards arising from the substance or mixture
Carbon oxides, Nitrogen oxides (NOx), Hydrogen chloride gas

Advice for firefighters:
Wear self-contained breathing apparatus for firefighting if necessary.
Accidental release measures:
Personal precautions, protective equipment and emergency procedures
Use personal protective equipment.

Avoid breathing vapours, mist or gas.
Evacuate personnel to safe areas.

Environmental precautions:
Prevent further leakage or spillage if safe to do so.
Do not let product enter drains.
Discharge into the environment must be avoided.

Methods and materials for containment and cleaning up:
Soak up with inert absorbent material and dispose of as hazardous waste.
Keep in suitable, closed containers for disposal.

Handling and storage:
Precautions for safe handling:
Avoid inhalation of vapour or mist.

Conditions for safe storage, including any incompatibilities:
Keep container tightly closed in a dry and well-ventilated place.
Containers which are opened must be carefully resealed and kept upright to prevent leakage.
Storage class (TRGS 510): 8A: Combustible, corrosive hazardous materials

Exposure controls/personal protection:
Control parameters:
Components with workplace control parameters
Contains no substances with occupational exposure limit values.
Exposure controls:
Appropriate engineering controls:
Handle in accordance with good industrial hygiene and safety practice.
Wash hands before breaks and at the end of workday.

Personal protective equipment:
Eye/face protection:
Tightly fitting safety goggles.
Faceshield (8-inch minimum).
Use equipment for eye protection tested and approved under appropriate government standards such as NIOSH (US) or EN 166(EU).

Skin protection:
Handle with gloves.
Gloves must be inspected prior to use.
Use proper glove
removal technique (without touching glove's outer surface) to avoid skin contact with this product.
Dispose of contaminated gloves after use in accordance with applicable laws and good laboratory practices.
Wash and dry hands.

Full contact:
Material: Nitrile rubber
Minimum layer thickness: 0.11 mm
Break through time: 480 min
Material tested:Dermatril (KCL 740 / Aldrich Z677272, Size M)
Splash contact
Material: Nitrile rubber
Minimum layer thickness: 0.11 mm
Break through time: 480 min
Material tested:Dermatril (KCL 740 / Aldrich Z677272, Size M)
It should not be construed as offering an approval for any specific use scenario.

Body Protection:
Complete suit protecting against chemicals, The type of protective equipment must be selected according to the concentration and amount of the dangerous substance at the specific workplace.
Respiratory protection:
Where risk assessment shows air-purifying respirators are appropriate use a fullface respirator with multi-purpose combination (US) or type ABEK (EN 14387) respirator cartridges as a backup to engineering controls.

If the respirator is the sole means of protection, use a full-face supplied air respirator.
Use respirators and components tested and approved under appropriate government standards such as NIOSH (US) or CEN (EU).
Control of environmental exposure
Prevent further leakage or spillage if safe to do so.
Do not let product enter drains.
Discharge into the environment must be avoided.

Stability and reactivity:
Chemical stability:
Stable under recommended storage conditions.
Incompatible materials:
Strong oxidizing agents:
Hazardous decomposition products:
Hazardous decomposition products formed under fire conditions.
Carbon oxides, Nitrogen oxides (NOx), Hydrogen chloride gas.

Disposal considerations:
Waste treatment methods:
Product:
Offer surplus and non-recyclable solutions to a licensed disposal company.
Contact a licensed professional waste disposal service to dispose of this material.
Contaminated packaging:
Dispose of as unused product.




TURPENTINE
DESCRIPTION:
Turpentine (which is also called spirit of turpentine, oil of turpentine, terebenthene, terebinthine and (colloquially) turps) is a fluid obtained by the distillation of resin harvested from living trees, mainly pines.
Turpentine is used as a specialized solvent.
Turpentine is also a source of material for organic syntheses.

CAS Number: 9005-90-7
EC Number: 232-688-5

Turpentine is composed of terpenes, primarily the monoterpenes alpha- and beta-pinene, with lesser amounts of carene, camphene, dipentene, and terpinolene.
Mineral turpentine or other petroleum distillates are used to replace turpentine – although the constituent chemicals are very different.
Turpentine is distilled from pine tree resins to create a superior, natural thinner that has become the artist’s choice for thinning oils and art-grade paints.
Turpentine improves bonding and penetration of most brush-applied alkyd and oil-type paints, varnishes, and enamels.
Turpentine is also used to clean brushes, rollers, spray equipment, and roller trays.

CHEMICAL AND PHYSICAL PROPERTIES OF TURPENTINE:
Chemical formula: C10H16
Molar mass: 136.238 g•mol−1
Appearance: Viscous liquid
Odor: Resinous
Melting point: −55 °C (−67 °F; 218 K)
Boiling point: 154 °C (309 °F; 427 K)
Solubility in water: 20 mg/L
Flash point: 35 °C (95 °F; 308 K)
Autoignition temperature: 220 °C (428 °F; 493 K)
Appearance: colorless to pale yellow clear liquid (est)
Food Chemicals Codex Listed: No
Specific Gravity: 0.85000 to 0.87000 @ 25.00 °C.
Pounds per Gallon - (est).: 7.073 to 7.239
Refractive Index: 1.46000 to 1.48000 @ 20.00 °C.
Melting Point: -55.00 °C. @ 760.00 mm Hg
Boiling Point: 153.00 to 175.00 °C. @ 760.00 mm Hg
Vapor Pressure: 4.000000 mmHg @ -6.70 °C.
Vapor Density: 4.84 ( Air = 1 )
Flash Point: 86.00 °F. TCC ( 30.00 °C. )
Soluble in:
alcohol
water, 5.875 mg/L @ 25 °C (est)
Insoluble in: water

Turpentine, the resinous exudate or extract obtained from coniferous trees, particularly those of the genus Pinus.
Turpentines are semifluid substances consisting of resins dissolved in a volatile oil; this mixture is separable by various distillation techniques into a volatile portion called oil (or spirit) of turpentine and a nonvolatile portion called rosin.
Although the term turpentine originally referred to the whole oleoresinous exudate, it now commonly refers to its volatile turpentine fraction only, which has various uses in industry and the visual arts.

Oil of turpentine is a colourless, oily, odorous, flammable, water-immiscible liquid with a hot, disagreeable taste.
It is a good solvent for sulphur, phosphorus, resins, waxes, oils, and natural rubber.
It hardens upon exposure to air.
Chemically, oil of turpentine is a mixture of cyclic monoterpene hydrocarbons, the predominant constituent being pinene.

Formerly, the largest use for turpentine oil was as a paint and varnish solvent.
Oil painters generally prefer it as a paint thinner and brush cleaner to petroleum solvents (mineral spirits), even though the latter are less expensive.
But the largest use of turpentine oil is now in the chemical industry, as a raw material in the synthesis of resins, insecticides, oil additives, and synthetic pine oil and camphor.
Turpentine oil is also used as a rubber solvent in the manufacture of plastics.

Turpentine oil is generally produced in countries that have vast tracts of pine trees.
The principal European turpentines are derived from the cluster pine (P. pinaster) and the Scotch pine (P. sylvestris), while the main sources of turpentine in the United States are the longleaf pine (P. palustris) and the slash pine (P. caribaea).

Turpentine oil is classified according to the way it is produced.
Sulfate turpentine, used widely in the chemicals industry, is obtained as a by-product of the kraft, or sulfate, process of cooking wood pulp in the course of the manufacture of kraft paper.
Wood turpentine is obtained by the steam distillation of dead, shredded bits of pine wood, while gum turpentine results from the distillation of the exudate of the living pine tree obtained by tapping.
Crude turpentine obtained from the living pine by tapping typically contains 65 percent gum rosin and 18 percent gum turpentine.

Various other oleoresins (solutions of resins dispersed in essential oils) are known as turpentines. Venice turpentine, for example, is a pale green, viscous liquid that is collected from the larch (Larix decidua, or L. europea).
Turpentine is used for lithographic work and in sealing wax and varnishes.

ETYMOLOGY:
The word turpentine derives (via French and Latin) from the Greek word τερεβινθίνη terebinthine, in turn the feminine form (to conform to the feminine gender of the Greek word, which means "resin") of an adjective (τερεβίνθινος) derived from the Greek noun (τερέβινθος) for the terebinth tree.

Although the word originally referred to the resinous exudate of terebinth trees (e.g. Chios turpentine, Cyprus turpentine, and Persian turpentine), it now refers to that of coniferous trees, namely crude turpentine (e.g. Venice turpentine is the oleoresin of larch), or the volatile oil part thereof, namely oil (spirit) of turpentine; the later usage is much more common today.

SOURCE TREES:
Important pines for turpentine production include: maritime pine (Pinus pinaster), Aleppo pine (Pinus halepensis), Masson's pine (Pinus massoniana), Sumatran pine (Pinus merkusii), longleaf pine (Pinus palustris), loblolly pine (Pinus taeda), slash pine (Pinus elliottii), and ponderosa pine (Pinus ponderosa).

To tap into the sap producing layers of the tree, turpentiners used a combination of hacks to remove the pine bark.
Once debarked, pine trees secrete crude turpentine (oleoresin) onto the surface of the wound as a protective measure to seal the opening, resist exposure to micro-organisms and insects, and prevent vital sap loss.

Turpentiners wounded trees in V-shaped streaks down the length of the trunks to channel the crude turpentine into containers.
It was then collected and processed into spirits of turpentine.
Crude turpentine yield may be increased by as much as 40% by applying paraquat herbicides to the exposed wood.

The V-shaped cuts are called "catfaces" for their resemblance to a cat's whiskers.
These marks on a pine tree signify it was used to collect resin for turpentine production.
Crude turpentine collected from the trees may be evaporated by steam distillation in a copper still. Molten rosin remains in the still bottoms after turpentine has been distilled out.
Such turpentine is called gum turpentine.
The term gum turpentine may also refer to crude turpentine, which may cause some confusion.

Turpentine may alternatively be extracted from destructive distillation of pine wood, such as shredded pine stumps, roots, and slash, using the light end of the heavy naphtha fraction (boiling between 90 and 115 °C or 195 and 240 °F) from a crude oil refinery.
Such turpentine is called wood turpentine.
Multi-stage counter-current extraction is commonly used so fresh naphtha first contacts wood leached in previous stages and naphtha laden with turpentine from previous stages contacts fresh wood before vacuum distillation to recover naphtha from the turpentine.
Leached wood is steamed for additional naphtha recovery prior to burning for energy recovery.

Sulfate turpentine:
When producing chemical wood pulp from pines or other coniferous trees, sulfate turpentine may be condensed from the gas generated in Kraft process pulp digesters.
The average yield of crude sulfate turpentine is 5–10 kg/t pulp.
Unless burned at the mill for energy production, sulfate turpentine may require additional treatment measures to remove traces of sulfur compounds.



CHEMISTRY OF TURPENTINE:
Turpentine is composed primarily of monoterpene hydrocarbons, the most prevalent of which are the pinenes, camphene, and 3-carene.
Rosin contains mostly diterpene resin acids, such as abietic acid, dehydroabietic acid, palustric acid, and isopimaric acid.
Numerous other compounds are present in small quantities in all turpentine products.
Canada turpentine, or Canada balsam, is an oleoresin obtained from the stems of the balsam fir (Abies balsamea [Family Pinaceae]).

USES AND PHARMACOLOGY:
Turpentine and its related products (the oil and rosin) are important in commerce and traditional medicine.
These products can pose a toxicity risk and should be handled and stored carefully.

Antibacterial effects:
In vitro data:
In an in vitro study, turpentine oil exerted antibacterial effects against Staphylococcus epidermidis and Escherichia coli.
Turpentine was also found to exert activity against 2 strains of yeast.

Anti-inflammatory effects:
Animal data:
Literature primarily documents turpentine use in experimental animal models of inflammation to induce a systemic inflammatory immune response, with demonstrated beneficial effects.

Antiparasitic effects:
Turpentine has been noted to possess varying antiparasitic effects.
Turpentine has been used in the treatment of myiasis.
Specifically, Turpentine is useful in helping to remove the larvae in cases of myiasis.

Clinical data:
A case report describes a 28-year-old male patient with a history of maxillofacial trauma who presented with oral myiasis.
He received topical cotton application of turpentine oil on the area infested with maggots.
After 10 to 12 minutes, the cotton was removed, and the maggots were subsequently removed.

Further treatment with surgical debridement and oral ivermectin was provided.
Another case report describes removal of blowfly larvae with turpentine oil in a neonatal patient.

Bone metabolism:
Animal data:
In a study of rats, inhibition of bone resorption occurred in a dose-dependent manner with turpentine.

Dermal injury:
Animal data:
When applied topically, turpentine causes skin irritation and, therefore, has been shown to exert rubefacient and counterirritant actions.
However, in a systematic study, a pine oil product derived from Pinus palustris and Pinus elliottii reduced dermal inflammation in a mouse ear model of contact irritant–induced dermal inflammation as well as second-degree burns to the mouse paw.

Neuropathy:
Clinical data:
Topical turpentine oil was found to be as effective as topical capsaicin cream for reducing pain in the feet of diabetic adults who suffered from painful diabetic neuropathy in a randomized, controlled trial (N=300).
Significant reductions were observed in both groups over the 3-month trial with 53% and 47%, respectively, experiencing at least a 3-point reduction in pain on the visual analogy scale.
The majority of patients were male (57%) with type 2 diabetes (89%).

Sclerosis:
Clinical data:
Abstract data from a study in Russia suggest turpentine baths may assist in the treatment of disseminated sclerosis, but the safety of this treatment has not been established.

Sexual dysfunction:
Clinical data:
One study from Russia documents the use of turpentine white emulsion baths in patients with sexual dysfunctions, but the safety of this treatment has not been established.

INDUSTRIAL AND OTHER END USES OF TURPENTINE:
Solvent:
As a solvent, turpentine is used for thinning oil-based paints, for producing varnishes, and as a raw material for the chemical industry.
Its use as a solvent in industrialized nations has largely been replaced by the much cheaper turpentine substitutes obtained from petroleum such as white spirit.
A solution of turpentine and beeswax or carnauba wax has long been used as a furniture wax.

Source of organic compounds:
Turpentine is also used as a source of raw materials in the synthesis of fragrant chemical compounds. Commercially used camphor, linalool, alpha-terpineol, and geraniol are all usually produced from alpha-pinene and beta-pinene, which are two of the chief chemical components of turpentine.
These pinenes are separated and purified by distillation.
The mixture of diterpenes and triterpenes that is left as residue after turpentine distillation is sold as rosin.

Medicinal elixir:
Turpentine and petroleum distillates such as coal oil and kerosene have been used medicinally since ancient times, as topical and sometimes internal home remedies.
Topically, Turpentine has been used for abrasions and wounds, as a treatment for lice, and when mixed with animal fat it has been used as a chest rub, or inhaler for nasal and throat ailments.
Vicks chest rubs still contain turpentine in their formulations, although not as an active ingredient.

Turpentine, now understood to be dangerous for consumption, was a common medicine among seamen during the Age of Discovery.
Turpentine was one of several products carried aboard Ferdinand Magellan's fleet during the first circumnavigation of the globe.
Taken internally Turpentine was used as a treatment for intestinal parasites.

Turpentine is dangerous, due to the chemical's toxicity.
Turpentine enemas, a very harsh purgative, had formerly been used for stubborn constipation or impaction.
Turpentine enemas were also given punitively to political dissenters in post-independence Argentina.

Niche uses:
Turpentine is also added to many cleaning and sanitary products due to its antiseptic properties and its "clean scent".
In early 19th-century America, turpentine was sometimes burned in lamps as a cheap alternative to whale oil.
Turpentine was most commonly used for outdoor lighting, due to its strong odour.

A blend of ethanol and turpentine called camphine served as the dominant lamp fuel replacing whale oil until the advent of kerosene.
In 1946, Soichiro Honda fueled the first Honda motorcycles with a blend of gasoline and turpentine to cover the smell of gasoline, due to the scarcity of gasoline in Japan following World War II.
In his book If Only They Could Talk, veterinarian and author James Herriot describes the use of the reaction of turpentine with resublimed iodine to "drive the iodine into the tissue" - or perhaps just impress the watching customer with a spectacular treatment (a dense cloud of purple smoke).
As an organic solvent, its vapour can irritate the skin and eyes, damage the lungs and respiratory system, as well as the central nervous system when inhaled, and cause damage to the renal system when ingested, among other things.
Ingestion can cause burning sensations, abdominal pain, nausea, vomiting, confusion, convulsions, diarrhea, tachycardia, unconsciousness, respiratory failure, and chemical pneumonia.

The Occupational Safety and Health Administration (OSHA) has set the legal limit (permissible exposure limit) for turpentine exposure in the workplace as 100 ppm (560 mg/m3) over an 8-hour workday.
The same threshold was adopted by the National Institute for Occupational Safety and Health (NIOSH) as the recommended exposure limit (REL).
At levels of 800 ppm (4480 mg/m3), turpentine is immediately dangerous to life and health.



SAFETY INFORMATION ABOUT TURPENTINE:
First aid measures:
Description of first aid measures:
General advice:
Consult a physician.
Show this safety data sheet to the doctor in attendance.
Move out of dangerous area:

If inhaled:
If breathed in, move person into fresh air.
If not breathing, give artificial respiration.
Consult a physician.
In case of skin contact:
Take off contaminated clothing and shoes immediately.
Wash off with soap and plenty of water.
Consult a physician.

In case of eye contact:
Rinse thoroughly with plenty of water for at least 15 minutes and consult a physician.
Continue rinsing eyes during transport to hospital.

If swallowed:
Do NOT induce vomiting.
Never give anything by mouth to an unconscious person.
Rinse mouth with water.
Consult a physician.

Firefighting measures:
Extinguishing media:
Suitable extinguishing media:
Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.
Special hazards arising from the substance or mixture
Carbon oxides, Nitrogen oxides (NOx), Hydrogen chloride gas

Advice for firefighters:
Wear self-contained breathing apparatus for firefighting if necessary.
Accidental release measures:
Personal precautions, protective equipment and emergency procedures
Use personal protective equipment.

Avoid breathing vapours, mist or gas.
Evacuate personnel to safe areas.

Environmental precautions:
Prevent further leakage or spillage if safe to do so.
Do not let product enter drains.
Discharge into the environment must be avoided.

Methods and materials for containment and cleaning up:
Soak up with inert absorbent material and dispose of as hazardous waste.
Keep in suitable, closed containers for disposal.

Handling and storage:
Precautions for safe handling:
Avoid inhalation of vapour or mist.

Conditions for safe storage, including any incompatibilities:
Keep container tightly closed in a dry and well-ventilated place.
Containers which are opened must be carefully resealed and kept upright to prevent leakage.
Storage class (TRGS 510): 8A: Combustible, corrosive hazardous materials

Exposure controls/personal protection:
Control parameters:
Components with workplace control parameters
Contains no substances with occupational exposure limit values.
Exposure controls:
Appropriate engineering controls:
Handle in accordance with good industrial hygiene and safety practice.
Wash hands before breaks and at the end of workday.

Personal protective equipment:
Eye/face protection:
Tightly fitting safety goggles.
Faceshield (8-inch minimum).
Use equipment for eye protection tested and approved under appropriate government standards such as NIOSH (US) or EN 166(EU).

Skin protection:
Handle with gloves.
Gloves must be inspected prior to use.
Use proper glove
removal technique (without touching glove's outer surface) to avoid skin contact with this product.
Dispose of contaminated gloves after use in accordance with applicable laws and good laboratory practices.
Wash and dry hands.

Full contact:
Material: Nitrile rubber
Minimum layer thickness: 0.11 mm
Break through time: 480 min
Material tested:Dermatril (KCL 740 / Aldrich Z677272, Size M)
Splash contact
Material: Nitrile rubber
Minimum layer thickness: 0.11 mm
Break through time: 480 min
Material tested:Dermatril (KCL 740 / Aldrich Z677272, Size M)
It should not be construed as offering an approval for any specific use scenario.

Body Protection:
Complete suit protecting against chemicals, The type of protective equipment must be selected according to the concentration and amount of the dangerous substance at the specific workplace.
Respiratory protection:
Where risk assessment shows air-purifying respirators are appropriate use a fullface respirator with multi-purpose combination (US) or type ABEK (EN 14387) respirator cartridges as a backup to engineering controls.

If the respirator is the sole means of protection, use a full-face supplied air respirator.
Use respirators and components tested and approved under appropriate government standards such as NIOSH (US) or CEN (EU).
Control of environmental exposure
Prevent further leakage or spillage if safe to do so.
Do not let product enter drains.
Discharge into the environment must be avoided.

Stability and reactivity:
Chemical stability:
Stable under recommended storage conditions.
Incompatible materials:
Strong oxidizing agents:
Hazardous decomposition products:
Hazardous decomposition products formed under fire conditions.
Carbon oxides, Nitrogen oxides (NOx), Hydrogen chloride gas.

Disposal considerations:
Waste treatment methods:
Product:
Offer surplus and non-recyclable solutions to a licensed disposal company.
Contact a licensed professional waste disposal service to dispose of this material.
Contaminated packaging:
Dispose of as unused product.


QUESTIONS AND ANSWERS ABOUT TURPENTINE:

1. What is TURPENTINE?
Turpentine is a yellow-colored, sticky liquid that comes from pine gum or pine wood.
Turpentine turns into a vapor very easily, and it can catch fire.
Oil of turpentine is a colorless liquid with a very strong smell.
Other names for turpentine are gum spirits, turps, gum thus, D.D. turpentine, wood turpentine, oil of turpentine, rectified turpentine oil, spirits of turpentine, sulfate wood turpentine, sulfate turpentine, gum turpentine, and steam-distilled turpentine.
2. Where can turpentine be found and how is turpentine used?
In the past, turpentine was the most widely used paint and varnish thinner.
Turpentine was also used in printing, hair products and medicines.
Turpentine is still used in some paints and coatings.
Today, less costly products have replaced the use of turpentine in paints.

Now, the major use of turpentine is as a raw material for the chemical industry.
Turpentine is also used for spray painting and pottery, ceramic coatings, artist’s paints and naval paints.
Turpentine is sometimes found in shoe and furniture polishes.
Turpentine is also used as a metal cleaner.

Compounds extracted from turpentine can be used for tires, plastics, adhesives, flavors, fragrances, makeup, paints and medicine.
3. How can people be exposed to turpentine?
People who work in pulp or paper factories may be exposed to turpentine.
Exposure at work can also occur at places that make flavorings, fragrances, coatings, metal cleaners or solvents.
At home, you can be exposed through food, personal care products, household products and medicine.

Pine forests are sources of natural, low level exposure to turpentine since trees release terpenes into the air.
You could be exposed to turpentine through:
Breathing vapors at work or at home, such as when painting.

Drinking turpentine in medicine.
Accidental drinking of turpentine is unlikely.
Touching paint thinners or other products containing turpentine.
Eye Contact by splashing turpentine in the eyes.

4. How does turpentine work?
Turpentine is easily taken into the intestines and the lungs.
Some turpentine leaves the body when air is breathed out.
The rest leaves the body in urine.
Turpentine irritates the stomach and intestines and affects the nervous system.

5. How can turpentine affect my health?
Turpentine is poisonous if swallowed.
Children and adults can die from drinking turpentine.
Fortunately, turpentine causes taste and odor problems before reaching toxic levels in humans. Turpentine is thought to be only mildly toxic when used according to manufacturers’ recommendations.

Turpentine can pass through the skin.
Some people develop an allergy to turpentine when exposed to it for a long time.
Turpentine exposure causes eye irritation, headache, dizziness and vomiting.
Breathing or swallowing also causes kidney and bladder irritation.

6. How is turpentine poisoning treated?
There is no treatment for turpentine poisoning.
A doctor will treat the symptoms.
Medicine may be given if seizures occur.
Pumping the stomach is only done if another poison has also been swallowed with the turpentine.

7. What should I do if exposed to turpentine?
If turpentine gets in your eyes, flush the eyes right away.
Use large amounts of water for at least 15 minutes.
Lift the lower and upper lids from time to time.
Get medical help.

If you touch turpentine, wash with soap and water.
If irritation does not stop, or if a large area of skin is affected, get medical help.
If you breathe turpentine, go to an area of fresh air.
Get medical help.

If it is hard to breathe, try to get oxygen.
Stay warm and quiet until help arrives.
If you swallow turpentine, drink several glasses of water.

Do not throw up.
Get medical help right away.
Stay warm and quiet until help arrives.

8. What factors limit use or exposure to turpentine?
When working with turpentine, have a source of fresh air and a ventilation system.
If this cannot be done, workers should wear a respirator.
Wear protective work clothing.

Wash well after exposure.
Wash again at the end of the work shift.

9. Is there a medical test to show whether I’ve been exposed to turpentine?
There is no medical test for turpentine poisoning.
TURPENTINE (Térébenthine)
turpentine; chian turpentine; turps; gum terpentine; spirit of turpentine; oleoresin; oil of turpentine CAS 9005-90-7
Turpentine
1-Hydroxyethane-1,1-diyl)diphosphonic acid; Etidronsaeure; Acetodiphosphonic acid; ethane-1-hydroxy-1,1- CAS No: 2809-21-4
TURPINAL SL
TURPINAL SL has been developed for the personal care industry in order to answer the need for high purity chemicals with strong chelation properties.
TURPINAL SL uses range from peroxide stabilization to bar soap oxidation prevention.
TURPINAL SL etidronic acid high purity cosmetics grade produced and tested to ensure quality and consistency.

CAS Number: 2809-21-4
EC Number: 220-552-8
Chemical Formula: C2H8O7P2
Molecular weight: 206 g/mol

TURPINAL SL provides hair damage control in bleaching/ coloring process.
TURPINAL SL acts as chelating agent.

TURPINAL SL has been developed for the personal care industry in order to answer the need for high purity chemicals with strong chelation properties.
TURPINAL SL uses range from peroxide stabilization to bar soap oxidation prevention.

TURPINAL SL etidronic acid high purity cosmetics grade produced and tested to ensure quality and consistency.
TURPINAL SL is ideally suited for personal care and cosmetic applications.

TURPINAL SL belongs to a group of medicines called bisphosphonates.
TURPINAL SL alters the cycle of bone formation and breakdown in the body.

TURPINAL SL is used to treat Paget's disease, and to treat conditions of irregular bone growth due to hip fracture or spinal cord injury.
TURPINAL SL may also be used for purposes not listed in this medication guide.

Incorporate TURPINAL SL at low levels in bar soap and hair care preparations.
TURPINAL SL is an excellent chelating agent for transition metals such as iron, copper, manganese and zinc.
TURPINAL SL is stable in oxygen bleaching conditions.

TURPINAL SL is a personal care products additive.
TURPINAL SL is produced and tested to meet the consistent high quality requirements encountered.

TURPINAL SL type is preferred for formulations based on neutral pH.
TURPINAL SL is miscible with water in all proportions and has a strong complexing capacity with polyvalent cations.

TURPINAL SL is a diphosphonate which affects calcium metabolism.
TURPINAL SL inhibits ectopic calcification and slows down bone resorption and bone turnover.

TURPINAL products are high purity grades of etidronic acid and sodium etidronate which are suitable for use in cosmetics and Personal Care or any applications requiring a very low metal content.
The high purity of these products is guaranteed by thorough quality control procedures (including testing for microbiological contamination).
Moreover, the certificate of analysis accompanying each batch contains detailed information covering chemical purity and trace metal content.

Their chelating properties make them outstanding candidates for the chelation of metal ions, in particular the transition metals (Fe, Cu, Mn, Zn) and the water hardness ions (Ca, Mg).
Thanks to the chelating properties and threshold effect, and added to TURPINAL SL chemical stability in oxidizing environment, TURPINAL can bring substantial benefits in many application fields and more specifically in the cosmetics industry.

These products are ideal chelants or additives in the following applications:
In the stabilization of peroxide bonds, in alkaline media specifically,
As a chelant in hair cosmetics containing mercaptan groups, i.e. thioglycolic acid, thiolactic acid,

As a means of limiting hair damage caused by bleaching or colouring,
In the stabilization of bar soaps, where TURPINAL is used as antioxidant and prevents discolouration and rancidity, in particular under the influence of day light,
In the stabilization of fragrances, which would otherwise lose their strength over time during storage of cosmetic formulations.

Uses of TURPINAL SL:
Use TURPINAL SL as directed by your doctor.
Check the label on the medicine for exact dosing instructions.

Take TURPINAL SL with 6 to 8 ounces (180 to 240 mL) of plain water first thing in the morning, at least 30 minutes before eating, drinking, or taking any other medicine.
TURPINAL SL works best if taken 60 minutes before eating, drinking, or taking any other medicine.

Taking TURPINAL SL with orange juice, coffee, or mineral water may decrease TURPINAL SL effectiveness.
Do not break, crush, suck, or chew the tablet before swallowing.

Do not lie down for at least 30 minutes after taking TURPINAL SL and until after you have had your first meal or snack of the day.
Do not take TURPINAL SL at bedtime or before getting out of bed.

Calcium or iron supplements, vitamins, or antacids containing calcium, magnesium, or aluminum may interfere with the absorption of TURPINAL SL.
These medicines must be taken at least 2 hours after taking TURPINAL SL.

If you miss a dose of TURPINAL SL, skip the missed dose and go back to your regular dosing schedule.
Do not take 2 doses at once.

Recommended Uses of TURPINAL SL:
TURPINAL SL ideally suited for use in personal care and cosmetic applications.
TURPINAL SL is added to bar soap and hair care preparations at low levels.

TURPINAL SL has a shelf life of at least 1 year in TURPINAL SL original sealed packaging at 5-30 oC.
TURPINAL SL is recommended to add TURPINAL at concentrations between 0.1-2% with reference to the finished product during production.

Usage Areas of TURPINAL SL:
TURPINAL SL is used in stabilization of peroxide bonds, especially in alkaline environments, as a complexing agent in hair cosmetics containing mercaptan groups (such as thioglycolic acid, thiolactic acid)

Limiting hair damage caused by bleaching and coloring,
TURPINAL SL is used in the stabilization of soap bars, especially under the influence of daylight, where TURPINAL is used as an antioxidant and protects TURPINAL SL from discoloration and molding (sour, smell).

Paget’s Disease:
TURPINAL SL disodium tablets are indicated for the treatment of symptomatic Paget’s disease of bone.

TURPINAL SL disodium therapy usually arrests or significantly impedes the disease process as evidenced by:
Symptomatic relief, including decreased pain and/or increased mobility (experienced by 3 out of 5 patients).

Reductions in serum alkaline phosphatase and urinary hydroxyproline levels (30% or more in 4 out of 5 patients).

Histomorphometry showing reduced numbers of osteoclasts and osteoblasts, and more lamellar bone formation.

Bone scans showing reduced radionuclide uptake at pagetic lesions.

In addition, reductions in pagetically elevated cardiac output and skin temperature have been observed in some patients.
In many patients, the disease process will be suppressed for a period of at least one year following cessation of therapy.
The upper limit of this period has not been determined.

The effects of the TURPINAL SL disodium treatment in patients with asymptomatic Paget’s disease have not been studied.
However, TURPINAL SL disodium treatment of such patients may be warranted if extensive involvement threatens irreversible neurologic damage, major joints, or major weight-bearing bones.

Applications of TURPINAL SL:
TURPINAL products are high purity grades of etidronic acid and sodium etidronate which are suitable for use in cosmetics or any applications requiring a very low metal content.

TURPINAL SL high purity of TURPINAL is guaranteed by thorough quality control procedures (including testing for microbiological contamination).
Moreover, the certificate of analysis accompanying each batch contains detailed information covering chemical purity and trace metal content.

TURPINAL SL and TURPINAL 4NL are respectively the acid form and the tetra sodium salt of etidronic acid.
They are colorless to slightly yellow liquids with a neutral odor.
TURPINAL 4NP is the tetrasodium powder form of etidronic acid.

These products can be mixed with water in all ratios and have a strong complexing capacity in relation to polyvalent cations.
The excellent complexing capacity for metals is exploited for the stabilization of H2O2-containing preparations and other preparations with active oxygen.

TURPINAL SL is also suited for application in mercaptan – containing formulations and enhances the color stability of bar soaps.
TURPINAL SL is recommended that TURPINAL be added during production with a concentration of 0.1 – 2% with reference to the finished preparation.

TURPINAL products are ideal chelants or additives in the following applications:
TURPINAL SL the stabilization of peroxide bonds, in alkaline media specifically.
As a chelant in hair cosmetics containing mercaptan groups, i.e. thioglycolic acid, thiolactic acid.

As a means of limiting hair damage caused by bleaching or coloring.
TURPINAL SL the stabilization of bar soaps, where TURPINAL is used as antioxidant and prevents discoloration and rancidity, in particular under the influence of day light.
TURPINAL SL the stabilization of fragrances, which would otherwise lose their strength over time during storage of cosmetic formulations.

Other Applications of TURPINAL SL:
Cooling water systems / industrial water treatment,
Industrial detergents,
Swimming pools,
Metal surface treatment as a corrosion inhibitor for steel,
Stabilizer in H2O2 solutions,
Sequestering agent in textile auxiliaries,
Cosmetics Oxygenated creams,
Liquid soap,
Bar soaps,
Shampoo,
Hair dyes.

Features of TURPINAL SL:
TURPINAL SL and 4NL are the acid form and tetra sodium salts of editronic acid, respectively.
TURPINAL SL are colorless to slightly yellow with neutral odor.

TURPINAL 2NZ and 4NP are the disodium and tetra sodium powder forms of editronic acid, respectively.
Miscible with water in all proportions and has a strong complexing capacity with polyvalent cations.

Excellent complexing capacity with metals.
TURPINAL SL is used for the stabilization of peroxide-containing preparations and other preparations to active oxygen.

TURPINAL SL is also suitable for application to formulations containing mercaptan and to increase the color stability of bar soaps.
TURPINAL SL is recommended to add TURPINAL at concentrations of 0.1-2% with reference to the finished product during production.

TURPINAL SL Indication:
TURPINAL SL is used for the treatment of symptomatic Paget's disease of bone and in the prevention and treatment of heterotopic ossification following total hip replacement or due to spinal cord injury.

Pharmacology of TURPINAL SL:
TURPINAL SL is a first generation (non-nitrogenous) bisphosphonate in the same family as clodronate and tiludronate.
TURPINAL SL affects calcium metabolism and inhibits bone resorption and soft tissue calcification.

TURPINAL SL is a high purity etidronic acid solution.
The TURPINAL series has been developed for the personal care industry in order to answer the need for high purity chemicals with strong chelation properties.
The microbiological and trace metal content in TURPINAL SL is carefully monitored in order to provide a high purity product that meets the stricter standards of the personal care product industry.

Of the etidronic acid that is resorbed (from oral preparation) or infused (for intravenous drugs), about 50% is excreted unchanged by the kidney.
The remainder has a very high affinity for bone tissue, and is rapidly absorbed onto the bone surface.
TURPINAL SL has been shown to prevent or delay skeletal-related events and decrease bone pain as well as normalize calcium levels in the presence of hypercalcemia.

Interactions of TURPINAL SL:
There have been isolated reports of patients experiencing increases in their prothrombin times when etidronate was added to warfarin therapy.
The majority of these reports concerned variable elevations in prothrombin times without clinically significant sequelae.
Although the relevance of these reports and any mechanism of coagulation alterations is unclear, patients on warfarin should have their prothrombin time monitored.

Contraindications of TURPINAL SL:
Didronel tablets are contraindicated in patients with known hypersensitivity to etidronate disodium or in patients with clinically overt osteomalacia.
TURPINAL SL disodium tablets, USP are indicated for the treatment of symptomatic Paget’s disease of bone and in the prevention and treatment of heterotopic ossification following total hip replacement or due to spinal cord injury.
TURPINAL SL disodium tablets are not approved for the treatment of osteoporosis.

Heterotopic Ossification of TURPINAL SL:
TURPINAL SL disodium tablets are indicated in the prevention and treatment of heterotopic ossification following total hip replacement or due to spinal cord injury.

TURPINAL SL disodium tablets reduce the incidence of clinically important heterotopic bone by about two-thirds.
Among those patients who form heterotopic bone, TURPINAL SL disodium tablets retard the progression of immature lesions and reduces the severity by at least half.
Follow-up data (at least 9 months post-therapy) suggests these benefits persist.

In total hip replacement patients, TURPINAL SL disodium tablets do not promote loosening of the prosthesis or impede trochanteric reattachment.
In spinal cord injury patients, TURPINAL SL disodium tablets do not inhibit fracture healing or stabilization of the spine.

Mechanism Of Action:
Bisphosphonates, when attached to bone tissue, are absorbed by osteoclasts, the bone cells that breaks down bone tissue.
Although the mechanism of action of non-nitrogenous bisphosphonates has not been fully elucidated, available data suggest that they bind strongly to hydroxyapatite crystals in the bone matrix, preferentially at the sites of increased bone turnover and inhibit the formation and dissolution of the crystals.

Other actions may include direct inhibition of mature osteoclast function, promotion of osteoclast apoptosis, and interference with osteoblast-mediated osteoclast activation.
TURPINAL SL does not interfere with bone mineralization.
In malignancy-related hypercalcemia, etidronic acid decreases serum calcium by inhibiting tumour-induced bone resorption and reducing calcium flow from the resorbing bone into the blood.

TURPINAL SL also reduces morbidity of osteolytic bone metastases by inhibiting tumour-induced bone resorption.
TURPINAL SL may promote osteoclast apoptosis by competing with adenosine triphosphate (ATP) in the cellular energy metabolism.
The osteoclast initiates apoptosis and dies, leading to an overall decrease in the breakdown of bone.

Drug Interactions of TURPINAL SL:
Aluminium Formation of non-absorbable complexes
Bismuth Formation of non-absorbable complexes
Calcium Formation of non-absorbable complexes
Iron Formation of non-absorbable complexes
Magnesium oxide Formation of non-absorbable complexes
Magnesium Formation of non-absorbable complexes
Sucralfate Formation of non-absorbable complexes

Food Interactions of TURPINAL SL:
Take on an empty stomach.
Avoid aluminium, calcium, iron and magnesium.

Identifiers of TURPINAL SL:
IUPAC Name: (1-hydroxy-1-phosphonoethyl)
CAS Number: 86159-18-4
Chemical Name: Etridonic Acid
Internal Tracking Number: 107607
Substance Type: Chemical Substance
Systematic Name: Phosphonic acid, P,P'-(1-hydroxyethylidene)bis-
CAS Number: 2809-21-4
EPA Registry Name: Etidronic acid
Molecular Weight: 206.03
Molecular Formula: C2H8O7P2

Properties of TURPINAL SL:
Chemical Formula: C2H8O7P2
Appearance: Clear, slightly yellow liquid
Density: 2.1±0.1 g/cm3
Boiling Point: 578.8±60.0 °C at 760 mmHg
Melting Point: 198~199℃
Molecular Formula: C2H8O7P2
Molecular Weight: 206.028
Flash Point: 303.8±32.9 °C
Exact Mass: 205.974518
PSA: 154.91000
LogP: -3.54
Vapour Pressure: 0.0±3.6 mmHg at 25°C
Index of Refraction: 1.586
Stability: Stable. Incompatible with strong oxidizing agents.

Appearance: clear Colorless To Pale Yellow Aqueous Solution
Specific Gravit: 1.42 - 1.46 G/ml At 25 C
Solubility: soluble In Water
Ph: < 2 (1% Solution)
Iron Content: 5 Ppm Max
Active Matter: 58 - 62%
Phosphoric Acid Content: 2.0% Max
Heavy Metals: as: < 2 Ppm; Cr/cd/mn/cu/co: < 1 Ppm
Chloride: 1.0% Max
Density (25°c): 1.43 - 1.45
Molecular Weight: 206.03

Specifications of TURPINAL SL:
Molecular weight: 206 g/mol
Freezing point: - 25 oC
Phosphoric acid: < 2%
pH (1% solution), 25 oC: < 2
Arsenic: < 2 ppm
Editronic acid: 60%
Chromium: < 1 ppm
Cobalt: < 1 ppm
Manganese: < 1 ppm
Cadmium: < 1 ppm
Iron: < 2 ppm
Copper: < 1 ppm
Specific gravity, 20/20 oC: 1.45

Other Descriptions of TURPINAL SL:

Drug Category:
Antihypocalcemic Agents
Antineoplastic Agents
Bisphosphonates
Osteoporosis Prophylactic

Drug Type:
Small Molecule
Approved

Generic Name:
Etidronic acid

Chemical Composition:
Etidronic Acid

Synonyms of TURPINAL SL:
Acetodiphosphonic acid
Acide etidronique [INN-French]
Acido etidronico [INN-Spanish]
Acidum etidronicum [INN-Latin]
EHDP
Etidronate Disodium
Etidronsaeure
HEDP
Hydroxyethanediphosphonic acid
Oxyethylidenediphosphonic acid
Etidronate
Etidronic acid
2809-21-4
etidronate
HEDP
1-Hydroxyethylidene-1,1-diphosphonic acid
EHDP
Etidronsaeure
Acetodiphosphonic acid
Hydroxyethanediphosphonic acid
TURPINAL SL
Oxyethylidenediphosphonic acid
Didronel
Dequest 2015
Dequest Z 010
Acido etidronico
Ferrofos 510
Acide etidronique
1-Hydroxyethane-1,1-diphosphonate
1-Hydroxyethane-1,1-diphosphonic acid
Phosphonic acid, (1-hydroxyethylidene)bis-
Diphosphonate (base)
(1-Hydroxyethane-1,1-diyl)diphosphonic acid
1-Hydroxyethanediphosphonic acid
Dequest 2010
Ethane-1-hydroxy-1,1-diphosphonic acid
(Hydroxyethylidene)diphosphonic acid
Ethane-1-hydroxy-1,1-diphosphonate
(1-Hydroxyethylene)diphosphonic acid
Acide etidronique [INN-French]
Acido etidronico [INN-Spanish]
Acidum etidronicum [INN-Latin]
(1-Hydroxyethylidene)diphosphonic acid
1,1,1-Ethanetriol diphosphonate
1-Hydroxyethylidene-1,1-bisphosphonate
1-Hydroxyethane-1,1-bisphosphonic acid
1-HYDROXY-1,1-DIPHOSPHONOETHANE
TURPINAL SL
Hydroxyethyl Cellulose; Hydroxyethyl cellulose ether; Hydroxyethyl ether cellulose; Natrosol; Natrasol 250 HHR ; Tylose HS 100000 YP2; Methyl 2-hydroxyethyl cellulose; TYLOSE MH 300 P2; Natrosol 250 M; Natrosol L 250; Natrosol LR; HEC; Natrasol 250 HR; TYLOSE HS 30000 YP2 CAS NO: 9032-42-2
TWEEN 20
TWEEN 20 is a polysorbate-type nonionic surfactant used as an emulsifier and solubilizer in pharmaceuticals, food, and cosmetics due to its stability and low toxicity.
In biochemical applications, TWEEN 20 is employed as a blocking agent in immunoassays and as a detergent for protein extraction and cell lysis.
TWEEN 20 is also utilized in various industrial applications, such as wetting agents in the elastomer industry and for removing residues from stamps.

CAS Number: 9005-64-5
EC Number: 500-018-3
Molecular Formula: C26H50O10
Molecular weight: 522.7

Synonyms: TWEEN 20, 9005-64-5, POLYOXYETHYLENE SORBITAN MONOLAURATE, Polyoxyethylene (20) sorbitan monolaurate, Polyoxyethylenesorbitan monolaurate, 2-[2-[3,4-bis(2-hydroxyethoxy)oxolan-2-yl]-2-(2-hydroxyethoxy)ethoxy]ethyl dodecanoate, Polysorbate (INN), 9005-66-7, Sorbimacrogol laurate 300, 2-{2-[3,4-bis(2-hydroxyethoxy)oxolan-2-yl]-2-(2-hydroxyethoxy)ethoxy}ethyl dodecanoate, 2-(2-(3,4-Bis(2-hydroxyethoxy)tetrahydrofuran-2-yl)-2-(2-hydroxyethoxy)ethoxy)ethyl dodecanoate, 2-[2-[3,4-bis(2-hydroxyethoxy)tetrahydrofuran-2-yl]-2-(2-hydroxyethoxy)ethoxy]ethyl dodecanoate, Alkest TW 20, Polyoxyethylene Sorbitan Monolaurate Kosher, FT-0645136, Polyoxyethylene Sorbitan Monolaurate 20 NF, D05565, D05566, D05567, 3,6-Anhydro-1-O-[2-(dodecanoyloxy)ethyl]-2,4,5-tris-O-(2-hydroxyethyl)hexitol, Polysorbate 20 (NF), Polysorbate 40 (NF), Polysorbate 60 (NF), TWEEN(R) 20, TWEEN (R) 20, TWEEN 20 (TN), TWEEN 40 (TN), TWEEN 60 (TN), SCHEMBL118527, POE (6) sorbitol monolaurate, POE(20) sorbitan monolaurate, CHEMBL371631, Ethoxylated Sorbitan monolaurate, POE (20) sorbitan monolaurate, DTXSID60922815, MFCD00165986, E432, Polysorbate 20 (NF), Polysorbate 40 (NF), Polysorbate 60 (NF), TWEEN(R) 20, TWEEN (R) 20, TWEEN 20 (TN), TWEEN 40 (TN), TWEEN 60 (TN), SCHEMBL118527, POE (6) sorbitol monolaurate, POE(20) sorbitan monolaurate, CHEMBL371631, Ethoxylated Sorbitan monolaurate, POE (20) sorbitan monolaurate, DTXSID60922815, MFCD00165986, E432, Polyoxyethylene Sorbitan Monolaurate Kosher, FT-0645136, Polyoxyethylene Sorbitan Monolaurate 20 NF, D05565, D05566, D05567, 3,6-Anhydro-1-O-[2-(dodecanoyloxy)ethyl]-2,4,5-tris-O-(2-hydroxyethyl)hexitol

TWEEN 20 is commonly used as an emulsifier and solubilizer in various applications, including pharmaceuticals, food, and cosmetics.

TWEEN 20 is a polysorbate-type nonionic surfactant formed by the ethoxylation of sorbitan before the addition of lauric acid.
TWEEN 20's stability and relative nontoxicity allows it to be used as a detergent and emulsifier in a number of domestic, scientific, and pharmacological applications.

As the name implies the ethoxylation process leaves the molecule with 20 repeat units of polyethylene glycol; in practice these are distributed across 4 different chains, leading to a commercial product containing a range of chemical species.
TWEEN 20 is used as a wetting agent in flavored mouth drops, helping to provide a spreading feeling to other ingredients like SD alcohol and mint flavor.

TWEEN 20 is also used as wetting agent in rubber balers in the elastomer industry.
TWEEN 20 has been used as a shape directing agent to synthesize spheroidal magnetite nanoassemblies
TWEEN 20 is a polyoxyethylene sorbitol ester that belongs to the polysorbate family.

TWEEN 20 is a nonionic detergent having a molecular weight of 1,225 daltons, assuming 20 ethylene oxide units, 1 sorbitol, and 1 lauric acid as the primary fatty acid.
TWEEN 20 is a nonionic detergent widely used in biochemical applications.

TWEEN 20 has been used as an emulsifying agent for the preparation of stable oil-in-water emulsions.
TWEEN 20 has been used in pre-extraction of membranes to remove peripheral proteins (used at 2% for extraction of membrane-bound proteins).
TWEEN 20 has been used as a blocking agent for membrane based immunoassays at a typical concentration of 0.05%.

TWEEN 20 can be used for lysing mammalian cells at a concentration of 0.005 to 0.5%.
TWEEN 20 lubricates the skin and has a soothing effect.

TWEEN 20 is used in oil-in-water emulsions (lotions, conditioners, cream rinses, shampoos, liquid soaps, body polishes or scrubs, etc.).
TWEEN 20 is widely used for body mist and linen sprays.

TWEEN 20 has been used as a blocking agent for membrane based immunoassays at a typical concentration of 0.05%.
TWEEN 20 is suitable for use as a solubilizing agent of membrane proteins and as a blocking agent in Western blotting.
TWEEN 20 can be used for lysing mammalian cells at a concentration of 0.05 to 0.5%.

TWEEN 20 is found as an ingredient in most body care products, cosmetics, and wet wipes.
TWEEN 20 is often used in combination with other emulsifiers such as mono- and diglycerides or sorbitan monostearates for a variety of purposes, such as dispersing flavors and colors, solubilizing essential oils and vitamins, and improving volume and texture in baked goods.

TWEEN 20 is a highly hydrophilic surfactant
TWEEN 20 is approved as food additives.

TWEEN 20 is a useful emulsifier, dispersant and solvent for aroma chemicals and oils.
TWEEN 20 is a nonionic solubilizing agent used in the textile industry.

TWEEN 20 is a polysorbate type nonionic surfactant formed by ethoxylation of sorbitan prior to the addition of lauric acid.
TWEEN 20 is used as a detergent and emulsifier in pharmacological practice.

TWEEN 20 is a nonionic surfactant.
TWEEN 20 is used as an emulsifier and a dispersing agent that allows oil and water to mix without the use of alcohol.

TWEEN 20 is a water-soluble yellowish liquid.
TWEEN 20 is an odor remover and stabilizer.

TWEEN 20 lubricates the skin and has a soothing effect.
TWEEN 20 is used in oil-in-water emulsions (lotions, conditioners, cream rinses, shampoos, liquid soaps, body polishes or scrubs, etc.).

In addition, TWEEN 20 is widely used for body mist and linen sprays.
TWEEN 20 is found as an ingredient in most body care products, cosmetics, and wet wipes.

TWEEN 20 is a nonionic surfactant
TWEEN 20 is used as an emulsifier and a dispersing agent that allows oil and water to mix without the use of alcohol.
TWEEN 20 is a water-soluble yellowish liquid.

TWEEN 20 is an odor remover and stabilizer.
TWEEN 20 is derived from coconut oil.

TWEEN 20 is non-toxic.
TWEEN 20 is used by philatelists to remove stamps from envelopes and to remove residues from stamps, without harming the stamp itself.

TWEEN 20 is a polysorbate-type nonionic surfactant formed by the ethoxylation of sorbitan before the addition of lauric acid.
TWEEN 20's stability and relative nontoxicity allows it to be used as a detergent and emulsifier in a number of domestic, scientific, and pharmacological applications.

TWEEN 20 is often used in combination with other emulsifiers such as mono- and diglycerides or sorbitan monostearates for a variety of purposes, such as dispersing flavors and colors, solubilizing essential oils and vitamins, and improving volume and texture in baked goods.
TWEEN 20 is a highly hydrophilic surfactant

TWEEN 20 is approved as food additives.
TWEEN 20 is a useful emulsifier, dispersant and solvent for aroma chemicals and oils.

TWEEN 20 is a nonionic solubilizing agent used in the textile industry.
TWEEN 20 is a polysorbate type nonionic surfactant formed by ethoxylation of sorbitan prior to the addition of lauric acid.
TWEEN 20 is used as a detergent and emulsifier in pharmacological practice.

Applications of TWEEN 20:

Biotechnical Applications:
In biological techniques and sciences, TWEEN 20 has a broad range of applications.
For example, TWEEN 20 is used as a washing agent in immunoassays.

TWEEN 20 helps to prevent non-specific antibody binding.
In this major application, TWEEN 20 is dissolved in Tris-buffered saline or phosphate buffered saline at dilutions of 0.05% to 0.5% v/v.

These buffers are used for washes beTWEEN each immunoreaction, to remove unbound immunologicals, and eventually for incubating solutions of immunoreagents (labeled antibodies) to reduce nonspecific background.
TWEEN 20 is used as an excipient in pharmaceutical applications to stabilize emulsions and suspensions.

Industrial and Domestic Applications:
TWEEN 20 is used by philatelists to remove stamps from envelopes and to remove residues from stamps, without harming the stamp itself.
TWEEN 20 is also used as wetting agent in rubber balers in the elastomer industry.
TWEEN 20 has been used as a shape directing agent to synthesize spheroidal magnetite nanoassemblies

TWEEN 20 is a polyoxyethylene sorbitol ester that belongs to the polysorbate family.
TWEEN 20 is a nonionic detergent having a molecular weight of 1,225 daltons, assuming 20 ethylene oxide units, 1 sorbitol, and 1 lauric acid as the primary fatty acid.

TWEEN 20 is responsible for the hydrophilic nature of the surfactant, while the hydrocarbon chains provide the hydrophobic environment.
TWEEN 20 is a nonionic detergent widely used in biochemical applications.

TWEEN 20 has been used as an emulsifying agent for the preparation of stable oil-in-water emulsions.
TWEEN 20 has been used in pre-extraction of membranes to remove peripheral proteins (used at 2% for extraction of membrane-bound proteins).

TWEEN 20 has been used as a blocking agent for membrane based immunoassays at a typical concentration of 0.05%.
TWEEN 20 can be used for lysing mammalian cells at a concentration of 0.005 to 0.5%.

TWEEN 20 has been used as a component of:
Washing buffer and blocking buffer in Western blotting
Blocking buffer in immunohistochemistry
Washing buffer in ELISA (enzyme linked immunosorbent assay)
Reaction mixture in PCR (polymerase chain reaction)

Other Applications:
Detergent production
Emulsifiers
Mouth droppers
Biotechnological Techniques
Immunoassays
Biochemistry laboratories
Suspension stabilizers
Pharmacological Applications
Elastomer Industry
Peripheral Protein Synthesis
Immunological Tests
Surfactants
Deodorizing Products
Shampoo production
Liquid soap manufacture
Body lotions
Wet Wipes production
Cosmetics industry
Skin care products
Textile industry

Preparation Instructions of TWEEN 20:
TWEEN 20 is miscible in water (100 mg/ml), yielding a clear, yellow solution.
TWEEN 20 is also miscible with alcohol, dioxane, and ethyl acetate; and is practically insoluble in liquid paraffin and fixed oils.

Storage/Stability of TWEEN 20:
Aqueous solutions of polysorbates undergo autoxidation during storage, with changes being catalyzed by light, increased temperature, and copper sulfate.
Autoclaving is not recommended without testing for changes in properties.

TWEEN 20 may not be stable to autoclaving, particularly with metal cations in buffer solutions.
TWEEN 20 is heat sensitive and will darken when exposed to elevated temperatures.

TWEENs have been reported to be incompatible with alkalis, heavy metal salts, phenols, and tannic acid.
TWEENs may reduce the activity of many preservatives.

Handling and Storage of TWEEN 20:

Storage:
Store in a cool, dry place away from direct sunlight and incompatible materials like strong acids or oxidizing agents.

Handling:
Use standard personal protective equipment (PPE) like gloves and safety glasses when handling large quantities or in an industrial setting.
Avoid inhaling aerosols or mist.

Stability and Reactivity of TWEEN 20:

Chemical Stability:
TWEEN 20 is stable under normal conditions of use and storage.

Conditions to Avoid:
Avoid exposure to extreme heat, open flames, and incompatible materials.

Incompatible Materials:
Strong oxidizing agents, strong acids, and strong bases may cause a reaction with TWEEN 20.

Hazardous Decomposition Products:
Under fire conditions, TWEEN 20 may decompose to produce toxic fumes, including carbon monoxide (CO) and carbon dioxide (CO2).

Hazardous Polymerization:
Hazardous polymerization will not occur.

First Aid Measures of TWEEN 20:

Ingestion:
If swallowed, rinse mouth with water.
Do not induce vomiting unless directed by medical personnel.
Seek medical advice if large quantities have been ingested.

Skin Contact:
Wash affected area with plenty of soap and water.
If skin irritation or rash occurs, get medical attention.

Eye Contact:
Rinse eyes immediately with plenty of water for at least 15 minutes, lifting the upper and lower eyelids.
Remove contact lenses if present and easy to do.
Seek medical attention if irritation persists.

Inhalation:
Move the affected person to fresh air.
If they experience any symptoms such as coughing or difficulty breathing, seek medical attention immediately.

Fire-Fighting Measures of TWEEN 20:

Suitable Extinguishing Media:
Use water spray, alcohol-resistant foam, dry chemical, or carbon dioxide (CO2) to extinguish fires involving TWEEN 20.

Unsuitable Extinguishing Media:
Avoid using a solid water stream as TWEEN 20 may scatter and spread the fire.

Specific Hazards:
TWEEN 20 may produce toxic fumes under fire conditions, including carbon monoxide (CO) and carbon dioxide (CO2).

Protective Equipment:
Firefighters should wear self-contained breathing apparatus (SCBA) and full protective gear to prevent exposure to toxic fumes.

Special Precautions:
Cool containers exposed to fire with water spray to prevent overheating and bursting.

Accidental Release Measures of TWEEN 20:

Personal Precautions:
Wear appropriate personal protective equipment (PPE), including gloves, eye protection, and, if necessary, a respirator. Ensure adequate ventilation.

Environmental Precautions:
Prevent entry into waterways, drains, or sewers.
Contain the spill if safe to do so.

Containment Methods:
Contain and collect spillage with non-combustible absorbent material (e.g., sand, earth, diatomaceous earth) and place TWEEN 20 in a container for disposal according to local regulations.

Cleaning Methods:
Clean the spill area thoroughly with water and detergent to remove residue.
Dispose of contaminated materials in accordance with local regulations.

Exposure Controls and Personal Protection of TWEEN 20:

Exposure Limits:
No specific occupational exposure limits have been established for TWEEN 20.
However, exposure controls should still be in place.

Engineering Controls:
Ensure adequate ventilation, particularly in areas where aerosols or vapors may be generated.
Use local exhaust ventilation or other engineering controls to minimize exposure.

Personal Protective Equipment (PPE):

Eye Protection:
Wear safety goggles or face shield if splashing is possible.

Skin Protection:
Wear protective gloves and clothing to prevent skin contact.
Nitrile or rubber gloves are recommended.

Respiratory Protection:
If exposure to aerosols or vapors is possible, wear an appropriate respirator (e.g., NIOSH-approved respirator with organic vapor/acid gas cartridge).

Hygiene Measures:
Wash hands thoroughly after handling and before eating, drinking, or smoking.
Remove contaminated clothing and wash before reuse.

Identifiers of TWEEN 20:
CAS Number: 9005-64-5
EC Number: 500-018-3
Molecular Formula: C26h50o10
Molecular Weight: 522.7
IUPAC Name: 2-[2-[3,4-bis(2-hydroxyethoxy)oxolan-2-yl]-2-(2-hydroxyethoxy)ethoxy]ethyl Dodecanoate

CAS Number: 9005-64-5
EC Number: 500-018-3
UNII (FDA Unique Ingredient Identifier): 7T1F30V5YH
PubChem CID: 5281955
RTECS Number: TR7400000
IUPAC Name: Polyoxyethylene (20) sorbitan monolaurate

Properties of TWEEN 20:
Molecular Weight: 522.7
XLogP3-AA: 2.5
Exact Mass: 522.34039779
Monoisotopic Mass: 522.34039779
Topological Polar Surface Area: 133 Ų
Hydrogen Bond Donor Count: 3
Hydrogen Bond Acceptor Count: 10
Rotatable Bond Count: 26
Heavy Atom Count: 36
Formal Charge: 0
Complexity: 507
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 4
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes

Physical Description: It is a lemon to amber-coloured oily liquid
Color: Lemon- to amber-colored
Form: liquid
Odor: Characteristic odor
Taste: Bitter
Melting Point: 110 °C
Solubility: Soluble in water, ethanol, methanol, ethyl acetate and dioxane. Insoluble in mineral oil and petroleum ether
Density: 1.095 g/mL
TWEEN 24
Tween 24 is a 100% bio-based ethoxylated sorbitan ester based on a natural fatty acid (lauric acid) and manufactured via the RSPO's Mass Balance System.
Tween 24 is highly effective at forming O/W emulsions.
Tween 24, a low moisture version of Tween 24, is a low logP adjuvant (0.25) and high HLB emulsifier (16.5) applicable for both built-in and tank mix adjuvants.

CAS: 9005-64-5
MF: C26H50O10
MW: 522.6692
EINECS: 500-018-3

Synonyms
Polisorbate 20- PS 20;Tween 20 (Trademark of ICI America, Inc.);Tween 20 ;Tween 20 1LT;Twain 20;TWEEN(R) 20 Vetec(TM) reagent grade, 40%;ACRYL/BIS 37.5:1 PREMIXED PWD ULTRA PURE;TWEEN 20 ELECTROPHORESIS GRADE

Tween 24 is recommended when formulating hydrolytically unstable actives, or when antagonistic interactions exist between formulation components.
Tween 24, much like Tween 24 LM, can improve a formulations performance through improved spray retention, spreading, leaf penetration and humectancy.
Offering enhanced surface activity to provide better wetting, lower equilibrium surface tension (EST) and lower contact angle, Tween 24 LM has the potential to increase yields and reduce land use.

Tween 24, whose common commercial names includes Alkest TW 20 and Polysorbate 20, is a mild nonionic surfactant formed by the ethoxylation of sorbitan before the addition of lauric acid which is a medium-chain fatty acid found mainly in coconut oil.
Tween 24 is allowed to be used as the emulsifier, detergent, dispersant, solvent and stabilizer, etc. in a number of fields such as pharmaceutical, chemical, food, textile and other industries due to its stability and relative non-toxicity.
Tween 24 is widely applied in biological techniques and sciences, which can be added to buffers and reagents for immunohistochemistry, such as Western blots and ELISAs, helping to prevent non-specific antibody binding, decrease background staining and enhance reagent spreading.
Besides, Tween 24 also has applications in food production as a common food grade additive which are found in many consumables on the market today.
Tween 24 can also be used as a wetting agent in flavored mouth drops such as Ice Drops, in oral or non-gastrointestinal suspensions and in rubber balers in the elastomer industry.

Tween 24 is a polymer composed of PEG-ylated sorbitan, where the total number of poly(ethylene glycol) units is 20 (w + x + y + z = 20) and a single terminal is capped by a dodecanoyl group.
Tween 24 is a surfactant and emulsifier used in cleaners and personal care products.
Tween 24 is a hydrophilic nonionic surfactant generally used as emulsifiers, dispersing agent and solubilizer.
Tween 24 is a polysorbate-type nonionic surfactant formed by the ethoxylation of sorbitan monolaurate.
Tween 24's stability and relative nontoxicity allows it to be used as a detergent and emulsifier in a number of domestic, scientific, and pharmacological applications.
As the name implies, the ethoxylation process leaves the molecule with 20 repeat units of polyethylene glycol; in practice these are distributed across 4 different chains, leading to a commercial product containing a range of chemical species

Tween 24 Chemical Properties
Melting point: 98.9 °C (decomp)
Boiling point: 100 °C
Density: 1.11 g/mL at 20 °C
Vapor pressure: FEMA: 2915 | POLYSORBATE 20
Refractive index: n20/D 1.468(lit.)
Fp: >230 °F
Storage temp.: Store below +30°C.
Solubility: 100 g/L
Form: viscous liquid
Color: Amber
Specific Gravity: 1.090~1.130 (20/20℃)
PH: 6-8 (50g/l, H2O, 20℃)
PH Range: 7
Odor: mild alcohol odor
Odor Type: alcoholic
Water Solubility: 100 g/L
Hydrophilic-Lipophilic Balance (HLB): 16.7
Stability: Stable. Incompatible with strong oxidizing agents.
EPA Substance Registry System: Tween 24 (9005-64-5)

Tween 24 is a mixture of laurate partial esters of sorbitol and sorbitol anhydrides condensed with approximately 20 mole of ethylene oxide (C2H4O) for each mole of sorbitol and its mono- and dianhydrides.
Tween 24 has a faint, characteristic odor and a warm, somewhat bitter taste.

Uses
Used for solubilizing membrane proteins during isolation and purification.
Tween 24 is used as a wetting agent in flavored mouth drops.
Tween 24 acts as a washing agent in Western blots and ELISAs and prevents antibody binding.
Tween 24 is a solubilizing agent of membrane proteins.
In pharmaceutical chemistry, Tween 24 is used as an excipient to stabilize emulsions and suspensions.
Further, Tween 24 is used as a dispersing agent, stabilizer, lubricator and also used in creams, salves, ointments, protective creams, balms, pomades, lipsticks, mascaras and glosses.
Tween 24 is a solubilizer, emulsifier, viscosity modifier, and stabilizer of essential oils in water.

Food applications
Tween 24 is used as a wetting agent in flavored mouth drops such as Ice Drops, helping to provide a spreading feeling to other ingredients like SD alcohol and mint flavor.
The World Health Organization has suggested acceptable daily intake limits of 0–25 mg of polyoxyethylene sorbitan esters per kg body weight.

Preparation
Tween 24 is prepared by condensing the partial esters of sorbitol and its anhydrides with ethylene oxide to effect an oxyethylene copolymerization at the free hydroxyl groups.

Health Effects
Tween 24 was a skin irritant in dermatitis patients but was reported not to induce irritant responses when applied to the intact skin of health volunteers.
Tween 24 produced, at worst, minimal irritation in the eyes of rabbits.
Only a small number of cases of skin sensitization have been reported in humans, although a moderate to strong sensitizing potential was seen in guinea-pigs treated by intradermal injection.
TWEEN 65
Tween 65 is a yellow-waxy solid.
Tween 65 is an oily liquid derived from PEG-ylated sorbitan (a derivative of sorbitol) esterified with fatty acids.


CAS Number: 9005-71-4
EC Number: 500-020-4
MDL number: MFCD00165348
Chemical name: Polyoxyethylene (20) sorbitan tristearate
Molecular Formula: C100H194O28



POLYOXYETHYLENE SORBITANTRISTEARATE, POE20, POLYOXYETHYLENE(20) SORBITAN TRISTEARATE, sorbimacrogoltristearate300, POLYOXYETHYLENE GLYCOL SORBITAN TRISTEARATE, polyoxyethylenesorbitan tristearate*(tween 65), TWEEN 65, emsorb6907, POLYETHYLENEGLYCOLSORBITANTRISTEARATE, POLYOXYETHYLENE-1,4-SORBITAN-TRISTEARATE, sorbitan,tristearate,polyoxyethylenederivs, TWEEN(TM) 65, T-65, sorbitan,trioctadecanoate,poly(oxy-1,2-ethanediyl)derivs., glycospersets20, POLYSORBATE 65, EmulsifierT-65, Tween 65, POE20, E 436, TS 30V, TWEEN 65, T-MAZ 65K, Komul NP 4, Ahco 7166T, emsorb6907, Montanox 65, TWEEN(R) 65, Polyoxyethylenesorbitan Tristearate, Emulsifier T-65, Polyoxyethylene Sorbitan Tristearate, Polyethylene glycol sorbitan tristearate. Polysorbate 65, Tween 65, 14BGY2Y3MJ, Peg-20 sorbitan tristearate, Polyoxyethylene (20) sorbitan tristearate, DTXSID30891988, E-436, Emsorb 6907, Glycosperse TS 20, INS NO.436,
INS-436, JEESORB STS-20, LIPOSORB TS-20, NIKKOL TS-30, POLYSORBATE 65 (II), Peg sorbitan tristearate, SORBAX PTS-20, Sorbimacrogol tristearate 300, Sorbitan, tristearate, polyoxyethylene derivs., UNII-14BGY2Y3MJ, Polysorbate 65, Polyoxyethylene glycol sorbitan tristearate, T-65, POE20, TWEEN 65, Tween-65, Ahco 7166T, emsorb6907, tween(R) 65, TWEEN(TM) 65, Polysprbate65, POLYSORBATE 65, EmulsifierT-65, glycospersets20, Tween 65 Polysorbate 65,
sorbimacrogoltristearate300, Sorbitantristearat, EO 20 mol, POLYOXYETHYLENE SORBITANTRISTEARATE, POLYETHYLENEGLYCOLSORBITANTRISTEARATE, POLYOXYETHYLENE(20) SORBITAN TRISTEARATE, POLYOXYETHYLENE-1,4-SORBITAN-TRISTEARATE, POLYOXYETHYLENE GLYCOL SORBITAN TRISTEARATE, sorbitan,tristearate,polyoxyethylenederivs, polyoxyethylenesorbitan tristearate*(tween 65), POLYOXYETHYLENE(20) SORBITAN TRISTEARATE(TWEEN (R) 65), sorbitan,trioctadecanoate,poly(oxy-1,2-ethanediyl)derivs, PEG-20 Sorbitan Tristearate, Polyoxyethylene (20) sorbitan tristearate, polyoxyethylenesorbitan tristearate*(tween 65), POLYOXYETHYLENE(20) SORBITAN TRISTEARATE, POLYOXYETHYLENE GLYCOL SORBITAN TRISTEARATE, POLYOXYETHYLENE SORBITANTRISTEARATE, POLYSORBATE 65, TWEEN 65, TWEEN(TM) 65, emsorb6907, EmulsifierT-65, glycospersets20, sorbimacrogoltristearate300, sorbitan,trioctadecanoate,poly(oxy-1,2-ethanediyl)derivs, sorbitan,tristearate,polyoxyethylenederivs., POE20, POLYETHYLENEGLYCOLSORBITANTRISTEARATE, POLYOXYETHYLENE-1,4-SORBITAN-TRISTEARATE, Sorbitantristearat, EO 20 mol, Tween-65, T-65,



Tween 65 is a yellow-waxy solid.
Tween 65 is an oily liquid derived from PEG-ylated sorbitan (a derivative of sorbitol) esterified with fatty acids.
Tween 65 is an ethoxylated sorbitan triester based on a natural fatty acid (stearic acid).


Tween 65 is highly effective at forming oil in water emulsions, particularly when used in combination with its non-ethoxylated precursor, Span 65.
Tween 65 is a sorbitan fatty acid ester ethoxylate and is an effective emulsifier.
Tween 65 is a yellow-waxy solid.


Tween 65 is an oily liquid derived from PEG-ylated sorbitan (a derivative of sorbitol) esterified with fatty acids.
Tween 65 is soluble in ethanol, isopropanol, and mineral oil.
HLB value of Tween 65 is 10.5.


Tween 65 emulsifier is also known as Polysorbate-65.
Tween 65, the full name polyoxyethylene (20) sorbitan tristearate.
Three stearic acids are in Tween 65's molecule structure, while polysorbate-60 only has one.


Tween 65 is unnatural as it is made from the chemical synthesis of sorbitan fatty acid and ethylene oxide.
Tween 65 is an ethoxylated (20) sorbitan ester based on a natural fatty acid (stearic acid).
Tween 65 is highly effective at forming O/W emulsions, particularly when used in combination with its non-ethoxylated derivative, Span 65V.


Tween 65 is a yellow-waxy solid.
Tween 65 is soluble in ethanol, isopropanol and mineral oil.
Tween 65 is an emulsifier manufactured by reacting stearic acid with sorbitol to yield a product which is then reacted with ethylene oxide.


Tween 65 is a nonionic surfaceactive agent which is dispersible in fat, oil, and water.
Tween 65 is also termed polysorbate 65.
Tween 65 is an ethoxylated (20) sorbitan ester derived from stearic acid, a natural fatty acid.


This highly effective ethoxylated, Tween 65, is known for its ability to form O/W emulsions, particularly in combination with Span 65V, its non-ethoxylated derivative.
Tween 65 is the abbreviation of “polyoxyethylene (20) sorbitan”.


Tween 65 is a surfactant type polysorbate whose stability and relative non-toxicity allow it to be used as a detergent and emulsifier in the food, industrial, cosmetic, and pharmaceutical industries.
Tween 65,also known as polyoxyethylene(20)sorbitan tristearate.


Tween 65 has a molecular formula of C100H194O28.
At roon temperature, Tween 65 is in the form of yellow viscous liquid or paste.
Tween 65 is an O/W emulsifier with an HLB value of 10.5.


Tween 65 is soluble in water.
Tween 65 is a fatty acid polyoxyethylene ester of sorbitan.
Tween 65 is highly effective emulsifier.


Tween 65 is stable and versatile.
Tween 65 is a polyoxyethylene sorbitan monooleate (polysorbate) surfactant that is used as a film-forming polymer and dispersing agent in solid preparations.


Tween 65 has been shown to inhibit the proliferation of prostate cancer cells, which may be due to its ability to bind to anti-prostate specific antigen (anti-pcsk9) antibody causing the antibody to aggregate and form a particle.
This process inhibits the interaction between the antibody and Tween 65's target, preventing it from binding with PCSK9 protein.


The addition of propranolol hydrochloride has been shown to increase the effectiveness of Tween 65.
Tween 65 is an ethoxylated sorbitan ester widely used in personal care products.
Tween 65 is a valuable polyol ester, resulting from the combination of sorbitol and stearic acid.


This white, waxy solid, Tween 65, possesses a melting point of 65-67 degrees Celsius and a molecular weight of 576.
Tween 65 is solid, or paste; or liquid.
Tween 65 is dispersible in water (soluble in water).


Tween 65 is stable.
Under strong acid or strong alkali condition, Tween 65 is easily hydrolyzed.
Tween 65 is a valuable polyol ester, resulting from the combination of sorbitol and stearic acid.


Tween 65 possesses a melting point of 65-67 degrees Celsius and a molecular weight of 576.
Tween 65 is a mixture of stearate esters of sorbitol and sorbitol anhydrides, consisting predominantly of the triester, condensed with approximately 20 moles of ethylene oxide.



USES and APPLICATIONS of TWEEN 65:
Tween 65 is used as an emulsifier in medicine, food, textiles, and cosmetics.
Tween 65 is also used as a stabilizer and wetting agent etc.
Tween 65 acts as o/w emulsifier.


Tween 65 is used in skin care creams, lotions, hair care, color cosmetics, sprayable emulsions, cleaners as well as toners, eye care, feet, hands, nails, specific skin care treatments, sun protection, after-sun, baby care, male grooming and shaving.
Tween 65 widely used in personal care products.


Tween 65 is used Chemicals manufacture Construction, Emulsification, and Nonwovens.
Tween 65 uses concentrated aqueous emulsions
Tween 65 is used as an emulsifier in medicine, food, textiles, and cosmetics.


Tween 65 is also used as a stabilizer and wetting agent etc.
Tween 65 is a mid-range HLB, nonionic surfactant suggested for use in textile chemicals (lubricant, emulsifier), household products (o/w emulsifier) and cosmetic formulations (o/w emulsifier).


Tween 65 is used as an emulsifier.
Suggested applications of Tween 65: ice cream, cakes and cake icings.
Tween 65 is used in frozen desserts, cakes, and coffee whiteners.


Tween 65 is frequently used with sorbitan monostearates or monoand diglycerides.
Typical usage range of Tween 65 is 0.10–0.40%.
Tween 65 is commonly used in vehicle care and waxes & polishes.


Tween 65 is used serving as an emulsifier and solubilized.
Tween 65 is used Food Additive, Ice Cream, Soft Drinks,
Cakes, Puddings, Desserts, Confectionery, Detergent, Emulsifier, Wetting Agent, and Pharmaceutical.


In these applications, Tween 65 proves itself indispensable as an emulsifying agent, stabilizer, and lubricant.
As an emulsifying agent, Tween 65 adeptly prevents the separation of two immiscible liquids, like oil and water, keeping them harmoniously combined.
Moreover, Tween 65's stabilizing capabilities contribute to maintaining the integrity of various formulations by preventing ingredient separation.


Lastly, as a lubricant, Tween 65 effectively reduces friction between surfaces.
The scientific community has dedicated substantial effort to studying Tween 65.
Tween 65's applications in diverse research areas have been explored extensively.


Furthermore, Tween 65 has been utilized to investigate the effects of surfactants on both human skin and the creation of innovative cosmetic products.
Overall, Tween 65 serves as a vital ingredient across industries, owing to its remarkable qualities as an emulsifying agent, stabilizing agent, and lubricant.


Tween 65's significance in various scientific studies underscores its versatility and potential for future applications.
Tween 65 acts as o/w emulsifier.
Tween 65 is used in skin care creams, lotions, hair care, color cosmetics, sprayable emulsions, cleaners as well as toners, eye care, feet, hands, nails, specific skin care treatments, sun protection, after-sun, baby care, male grooming and shaving.


Tween 65 is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
Tween 65 is used as emulsifier, stabilizer, wetting agent, diffusing agent, osmotic agent.
Tween 65 has been used in a study as a carbon source for the reductive dechlorination of hexachlorobenzene in a mixed, methanogenic culture.


Tween 65 has also been used in a study to investigate its ability to stimulate growth of the hypocotyl of Amaranthus caudatus L.
Tween 65 improves texture and appearance.
Tween 65 enhances product stability.


Tween 65 is suitable for different formulations.
Tween 65 is a high-quality ingredient used in various applications.
Tween 65 is known for its excellent emulsifying properties and is widely used in the pharmaceutical, cosmetics, and food industries.


Tween 65 possesses a melting point of 65-67 degrees Celsius and a molecular weight of 576.
In these applications, Tween 65 proves itself indispensable as an emulsifying agent, stabilizer, and lubricant.
As an emulsifying agent, Tween 65 adeptly prevents the separation of two immiscible liquids, like oil and water, keeping them harmoniously combined.


Moreover, Tween 65's stabilizing capabilities contribute to maintaining the integrity of various formulations by preventing ingredient separation.
Lastly, as a lubricant, Tween 65 effectively reduces friction between surfaces.
The scientific community has dedicated substantial effort to studying Tween 65.


Tween 65's applications in diverse research areas have been explored extensively.
Furthermore, Tween 65 has been utilized to investigate the effects of surfactants on both human skin and the creation of innovative cosmetic products.


Overall, Tween 65 serves as a vital ingredient across industries, owing to its remarkable qualities as an emulsifying agent, stabilizing agent, and lubricant.
Tween 65's significance in various scientific studies underscores its versatility and potential for future applications.



FUNCTIONS OF TWEEN 65:
*Dispersing agents
*Emulsifiers
*Surfactants / detergents
*O/W emulsifier
*Wetting agent
*Emulsifier,
*Solubilizer



CHEMICAL PROPERTIES OF TWEEN 65:
Tween 65 is tan, waxy solid; faint odor, bitter taste.
Tween 65 is a sol in mineral oil, vegetable oil, mineral spirits, acetone, ether, dioxane, alc, and methanol; dispersible in water, carbon tetrachloride.



KEY FEATURES OF TWEEN 65:
*Highly effective emulsifier – Tween 65 excels at creating stable emulsions in a wide range of products.
*Stable and versatile – Tween 65 offers reliable performance and can be used in various formulations.
*Improves texture and appearance – By optimizing the emulsification process, Tween 65 enhances the overall texture and appearance of products.
*Enhances product stability – With its emulsifying properties, Tween 65 helps maintain the stability of formulations over time.
*Suitable for different formulations – This high-quality emulsifier, Tween 65, is compatible with a wide range of raw materials and formulations.



PHYSICAL and CHEMICAL PROPERTIES of TWEEN 65:
Appearance: Amber to light yellow oily liquid
Acid value: 2mgKOH/g Max.
Saponification value: 45-55mgKOH/g
Hydroxyl value: 65-80mgKOH/g
Water: 3.0% Max.
Physical state: paste
Color: No data available
Odor: No data available
Melting point/freezing point: No data available
Initial boiling point and boiling range: No data available
Flammability (solid, gas): No data available
Upper/lower flammability or explosive limits: No data available

Flash point: 149,00 °C - closed cup
Autoignition temperature: No data available
Decomposition temperature: No data available
pH: No data available
Viscosity
Viscosity, kinematic: No data available
Viscosity, dynamic: No data available
Water solubility: No data available
Partition coefficient: n-octanol/water: No data available
Vapor pressure: No data available
Density: No data available
Relative density: No data available
Relative vapor density: No data available

Particle characteristics:
No data available
Explosive properties: No data available
Oxidizing properties: No data available
Other safety information: No data available
Flash point: 149 °C
storage temp.: Store at RT.
Hydrophilic-Lipophilic Balance (HLB): 10.5
FDA 21 CFR: 172.838; 172.836; 172.840; 172.842; 173.340
Substances Added to Food (formerly EAFUS): POLYSORBATE 65
FDA UNII: 14BGY2Y3MJ
EPA Substance Registry System: Polysorbate 65 (9005-71-4)
Flash Point: 149°C
Storage Condition: Store at RT.
MDL: MFCD00165348



FIRST AID MEASURES of TWEEN 65:
-Description of first-aid measures:
*If inhaled:
If breathed in, move person into fresh air.
*In case of skin contact:
Wash off with soap and plenty of water.
*In case of eye contact:
Flush eyes with water as a precaution.
*If swallowed:
Never give anything by mouth to an unconscious person.
Rinse mouth with water.
-Indication of any immediate medical attention and special treatment needed:
No data available



ACCIDENTAL RELEASE MEASURES of TWEEN 65:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Keep in suitable, closed containers for disposal.



FIRE FIGHTING MEASURES of TWEEN 65:
-Extinguishing media:
*Suitable extinguishing media:
Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.
-Further information:
No data available


EXPOSURE CONTROLS/PERSONAL PROTECTION of TWEEN 65:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
*Skin protection:
Handle with gloves.
Wash and dry hands.
Full contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min
Splash contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min
*Body Protection:
Impervious clothing
*Respiratory protection:
Respiratory protection not required.
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of TWEEN 65:
-Precautions for safe handling:
*Hygiene measures:
General industrial hygiene practice.
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Store in cool place.
Keep container tightly closed in a dry and well-ventilated place



STABILITY and REACTIVITY of TWEEN 65:
-Reactivity:
No data available
-Chemical stability:
Stable under recommended storage conditions.
-Possibility of hazardous reactions:
No data available
-Conditions to avoid:
No data available