Hydroxyethyl cellulose; MH 15003 P6; Cellulose, 2 - hydroxyethyl ether; hydroxyethyl cellulose ;Methyl 2-hydroxyethyl cellulose cas no: 9004-62-0

Hydroxyethyl cellulose; MH 200 YP2; Cellulose, 2 - hydroxyethyl ether; hydroxyethyl cellulose ;Methyl 2-hydroxyethyl cellulose cas no: 9004-62-0

Hydroxyethyl cellulose; MH 2000 YP2; Cellulose, 2 - hydroxyethyl ether; hydroxyethyl cellulose ;Methyl 2-hydroxyethyl cellulose cas no: 9004-62-0

TYLOSE MH 2000 YP2 IUPAC Name 5-[6-[[3,4-dihydroxy-6-(hydroxymethyl)-5-methoxyoxan-2-yl]oxymethyl]-3,4-dihydroxy-5-[4-hydroxy-3-(2-hydroxyethoxy)-6-(hydroxymethyl)-5-methoxyoxan-2-yl]oxyoxan-2-yl]oxy-6-(hydroxymethyl)-2-methyloxane-3,4-diol TYLOSE MH 2000 YP2 InChI InChI=1S/C29H52O21/c1-10-15(34)16(35)24(13(8-33)45-10)49-28-20(39)18(37)25(50-29-26(43-5-4-30)21(40)23(42-3)12(7-32)47-29)14(48-28)9-44-27-19(38)17(36)22(41-2)11(6-31)46-27/h10-40H,4-9H2,1-3H3 TYLOSE MH 2000 YP2 InChI Key CWSZBVAUYPTXTG-UHFFFAOYSA-N TYLOSE MH 2000 YP2 Canonical SMILES CC1C(C(C(C(O1)CO)OC2C(C(C(C(O2)COC3C(C(C(C(O3)CO)OC)O)O)OC4C(C(C(C(O4)CO)OC)O)OCCO)O)O)O)O TYLOSE MH 2000 YP2 Molecular Formula (C2H602)x TYLOSE MH 2000 YP2 CAS 9004-62-0 TYLOSE MH 2000 YP2 European Community (EC) Number 618-387-5 TYLOSE MH 2000 YP2 ICSC Number 1559 TYLOSE MH 2000 YP2 RTECS Number FJ5958000 TYLOSE MH 2000 YP2 Physical Description WHITE POWDER. TYLOSE MH 2000 YP2 Solubility Solubility in water: good TYLOSE MH 2000 YP2 Autoignition Temperature 380 °C TYLOSE MH 2000 YP2 Molecular Weight 736.7 g/mol TYLOSE MH 2000 YP2 XLogP3-AA -7.7 TYLOSE MH 2000 YP2 Hydrogen Bond Donor Count 11 TYLOSE MH 2000 YP2 Hydrogen Bond Acceptor Count 21 TYLOSE MH 2000 YP2 Rotatable Bond Count 15 TYLOSE MH 2000 YP2 Exact Mass 736.300109 g/mol TYLOSE MH 2000 YP2 Monoisotopic Mass 736.300109 g/mol TYLOSE MH 2000 YP2 Topological Polar Surface Area 315 Ų TYLOSE MH 2000 YP2 Heavy Atom Count 50 TYLOSE MH 2000 YP2 Formal Charge 0 TYLOSE MH 2000 YP2 Complexity 999 TYLOSE MH 2000 YP2 Isotope Atom Count 0 TYLOSE MH 2000 YP2 Defined Atom Stereocenter Count 0 TYLOSE MH 2000 YP2 Undefined Atom Stereocenter Count 20 TYLOSE MH 2000 YP2 Defined Bond Stereocenter Count 0 TYLOSE MH 2000 YP2 Undefined Bond Stereocenter Count 0 TYLOSE MH 2000 YP2 Covalently-Bonded Unit Count 1 TYLOSE MH 2000 YP2 Compound Is Canonicalized Yes Tylose® MHEC (methyl hydroxyethyl cellulose/Tylose MH-grades) are water soluble, nonionic cellulose ethers, which are offered as free flowing powder or in granular form. Tylose MHEC may contain further additives which for example control the dissolution behavior or the thickening power.Methylhydroxyethyl cellulose. Offers very high water retention, low gloss, low pigment compatibility, low pseudoplasticity, moderate thickening effect, and moderate wet scrub resistance. Exhibits good anti-spattering. Used for paint applications like solid paints, powder paints, limewash paints, cement paints, distempers, and emulsion based plasters.Tylose® MH 2000 YP2 is a water-soluble, non-ionic methyl hydroxyethyl cellulose powder with standard etherification. It provides increased biostability, low gloss appearance, good anti-spattering properties, and moderate wet scrub resistance. This grade of methyl hydroxyethyl cellulose (MHEC) is ideal for use in cement paints, distempers, and lime-wash paints.Constitution: Methyl hydroxyethyl cellulose Appearance:powder Etherification:standard Particle size:powder Delayed solubility:yes Level of viscosity:2000 mPa•sTYLOSE MH 2000 YP2 Biostability:yes TYLOSE MH 2000 YP2 Gloss:low TYLOSE MH 2000 YP2 Pigment Compatibility:low TYLOSE MH 2000 YP2 Anti-spattering:good TYLOSE MH 2000 YP2 Pseudoplasticity:low TYLOSE MH 2000 YP2 Thickening effect:low TYLOSE MH 2000 YP2 Wet scrub resistance:moderate TYLOSE MH 2000 YP2 Water retention:lowCementitious thin bed adhesives are used to adhere ceramic tiles, to build walls of aerated concrete or lime stone bricks and to install exterior insulating finishing systems(EIFS). They offer an easy and light workability,a high efficiency and guarantee a long durability.Cement tile adhesives have to be easy to trowel. They must provide long embedding time, high slip resistance and sufficient adhesion strength. These properties can be influenced by Tylose® MC. Adhesives for block laying are used to build up walls of aerated concrete blocks, sand-lime bricks or standard bricks. EIFS adhesives ensure an excellent bond between substrate and insulating boards. Tylose MC improves the workability of EIFS adhesives and increases both adhesion and sag resistance.Renders are mixtures of mineral binders, aggregates and auxiliaries. Depending on the process, there is a distinction between hand and machine application.Renders are used for base coating, insulation, renovation and decorative purposes. Renders based on cement or cement/hydrated lime can be employed for exterior and interior work.Cement based jointing and trowelling compounds are used for repairing systems and to smooth coarse walls and floors. Grouts are applied to fill the gaps between ceramic or stone tiles.Tylose MC is an important additive ensuring there is sufficient water retention in renders and trowelling compounds. Additional advantages are better workability and an increase of the adhesion strength.Machine applied renders are mixed in continuously or discontinuously working plastering machines.These enable coverage of large wall and ceiling areas by a highly efficient technique. Continuously operating plastering machines need to be fed with premixed renders containing Tylose. Other additives can be added as required.What is TYLOSE MH 2000 YPS? TYLOSE MH 2000 YPS (hydroxyethyl starch) is made from natural sources of starch. TYLOSE MH 2000 YPS increases the volume of blood plasma that can be lost from bleeding or severe injury. Plasma is needed to circulate red blood cells that deliver oxygen throughout the body.TYLOSE MH 2000 YPS is used to treat or prevent hypovolemia (decreased blood plasma volume, also called "shock") that may occur as a result of serious injury, surgery, severe blood loss, burns, or other trauma.TYLOSE MH 2000 YPS may also be used for purposes not listed in this medication guide.Important Information You should not receive this medication if you have a bleeding or blood clotting disorder, congestive heart failure, kidney disease, or urination problems not caused by hypovolemia (decreased blood plasma volume).TYLOSE MH 2000 YPS can harm your kidneys. Call your doctor at once if you have any of these symptoms of kidney damage: swelling, rapid weight gain, unusual tiredness, nausea, vomiting, feeling short of breath, red or pink urine, painful or difficult urination, or little or no urinating.Before taking this medicine You should not receive this medication if you are allergic to TYLOSE MH 2000 YPS, or if you have:a bleeding or blood clotting disorder;kidney disease;congestive heart failure; or urination problems not caused by hypovolemia (decreased blood plasma volume).If possible before you receive TYLOSE MH 2000 YPS, tell your doctor if you have:liver disease;a history of heart disease; or if you are allergic to corn.FDA pregnancy category C. It is not known whether TYLOSE MH 2000 YPS will harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant while using this medication.It is not known whether TYLOSE MH 2000 YPS passes into breast milk or if it could harm a nursing baby. Tell your doctor if you are breast-feeding a baby.In an emergency situation it may not be possible to tell your caregivers about your health conditions, or if you are pregnant or breast-feeding. Make sure any doctor caring for your pregnancy or your baby knows you have received TYLOSE MH 2000 YPS.How is TYLOSE MH 2000 YPS given?TYLOSE MH 2000 YPS is injected into a vein through an IV. A healthcare provider will give you this injection.Your breathing, blood pressure, oxygen levels, kidney function, and other vital signs will be watched closely while you are receiving TYLOSE MH 2000 YPS. Your blood will also need to be tested daily during treatment.What happens if I miss a dose?Because you will receive TYLOSE MH 2000 YPS in a clinical setting, you are not likely to miss a dose.What happens if I overdose?Since TYLOSE MH 2000 YPS is given by a healthcare professional in a medical setting, an overdose is unlikely to occur.What should I avoid after receiving TYLOSE MH 2000 YPS?Follow your doctor's instructions about any restrictions on food, beverages, or activity.TYLOSE MH 2000 YPS side effects Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat.Tell your caregivers right away if you have:wheezing or gasping for breath, rapid breathing, sweating, and anxiety;a light-headed feeling, like you might pass out;weak pulse, slow breathing;chest pain, fever, chills, cough; or easy bruising, unusual bleeding, or any bleeding that will not stop.Rare but serious side effects may include:severe headache, vision or speech problems, mental changes;drooping eyelids, loss of feeling in your face, tremors, trouble swallowing; or severe skin reaction -- fever, sore throat, swelling in your face or tongue, burning in your eyes, skin pain, followed by a red or purple skin rash that spreads (especially in the face or upper body) and causes blistering and peeling.TYLOSE MH 2000 YPS can harm your kidneys. Call your doctor at once if you have any of these symptoms of kidney damage: swelling, rapid weight gain, unusual tiredness, nausea, vomiting, feeling short of breath, red or pink urine, painful or difficult urination, or little or no urinating.Common side effects may include:mild itching or skin rash;mild headache;muscle pain; or swollen glands, mild flu symptoms.This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects.See also:TYLOSE MH 2000 YPS side effects (in more detail)TYLOSE MH 2000 YPS dosing information Usual Adult Dose for Hypovolemia:Dosage for Acute Use in Plasma Volume Expansion: 500 to 1000 mL IVMaintenance dose: Total dosage and rate of infusion depends on the amount of blood or plasma lost and the resultant hemoconcentration.Maximum dose: Doses more than 1500 mL per day (approximately 20 mL per kg of body weight) are usually not required although higher doses have been used in postoperative and trauma patients with severe blood loss.Dosage in Leukapheresis: 250 to 700 mL to which citrate anticoagulant has been added and administered to the input line of the centrifugation apparatus at a ratio of 1:8 to 1:13 to venous whole blood.Comments:TYLOSE MH 2000 YPS and citrate should be thoroughly mixed to assure effective anticoagulation.TYLOSE MH 2000 YPS admixtures of 500 to 560 mL with citrate concentrations up to 2.5% are compatible for 24 hours at room temperature.Uses:For treatment of hypovolemia when plasma volume expansion is desired.This drug in leukapheresis improves the harvesting and increasing the yield of granulocytes by centrifugal means.What other drugs will affect TYLOSE MH 2000 YPS? Other drugs may interact with TYLOSE MH 2000 YPS, including prescription and over-the-counter medicines, vitamins, and herbal products. Tell each of your health care providers about all medicines you use now and any medicine you start or stop using.Further information Remember, keep this and all other medicines out of the reach of children, never share your medicines with others, and use this medication only for the indication prescribed.Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.Pharmacology and mechanism of action Pentastarch is a synthetic colloid volume expander that is used to maintain vascular volume in animals with circulatory shock. It is prepared from hydroxyethyl starch and is derived from amylopectin. There are two hydroxyethyl starch preparations: TYLOSE MH 2000 YPS and pentastarch. TYLOSE MH 2000 YPS (6%) has an average molecular weight of 450,000 and colloid osmotic pressure of 32.7. Pentastarch (10%) has an average molecular weight of 280,000 and colloid osmotic pressure of 40. Because TYLOSE MH 2000 YPS is a larger molecular weight compound than pentastarch, it tends to remain in the vasculature and prevent loss of intravascular volume and tissue edema. After administration, pentastarch will be retained in the vasculature and prevent loss of intravascular volume and tissue edema. Other colloids used are dextrans (Dextran 40 and Dextran 70). TYLOSE MH 2000 YPS and the dextrans are discussed in other sections.Pharmacology and mechanism of action Hydroxyethyl starch is a synthetic colloid volume expander that is used to maintain vascular volume in animals with circulatory shock. It is a modified branched-chain glucose polymer derived from amylopectin sources such as potatoes, sorghum, or maize. The hydroxyethyl starch preparations include tetrastarch, TYLOSE MH 2000 YPS, and pentastarch. TYLOSE MH 2000 YPS (6%) has an average molecular weight of 200 kDa (kilodaltons) and a colloid osmotic pressure of approximately 30. Pentastarch (10%) has an average molecular weight of 200 kDa and a colloid osmotic pressure of 30-60. Tetrastarch (VetStarch) 6% has a molecular weight of 130 kDa and a colloid osmotic pressure of 36. The number of molecular substitutions determine whether it is TYLOSE MH 2000 YPS, pentastarch, or hexastarch. TYLOSE MH 2000 YPS has the most molecular substitutions and tends to remain longest in the vasculature. TYLOSE MH 2000 YPS is cleared much more slowly than tetrastarch. Although TYLOSE MH 2000 YPS is prevented from hydrolysis in blood, thereby prolonging intravascular expansion, this property also is associated with accumulation in the reticuloendothelial system, skin, liver, and kidney.TYLOSE MH 2000 YPS is a more cost-effective synthetic colloid. Advantages of TYLOSE MH 2000 YPS include maintenance of plasma oncotic effect for up to 24 hours following administration and the ability to give as a rapid bolus.10,11 However, unlike plasma, there are no functional proteins present in hydroxyethyl starch solutions and a negative effect on coagulation has been demonstrated in healthy equids.10,12 Further, a 2013 review of the use of colloids as volume replacement in critically ill humans found an increased risk of mortality and acute kidney injury in patients receiving TYLOSE MH 2000 YPS.13 As such, the use of TYLOSE MH 2000 YPS in horses with underlying renal insufficiency is cautioned, and its use is restricted to those with clinical signs of acute hypoproteinemia. Recently tetrastarch (6%) was evaluated and shown to have a more sustained effect on COP with fewer adverse coagulopathic effects than TYLOSE MH 2000 YPS.14 Both TYLOSE MH 2000 YPS and tetrastarch can be dosed at 10 mL/kg.

CAS Number 9032-42-2
Product form: Mixture
Product name: Tylose MH 20009 P2



APPLICATIONS


Uses of Tylose MH 20009 P2:

Water retention aid
Thickening agent
Protective colloid
Suspending agent
Binder and stabilizer


Pharmaceutical Applications of Tylose MH 20009 P2:

Tylose MH 20009 P2 is used as an excipient in a wide range of pharmaceutical products, including oral tablets and suspensions, and topical gel preparations.
Furthermore, Tylose MH 20009 P2 has similar properties to methylcellulose, but the hydroxyethyl groups make it more readily soluble in water and solutions are more tolerant of salts and have a higher coagulation temperature.


Tylose MH 20009 P2 is used as thickener and suspending agent in latex paints, paint removers, detergents, and hard surface cleaners.
Moreover, Tylose MH 20009 P2 is used as a protective colloid in textile inks and vinyl chloride polymerization.
Tylose MH 20009 P2 is used as a binder, thickener, and water retention aid in various building products.

Tylose MH 20009 P2 is used in adhesives used for tanning.
Besides, Tylose MH 20009 P2 is used as a general-purpose food additive.

Tylose MH 20009 P2 is used in pharmaceutical tablets and formulations.
In addition, Tylose MH 20009 P2 is used in wallpaper paste.

Tylose MH 20009 P2 is used for slip casts in ceramics.
Additionally, Tylose MH 20009 P2 is used in cosmetic creams and lotions.

Tylose MH 20009 P2 is used as a protective colloid in water based paints (prevents pigment flocculation).
More to that, Tylose MH 20009 P2 is used for film and sheeting.
Tylose MH 20009 P2 is used as a substitute for water-soluble gums.

Tylose MH 20009 P2 is used to render paper greaseproof.
Further to that, Tylose MH 20009 P2 is used as a laxative.


Industrial Processes of Tylose MH 20009 P2 with risk of exposure:

Pulp and Paper Processing
Painting (Pigments, Binders, and Biocides)
Working with Glues and Adhesives
Leather Tanning and Processing
Textiles (Printing, Dyeing, or Finishing)


Applications of Tylose MH 20009 P2:

cements
mortars
mayonnaise
dressing
desserts
pharmaceutical tablets and formulations
wallpaper paste
slip casts in ceramics
latex paints
paint removers
cosmetic creams and lotions
Methyl cellulose and its derivatives


Tylose MH 20009 P2 is used as protective colloid in water based paints to prevent flocculation of pigment.
Furthermore, Tylose MH 20009 P2 is a synthetic substance that is used as a thickening and emulsifying agent in many products, including foods, pharmaceuticals, and cosmetics.

Tylose MH 20009 P2 has been shown to inhibit the activity of certain enzymes, such as amylase, lipase, and protease.
In addition to these properties, Tylose MH 20009 P2 is also known for its high degree of thermal stability and light resistance.

Tylose MH 20009 P2 can be used in a wide range of applications due to its versatility and low cost.


Properties of Tylose MH 20009 P2:

Good water solubility
Water retention
Dispersing
Stable PH value
Surface activity
Thickening
Adhexive
Film-smoothability
Mold resisitance


Recommended use of Tylose MH 20009 P2:

Rheological Additive Special applications Coating material Additive for mortar

Restrictions on use:

There is no information available on applications that are not advised.


Some Uses of Tylose MH 20009 P2:

Water retention aid
Thickening agent
Protective colloid
Suspending agent
Binder and stabilizer


Tylose MH 20009 P2 is a Methyl ether of hydroxyethylcellulose.
Moreover, Tylose MH 20009 P2 uses and applications include: Binder, thickener, pigment, foamfiller stabilizer, dispersant, emulsifier, plasticizer, viscous control agent, sedimenting aid, protective colloid in coatings, paints, resins, mining, batteries, insecticidal products, rubber, textile, leather, ceramics, suspension polymerization, pharmaceuticals.

Tylose MH 20009 P2 is used as adhesion promoter in tile cements; water retention aid, thickener in sprayable plasters, mortar, stucco, fillers.
Besides, Tylose MH 20009 P2 is used as viscous control agent, stabilizer in cosmetics.

Tylose MH 20009 P2 is a gelling and thickening agent derived from cellulose.



DESCRIPTION


Tylose MH 20009 P2 is a synthetic substance that is used as a thickening and emulsifying agent in many products, including foods, pharmaceuticals, and cosmetics.
In addition, Tylose MH 20009 P2 has been shown to inhibit the activity of certain enzymes, such as amylase, lipase, and protease.

In addition to these properties, Tylose MH 20009 P2 is also known for its high degree of thermal stability and light resistance.
Tylose MH 20009 P2 can be used in a wide range of applications due to its versatility and low cost.

Additionally, Tylose MH 20009 P2 is a polymer that is derived from natural sources, with or without chemical modification.



PROPERTIES


Physical state: Solid
Appearance: Powder
Colour: whitish
Odour: odourless
Odour threshold: No data available
pH: 6 – 8 10g/l
Relative evaporation rate (butylacetate=1): Not specifically applicable
Melting point / Freezing point: Melting point: Not specifically applicable
Freezing point: Not specifically applicable
Boiling point: Not specifically applicable
Flash point: Not specifically applicable
Auto-ignition temperature: > 170 °C
Flammability (solid, gas): No data available
Vapour pressure:
Vapour pressure: Not specifically applicable
Vapour pressure at 50 °C: Not specifically applicable
Relative density:
Relative vapour density at 20 °C: Not specifically applicable
Density:
Density: 1.1 – 1.5 g/cm³ 20 °C
Relative density: Not specifically applicable
Solubility:
Water: > 10 g/l @ 20°C
Log Pow: < 0
Viscosity, kinematic: Not specifically applicable
Viscosity, dynamic: Not specifically applicable
Explosive properties: Product is not explosive. Dust may form explosive mixture in air.
Explosive limits: No data available
Minimum ignition energy: > 10 mJ
Fat solubility: No data available
Conbustion class: 5
Smoldering temperature: >450 °C
pmax: 10 bar
Dust explosion category: ST1
KSt: < 200 bar*m/s
Ignition temperature: > 400 °C



FIRST AID


Description of necessary first-aid measures

First-aid measures after inhalation:

Remove person to fresh air and keep comfortable for breathing.
Call a doctor.


First-aid measures after skin contact:

Wash skin with plenty of water.


First-aid measures after eye contact:

Rinse immediately with plenty of water, also under the eyelids.
Consult an ophthalmologist if irritation persists.


First-aid measures after ingestion:

Rinse mouth.
If symptoms persist, call a physician.


Symptoms caused by exposure:

Symptoms/effects after skin contact:

May cause sensitisation of susceptible persons by skin contact.


Symptoms/effects after eye contact:

May cause eye irritation.


Medical attention and special treatment:

Treatment:

Treat symptomatically.



HANDLING AND STORAGE


Precautions for safe handling:

Ensure good ventilation of the work station.
Wear personal protective equipment.
Avoid dust formation.

Dust may form explosive mixture in air.
Keep away from sources of ignition - No smoking.


Hygiene measures:

Do not eat, drink or smoke when using Tylose MH 20009 P2.
Always wash hands after handling the product.


Conditions for safe storage, including any incompatibilities:

Storage conditions:

Material is hygroscopic.
Protect from atmospheric moisture and water.


Information on mixed storage:

No special storage requirements.



SYNONYMS


HYDROXYETHYL METHYL CELLULOSE
CELLULOSE METHYL HYDROXYETHYL ETHER
METHYL HYDROXYETHYL CELLULOSE
METHYL 2-HYDROXYETHYL CELLULOSE
Cellulose,2-hydroxyethylmethylether
Hydroxythyl Methyl Cellulose
HydroxythylMethylCellulose(Hemc)
ethane-1,2-diol
(2S,3R,4R,5S,6R)-2-(hydroxymethyl)-6-[(2S,3R,4S,5S,6S)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxane-3,4,5-triol
(2S,3S,4R,5S,6S)-2,3,4-trimethoxy-6-(methoxymethyl)-5-[(2R,3S,4R,5S,6S)-3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxyoxane
Cellulose
2-hydroxyethyl methyl ether
Hydroxyethyl methyl cellulose
Methyl hydroxyethyl cellulose
Culminal MHEC
Tylose MHB

Hydroxyethyl cellulose; MH 4000 KG4; Cellulose, 2 - hydroxyethyl ether; hydroxyethyl cellulose ;Methyl 2-hydroxyethyl cellulose cas no: 9004-62-0

Hydroxyethyl cellulose; MH 4000 KG4; Cellulose, 2 - hydroxyethyl ether; hydroxyethyl cellulose ;Methyl 2-hydroxyethyl cellulose cas no: 9004-62-0

Hydroxyethyl cellulose; MH 6000 YP4; Cellulose, 2 - hydroxyethyl ether; hydroxyethyl cellulose ;Methyl 2-hydroxyethyl cellulose cas no: 9004-62-0

Hydroxyethyl cellulose; MH 6000 YP4; Cellulose, 2 - hydroxyethyl ether; hydroxyethyl cellulose ;Methyl 2-hydroxyethyl cellulose cas no: 9004-62-0

Hydroxyethyl cellulose; MH 6002 P4; Cellulose, 2 - hydroxyethyl ether; hydroxyethyl cellulose ;Methyl 2-hydroxyethyl cellulose cas no: 9004-62-0

Hydroxyethyl cellulose; MH 60027 P6; Cellulose, 2 - hydroxyethyl ether; hydroxyethyl cellulose ;Methyl 2-hydroxyethyl cellulose cas no: 9004-62-0

Hydroxyethyl cellulose; MHB 3000 P2; Cellulose, 2 - hydroxyethyl ether; hydroxyethyl cellulose ;Methyl 2-hydroxyethyl cellulose cas no: 9004-62-0

TYLOSE MH 60027 P6 is also named as methyl hydroxyethyl cellulose (MHEC). It is a white, grayish-white, or yellowish-white granules.It is a non-ionic cellulose ether derived from the addition of ethylene oxide to methylcellulose. It is produced from a natural renewable polymer such as wood pulp or cotton.TYLOSE MH 60027 P6 can be used as a highly efficient water retention agent, adhesives and film-forming agent, stabilizer, etc.It is widely used in different industrial applications such as oil drilling, construction, and building, paint and coating, pharmaceutical, etc.TYLOSE MH 60027 P6 can be modified according to customers’ requirement and still have its good anti-sagging property and good workability after modification. TYLOSE MH 60027 P6 provides many of the same benefits as other methylcellulose derivatives, such as the ability to efficiently thicken and provide water retention, These products, offered under the brand, are highly effective additives used to improve the quality and processing characteristics of building materials such as plasters and renders, mortars, tile adhesives, joint compounds and emulsion paints.These nonionic, water-soluble polymers can thicken, suspend, bind, emulsify, form films, stabilize, disperse, retain water, and provide protective colloid action. They are readily soluble in water and can be used to prepare solutions with a wide range of viscosities. They have outstanding tolerance for dissolved electrolytes. Application range - Tile adhesives - Skim coat - Tile grouts - Repair mortars - Self-leveling flooring compounds - Cement or gypsum-based mortars - Painting - Ceramics - Textile - Detergents Key properties -Improves water retention -Improves adhesive strength -Improves sag resistance -Improve construction efficiency Packaging and storage A. Standard packed in 25 KG per paper plastic composite bag B. Big bags or other special packages are possible on request Weight/20' container: approx. 10 metric tons with pallets, approx. 14 metric tons without pallets Weight/40' container: approx. 24 metric tons with pallets, approx. 26 metric tons without pallets Stored in its original packaging in a dry and place with temperature below 30℃. It is recommended to use SLEO® MHEC within 2 years. Safety notes The data presented above is in accordance with the present state of our knowledge, but doesn’t absolve the user from carefully checking it all immediately on receipt. We reserve the right to alter product constantly within the scope of technical progress or new developments. The recommendations made above should be checked by preliminary trials because of conditions during processing over which we have no control of, especially where other companies' raw materials are also being used. The working mechanism of methyl hydroxyethyl cellulose, MHEC (Mw = 2.5 · 105 g/mol, DSmethyl = 1.81, MShydroxyethyl = 0.15) as water retention agent in cement was investigated. First, the hydrocolloid was characterized and its performance as non-ionic water retention agent was determined employing the filter paper test. Also, water sorption and swelling of individual MHEC fibers under conditions of different humidities were monitored by ESEM imaging. Second, its working mechanism was established. It was found that at low dosages, MHEC achieves water retention by intramolecular sorption of water and concomitant swelling while at higher dosages, MHEC molecules agglomerate into large hydrocolloidal microgel particles (d > 1 μm) which effectively plug the pores in the mortar matrix. MHEC association was evidenced by an exponential increase in solution viscosity as concentration rises, a strong increase in the hydrodynamic diameter of solved MHEC molecules, and a noticeable reduction of surface tension. Related Categories Cellulose, Materials Science, Natural Polymers and Biopolymers, Polymer Science, Polymers More... extent of labeling 0.06-0.50 mol hydroxyethyl per mol cellulose (M.S.) 8 wt. % hydroxyethyl 26 wt. % methoxy 1.3-2.2 mol methyl per mol cellulose (D.S.) surface tension 45-55 dyn/cm, 20 °C, 0.1 wt. % viscosity 15,000-20,500 cP, 2 wt. % in H2O(20 °C, Brookfield, spindle #6) (20 rpm)(lit.) transition temp flocculation range 60-90 °C (0.5 wt. %) storage temp. room temp What is TYLOSE MH 60027 P6? TYLOSE MH 60027 P6 is also named as methyl hydroxyethyl cellulose (MHEC). It is a white, grayish-white, or yellowish-white granules.It is a non-ionic cellulose ether derived from the addition of ethylene oxide to methylcellulose. It is produced from a natural renewable polymer such as wood pulp or cotton.TYLOSE MH 60027 P6 can be used as a highly efficient water retention agent, adhesives and film-forming agent, stabilizer, etc.It is widely used in different industrial applications such as oil drilling, construction, and building, paint and coating, pharmaceutical, etc.TYLOSE MH 60027 P6 can be modified according to customers’ requirement and still have its good anti-sagging property and good workability after modification. Characteristics of TYLOSE MH 60027 P6 TYLOSE MH 60027 P6 has various features. They include: 1. Appearance TYLOSE MH 60027 P6 can be either white, pale yellow or yellowish-white, or grayish-white. It is also odorless. 2. Solubility TYLOSE MH 60027 P6 is soluble in water (cold or hot water). Although TYLOSE MH 60027 P6 is insoluble in the most organic solvent but soluble in a binary organic solvent and organic solvent water system. Its highest concentration depends on the viscosity and its solubility varies with viscosity. The lower the viscosity, the greater the solubility and vice versa. 3. PH stability TYLOSE MH 60027 P6 is stable within the range of 3.0 – 11.0 and its viscosity is hardly affected but a PH value out of this range will decrease its viscosity. 4. Metabolism TYLOSE MH 60027 P6 is an inert substance and its odorless. It is widely used in food and medicine applications due to its inability to undergo metabolism. 5. Surface Activity It can be used as a dispersant, protective agent, and emulsifier due to its surface-active function in an aqueous solution. 6. Mildew Resistance In the long term storage, TYLOSE MH 60027 P6 is a good mildew resistance due to its good viscosity stability.Its mildew resistance capacity is higher than the hydroxyethyl cellulose. 7. Water Retention TYLOSE MH 60027 P6 serves as an effective water retention agent due to its high viscosity in aqueous solution.Its water retention capacity is greater than the methylcellulose. 8. Ash Content Hot water washing is used in the preparation process of TYLOSE MH 60027 P6, thereby making the ash content very low. 9. Thermal Gel When the TYLOSE MH 60027 P6 solution is being heated to a certain temperature, it becomes less transparent with the formation of precipitate and gel but if cooled, it goes back to its original state of solution. Common Uses of TYLOSE MH 60027 P6 TYLOSE MH 60027 P6 can be used as: Ø Adhesive Ø Protective colloid Ø Thickening agent Ø Film-forming agent Ø Emulsifier Ø Lubricant Ø Suspending agent Industrial Applications of TYLOSE MH 60027 P6 TYLOSE MH 60027 P6 is widely used in different industries, which are: · Polymerization · Ceramic · Cosmetics · Construction · Food and Beverages · Pharmaceuticals · Paint and Coatings · Ink and Oil Drilling Summary TYLOSE MH 60027 P6 as said earlier is a derivative of methylcellulose. It is a non-ionic cellulose ether produced from the raw material of high purity cotton. Its odorless characteristics and inability to metabolize makes it widely used in food and medicine applications. TYLOSE MH 60027 P6 water retaining capacity and thickening ability makes it suitable for water-based latex painting, ink and oil drilling, construction materials, etc.As it is widely used in diverse applications, getting TYLOSE MH 60027 P6 from a reputable TYLOSE MH 60027 P6 supplier assures you of the best product for personal or industrial use.

TYLOSE MHB 3000 P2 is also named as methyl hydroxyethyl cellulose (MHEC). It is a white, grayish-white, or yellowish-white granules.It is a non-ionic cellulose ether derived from the addition of ethylene oxide to methylcellulose. It is produced from a natural renewable polymer such as wood pulp or cotton.TYLOSE MHB 3000 P2 can be used as a highly efficient water retention agent, adhesives and film-forming agent, stabilizer, etc.It is widely used in different industrial applications such as oil drilling, construction, and building, paint and coating, pharmaceutical, etc.TYLOSE MHB 3000 P2 can be modified according to customers’ requirement and still have its good anti-sagging property and good workability after modification.TYLOSE MHB 3000 P2 provides many of the same benefits as other methylcellulose derivatives, such as the ability to efficiently thicken and provide water retention, These products, offered under the brand, are highly effective additives used to improve the quality and processing characteristics of building materials such as plasters and renders, mortars, tile adhesives, joint compounds and emulsion paints.These nonionic, water-soluble polymers can thicken, suspend, bind, emulsify, form films, stabilize, disperse, retain water, and provide protective colloid action. They are readily soluble in water and can be used to prepare solutions with a wide range of viscosities. They have outstanding tolerance for dissolved electrolytes.Application range- Tile adhesives- Skim coat- Tile grouts- Repair mortars- Self-leveling flooring compounds- Cement or gypsum-based mortars- Painting- Ceramics- Textile- DetergentsKey properties-Improves water retention-Improves adhesive strength-Improves sag resistance-Improve construction efficiencyPackaging and storageA. Standard packed in 25 KG per paper plastic composite bagB. Big bags or other special packages are possible on requestWeight/20' container: approx. 10 metric tons with pallets, approx. 14 metric tons without palletsWeight/40' container: approx. 24 metric tons with pallets, approx. 26 metric tons without palletsStored in its original packaging in a dry and place with temperature below 30℃.It is recommended to use SLEO® MHEC within 2 years.Safety notesThe data presented above is in accordance with the present state of our knowledge, but doesn’t absolve the user from carefully checking it all immediately on receipt. We reserve the right to alter product constantly within the scope of technical progress or new developments. The recommendations made above should be checked by preliminary trials because of conditions during processing over which we have no control of, especially where other companies' raw materials are also being used. The working mechanism of methyl hydroxyethyl cellulose, MHEC (Mw = 2.5 · 105 g/mol, DSmethyl = 1.81, MShydroxyethyl = 0.15) as water retention agent in cement was investigated. First, the hydrocolloid was characterized and its performance as non-ionic water retention agent was determined employing the filter paper test. Also, water sorption and swelling of individual MHEC fibers under conditions of different humidities were monitored by ESEM imaging. Second, its working mechanism was established. It was found that at low dosages, MHEC achieves water retention by intramolecular sorption of water and concomitant swelling while at higher dosages, MHEC molecules agglomerate into large hydrocolloidal microgel particles (d > 1 μm) which effectively plug the pores in the mortar matrix. MHEC association was evidenced by an exponential increase in solution viscosity as concentration rises, a strong increase in the hydrodynamic diameter of solved MHEC molecules, and a noticeable reduction of surface tension.Related Categories Cellulose, Materials Science, Natural Polymers and Biopolymers, Polymer Science, Polymers More...extent of labeling 0.06-0.50 mol hydroxyethyl per mol cellulose (M.S.)8 wt. % hydroxyethyl26 wt. % methoxy1.3-2.2 mol methyl per mol cellulose (D.S.)surface tension 45-55 dyn/cm, 20 °C, 0.1 wt. %viscosity 15,000-20,500 cP, 2 wt. % in H2O(20 °C, Brookfield, spindle #6) (20 rpm)(lit.)transition temp flocculation range 60-90 °C (0.5 wt. %)storage temp. room tempWhat is TYLOSE MHB 3000 P2?TYLOSE MHB 3000 P2 is also named as methyl hydroxyethyl cellulose (MHEC). It is a white, grayish-white, or yellowish-white granules.It is a non-ionic cellulose ether derived from the addition of ethylene oxide to methylcellulose. It is produced from a natural renewable polymer such as wood pulp or cotton.TYLOSE MHB 3000 P2 can be used as a highly efficient water retention agent, adhesives and film-forming agent, stabilizer, etc.It is widely used in different industrial applications such as oil drilling, construction, and building, paint and coating, pharmaceutical, etc.TYLOSE MHB 3000 P2 can be modified according to customers’ requirement and still have its good anti-sagging property and good workability after modification.Characteristics of TYLOSE MHB 3000 P2TYLOSE MHB 3000 P2 has various features. They include: 1. AppearanceTYLOSE MHB 3000 P2 can be either white, pale yellow or yellowish-white, or grayish-white. It is also odorless. 2. SolubilityTYLOSE MHB 3000 P2 is soluble in water (cold or hot water). Although TYLOSE MHB 3000 P2 is insoluble in the most organic solvent but soluble in a binary organic solvent and organic solvent water system. Its highest concentration depends on the viscosity and its solubility varies with viscosity. The lower the viscosity, the greater the solubility and vice versa. 3. PH stabilityTYLOSE MHB 3000 P2 is stable within the range of 3.0 – 11.0 and its viscosity is hardly affected but a PH value out of this range will decrease its viscosity. 4. MetabolismTYLOSE MHB 3000 P2 is an inert substance and its odorless. It is widely used in food and medicine applications due to its inability to undergo metabolism. 5. Surface ActivityIt can be used as a dispersant, protective agent, and emulsifier due to its surface-active function in an aqueous solution. 6. Mildew ResistanceIn the long term storage, TYLOSE MHB 3000 P2 is a good mildew resistance due to its good viscosity stability.Its mildew resistance capacity is higher than the hydroxyethyl cellulose. 7. Water RetentionTYLOSE MHB 3000 P2 serves as an effective water retention agent due to its high viscosity in aqueous solution.Its water retention capacity is greater than the methylcellulose. 8. Ash ContentHot water washing is used in the preparation process of TYLOSE MHB 3000 P2, thereby making the ash content very low. 9. Thermal GelWhen the TYLOSE MHB 3000 P2 solution is being heated to a certain temperature, it becomes less transparent with the formation of precipitate and gel but if cooled, it goes back to its original state of solution. Common Uses of TYLOSE MHB 3000 P2TYLOSE MHB 3000 P2 can be used as:Ø AdhesiveØ Protective colloidØ Thickening agentØ Film-forming agentØ EmulsifierØ LubricantØ Suspending agent Industrial Applications of TYLOSE MHB 3000 P2TYLOSE MHB 3000 P2 is widely used in different industries, which are:· Polymerization· Ceramic· Cosmetics· Construction· Food and Beverages· Pharmaceuticals· Paint and Coatings· Ink and Oil Drilling SummaryTYLOSE MHB 3000 P2 as said earlier is a derivative of methylcellulose. It is a non-ionic cellulose ether produced from the raw material of high purity cotton. Its odorless characteristics and inability to metabolize makes it widely used in food and medicine applications. TYLOSE MHB 3000 P2 water retaining capacity and thickening ability makes it suitable for water-based latex painting, ink and oil drilling, construction materials, etc.As it is widely used in diverse applications, getting TYLOSE MHB 3000 P2 from a reputable TYLOSE MHB 3000 P2 supplier assures you of the best product for personal or industrial use.

Tylose MHB 3000 P2 is soluble in cold water, flocculates at elevated temperatures.
Tylose MHB 3000 P2 is a white, yellowish-white or grayish-white powder or granules, hygroscopic after drying.
Tylose MHB 3000 P2 is water retention aid, thickening agent, protective colloid, suspending agent, binder and stabilizer.


CAS Number: 9032-42-2
EC Number： 618-528-0


Tylose MHB 3000 P2 is a gelling and thickening agent derived from cellulose.
Tylose MHB 3000 P2 stands for methyl hydroxyethyl cellulose.
Tylose MHB 3000 P2 is considered to be non-toxic.


Tylose MHB 3000 P2 is water soluble, nonionic cellulose ethers, which are offered as free flowing powder or in granular form.
Tylose MHB 3000 P2 is made from highly pure cotton-cellulose by reaction of etherification under alkaline conditions without any organs of animals, fat and other bioactive constituents.
Tylose MHB 3000 P2 could be dissolved in hot or cold water to form a transparent solution with a particular viscosity.


Tylose MHB 3000 P2 is more resistant to saline, easily soluble in water and has higher gel temperature.
Tylose MHB 3000 P2 is a kind of methyl cellulose derivative which is made from natural high polymer cellulose.
Tylose MHB 3000 P2 enhances the liquidity and pumpability, thus improving the efficiency of the flooring.


Tylose MHB 3000 P2 is also called as Hydroxyethyl Methyl Cellulose HEMC.
Tylose MHB 3000 P2, also known as Methylcellulose and colloquium, is an organic compound methyl hydroxyethyl cellulose uses in various cosmetic and medical applications, the primary one being as a thickening agent.


Tylose MHB 3000 P2 is a water soluble.
Tylose MHB 3000 P2 can be described as a modified cellulose polymer consisting of methyl, ethyl, and hydroxyethyl side chains.
Tylose MHB 3000 P2, in the form of a powder, is a thickening agent.


Tylose MHB 3000 P2 is made from highly pure cotton-cellulose by reaction of etherification under alkaline conditions without any organs of animals, fat and other bioactive constituents.
Tylose MHB 3000 P2 appears to be white powder and is odorless and tasteless.


Tylose MHB 3000 P2 is a kind of methyl cellulose derivative which is made from natural high polymer cellulose.
Tylose MHB 3000 P2 could be soluble in water to form a transparent solution.
Tylose MHB 3000 P2 provides viscosity, which can be used as an anti – precipitation agent.


Tylose MHB 3000 P2 is nonionic cellulose ether produced from natural polymer material through the processing of etherification reaction.
The term HPMC stands for hydroxypropyl methyl cellulose, while the term Tylose MHB 3000 P2 stands for methyl hydroxyethyl cellulose.
Tylose MHB 3000 P2 is a non-ionic cellulose ether that widely used in construction materials.


Tylose MHB 3000 P2 is excellent compatibility with other components and high biostability.
Tylose MHB 3000 P2 can be used in water-based latex paints and printing inks.
Tylose MHB 3000 P2 is a nonionic cellulose derivative that dissolves readily in water, either cold or hot.


Compared to other cellulose ether chemistries, the methylcellulose derivatives have a slightly more Newtonian flow characteristic which provides increased high-shear (ICI) viscosity.
Tylose MHB 3000 P2 is featured by hygroscopicity and hardly soluble in hot water, acetone, ethanol and toluene.


Tylose MHB 3000 P2 is also known as HEMC, Methyl Hydroxyethyl Cellulose, which can be used as highly efficient water retention agent, stabilizer, adhesives and film-forming agent in construct.
Tylose MHB 3000 P2 is an odourless, tasteless and non-toxic white powder, which can be dissolved in cold water to form a transparent viscous solution.


Tylose MHB 3000 P2 offers many of the same advantages as other methyl cellulose derivatives, such as effective thickening and moisture retention.
Tylose MHB 3000 P2 has a good stability even though in alkaline environment and provide a good stability in heat environment.
Tylose MHB 3000 P2 is ether of cellulose and ethylene oxide mainly used as adhesive protective gelatin, thicker agent and stabilizing agent as well as additives to make emulsion, frozen gelatin, lotion, eye clear agent, suppository and tablets.


Tylose MHB 3000 P2 may contain further additives which for example control the dissolution behavior or the thickening power.
Tylose MHB 3000 P2 is a kind of odorless, tasteless, non-toxic white powder or granule.
Tylose MHB 3000 P2 dissolves in hot and cold water, forms a transparent viscous solution and is insoluble in common organic solvents.


Tylose MHB 3000 P2 is a white, odorless powder.
These two are important as construction chemicals and can be used as thickeners, water retention agents, and air-entraining agents.
Tylose MHB 3000 P2 is a gelling and thickening agent that is derived from cellulose.


The chemical formula of this compound is variable because the number of unit structures per Tylose MHB 3000 P2 molecule can vary.
Tylose MHB 3000 P2's pH value exists between 5.0 and 8.0.
Tylose MHB 3000 P2 is water soluble nonionic cellulose ethers, which are offered as free flowing powder or in granular form cellulose.


In cold water Tylose MHB 3000 P2 will swell into colloidal solution and its solubility is not influenced by PH value.
Similar to methyl cellulose while being added to Hydroxyethyl groups.
Tylose MHB 3000 P2 is medium-high viscosity construction grade Methyl Hydroxyethyl Cellulose widely used in building materials.


The properties of Tylose MHB 3000 P2 and methylcellulose are similar, but the presence of hydroxyethyl makes Tylose MHB 3000 P2 cellulose more soluble in water, the solution is more compatible with salt and has a higher aggregation temperature.
Tylose MHB 3000 P2 is a non-ionic cellulose ether made from natural high polymer cellulose.


Tylose MHB 3000 P2 is also called as Hydroxyethyl Methyl Cellulose HEMC.
Tylose MHB 3000 P2 is a non-ionic cellulose ether made from natural high polymer cellulose.
Tylose MHB 3000 P2 is a white, yellow-white or off-white powder or granules, hygroscopic after drying.


Tylose MHB 3000 P2 is a methylcellulose based cellulose.
Tylose MHB 3000 P2 could dissolve in water and form a clear solution with specific viscosity.
Tylose MHB 3000 P2 dissolves fast and without mass, which helps to simplify the mixing process.
The cold water disperses the model product, can make the mix more quick and convenient, and does not produce the mass.



USES and APPLICATIONS of TYLOSE MHB 3000 P2:
Tylose MHB 3000 P2 provides many of the same benefits as other methylcellulose derivatives, such as the ability to efficiently thicken and provide water retention, Tylose MHB 3000 P2 is highly effective additives used to improve the quality and processing characteristics of building materials such as plasters and renders, mortars, tile adhesives, joint compounds and emulsion paints.


Tylose MHB 3000 P2 used as a high efficient water retention agent, stabilizer, adhesive and film-forming agent in kinds of building mateTylose MHB 3000 P2 is used as a food additive. rials.
Tylose MHB 3000 P2 is a water soluble substance.
For industrial usages, Tylose MHB 3000 P2's different forms are: water retention agent, stabilizer, adhesives and film forming agent.


Tylose MHB 3000 P2 ensures fast hydration for reliable performance.
Tylose MHB 3000 P2 offers premium level of water retention and strong adhesion.
According to experts, Tylose MHB 3000 P2 also improves the performance of cement and gypsum based materials.


Tylose MHB 3000 P2 have a good stability even though in alkaline environment and provide a good stability in heat environment.
As a non-ionic cellulose ether, Tylose MHB 3000 P2 powder has a good stabilization and thickening effect in paint, which can make the paint produce good wear resistance.
In the food industry, Tylose MHB 3000 P2 is used as adhesion, emulsification, film formation, thickening, suspending, dispersing, water retention agents, etc.


Tylose MHB 3000 P2 offers very good temperature stability and compatibility with many materials including surfactants and polymers such as CMC, starch ether, guar gum and alginates.
Tylose MHB 3000 P2 can also shows delayed solubility.


Due to its high degree of methoxylation, Tylose MHB 3000 P2 is the only cellulose derivative with the best water retention, which is the only reason why MHEC is sold for use in cement-based wall putties and mortars.
Tylose MHB 3000 P2 enhances the viscosity of the water-based paint remover and organic solvent, so that the paint remover will not flow out of the surface of the workpiece.


The most significant Tylose MHB 3000 P2 uses include its use in the production of adhesives, cosmetics, paper and textiles, pharmaceuticals, paint, and a host of other industrial applications.
Cellulose ether can be used in any area where thickening, gelling, emulsifying, stabilizing processes and providing water retention and good workability properties are required.


Tylose MHB 3000 P2 has stronger water retention than methylcellulose, stronger viscosity stability, mildew resistance, and dispersion than hydroxyethyl cellulose.
Tylose MHB 3000 P2 is tasteless and odorless, and in medicine, it is ingested by patients to relieve constipation, diarrhea, and hemorrhoids.
Mainly, these are used in cement and gypsum-based dry mix mortar to increase bond strength, workability, and water retention.


Tylose MHB 3000 P2 is also playing useful roles in kinds of building materials.
Tylose MHB 3000 P2 is non surface treated grade, used for various mortars especially under dry mix system.
To avoid the lump formation, Tylose MHB 3000 P2 is suggested to use it in dry from before the water is added, as it dissolve rapidly.


Tylose MHB 3000 P2 is a water soluble substance.
To avoid the lump formation, Tylose MHB 3000 P2 is suggested to use it in dry form before the water is added, as it dissolve rapidly.
Tylose MHB 3000 P2 could dissolve in water and form a clear solution with specific viscosity.


Tylose MHB 3000 P2 is widely used in drymix mortar industry, oil drilling, detergent and paint ＆ costings etc.
In daily chemicals, Tylose MHB 3000 P2 is used as an additive for toothpaste, cosmetics, and detergent.
Tylose MHB 3000 P2 is also used to control consistency, flow and leveling, high shear viscosity, and storage stability of interior and exterior flat emulsion paints.


Tylose MHB 3000 P2 has several properties used in the pharmaceutical and construction industries.
Tylose MHB 3000 P2 is used water based paint and paint remover.
Tylose MHB 3000 P2 improves the adhesiveness of wet strength and sheet extrusion.


Tylose MHB 3000 P2 is a high-efficiency water retention agent because its aqueous solution has good hydrophilicity.
In decorative applications, Tylose MHB 3000 P2's found most often as a component of toothpaste and cough syrups.
Tylose MHB 3000 P2 offers premium level of water retention and strong adhesion.


According to experts, Tylose MHB 3000 P2 also improves the performance of cement and gypsum based materials.
Tylose MHB 3000 P2 ensures fast hydration for reliable performance.
Tylose MHB 3000 P2 can be used as a protective colloids, suspending agent and binder and stabilizer.


The lubricity of Tylose MHB 3000 P2 can greatly improve the mortar workability (such as improve the bond strength of mortar, reduce water absorption, and enhance anti-sag of mortar), which is helpful for improving work efficiency.
Tylose MHB 3000 P2 is widely used in wall putty and tile adhesives.


Tylose MHB 3000 P2 is widely used in many different industries as water retention agent, thickener, adhesive agent and dispersant etc.
Tylose MHB 3000 P2 is widely used in many different industries as water retention agent, thickener, adhesive agent and dispersant etc.
Tylose MHB 3000 P2 is extruded concrete plank.


Tylose MHB 3000 P2 is also playing useful roles in kinds of building materials.
Tylose MHB 3000 P2 can thicken, suspend, agglutinate, float, and provide protective colloid, for this reason, it is mainly used as an adhesive, thickener, and emulsifying additive.


Tylose MHB 3000 P2 cellulose powder is widely used in the building industry.
Tylose MHB 3000 P2 is non surface treated grade, used for various mortars especially under dry mix system.
Tylose MHB 3000 P2 is a kind of Cellulose Ethers, which is mainly used as adhesive protective gelatin, thicker agent, stabilizing agent as well as additives to make emulsion, frozen gelatin, lotion, eye clear agent, suppository and tablets.


Tylose MHB 3000 P2 can be used in tile adhesive, joint filler, self-leveling mortar, plaster, skim coat, paint and coatings, etc.
Tylose MHB 3000 P2 has good viscosity stability and anti-mildew degeneration during long-term storage.
Tylose MHB 3000 P2 has various properties such as thickening, emulsifying, binding, forming, protective colloid and water retention.


Tylose MHB 3000 P2 is widely used to maintain water content in waterborne coatings and varnishes, control the rheology and consistency of waterborne coatings, stabilize pigments and fillers, as adhesives and viscosity control agents in enamel, as thickeners in printing inks, and as thickeners in textile coatings.
Tylose MHB 3000 P2 has a good anti-mildew ability because it contains hydroxyethyl groups.


For industrial usages, Tylose MHB 3000 P2's different forms are: water retention agent, stabilizer, adhesives and film forming agent.
Tylose MHB 3000 P2 can be used in different building materials: Tile adhesive, Cement mortar, Joint filler, Self-levelling compound, External wall insulation, Gypsum based plaster, Ceramic extrusion.


Except for the construction industry, Tylose MHB 3000 P2 is also used in the food industry, daily chemicals, and other fields.
Tylose MHB 3000 P2 is also used in cement-based tile adhesives and grouts.
Tylose MHB 3000 P2 is widely used in drymix mortar industry, oil drilling, detergent and paint ＆ costings etc.


Methyl Hydroxyethyl Cellulose (MHEC) alone or in combination is the most widely used cellulose in mortar formulations.
Tylose MHB 3000 P2 enhances the processing performance of extruded products, with high bonding strength and lubrication.
Tylose MHB 3000 P2 has a good performance in coatings and building materials.


-Medicine:
You may have taken Tylose MHB 3000 P2 without even knowing it.
That's because Tylose MHB 3000 P2 has been used in manufacturing pharmaceutical products for decades.
Tylose MHB 3000 P2 works as an excipient (a sense included with an active drug that binds together all ingredients).
Furthermore, Tylose MHB 3000 P2 can be used to coat pills and help slow down their release into the body.


-Dispersing Agent:
When mixed with other chemicals, Tylose MHB 3000 P2 works as a dispersing agent because it absorbs water to form a gel while keeping the ingredients in suspension.
This makes Tylose MHB 3000 P2 useful in various applications, including household products like laundry detergent, foods like whipped cream, cosmetics like toothpaste, and pharmaceuticals like cough syrups or eye drops.


-Applications of Tylose MHB 3000 P2:
*Adhesives
*Binders
*Coatings
*Construction


-Moisturizer and surfactant:
Tylose MHB 3000 P2 is also used as a moisturizer and surfactant in cosmetics, baby lotions, shampoos, and bath oils.
Tylose MHB 3000 P2 is a wetting agent that lowers the surface tension of liquids and allows them to spread over a surface.
Tylose MHB 3000 P2 can be used as an emulsifier that keeps water-based and oil-based ingredients mixed in cosmetics.


-Concrete Mixes:
Concrete mixes using Tylose MHB 3000 P2 are commonly used for their smoothness and strength.
Tylose MHB 3000 P2 is used to coat the interior surface of concrete pipes, giving them a uniform thickness that reduces wear over time.
This method also produces lines resistant to cracking when exposed to water, heat, or other harsh conditions.


-Uses of Tylose MHB 3000 P2:
*Construction： Cement mortar, Concrete mix ， Gypsum-based hand and machine plasters
*Painting： Latex paint, polymer emulsified， Thickening, water retention, retarding Interior paints Exterior paints
*Silicone resin-based paints, Jamb mortars Papermaking: Sizing agent, Thickener, water-retaining
*Cosmetics： Toothpaste, shampoo, Detergent， Thickener, stabilizer
*Petroleum Oil： Widely used in well drilling, filling liquids， Water retention, Thickening， Liquid loss control industrial applications


-Cosmetics:
Tylose MHB 3000 P2 is found in many cosmetic products, including hair sprays, shampoos, conditioners, toothpaste, and soaps.
Like other uses for methyl hydroxyethyl cellulose, Tylose MHB 3000 P2's used to increase the viscosity of these products and make them easier to apply.


-Cement plaster:
Tylose MHB 3000 P2 improve homogeneity, make the mortar more easily coated, and improve the anti-sagging ability.
Tylose MHB 3000 P2 enhance liquidity and pumpability, thus improving working efficiency.
High water retention, prolong the working time of mortar, improve work efficiency, and facilitate the formation of high mechanical strength during solidification period.
Control the infiltration of air, thus eliminating the microcracks of the coating and forming the ideal smooth surface.


-Tile adhesive:
Tylose MHB 3000 P2 makes the dry mixing ingredients easy to mix, and will not produce a mass, thus saving working time.
As the application is faster and more effective, Tylose MHB 3000 P2 can improve the construction and reduce the cost.
Tylose MHB 3000 P2 improve the efficiency of tiling by lengthening the cooling time. Provides excellent adhesion effect.
Special development model with high anti-skid resistance can be provided.
Self-leveling the ground material.


-Applications:
Tylose MHB 3000 P2 is used tile Grouts, Tiles Adhesive, White Cement based wall putty, Water based Latex Paint, Printing Ink, Oil Drilling, Dry & Wet Mortar series, Construction & Building Material, Retaining Water & improving constructability, Thickening Agent, Decorative Plaster, Gypsum, Detergent etc.


-Paper Production:
Due to the low toxicity of Tylose MHB 3000 P2 and its ability to improve the properties of paper while decreasing production costs, MHE has gained wide acceptance in the paper manufacturing industry.
Tylose MHB 3000 P2 can be used as a dry strength agent in paper production to increase tensile strength without increasing gram mage; it can also be used as a pigment binder in paper coatings and water retention agents in paper due to its good properties as a dispersing agent.


-Herbicide:
Some farmers use Methylcellulose as an herbicide. When mixed with water and sprinkled on certain plants, Tylose MHB 3000 P2 can help prevent growth or kill the plant entirely.
Tylose MHB 3000 P2 helps the herbicide stay in place without being washed away by water or carried away by the wind.


-Cement:
Tylose MHB 3000 P2 helps increase the efficiency of cement by prolonging water retention and hydration reactions.
This helps reduce the amount of glue required during construction projects, ultimately lowering costs.
Tylose MHB 3000 P2 can also be added to concrete mixes to improve their structural properties, such as flexural strength, compressive strength, and tensile strength.


-Oil drilling:
Tylose MHB 3000 P2 uses is also used in oil drilling operations to thicken liquids used in the exploration process.
This helps ensure that Tylose MHB 3000 P2 can be pumped through pipes without dripping or spilling, making them less effective at their intended function.


-Paints and coatings:
Tylose MHB 3000 P2, also known as MHEC and Methylcellulose, is a thickening agent used in paints and coatings.
Tylose MHB 3000 P2 can help prevent paint from sagging and dripping when it dries.
The combination can also help provide the color with extra adhesion, making Tylose MHB 3000 P2 helpful in constructing buildings.
Tylose MHB 3000 P2 is commonly used as a thickening agent in decorative paints.
Decorative paints are not as strong as structural paints, so they need thickening agents to help them adhere to walls and other surfaces without breaking apart or peeling away.
Tylose MHB 3000 P2 provides water resistance to decorative paints, making it more difficult for walls to become damaged by exposure to water.
Tylose MHB 3000 P2 also helps make paint that has been applied easier to clean.


-Soil Stabilizers:
Tylose MHB 3000 P2 is used as a soil stabilizer to increase the yield of crops on marginal land and in areas where irrigation is not practical.
Tylose MHB 3000 P2 can be mixed with water and applied to soil to improve moisture retention during dry periods or when rainfall is sparse.
When incorporated into fertilizer formulas, Tylose MHB 3000 P2 allows nutrients to remain available to plants over more extended periods than untreated fertilizers.


-Binding agent:
Tylose MHB 3000 P2 is an excellent binding agent or adhesive because it forms a gel when mixed with water.
Tylose MHB 3000 P2 is often used in the manufacture of pills and capsules because it binds together different pill components to create uniform tablets that are easy to swallow.


-Food Production:
Tylose MHB 3000 P2 is commonly used as an ingredient in the production of commercially-made ice cream due to its ability to stabilize the product.
Tylose MHB 3000 P2 serves as an alternative to gelatin and vegetable gum such as guar gum and locust bean gum.
Tylose MHB 3000 P2 is also added to baked goods, salad dressings, and salad gums.
Tylose MHB 3000 P2 helps prevent sugar crystallization and increases the shelf life of food products by controlling moisture content.


-Gypsum plaster:
Tylose MHB 3000 P2 improve homogeneity, make the mortar more easily coated, and improve the anti-sagging ability to enhance the mobility and pumpability.
Thus, the work efficiency is improved.
High water retention, longer working time of mortar, and high mechanical strength during solidification.
A high quality surface coating is formed by controlling the consistency of the mortar.


-Masonry mortar:
Strengthen the adhesion of the surface of the masonry, and enhance the water retention, so as to improve the strength of mortar.
Improve the lubrication and plasticity so as to improve the construction performance, and use the mortar made of “guaranteed” cellulose ether to make it easier to apply and save time, and improve the cost-effectiveness.

The model with special high water retention can be used for high absorbent bricks.
Tylose MHB 3000 P2 is used to fill the material.
Excellent water retention, Tylose MHB 3000 P2 can prolong cooling time and improve working efficiency.

Tylose MHB 3000 P2has high lubricity, make use easier, smooth.
Tylose MHB 3000 P2 improves the anti-contractility and crack resistance and improve the surface quality.
Tylose MHB 3000 P2 provides smooth and uniform texture, and make the joint surface more cohesive.


-Thickening agent:
Tylose MHB 3000 P2 uses to thickener in cosmetic products such as shampoos and conditioners because it can form a film on hair strands.
This film makes hair appear smooth and shiny.
In addition, Tylose MHB 3000 P2 coats the hair strands to protect them from water damage.
Because Tylose MHB 3000 P2 is water-soluble, it does not cause build-up on hair strands after repeated use of the product containing it.



PROPERTIES OF TYLOSE MHB 3000 P2:
● Good thickening / thickening efficiency
● Available in a wide range of molecular weight and viscosity
● Excellent properties as a water-retaining agent
● Excellent resistance to dissolved inorganic salts
● Excellent solution clarity
● Low toxicity and environmental protection



WHAT IS THE DIFFERENCE BETWEEN HPMC AND TYLOSE MHB 3000 P2?
HPMC and Tylose MHB 3000 P2 are modified cellulose forms that are mainly used as gelling agents for thickening properties in different items.
The key difference between HPMC and Tylose MHB 3000 P2 is that the gel temperature of HPMC is around 60 – 75 ℃ depending on the group content and different production techniques, whereas the gel temperature of MHEC is usually higher than 80 ℃.



KEY PROPERTIES OF TYLOSE MHB 3000 P2:
- Improves workability
- Reduce water absorption
- Increase adhesion strength



PHYSICAL PROPERTIES OF TYLOSE MHB 3000 P2:
Tylose MHB 3000 P2 appears to be white powder and is odorless and tasteless.
Tylose MHB 3000 P2 is featured by hygroscopicity and hardly soluble in hot water, acetone, ethanol and toluene.
In cold water Tylose MHB 3000 P2 will swell into colloidal solution and its solybility is not influenced by PH value.
Similar to methyl cellulose while being added to Hdroxyethyl groups.
Tylose MHB 3000 P2 is more resistant to saline, easily soluble in water and has higher gel temperature.



WHY TYLOSE MHB 3000 P2 IS BEING PREFERRED OVER HPMC FOR CELLULOSE ETHER?
Cellulose Ether is derived from Cellulose and is a water-soluble compound used in several industries.
It finds its usage mainly in the construction, food, pharmaceutical, and cosmetics industries.
Specifically, Cellulose Ether is primarily used in the construction sector as it acts as a binder, thickener, and water retention agent in construction.

There are different grades of Cellulose Ether, which have their applicability and properties.
The two primary grades of Cellulose Ether HPMC (Hydroxypropyl Methyl Cellulose) and Tylose MHB 3000 P2 have varied similarities, yet one is more preferred than the other in recent days.

Nowadays, Tylose MHB 3000 P2 grade of Cellulose Ether is more preferred than the HPMC grade in the construction industry.
Though, both are being utilized widely for increasing bond strength and water retention capacity of a dry mixture of cement and gypsum, few properties differentiate them.
The first property differentiating Tylose MHB 3000 P2 from HPMC is gel temperature; the gel temperature of MHEC is higher than that of Tylose MHB 3000 P2.

The gel temperature of HPMC is around 60°c - 70°c, which varies as per its content and production technique; however, the gel temperature of Tylose MHB 3000 P2 is generally more than 80°C, which makes it a better alternative.
Tylose MHB 3000 P2 has better thermal stability owing to its high gel temperature, causing better water retention capacity during summers in South Asian Countries.

Furthermore, Tylose MHB 3000 P2 has a more significant number of Hydrophilic groups in its structure, eventually leading to more hydrophilicity than the HPMC grade.
Having more Hydrophilic groups makes Tylose MHB 3000 P2 better in water retention, and hence it is preferred more.
In addition, the prices of Tylose MHB 3000 P2 grades have been lesser than that of HPMC, making them more economical to use.
In India, the prices of Cellulose Ether, with respective to all grades, have been marginally increasing from the first week of April.

According to ChemAnalyst, “Tylose MHB 3000 P2grade would be chosen over HPMC grade in countries including India as summers have already approached.
Construction industries would go for having cellulose ether with higher gel temperature and better hydrophilicity.
Furthermore, the Indian domestic market of Cellulose Ether is most likely to showcase stagnant to a marginal rise in the prices.”



PHYSICAL and CHEMICAL PROPERTIES of TYLOSE MHB 3000 P2:
Molecular Weight:858.9
Hydrogen Bond Donor Count:10
Hydrogen Bond Acceptor Count:24
Rotatable Bond Count:17
Exact Mass:858.39440297
Monoisotopic Mass:858.39440297
Topological Polar Surface Area:332
Heavy Atom Count:58
Complexity:884
Defined Atom Stereocenter Count:20
Covalently-Bonded Unit Count:3
Compound Is Canonicalized:Yes
Molecular Weight: 858.9
Hydrogen Bond Donor Count: 10
Hydrogen Bond Acceptor Count: 24
Rotatable Bond Count: 17
Exact Mass: 858.39440297
Monoisotopic Mass: 858.39440297
Topological Polar Surface Area: 332 Ų
Heavy Atom Count: 58
Formal Charge: 0
Complexity: 884
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 20
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 3
Compound Is Canonicalized: Yes
Appearance: White powder
Loss on drying: ≤5%
PH: 4.0-8.0



FIRST AID MEASURES of TYLOSE MHB 3000 P2:
-Description of first-aid measures:
*General advice:
Show this material safety data sheet to the doctor in attendance.
*If inhaled
After inhalation:
Fresh air.
Call in physician.
*In case of skin contact:
Take off immediately all contaminated lothing.
Rinse skin with water/ shower.
Consult a physician.
*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 TYLOSE MHB 3000 P2:
-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 TYLOSE MHB 3000 P2:
-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:
Remove container from danger zone and cool with water.
Prevent fire extinguishing water from contaminating surface water or the ground water system.



EXPOSURE CONTROLS/PERSONAL PROTECTION of TYLOSE MHB 3000 P2:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Safety glasses
*Skin protection:
Full contact:
Material: butyl-rubber
Minimum layer thickness: 0,7 mm
Break through time: 480 min
Splash contact:
Material: Chloroprene
Minimum layer thickness: 0,65 mm
Break through time: 240 min
*Body Protection:
Flame retardant antistatic protective clothing.
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of TYLOSE MHB 3000 P2:
-Precautions for safe handling:
*Advice on protection against fire and explosion:
Take precautionary measures against static discharge.
*Hygiene measures:
Change contaminated clothing.
Preventive skin protection recommended.
Wash hands after working with substance.
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Keep container tightly closed in a dry and well-ventilated place.



STABILITY and REACTIVITY of TYLOSE MHB 3000 P2:
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .
-Possibility of hazardous reactions:
No data available



SYNONYMS:
Cellulose,2-hydroxyethyl methyl ether
Hydroxyethyl methyl cellulose
Methyl hydroxyethyl cellulose
Culminal MHEC
Tylose MHB
Walocel MT 10.000GO
Walocel MKS 8.000PP11
Tylopur MH
Tylose MHB 1000
Tylose MHB 30000
Tylose MH 4000
Tylose MH 300P
Tylose MH 1000P
Tylose MH 1000
Tylose MH 2000
Tylose MH 50
Tylose MH 300
Tylose MH 2000P
Tylose MH 20
Tylose MH 4000P
Tylose MH
2-Hydroxyethyl methyl cellulose
Tylose MH 200XP
Tylose 4000
Tylose MH 200K
Tylose MHB 50
Unishot A 10
Tylose MH 2000XP
Metolose SEB 15T
Benecel ME 233P
SNB 100T
Culminal MHEC 15000PFF
Metolose SEB 02T
Tylose MH 10000K
Tylose MHB 3000P
Tylose MHB 3000
Tylose MG 50
Metolose SEB 30T
Metolose SEB 30000
Modocoll E 20
Modocoll E 100
SEW 04T
Tylose MH 6000XP
Cesca MHEC 6000PR
Metolose SEB 04T
Walocel MKX 30.000PF01
Metolose SEB 4000
Metolose SEW 4000
Tylopur MH 300
OMC 181
Metolose SE
Tylose MN
Metolose SEB 15000
Tylose MH 200KG4
Hymetellose
Culminal MHEC 300000PR
SHV-WF
Metolose SEW 30T
Tylose MH 200YP2
Tylose MH 10000
Culminal MHEC 40000
MH 4000
SNB
SNB (binder)
90SHV-WF
Walocel VP-M 20677
Tylose MG 15003P6
Tylose MH 50G4
Walocel MKX 60000PF01
Walocel MKX 40000PP01
Walocel VP-M 20678
Walocel MKX 45000
Walocel 400PFV
Marpolose ME 300000
Tylopur MH 50G4
Tylose MH 3001P6
SEB 4000
Culminal C 8315
Methocel 267
Metolose SNB 60T
Tylose MB 10000P6
Walocel MKX 20000PF40
Walocel MW 15000GB
Tylose MH 10000P6
Mecellose HEMC
51990-47-7
457603-24-6
1089092-83-0
1884332-09-5
2097341-71-2
2-hydroxyethyl methyl cellulose
Cellulose, 2-hydroxyethyl methyl ether
Methyl hydroxyethyl cellulose
9032-42-2
methyl 2-hydroxyethyl cellulose
ethane-1,2-diol
(2S,3R,4R,5S,6R)-2-(hydroxymethyl)-6-[(2S,3R,4S,5S,6S)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxane-3,4,5-triol
(2S,3S,4R,5S,6S)-2,3,4-trimethoxy-6-(methoxymethyl)-5-[(2R,3S,4R,5S,6S)-3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxyoxane

Hydroxyethyl cellulose; MHF 10015 P4; Cellulose, 2 - hydroxyethyl ether; hydroxyethyl cellulose ;Methyl 2-hydroxyethyl cellulosecas no: 9004-62-0

TYLOSE MHB 3000 YP2 is also named as methyl hydroxyethyl cellulose (MHEC). It is a white, grayish-white, or yellowish-white granules.It is a non-ionic cellulose ether derived from the addition of ethylene oxide to methylcellulose. It is produced from a natural renewable polymer such as wood pulp or cotton.TYLOSE MHB 3000 YP2 can be used as a highly efficient water retention agent, adhesives and film-forming agent, stabilizer, etc.It is widely used in different industrial applications such as oil drilling, construction, and building, paint and coating, pharmaceutical, etc.TYLOSE MHB 3000 YP2 can be modified according to customers’ requirement and still have its good anti-sagging property and good workability after modification. TYLOSE MHB 3000 YP2 provides many of the same benefits as other methylcellulose derivatives, such as the ability to efficiently thicken and provide water retention, These products, offered under the brand, are highly effective additives used to improve the quality and processing characteristics of building materials such as plasters and renders, mortars, tile adhesives, joint compounds and emulsion paints.These nonionic, water-soluble polymers can thicken, suspend, bind, emulsify, form films, stabilize, disperse, retain water, and provide protective colloid action. They are readily soluble in water and can be used to prepare solutions with a wide range of viscosities. They have outstanding tolerance for dissolved electrolytes. Application range - Tile adhesives - Skim coat - Tile grouts - Repair mortars - Self-leveling flooring compounds - Cement or gypsum-based mortars - Painting - Ceramics - Textile - Detergents Key properties -Improves water retention -Improves adhesive strength -Improves sag resistance -Improve construction efficiency Packaging and storage A. Standard packed in 25 KG per paper plastic composite bag B. Big bags or other special packages are possible on request Weight/20' container: approx. 10 metric tons with pallets, approx. 14 metric tons without pallets Weight/40' container: approx. 24 metric tons with pallets, approx. 26 metric tons without pallets Stored in its original packaging in a dry and place with temperature below 30℃. It is recommended to use SLEO® MHEC within 2 years. Safety notes The data presented above is in accordance with the present state of our knowledge, but doesn’t absolve the user from carefully checking it all immediately on receipt. We reserve the right to alter product constantly within the scope of technical progress or new developments. The recommendations made above should be checked by preliminary trials because of conditions during processing over which we have no control of, especially where other companies' raw materials are also being used. The working mechanism of methyl hydroxyethyl cellulose, MHEC (Mw = 2.5 · 105 g/mol, DSmethyl = 1.81, MShydroxyethyl = 0.15) as water retention agent in cement was investigated. First, the hydrocolloid was characterized and its performance as non-ionic water retention agent was determined employing the filter paper test. Also, water sorption and swelling of individual MHEC fibers under conditions of different humidities were monitored by ESEM imaging. Second, its working mechanism was established. It was found that at low dosages, MHEC achieves water retention by intramolecular sorption of water and concomitant swelling while at higher dosages, MHEC molecules agglomerate into large hydrocolloidal microgel particles (d > 1 μm) which effectively plug the pores in the mortar matrix. MHEC association was evidenced by an exponential increase in solution viscosity as concentration rises, a strong increase in the hydrodynamic diameter of solved MHEC molecules, and a noticeable reduction of surface tension. Related Categories Cellulose, Materials Science, Natural Polymers and Biopolymers, Polymer Science, Polymers More... extent of labeling 0.06-0.50 mol hydroxyethyl per mol cellulose (M.S.) 8 wt. % hydroxyethyl 26 wt. % methoxy 1.3-2.2 mol methyl per mol cellulose (D.S.) surface tension 45-55 dyn/cm, 20 °C, 0.1 wt. % viscosity 15,000-20,500 cP, 2 wt. % in H2O(20 °C, Brookfield, spindle #6) (20 rpm)(lit.) transition temp flocculation range 60-90 °C (0.5 wt. %) storage temp. room temp What is TYLOSE MHB 3000 YP2? TYLOSE MHB 3000 YP2 is also named as methyl hydroxyethyl cellulose (MHEC). It is a white, grayish-white, or yellowish-white granules.It is a non-ionic cellulose ether derived from the addition of ethylene oxide to methylcellulose. It is produced from a natural renewable polymer such as wood pulp or cotton.TYLOSE MHB 3000 YP2 can be used as a highly efficient water retention agent, adhesives and film-forming agent, stabilizer, etc.It is widely used in different industrial applications such as oil drilling, construction, and building, paint and coating, pharmaceutical, etc.TYLOSE MHB 3000 YP2 can be modified according to customers’ requirement and still have its good anti-sagging property and good workability after modification. Characteristics of TYLOSE MHB 3000 YP2 TYLOSE MHB 3000 YP2 has various features. They include: 1. Appearance TYLOSE MHB 3000 YP2 can be either white, pale yellow or yellowish-white, or grayish-white. It is also odorless. 2. Solubility TYLOSE MHB 3000 YP2 is soluble in water (cold or hot water). Although TYLOSE MHB 3000 YP2 is insoluble in the most organic solvent but soluble in a binary organic solvent and organic solvent water system. Its highest concentration depends on the viscosity and its solubility varies with viscosity. The lower the viscosity, the greater the solubility and vice versa. 3. PH stability TYLOSE MHB 3000 YP2 is stable within the range of 3.0 – 11.0 and its viscosity is hardly affected but a PH value out of this range will decrease its viscosity. 4. Metabolism TYLOSE MHB 3000 YP2 is an inert substance and its odorless. It is widely used in food and medicine applications due to its inability to undergo metabolism. 5. Surface Activity It can be used as a dispersant, protective agent, and emulsifier due to its surface-active function in an aqueous solution. 6. Mildew Resistance In the long term storage, TYLOSE MHB 3000 YP2 is a good mildew resistance due to its good viscosity stability.Its mildew resistance capacity is higher than the hydroxyethyl cellulose. 7. Water Retention TYLOSE MHB 3000 YP2 serves as an effective water retention agent due to its high viscosity in aqueous solution.Its water retention capacity is greater than the methylcellulose. 8. Ash Content Hot water washing is used in the preparation process of TYLOSE MHB 3000 YP2, thereby making the ash content very low. 9. Thermal Gel When the TYLOSE MHB 3000 YP2 solution is being heated to a certain temperature, it becomes less transparent with the formation of precipitate and gel but if cooled, it goes back to its original state of solution. Common Uses of TYLOSE MHB 3000 YP2 TYLOSE MHB 3000 YP2 can be used as: Ø Adhesive Ø Protective colloid Ø Thickening agent Ø Film-forming agent Ø Emulsifier Ø Lubricant Ø Suspending agent Industrial Applications of TYLOSE MHB 3000 YP2 TYLOSE MHB 3000 YP2 is widely used in different industries, which are: · Polymerization · Ceramic · Cosmetics · Construction · Food and Beverages · Pharmaceuticals · Paint and Coatings · Ink and Oil Drilling Summary TYLOSE MHB 3000 YP2 as said earlier is a derivative of methylcellulose. It is a non-ionic cellulose ether produced from the raw material of high purity cotton. Its odorless characteristics and inability to metabolize makes it widely used in food and medicine applications. TYLOSE MHB 3000 YP2 water retaining capacity and thickening ability makes it suitable for water-based latex painting, ink and oil drilling, construction materials, etc.As it is widely used in diverse applications, getting TYLOSE MHB 3000 YP2 from a reputable TYLOSE MHB 3000 YP2 supplier assures you of the best product for personal or industrial use.

Tylose MHF 10015 P4 is a water-soluble, non-ionic, modified methyl hydroxyethyl cellulose powder with standard etherification. It provides fast consistency development, very high sag resistance and water demand, moderate water retention and influence on cement hydration, and high heat stability. This grade of methyl hydroxyethyl cellulose (MHEC) is ideal for use in cement tile adhesives.

CAS NO: 9032-42-2
EC NO: 618-528-0

IUPAC NAMES
ethane-1,2-diol;(2S,3R,4R,5S,6R)-2-(hydroxymethyl)-6-[(2S,3R,4S,5S,6S)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxane-3,4,5-triol;(2S,3S,4R,5S,6S)-2,3,4-trimethoxy-6-(methoxymethyl)-5-[(2R,3S,4R,5S,6S)-3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxyoxane

SYNONYMS

9032-42-2
methyl 2-hydroxyethyl cellulose
METHYL HYDROXYETHYL CELLULOSE
METHYL 2-HYDROXYETHYL CELLULOSE
Hymetellose
Cellulose,2-hydroxyethylmethylether
'Tylose'® MH 300
Hydroxythyl Methyl Cellulose
HydroxythylMethylCellulose(Hemc)
HEMC
HYDROETHYLMETHYL CELLULOSE (HEMC)
METHYL HYDROXYETHYL CELLULOSE (20-40CPS: 2% IN WATER)
Methyl Hydroxyethyl Cellulose (20-40mPa.s, 2% in Water at 20deg C)
Methyl hydroxyethyl cellulose (20-40cps
(20-40MPa.s, 2% in Water at 20deg C)
Methyl Hydroxyethyl Cellulose
HEMC(Hydroxyethyl Methyl Cellulose)
Methyl Hydroxyethyl Cellulose (MHEC)
Methylhydroxyethylcellulose for synthesis
HYDROXYETHYL METHYL CELLULOSE
CELLULOSE METHYL HYDROXYETHYL ETHER
Hydroxyethyl Methyl Cellulose(Hemc)
METHYLHYDROXYETHYLCELLULOSE FOR SYNTHESI


Tylose MH 10015 P4
DOCUMENTS

Tylose MH 10015 P4 is a water soluble, nonionic, modified methylhydroxyethylcellulose powder with standard etherification. It provides rapid development of consistency, very high sag resistance and water demand, moderate water retention and influence on cement hydration, and high thermal stability. This grade of methylhydroxyethylcellulose (MHEC) is ideal for use in cement tile adhesives.


TYLOSE MHF 10015 P4

Areas of use for TYLOSE MHF 10015 P4:
In paint strippers
Friction fuel thickener

CELLULOSE ETER (HEC) HYDROXYETHYL CELLULOSE
TYLOSE MHF 10015 P4 is a nonionic cellulose ether which is produced using natural polymeric cellulose as a raw material and through a series of etherization reactions.

TYLOSE MHF 10015 P4
General detail
TYLOSE MHF 10015 P4 AREAS OF USE:

TYLOSE MHF 10015 P4 in the latex paint composition prevents gel from gelling, contributes to its dispersion, stabilizes the latex paint and increases the viscosity of the component. TYLOSE MHF 10015 P4 has good compatibility with other materials such as pigments, auxiliary substances, fillers and salts in its components.

Coatings thickened with TYLOSE MHF 10015 P4 have good rheology at different cutting speeds and are pseudoplastic.

The machinability and leveling properties of TYLOSE MHF 10015 P4 are good: brush, roller, sprayer and
can be applied with other construction methods; it doesn't drip, sag or bounce back easily.

TYLOSE MHF 10015 P4 high viscosity is primarily used as an adhesive for finishing and finishing fluids in oil drilling. TYLOSE MHF 10015 P4 low viscosity is used as a fluid loss additive. Among the various solutions required for drilling, finishing, cementing and crushing, TYLOSE MHF 10015 P4 offers good fluidity and mud stability.

TYLOSE MHF 10015 P4 is used as a binder, thickener, stabilizer and dispersant in toothpastes, detergents and cosmetics.

TYLOSE MHF 10015 P4 offers easy application thanks to its shear resistance and its binding effect in products thanks to its water retention function.
TYLOSE MHF 10015 P4 helps create movies.

TYLOSE MHF 10015 P4 CHARACTERISTICS:
TYLOSE MHF 10015 P4 has thickening, binding, dispersing, film-forming and suspending properties.

When the pH of TYLOSE MHF 10015 P4 aqueous solution is between 2 and 12, the viscosity is stable. If TYLOSE MHF 10015 P4 exceeds this range, acidic or alkaline oxidative degradation occurs and viscosity decreases.

The viscosity of TYLOSE MHF 10015 P4 aqueous solution decreases as the temperature increases and the viscosity can be recovered as the temperature drops to the original temperature. TYLOSE MHF 10015 P4 If there is no high salt concentration, no gel or precipitate will form when the solution is heated to the boiling point; TYLOSE MHF 10015 P4 is therefore very resistant to temperature.

TYLOSE MHF 10015 P4 aqueous solution is a nonionic system and can be used in other water soluble polymers, surfactants, salts, etc. can be found with. For this reason, TYLOSE MHF 10015 P4 is widely used in the daily chemical industry.

TYLOSE MHF 10015 P4 CAS number: 9032-42-2
TYLOSE MHF 10015 P4 Decorative mineral-based plasters
TYLOSE MHF 10015 P4 Tile adhesive, standard
TYLOSE MHF 10015 P4 Cement based trowel compounds
TYLOSE MHF 10015 P4 grout, cement-based
Chemical Properties-soluble in cold water, flocculates at elevated temperatures
Chemical Properties-A white, yellowish-white or grayish-white powder or granules, hygroscopic after drying.
Uses-Water retention aid, thickening agent, protective colloid, suspending agent, binder and stabilizer.
Pharmaceutical Applications-TYLOSE MHF 10015 P4 is used as an excipient in a wide range of pharmaceutical products, including oral tablets and suspensions, and topical gel preparations. It has similar properties to methylcellulose, but the hydroxyethyl groups make it more readily soluble in water and solutions are more tolerant of salts and have a higher coagulation temperature.
Safety-TYLOSE MHF 10015 P4 is used as an excipient in various oral and topical pharmaceutical preparations, and is generally regarded as an essentially nontoxic and nonirritant material.
storage-TYLOSE MHF 10015 P4 is hygroscopic and should therefore be stored under dry conditions away from heat.
Regulatory Status-GRAS listed. Included in nonparenteral medicines licensed in Europe (oral suspensions, tablets, and topical preparations).
TYLOSE MHF 10015 P4 is a thickening and gelling agent that comes from cellulose which is used in cleaning solutions and in cosmetics. 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.
1. Product identifier
Product form : Mixture
Product name : Tylose MHF 10015 P4
Product code : (MHEC_M-2)
1.2. Relevant identified uses of the substance or mixture and uses advised against
1.2.1. Relevant identified uses
Use of the substance/mixture : Rheological Additive
Special applications
Coating material
Additive for mortar
1.2.2. Uses advised against
Restrictions on use : There is no information available on applications that are not advised
SECTION 2: Hazards identification
2.1. Classification of the substance or mixture
Classification according to Regulation (EC) No. 1272/2008 [CLP]
Not classified
Adverse physicochemical, human health and environmental effects
No additional information available
2.2. Label elements
Handle in accordance with good industrial hygiene and safety practice.
2.3. Other hazards
Other hazards not contributing to the classification : Dust may form explosive mixture in air.
Physical state : Solid
Appearance : Powder.
Colour : whitish.
Odour : Odourless.
Odour threshold : No data available
pH : 6 - 8 10g/l
Relative evaporation rate (butylacetate=1) : Not specifically applicable
Melting point : Not specifically applicable
Freezing point : Not specifically applicable
Boiling point : Not specifically applicable
Flash point : Not specifically applicable
Auto-ignition temperature : > 170 °C
Decomposition temperature : No data available
Flammability (solid, gas) : No data available
Vapour pressure : Not specifically applicable
Vapour pressure at 50 °C : Not specifically applicable
Relative vapour density at 20 °C : Not specifically applicable
Relative density : Not specifically applicable
Density : 1.1 - 1.5 g/cm³ 20 °C
Solubility : Water: > 10 g/l @ 20°C
Log Pow : < 0
Viscosity, kinematic : Not specifically applicable
Viscosity, dynamic : Not specifically applicable
Explosive properties : Product is not explosive. Dust may form explosive mixture in air.
Tylose MHF 10015 P4
Persistence and degradability Product is biodegradable. Does not affect the functioning of waste-water treatment plants.
In case of loss of large quantities, advice local authorities.
Chemical oxygen demand (COD) < 1500 mg/g
Recommended fields of application

 Tile adhesives, premium Application performance

Consistency development: fast

Final consistency: very high

Sag resistance: very high

Water demand: very high

Water retention: moderate

Cement retardation: moderate

Heat stability: high

Application properties

Tylose MHF 10015 P4 is mainly recommended for premium cement based tile adhesives. It ensures sufficient water retention and gives very good adhesion strength. The special modification increases the thickening effect, improves the workability and leads to outstanding slip resistance and extra-long open time.

Packaging, storage and safety instructions

This Tylose type is supplied in multilayer paper bags with polyethylene intermediate layer and/or in big bags. When kept in clean, dry conditions in its original packing, Tylose can be stored for a long time. During storage a slow loss of viscosity can be measured. Tylose absorbs water from moist air. Once opened, container must be resealed and kept tightly closed. Like all fine particle organic substances, cellulose ethers constitute a dust explosion hazard.

Dust formation and deposits must be kept to a minimum so that no ignitable dust/air mixtures can form. Ignition sources such as naked flames, hot surfaces, sparks and static electricity should be avoided.

TYLOSE MHF 10015 P4 is also named as methyl hydroxyethyl cellulose (MHEC). It is a white, grayish-white, or yellowish-white granules.It is a non-ionic cellulose ether derived from the addition of ethylene oxide to methylcellulose. It is produced from a natural renewable polymer such as wood pulp or cotton.TYLOSE MHF 10015 P4 can be used as a highly efficient water retention agent, adhesives and film-forming agent, stabilizer, etc.It is widely used in different industrial applications such as oil drilling, construction, and building, paint and coating, pharmaceutical, etc.TYLOSE MHF 10015 P4 can be modified according to customers’ requirement and still have its good anti-sagging property and good workability after modification. TYLOSE MHF 10015 P4 provides many of the same benefits as other methylcellulose derivatives, such as the ability to efficiently thicken and provide water retention, These products, offered under the brand, are highly effective additives used to improve the quality and processing characteristics of building materials such as plasters and renders, mortars, tile adhesives, joint compounds and emulsion paints.These nonionic, water-soluble polymers can thicken, suspend, bind, emulsify, form films, stabilize, disperse, retain water, and provide protective colloid action. They are readily soluble in water and can be used to prepare solutions with a wide range of viscosities. They have outstanding tolerance for dissolved electrolytes. Application range - Tile adhesives - Skim coat - Tile grouts - Repair mortars - Self-leveling flooring compounds - Cement or gypsum-based mortars - Painting - Ceramics - Textile - Detergents Key properties -Improves water retention -Improves adhesive strength -Improves sag resistance -Improve construction efficiency Packaging and storage A. Standard packed in 25 KG per paper plastic composite bag B. Big bags or other special packages are possible on request Weight/20' container: approx. 10 metric tons with pallets, approx. 14 metric tons without pallets Weight/40' container: approx. 24 metric tons with pallets, approx. 26 metric tons without pallets Stored in its original packaging in a dry and place with temperature below 30℃. It is recommended to use SLEO® MHEC within 2 years. Safety notes The data presented above is in accordance with the present state of our knowledge, but doesn’t absolve the user from carefully checking it all immediately on receipt. We reserve the right to alter product constantly within the scope of technical progress or new developments. The recommendations made above should be checked by preliminary trials because of conditions during processing over which we have no control of, especially where other companies' raw materials are also being used. The working mechanism of methyl hydroxyethyl cellulose, MHEC (Mw = 2.5 · 105 g/mol, DSmethyl = 1.81, MShydroxyethyl = 0.15) as water retention agent in cement was investigated. First, the hydrocolloid was characterized and its performance as non-ionic water retention agent was determined employing the filter paper test. Also, water sorption and swelling of individual MHEC fibers under conditions of different humidities were monitored by ESEM imaging. Second, its working mechanism was established. It was found that at low dosages, MHEC achieves water retention by intramolecular sorption of water and concomitant swelling while at higher dosages, MHEC molecules agglomerate into large hydrocolloidal microgel particles (d > 1 μm) which effectively plug the pores in the mortar matrix. MHEC association was evidenced by an exponential increase in solution viscosity as concentration rises, a strong increase in the hydrodynamic diameter of solved MHEC molecules, and a noticeable reduction of surface tension. Related Categories Cellulose, Materials Science, Natural Polymers and Biopolymers, Polymer Science, Polymers More... extent of labeling 0.06-0.50 mol hydroxyethyl per mol cellulose (M.S.) 8 wt. % hydroxyethyl 26 wt. % methoxy 1.3-2.2 mol methyl per mol cellulose (D.S.) surface tension 45-55 dyn/cm, 20 °C, 0.1 wt. % viscosity 15,000-20,500 cP, 2 wt. % in H2O(20 °C, Brookfield, spindle #6) (20 rpm)(lit.) transition temp flocculation range 60-90 °C (0.5 wt. %) storage temp. room temp What is TYLOSE MHF 10015 P4? TYLOSE MHF 10015 P4 is also named as methyl hydroxyethyl cellulose (MHEC). It is a white, grayish-white, or yellowish-white granules.It is a non-ionic cellulose ether derived from the addition of ethylene oxide to methylcellulose. It is produced from a natural renewable polymer such as wood pulp or cotton.TYLOSE MHF 10015 P4 can be used as a highly efficient water retention agent, adhesives and film-forming agent, stabilizer, etc.It is widely used in different industrial applications such as oil drilling, construction, and building, paint and coating, pharmaceutical, etc.TYLOSE MHF 10015 P4 can be modified according to customers’ requirement and still have its good anti-sagging property and good workability after modification. Characteristics of TYLOSE MHF 10015 P4 TYLOSE MHF 10015 P4 has various features. They include: 1. Appearance TYLOSE MHF 10015 P4 can be either white, pale yellow or yellowish-white, or grayish-white. It is also odorless. 2. Solubility TYLOSE MHF 10015 P4 is soluble in water (cold or hot water). Although TYLOSE MHF 10015 P4 is insoluble in the most organic solvent but soluble in a binary organic solvent and organic solvent water system. Its highest concentration depends on the viscosity and its solubility varies with viscosity. The lower the viscosity, the greater the solubility and vice versa. 3. PH stability TYLOSE MHF 10015 P4 is stable within the range of 3.0 – 11.0 and its viscosity is hardly affected but a PH value out of this range will decrease its viscosity. 4. Metabolism TYLOSE MHF 10015 P4 is an inert substance and its odorless. It is widely used in food and medicine applications due to its inability to undergo metabolism. 5. Surface Activity It can be used as a dispersant, protective agent, and emulsifier due to its surface-active function in an aqueous solution. 6. Mildew Resistance In the long term storage, TYLOSE MHF 10015 P4 is a good mildew resistance due to its good viscosity stability.Its mildew resistance capacity is higher than the hydroxyethyl cellulose. 7. Water Retention TYLOSE MHF 10015 P4 serves as an effective water retention agent due to its high viscosity in aqueous solution.Its water retention capacity is greater than the methylcellulose. 8. Ash Content Hot water washing is used in the preparation process of TYLOSE MHF 10015 P4, thereby making the ash content very low. 9. Thermal Gel When the TYLOSE MHF 10015 P4 solution is being heated to a certain temperature, it becomes less transparent with the formation of precipitate and gel but if cooled, it goes back to its original state of solution. Common Uses of TYLOSE MHF 10015 P4 TYLOSE MHF 10015 P4 can be used as: Ø Adhesive Ø Protective colloid Ø Thickening agent Ø Film-forming agent Ø Emulsifier Ø Lubricant Ø Suspending agent Industrial Applications of TYLOSE MHF 10015 P4 TYLOSE MHF 10015 P4 is widely used in different industries, which are: · Polymerization · Ceramic · Cosmetics · Construction · Food and Beverages · Pharmaceuticals · Paint and Coatings · Ink and Oil Drilling Summary TYLOSE MHF 10015 P4 as said earlier is a derivative of methylcellulose. It is a non-ionic cellulose ether produced from the raw material of high purity cotton. Its odorless characteristics and inability to metabolize makes it widely used in food and medicine applications. TYLOSE MHF 10015 P4 water retaining capacity and thickening ability makes it suitable for water-based latex painting, ink and oil drilling, construction materials, etc.As it is widely used in diverse applications, getting TYLOSE MHF 10015 P4 from a reputable TYLOSE MHF 10015 P4 supplier assures you of the best product for personal or industrial use.

Hydroxyethyl cellulose; MHF 10016 P4; Cellulose, 2 - hydroxyethyl ether; hydroxyethyl cellulose ;Methyl 2-hydroxyethyl cellulose cas no: 9004-62-0

Hydroxyethyl cellulose; MHS 150003 P4; Cellulose, 2 - hydroxyethyl ether; hydroxyethyl cellulose ;Methyl 2-hydroxyethyl cellulose cas no: 9004-62-0

Tylose MHF 10016 P4 is a complex mixture of ethoxylated amylopectins ranging in molecular weight from 10 to 1,000 kDa (average molecular weight, ~450 kDa).
When infused as a 6% solution, Tylose MHF 10016 P4 approximates the activity of human albumin.
The larger molecular weights, however, increase Tylose MHF 10016 P4's intravascular residence time as well as its plasma expansion effects relative to albumin.

CAS: 9004-62-0
MF: C29H52O21
EINECS: 618-387-5

Tylose MHF 10016 P4 is synthetically produced, so it is degraded more slowly and is less antigenic than other colloids.
Despite these advantages, Tylose MHF 10016 P4 is quite expensive and also has no oxygen-carrying capacity.
Tylose MHF 10016 P4 is a commonly used cellulose ethers organic water-based ink thickening agent, belongs to a water-soluble non-ionic compound, with good water thickening ability, degraded by oxygen, acid and enzyme, under alkaline conditions can be crosslinked by Cu2 +.

Has thermal stability, when heated, does not appear gelation, does not occur precipitation under acidic conditions, the film-forming property is good, the aqueous solution can be made of a transparent film, can be derived from the reaction of alkali Tylose MHF 10016 P4 with ethylene oxide, having properties such as thickening, emulsifying, adhesive, suspension, film-forming, maintaining moisture and protectiving colloid.

The role of thickener in the aqueous ink is thickened.
The viscosity of the ink added a thickening agent increases, can improve the physical and chemical stability of the ink; due to the increased viscosity, rheology of the ink can be controlled at the time of printing; the pigment and filler in ink is not easy to precipitate, increasing the storage stability of the water-based ink.
Thickening agent is a cellulose-based material and (or) polyvinyl alcohol substances.
Tylose MHF 10016 P4 may be methyl cellulose, ethyl cellulose, hydroxymethyl cellulose, carboxymethyl cellulose, hydroxypropyl cellulose, Hydroxyethyl cellulose and hydroxypropylmethyl cellulose; polyvinyl alcohol material may be an or several species of polyethylene 400, 600, 800, 1000, 1600, 2000, 4000, 6000.

Tylose MHF 10016 P4 is a gelling and thickening agent derived from cellulose.
Tylose MHF 10016 P4 is widely used in cosmetics, cleaning solutions, and other household products.
Tylose MHF 10016 P4 and methyl cellulose are frequently used with hydrophobic drugs in capsule formulations, to improve the drugs' dissolution in the gastrointestinal fluids.
This process is known as hydrophilization.
Tylose MHF 10016 P4 is also used extensively in the oil and gas industry as a drilling mud additive under the name HEC as well in industrial applications, paint and coatings, ceramics, adhesives, emulsion polymerization, inks, construction, welding rods, pencils and joint fillers.

Tylose MHF 10016 P4 can be one of the main ingredients in water-based personal lubricants.
Tylose MHF 10016 P4 is also a key ingredient in the formation of large bubbles as it possesses the ability to dissolve in water but also provide structural strength to the soap bubble.
Among other similar chemicals, Tylose MHF 10016 P4 is often used as slime (and gunge, in the UK).
Tylose MHF 10016 P4 is a commonly used thickener in paint & coating formulations.
Tylose MHF 10016 P4 thickeners are used in paint & coating formulations to increase the viscosity of the paint and to improve its flow and leveling properties.

Tylose MHF 10016 P4 Chemical Properties
Melting point: 288-290 °C (dec.)
Density: 0.75 g/mL at 25 °C(lit.)
Storage temp.: 2-8°C
Solubility H2O: ≤5 wt. % at 20 °C
Form: powder
Color: Light brown powder
Odor: Odorless
PH: pH(20g/l,25℃) : 5.0～8.0
Water Solubility: almost transparency
Merck: 14,4673
Stability: Stable. Incompatible with strong oxidizing agents, acid chlorides, acid anhydrides
InChI: InChI=1S/C29H52O21/c1-10-15(34)16(35)24(13(8-33)45-10)49-28-20(39)18(37)25(50-29-26(43-5-4-30)21(40)23(42-3)12(7-32)47-29)14(48-28)9-44-27-19(38)17(36)22(41-2)11(6-31)46-27/h10-40H,4-9H2,1-3H3
InChIKey: CWSZBVAUYPTXTG-UHFFFAOYSA-N
CAS DataBase Reference: 9004-62-0(CAS DataBase Reference)
EPA Substance Registry System: Tylose MHF 10016 P4 (9004-62-0)

Tylose MHF 10016 P4 is white to yellowish fibrous or powdery solid, non-toxic, tasteless and soluble in water.
Insoluble in common organic solvents.
Having properties such as thickening, suspending, adhesive, emulsifying, dispersing, water holding.
Different viscosity range of solution can be prepared.
Having exceptionally good salt solubility to electrolyte.

Tylose MHF 10016 P4 is soluble in hot or cold water, and does not precipitate at high temperature or boiling, so it has a wide range of solubility and viscosity characteristics, as well as non-thermal gelling properties.
Tylose MHF 10016 P4 is a non-ionic polymer material , can coexist with a wide range of other water-soluble polymers, surfactants, and salts, and is an excellent colloidal thickener for high-concentration dielectric solutions.
The water retention capacity of Tylose MHF 10016 P4 is twice that of methyl cellulose, and it has better flow regulation; the dispersing ability of Tylose MHF 10016 P4 is comparable to that of methyl cellulose and hydroxypropyl methyl cellulose.
The specific dispersing ability is the worst, but the protective colloid ability is the strongest.
Tylose MHF 10016 P4 occurs as a white, yellowish-white or grayish-white, odorless and tasteless, hygroscopic powder.

Uses
1. Tylose MHF 10016 P4 is used for cracking method to extract polymerized dispersing agents such as oil water base gel fracturing fluid, polystyrene and polyvinyl chloride.
Also for latex thickening agent in paint industry, hygristor in electronics industry, cement anti-coagulant agent and water retention agent in construction industry.
Glazing in ceramic industry and toothpaste binder.
Also widely used in many aspects such as printing and dyeing, textile, paper, pharmaceutical, health, food, cigarettes, pesticides and fire extinguishing agent.

2. Used as a water-based drilling fluids, and thickening agent and filtrate reducer of completion fluids, thickening agent has obvious effect on brine drilling fluid.
Also can be used for filtrate reducer of oil well cement.
Cross-linking with the polyvalent metal ions into a gel.

3. As surfactants, protective colloids, emulsion stabilizers in combination with emulsion such as vinyl chloride, vinyl acetate emulsion, and a tackifier, dispersant, dispersion stabilizer of emulsion.
Tylose MHF 10016 P4 widely used in many aspects such as coatings, fibers, dyeing, paper, cosmetics, pharmaceuticals, pesticides.
There are many uses in oil exploitation and machinery industry.
4. As surfactants, latex thickening agent, protective colloid, oil exploitation fracturing fluid and polystyrene and polyvinyl chloride dispersing agents, etc.

Thickener, protective colloid, binder, stabilizer and suspending agent.
Tylose MHF 10016 P4 is a thickener, protective colloid, binder, stabilizer, and suspending agent.
Tylose MHF 10016 P4 is obtained from wood pulp Copyright 2014 Cengage Learning.
Tylose MHF 10016 P4 may not be copied, scanned, or duplicated, in whole or in part.
Due to electronic rights, some third party content may be suppressed from the eBook and/or eChapter(s).
Editorial Review has deemed that any suppressed content does not materially affect the overall learning experience.
Cengage Learning reserves the right to remove additional content at any time if subsequent rights restrictions require it or chemical cotton by treatment with an alkali.

Pharmaceutical Applications
Tylose MHF 10016 P4 is a nonionic, water-soluble polymer widely used in pharmaceutical formulations.
Tylose MHF 10016 P4 is primarily used as a thickening agent in ophthalmic and topical formulations, although it is also used as a binder and film-coating agent for tablets.
Tylose MHF 10016 P4 is present in lubricant preparations for dry eye, contact lens care, and dry mouth.
The concentration of Tylose MHF 10016 P4 used in a formulation is dependent upon the solvent and the molecular weight of the grade.
Tylose MHF 10016 P4 is also widely used in cosmetics.

Production methods
1. Alkali cellulose is a natural polymer, each of a fiber-based ring contains three hydroxyl groups, the most active hydroxyl reaction to give Tylose MHF 10016 P4.
The raw material cotton linter or refined pulp meal were immersed in 30% liquid caustic soda, took out to squeeze after half an hour.
Squeezed water containing soda to 1: 2.8, pulverized.
Pulverized alkali cellulose was added into the reaction kettle, sealed, vacuumized, nitrogen charge, repeated to vacuumize and nitrogen charge to replace atmosphere in the reaction kettle.
Precooled the liquid ethylene oxide was pressed into, cooling water was pumped in jacket of reaction kettle, controlled at about 25 ℃ and reacted for 2 h, crude product of Tylose MHF 10016 P4 was obtained.
The crude product was washed with alcohol, added acetic acid to adjust pH value to 4-6, added glyoxal to crosslink and aging.
Then washed with water, centrifugal dewatering, dryed, milled to obtain Tylose MHF 10016 P4.
Raw material consumption (kg/t) linter or low pulp meal 730-780 liquid caustic soda (30%) 2400 ethylene oxide 900 alcohol (95%) 4500 acetic acid 240 Glyoxal (40%) 100-300.

2. The raw material cotton linter or refined pulp meal were immersed in 30% liquid caustic soda, after half an hour took out to squeeze.
Squeezed water containing soda to 1: 2.8, pulverized alkali cellulose was added into the reaction kettle, sealed and vacuumized, nitrogen charge, used nitrogen to replace all atmosphere in the reaction kettle,Precooled the liquid ethylene oxide was pressed into.
In the cooling, controlled at 25 ℃ and reacted for 2 h, to give the crude product of crude Tylose MHF 10016 P4.
The crude product was washed with ethanol and acetic acid was added to adjust the pH value to 4-6. added glyoxal to crosslink and aging, washed with water fast, finally centrifugal dehydration, dried, milled, obtained low salt Tylose MHF 10016 P4.

Toxicology
Considered to be non toxic.
Use as a food additive indicates good tolerance of small amounts, but excessive amounts or overuse may bring irritant and /or harmful effects.
Polysaccharides are not substantially absorbed from the gastrointestinal tract but may produce a laxative effect.

Synonyms
Hydroxyethyl cellulose
9004-62-0
Hespan
Cellulose, 2-hydroxyethyl ether
2-Hydroxyethyl cellulose
5-[6-[[3,4-dihydroxy-6-(hydroxymethyl)-5-methoxyoxan-2-yl]oxymethyl]-3,4-dihydroxy-5-[4-hydroxy-3-(2-hydroxyethoxy)-6-(hydroxymethyl)-5-methoxyoxan-2-yl]oxyoxan-2-yl]oxy-6-(hydroxymethyl)-2-methyloxane-3,4-diol
Cellulosize
Cellosize
Natrosol
Cellosize QP
Cellosize WP
Tylose H series
Natrosol LR
Tylose P
Cellosize QP3
OETs
Tylose P-X
Tylose PS-X
Cellosize UT 40
Cellosize WP 09
Tylose P-Z series
Glutofix 600
Natrosol 150L
Natrosol 180HH
Natrosol 180L
Natrosol 240JR
Natrosol 250
Natrosol 250G
Natrosol 250H
Natrosol 250HHP
Natrosol 250HHR
Natrosol 250HR
Natrosol 250HX
Natrosol 250L
Natrosol 250M
Natrosol 250MH
Natrosol 300H
Hercules N 100
Hydroxyethyl-cellulose
Natrosol 250H4R
Cellosize WP 300
Tylose H 20
Fuji hec-BL 20
Caswell No. 487
Natrosol 250 HHR
Cellosize WP 300H
Cellosize WP 400H
Unicel QP 100MH
Tylose H 300
Cellosize QP 1500
Cellosize QP 4400
Cellosize WP 4400
Cellosize WPO 9H17
Unicel QP 300 H
Cellosize 4400H16
Cellosize QP 30000
UNII-12VCE9HR9E
UNII-7Q6P4JN1QT
UNII-B24JYI97VR
UNII-R33S7TK2EP
UNII-X70SE62ZAR
UNII-ZYD53NBL45
Hydroxyethyl cellulose ether
Hydroxyethyl ether cellulose
Hec-Al 5000
Unicel QP 52000 H
Hydroxyethyl cellulose [NF]
UNII-6OX6A5C7B6
UNII-S38J6RZN16
Walocel HT 6.000 PFV
UNII-273FM27VK1
UNII-2Q40985DRM
UNII-I2N4ZF9233
UNII-M825OX60H9
Cellulose 2-hydroxyethyl ether
HSDB 578
SCHEMBL23306563
UNII-8136Y38GY5
UNII-L605B5892V
Cellulose, 2- hydroxyethyl ether
Cellulose, ethylene oxide-grafted
DTXSID60873934
AH 15
BL 15
EPA Pesticide Chemical Code 046201
LS-146657
FT-0627136
J 164
H11622
2-Hydroxyethyl cellulose; Cellulose hydroxyethyl ether
2-O-(2-Hydroxyethyl)-4-O-methylhexopyranosyl-(1->4)-[4-O-methylhexopyranosyl-(1->6)]hexopyranosyl-(1->5)-2,6-anhydro-1-deoxyheptitol

Tylose MHS 150003 P4 is a commonly used cellulose ethers organic water-based ink thickening agent, belongs to a water-soluble non-ionic compound, with good water thickening ability, degraded by oxygen, acid and enzyme, under alkaline conditions can be crosslinked by Cu2 +.

CAS NO : 9004-62-0
EC NO :618-387-5

IUPAC NAME
5-[6-[[3,4-dihydroxy-6-(hydroxymethyl)-5-methoxyoxan-2-yl]oxymethyl]-3,4-dihydroxy-5-[4-hydroxy-3-(2-hydroxyethoxy)-6-(hydroxymethyl)-5-methoxyoxan-2-yl]oxyoxan-2-yl]oxy-6-(hydroxymethyl)-2-methyloxane-3,4-diol

SYNONYMS

Hetastarch
9004-62-0
Hespan
5-[6-[[3,4-dihydroxy-6-(hydroxymethyl)-5-methoxyoxan-2-yl]oxymethyl]-3,4-dihydroxy-5-[4-hydroxy-3-(2-hydroxyethoxy)-6-(hydroxymethyl)-5-methoxyoxan-2-yl]oxyoxan-2-yl]oxy-6-(hydroxymethyl)-2-methyloxane-3,4-diol
Plasmasteril
Pentaspan
Hespander
Onkohas
Voluven
Hespander injection
HAS [German]
Penford 260
Penford 280
Penford 290
Ethylex gum 2020
Penford P 208
Essex gum 1360
Essex 1360
Hetastarch [USAN:BAN]
Pentastarch [USAN:BAN]
O-(2-Hydroxyethyl)starch
Hydroxyathylstarke [German]
2-Hydroxyethyl starch ether
Starch 2-hydroxyethyl ether
Tapioca starch hydroxyethyl ether
ASL 607
DTXSID60873934
VZ36173
LS-146657
FT-0627136
2-O-(2-Hydroxyethyl)-4-O-methylhexopyranosyl-(1->4)-[4-O-methylhexopyranosyl-(1->6)]hexopyranosyl-(1->5)-2,6-anhydro-1-deoxyheptitol
2-hydroxyethylcelluloseether;ah15;aw15(polysaccharide);aw15[polysaccharide];bl15;cellosize;The blood coHydroxyethyl cellulose etherngeals the appearance board;5-[6-[[3,4-dihydroxy-6-(hydroxymethyl)-5-methoxyoxan-2-yl]oxymethyl]-3,4-dihydroxy-5-[4-hydroxy-3-(2-hydroxyethoxy)-6-(hydroxymethyl)-5-methoxyoxan-2-yl]oxyoxan-2-yl]oxy-6-(hydroxymethyl)-2-methyloxane-3,4-diol
HYPROMELLOSE
Hydroxypropyl Methylcellulose
K100M USP Grade
9004-65-3 Active CAS-RN
Cellulose, 2-hydroxypropyl methyl ether
2-Hydroxypropyl methyl cellulose
2-Hydroxypropyl methyl cellulose ether
2-Hydroxypropyl cellulose methyl ether
Hydroxypropylmethylcellulosum
Isopto alkaline
Isopto plain
Isopto Tears
Methocel E,F,K
Methyl cellulose, propylene glycol ether
Methylhydroxypropylcellulosum
Metolose
Tearisol
Hipromelosa
Hypromellosum
Hydroxypropyl methyl cellulose (464)
cellulose hydroxypropyl methyl ether
cellulose,
2-hydroxypropyl methyl ether
2-hydroxypropyl cellulose methyl ether
2-hydroxypropyl methyl cellulose
hydroxypropyl methylcellulose
hydroxypropylmethyl cellulose
hydroxypropylmethylcellulose
hydroxypropylmethylcellulosum
methyl cellulose,
propylene glycol ether
methyl hydroxypropyl cellulose
methylhydroxypropylcellulose
methylhydroxypropylcellulosum
E464, hydroxypropyl methylcellulose, HPMC
hypromellose(noun)
Hydroxypropyl methylcellulose,


TYLOSE MHS 150003 P4

Thickeners and binders
TYLOSE MHS 150003 P4 is a commonly used cellulose ethers organic water-based ink thickening agent, belongs to a water-soluble non-ionic compound, with good water thickening ability, degraded by oxygen, acid and enzyme, under alkaline conditions can be crosslinked by Cu2 +. Has thermal stability, when heated, does not appear gelation, does not occur precipitation under acidic conditions, the film-forming property is good, the aqueous solution can be made of a transparent film, can be derived from the reaction of alkali cellulose with ethylene oxide, having properties such as thickening, emulsifying, adhesive, suspension, film-forming, maintaining moisture and protectiving colloid. The role of thickener in the aqueous ink is thickened. The viscosity of the ink added a thickening agent increases, can improve the physical and chemical stability of the ink; due to the increased viscosity, rheology of the ink can be controlled at the time of printing; the pigment and filler in ink is not easy to precipitate, increasing the storage stability of the water-based ink.
Thickening agent is a cellulose-based material and (or) polyvinyl alcohol substances. Cellulose substances may be methyl cellulose, ethyl cellulose, hydroxymethyl cellulose, carboxymethyl cellulose, hydroxypropyl cellulose, Hydroxyethyl cellulose and hydroxypropylmethyl cellulose; polyvinyl alcohol material may be an or several species of polyethylene 400, 600, 800, 1000, 1600, 2000, 4000, 6000.

Chemical properties
This product is white to yellowish fibrous or powdery solid, non-toxic, tasteless and soluble in water. Insoluble in common organic solvents. Having properties such as thickening, suspending, adhesive, emulsifying, dispersing, water holding. Different viscosity range of solution can be prepared. Having exceptionally good salt solubility to electrolyte.

Uses
1. TYLOSE MHS 150003 P4 is used for cracking method to extract polymerized dispersing agents such as oil water base gel fracturing fluid, polystyrene and polyvinyl chloride. Also for latex thickening agent in paint industry, hygristor in electronics industry, cement anti-coagulant agent and water retention agent in construction industry. Glazing in ceramic industry and toothpaste binder. Also widely used in many aspects such as printing and dyeing, textile, paper, pharmaceutical, health, food, cigarettes, pesticides and fire extinguishing agent.
2. Used as a water-based drilling fluids, and thickening agent and filtrate reducer of completion fluids, thickening agent has obvious effect on brine drilling fluid. Also can be used for filtrate reducer of oil well cement. Cross-linking with the polyvalent metal ions into a gel.
3. As surfactants, protective colloids, emulsion stabilizers in combination with emulsion such as vinyl chloride, vinyl acetate emulsion, and a tackifier, dispersant, dispersion stabilizer of emulsion. Widely used in many aspects such as coatings, fibers, dyeing, paper, cosmetics, pharmaceuticals, pesticides. There are many uses in oil exploitation and machinery industry.
4. As surfactants, latex thickening agent, protective colloid, oil exploitation fracturing fluid and polystyrene and polyvinyl chloride dispersing agents, etc.
Production methods
1. Alkali cellulose is a natural polymer, each of a fiber-based ring contains three hydroxyl groups, the most active hydroxyl reaction to give Tylose MHS 150003 p4. The raw material cotton linter or refined pulp meal were immersed in 30% liquid caustic soda, took out to squeeze after half an hour. Squeezed water containing soda to 1: 2.8, pulverized. Pulverized alkali cellulose was added into the reaction kettle, sealed, vacuumized, nitrogen charge, repeated to vacuumize and nitrogen charge to replace atmosphere in the reaction kettle. Precooled the liquid ethylene oxide was pressed into, cooling water was pumped in jacket of reaction kettle, controlled at about 25 ℃ and reacted for 2 h, crude product of Tylose MHS 150003 p4. was obtained. The crude product was washed with alcohol, added acetic acid to adjust pH value to 4-6, added glyoxal to crosslink and aging. Then washed with water, centrifugal dewatering, dryed, milled to obtain Tylose MHS 150003 p4. Raw material consumption (kg/t) linter or low pulp meal 730-780 liquid caustic soda (30%) 2400 ethylene oxide 900 alcohol (95%) 4500 acetic acid 240 Glyoxal (40%) 100-300.
2. The raw material cotton linter or refined pulp meal were immersed in 30% liquid caustic soda, after half an hour took out to squeeze. Squeezed water containing soda to 1: 2.8, pulverized alkali cellulose was added into the reaction kettle, sealed and vacuumized, nitrogen charge, used nitrogen to replace all atmosphere in the reaction kettle,Precooled the liquid ethylene oxide was pressed into. In the cooling, controlled at 25 ℃ and reacted for 2 h, to give the crude product of crude Tylose MHS 150003 p4. The crude product was washed with ethanol and acetic acid was added to adjust the pH value to 4-6. added glyoxal to crosslink and aging, washed with water fast, finally centrifugal dehydration, dried, milled, obtained low salt Tylose MHS 150003 p4.
Description
Hetastarch, another nonproteinaceous colloid, is a complex mixture of ethoxylated amylopectins ranging in molecular weight from 10 to 1,000 kDa (average molecular weight, ~450 kDa). When infused as a 6% solution, hetastarch approximates the activity of human albumin. The larger molecular weights, however, increase its intravascular residence time as well as its plasma expansion effects relative to albumin.
Hetastarch is synthetically produced, so it is degraded more slowly and is less antigenic than other colloids. Despite these advantages, hetastarch is quite expensive and also has no oxygen-carrying capacity.
Chemical Properties
light yellow powder
Chemical Properties
TYLOSE MHS 150003 P4 occurs as a white, yellowish-white or grayish-white, odorless and tasteless, hygroscopic powder.
Uses
TYLOSE MHS 150003 P4 is a thickener, protective colloid, binder, stabilizer, and suspending agent. It is obtained from wood pulp Copyright 2014 Cengage Learning. All Rights Reserved. May not be copied, scanned, or duplicated, in whole or in part. Due to electronic rights, some third party content may be suppressed from the eBook and/or eChapter(s). Editorial Review has deemed that any suppressed content does not materially affect the overall learning experience. Cengage Learning reserves the right to remove additional content at any time if subsequent rights restrictions require it. or chemical cotton by treatment with an alkali.
Pharmaceutical Applications
TYLOSE MHS 150003 P4 is a nonionic, water-soluble polymer widely used in pharmaceutical formulations. It is primarily used as a thickening agent in ophthalmic and topical formulations, although it is also used as a binder and film-coating agent for tablets.It is present in lubricant preparations for dry eye, contact lens care, and dry mouth.
The concentration of TYLOSE MHS 150003 P4 used in a formulation is dependent upon the solvent and the molecular weight of the grade.
TYLOSE MHS 150003 P4 is also widely used in cosmetics.
storage
TYLOSE MHS 150003 P4 powder is a stable though hygroscopic material.
Aqueous solutions of hydroxyethyl cellulose are relatively stable at pH 2–12 with the viscosity of solutions being largely unaffected. However, solutions are less stable below pH 5 owing to hydrolysis. At high pH, oxidation may occur.
Increasing the temperature reduces the viscosity of aqueous TYLOSE MHS 150003 P4 solutions. However, on cooling, the original viscosity is restored. Solutions may be subjected to freeze–thawing, high-temperature storage, or boiling without precipitation or gelation occurring.
TYLOSE MHS 150003 P4 is subject to enzymatic degradation, with consequent loss in viscosity of its solutions. Enzymes that catalyze this degradation are produced by many bacteria and fungi present in the environment. For prolonged storage, an antimicrobial preservative should therefore be added to aqueous solutions. Aqueous solutions of TYLOSE MHS 150003 P4 may also be sterilized by autoclaving.
TYLOSE MHS 150003 P4 powder should be stored in a well-closed container, in a cool, dry place.

Incompatibilities
TYLOSE MHS 150003 P4 is insoluble in most organic solvents. It is incompatible with zein and partially compatible with the following water-soluble compounds: casein; gelatin; methylcellulose; polyvinyl alcohol, and starch.
TYLOSE MHS 150003 P4 can be used with a wide variety of watersoluble antimicrobial preservatives. However, sodium pentachlorophenate produces an immediate increase in viscosity when added to hydroxyethyl cellulose solutions.
TYLOSE MHS 150003 P4 has good tolerance for dissolved electrolytes, although it may be salted out of solution when mixed with certain salt solutions. For example, the following salt solutions will precipitate a 10% w/v solution of Cellosize WP-09 and a 2% w/v solution of Cellosize WP-4400: sodium carbonate 50% and saturated solutions of aluminum sulfate; ammonium sulfate; chromic sulfate; disodium phosphate; magnesium sulfate; potassium ferrocyanide; sodium sulfate; sodium sulfite; sodium thiosulfate; and zinc sulfate.
Natrosol is soluble in most 10% salt solutions, excluding sodium carbonate and sodium sulfate, and many 50% salt solutions with the exception of the following: aluminum sulfate; ammonium sulfate; diammonium phosphate; disodium phosphate; ferric chloride; magnesium sulfate; potassium ferrocyanide; sodium metaborate; sodium nitrate; sodium sulfite; trisodium phosphate; and zinc sulfate. Natrosol 150 is generally more tolerant of dissolved salts than is Natrosol 250.
TYLOSE MHS 150003 P4 is also incompatible with certain fluorescent dyes or optical brighteners, and certain quaternary disinfectants which will increase the viscosity of aqueous solutions.
Information on basic physical and chemical properties
TYLOSE MHS 150003 P4 Physical state : Solid
TYLOSE MHS 150003 P4 Appearance : Powder.
TYLOSE MHS 150003 P4 Colour : whitish.
TYLOSE MHS 150003 P4 Odour : Odourless.
TYLOSE MHS 150003 P4 Odour threshold : No data available
TYLOSE MHS 150003 P4 pH : 6 - 8 10g/l
TYLOSE MHS 150003 P4 Relative evaporation rate (butylacetate=1) : Not specifically applicable
TYLOSE MHS 150003 P4 Melting point : Not specifically applicable
TYLOSE MHS 150003 P4 Freezing point : Not specifically applicable
TYLOSE MHS 150003 P4 Boiling point : Not specifically applicable
TYLOSE MHS 150003 P4 Flash point : Not specifically applicable
TYLOSE MHS 150003 P4 Auto-ignition temperature : > 170 °C
TYLOSE MHS 150003 P4 Decomposition temperature : No data available
TYLOSE MHS 150003 P4 Flammability (solid, gas) : No data available
TYLOSE MHS 150003 P4 Vapour pressure : Not specifically applicable
TYLOSE MHS 150003 P4 Vapour pressure at 50 °C : Not specifically applicable
TYLOSE MHS 150003 P4 Relative vapour density at 20 °C : Not specifically applicable
TYLOSE MHS 150003 P4 Relative density : Not specifically applicable
TYLOSE MHS 150003 P4 Density : 1.1 - 1.5 g/cm³ 20 °C
TYLOSE MHS 150003 P4 Solubility : Water: > 10 g/l @ 20°C
TYLOSE MHS 150003 P4 Log Pow : < 0
TYLOSE MHS 150003 P4 Viscosity, kinematic : Not specifically applicable
TYLOSE MHS 150003 P4 Viscosity, dynamic : Not specifically applicable
TYLOSE MHS 150003 P4 Explosive properties : Product is not explosive. Dust may form explosive mixture in air.
TYLOSE MHS 150003 P4 Oxidising properties : No data available
TYLOSE MHS 150003 P4 Lower explosive limit (LEL) : 30 g/m³
TYLOSE MHS 150003 P4 Minimum ignition energy : > 10 mJ
TYLOSE MHS 150003 P4 Bulk density : 200 - 600 g/l
TYLOSE MHS 150003 P4 Conbustion class : 5
TYLOSE MHS 150003 P4 Smst explosion category : ST1
TYLOSE MHS 150003 P4 KSt : < 200 bar*m/s

Tylose MHS 150003 P4
Persistence and degradability Product is biodegradable. Does not affect the functioning of waste-water treatment plants.
In case of loss of large quantities, advice local authorities.
Chemical oxygen demand (COD) < 1500 mg/g
Tylose MHS 150003 P4
Log Pow < 0
Bioaccumulative potential Not potentially bioaccumulable

Tylose MHS 150003 P4 is a water-soluble, non-ionic, highly etherified, modified methyl hydroxyethyl cellulose powder. It provides very fast consistency development, high water demand, water retention, and heat stability, and moderate sag resistance and influence on cement hydration. This grade of methyl hydroxyethyl cellulose (MHEC) is ideal for use in block laying adhesives and gypsum mounting binders and spray plasters.
Recommended fields of application

 Plasters, gypsum based Thin layer plasters, gypsum based Gypsum-Lime-Plasters Tile adhesives

Application performance

Consistency development: very fast

Water retention: very high

Final consistency: moderate

Influence on cement hydration: moderate

Sag resistance: moderate

Heat stability: high

Water demand: high

Packaging, Storage, Safety instructions Packaging, Storage, Safety instructions Like all fine-particle organic substances, cellulose ethers constitute a dust explosion hazard. Dust formation and deposits must be kept to a minimum so that no ignitable dust/air mixtures can form. Ignition sources such as naked flames, hot surfaces, sparks and static electricity should be avoided. Tylose starts to decompose at about 200°C. Its ignition temperature is >360°C.

Tylose burns easily and the fire may spread. When stored in closed containers, or in its original packaging in a dry place. at room temperature, Tylose can be kept for a long time. In the case of high viscosity grades, a slow loss of viscosity can be measured after lengthy storage (>1 year). Tylose absorbs water from moist air. Once opened, container must be resealed and kept tightly closed. This Tylose-type is supplied in multi-ply paper bags with polyethylene intermediate layer and/or in big bags.
Application Performance
Consistent development of Tylose MHS 150009 P4: fast Water retention: very high
Final consistency of Tylose MHS 150009 P4: moderate Effect on cement hydration: medium
Tylose MHS 150009 P4 sag resistance: medium Heat stability: high
Water demand: high
Packaging, Storage, Safety instructions Packaging, Storage, Safety instructions Tylose MHS 150009 P4
Like all fine organic matter, Tylose MHS 150009 P4 poses a dust explosion hazard. Dust formation
Deposits should be kept to a minimum so that no sediment / air mixture can form. Sources of ignition
naked flames, hot surfaces, sparks and static electricity should be avoided. Tylose also begins to decompose
approx. 200 ° C. Ignition temperature> 360 ° C. Tylose MHS 150009 P4 easily burns and a fire could occur.
When Tylose MHS 150009 P4 is stored in closed containers or in its original packaging in a dry place at room temperature,
should be stored for a long time. In case of high viscosity grades, a slow loss of viscosity
long-term storage (> 1 year). Tylose absorbs water from moist air. After opening, the container should be closed and
it is kept tightly closed.
Tylose MHS 150009 P4 Effect on cement hydration: medium
Tylose MHS 150009 P4 Heat stability: high
Tylose MHS 150009 P4 Recommended Application Areas
Tylose MHS 150009 P4 Used in building materials.
Tylose MHS 150009 P4 is used as block flooring adhesive.
Tylose MHS 150009 P4 Used as plaster mounting binders.
Tylose MHS 150009 P4 Used in gypsum spray plaster.
TYLOSE MHS ​​150009 P4 Usage Areas:
Gypsum-based hand and machine plasters
Gypsum-based satin (thin layer) plaster
Gypsum-Lime based plasters
Tile adhesives
Gypsum Based Hand and Machine Plasters
Product Name Chemical Description Uses
TYLOSE MH 10.001 P4 Methyl Hydroxy Ethyl Cellulose Höppler falling ball viscometer 10.000 mPas Decorative mineral based plasters, Smooth block adhesives, Tile adhesives, Exterior coating and insulation systems
TYLOSE MH 10.007 P4 Methyl Hydroxy Ethyl Cellulose Höppler falling ball viscometer 10.000 mPas Decorative mineral based plasters, Smooth block adhesives, Tile adhesives, Exterior coating and insulation systems
TYLOSE MH 15.000 P4 Methyl Hydroxy Ethyl Cellulose Höppler falling ball viscometer 15.000 mPas Ready-mixed concrete joint fillers, Tile adhesives Exterior coating and insulation systems, Gypsum-based joint compounds, Insulation Plasters
TYLOSE MH 15.002 P6 Methyl Hydroxy Ethyl Cellulose Höppler falling ball viscometer 15.000 mPas Cement-lime based plaster, Gypsum-Lime based plaster, Smooth block adhesive, Exterior Coating and insulation systems, thin layer plaster, Repair plaster
TYLOSE MH 2.000 YP2 Methyl Hydroxy Ethyl Cellulose Höppler falling ball viscometer 2.000 mPas Cement based screed plaster, Repair plasters, Cement based plasters
TYLOSE MH 30.000 P4 Methyl Hydroxy Ethyl Cellulose Höppler falling ball viscometer 30.000 mPas Cement Based plaster compounds, Masonry Mortars, Ready mixed concrete joint filler, Cement based paints
TYLOSE MH 6.000 YP4 Methyl Hydroxy Ethyl Cellulose Höppler falling ball viscometer 6.000 mPas Cement based screed plaster, Cement based Plaster compounds Decorative surface coatings
TYLOSE MH 60.004 P6 Methyl Hydroxy Ethyl Cellulose Höppler falling ball viscometer 60.000 mPas. Tile adhesives, cement-based hand plasters, cement-lime-based plasters, gypsum-based plasters.
TYLOSE MH 60.027 P6 Methyl Hydroxy Ethyl Cellulose Höppler falling ball viscometer 60.000 mPas. Tile adhesives, cement-based hand plasters, cement-lime-based plasters, gypsum-based plasters.
TYLOSE MH 60.028 P6 Methyl Hydroxy Ethyl Cellulose Höppler falling ball viscometer 60.000 mPas. Tile adhesives, cement-based hand plasters, cement-lime-based plasters, gypsum-based plasters and sheathing products.
TYLOSE MH 150009 P4 Methyl Hydroxy Ethyl Cellulose.
TYLOSE MH 150009 P4 Physical State: Free Powder
TYLOSE MH 150009 P4 Humidity: ≤ 6%
TYLOSE MH 150009 P4 NaCl content: ≤ 1.5%
TYLOSE MH 150009 P4 Grain size: <100μm: min. 90%
TYLOSE MH 150009 P4 Grain size: <63μm: min. 65%

Hydroxyethyl cellulose; MHS 150009 P4; Cellulose, 2 - hydroxyethyl ether; hydroxyethyl cellulose ;Methyl 2-hydroxyethyl cellulose cas no: 9004-62-0

Tylose MHS 150009 P4 is a water soluble substance. Tylose MHS 150009 P4 is non-ionic. Tylose MHS 150009 P4 is highly etherified. Tylose MHS 150009 P4 is a modified methyl hydroxyethyl cellulose powder.

CAS NO 9004-62-0
SYNONYMS:
2-Hydroxyethyl cellulose;2-Hydroxyethyl cellulose ether;AH 15;AW 15 (Polysaccharide);BL 15;Caswell No. 487;Cellosize4400H16;Cellosize QP;Cellosize QP 1500;Cellosize QP 30000;Cellosize QP 4400;Cellosize QP3;Cellosize UT 4;Cellosize WP;Cellosize WP 09;Cellosize WP 300;Cellosize WP 300H;Cellosize WP 400H;Cellosize WP 4400;Cellosize WPO 9H17;Cellulose 2-hydroxyethyl ether;Cellulose hydroxyethyl ether;Cellulose hydroxyethylate;Cellulose, 2-hydroxyethyl ether;Cellulose, ethylene oxide-grafted;Cellulosize;EPA Pesticide Chemical Code 046201;Fuji hec-BL 20;Glutofix 600;HEC;Hec-Al 5000;Hespan;HSDB 578;Hydroxyethyl cellulose;Hydroxyethyl cellulose ether;Hydroxyethyl ether cellulos;Hydroxyethylcellulose;Hyetellos;Natrosol;Natrosol 150L;Natrosol 180HH;Natrosol 180L;Natrosol 250;Natrosol 250 HHR;Natrosol 250G;Natrosol 250H;Natrosol 250H4R;Natrosol 250HHP;Natrosol 250HHR;Natrosol 250HR;Natrosol 250HX;Natrosol 250L;Natrosol 250M;Natrosol 250MH;Natrosol 300H;Natrosol LR;OETs;Oxirane, polymer with cellulose;Tylose H 20;Tylose300;Tylose H series;tylose P;Tylose P-X;Tylose P-Z series;Tylose PS-X;Unicel QP 100MH;Unicel QP 300 H;Unicel QP 52000 H;UNII-12VCE9HR9E;UNII-2Q40985DRM;UNII-6OX6A5C7B6;UNII-7Q6P4JN1QT;UNII-8136Y38GY5;UNII-B24JYI97VR;UNII-I2N4ZF9233;UNII-L605B5892V;UNII-M825OX60H9;UNII-S38J6RZN16;UNII-T4V6TWG28D;UNII-X70SE62ZA;UNII-ZYD53NBL45;Walocel HT 6.000 PFV;Tylose MHS 150009 P4
Hetastarch;9004-62-0;5-[6-[[3,4-dihydroxy-6-(hydroxymethyl)-5-methoxyoxan-2-yl]oxymethyl]-3,4-dihydroxy-5-[4-hydroxy-3-(2-hydroxyethoxy)-6-(hydroxymethyl)-5-methoxyoxan-2-yl]oxyoxan-2-yl]oxy-6-(hydroxymethyl)-2-methyloxane-3,4-diol;DTXSID60873934;VZ36173;FT-0627136;2-O-(2-Hydroxyethyl)-4-O-methylhexopyranosyl-(1->4)-[4-O-methylhexopyranosyl-(1->6)]hexopyranosyl-(1->5)-2,6-anhydro-1-deoxyheptitol
2-hydroxyethylcelluloseether
ah15
aw15(polysaccharide)
aw15[polysaccharide]
bl15
cellosize
The blood coHydroxyethyl cellulose etherngeals the appearance board
5-[6-[[3,4-dihydroxy-6-(hydroxymethyl)-5-methoxyoxan-2-yl]oxymethyl]-3,4-dihydroxy-5-[4-hydroxy-3-(2-hydroxyethoxy)-6-(hydroxymethyl)-5-methoxyoxan-2-yl]oxyoxan-2-yl]oxy-6-(hydroxymethyl)-2-methyloxane-3,4-diol
2-HYDROXYETHYL CELLULOSE
Natrosol L 250
hydrdoxyethyl cellulose
2-HYDROXYETHYL CELLULOSE, AVERAGE MV CA. 90,000
2-HYDROXYETHYL CELLULOSE, AVERAGE MV CA. 1,300,000
HYDROXYETHYL-CELLULOSE 90'000-105'000
2-HYDROXYETHYL CELLULOSE, AVERAGE MV CA. 720,000
HydroxyethylCelluloseHighViscosity(200)
HydroxyethylCellulose(Hec),Cas
HYDROXYETHYL CELLULOSE (HEC)
NATROSOL(R)250
hydroxyethy cellulolse
HYDROXYETHYL CELLULOSE: 200-300CPS (2% IN WATER)
Hydroxyethyl Cellulose (200-300mPa.s, 2% in Water at 20deg C)
Hydroxyethyl Cellulose (4,500-6,500mPa.s, 2% in Water at 25deg C)
Hydroxyethyl Cellulose (800-1,500mPa.s, 2% in Water at 20deg C)
HYDROXYETHYLCELLULOSE,100CPS,NF
HYDROXYETHYLCELLULOSE,2000CPS,NF
HYDROXYETHYLCELLULOSE,3,400CPS
HYDROXYETHYLCELLULOSE,5,000CPS
HYDROXYETHYLCELLULOSE,5,000CPS,NF
2-Hydroxyethyl cellulose, hydrophobically modified
cellosize4400h16
cellosizeqp
cellosizeqp1500
cellosizeqp3
cellosizeqp30000
cellosizeqp4400
cellosizeut40
cellosizewp
cellosizewp09
cellosizewp300
cellosizewp300h
cellosizewp400h
cellosizewp4400
cellosizewpo9h17
cellulose,ethyleneoxide-grafted
cellulosehydroxyethylate
fujihec-bl20
glutofix600
hec-al5000
herculesn100
hespan
hetastarch
hydroxyethylethercellulose
j164
natrosol
natrosol150l
natrosol180hh
natrosol180l

Tylose MHS 150009 P4

DOCUMENTS

Tylose MHS 150009 P4 is a water-soluble, non-ionic, highly etherified, modified methyl hydroxyethyl cellulose powder.Tylose MHS 150009 P4 provides very fast consistency development, high water demand, water retention, and heat stability, and moderate sag resistance and influence on cement hydration. This grade Tylose MHS 150009 P4 is ideal for use in block laying adhesives and gypsum mounting binders and spray plasters.
 water-soluble cellulose ethers under the Tylose® trade name - including methyl hydroxyethyl cellulose (MHEC), methyl hydroxypropyl cellulose (MHPC), and hydroxyethyl cellulose (HEC) - for applications such as construction and ceramic coatings & paints.
Tylose MHS 150009 P4
Technical Data Sheet
O OH CH, CH2, CH3
Product properties Product properties of Tylose MHS 150009 P4 
Constitution: Methylhydroxyethyl cellulose modified
Appearance of Tylose MHS 150009 P4 : powder Delayed solubility: no
Etherification of Tylose MHS 150009 P4 : high etherification Thickening effect: moderate
Particle size of Tylose MHS 150009 P4 : fine powder Level of viscosity: 150000 mPas
according to Höppler
Product specification Product specification of Tylose MHS 150009 P4 Recommended fields of application Recommended fields of application
Moisture of Tylose MHS 150009 P4 : ≤ 6 %
Content of NaCl of Tylose MHS 150009 P4 : ≤ 1.5 %
Particle size of Tylose MHS 150009 P4 : <125µm: min. 85%
Particle size of Tylose MHS 150009 P4 : <100µm: min. 70%
Viscosity of Tylose MHS 150009 P4 : 5600 - 8000 mPas
Brookfield RV,20rpM, 1.0%,20°C,20° GH
Plasters, gypsum based
Thin layer plasters, gypsum based
Gypsum-Lime-Plasters
Tile adhesives
Product properties 
Constitution:Methyl hydroxyethyl cellulose modified
Appearance:powder
Etherification:high
Particle size:fine powder
Delayed solubility:no
Level of viscosity:
according to Höppler 150000 mPa•s
Tylose® MHS grades - water soluble, non-ionic, highly etherified methyl hydroxyethyl cellulose 

Application performance 
Building materials 
Consistency development:very fast
Final consistency:moderate
Sag resistance:moderate
Water demand:high
Water retention:very high
Influence on cement hydration:moderate
Heat stability:high

Tylose MHS 150009 P4
Technical Data Sheet
Application performance Application performance
Consistency development of Tylose MHS 150009 P4 : fast Water retention: very high
Final consistency of Tylose MHS 150009 P4 : moderate Influence on cement hydration: moderate
Sag resistance of Tylose MHS 150009 P4 : moderate Heat stability: high
Water demand: high
Packaging, Storage, Safety instructions Packaging, Storage, Safety instructions of Tylose MHS 150009 P4 
Like all fine-particle organic substances, of Tylose MHS 150009 P4 constitute a dust explosion hazard. Dust formation
and deposits must be kept to a minimum so that no ignitable dust/air mixtures can form. Ignition sources such
as naked flames, hot surfaces, sparks and static electricity should be avoided. Tylose starts to decompose at
about 200°C. Its ignition temperature is >360°C. of Tylose MHS 150009 P4 burns easily and the fire may spread.
When stored in closed containers, or in its original packaging in a dry place at room temperature, of Tylose MHS 150009 P4 can
be kept for a long time. In the case of high viscosity grades, a slow loss of viscosity can be measured after
lengthy storage (>1 year). Tylose absorbs water from moist air. Once opened, container must be resealed and
kept tightly closed.
 of Tylose MHS 150009 P4 is supplied in multi-ply paper bags with polyethylene intermediate layer and/or in big bags. 

Tylose MHS 150009 P4
Product Properties
Constitution: Methyl hydroxyethyl cellulose modified
Appearance: powder
Etherification: high
Particle size: fine powder
Delayed solubility: no
Level of viscosity:
according to Höppler 15000 mPa•s
Tylose® MHS grades – water soluble, non-ionic, highly etherified methyl hydroxyethyl cellulose

Application Performance
Building Materials
Consistency development: very fast
Final consistency: moderate
Sag resistance: moderate
Water demand: high
Water retention: very high
Influence on cement hydration: moderate
Heat stability: high
Recommended Fields Of Application
Building Materials
Block laying adhesive
Gypsum mounting binder
Gypsum spray plaster
Nomenclature Information
Type of ether Viscosity level Chemical refinement
M Methyl 60000 
The viscosity level is based on
Hoeppler: 2%
solution of the
commercial product
with 5% moisture
content, 20ºC,
20º dH
(German hardness)

Y Delayed solubility products
H Hydroxyethyl 30000 K Readily soluble granules
O Hydroxypropyl 15000 N non-delayed solubility products
A Allyl 10000 (only for Tylose H grades) *
X Hydrophobe 6000 
etherification 4000 Degree of particle size
2000 Types of granules:
Degree of 1000 G4 Granules (< 500 μm)
B etherification 300 G6 Granules (< 400 μm)
F Special higher 200 G6 Granules (< 400 μm)
S degrees of . Powder types:
T etherification, . P2 Powder (< 180 μm)
depending on the . P3 Fine Powder (< 125 μm)
individual type of 01 P4 Fine powder (< 125 μm)
ether 02 P6 Ultra fine powder (< 100 μm)

Tylose MHS grades
Grades Knowledge Base
Tylose MHS 10012 P6 
Tylose MHS 30024 P4 
Tylose MHS 30027 P6 
Tylose MHS 60000 YP4 
Tylose MHS 100005 P3 
Tylose MHS 100006 P3 
Tylose MHS 150009 P4 
Tylose MHS 150012 P4 
Tylose MHS 300000 P4 ,

Gypsum Based Hand and Machine Plasters
Product Name Chemical Description Usage Areas
TYLOSE MH 10.001 P4 Methyl Hydroxy Ethyl Cellulose Höppler falling ball viscometer 10.000 mPas Decorative mineral based plasters, Smooth block adhesives, Tile adhesives, Exterior coating and insulation systems
TYLOSE MH 10.007 P4 Methyl Hydroxy Ethyl Cellulose Höppler falling ball viscometer 10,000 mPas Decorative mineral based plasters, Smooth block adhesives, Tile adhesives, Exterior coating and insulation systems
TYLOSE MH 15.000 P4 Methyl Hydroxy Ethyl Cellulose Höppler falling ball viscometer 15.000 mPas Ready-mixed concrete joint fillers, Tile adhesives External coating and insulation systems, Gypsum-based joint compounds, Insulation Plasters
TYLOSE MH 15.002 P6 Methyl Hydroxy Ethyl Cellulose Höppler falling ball viscometer 15.000 mPas Cement-lime-based plasters, Gypsum-Lime-based plasters, Smooth block adhesives, Exterior Coating and insulation systems, thin layer plasters, Repair plasters
TYLOSE MH 2.000 YP2 Methyl Hydroxy Ethyl Cellulose Höppler falling ball viscometer 2.000 mPas Cement-based screed plaster, Repair plasters, Cement-based plasters
TYLOSE MH 30.000 P4 Methyl Hydroxy Ethyl Cellulose Höppler falling ball viscometer 30.000 mPas Cement Based plastering compounds, Masonry Mortars, Ready-mixed concrete grouting, Cement-based paints
TYLOSE MH 6.000 YP4 Methyl Hydroxy Ethyl Cellulose Höppler falling ball viscometer 6.000 mPas Cement-based screed plaster, Cement-based Plastering compounds Decorative surface coatings
TYLOSE MH 60.004 P6 Methyl Hydroxy Ethyl Cellulose Höppler falling ball viscometer 60.000 mPas. Tile adhesives, cement based hand applied plasters, cement lime based plasters, gypsum based plasters.
TYLOSE MH 60.027 P6 Methyl Hydroxy Ethyl Cellulose Höppler falling ball viscometer 60.000 mPas. Tile adhesives, cement based hand applied plasters, cement lime based plasters, gypsum based plasters.
TYLOSE MH 60.028 P6 Methyl Hydroxy Ethyl Cellulose Höppler falling ball viscometer 60.000 mPas. Tile adhesives, cement based hand applied plasters, cement lime based plasters, gypsum based plasters and jacketing products.

TYLOSE MHS 150009 P4

DOCUMENTS
Tylose MHS 150009 P4 

 Tylose MHS 150009 P4 is a water-soluble. Tylose MHS 150009 P4 is non-ionic. Tylose MHS 150009 P4 is highly etherified. Tylose MHS 150009 P4 is modified methyl hydroxyethyl cellulose powder. Tylose MHS 150009 P4 provides very fast consistency development, high water demand, water retention, and heat stability, and moderate sag resistance and influence on cement hydration. Tylose MHS 150009 P4 is a water-soluble, non-ionic, highly etherified, modified methyl hydroxyethyl cellulose powder.Tylose MHS 150009 P4 provides very fast consistency development, high water demand, water retention, and heat stability, and moderate sag resistance and influence on cement hydration. This grade Tylose MHS 150009 P4 is ideal for use in block laying adhesives and gypsum mounting binders and spray plasters.
water-soluble cellulose ethers under the Tylose trade name - including methyl hydroxyethyl cellulose (MHEC), methyl hydroxypropyl cellulose (MHPC), and hydroxyethyl cellulose (HEC) - for applications such as construction and ceramic coatings & paints. Tylose MHS 150009 P4 of methyl hydroxyethyl cellulose (MHEC) is ideal for use in block laying adhesives and gypsum mounting binders and spray plasters. Tylose MHS 150009 P4 grades – water soluble, non-ionic, highly etherified methyl hydroxyethyl cellulose.Tylose MHS 150009 P4 is a water-soluble. Tylose MHS 150009 P4 is non-ionic. Tylose MHS 150009 P4 is highly etherified. Tylose MHS 150009 P4 is modified methyl hydroxyethyl cellulose powder. Tylose MHS 150009 P4 provides very fast consistency development, high water demand, water retention, and heat stability, and moderate sag resistance and influence on cement hydration. This grade Tylose MHS 150009 P4 of methyl hydroxyethyl cellulose (MHEC) is ideal for use in block laying adhesives and gypsum mounting binders and spray plasters. Tylose MHS 150009 P4 grades – water soluble, non-ionic, highly etherified methyl hydroxyethyl cellulose. Tylose MHS 150009 P4 is a water-soluble, non-ionic, highly etherified, modified methyl hydroxyethyl cellulose powder.Tylose MHS 150009 P4 provides very fast consistency development, high water demand, water retention, and heat stability, and moderate sag resistance and influence on cement hydration. This grade Tylose MHS 150009 P4 is ideal for use in block laying adhesives and gypsum mounting binders and spray plasters..

 Tylose MHS 150009 P4 Technical Data Sheet

MHS 150003 P4O OH CH, CH2, CH3
Product properties Product properties of Tylose MHS 150009 P4
Constitution: Methylhydroxyethyl cellulose modified
Appearance of Tylose MHS 150009 P4 : powder Delayed solubility: no
Etherification of Tylose MHS 150009 P4 : high etherification Thickening effect: moderate
Particle size of Tylose MHS 150009 P4 : fine powder Level of viscosity: 150000 mPas according to Höppler
Product specification Product specification of Tylose MHS 150009 P4 Recommended fields of application Recommended fields of application
Moisture of Tylose MHS 150009 P4 : ≤ 6 %
Content of NaCl of Tylose MHS 150009 P4 : ≤ 1.5 %
Particle size of Tylose MHS 150009 P4 : <125µm: min. 85%
Particle size of Tylose MHS 150009 P4 : <100µm: min. 70%
Viscosity of Tylose MHS 150009 P4 : 5600 - 8000 mPas
Brookfield RV,20rpM, 1.0%,20°C,20° GH
Tylose MHS 150009 P4 is used as Plasters, gypsum based
Tylose MHS 150009 P4 is used as Thin layer plasters, gypsum based
Tylose MHS 150009 P4 is used as Gypsum-Lime-Plasters
Tylose MHS 150009 P4 is used as Tile adhesives.

Product properties 
Constitution:Methyl hydroxyethyl cellulose modified
Appearance:powder
Etherification:high
Particle size:fine powder
Delayed solubility:no
Level of viscosity:
according to Höppler 150000 mPa•s
Tylose MHS grades - water soluble, non-ionic, highly etherified methyl hydroxyethyl cellulose
 
Tylose MHS 150009 P4 of methyl hydroxyethyl cellulose (MHEC) is ideal for use in block laying adhesives and gypsum mounting binders and spray plasters. Tylose MHS 150009 P4 grades – water soluble, non-ionic, highly etherified methyl hydroxyethyl cellulose. Tylose MHS 150009 P4 provides very fast consistency development, high water demand, water retention, and heat stability, and moderate sag resistance and influence on cement hydration Tylose MHS 150009 P4 is a water-soluble. Tylose MHS 150009 P4 is non-ionic. Tylose MHS 150009 P4 is highly etherified. Tylose MHS 150009 P4 is modified methyl hydroxyethyl cellulose powder. Tylose MHS 150009 P4 provides very fast consistency development, high water demand, water retention, and heat stability, and moderate sag resistance and influence on cement hydration. This grade Tylose MHS 150009 P4 of methyl hydroxyethyl cellulose (MHEC) is ideal for use in block laying adhesives and gypsum mounting binders and spray plasters.
Application performance of 
Building materials 
Consistency development:very fast
Final consistency:moderate
Sag resistance:moderate
Water demand:high
Water retention:very high
Influence on cement hydration:moderate
Heat stability:high
 
 
Tylose MHS 150003 P4
Technical Data Sheet
Application performance Application performance
Consistency development of Tylose MHS 150009 P4 : fast Water retention: very high
Final consistency of Tylose MHS 150009 P4 : moderate Influence on cement hydration: moderate
Sag resistance of Tylose MHS 150009 P4 : moderate Heat stability: high
Water demand of Tylose MHS 150009 P4 : high

Packaging, Storage, Safety instructions of Tylose MHS 150009 P4

Like all fine-particle organic substances, of Tylose MHS 150009 P4 constitute a dust explosion hazard. Dust formation and deposits must be kept to a minimum so that no ignitable dust/air mixtures can form. Ignition sources such as naked flames, hot surfaces, sparks and static electricity should be avoided. Tylose starts to decompose at about 200°C. Its ignition temperature is >360°C. of Tylose MHS 150009 P4 burns easily and the fire may spread. When stored in closed containers, or in its original packaging in a dry place at room temperature, of Tylose MHS 150009 P4 can be kept for a long time. In the case of high viscosity grades, a slow loss of viscosity can be measured after lengthy storage (>1 year). Tylose absorbs water from moist air. Once opened, container must be resealed and kept tightly closed. of Tylose MHS 150009 P4 is supplied in multi-ply paper bags with polyethylene intermediate layer and/or in big bags.
 
TYLOSE MHS 150009 P4 
Tylose MHS 150009 P4 
Tylose MHS 150009 P4 is a water soluble substance. Tylose MHS 150009 P4 is non-ionic. Tylose MHS 150009 P4 is highly etherified. Tylose MHS 150009 P4 is a modified methyl hydroxyethyl cellulose powder. Tylose MHS 150009 P4 provides very fast consistency development, high water demand, water retention and heat stability, and an effect on moderate sag resistance and cement hydration. Consisting of methyl hydroxyethyl cellulose (MHEC), this Tylose MHS 150009 P4 grade is ideal for use in block floor adhesives and gypsum mounting binders and spray plasters. Tylose MHS 150009 P4 grades - water soluble, nonionic, highly etherified methyl hydroxyethyl cellulose. Tylose MHS 150009 P4 Like all fine organic matter, Tylose MHS 150009 P4 poses a dust explosion hazard. Deposits should be kept to a minimum so that no sediment / air mixture is formed. Tylose MHS 150009 P4 Sources of ignition: bare flames, hot surfaces, sparks and static electricity should be avoided. Tylose MHS 150009 P4 begins to decompose about 200 ° C. Ignition temperature> 360 ° C. Tylose MHS 150009 P4 easily burns and a fire could occur. Tylose MHS 150009 P4 should be stored for a long time when stored in closed containers or Tylose MHS 150009 P4 in its original packaging in a dry place at room temperature. This type of Tylose MHS 150009 P4 is ideal for use in block flooring adhesives and gypsum mounting binders and spray plasters. Tylose MHS 150009 P4 for applications such as construction and ceramic coatings and paints, including water soluble cellulose ethers - methyl hydroxyethyl cellulose (MHEC), methyl hydroxypropyl cellulose (MHPC) and hydroxyethyl cellulose (HEC) under the trade name Tylose MHS 150009 P4 .
Tylose MHS 150009 P4 
Technical data sheet Tylose MHS 150009 P4 OOH CH, CH2, CH3
Tylose MHS 150009 P4 Product features
Constitution: Methylhydroxyethyl cellulose modified
The appearance of Tylose MHS 150009 P4 : powder Delayed resolution: no
Tylose MHS 150009 P4 : high etherification Thickening effect: medium
Tylose MHS 150009 P4 particle size: fine powder Viscosity level: 150000 mPas
Moisture of Tylose MHS 150009 P4 : 6%
NaCl content of Tylose MHS 150009 P4 : ≤ 1.5%
Particle size of Tylose MHS 150009 P4 : <125um: min. 85%
Particle size of Tylose MHS 150009 P4 : <100um: min. 70%
Viscosity of Tylose MHS 150009 P4 : 5600-8000 mPas
Tylose MHS 150009 P4 Brookfield RV, 20rpM, 1.0%, 20 ° C, 20 ° GH
Tylose MHS 150009 P4 Used in gypsum based plasters.
Tylose MHS 150009 P4 Thin layer plasters are used based on gypsum. Used in Tylose MHS 150009 P4 Gypsum-Lime-Plasters.
Tylose MHS 150009 P4 is used in tile adhesives.
 
 Tylose MHS 150009 P4 
Technical data sheet
Application performance Application performance
Consistent development of Tylose MHS 150009 P4 : fast Water retention: very high
Final consistency of Tylose MHS 150009 P4 : moderate Effect on cement hydration: medium
Tylose MHS 150009 P4 sag resistance: medium Heat stability: high
Tylose MHS 150009 P4 Water demand: high

Tylose MHS 150009 P4 long-term storage (> 1 year). Tylose absorbs water from moist air. Tylose MHS 150009 P4 After opening, the container should be closed and kept tightly closed. Tylose MHS 150009 P4 is supplied in multi-layer paper bags with a polyethylene interlayer and / or big bags. Tylose MHS 150009 P4 is a water soluble substance. Tylose MHS 150009 P4 is non-ionic. Tylose MHS 150009 P4 is highly etherified. Tylose MHS 150009 P4 is a modified methyl hydroxyethyl cellulose powder. Tylose MHS 150009 P4 provides very fast consistency development, high water demand, water retention and heat stability, and an effect on moderate sag resistance and cement hydration. Consisting of methyl hydroxyethyl cellulose (MHEC), this Tylose MHS 150009 P4 grade is ideal for use in block flooring adhesives and gypsum mounting binders and spray plasters. Tylose MHS 150009 P4 grades - water soluble, non-ionic, highly etherified methyl hydroxyethyl cellulose..Tylose MHS 150009 P4 Application Performance.Tylose MHS 150009 P4 Used in building materials. Consistency improvement of Tylose MHS 150009 P4 : very fast Tylose MHS 150009 P4 Final consistency: medium.Tylose Tylose MHS 150009 P4 Packaging, Storage, Safety instructions Packaging, Storage, Safety instructions Tylose MHS 150009 P4 
Tylose MHS 150009 P4 Like all fine organic matter, Tylose MHS 150009 P4 poses a dust explosion hazard. Deposits should be kept to a minimum so that no sediment / air mixture is formed. Tylose MHS 150009 P4 Sources of ignition: bare flames, hot surfaces, sparks and static electricity should be avoided. Tylose MHS 150009 P4 begins to decompose about 200 ° C. Ignition temperature> 360 ° C. Tylose MHS 150009 P4 easily burns and a fire could occur. Tylose MHS 150009 P4 should be stored for a long time when stored in closed containers or Tylose MHS 150009 P4 in its original packaging in a dry place at room temperature. In case of high viscosity grades, a slow loss of viscosity
 
Tylose MHS 150009 P4 Application Performance.Tylose MHS 150009 P4 Used in building materials. Consistency improvement of Tylose MHS 150009 P4 : very fast Tylose MHS 150009 P4 Final consistency: medium. Deposits should be kept to a minimum so that no sediment / air mixture is formed. Tylose MHS 150009 P4 Sources of ignition: bare flames, hot surfaces, sparks and static electricity should be avoided. Tylose MHS 150009 P4 begins to decompose about 200 ° C. Ignition temperature> 360 ° C. Tylose MHS 150009 P4 easily burns and a fire could occur. Tylose MHS 150009 P4 should be stored for a long time when stored in closed containers or Tylose MHS 150009 P4 in its original packaging in a dry place at room temperature. This type of Tylose MHS 150009 P4 is ideal for use in block flooring adhesives and gypsum mounting binders and spray plasters. Tylose MHS 150009 P4 for applications such as construction and ceramic coatings and paints, including water soluble cellulose ethers - methyl hydroxyethyl cellulose (MHEC), methyl hydroxypropyl cellulose (MHPC) and hydroxyethyl cellulose (HEC) under the trade name Tylose MHS 150009 P4 . Tylose MHS 150009 P4 is a water soluble substance. Tylose MHS 150009 P4 is non-ionic. Tylose MHS 150009 P4 is highly etherified. Tylose MHS 150009 P4 is a modified methyl hydroxyethyl cellulose powder. Tylose MHS 150009 P4 provides very fast consistency development, high water demand, water retention and heat stability, and an effect on moderate sag resistance and cement hydration. Consisting of methyl hydroxyethyl cellulose (MHEC), this Tylose MHS 150009 P4 grade is ideal for use in block floor adhesives and gypsum mounting binders and spray plasters. Tylose MHS 150009 P4 grades - water soluble, nonionic, highly etherified methyl hydroxyethyl cellulose. Tylose MHS 150009 P4 Like all fine organic matter, Tylose MHS 150009 P4 poses a dust explosion hazard. Tylose MHS 150009 P4 provides very fast consistency development, high water demand, water retention and heat stability, and an effect on moderate sag resistance and cement hydration. Consisting of methyl hydroxyethyl cellulose (MHEC), this Tylose MHS 150009 P4 grade is ideal for use in block flooring adhesives and gypsum mounting binders and spray plasters. Tylose MHS 150009 P4 grades - water soluble, non-ionic, highly etherified methyl hydroxyethyl cellulose..
Tylose MHS 150009 P4 
Technical data sheet Tylose MHS 150009 P4 OOH CH, CH2, CH3

Tylose MHS 150009 P4 Brookfield RV, 20rpM, 1.0%, 20 ° C, 20 ° GH
Tylose MHS 150009 P4 Used in gypsum based plasters.
Tylose MHS 150009 P4 Thin layer plasters are used based on gypsum. Used in Tylose MHS 150009 P4 Gypsum-Lime-Plasters.
Tylose MHS 150009 P4 is used in tile adhesives.
 
 Tylose MHS 150009 P4 
Technical data sheet
Consistent development of Tylose MHS 150009 P4 : fast Water retention: very high
Tylose MHS 150009 P4 Product features
Constitution: Methylhydroxyethyl cellulose modified
The appearance of Tylose MHS 150009 P4 : powder Delayed resolution: no
Tylose MHS 150009 P4 : high etherification Thickening effect: medium
Tylose MHS 150009 P4 particle size: fine powder Viscosity level: 150000 mPas
Moisture of Tylose MHS 150009 P4 : 6%
NaCl content of Tylose MHS 150009 P4 : ≤ 1.5%
Particle size of Tylose MHS 150009 P4 : <125um: min. 85%
Particle size of Tylose MHS 150009 P4 : <100um: min. 70%
Viscosity of Tylose MHS 150009 P4 : 5600-8000 mPas

Final consistency of Tylose MHS 150009 P4 : moderate Effect on cement hydration: medium
Tylose MHS 150009 P4 sag resistance: medium Heat stability: high
Tylose MHS 150009 P4 Water demand: high
Tylose MHS 150009 P4 Packaging, Storage, Safety instructions Packaging, Storage, Safety instructions Tylose MHS 150009 P4 
Tylose MHS 150009 P4 Like all fine organic matter, Tylose MHS 150009 P4 poses a dust explosion hazard. Deposits should be kept to a minimum so that no sediment / air mixture is formed. Tylose MHS 150009 P4 Sources of ignition: bare flames, hot surfaces, sparks and static electricity should be avoided. Tylose MHS 150009 P4 begins to decompose about 200 ° C. Ignition temperature> 360 ° C. Tylose MHS 150009 P4 easily burns and a fire could occur. Tylose MHS 150009 P4 should be stored for a long time when stored in closed containers or Tylose MHS 150009 P4 in its original packaging in a dry place at room temperature. In case of high viscosity grades, a slow loss of viscosity
long-term storage (> 1 year). Tylose absorbs water from moist air. Tylose MHS 150009 P4 After opening, the container should be closed and kept tightly closed. Tylose MHS 150009 P4 is supplied in multi-layer paper bags with a polyethylene interlayer and / or big bags. Tylose MHS 150009 P4 is a water soluble substance. Tylose MHS 150009 P4 is non-ionic. Tylose MHS 150009 P4 is highly etherified. Tylose MHS 150009 P4 is a modified methyl hydroxyethyl cellulose powder. Tylose MHS 150009 P4 provides very fast consistency development, high water demand, water retention and heat stability, and an effect on moderate sag resistance and cement hydration. Consisting of methyl hydroxyethyl cellulose (MHEC), this Tylose MHS 150009 P4 grade is ideal for use in block flooring adhesives and gypsum mounting binders and spray plasters. Tylose MHS 150009 P4 grades - water soluble, non-ionic, highly etherified methyl hydroxyethyl cellulose..Tylose MHS 150009 P4 Application Performance.Tylose MHS 150009 P4 Used in building materials. Consistency improvement of Tylose MHS 150009 P4 : very fast Tylose MHS 150009 P4 Final consistency: medium.
Tylose MHS 150009 P4 
Product Properties
Constitution: Methyl hydroxyethyl cellulose modified
Appearance: powder
Etherification: high
Particle size: fine powder
Delayed solubility: no
Level of viscosity:
according to Höppler 15000 mPa•s
Tylose MHS grades - water soluble, non-ionic, highly etherified methyl hydroxyethyl cellulose
 
 Application Performance
Building Materials
Consistency development: very fast
Final consistency: moderate
Sag resistance: moderate
Water demand: high
Water retention: very high
Influence on cement hydration: moderate
Heat stability: high
Recommended Fields Of Application
Building Materials
Block laying adhesive
Gypsum mounting binder
Gypsum spray plaster
Nomenclature Information
MHS 150003 P4 Sag resistance: medium.Tylose MHS 150009 P4 Water demand: high.Tylose MHS 150009 P4 Water retention: very high.Tylose MHS 150009 P4 Effect on cement hydration: medium.Tylose MHS 150009 P4 Heat stability: high.Tylose MHS 150009 P4 Recommended Application Areas. Tylose MHS 150009 P4 is used in building materials.
Tylose MHS 150009 P4 
TYLOSE MH 150003 P4 Physical State: Free Powder
TYLOSE MH 150003 P4 Humidity: ≤ 6%
TYLOSE MH 150003 P4 NaCl content: ≤ 1.5%
TYLOSE MH 150003 P4 Grain size: <100μm: min. 90%
TYLOSE MH 150003 P4 Grain size: <63μm: min. 65%
Tylose MHS 150009 P4 Properties: Methyl hydroxyethyl cellulose modified
Tylose MHS 150009 P4 Appearance: powder
Tylose MHS 150009 P4 Etherification: High
Tylose MHS 150009 P4 Particle size: fine powder
Tylose MHS 150009 P4 Delayed resolution: no
Tylose MHS 150009 P4 Viscosity level: according to Höppler 15000 mPa s
Tylose MHS 150009 P4 is soluble in water,
Tylose MHS 150009 P4 nonionic, highly etherified methyl hydroxyethyl cellulose
Tylose MHS 150009 P4 Application Performance
Tylose MHS 150009 P4 Used in building materials.
Consistency improvement of Tylose MHS 150009 P4 : very fast
Tylose MHS 150009 P4 Final consistency: medium
Tylose MHS 150009 P4 Sag resistance: medium
Tylose MHS 150009 P4 Water demand: high
Tylose MHS 150009 P4 Water retention: very high
Tylose MHS 150009 P4 Effect on cement hydration: medium
Tylose MHS 150009 P4 Heat stability: high
Tylose MHS 150009 P4 Recommended Application Areas
Tylose MHS 150009 P4 Used in building materials.
Tylose MHS 150009 P4 is used as block flooring adhesive.
Tylose MHS 150009 P4 Used as plaster mounting binders.
Tylose MHS 150009 P4 is used in plaster spray plaster.
Nomenclature Information
Gypsum Based Hand and Machine Plasters
Product Name Chemical Description Uses
Type MH
 Tylose MHS 150009 P4 Packaging, Storage, Safety instructions Packaging, Storage, Safety instructions Tylose MHS 150009 P4 
Tylose MHS 150009 P4 begins to decompose about 200 ° C. Ignition temperature> 360 ° C. Tylose MHS 150009 P4 easily burns and a fire could occur. Tylose MHS 150009 P4 should be stored for a long time when stored in closed containers or Tylose MHS 150009 P4 in its original packaging in a dry place at room temperature. In case of high viscosity grades, a slow loss of viscosity. Long-term storage (> 1 year). Tylose absorbs water from moist air. Tylose MHS 150009 P4 After opening, the container should be closed and kept tightly closed. Tylose MHS 150009 P4 is supplied in multi-layer paper bags with a polyethylene interlayer and / or big bags. Tylose MHS 150009 P4 is a water soluble substance. Tylose MHS 150009 P4 is non-ionic. Tylose MHS 150009 P4 is highly etherified. Tylose MHS 150009 P4 should be stored for a long time when stored in closed containers or Tylose MHS 150009 P4 in its original packaging in a dry place at room temperature. In case of high viscosity grades, a slow loss of viscosity long-term storage (> 1 year). Tylose absorbs water from moist air. Tylose MHS 150009 P4 After opening, the container should be closed and kept tightly closed. Tylose MHS 150009 P4 is supplied in multi-layer paper bags with a polyethylene interlayer and / or big bags. Tylose MHS 150009 P4 is a water soluble substance. Tylose MHS 150009 P4 is non-ionic. Tylose MHS 150009 P4 is highly etherified. Tylose MHS 150009 P4 is a modified methyl hydroxyethyl cellulose powder. Tylose MHS 150009 P4 is a modified methyl hydroxyethyl cellulose powder. Tylose MHS 150009 P4 provides very fast consistency development, high water demand, water retention and heat stability, and an effect on moderate sag resistance and cement hydration. Consisting of methyl hydroxyethyl cellulose (MHEC), this Tylose MHS 150009 P4 grade is ideal for use in block flooring adhesives and gypsum mounting binders and spray plasters. Tylose MHS 150009 P4 grades - water soluble, nonionic, highly etherified methyl hydroxyethyl cellulose..Tylose MHS 150009 P4 Application Performance.Tylose MHS 150009 P4 Used in building materials. Consistency improvement of Tylose MHS 150009 P4 : very fast. 150003 P4 Final consistency: medium Tylose MHS 150009 P4 Sagging resistance: medium.Tylose MHS 150009 P4 Water demand: high.Tylose MHS 150009 P4 Water retention: very high Tylose MHS 150009 P4 Effect on cement hydration: medium.Tylose MHS 150009 P4 Heat Tylose MHS 150009 P4 Recommended Application Areas Tylose MHS 150009 P4 Used in building materials Tylose MHS 150009 P4 Like all fine organic materials, Tylose MHS 150009 P4 poses a dust explosion hazard. Deposits should be kept to a minimum so that no sediment / air mixture is formed. Tylose MHS 150009 P4 Sources of ignition: bare flames, hot surfaces, sparks and static electricity should be avoided.
 
Gypsum Based Hand and Machine Plasters
Product Name Chemical Description Uses
TYLOSE MH 10.001 P4 Methyl Hydroxy Ethyl Cellulose Höppler falling ball viscometer 10.000 mPas Decorative mineral based plasters, Smooth block adhesives, Tile adhesives, Exterior coating and insulation systems
TYLOSE MH 10.007 P4 Methyl Hydroxy Ethyl Cellulose Höppler falling ball viscometer 10.000 mPas Decorative mineral based plasters, Smooth block adhesives, Tile adhesives, Exterior coating and insulation systems
TYLOSE MH 15.000 P4 Methyl Hydroxy Ethyl Cellulose Höppler falling ball viscometer 15.000 mPas Ready-mixed concrete joint fillers, Tile adhesives Exterior coating and insulation systems, Gypsum-based joint compounds, Insulation Plasters
TYLOSE MH 15.002 P6 Methyl Hydroxy Ethyl Cellulose Höppler falling ball viscometer 15.000 mPas Cement-lime based plaster, Gypsum-Lime based plaster, Smooth bl
Y Delayed solubility products
H Hydroxyethyl 30000 K Readily soluble granules
O Hydroxypropyl 15000 N non-delayed solubility products
A Allyl 10000 (only for Tylose H grades) *
X Hydrophobe 6000 
etherification 4000 Degree of particle size
2000 Types of granules:
Degree of 1000 G4 Granules (< 500 μm)
B etherification 300 G6 Granules (< 400 μm)
F Special higher 200 G6 Granules (< 400 μm)
S degrees of . Powder types:
T etherification, . P2 Powder (< 180 μm)
depending on the . P3 Fine Powder (< 125 μm)
individual type of 01 P4 Fine powder (< 125 μm)
ether 02 P6 Ultra fine powder (< 100 μm)

Recommended fields of application 
Gypsum based joint filler Plaster adhesives, gypsum based
Application performance
Consistency development: fast
Water retention: very high
Final consistency: very high
Influence on cement hydration: moderate
Sag resistance: high
Heat stability: high
Water demand: very high
Packaging, Storage, Safety instructions Like all fine-particle organic substances, cellulose ethers constitute a dust explosion hazard. Dust formation and deposits must be kept to a minimum so that no ignitable dust/air mixtures can form. Ignition sources such as naked flames, hot surfaces, sparks and static electricity should be avoided. Tylose starts to decompose at about 200°C. Its ignition temperature is >360°C. Tylose burns easily and the fire may spread. When stored in closed containers, or in its original packaging in a dry place at room temperature, Tylose can be kept for a long time. In the case of high viscosity grades, a slow loss of viscosity can be measured after lengthy storage (>1 year). Tylose absorbs water from moist air. Once opened, container must be resealed and kept tightly closed. This Tylose-type is supplied in multi-ply paper bags with polyethylene intermediate layer and/or in big bags.

Starch, 2-hydroxypropyl ether; tylovis se 7 cas no: 9049-76-7

DESCRIPTION:
TYLOSE MHS 60000 YP4 is Methyl hydroxyethyl cellulose.
TYLOSE MHS 60000 YP4 Acts as a rheology modifier.
TYLOSE MHS 60000 YP4 Offers low gloss, low pigment compatibility and high thickening effect as well as moderate water retention, high wet scrub resistance, moderate anti-spattering and moderate pseudoplasticity.

TYLOSE MHS 60000 YP4 Has no bio stability.
TYLOSE MHS 60000 YP4 is Used in emulsion based tile adhesives.
TYLOSE MHS 60000 YP4 is water soluble, non-ionic, highly etherified methyl hydroxyethyl cellulose.


APPLICATIONS OF TYLOSE MHS 60000 YP4:
TYLOSE MHS 60000 YP4 is Used as Emulsion tile adhesive
TYLOSE MHS 60000 YP4 is Used as Emulsion glue
TYLOSE MHS 60000 YP4 is Used as Wet joints


SAFETY INFORMATION ABOUT TYLOSE MHS 60000 YP4:
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

Packaging, storage, safety instructions:

Like all organic powder substances, cellulose ethers present a dust explosion hazard.
In order to avoid combustible dust-air mixtures, the risk of dust generation and accumulation must be minimised.
Avoid sources of ignition such as open flames, hot surfaces, sparks, and electrical disturbances.

Tylose begins to decompose at around 200˚C.
The flash point is greater than 360˚C.
Tylose burns easily and fire can spread.

Tylose can be stored for a long time if stored in a closed container or in its original packaging in a dry place at room temperature.
For high-viscosity types, a slight loss of viscosity may occur after long-term storage (more than 1 year).
Tylose absorbs water from humid air.
An opened container must be resealed tightly.


PHYSICAL AND CHEMICAL PROPERTIES OF TYLOSE MHS 60000 YP4:
Physical state : Solid
Appearance : Powder.
Colour : whitish
Odour : odourless
pH : 6 – 8 10g/l
Auto-ignition temperature : > 170 °C
Density : Density: 1.1 – 1.5 g/cm³ 20 °C
Solubility : Water: > 10 g/l @ 20°C
Log Pow : < 1
Explosive properties : Product is not explosive. Dust may form explosive mixture in air.
Minimum ignition energy : > 10 mJ
Conbustion class : 5
Smoldering temperature : >450 °C
pmax : 10 bar
Dust explosion category : ST1
KSt : < 200 bar*m/s
Ignition temperature : > 400 °C
Constitution: Methyl hydroxypropyl cellulose
Appearance: powder
Etherification: high
Particle size: fine powder
Delayed solubility: yes
Level of viscosity according to Höppler: 60000 mPa•s
Humidity : ≤6%
NaCl content: ≤1.5%
Grain size: <125µm: min. 85%
Grain size: <100µm: min. 70%
Viscosity: 27000 – 34000 mPas
Brookfield RV, 20rpM, 1.9%20°C, 20°GH


APPLICATION PERFORMANCE WITH BUILDING MATERIALS:
Consistency development: fast
Final consistency: low
Sag resistance: low
Water demand: low
Water retention: very high
Influence on cement hydration: low
Heat stability: high

DESCRIPTION:

Tylose PSO 810001, a methyl hydroxypropyl cellulose (MHPC) which acts as a thickener for a much broader range of organic solvents.
Tylose PSO 810001 performs exceedingly well in most polar organic solvents, organic solvent mixtures and organic solvent/water systems.
Fields of application include paint strippers, adhesives and fuel pastes.

CAS NO: 9004-65-3


APPROPRIATE SOLVENTS FOR TYLOSE PSO 810001 – SOME TYPICAL EXAMPLES:
Alcohols:
Methanol Ethanol Propanol Isopropanol Octanol Butyl diglycol 1,3-Butanediol Glycerol Diethylene glycol
Aldehydes/Ketones:
Acetone (propanone) 2-Butanone
Amides:
DMF (Dimethyl formamide) NEP (N-Ethyl-2-pyrrolidone) NMP (N-Methyl-2-pyrrolidone)
Esters:
Dibasic Esters BDGA (2-(2-Butoxyethoxy)ethyl acetate)
Ethers:
DPM (Dipropylene glycol methyl ether) TPM (Tripropylene glycol methyl ether) THF (Tetrahydrofuran) 1,3-Dioxolane



Halogenated Carbohydrates:
Methylene chloride Chloroform (trichloromethane)
Others:
DMSO (Dimethyl sulfoxide) Pyridine


SAFETY INFORMATION ABOUT TYLOSE PSO 810001:
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




PHYSICAL AND CHEMICAL PROPERTIES OF TYLOSE PSO 810001:
Physical state : Solid
Appearance : Powder.
Colour : whitish
Odour : odourless
pH : 6 – 8 10g/l
Auto-ignition temperature : > 170 °C
Density : Density: 1.1 – 1.5 g/cm³ 20 °C
Solubility : Water: > 10 g/l @ 20°C
Log Pow : < 0
Explosive properties : Product is not explosive. Dust may form explosive mixture in air.
Minimum ignition energy : > 10 mJ
Conbustion class : 5
Smoldering temperature : > 450 °C
pmax : 10 bar
Dust explosion category : ST1
KSt : < 200 bar*m/s
Ignition temperature : > 400 °C

C.I. Pigment Blue 29; C.I. 77007; Ultramarine; Ultramarine blue pigment; Azure blue; Azzurrum ultramarine; Azzurrum transmarinum; Azzuro oltramarino; azur d'Acre; pierre d'azur; Lazurstein; cas no: 57455-37-5, 67053-79-6

UCAR Ester EEP is a slow evaporating ether–ester solvent with excellent solvent properties for a wide range of coating applications.
UCAR Ester EEP provides excellent film formation due to its enhanced flow and leveling characteristics.
UCAR Ester EEP is a flammable, colorless liquid.

CAS: 763-69-9
MF: C7H14O3
MW: 146.18
EINECS: 212-112-9

UCAR Ester EEP is a low volatility ether ester with good solubility for a wide range of coating polymers.
The ether ester group, linear structure, and propionyl group at the molecular center allow this material to combine some properties not found in other solvents, such as slow volatilization rate, resistance to solvent cracking in baking applications, and compatibility with a wide range of polymers.

UCAR Ester EEP has high solubility, low solution viscosity (relative to its evaporation rate), good solvent release from the film, good flow and leveling properties in a wide range of coatings.
UCAR Ester EEP solvent has moderate odor, low surface tension and high resistivity; it has the special function of preventing silver powder from thickening and blackening; UCAR Ester EEP also has the effect of preventing sedimentation in the use of aluminum silver paste.

UCAR Ester EEP is a cycloaddition product of ethyl 3-ethoxypropanoate.
UCAR Ester EEP has been shown to be more chemically stable than the reactants and has an increased uptake in the reaction solution.
UCAR Ester EEP is able to undergo a cycloaddition process with diethyl succinate under conditions of high temperature and pressure, leading to the formation of methyl ethyl malonic acid.

This chemical reaction takes place via an intermolecular hydrogen bonding interaction between the ethoxy group on one molecule and the ester group on the other molecule.
The cyclohexane ring on each molecule also forms a hydrogen bonding interaction with UCAR Ester EEP's corresponding methyl or ethyl groups.
UCAR Ester EEP is not reactive in its pure form but can undergo reactions when exposed to chemicals such as potassium hydroxide, which leads to its degradation into propionic acid and ethanol.

UCAR Ester EEP Chemical Properties
Melting point: -75 °C
Boiling point: 166 °C (lit.)
Density: 0.95 g/mL at 25 °C (lit.)
Vapor density: 5.03 (vs air)
Vapor pressure: 2.0 hPa (25 °C)
Refractive index: n20/D 1.405(lit.)
Fp: 126 °F
Storage temp.: Store below +30°C.
Solubility water: soluble54.1 g/L at 20°C
Form: Liquid
Color: Clear
Water Solubility: 1.6 g/100 mL (20 ºC)
InChIKey: BHXIWUJLHYHGSJ-UHFFFAOYSA-N
LogP: 1.47 at 20℃
CAS DataBase Reference: 763-69-9(CAS DataBase Reference)
NIST Chemistry Reference: UCAR Ester EEP (763-69-9)
EPA Substance Registry System: UCAR Ester EEP (763-69-9)

Uses
UCAR Ester EEP is used in the synthesis of phenols and selective inhibitors of cyclin-dependant kinase 4/6 for novel cancer therapies.
UCAR Ester EEP is also used as a solvent to prepare polymers.
Further, UCAR Ester EEP is used in paints and coatings.
UCAR Ester EEP used as solvent in preparing new polymers.
UCAR Ester EEP is mainly used in automotive coatings (original paint, refinishing paint), plastic paint, paint for household appliances, and can be used in screen printing inks, other inks and graphic products, and slow-drying solvents for high-grade inks.

Reactivity Profile
UCAR Ester EEP is an ester.
Esters react with acids to liberate heat along with alcohols and acids.
Strong oxidizing acids may cause a vigorous reaction that is sufficiently exothermic to ignite the reaction products.
Heat is also generated by the interaction of esters with caustic solutions.
Flammable hydrogen is generated by mixing esters with alkali metals and hydrides.
Liquid or mist may irritate th eyes and skin.
May cause headache, nausea and vomiting, central nervous system depression with dizziness, drowsiness and unconsciousness.

Synonyms
Ethyl 3-ethoxypropionate
Ethyl 3-ethoxypropanoate
763-69-9
3-Ethoxypropionic acid ethyl ester
Propanoic acid, 3-ethoxy-, ethyl ester
Ethyl-3-ethoxypropionate
Ethoxypropionic acid, ethyl ester
Ethyl beta-ethoxypropionate
NSC 8870
PROPIONIC ACID, 3-ETHOXY-, ETHYL ESTER
EINECS 212-112-9
Ethylester kyseliny 3-ethoxypropionove
UNII-EC38RSJ79J
BRN 1751976
EC38RSJ79J
Ethyl .beta.-ethoxypropionate
AI3-03254
DTXSID0027309
Ethylester kyseliny 3-ethoxypropionove [Czech]
NSC-8870
3-Ethoxy-propionic acid ethyl ester
EC 212-112-9
EEP Solvent
Ektapro EEP
MFCD00051356
Ethyl3-ethoxypropanoate
ethyl-3-ethoxypropionat
EEP (CHRIS Code)
Ethyl 3-Ethyoxypropionate
3-ethoxypropionic acid ethyl
SCHEMBL37036
WLN: 2OV2O2
DTXCID907309
CHEMBL3561286
Ethyl 3-ethoxypropionate, 99%
BHXIWUJLHYHGSJ-UHFFFAOYSA-
NSC8870
Ethyl 3-ethoxypropionate, >=99%
3-ethoxy-propanoic acid ethyl ester
Tox21_200179
Ethyl ester of 3-ethoxypropanoic acid
AKOS000120095
CS-W013312
.beta.-Ethoxypropionic acid ethyl ester
NCGC00248553-01
NCGC00257733-01
CAS-763-69-9
LS-124674
E0319
FT-0625748
FT-0652028
EN300-20634
E83003
A838683
J-520873
Q22829038
InChI=1/C7H14O3/c1-3-9-6-5-7(8)10-4-2/h3-6H2,1-2H3
EEP

UCAR n-Butyl Propionate is a butyl ester of propionic acid.
UCAR n-Butyl Propionate has the chemical formula CH3CH2COO(CH2)3CH3.
UCAR n-Butyl Propionate is a plant metabolite, a human metabolite and an insect attractant.

CAS: 590-01-2
MF: C7H14O2
MW: 130.18
EINECS: 209-669-5

UCAR n-Butyl Propionate is a propanoate ester of butan-1-ol.
UCAR n-Butyl Propionate has a role as a plant metabolite, a human metabolite, an insect attractant and a flavouring agent.
UCAR n-Butyl Propionate is functionally related to a butan-1-ol.
A water-white liquid with an apple-like odor.
Less dense than water.
Flash point 90°F.

May irritate skin and eyes.
UCAR n-Butyl Propionate used to make perfumes and flavorings.
UCAR n-Butyl Propionate is used as a solvent or lacquer thinner; and in perfumes and flavoring
UCAR n-Butyl Propionate is an ester of propionic acid, which is a naturally occurring fatty acid found in many plants and animals.

UCAR n-Butyl Propionate is a colorless liquid with a sweet, fruity odor and a low vapor pressure.
UCAR n-Butyl Propionate is used as a flavoring agent and a solvent in food, pharmaceutical, and cosmetic products.
UCAR n-Butyl Propionate is also used as a plasticizer and in the manufacture of perfumes, dyes, and other chemicals.
In addition, UCAR n-Butyl Propionate is used as a solvent in the production of paints, varnishes, and other coatings.

UCAR n-Butyl Propionate Chemical Properties
Melting point: -75 °C
Boiling point: 145 °C/756 mmHg (lit.)
Density: 0.875 g/mL at 25 °C (lit.)
Vapor density: 4.5 (vs air)
Vapor pressure: 4.6hPa at 20℃
Refractive index: n20/D 1.401(lit.)
FEMA: 2211 | BUTYL PROPIONATE
Fp: 101 °F
Storage temp.: Flammables area
Solubility: 1.5g/l
Form: Liquid
Color: Clear colorless
Odor: at 100.00 %. earthy sweet weak rose
Odor Type: fruity
Odor Threshold: 0.036ppm
Water Solubility: 0.2 g/100 mL (20 ºC)
JECFA Number: 143
Merck: 14,1587
LogP: 2.67 at 20℃
CAS DataBase Reference: 590-01-2(CAS DataBase Reference)
NIST Chemistry Reference: PUCAR n-Butyl Propionate(590-01-2)
EPA Substance Registry System: UCAR n-Butyl Propionate (590-01-2)

UCAR n-Butyl Propionate is a flammable, colorless to straw-yellow liquid with an apple-like odor.
UCAR n-Butyl Propionate has a characteristic earthy, faintly sweet odor and apricot-like taste.
Reported found in fresh apple, apple juice, melon, strawberry, Gruyere de Comte cheese and plum.
UCAR n-Butyl Propionate is a colorless liquid with a pear drops-like or apple-like odor.
The liquid is less dense than water.
UCAR n-Butyl Propionate's vapor is 4.5 times denser than the air at the mean ocean level.

Uses
UCAR n-Butyl Propionate is a moderately fast evaporating solvent.
UCAR n-Butyl Propionate's linear structure contributes to effective viscosity reduction and improves solvent diffusion from coating films.
UCAR n-Butyl Propionate is used solvent for nitrocellulose, retarder in lacquer thinner, ingredient of perfumes, flavors.

UCAR n-Butyl Propionate is used to make fragrances, perfumes and as a flavoring.
UCAR n-Butyl Propionate is also used in paints and primers for auto body or engine, appliance coatings (paints designed specifically for painting household items and vehicles like microwave ovens, refrigerators and automobiles), enamels, lacquers, and printing inks, as a solvent for adhesives and nitrocellulose, and in polymerization reactions for acrylic resins.

Preparation
By esterification of propionic acid with n-butyl alcohol in the presence of concentrated H2SO4 or p-toluene sulfonic acid.
UCAR n-Butyl Propionate is derived by esterification of propionic acid with butanol.

CH3CH2COOH + CH3(CH2)3OH ⇌ CH3CH2COO(CH2)3CH3 + H2O

Hazards and Toxicity
UCAR n-Butyl Propionate may irritate skin and eyes.
Exposure to its vapor may cause eye and respiratory system irritation.
Upon ingestion, causes abdominal pain and nausea.
UCAR n-Butyl Propionate is very flammable.
UCAR n-Butyl Propionate may ignite even at ambient temperatures.
Above 32 °C (90 °F), explosive mixtures with air may be formed.
Strong oxidizing acids may cause a violent reaction that is sufficiently exothermic to ignite UCAR n-Butyl Propionate and the reaction products.
Upon catching a fire, irritating, toxic and suffocating gases may be produced, such as carbon dioxide and carbon monoxide.

Reactivity Profile
UCAR n-Butyl Propionate is an ester.
Esters react with acids to liberate heat along with alcohols and acids.
Strong oxidizing acids may cause a vigorous reaction that is sufficiently exothermic to ignite the reaction products.
Heat is also generated by the interaction of esters with caustic solutions.
Flammable hydrogen is generated by mixing esters with alkali metals and hydrides.

Synonyms
Butyl propionate
Butyl propanoate
590-01-2
N-BUTYL PROPIONATE
Propanoic acid, butyl ester
n-Butyl propanoate
Propionic acid, butyl ester
Propionic Acid Butyl Ester
FEMA No. 2211
Butyl propionate (natural)
NSC 8449
n-Butyl n-propionate
EINECS 209-669-5
propanoic acid butyl ester
UN1914
UNII-2NXC4AK99E
BRN 1700932
2NXC4AK99E
Butyl ester of propanoic acid
AI3-24352
DTXSID5027223
NSC-8449
Butyl propionate [UN1914] [Flammable liquid]
4-02-00-00708 (Beilstein Handbook Reference)
n-butylpropionate
propionic acid butyl
MFCD00009448
Butyl propionate, 99%
Propionic acid-butyl ester
SCHEMBL26794
DTXCID907223
BUTYL PROPIONATE [FHFI]
CHEMBL3561586
N-BUTYL PROPIONATE [MI]
CHEBI:89831
FEMA 2211
Butyl propionate, >=98%, FG
NSC8449
Tox21_201691
Butyl propionate, analytical standard
NA1914
AKOS015907872
LS-2607
UN 1914
NCGC00249097-01
NCGC00259240-01
CAS-590-01-2
FT-0623318
FT-0623319
P0502
Butyl propanoate; (Propanoic acid, butyl ester)
Butyl propionate [UN1914] [Flammable liquid]
A832103
Q2726127
InChI=1/C7H14O2/c1-3-5-6-9-7(8)4-2/h3-6H2,1-2H

A propanoate ester of pentan-1-ol.
Colorless liquid with an apple-like odor.
Floats on water.

CAS: 624-54-4
MF: C8H16O2
MW: 144.21
EINECS: 210-852-7

UCAR n-Pentyl Propionate is an organic ester formed by the condensation of pentan-1-ol and propanoic acid.
UCAR n-Pentyl Propionate is a colorless liquid with an apple-like odor, that floats on water.

UCAR n-Pentyl Propionate Chemical Properties
Melting point: -75 °C
Boiling point: 169 °C(lit.)
Density: 0.873 g/mL at 25 °C(lit.)
Vapor pressure: 1.7hPa at 20℃
FEMA: 2082 | ISOAMYL PROPIONATE
Refractive index: n20/D 1.4074(lit.)
Fp: 133 °F
Storage temp.: Flammables area
Color: Colorless liquid
Odor: fruity, apricot-pineapple odor
Odor Type: fruity
Water Solubility: 706.7mg/L(20 ºC)
LogP: 2.83 at 25℃
EPA Substance Registry System: UCAR n-Pentyl Propionate (624-54-4)

Uses
UCAR n-Pentyl Propionate, an ester, has been employed for the evaluation of experimental values of HEm and VEm at 318.15K for the binary mixtures of alkyl propanoates with alkanes.

Reactivity Profile
UCAR n-Pentyl Propionate is an ester.
Esters react with acids to liberate heat along with alcohols and acids.
Strong oxidizing acids may cause a vigorous reaction that is sufficiently exothermic to ignite the reaction products.
Heat is also generated by the interaction of esters with caustic solutions.
Flammable hydrogen is generated by mixing esters with alkali metals and hydrides.
Special Hazards of Combustion Products: Irritating vapors and toxic gases, such as carbon dioxide and carbon monoxide, may be formed when involved in fire.
Exposure can cause irritation of eyes, nose and throat.

Synonyms
Pentyl propionate
Pentyl propanoate
AMYL PROPIONATE
n-Pentyl propionate
624-54-4
Amyl propanoate
Propanoic acid, pentyl ester
Pentyl propanate
n-Amyl propionate
n-Pentyl propanoate
Propionic acid, pentyl ester
NSC 7931
n-Amyl propionate (natural)
N-Amyl n-propionate
EINECS 210-852-7
propionic acid pentyl ester
BRN 1747102
AI3-24356
UNII-826P0596UJ
NSC-7931
826P0596UJ
EC 210-852-7
Propionic acid, pentyl ester (6CI,7CI,8CI)
PPE (CHRIS Code)
Pentyl propionate, >=99%
SCHEMBL20847
DTXSID4041606
CHEBI:87373
NSC7931
TWSRVQVEYJNFKQ-UHFFFAOYSA-N
MFCD00048849
AKOS015902810
LS-121581
FT-0622381
Q3050158

Acts as a fast evaporating, non-HAP solvent.
Offers stronger solvency for high solids coatings.
Provides proper volatility for high solids coatings and printing inks applications.

CAS: 106-36-5
MF: C6H12O2
MW: 116.16
EINECS: 203-389-7

Improves solvent diffusion from coating films.
Possesses linear structure giving faster diffusion through coating and ink films.
Imparts high electrical resistance for electrostatically sprayed coatings.
Used in automotive refinish, OEM coatings, appliance coatings, and printing inks.
Reported found among the volatile constituents of grape var. white sauvignon.
Also reported found in fresh apple, apple juice, apricot, melon, papaya, pear, Gruyere de Comte cheese, rum, cider, popcorn, durian, olive, malt whiskey and coffee.
UCAR n-Propyl Propionate is a propanoate ester resulting from the formal condensation of the hydroxy group of propanol with the carboxy group of propanoic acid.

UCAR n-Propyl Propionate has a role as a human metabolite, a rat metabolite, a biomarker and a fungal metabolite.
UCAR n-Propyl Propionate is functionally related to a propan-1-ol.
UCAR n-Propyl Propionate and water mixtures can be separated by pervaporation using PEBA membranes.
The diffusivity of pure UCAR n-Propyl Propionate in the PEBA membrane is about 28 times higher than pure water diffusivity.
UCAR n-Propyl Propionate is the organic compound with the molecular formula C6H12O2.

UCAR n-Propyl Propionate is the ester of propanol and propionic acid.
Like most esters, UCAR n-Propyl Propionate is a colorless liquid with a fruity odor.
The scent of UCAR n-Propyl Propionate is described as a chemically tinged pineapple or pear.
UCAR n-Propyl Propionate is used in perfumery and as a solvent.
The refractive index at 20 °C is 1.393.
Because UCAR n-Propyl Propionate is a low-odor, moderately volatile, non-HAP ester solvent with good solvent activity and versatility, UCAR n-Propyl Propionate is considered a safer substitute for toluene.

UCAR n-Propyl Propionate Chemical Properties
Melting point: −76 °C(lit.)
Boiling point: 122-124 °C(lit.)
Density: 0.881 g/mL at 25 °C(lit.)
Vapor density: 4 (vs air)
Vapor pressure: 18.53hPa at 25℃
Refractive index: n20/D 1.393(lit.)
FEMA: 2958 | PROPYL PROPIONATE
Fp: 76 °F
Storage temp.: Flammables area
Solubility: 5g/l
Form: Liquid
Color: Clear colorless
Specific Gravity: 0.882 (20/4℃)
Odor: at 100.00 %. sharp chemical pungent sweet fruity pineapple winey
Odor Type: chemical
Odor Threshold: 0.058ppm
Explosive limit: 1.3%(V)
Water Solubility: Soluble in water. (5g/L).
JECFA Number: 142
Merck: 14,7867
BRN: 1699993
LogP: 1.85 at 25℃
CAS DataBase Reference: 106-36-5(CAS DataBase Reference)
NIST Chemistry Reference: UCAR n-Propyl Propionate (106-36-5)
EPA Substance Registry System: UCAR n-Propyl Propionate (106-36-5)

UCAR n-Propyl Propionate has a complex, fruity odor reminiscent of apple, banana and pineapple.
UCAR n-Propyl Propionate has a somewhat pleasant, bitter flavor.

Uses
UCAR n-Propyl Propionate is a general reagent which can be used in various transesterification reactions.
UCAR n-Propyl Propionate is used as Solvent for nitrocellulose, paints, varnishes, lacquers, coating agents.
UCAR n-Propyl Propionate is a fast evaporating solvent.
UCAR n-Propyl Propionate's linear structure contributes to effective viscosity reduction and improves solvent diffusion from coating films.
UCAR n-Propyl Propionate has application in automotive refinish, OEM coatings, appliance coatings, printing inks and as polymerization solvent.
UCAR n-Propyl Propionate's good activity yields efficient resin viscosity reduction that enables the development of lower VOC coatings.
UCAR n-Propyl Propionate's high electrical resistivity is beneficial in optimizing transfer efficiency in coatings applied via electrostatic spray equipment.

Preparation
UCAR n-Propyl Propionate was synthesized by esterification of propyl alcohol with the corresponding acid in the presence of concentrated H2SO4, or in the presence of BF3.

Synonyms
PROPYL PROPIONATE
Propyl propanoate
106-36-5
Propanoic acid, propyl ester
n-Propyl propionate
n-Propyl propanoate
Propionic acid, propyl ester
n-Propyl n-propionate
Propylester kyseliny propionove
FEMA No. 2958
Propionic Acid Propyl Ester
Propyl propionate (natural)
NSC 72022
Propionic acid n-propyl ester
n-Propylpropropionate
Propyl ester of propanoic acid
EINECS 203-389-7
UNII-G09TRV00GK
Propanoic acid propyl ester
Propionic acid-propyl ester
Propylester kyseliny propionove [Czech]
BRN 1699993
G09TRV00GK
AI3-24357
DTXSID4042337
CHEBI:89828
NSC-72022
WE(3:0/3:0)
4-02-00-00707 (Beilstein Handbook Reference)
Propyl-propanoate
chlorhexidineacetate
propionic acid propyl
Propionate de propyle
n-Propyl n-propanoate
Propyl propionate, 99%
Propionoic acid propyl ester
SCHEMBL62961
WLN: 3OV2
PROPYL PROPANOATE [MI]
PROPYL PROPIONATE [FCC]
CHEMBL3185284
DTXCID2022337
PROPYL PROPIONATE [FHFI]
FEMA 2958
AMY21939
NSC72022
Tox21_301107
LMFA07010412
MFCD00009373
AKOS008947790
LS-3080
Propyl propionate, >=98%, FCC, FG
NCGC00248289-01
NCGC00255007-01
CAS-106-36-5
LS-13177
FT-0631593
P0511
F87292
J-001582
Q3119221
Propyl propionate, natural (US), >=98%, FCC, FG

UltimoPure Isostearic Acid is a unique fatty acid.
UltimoPure Isostearic Acid is useful in pharmaceutical, personal care, and cosmetic products.


CAS Number: 30399-84-9 / 2724-58-5
EC Number: 250-178-0
MDL number: MFCD00044082
Chem/IUPAC Name: Isooctadecanoic acid
INCI NAME: Isostearic Acid
Empirical Formula (Hill Notation): C18H36O2



SYNONYMS:
ISOOCTADECANOIC ACID, isostearic, 16-METHYLHEPTADECANOIC ACID, Isostearinsure, ISOSTEARIC ACID, 16-methyl-heptadecanoicaci, ISOSTEARIC ACID MIXED ISOMERS, Heptadedecanoicacid,16-Methyl, Heptadecanoic acid, 16-methyl-, Iso Octadecanoic Acid, Isooctadecanoic acid, Iso-octadecanoic acid, 16-methyl Heptadecanoic acid, ISOOCTADECANOIC ACID,Heptadecanoic acid, 16-methyl-, 16-Methylmargaric acid, Ar Prisorine 3505, Emersol 873, Isooctadecanoic acid, Prisorine 3509



Isostearic acid is a fatty acid molecule with an 18-carbon atom chain backbone.
UltimoPure Isostearic Acid is an isomer of stearic acid, meaning that they both have a chemical formula of C18H36O2, but differ in the arrangement of their atoms.


While stearic acid has a linear carbon chain with 18 carbon atoms, UltimoPure Isostearic Acid as a carbon chain with 17 atoms and a single carbon branch at the 16th carbon atom.
UltimoPure Isostearic Acid's chemical structure can be represented as (CH3)2CH(CH2)14CO2H.


UltimoPure Isostearic Acid is found naturally in meat products and vegetable oils.
UltimoPure Isostearic Acid is a methyl-branched fatty acid that is heptadecanoic acid (margaric acid) substituted by a methyl group at position 16.


UltimoPure Isostearic Acid, also known as iso-octadecanoic acid, is an branched saturated fatty acid derived from vegetable oils.
With the chemical formula of CH3(CH2)14COOH and CAS number30399-84-9 / 2724-58-5, UltimoPure Isostearic Acid appears as a waxy white solid at room temperature.


Compared to straight-chain stearic acid, UltimoPure Isostearic Acid contains a methyl branch on its carbon chain that gives it exceptional properties.
The methyl branch results in a lower melting point (around 52-55°C) and imparts greater solubility in oil phases.


UltimoPure Isostearic Acid also exhibits superior viscosity characteristics.
UltimoPure Isostearic Acid is a unique fatty acid.
UltimoPure Isostearic Acid is useful in pharmaceutical, personal care, and cosmetic products.


UltimoPure Isostearic Acid is an ester that acts as a dry emollient (smooth & dry) as well as being a co-emulsifier.
UltimoPure Isostearic Acid is a fatty acid that is used as an emollient in pharmaceutical preparations.
UltimoPure Isostearic Acid is a unique fatty acid.


UltimoPure Isostearic Acid is useful in pharmaceutical, personal care, and cosmetic products.
UltimoPure Isostearic Acid, derived from natural fats, is a crucial ingredient in cosmetics, lubricants, and industrial formulations.
UltimoPure Isostearic Acid's stable properties and emulsifying capabilities enhance the performance of diverse products.


Trusted for its versatility, UltimoPure Isostearic Acid ensures quality and functionality across various applications.
UltimoPure Isostearic Acid is a lightly-branched, liquid fatty acid produced by the reaction of oleic acid with a natural mineral
catalyst - there is no chemical addition in this reaction, isostearic acid is based 100% on the parent oil or fat.


UltimoPure Isostearic Acid is a liquid fatty acid derived from vegetables that offers a light sensation of lubricated skin, avoiding the dry sensation of topical products.
UltimoPure Isostearic Acid generates low viscosity for good spread and acts as a cleaning agent, emollient and greasing agent.


UltimoPure Isostearic Acid is used in applications which require a liquid fatty acid with exceptional stability: thermal stability in the
case of a lubricant, odour stability for a cosmetic formulation, and oxidation stability for products with long shelf-life requirements.
The branching structure of UltimoPure Isostearic Acid also enhances its dispersing power.


UltimoPure Isostearic Acid is an exceptionally mild liquid fatty acid that offers a light lubricious feel and can be used in many skin care and colour cosmetic applications.
UltimoPure Isostearic Acid is a clear, oily liquid that is used in a wide variety of cosmetics and personal care products.


UltimoPure Isostearic Acid is a vegetable-derived liquid fatty acid that offers a light lubricious skin feel, preventing a dry afterfeel from topical products.
UltimoPure Isostearic Acid promotes low viscosity for good spreading and acts as a cleansing agent, emollient and superfatting agent and is compatible with cold processing.


UltimoPure Isostearic Acid is a mixture of branched chain 18 carbon aliphatic acids.
100% vegetable based UltimoPure Isostearic Acid.
Due to its branched structure UltimoPure Isostearic Acid has a soft skin feel; forms a highly substantive lipid film and leaves a glossy appearance.


UltimoPure Isostearic Acid is unique, highly branched, saturated fatty acid.
Additionally, UltimoPure Isostearic Acid has excellent heat stability, oxidation resistance, pigment dispensing ability, defoaming property and is compatible with various organic solvents.


UltimoPure Isostearic Acid is a liquid fatty acid created from oleic acid.
UltimoPure Isostearic Acid's claimed to have great odour, thermal and oxidation stability and is great for the stabilization of pigments and mineral particles in oils and solvents. It's quite popular in foundations.


UltimoPure Isostearic Acid is a saturated fatty acid found in a variety of animal and plant species.
UltimoPure Isostearic Acid is light light-colored, liquid fatty acid consisting of methyl branched C18 fatty acid isomers with smaller amounts of linear staurated fatty acids and oleic acid.


The low unsaturation and especially the absence of poly-unsaturation results in excellent oxidation resistance and color stability.
UltimoPure Isostearic Acid is a long chain hydrocarbon with excellent color and thermo-oxidative stability for automotive and industrial coatings


UltimoPure Isostearic Acid is recommended for polyol esters in synthetic lubricants, for textile lubricants and hydraulic fluids among other general applications
UltimoPure Isostearic Acid is a top grade for cosmetics esters applications


UltimoPure Isostearic Acid is a vegetable derived recommended for less critical applications, but with oxidation stability better than oleic acid and its derivatives
UltimoPure Isostearic Acid has some features that are transparent and odorless, unlike straight chain fatty acids.



USES and APPLICATIONS of ULTIMOPURE ISOSTEARIC ACID:
UltimoPure Isostearic Acid is used for research use only.
UltimoPure Isostearic Acid is used similar to stearic or oleic acids.
UltimoPure Isostearic Acid is used in the synthesis of methyl-branched poly(hydroxyalkanoate)s, biosurfactants and silver nanoparticles.


UltimoPure Isostearic Acid helps the formula have higher stability.
UltimoPure Isostearic Acid is commonly used in place of some stearic acid in formulas.
UltimoPure Isostearic Acid is used to make the skin feel better.


UltimoPure Isostearic Acid has been shown to have skin-moisturizing and anti-inflammatory properties, which are due to its ability to inhibit the activity of phospholipase A2.
UltimoPure Isostearic Acid also has a high degree of chemical stability and adsorption capacity.


Its adsorption mechanism is not yet well understood, but UltimoPure Isostearic Acid appears to be related to its hydroxyl group.
UltimoPure Isostearic Acid has been used successfully in the treatment of congestive heart failure and can prevent the accumulation of lipids on the surface of blood vessels, thereby reducing atherosclerosis.


UltimoPure Isostearic Acid also functions as a substrate for the synthesis of isovaleric acid, which can be used as a fragrance ingredient in cosmetic products.
UltimoPure Isostearic Acid is a high quality 16-Methylheptadecanoic acid used in synthesis.


UltimoPure Isostearic Acid has been used as molecular tool for various biochemical applications.
UltimoPure Isostearic Acid has also been used in a wide array of other chemical and immunological applications.
UltimoPure Isostearic Acid has a wide range of industrial uses.


UltimoPure Isostearic Acid functions as a surfactant – cleansing agent, and a binder.
UltimoPure Isostearic Acid is used resin modification, Metallic pastes, Inks, Waxes and wax emulsifiers, Quaternary derivatives for textile softeners and antistats, Liquid stabilizers (metal soaps), and Anti-corrosion additives.


Cosmetic Uses of UltimoPure Isostearic Acid: binding agents, cleansing agents, surfactants, and surfactant - emulsifying
UltimoPure Isostearic Acid is a component of many cell membranes and is used in the synthesis of methyl-branched poly(hydroxyalkanoate)s, biosurfactants and silver nanoparticles.


Additionally, UltimoPure Isostearic Acid can modulate the activity of certain enzymes, including lipoxygenase, cyclooxygenase, and cytochrome P450, as well as inhibit the activity of certain transcription factors, such as NF-κB and AP-1.
Moreover, UltimoPure Isostearic Acid inhibits the growth of cancer cells.


UltimoPure Isostearic Acid has also been found to have anti-inflammatory and antioxidant properties.
UltimoPure Isostearic Acid is used bath, shower & soaps, Antiperspirants & deodorants, After sun, Body care, Eye colour, Face / neck skin care, Face colour, Hair colour, Lip colour, Shaving / hair removal, and Sun protection.


UltimoPure Isostearic Acid also offers film forming properties, making it ideal for use in soaps, shaving foams and liquid cleansers.
UltimoPure Isostearic Acid is compatible with cold processing.
Recommended topical use levels of UltimoPure Isostearic Acid is 0.5-5%


UltimoPure Isostearic Acid is used in cosmetic and industrial applications for the stabilisation of pigments and mineral particles in oils and solvents.
UltimoPure Isostearic Acid is mainly used as an additive in adhesives or lubricants for both paints and personal care products.


UltimoPure Isostearic Acid is used treatment / Conditioner, Leave-in treatment / Styling, Cleansing, Lotion / Toner, Milk / Cream / Serum, Foundation / Make-up Base, and Suncare, Lipstick / Gloss.
UltimoPure Isostearic Acid is a lightly-branched, liquid fatty acid produced by the reaction of oleic acid with a natural mineral catalyst – there is no chemical addition in this reaction, isostearic acid is based 100% on the parent oil or fat.


UltimoPure Isostearic Acid is used in applications which require a liquid fatty acid with exceptional stability: thermal stability in the case of a lubricant, odour stability for a cosmetic formulation, and oxidation stability for products with long shelf-life requirements.
UltimoPure Isostearic Acid is used for a cosmetic formulation.


UltimoPure Isostearic Acid is used industrial applications for the stabilisation of pigments mineral particles in oils and solvents.
The branching structure of UltimoPure Isostearic Acid also enhances its dispersing power, and it is used in cosmetic and industrial applications for the stabilisation of pigments and mineral particles in oils and solvents.



WHAT DOES ULTIMOPURE ISOSTEARIC ACID DO IN A FORMULATION?
*Binding
*Cleansing
*Emulsifying
*Surfactant



FEATURES OF ULTIMOPURE ISOSTEARIC ACID:
*Vegetable-based methyl-branched saturated fatty acid.
*Good solubility with ceramides.
*Low odor with our unique purification technology.



BENEFITS OF ULTIMOPURE ISOSTEARIC ACID:
*Flexibility - allows product to deform under stress and prevents cracking.
UltimoPure Isostearic Acid can also be used in conjunction with flexible substrates
*Easy to handle offering manufacturing flexibility
*Low color for low color applications and improved aesthetics
*Thermo-oxidative stability for longer product lifetime, and allowing for exposure to high temperature conditions
*Pigment wetting - allows high loading of pigment/fillers which can bring cost savings



SCIENTIFIC FACTS OF ULTIMOPURE ISOSTEARIC ACID:
UltimoPure Isostearic Acid, a fatty acid, is a blend of different forms of octadecanoic acid, which is obtained from animal and vegetable fats and oils.
UltimoPure Isostearic Acid can be prepared from many sources including soybean oil or tallow



FUNCTIONS OF ULTIMOPURE ISOSTEARIC ACID:
*Spreading agents



PHYSICAL and CHEMICAL PROPERTIES of ULTIMOPURE ISOSTEARIC ACID:
Molecular Weight: 284.48 g/mol
Molecular Formula: C18H36O2
Canonical SMILES: CC(C)CCCCCCCCCCCCCCC(=O)O
InChI: InChI=1S/C18H36O2/c1-17(2)15-13-11-9-7-5-3-4-6-8-10-12-14-16-18(19)20/h17H,3-16H2,1-2H3,(H,19,20)
InChIKey: XDOFQFKRPWOURC-UHFFFAOYSA-N
Boiling Point: 400.8±13.0°C at 760 Torr (estimate)
Melting Point: 67.8-68.5°C
Flash Point: 225.6°C
Purity: ≥95%
Density: 0.887±0.06 g/cm3
Appearance: White powder; White to pale yellow solid
Storage: Store at 2-8°C
Assay: 0.99
EINECS: 220-336-3

MDL: MFCD00044082
Refractive Index: 1.444
Stability: Stable
Solubility: Soluble in organic solvents, insoluble in water; Soluble in acids
Chemical Properties:
pH of aqueous solution: 6.5 (slightly acidic)
Toxicity: Non-toxic
Flammability: Flammable
Hygroscopicity: Low hygroscopicity
LogP: 7.674 (estimated)
IUPAC Name: 16-methylheptadecanoic acid
Appearance: White solid (estimated)
Assay: 95.00 to 100.00%
Boiling Point: 400.00 to 401.00 °C @ 760.00 mm Hg (estimated)

Flash Point: 438.00 °F TCC (225.70 °C) (estimated)
logP (o/w): 7.674 (estimated)
Soluble in water: 0.007116 mg/L @ 25 °C (estimated)
Physical State: Solid
Color: Not available
Odor: Not available
Melting Point/Freezing Point: Not available
Initial Boiling Point and Boiling Range: Not available
Flammability (Solid, Gas): Not available
Upper/Lower Flammability or
Explosive Limits: Not available
Flash Point: Not available
Autoignition Temperature: Not available

Decomposition Temperature: Not available
pH: Not available
Viscosity: Not available
Water Solubility: Not available
Partition Coefficient (n-octanol/water): Not available
Vapor Pressure: Not available
Density: Not available
Relative Density: Not available
Relative Vapor Density: Not available
Particle Characteristics: Not available
Explosive Properties: Not available
Oxidizing Properties: Not available
Other Safety Information: Not available



FIRST AID MEASURES of ULTIMOPURE ISOSTEARIC ACID:
-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 ULTIMOPURE ISOSTEARIC ACID:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Sweep up and shovel.
Keep in suitable, closed containers for disposal.



FIRE FIGHTING MEASURES of ULTIMOPURE ISOSTEARIC ACID:
-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 ULTIMOPURE ISOSTEARIC ACID:
-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:
Choose body protection in relation to its type.
*Respiratory protection:
Respiratory protection is not required.
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of ULTIMOPURE ISOSTEARIC ACID:
-Precautions for safe handling:
*Advice on protection against fire and explosion:
Normal measures for preventive fire protection.
*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.
*Storage stability:
Recommended storage temperature: 2 - 8 °C
*Storage class:
Storage class (TRGS 510): 13: Non Combustible Solids



STABILITY and REACTIVITY of ULTIMOPURE ISOSTEARIC ACID:
-Reactivity:
No data available
-Chemical stability:
Stable under recommended storage conditions.
-Possibility of hazardous reactions:
No data available
-Conditions to avoid:
No data available

Ultramarine Blue Pigment is a commonly used blue pigment, widely employed in the production of paints and inks across various industries.
Known for Ultramarine Blue Pigment high color durability and stability, this pigment is a popular choice in the plastic, paint, and printing sectors.
Offering a broad color range, Ultramarine Blue Pigment contributes to both aesthetic and functional qualities in diverse applications.

CAS: 57455-37-5
MF: Al6Na8O24S3Si6
MW: 994.500988

Synonyms
Ultramarine Blue, Azure blue, 57455-37-5, UNII-I39WR998BI, I39WR998BI, C. I. 77007, Lazurite, Ultramarine, LAZURITE [MI], ULTRAMARINE [MI], 3516 ULTRA BLUE, 3522 ULTRA BLUE, ULTRAMARINE (MINERAL), CI 77007 [INCI], ULTRAMARINE BLUE (MINERAL), ULTRAMARINE BLUE CI 77007, AKOS032950034, ALUMINUM SODIUM THIOSILICATE BLUE, LAZURITE (NA5(AL3(SIO4)3S)), LAZURITE (CA2NA6(AL6(SIO4)6(SO4)S)), Q219660.

One of the distinguishing features of Ultramarine Blue Pigment is its exceptional colorfastness, ensuring that the vivid blue tones remain vibrant over time, even in challenging environmental conditions.
This quality makes Ultramarine Blue Pigment a preferred choice in sectors such as automotive coatings, where longevity and resistance to fading are paramount.

In the realm of plastic manufacturing, Ultramarine Blue Pigment plays a crucial role in providing diverse products with an attractive and consistent blue coloration.
From packaging materials to a myriad of plastic goods, Ultramarine Blue Pigment adds an aesthetic appeal while maintaining durability.
Moreover, Ultramarine Blue Pigment is a staple in the world of textile dyeing, offering textile manufacturers the means to achieve a range of blue shades with reliability and reproducibility.
Ultramarine Blue Pigment compatibility with various substrates and dyeing processes enhances its versatility in the textile industry.

Beyond its application in coloration, Ultramarine Blue Pigment is known for its chemical stability, ensuring compatibility with different formulations in the ink industry.
This stability translates into consistent performance in printing processes, making Ultramarine Blue Pigment a valuable component in the production of inks for diverse printing applications.
In summary, Ultramarine Blue Pigment stands out as a go-to blue pigment, appreciated for its enduring color qualities and versatility across industries.
Ultramarine Blue Pigment widespread use in paints, inks, plastics, textiles, and more underscores its significance in contributing to the visual appeal and functionality of a diverse array of products.

Ultramarine Blue Pigment Chemical Properties
Specific Gravity: 2.3
Hydrolytic Sensitivity 1: no significant reaction with aqueous systems
Stability: Stable. Incompatible with strong oxidizing agents.
CAS DataBase Reference: 57455-37-5(CAS DataBase Reference)
EPA Substance Registry System: C.I. Ultramarine Blue Pigment (57455-37-5)

Uses
During the Middle Ages, Ultramarine Blue Pigment was used by artists as the blue from over the sea.
Ultramarine Blue Pigment was derived from the semiprecious stone, lapis lazuli, imported from Afghanistan.
Since 1828 when it was first synthesized, the supply of the pigment has become abundant.
Ultramarine pigments are used in plastics, paints, printing inks, paper, artist colors, laundry detergents (optical brightener), and toys.

Synthetic production
In 1990, an estimated 20,000 tons of ultramarine were produced industrially. The raw materials used in the manufacture of synthetic ultramarine are the following:

White kaolin,
Anhydrous sodium sulfate (Na2SO4),
Anhydrous sodium carbonate (Na2CO3),
Powdered sulfur,
Powdered charcoal or relatively ash-free coal, or colophony in lumps.[19]

The preparation is typically made in steps:
The first part of the process takes place at 700 to 750 °C in a closed furnace, so that sulfur, carbon and organic substances give reducing conditions.
This yields a yellow-green product sometimes used as a pigment.
In the second step, air or sulfur dioxide at 350 to 450 °C is used to oxidize sulfide in the intermediate product to S2 and Sn chromophore molecules, resulting in the blue (or purple, pink or red) pigment.
The mixture is heated in a kiln, sometimes in brick-sized amounts.

The resultant solids are then ground and washed, as is the case in any other insoluble pigment's manufacturing process; the chemical reaction produces large amounts of sulfur dioxide.
Ultramarine Blue Pigment poor in silica is obtained by fusing a mixture of soft clay, sodium sulfate, charcoal, sodium carbonate, and sulfur.
The product is at first white, but soon turns green "green ultramarine" when it is mixed with sulfur and heated.
The sulfur burns, and a fine blue pigment is obtained.
Ultramarine rich in silica is generally obtained by heating a mixture of pure clay, very fine white sand, sulfur, and charcoal in a muffle furnace.
A blue product is obtained at once, but a red tinge often results.
The different ultramarines—green, blue, red, and violet—are finely ground and washed with water.

Synthetic ultramarine is a more vivid blue than natural ultramarine, since the particles in synthetic ultramarine are smaller and more uniform than the particles in natural ultramarine and therefore diffuse light more evenly.
Ultramarine Blue Pigment color is unaffected by light nor by contact with oil or lime as used in painting.
Hydrochloric acid immediately bleaches it with liberation of hydrogen sulfide.
Even a small addition of zinc oxide to the reddish varieties especially causes a considerable diminution in the intensity of the color.
Modern, synthetic ultramarine blue is a non-toxic, soft pigment that does not need much mulling to disperse into a paint formulation.

UNDECANE N° CAS : 1120-21-4 "Satisfaisant" dans toutes les catégories. Origine(s) : Minérale Nom INCI : UNDECANE N° EINECS/ELINCS : 214-300-6 Classification : COV Compatible Bio (Référentiel COSMOS) Ses fonctions (INCI) Emollient : Adoucit et assouplit la peau Agent d'entretien de la peau : Maintient la peau en bon état

Ultramoll® VII is a high-performance plasticizer used in various polymer applications for its excellent flexibility and compatibility.
Ultramoll® VII is characterized by its ability to enhance the flexibility and durability of polymer products.
The chemical formula for Ultramoll® VII is proprietary, and it is commonly used in various industrial applications due to its superior properties.

CAS Number: 68515-49-1
EC Number: 271-091-4

Synonyms: Plasticizer, Ultramoll® VII, Polymer plasticizer, Ultramoll Polymer Plasticizer VII, Plasticizing Agent VII, Polymer Additive VII, Plasticizer Additive VII, PU Plasticizer VII, Ultramoll Plasticizer VII, Flexible Additive VII



APPLICATIONS


Ultramoll® VII is widely used in the formulation of flexible PVC products, providing excellent flexibility and durability.
Ultramoll® VII is essential in the manufacture of high-performance polyurethane foams, enhancing their flexibility.
Ultramoll® VII is utilized in the production of elastomers, improving their flexibility and longevity.

Ultramoll® VII is a preferred plasticizer for flexible and rigid foams due to its efficiency in enhancing flexibility.
Ultramoll® VII is used in automotive applications for its excellent flexibility and durability under various conditions.
Ultramoll® VII is found in the production of sealants and caulks, contributing to their flexibility and performance.

Ultramoll® VII is used in water-based polymer systems for its compatibility and efficiency in enhancing flexibility.
Ultramoll® VII is a key component in solvent-based polymer formulations, providing improved flexibility.
Ultramoll® VII is used in the textile industry to improve the flexibility and performance of coatings on fabrics.

Ultramoll® VII is employed in the production of rubber materials for its plasticizing properties.
Ultramoll® VII is used in the manufacturing of synthetic fibers, enhancing their flexibility and resilience.
Ultramoll® VII is used in the construction industry for high-performance coatings and sealants.

Ultramoll® VII is used in the creation of high-performance adhesives, providing improved flexibility and durability.
Ultramoll® VII is a key component in the production of plastics, enhancing their flexibility and mechanical properties.
Ultramoll® VII is utilized in the formulation of industrial coatings, ensuring improved flexibility and performance.

Ultramoll® VII is applied in the creation of specialty coatings for various industrial applications, ensuring enhanced flexibility and performance.
Ultramoll® VII is used in the production of coatings for metal surfaces, providing improved flexibility and durability.
Ultramoll® VII is essential in the creation of high-quality printing inks, enhancing flexibility and performance during printing.

Ultramoll® VII is used in the production of rubber products, ensuring consistent flexibility and performance.
Ultramoll® VII is employed in the automotive industry, used in high-performance coatings and adhesives for improved flexibility.
Ultramoll® VII is utilized in the production of wood coatings, enhancing their flexibility and durability.

Ultramoll® VII is found in the manufacture of specialty coatings for industrial machinery, providing improved flexibility and performance.
Ultramoll® VII is utilized in the formulation of adhesives and sealants, ensuring enhanced flexibility and performance.
Ultramoll® VII is a key ingredient in the production of polyurethane elastomers, enhancing their flexibility and longevity.

Ultramoll® VII is employed in the textile industry to improve the performance and flexibility of coatings on fabrics.
Ultramoll® VII is used in the rubber industry for its plasticizing properties, improving flexibility and performance.
Ultramoll® VII is essential in the production of high-performance industrial coatings, providing improved flexibility and durability.

Ultramoll® VII is a vital component in water-based and solvent-based polymer systems, ensuring enhanced flexibility and performance.
Ultramoll® VII is applied in the creation of high-performance industrial products, providing improved flexibility and durability.
Ultramoll® VII is used in the formulation of household and industrial coatings, enhancing their flexibility and performance.

Ultramoll® VII is utilized in the production of specialty coatings for electronic devices, providing improved flexibility.
Ultramoll® VII is found in the creation of specialty inks for various applications, enhancing flexibility and performance.
Ultramoll® VII is used in the production of ceramic and glass coatings, improving their flexibility and application properties.

Ultramoll® VII is applied in the creation of coatings for plastic surfaces, ensuring improved flexibility and performance.
Ultramoll® VII is utilized in the formulation of coatings for wood surfaces, providing enhanced flexibility and durability.
Ultramoll® VII is essential in the production of high-performance adhesives, ensuring improved flexibility and application properties.

Ultramoll® VII is used in the formulation of coatings for automotive applications, providing improved flexibility and performance.
Ultramoll® VII is utilized in the production of specialty adhesives and sealants, ensuring enhanced flexibility and durability.
Ultramoll® VII is found in the manufacture of coatings for industrial machinery, providing improved flexibility and performance.

Ultramoll® VII is employed in the creation of specialty coatings for various substrates, ensuring improved flexibility and performance.
Ultramoll® VII is used in the formulation of high-performance coatings for various applications, providing enhanced flexibility and performance.
Ultramoll® VII is a key component in the production of specialty inks for flexographic and gravure printing, ensuring improved flexibility and performance.

Ultramoll® VII is used in the creation of specialty inks for digital printing, providing enhanced flexibility and application properties.
Ultramoll® VII is essential in the production of high-performance industrial products, ensuring improved flexibility and performance.
Ultramoll® VII is utilized in the manufacture of environmentally friendly industrial products, providing enhanced flexibility and durability.

Ultramoll® VII is used in the creation of water-based and solvent-based products, ensuring improved flexibility and performance.
Ultramoll® VII is a critical ingredient in the formulation of specialty coatings for metal and plastic surfaces, providing enhanced flexibility and application properties.



DESCRIPTION


Ultramoll® VII is a high-performance plasticizer used in various polymer applications for its excellent flexibility and compatibility.
Ultramoll® VII is characterized by its ability to enhance the flexibility and durability of polymer products.

Ultramoll® VII is a versatile chemical compound used in various polymer applications.
Ultramoll® VII is known for its strong plasticizing properties, which improve the flexibility and performance of polymer products.
Ultramoll® VII provides excellent compatibility with a wide range of polymers, making it ideal for industrial coatings and adhesives.

Ultramoll® VII is compatible with a wide range of polymer systems, enhancing its versatility in different formulations.
Ultramoll® VII is widely used in the coatings, adhesives, elastomers, and sealants industries, among others.
Ultramoll® VII's non-toxic nature makes it safe for use in various industrial and consumer products.

Ultramoll® VII offers excellent flexibility, making it suitable for applications requiring enhanced flexibility and durability.
Ultramoll® VII is known for its ease of dispersion, ensuring uniform plasticizing in various systems.
Ultramoll® VII is essential in the creation of durable and high-performance polymer products.

Ultramoll® VII's strong plasticizing properties make it a preferred choice in the creation of high-quality industrial coatings.
Ultramoll® VII is an important precursor in the production of high-performance adhesives and sealants, providing improved flexibility.
Ultramoll® VII is widely used in the manufacture of durable and resilient polymer products, ensuring enhanced flexibility and performance.



PROPERTIES


Chemical Formula: Proprietary
Common Name: Ultramoll® VII
Molecular Structure: Proprietary
Appearance: Clear liquid
Density: 1.05 g/cm³
Viscosity: Low
Solubility: Miscible with most organic solvents
Reactivity: Low
Chemical Stability: Excellent
Compatibility: Wide range of polymer systems
Flexibility: Excellent
Dispersion: Easy



FIRST AID


Inhalation:
If Ultramoll® VII is inhaled, move the affected person to fresh air immediately.
If breathing difficulties persist, seek immediate medical attention.
If the person is not breathing, administer artificial respiration.
Keep the affected person warm and at rest.

Skin Contact:
Remove contaminated clothing and footwear.
Wash the affected skin area thoroughly with soap and water.
If skin irritation or rash develops, seek medical attention.
Launder contaminated clothing before reuse.

Eye Contact:
Flush the eyes with plenty of water for at least 15 minutes, lifting upper and lower eyelids.
Seek immediate medical attention if irritation or redness persists.
Remove contact lenses if present and easy to do; continue rinsing.

Ingestion:
Do not induce vomiting unless directed to do so by medical personnel.
Rinse the mouth thoroughly with water.
Seek immediate medical attention.
If the person is conscious, give small sips of water to drink.

Note to Physicians:
Treat symptomatically.
No specific antidote.
Provide supportive care.



HANDLING AND STORAGE


Handling:

Personal Protection:
Wear appropriate personal protective equipment (PPE), including chemical-resistant gloves, safety goggles or face shield, and protective clothing.
Use respiratory protection if ventilation is insufficient or if exposure limits are exceeded.

Ventilation:
Ensure adequate ventilation in the working area to control airborne concentrations below occupational exposure limits.
Use local exhaust ventilation or other engineering controls to minimize exposure.

Avoidance:
Avoid direct skin contact and inhalation of vapors.
Do not eat, drink, or smoke while handling Ultramoll® VII.
Wash hands thoroughly after handling.

Spill and Leak Procedures:
Use appropriate personal protective equipment.
Contain spills to prevent further release and minimize exposure.
Absorb spills with inert materials (e.g., sand, vermiculite) and collect for disposal.

Storage:
Store Ultramoll® VII in a cool, well-ventilated area away from incompatible materials (see SDS for specific details).
Keep containers tightly closed when not in use to prevent contamination.
Store away from heat sources, direct sunlight, and ignition sources.

Handling Cautions:
Avoid generating aerosols or mists.
Ground and bond containers during transfer operations to prevent static electricity buildup.
Use explosion-proof electrical equipment in areas where vapors may be present.


Storage:

Temperature:
Store Ultramoll® VII at temperatures recommended by the manufacturer.
Avoid exposure to extreme temperatures.

Containers:
Use approved containers made of compatible materials.
Check for leaks or damage in storage containers regularly.

Separation:
Store Ultramoll® VII away from incompatible materials, including strong acids, bases, oxidizing agents, and reducing agents.

Handling Equipment:
Use dedicated equipment for handling Ultramoll® VII to avoid cross-contamination.
Ensure all handling equipment is in good condition.

Security Measures:
Restrict access to storage areas.
Follow all applicable local regulations regarding the storage of hazardous materials.

Emergency Response:
Have emergency response equipment and materials readily available, including spill cleanup materials, fire extinguishers, and emergency eyewash stations.

cat's claw extract; cats claw extract; extract of the uncaria tomentosa, rubiaceae; UNCARIA TOMENTOSA EXTRACT CAS NO:999999-999-4

Undecanedioic Acid; 1,11-Undecanedioic acid; 1,9-Nonanedicarboxylic acid; Undecandiäure; ácido undecanodioico; Acide undécanedioïque; n-Nonane-omega,omega'-dicarboxylic acid; Undecane-1,11-dioic acid; CAS NO: 1852-04-6

UNDECETH-10; N° CAS : 34398-01-1; "Pas terrible" dans toutes les catégories.; Nom INCI : UNDECETH-10; Classification : Composé éthoxylé, Tensioactif non ionique Ses fonctions (INCI); Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation.Noms français : Éther de polyéthylène glycol (10) et d'undécyle ; Noms anglais : Poly(oxy-1,2-ethanediyl), alpha-undecyl-omega-hydroxy-

Undecanol, also known as N-undecyl alcohol or undecan-1-ol, belongs to the class of organic compounds known as fatty alcohols.
These are aliphatic alcohols consisting of a chain of a least six carbon atoms.
Thus, Undecanol is considered to be a fatty alcohol.

CAS Number: 112-42-5
EC Number: 203-970-5
Chemical Formula: CH3(CH2)10OH
Molar Mass: 172.31 g/mol

Undecanol, also known as N-undecyl alcohol or undecan-1-ol, belongs to the class of organic compounds known as fatty alcohols.
These are aliphatic alcohols consisting of a chain of a least six carbon atoms.

Thus, Undecanol is considered to be a fatty alcohol lipid molecule.
Undecanol is a very hydrophobic molecule, practically insoluble in water, and relatively neutral.

Undecanol is a colorless, water-insoluble liquid.
Undecanol has a floral citrus like odor, and a fatty taste and is used as a flavoring ingredient in foods.

Undecanol can be found in fruits including apples and bananas.
Undecanol is commonly produced by the reduction of 1-undecanal, the analogous aldehyde.

Undecanol, also known as Undecyl alcohol or 1-Hendecanol, is a fatty alcohol which can be found in foods like fruits, eggs, and cooked pork.
Ungraded products supplied by TCI America are generally suitable for common industrial uses or for research purposes but typically are not suitable for human consumption or therapeutic use.

Undecanol can be used as a precursor in the synthesis of undecanal by chemoselective oxidation using a fluorous derivative of TEMPO (2,2,6,6-tetramethylpiperidine-1-oxyl) radical as a catalyst.
Undecanol can be also used as a solvent in homogeneous liquid-liquid microextraction method.

Undecanol, also known by its IUPAC name 1-undecanol or undecan-1-ol, and by Undecanol trivial names undecyl alcohol and hendecanol, is a fatty alcohol.
Undecanol is a colorless, water-insoluble liquid of melting point 19 °C and boiling point 243 °C.

Undecanol appears as a water-white liquid with a mild odor.
Flash point 250 °F.
Slightly soluble in water.

Considered a marine pollutant by DOT.
Immediate steps should be taken to limit Undecanol spread to the environment.

As a liquid Undecanol can easily penetrate the soil and contaminate groundwater or streams.
Mildly irritating to both the eyes and skin.

Undecanol is a fatty alcohol that is undecane substituted by a hydroxy group at position 1.
Undecanol has a role as a metabolite.
Undecanol is a fatty alcohol and a primary alcohol.

Uses of Undecanol:
Undecanol can be used as a precursor in the synthesis of undecanal by chemoselective oxidation using a fluorous derivative of TEMPO (2,2,6,6-tetramethylpiperidine-1-oxyl) radical as a catalyst.
Undecanol can be also used as a solvent in homogeneous liquid-liquid microextraction method.

Consumer Uses:
Functional fluids (closed systems)
Intermediates
Processing aids, specific to petroleum production
Surface active agents

Industry Uses:
Functional fluids (closed systems)
Intermediate
Intermediates
Processing aids, specific to petroleum production
Surface active agents

Industrial Uses and Production of Undecanol:
Undecanol has a floral citrus like odor, and a fatty taste and is used as a flavoring ingredient in foods.
Undecanol is commonly produced by the reduction of undecanal, the analogous aldehyde.

General Manufacturing Information of Undecanol:

Industry Processing Sectors:
All Other Chemical Product and Preparation Manufacturing
Oil and Gas Drilling, Extraction, and Support activities
Soap, Cleaning Compound, and Toilet Preparation Manufacturing

Natural Occurrence of Undecanol:
Undecanol is found naturally in many foods such as fruits (including apples and bananas), butter, eggs and cooked pork.

Pharmacology and Biochemistry of Undecanol:

Action Mechanism:
Undecanol was the most potent fungicide followed by decanol.
The time-kill curve study showed that undecanol was fungicidal against S. cerevisiae at any growth stages was not influenced by pH values.

The alcohols tested inhibited glucose-induced acidification by inhibiting the plasma membrane H(+)-ATPase.
The primary antifungal action of amphipathic medium-chain (C(9)-C(12)) alkanols comes mainly from their ability as nonionic surfactants to disrupt the native membrane-associated function of the integral proteins.

Human Metabolite Information of Undecanol:

Cellular Locations:
Extracellular
Membrane

Handling and Storage of Undecanol:

Nonfire Spill Response:
Do not touch or walk through spilled material.
Stop leak if you can do Undecanol without risk.

Prevent dust cloud.
For Asbestos, avoid inhalation of dust.

Cover spill with plastic sheet or tarp to minimize spreading.
Do not clean up or dispose of, except under supervision of a specialist.

SMALL DRY SPILL:
With clean shovel, place material into clean, dry container and cover loosely; move containers from spill area.

SMALL SPILL:
Pick up with sand or other non-combustible absorbent material and place into containers for later disposal.

LARGE SPILL:
Dike far ahead of liquid spill for later disposal.
Cover powder spill with plastic sheet or tarp to minimize spreading.
Prevent entry into waterways, sewers, basements or confined areas.

Fire Fighting of Undecanol:

SMALL FIRE:
Dry chemical, CO2, water spray or regular foam.

LARGE FIRE:
Water spray, fog or regular foam. Do not scatter spilled material with high-pressure water streams.
If Undecanol can be done safely, move undamaged containers away from the area around the fire.
Dike runoff from fire control for later disposal.

FIRE INVOLVING TANKS:
Cool containers with flooding quantities of water until well after fire is out.
Withdraw immediately in case of rising sound from venting safety devices or discoloration of tank.
ALWAYS stay away from tanks engulfed in fire.

Accidental Release Measures of Undecanol:

IMMEDIATE PRECAUTIONARY MEASURE:
Isolate spill or leak area in all directions for at least 50 meters (150 feet) for liquids and at least 25 meters (75 feet) for solids.

SPILL:
Increase the immediate precautionary measure distance, in the downwind direction, as necessary.

FIRE:
If tank, rail car or tank truck is involved in a fire, ISOLATE for 800 meters (1/2 mile) in all directions; also, consider initial evacuation for 800 meters (1/2 mile) in all directions.

Spillage Disposal of Undecanol:

Personal protection:
Filter respirator for organic gases and vapours adapted to the airborne concentration of the substance.
Collect leaking and spilled liquid in covered containers as far as possible.

Cleanup Methods of Undecanol:
Using acclimated mixed microbial cultures, the theoretical and 5-day BOD for Undecanol were determined to be 16.50% and 4.5 mmol/mmol chemical, respectively.
After 5 days at 21 °C in sewage, the theoretical BOD for Undecanol was 27.6%.

Undecanol had a zero order biodegradation rate of 0.125 ppm/hour and a first order biodegradation rate constant of 6.1X10-3/hour by activated sludge.
Using this biodegradation rate constant a half-life of 4.7 days can be calculated.

Disposal Methods of Undecanol:
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 its approved use or return Undecanol 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.

Safety Profile of Undecanol:
Moderately toxic by ingestion.
A skin irritant.

Combustible liquid.
Mutation data reported.
When heated to decomposition Undecanol emits acrid smoke and irritating fumes.

Identifiers of Undecanol:
CAS Number: 112-42-5
ChEBI: CHEBI:87499
ChEMBL: ChEMBL444525
ChemSpider: 7892
ECHA InfoCard: 100.003.609
PubChem CID: 8184
UNII: 06MJ0P28T3
CompTox Dashboard (EPA): DTXSID0026915
InChI: InChI=1S/C11H24O/c1-2-3-4-5-6-7-8-9-10-11-12/h12H,2-11H2,1H3
Key: KJIOQYGWTQBHNH-UHFFFAOYSA-N
SMILES: OCCCCCCCCCCC

CAS number: 112-42-5
EC number: 203-970-5
Hill Formula: C₁₁H₂₄O
Chemical formula: CH₃(CH₂)₁₀OH
Molar Mass: 172.31 g/mol
HS Code: 2905 19 00

Synonym(s): Alcohol C11, Undecyl alcohol
Linear Formula: CH3(CH2)10OH
CAS Number: 112-42-5
Molecular Weight: 172.31
Beilstein: 1698334
EC Number: 203-970-5
MDL number: MFCD00004751
PubChem Substance ID: 24900621
NACRES: NA.22

Product Number: U0005
Purity / Analysis Method: >99.0%(GC)
Molecular Formula / Molecular Weight: C11H24O = 172.31
Physical State (20 deg.C): Liquid
CAS RN: 112-42-5
Reaxys Registry Number: 1698334
PubChem Substance ID: 87577736
SDBS (AIST Spectral DB): 2531
MDL Number: MFCD00004751

Density: 0.83 g/mL at 25 °C
CAS No.: 112-42-5
Storage: 2 years -20°C liquid
Shipping: Room temperature shipping(Stability testing shows this product can be shipped without any cooling measures.)
Smiles: CCCCCCCCCCCO

CAS: 1653-30-1
Molecular Formula: C11H24O
Molecular Weight (g/mol): 172.31
MDL Number: MFCD00021958
InChI Key: XMUJIPOFTAHSOK-UHFFFAOYNA-N
PubChem CID: 15448
ChEBI: CHEBI:77930
IUPAC Name: undecan-2-ol
SMILES: CCCCCCCCCC(C)O

Properties of Undecanol:
Chemical formula: C11H24O
Molar mass: 172.31 g/mol
Appearance: Colorless liquid
Density: 0.8298 g/mL
Melting point: 19 °C (66 °F; 292 K)
Boiling point: 243 °C (469 °F; 516 K)
Solubility in water: Insoluble
Solubility in Ethanol and diethyl ether: Soluble

Density: 0.83 g/cm3 (20 °C)
Flash point: 108 °C
Melting Point: 16 °C
Vapor pressure: Viscosity kinematic: 20.03 mm2/s (20 °C)
Solubility: 0.0057 g/l insoluble

Physical State: Liquid
Storage: Store at 4° C
Melting Point: 11° C (lit.)
Boiling Point: 146° C (lit.) at 30 mmHg
Density: 0.83 g/cm3 at 25° C

Quality Level: 100
Assay: 99%
Refractive index: n20/D 1.44 (lit.)
bp: 146 °C/30 mmHg (lit.)
mp: 11 °C (lit.)
Density: 0.83 g/mL at 25 °C (lit.)
Storage temp.: 2-8°C
SMILES string: CCCCCCCCCCCO
InChI: 1S/C11H24O/c1-2-3-4-5-6-7-8-9-10-11-12/h12H,2-11H2,1H3
InChI key: KJIOQYGWTQBHNH-UHFFFAOYSA-N

Molecular Weight: 172.31
XLogP3: 4.6
Hydrogen Bond Donor Count: 1
Hydrogen Bond Acceptor Count: 1
Rotatable Bond Count: 9
Exact Mass: 172.182715385
Monoisotopic Mass: 172.182715385
Topological Polar Surface Area: 20.2 Ų
Heavy Atom Count: 12
Complexity: 71.4
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

Specifications of Undecanol:
Assay (GC, area%): ≥ 97.5 % (a/a)
Density (d 20 °C/ 4 °C): 0.832 - 0.833
Identity (IR): passes test

Melting Point: 1°C to 3°C
Density: 0.828
Boiling Point: 228°C to 229°C
Flash Point: 107°C (225°F)
Odor: Mild
Beilstein: 1719795
Refractive Index: 1.437
Quantity: 50 g
Solubility Information: Not miscible or difficult to mix in water. Soluble in alcohol and ethyl ether.
Formula Weight: 172.31
Percent Purity: ≥98%
Chemical Name or Material: 2-Undecanol

Solubility: (20 °C) insoluble
Melting Point: 13 - 15 °C
Molar Mass: 172.31 g/mol
Boiling Point: 129 - 131 °C (16 hPa)
Flash Point: 113 °C
Refractive Index: 1.44 (20 °C, 589 nm)
Density: 0.83 g/cm3 (20 °C)
pH: 7 (H2O, 20 °C)
Synonyms: Undecyl alcohol
Hill Formula: C11H24O
Chemical Formula: CH3(CH2)10OH

Related Products of Undecanol:
N,N-Diethyl-2,2,2-trifluoroacetamide
1-Bromo-2,4-difluoro-3-methylbenzene
(2,3-Difluoro-4-methylphenyl)methanol
a-Hydroxy-γ-butyrolactone
3-Isobutylaniline

Names of Undecanol:

Preferred IUPAC name:
Undecan-1-ol

Other names:
Undecanol
1-Undecanol
Undecyl alcohol
1-Hendecanol

Synonyms of Undecanol:
1-UNDECANOL
Undecan-1-ol
Undecyl alcohol
112-42-5
Undecanol
n-Undecanol
n-Undecyl alcohol
1-Hendecanol
Hendecanoic alcohol
Hendecyl alcohol
Alcohol C-11
n-Hendecylenic alcohol
Tip-Nip
1-Undecyl alcohol
n-Undecan-1-ol
Decyl carbinol
C11 alcohol
Neodol 1
FEMA No. 3097
Alcohol C11
Undecanol-(1)
NSC 403667
CHEBI:87499
06MJ0P28T3
NSC-403667
Alcohol, undecyl
CAS-112-42-5
UMQ
UNA
HENDECANOL
HSDB 1089
EINECS 203-970-5
BRN 1698334
Decane, hydroxymethyl deriv.
UNII-06MJ0P28T3
AI3-00330
Neoflex 11
Pri-n-undecyl alcohol
1-Undecanol, 99%
Dlcohol c-11 undecylic
EC 203-970-5
1-UNDECANOL [HSDB]
SCHEMBL20655
n-C11H23OH
Undecyl alcohol, 97%, FG
4-01-00-01835 (Beilstein Handbook Reference)
UNDECYL ALCOHOL [FCC]
UNDECYL ALCOHOL [FHFI]
UNDECYL ALCOHOL [INCI]
CHEMBL444525
DTXSID0026915
AMY5947
ZINC1596062
Tox21_201585
Tox21_300548
LMFA05000144
MFCD00004751
NSC403667
s9450
STL280304
AKOS009031434
CS-W004292
HY-W004292
6-(methylamino)pyridin-3-ylboronic?acid
NCGC00164024-01
NCGC00164024-02
NCGC00164024-03
NCGC00254401-01
NCGC00259134-01
1-Undecanol, purum, >=98.0% (GC)
143819-62-9
BP-31088
LS-14031
FT-0608326
U0005
EN300-20041
Q161686
J-002774
F8881-3903
112-42-5 [RN]
1-Undecanol [ACD/Index Name] [ACD/IUPAC Name]
1-Undecanol [German] [ACD/Index Name] [ACD/IUPAC Name]
1-Undécanol [French] [ACD/IUPAC Name]
250-092-3 [EINECS]
30207-98-8 [RN]
MFCD00004751 [MDL number]
undecan-1-ol
Undecanol [Wiki]
Undecyl alcohol
YQ3155000
11-Undecanolactone
143819-62-9 [RN]
1-Hendecanol
1-Hydroxyundecane
1-UNDECANOL-D23
1-Undecyl alcohol
349553-88-4 [RN]
4-01-00-01835 (Beilstein Handbook Reference) [Beilstein]
Alcohol, undecyl
bovine albumin
Hendecanoic alcohol
hendecanol
Hendecyl alcohol
methyl butylhexanol
NCGC00164024-01
Neodol 1
Neoflex 11
n-Hendecylenic alcohol
n-Undecan-1-ol
n-Undecanol
N-UNDECYL ALCOHOL
n-Undecyl-d23 Alcohol
Pri-N-undecyl alcohol
pUndecanol
Tip-Ni
Tip-Nip
UMQ
UNA
Undecanol-(1)
UNDECYL-MALTOSIDE

Accueil Ingrédients UNDECETH-11 UNDECETH-11 Nom INCI : UNDECETH-11 Classification : Composé éthoxylé Ses fonctions (INCI) Emollient : Adoucit et assouplit la peau Agent émulsifiant : Favorise la formation de mélanges intimes entre des liquides non miscibles en modifiant la tension interfaciale (eau et huile) Agent d'entretien de la peau : Maintient la peau en bon état Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation

UNDECETH-3 Nom INCI : UNDECETH-3 Classification : Composé éthoxylé Ses fonctions (INCI) Emollient : Adoucit et assouplit la peau Agent émulsifiant : Favorise la formation de mélanges intimes entre des liquides non miscibles en modifiant la tension interfaciale (eau et huile) Agent d'entretien de la peau : Maintient la peau en bon état Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation

UNDECETH-5 N° CAS : 34398-01-1 Nom INCI : UNDECETH-5 Classification : Composé éthoxylé 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

UNDECETH-8 "Pas terrible" dans toutes les catégories. Nom INCI : UNDECETH-8 Classification : Composé éthoxylé Ses fonctions (INCI) Emollient : Adoucit et assouplit la peau Agent émulsifiant : Favorise la formation de mélanges intimes entre des liquides non miscibles en modifiant la tension interfaciale (eau et huile) Agent d'entretien de la peau : Maintient la peau en bon état Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation

Poly(oxy-1,2-ethanediyl), alpha-undecyl-omega-hydroxy-, branched and linear; UNII-R6B5PCO2JN; alpha-Alkyl-omega-hydroxypoly(oxypropylene) and/or poly(oxyethylene) polymers where the alkyl chain contains a minimum of six carbons, minimum number average molecular weight (in amu) 1,100 CAS NO:127036-24-2

UNDECYL ALCOHOL N° CAS : 112-42-5 "Satisfaisant" dans toutes les catégories. Nom INCI : UNDECYL ALCOHOL Nom chimique : Undecan-1-ol N° EINECS/ELINCS : 203-970-5 Classification : Alcool Ses fonctions (INCI) Anti-séborrhée : Aide à contrôler la production de sébum Emollient : Adoucit et assouplit la peau Agent masquant : Réduit ou inhibe l'odeur ou le goût de base du produit Agent d'entretien de la peau : Maintient la peau en bon état Agent de contrôle de la viscosité : Augmente ou diminue la viscosité des cosmétiques

Alphadrate; Amide of carbonic acid; Carbamimidic acid; Carbamide resin; Carbamimidic acid; Carbonyl diamide; Carbonyldiamine; Isourea cas no: 57-13-6

Undecyl alcohol 97%, FG Synonym: 1-Undecanol, Alcohol C11, Undecyl alcohol CAS Number 112-42-5 Linear Formula CH3(CH2)10OH Molecular Weight 172.31 FEMA Number 3097 Beilstein/REAXYS Number 1698334 EC Number 203-970-5 Council of Europe no. 751 MDL number MFCD00004751 PubChem Substance ID 24901463 Flavis number 2.057 NACRES NA.21 Undecyl alcohol has been reported as a key volatile constituent of Senecio tenuifolius and Flacourtia montana. Undecanol, also known by its IUPAC name 1-undecanol or undecan-1-ol, and by its trivial names undecyl alcohol and hendecanol, is a fatty alcohol. Undecanol is a colorless, water-insoluble liquid of melting point 19 °C and boiling point 243 °C. It has a floral citrus like odor, and a fatty taste and is used as a flavoring ingredient in foods. It is commonly produced by the reduction of undecanal, the analogous aldehyde. 1-Undecanol is found naturally in many foods such as fruits (including apples and bananas), butter, eggs and cooked pork. Undecanol can irritate the skin, eyes and lungs. Ingestion can be harmful, with the approximate toxicity of ethanol. 1-undecanol appears as a water-white liquid with a mild odor. Flash point 250°F. Slightly soluble in water. Considered a marine pollutant by DOT. Immediate steps should be taken to limit its spread to the environment. As a liquid it can easily penetrate the soil and contaminate groundwater or streams. Mildly irritating to both the eyes and skin.COLOURLESS LIQUID.Citrus.FATTY FLAVOR.473 °F at 760 mm Hg.Soluble in ethanol; very soluble in ether.Soluble in 60% alcohol.When heated to decomposition it emit acrid smoke and irritating fumes..Undecanol was the most potent fungicide followed by decanol. The time-kill curve study showed that undecanol was fungicidal against S. cerevisiae at any growth stages was not influenced by pH values. The alcohols tested inhibited glucose-induced acidification by inhibiting the plasma membrane H(+)-ATPase. The primary antifungal action of amphipathic medium-chain (C(9)-C(12)) alkanols comes mainly from their ability as nonionic surfactants to disrupt the native membrane-associated function of the integral proteins. Industry Uses Functional fluids (closed systems) Processing aids, specific to petroleum production Surface active agents Consumer Uses Fuels and related products Laundry and dishwashing products Personal care products By reduction of the corresponding aldehyde.Purity: a minimum of 97-98.5% undecyl alcohol.This chemical is listed as a High Production Volume (HPV) (65FR81686). Chemicals listed as HPV were produced in or imported into the U.S. in >1 million pounds in 1990 and/or 1994. The HPV list is based on the 1990 Inventory Update Rule.Commercial products from the family of 6 to 11 carbon alcohols that make up the plasticizer range are available both as ... pure single carbon chain materials and as complex isomeric mixtures. Commercial descriptions of plasticizer range alcohols are ... in general a ... pure material is called "-anol" /eg, 1-undecanol/, and the mixtures are called "-yl alcohol /eg, undecyl alcohol/ or "iso...yl alcohol" /eg, isoundecyl alcohol/.Reported uses /include/ non-alcoholic beverages 4.09 ppm; ice cream, ices, etc 15.47 ppm; candy 17.65 ppm; baked goods 17.66 ppm; alcoholic beverages 4.50 ppm.Excerpt from ERG Guide 171 [Substances (Low to Moderate Hazard)]: Some may burn but none ignite readily. Containers may explode when heated. Some may be transported hot. For UN3508, be aware of possible short circuiting as this product is transported in a charged state.Wash eyes with water for at least 15 min.Fresh air, rest. Refer for medical attention.Remove contaminated clothes. Rinse and then wash skin with water and soap.First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then refer for medical attention.Rinse mouth. Do NOT induce vomiting. Give one or two glasses of water to drink. Refer for medical attention .Excerpt from ERG Guide 171 [Substances (Low to Moderate Hazard)]: SMALL FIRE: Dry chemical, CO2, water spray or regular foam. LARGE FIRE: Water spray, fog or regular foam. Do not scatter spilled material with high-pressure water streams. Move containers from fire area if you can do it without risk. Dike fire-control water for later disposal. FIRE INVOLVING TANKS: Cool containers with flooding quantities of water until well after fire is out. Withdraw immediately in case of rising sound from venting safety devices or discoloration of tank. ALWAYS stay away from tanks engulfed in fire.Excerpt from ERG Guide 171 [Substances (Low to Moderate Hazard)]: As an immediate precautionary measure, isolate spill or leak area in all directions for at least 50 meters (150 feet) for liquids and at least 25 meters (75 feet) for solids. SPILL: Increase, in the downwind direction, as necessary, the isolation distance shown above. FIRE: If tank, rail car or tank truck is involved in a fire, ISOLATE for 800 meters (1/2 mile) in all directions; also, consider initial evacuation for 800 meters (1/2 mile) in all directions. Personal protection: filter respirator for organic gases and vapours adapted to the airborne concentration of the substance. Collect leaking and spilled liquid in covered containers as far as possible.Using acclimated mixed microbial cultures, the theoretical and 5-day BOD for 1-undecanol were determined to be 16.50% and 4.5 mmol/mmol chemical, respectively(1). After 5 days at 21 °C in sewage, the theoretical BOD for 1-undecanol was 27.6%(2). 1-Undecanol had a zero order biodegradation rate of 0.125 ppm/hour and a first order biodegradation rate constant of 6.1X10-3/hour by activated sludge(3). Using this biodegradation rate constant a half-life of 4.7 days can be calculated.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 its approved use or return it 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.Excerpt from ERG Guide 171 [Substances (Low to Moderate Hazard)]: Do not touch or walk through spilled material. Stop leak if you can do it without risk. Prevent dust cloud. Avoid inhalation of asbestos dust. SMALL DRY SPILL: With clean shovel, place material into clean, dry container and cover loosely; move containers from spill area. SMALL SPILL: Pick up with sand or other non-combustible absorbent material and place into containers for later disposal. LARGE SPILL: Dike far ahead of liquid spill for later disposal. Cover powder spill with plastic sheet or tarp to minimize spreading. Prevent entry into waterways, sewers, basements or confined areas. (ERG, 2016)Residues of nonyl, decyl, and undecyl glycoside mixture with a mixture of nonyl, decyl, and undecyl oligosaccharides and related reaction products (primarily decanol and undecanol) produced as an aqueous-based liquid (50 to 65% solids) from the reaction of primary alcohols (containing 15 to 20% secondary alcohol isomers) in a ratio of 20% C9, 40% C10, and 40% C11 with carbohydrates (average glucose to alkyl chain ratio 1.3 to 1.8) are exempted from the requirement of a tolerance when used as a surfactant in accordance with good agricultural practice as inert (or occasionally active) ingredients in pesticide formulations applied to growing crops or to raw agricultural commodities after harvest.Residues of nonyl, decyl, and undecyl glycoside mixture with a mixture of nonyl, decyl, and undecyl oligosaccharides and related reaction products (primarily decanol and undecanol) produced as an aqueous-based liquid (50 to 65% solids) from the reaction of primary alcohols (containing 15 to 20% secondary alcohol isomers) in a ratio of 20% C9, 40% C10, and 40% C11 with carbohydrates (average glucose to alkyl chain ratio 1.3 to 1.8) are exempted from the requirement of a tolerance when used as a surfactant in accordance with good agricultural practice as inert (or occasionally active) ingredients in pesticide formulations applied to animals.UNDECANOL is an alcohol. Flammable and/or toxic gases are generated by the combination of alcohols with alkali metals, nitrides, and strong reducing agents. They react with oxoacids and carboxylic acids to form esters plus water. Oxidizing agents convert them to aldehydes or ketones. Alcohols exhibit both weak acid and weak base behavior. They may initiate the polymerization of isocyanates and epoxides.Residues of nonyl, decyl, and undecyl glycoside mixture with a mixture of nonyl, decyl, and undecyl oligosaccharides and related reaction products (primarily decanol and undecanol) produced as an aqueous-based liquid (50 to 65% solids) from the reaction of primary alcohols (containing 15 to 20% secondary alcohol isomers) in a ratio of 20% C9, 40% C10, and 40% C11 with carbohydrates (average glucose to alkyl chain ratio 1.3 to 1.8) are exempted from the requirement of a tolerance when used as a surfactant in accordance with good agricultural practice as inert (or occasionally active) ingredients in pesticide formulations applied to growing crops or to raw agricultural commodities after harvest.Residues of nonyl, decyl, and undecyl glycoside mixture with a mixture of nonyl, decyl, and undecyl oligosaccharides and related reaction products (primarily decanol and undecanol) produced as an aqueous-based liquid (50 to 65% solids) from the reaction of primary alcohols (containing 15 to 20% secondary alcohol isomers) in a ratio of 20% C9, 40% C10, and 40% C11 with carbohydrates (average glucose to alkyl chain ratio 1.3 to 1.8) are exempted from the requirement of a tolerance when used as a surfactant in accordance with good agricultural practice as inert (or occasionally active) ingredients in pesticide formulations applied to animals.Undecyl alcohol is a food additive permitted for direct addition to food for human consumption as a synthetic flavoring substance and adjuvant in accordance with the following conditions: a) they are used in the minimum quantity required to produce their intended effect, and otherwise in accordance with all the principles of good manufacturing practice, and 2) they consist of one or more of the following, used alone or in combination with flavoring substances and adjuvants generally recognized as safe in food, prior-sanctioned for such use, or regulated by an appropriate section in this part.ALCOHOL-INDUCED NUTRITIONAL ENCEPHALOMALACIA IN STARTING CHICKS COULD BE COMPLETELY PREVENTED BY DIETARY SUPPLEMENTATION OF D,L-ALPHA-TOCOPHERYL ACETATE.WITH USE OF SURFACTANTS EG TWEEN 80, ALCOHOL EMULSIONS WERE PHYTOTOXIC ONLY TO YOUNG MERISTEMATIC TISSUE. WITHOUT THE SURFACANT, C11 ALCOHOLS & ESTERS SHOWED NONSELECTIVE TISSUE KILL.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 necessary. Administer oxygen by nonrebreather mask at 10 to 15 L/min. Monitor for shock and treat if necessary ... . Monitor for pulmonary edema 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. Administer activated charcoal ... . /Higher alcohols (>3 carbons) and related compounds/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 ... . Monitor cardiac rhythm and treat arrhythmias as necessary ... . Start IV administration of D5W /SRP: "To keep open", minimal flow rate/. Use 0.9% saline (NS) or lactated Ringer's (LR) if signs of hypovolemia are present. For hypotension with signs of hypovolemia, administer fluid cautiously. Consider vasopressors if patient is hypotensive with a normal fluid volume. Watch for signs of fluid overload ... . Monitor for signs of hypoglycemia (decreased LOC, tachycardia, pallor, dilated pupils, diaphoresis, and/or dextrose strip or glucometer readings below 50 mg) and administer 50% dextrose if necessary ... . Treat seizures with diazepam or lorazepam ... . Use proparacaine hydrochloride to assist eye irrigation ... . /Higher alcohols (>3 carbons) and related compounds//SIGNS AND SYMPTOMS/ The substance is severely irritating to the eyes, and is irritating to the skin and the respiratory tract.1-Undecanol's production and use as a food additive, synthetic flavor, and in perfumery may result in its release to the environment through various waste streams. 1-Undecanol exists naturally in citrus fruits. If released to air, a vapor pressure of 2.97X10-3 mm Hg at 25 °C indicates 1-undecanol will exist solely as a vapor in the atmosphere. Vapor-phase 1-undecanol 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 23 hours. If released to soil, 1-undecanol is expected to have no mobility based upon an estimated Koc of 8,800. Volatilization from moist soil surfaces is expected to be an important fate process based upon an estimated Henry's Law constant of 7.3X10-5 atm-cu m/mole. However, adsorption to soil is expected to attenuate volatilization. 1-Undecanol is expected to biodegrade rapidly in soil and water based on sewage and sludge studies. If released into water, 1-undecanol 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 20 hours and 10 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 9 months if adsorption is considered. An estimated BCF of 86 suggests the potential for bioconcentration in aquatic organisms is moderate. Hydrolysis is not expected to be an important environmental fate process since this compound lacks functional groups that hydrolyze under environmental conditions. Occupational exposure to 1-undecanol may occur through dermal contact with this compound at workplaces where 1-undecanol is produced or used. Monitoring data indicate that the general population may be exposed to 1-undecanol via ingestion of food and drinking water, and dermal contact with this compound and other consumer products containing 1-undecanol. (SRC)TERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 8,800(SRC), determined from a log Kow of 4.72(2) and a regression-derived equation(3), indicates that 1-undecanol is expected to be immobile in soil(SRC). Volatilization of 1-undecanol from moist soil surfaces is expected to be an important fate process(SRC) given an estimated Henry's Law constant of 7.3X10-5 atm-cu m/mole(SRC), using a fragment constant estimation method(4). However, adsorption to soil is expected to attenuate volatilization(SRC). 1-Undecanol is not expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 2.97X10-3 mm Hg(5). The theoretical BOD for 1-undecanol was 27.6% after 5-day incubation in sewage(6), indicating that biodegradation may be an important environmental fate process in soil(SRC).AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 8,800(SRC), determined from a log Kow of 4.72(2) and a regression-derived equation(3), indicates that 1-undecanol is expected to adsorb to suspended solids and sediment(SRC). Volatilization from water surfaces is expected(3) based upon an estimated Henry's Law constant of 7.3X10-5 atm-cu m/mole(SRC), developed using a fragment constant estimation method(4). Using this Henry's Law constant and an estimation method(3), volatilization half-lives for a model river and model lake are 20 hours and 10 days, respectively(SRC). 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 9 months if adsorption is considered(5). According to a classification scheme(6), an estimated BCF of 86(SRC), from its log Kow(2) and a regression-derived equation(7), suggests the potential for bioconcentration in aquatic organisms is moderate(SRC). The theoretical BOD for 1-undecanol was 27.6% after 5-day incubation in sewage(8), indicating that biodegradation may be an important environmental fate process in water(SRC).ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), 1-undecanol, which has a vapor pressure of 2.97X10-3 mm Hg at 25 °C(2), is expected to exist solely as a vapor in the ambient atmosphere. Vapor-phase 1-undecanol is degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals(SRC); the half-life for this reaction in air is estimated to be 23 hours(SRC), calculated from its rate constant of 1.7X10-11 cu cm/molecule-sec at 25 °C(SRC) that was derived using a structure estimation method(3).AEROBIC: Using acclimated mixed microbial cultures, the theoretical and 5-day BOD for 1-undecanol were determined to be 16.50% and 4.5 mmol/mmol chemical, respectively(1). After 5 days at 21 °C in sewage, the theoretical BOD for 1-undecanol was 27.6%(2). 1-Undecanol had a zero order biodegradation rate of 0.125 ppm/hour and a first order biodegradation rate constant of 6.1X10-3/hour by activated sludge(3). Using this biodegradation rate constant a half-life of 4.7 days can be calculated(SRC).The rate constant for the vapor-phase reaction of 1-undecanol with photochemically-produced hydroxyl radicals has been estimated as 1.7X10-11 cu cm/molecule-sec at 25 °C(SRC) using a structure estimation method(1). This corresponds to an atmospheric half-life of about 23 hours at an atmospheric concentration of 5X10+5 hydroxyl radicals per cu cm(1). 1-Undecanol is not expected to undergo hydrolysis in the environment due to the lack of functional groups that hydrolyze under environmental conditions(2).An estimated BCF of 86 was calculated for 1-undecanol(SRC), using a log Kow of 4.72(1) and a regression-derived equation(2). According to a classification scheme(3), this BCF suggests the potential for bioconcentration in aquatic organisms is moderate(SRC), provided the compound is not metabolized by the organism(SRC).The Koc of 1-undecanol is estimated as 8,800(SRC), using a log Kow of 4.72(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that 1-undecanol is expected to be immobile in soil.The Henry's Law constant for 1-undecanol is estimated as 7.23X10-5 atm-cu m/mole(SRC) using a fragment constant estimation method(1). This Henry's Law constant indicates that 1-undecanol is expected to volatilize from water surfaces(2). Based on this Henry's Law constant, the volatilization half-life from a model river (1 m deep, flowing 1 m/sec, wind velocity of 3 m/sec)(2) is estimated as 20 hours(SRC). The volatilization half-life from a model lake (1 m deep, flowing 0.05 m/sec, wind velocity of 0.5 m/sec)(2) is estimated as 10 days(SRC). 1-Undecanol's Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). However, volatilization from water surfaces is expected to be attenuated by adsorption to suspended solids and sediment in the water column. The volatilization half-life from a model pond is about 9 months when adsorption is considered(3). 1-Undecanol is not expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 2.97X10-3 mm Hg(4).SURFACE WATER: 1-Undecanol has been qualitatively identified in the Northern Basin of Lake Michigan(1).1-Undecanol was identified as a volatile component of beef.1-Undecanol was qualitatively identified in Lake Michigan lake trout at Charlevoix, MI on 9/25/77(1).Occupational exposure to 1-undecanol may occur through dermal contact with this compound at workplaces where 1-undecanol is produced or used. Monitoring data indicate that the general population may be exposed to 1-undecanol via ingestion of food and drinking water, and dermal contact with this compound and other consumer products containing 1-undecanol. (SRC) UNDECYL ALCOHOL UNDECYL ALCOHOL is classified as : Antiseborrhoeic Emollient Masking Skin conditioning Viscosity controlling CAS Number 112-42-5 EINECS/ELINCS No: 203-970-5 COSING REF No: 80494 Chem/IUPAC Name: Undecan-1-ol FORMULA C11 H24 O MOLECULAR WEIGHT 172 CAS 112-42-5 EINECS 203-970-5 FEMA 3097 APPEARANCE AT 20°C CLEAR MOBILE LIQUID / SOLID COLOR COLORLESS TO PALE YELLOW ODOR CITRUS, MILD, SLIGHTLY FATTY-WAXY TASTE ALDEHIDIC, SOAPY, WAXY, SWEET OPTICAL ROTATION (°) 0 / 0 DENSITY AT 20°C (g/ml)) 0,823 - 0,843 REFRACTIVE INDEX nD20 1,4370 - 1,4430 FLASHPOINT (°C) 113 SOLUBILITY 1:1 v/v ETHANOL 80% ASSAY (% GC) > 98 ACID VALUE (mg KOH/g) < 3 Flavouring Undecyl alcohol Synonym(s) Alcohol C-11 Latest JECFA evaluation 1997 (Session 49) Status of specification Full Chemical name 1-Undecanol JECFA number 106 CAS number 112-42-5 FEMA number 3097 COE number 751 FLAVIS number - Molecular weight 172.31 Chemical formula C11H24O Physical form/odour colourless liquid/fatty-floral odour Solubility soluble in most fixed oils; insoluble in water Solubility in ethanol 1ml in 4 ml of 60% alcohol Boiling point (°C) 146° (30 mm Hg) Assay min % 97.0% Acid value max - Refractive index 1.437-1.443 Specific gravity 0.820-0.840 Other requirements - ID Test IR 1-undecanol, being an organic chemical with molecular formula C11H24O and scented with lemon, is a colorless or pale yellow , water insoluble but alcohol and ether soluble liquid. It is prepared from metal sodium reduction of Ethyl undecanoate, or pressurization and catalytic hydrogenation of ethyl ω- undecanoate , or even obtained by the Grignard reaction of nonyl magnesium bromide and with ethylene oxide. The application of this alcohol is limited. It is only used for some typical aroma oil and fragrance as the fat is solid at low temperature. The citrus rose type and the like only play a secondary and harmonious role and are taken as deodorant. In addition, it is also used to manufacture spices with the scent of acacia, polianthes tuberosa and the like.It is colorless liquid at room temperature; scented with light sweet fat wax mixed with the scent of roses and fruity flavor of citrus, pineapple and the like. But generally the whole body smells scent of rose, as if a little bit of rue flavor. It will smell like orange after highly diluted with the soft sweet flavor of citrus fruit oil. Its concentration is less than 20 × 10-6 with fruity and sweet scent. Unpleasant fat and smell will be produced when the concentration is higher; Melting point :15 ~ 19 ℃; Flash point> 82 ℃; Density: D4250 .828 ~ 0.834; Refractive index: nD200.4370 ~ 1.4430; water insoluble, soluble in most organic solvents, 1: 4.soluble in 60% ethanol.It is prepared from undecaethylene reduction. Put 200 ml of anhydrous toluene and 70 g of sodium into a 5-liter three-necked flask, and then heat reflux it until sodium is completely melted. Then stop heating, stir quickly to get the sodium to disperse into sand until the temperature drops to 60 ~ C. Then put 107 grams of ethyl undecanoate into 150ml absolute ethanol solution followed by adding 500ml of absolute ethanol. When the reaction is weakened, heat it in an oil bath until the sodium is completely dissolved. Next remove the ethanol and toluene through the method of steam distillation. Then wash the remaining oily substances with 200ml × 3 hot water. Then wash ether layer with a sequence of water, sodium carbonate and then water after the ethyl ether was extracted. Also dry with magnesium sulfate, boil off the ethyl ether. The product will be finally extracted from the residue after reduced pressure distillation. The yield is 70%. Uses Although this undecanol is among the common varieties, but it is still not widely used. It is often used together with undecylenic aldenyde or other fat and aldehydes as the integrator of fragrant volatile of aldehyde. Also it can be well integrated with floral fragrance, citrus cologne, acacia, robinia pseudoacacia, tuberose, violets, clean and grass smell, usually used for rose base. Few application is also available in such pineapple, orange, lemon, lime, orange , cassis, rose food flavors. Storage Be sealed and stored in a cool dry place. Also be kept away from fire. Chemical Properties Colorless liquid; citrus odor. Soluble in 60% alcohol. Combustible. Chemical Properties Undecyl alcohol has a floral, citrus-like odor and fatty flavor. Occurrence Reported found in citrus fruits, fresh apple, banana, sour cherry, orange juice, orange peel oil, American cranberry, Vitis vinifera L., parmesan cheese, mushroom, tamarind, coriander seed and leaf, white wine, butter, heated butter, boiled eggs, boiled or uncured pork, plum brandy, coriander leaf, crayfish and oysters. Uses 1-Undecanol is an antifungal, antioxidant compound. As well, it is used in the synthesis Definition ChEBI: A fatty alcohol that is undecane substituted by a hydroxy group at position 1. Preparation By reduction of the corresponding aldehyde. Synthesis Reference(s) The Journal of Organic Chemistry, 60, p. 5961, 1995 DOI: 10.1021/jo00123a038 Health Hazard Recommended Personal Protective Equipment: Goggles and face shield; Symptoms Following Exposure: Liquid can irritate eyes; General Treatment for Exposure: Wash eyes with water for at least 15 min.; Toxicity by Inhalation (Threshold Limit Value): Not pertinent; Short-Term Exposure Limits: Not pertinent; Toxicity by Ingestion: Grade 2, LD50 = 0.5-5 g/kg; Late Toxicity: Data not available; Vapor (Gas) Irritant Characteristics: None; Liquid or Solid Irritant Characteristics: No appreciable hazard. Practically harmless to the skin; Odor Threshold: Not pertinent. Chemical Reactivity Reactivity with Water No reaction; Reactivity with Common Materials: No reactions; Stability During Transport: Stable; Neutralizing Agents for Acids and Caustics: Not pertinent; Polymerization: Not pertinent; Inhibitor of Polymerization: Not pertinent. Safety Profile Moderately toxic by ingestion. A skin irritant. Combustible liquid. Mutation data reported. When heated to decomposition it emits acrid smoke and irritating fumes. See also ALCOHOLS. Metabolism See alcohol C-8. Purification Methods Purify the alcohol by repeated fractional crystallisation from its melt or by distillation in a vacuum. [Beilstein 1 H 427, 1 IV 1835.] 1-Undecanol, also known as N-undecyl alcohol or undecan-1-ol, belongs to the class of organic compounds known as fatty alcohols. These are aliphatic alcohols consisting of a chain of a least six carbon atoms. Thus, 1-undecanol is considered to be a fatty alcohol lipid molecule. 1-Undecanol is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral. Higher alcohols are not highly toxic in the industrial setting; Can cause liver injury, somnolence, and respiratory depression in experimental animals; A skin, eye, and respiratory tract irritant; [HSDB] Safe when used as a flavoring agent in food; [JECFA] An irritant; [MSDSonline] 1-Undecanol Formula: C11H24O Molecular weight: 172.3077 IUPAC Standard InChI: InChI=1S/C11H24O/c1-2-3-4-5-6-7-8-9-10-11-12/h12H,2-11H2,1H3 Download the identifier in a file. INChI Trust 2011 Certified Logo IUPAC Standard InChIKey: KJIOQYGWTQBHNH-UHFFFAOYSA-N CAS Registry Number: 112-42-5 Chemical structure: C11H24O This structure is also available as a 2d Mol file or as a computed 3d SD file The 3d structure may be viewed using Java or Javascript. Other names: Undecyl alcohol; n-Undecan-1-ol; n-Undecanol; n-Undecyl alcohol; Hendecanoic alcohol; Hendecyl alcohol; 1-Hendecanol; Alcohol c-11; n-Hendecylenic alcohol; Undecanol-(1); Tip-Nip; Undecanol; Decyl carbinol; Neodol 1; Undecan-1-ol; 1-Undecyl alcohol; NSC 403667 Permanent link for this species. Use this link for bookmarking this species for future reference. Information on this page: Reaction thermochemistry data References Notes Other data available: Condensed phase thermochemistry data Phase change data IR Spectrum Mass spectrum (electron ionization) Gas Chromatography Options: Switch to calorie-based units

Undecyl alcohol (undecanol), being an organic chemical with molecular formula C11H24O and scented with lemon, is a colorless or pale yellow , water insoluble but alcohol and ether soluble liquid.
Undecyl alcohol (undecanol) is prepared from metal sodium reduction of Ethyl undecanoate, or pressurization and catalytic hydrogenation of ethyl ω- undecanoate , or even obtained by the Grignard reaction of nonyl magnesium bromide and with ethylene oxide.
The application of this alcohol is limited.

CAS: 112-42-5
MF: C11H24O
MW: 172.31
EINECS: 203-970-5

Undecyl alcohol (undecanol) is only used for some typical aroma oil and fragrance as the fat is solid at low temperature.
The citrus rose type and the like only play a secondary and harmonious role and are taken as deodorant.
In addition, Undecyl alcohol (undecanol) is also used to manufacture spices with the scent of acacia, polianthes tuberosa and the like.
A fatty alcohol that is undecane substituted by a hydroxy group at position 1.
Undecyl alcohol (undecanol) appears as a water-white liquid with a mild odor. Flash point 250 °F.
Slightly soluble in water.
Considered a marine pollutant by DOT.
Immediate steps should be taken to limit its spread to the environment.
As a liquid Undecyl alcohol (undecanol) can easily penetrate the soil and contaminate groundwater or streams.
Mildly irritating to both the eyes and skin.
Undecyl alcohol (undecanol), also known by its IUPAC name 1-undecanol or undecan-1-ol, and by its trivial names undecyl alcohol and hendecanol, is a fatty alcohol.
Undecyl alcohol (undecanol) is a colorless, water-insoluble liquid of melting point 19 °C and boiling point 243 °C.

Undecyl alcohol (undecanol) Chemical Properties
Melting point: 11 °C (lit.)
Boiling point: 146 °C/30 mmHg (lit.)
Density: 0.83 g/mL at 25 °C (lit.)
Vapor pressure: <1 hPa (20 °C)
FEMA: 3097 | UNDECYL ALCOHOL
Refractive index: n20/D 1.44(lit.)
Fp: >230 °F
Storage temp.: Store below +30°C.
Solubility: 0.0057g/l insoluble
Form: Liquid
Pka: 15.20±0.10(Predicted)
Color: Clear colorless to pale yellow
Odor: Faint alcohol.
Odor Type: waxy
Water Solubility: Not miscible or difficult to mix with water. Soluble in chloroform and ethyl acetate.
JECFA Number: 106
BRN: 1698334
Stability: Stable. Combustible. Incompatible with strong oxidizing agents, strong acids.
LogP: 4.9 at 20℃
CAS DataBase Reference: 112-42-5(CAS DataBase Reference)
EPA Substance Registry System: Undecyl alcohol (undecanol) (112-42-5)

Undecyl alcohol (undecanol) is colorless liquid at room temperature; scented with light sweet fat wax mixed with the scent of roses and fruity flavor of citrus, pineapple and the like.
But generally the whole body smells scent of rose, as if a little bit of rue flavor.
Undecyl alcohol (undecanol) will smell like orange after highly diluted with the soft sweet flavor of citrus fruit oil.
Undecyl alcohol (undecanol)'s concentration is less than 20 × 10-6 with fruity and sweet scent.

Unpleasant fat and smell will be produced when the concentration is higher; Melting point :15 ~ 19 ℃; Flash point> 82 ℃; Density: D4250 .828 ~ 0.834; Refractive index: nD200.4370 ~ 1.4430; water insoluble, soluble in most organic solvents, 1: 4.soluble in 60% ethanol
Undecyl alcohol (undecanol) has a floral, citrus-like odor and fatty flavor.
Undecyl alcohol (undecanol) is an antifungal, antioxidant compound.
As well, Undecyl alcohol (undecanol) is used in the synthesis
Undecyl alcohol (undecanol) can be used as a precursor in the synthesis of undecanal by chemoselective oxidation using a fluorous derivative of TEMPO (2,2,6,6-tetramethylpiperidine-1-oxyl) radical as a catalyst.
Undecyl alcohol (undecanol) can be also used as a solvent in homogeneous liquid-liquid microextraction method.

Uses
Although Undecyl alcohol (undecanol) is among the common varieties, but it is still not widely used.
Undecyl alcohol (undecanol) is often used together with undecylenic aldenyde or other fat and aldehydes as the integrator of fragrant volatile of aldehyde.
Also Undecyl alcohol (undecanol) can be well integrated with floral fragrance, citrus cologne, acacia, robinia pseudoacacia, tuberose, violets, clean and grass smell, usually used for rose base.
Few application is also available in such pineapple, orange, lemon, lime, orange , cassis, rose food flavors.
Undecyl alcohol (undecanol) has a floral citrus like odor, and a fatty taste and is used as a flavoring ingredient in foods.
Undecyl alcohol (undecanol) is commonly produced by the reduction of undecanal, the analogous aldehyde.

Preparation
Undecyl alcohol (undecanol) is prepared from undecaethylene reduction.
Put 200 ml of anhydrous toluene and 70 g of sodium into a 5-liter three-necked flask, and then heat reflux Undecyl alcohol (undecanol) until sodium is completely melted.
Then stop heating, stir quickly to get the sodium to disperse into sand until the temperature drops to 60 ~ C.
Then put 107 grams of ethyl undecanoate into 150ml absolute ethanol solution followed by adding 500ml of absolute ethanol.
When the reaction is weakened, heat Undecyl alcohol (undecanol) in an oil bath until the sodium is completely dissolved.

Next remove the ethanol and toluene through the method of steam distillation.
Then wash the remaining oily substances with 200ml × 3 hot water.
Then wash ether layer with a sequence of water, sodium carbonate and then water after the ethyl ether was extracted.
Also dry with magnesium sulfate, boil off the ethyl ether.
Undecyl alcohol (undecanol) will be finally extracted from the residue after reduced pressure distillation.
The yield is 70%.

Health Hazard
Recommended Personal Protective Equipment: Goggles and face shield; Symptoms Following Exposure: Liquid can irritate eyes; General Treatment for Exposure: Wash eyes with water for at least 15 min.; Toxicity by Inhalation (Threshold Limit Value): Not pertinent; Short-Term Exposure Limits: Not pertinent; Toxicity by Ingestion: Grade 2, LD50 = 0.5-5 g/kg; Late Toxicity: Data not available; Vapor (Gas) Irritant Characteristics: None; Liquid or Solid Irritant Characteristics: No appreciable hazard.
Practically harmless to the skin; Odor Threshold: Not pertinent.
Undecyl alcohol (undecanol) can irritate the skin, eyes and lungs.
Ingestion can be harmful, with the approximate toxicity of ethanol.

Synonyms
1-UNDECANOL
Undecan-1-ol
Undecyl alcohol
112-42-5
Undecanol
n-Undecanol
n-Undecyl alcohol
1-Hendecanol
Hendecanoic alcohol
Hendecyl alcohol
Alcohol C-11
n-Hendecylenic alcohol
Tip-Nip
1-Undecyl alcohol
n-Undecan-1-ol
Decyl carbinol
C11 alcohol
Neodol 1
FEMA No. 3097
Alcohol, undecyl
Alcohol C11
Undecanol-(1)
NSC 403667
HSDB 1089
EINECS 203-970-5
BRN 1698334
Decane, hydroxymethyl deriv.
UNII-06MJ0P28T3
AI3-00330
DTXSID0026915
CHEBI:87499
06MJ0P28T3
NSC-403667
EC 203-970-5
4-01-00-01835 (Beilstein Handbook Reference)
DTXCID706915
143819-62-9
CAS-112-42-5
UMQ
UNA
HENDECANOL
Undcanol
1-Hydroxyundecane
Neoflex 11
Alchem 11
Undecan- 1- ol
Pri-n-undecyl alcohol
undecan - 1 - ol
C(CCCCC)CCCCCO
1-Undecanol, 99%
Dlcohol c-11 undecylic
1-UNDECANOL [HSDB]
SCHEMBL20655
n-C11H23OH
Undecyl alcohol, 97%, FG
Undecyl alcohol (6CI 8CI)
UNDECYL ALCOHOL [FCC]
UNDECYL ALCOHOL [FHFI]
UNDECYL ALCOHOL [INCI]
CHEMBL444525
AMY5947
Tox21_201585
Tox21_300548
LMFA05000144
MFCD00004751
NSC403667
s9450
STL280304
AKOS009031434
ALCOHOL C-11 (1-UNDECANOL)
CS-W004292
HY-W004292
LS-3149
6-(methylamino)pyridin-3-ylboronic?acid
NCGC00164024-01
NCGC00164024-02
NCGC00164024-03
NCGC00254401-01
NCGC00259134-01
1-Undecanol, purum, >=98.0% (GC)
BP-31088
FT-0608326
U0005
EN300-20041
Q161686
J-002774
F8881-3903
Z104476546

SynonymsN-(1-oxo-10-undecen-1-yl)Glycine;Thiazolium,3-heptyl-2-[(3-heptyl-4-methyl-2(3H)-thiazolylidene)methyl]-4-methyl- cas :54301-26-7

Synonyms: UNDECYLENOYL PHENYLALANINE;N-(1-Oxo-10-undecen-1-yl)-L-phenylalanine;L-Phenylalanine, N-(1-oxo-10-undecen-1-yl)- CAS: 175357-18-3

DESCRIPTION:

UNIPLEX FRP-45 is Liquid flame retardant that imparts efficient flame retardance to a large number of polymers (e. g. flexible PVC, TPO, PU and elastomers) due to its high bromine content.
UNIPLEX FRP-45 offers a very low volatility combined with a superior thermal and color stability.


CAS# 26040-51-7
EC Number 247-426-5
Molecular Formula C24H34Br4O4
Molecular Weight 706.14

SYNONYMS OF UNIPLEX FRP-45:
FRP 45; Pyronil 45; Uniplex FRP 45, Di-(2-ethylhexyl) tetrabromophthalate


APPLICATIONS OF UNIPLEX FRP-45:
UNIPLEX FRP-45 is especially recommended for applications like cable & wires or conveyer belts (e. g. made of PVC-P).
UNIPLEX FRP-45 is also suitable for adhesives, coatings, films and coated fabrics.
Product is compatible with PVC, PVC-P, flexible PUR, EPDM and PF.
Outstanding thermostability, good hydrolytic stability, and low volatility.


UNIPLEX FRP-45 is di-(2-ethylhexyl) tetrabromo phthalate.
UNIPLEX FRP-45 Acts as a flame retardant.
UNIPLEX FRP-45 offers a very low volatility combined with a superior thermal and color stability.

Due to its high bromine content, UNIPLEX FRP-45 can be used in number of polymers.
UNIPLEX FRP-45 is Compatible with flexible PVC, TPO and elastomers.

UNIPLEX FRP-45 is Suitable for use in cable & wires or conveyer belts (e.g. made of PVC-P).
Uniplex FRP-45 has a shelf life of at least 1 year.

UNIPLEX FRP-45 is a Di-2-ethylhexyl tetra bromo phthalate appearing as a clear amber liquid.
This liquid flame retardant imparts efficient flame retardance to commonly used polymers due to its high bromine content.
UNIPLEX FRP-45 provides low volatility and thermal and colour stability, finding application in adhesives, coatings, films, and coated fabrics.


UNIPLEX FRP-45 is a flame retardant.
UNIPLEX FRP-45 is di-(2-ethylhexyl) tetrabromo phthalate (bromine content is 45%).
UNIPLEX FRP-45 offers a very low volatility combined with a superior thermal and color stability.

UNIPLEX FRP-45 is compatible with a large number of polymers (e.g. flexible PVC, TPO and elastomers) due to its high bromine content.
UNIPLEX FRP-45 is suitable for adhesives.
UNIPLEX FRP-45 has a shelf life of at least 1 year.

UNIPLEX FRP-45 is a liquid flame retardant that imparts efficient flame retardance to a large number of polymers (e.g. flexible PVC, TPO and elastomers) due to its high bromine content.
UNIPLEX FRP-45 offers a very low volatility combined with a superior thermal and colour stability.
UNIPLEX FRP-45 is Di-(2-ethylhexyl) tetrabromo phthalate.

UNIPLEX FRP-45 is often used in the construction industry , electronics industry and polymer/rubber industry
UNIPLEX FRP-45 is a liquid flame retardant for polyvinyl chloride that provides excellent plasticizing properties, in addition to flame retardancy.

UNIPLEX FRP-45 provides the following advantages in polyvinyl chloride, as well as in other elastomers such as SBR, Neoprene, and EPDM:
UNIPLEX FRP-45 has High oxygen index values for efficient flame retardancy
UNIPLEX FRP-45 is Highly effective plasticization
UNIPLEX FRP-45 is Superior thermal and color stability
UNIPLEX FRP-45 has Low volatility
UNIPLEX FRP-45 has Excellent electrical properties

USES OF UNIPLEX FRP-45:
Bis(2-ethylhexyl) tetrabromophthalate is for use as a flame retardant and plasticizer in vinyl products.
UNIPLEX FRP-45 is also used as a flame retardant in wire and cable insulation, carpet backing, fabrics, wall coverings, adhesives, coatings and polyurethane foam.


CHEMICAL AND PHYSICAL PROPERTIES OF UNIPLEX FRP-45:
Appearance Clear amber liquid
Bromine content 45%
Assay > 95%
2-Ethylhexanol content < 0.3%
Tetrabromophthalic anhydride content < 0.1%
Acidity < 0.05 mEq/100 g
Water content < 0.1%
Colour, Gardner < 3#
Density at 20 °C 1.541 g/cm3
Viscosity at 25 °C 1595 mPa • s
Solubility Insoluble (3.3E-6 g/L) (25 ºC), Calc.*
Density 1.529±0.06 g/cm3 (20 ºC 760 Torr), Calc.*
CAS# 26040-51-7
EC Number 247-426-5
Molecular Formula C24H34Br4O4
Molecular Weight 706.14
Melting Point: -27°C (-16.6°F)
Boiling Point: >=300°C (572°F)
Flash Point: 207°C (404.6°F) closed cup
Auto-ignition: 370°C (698°F)
Solubility in Water: Slight


SAFETY INFORMATION ABOUT UNIPLEX FRP-45:
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.

DESCRIPTION:

UNIPLEX FRX 44-94 is Liquid flame retardant that imparts efficient flame retardance to a large number of polymers (e. g. flexible PVC, TPO, PU and elastomers) due to its high bromine content.
UNIPLEX FRX 44-94 offers a very low volatility combined with a superior thermal and color stability.


CAS# 26040-51-7
EC Number 247-426-5
Molecular Formula C24H34Br4O4
Molecular Weight 706.14

SYNONYMS OF UNIPLEX FRX 44-94:
FRP 45; Pyronil 45; Uniplex FRP 45, Di-(2-ethylhexyl) tetrabromophthalate


UNIPLEX FRX 44-94 is a nitrogen and phosphorous containing blend appearing as a white powder.
UNIPLEX FRX 44-94 provides ultraviolet stability, is non-hydroscopic, and forms an intumescent layer under heat and fire exposure.
UNIPLEX FRX 44-94 finds application in thermosets, polyolefin compounds, and paints and coatings.

UNIPLEX FRX 44-94 is a nitrogen (27%) and phosphorus (15.7%) blend.
UNIPLEX FRX 44-94 Acts as a flame retardant.
The blend forms an intumescent layer under heat and fire exposure.

UNIPLEX FRX 44-94 offers an excellent UV stability and is non-hydroscopic.
UNIPLEX FRX 44-94 can be processed at temperatures up to 225°C.

UNIPLEX FRX 44-94 is Compatible with thermosets and polyolefin compounds and suitable for paints and coatings.
UNIPLEX FRX 44-94 has a shelf life of at least 3 years.

UNIPLEX FRX 44-94 is a nitrogen and phosphorous containing blend appearing as a white powder.
UNIPLEX FRX 44-94 provides ultraviolet stability, is non-hydroscopic, and forms an intumescent layer under heat and fire exposure.
UNIPLEX FRX 44-94 finds application in thermosets, polyolefin compounds, and paints and coatings.



APPLICATIONS OF UNIPLEX FRX 44-94:
UNIPLEX FRX 44-94 is especially recommended for applications like cable & wires or conveyer belts (e. g. made of PVC-P).
UNIPLEX FRX 44-94 is also suitable for adhesives, coatings, films and coated fabrics.
Product is compatible with PVC, PVC-P, flexible PUR, EPDM and PF.
Outstanding thermostability, good hydrolytic stability, and low volatility.


UNIPLEX FRX 44-94 is di-(2-ethylhexyl) tetrabromo phthalate.
UNIPLEX FRX 44-94 Acts as a flame retardant.
UNIPLEX FRX 44-94 offers a very low volatility combined with a superior thermal and color stability.

Due to its high bromine content, UNIPLEX FRX 44-94 can be used in number of polymers.
UNIPLEX FRX 44-94 is Compatible with flexible PVC, TPO and elastomers.

UNIPLEX FRX 44-94 is Suitable for use in cable & wires or conveyer belts (e.g. made of PVC-P).
UNIPLEX FRX 44-94 has a shelf life of at least 1 year.

UNIPLEX FRX 44-94 is a Di-2-ethylhexyl tetra bromo phthalate appearing as a clear amber liquid.
This liquid flame retardant imparts efficient flame retardance to commonly used polymers due to its high bromine content.
UNIPLEX FRX 44-94 provides low volatility and thermal and colour stability, finding application in adhesives, coatings, films, and coated fabrics.


UNIPLEX FRX 44-94 is a flame retardant.
UNIPLEX FRX 44-94 is di-(2-ethylhexyl) tetrabromo phthalate (bromine content is 45%).
UNIPLEX FRX 44-94 offers a very low volatility combined with a superior thermal and color stability.

UNIPLEX FRX 44-94 is compatible with a large number of polymers (e.g. flexible PVC, TPO and elastomers) due to its high bromine content.
UNIPLEX FRX 44-94 is suitable for adhesives.
UNIPLEX FRX 44-94 has a shelf life of at least 1 year.

UNIPLEX FRX 44-94 is a liquid flame retardant that imparts efficient flame retardance to a large number of polymers (e.g. flexible PVC, TPO and elastomers) due to its high bromine content.
UNIPLEX FRX 44-94 offers a very low volatility combined with a superior thermal and colour stability.
UNIPLEX FRX 44-94 is Di-(2-ethylhexyl) tetrabromo phthalate.

UNIPLEX FRX 44-94 is often used in the construction industry , electronics industry and polymer/rubber industry
UNIPLEX FRX 44-94 is a liquid flame retardant for polyvinyl chloride that provides excellent plasticizing properties, in addition to flame retardancy.

UNIPLEX FRX 44-94 provides the following advantages in polyvinyl chloride, as well as in other elastomers such as SBR, Neoprene, and EPDM:
UNIPLEX FRX 44-94 has High oxygen index values for efficient flame retardancy
UNIPLEX FRX 44-94 is Highly effective plasticization
UNIPLEX FRX 44-94 is Superior thermal and color stability
UNIPLEX FRX 44-94 has Low volatility
UNIPLEX FRX 44-94 has Excellent electrical properties

USES OF UNIPLEX FRX 44-94:
Bis(2-ethylhexyl) tetrabromophthalate is for use as a flame retardant and plasticizer in vinyl products.
UNIPLEX FRX 44-94 is also used as a flame retardant in wire and cable insulation, carpet backing, fabrics, wall coverings, adhesives, coatings and polyurethane foam.


CHEMICAL AND PHYSICAL PROPERTIES OF UNIPLEX FRX 44-94:
Appearance Clear amber liquid
Bromine content 45%
Assay > 95%
2-Ethylhexanol content < 0.3%
Tetrabromophthalic anhydride content < 0.1%
Acidity < 0.05 mEq/100 g
Water content < 0.1%
Colour, Gardner < 3#
Density at 20 °C 1.541 g/cm3
Viscosity at 25 °C 1595 mPa • s
Solubility Insoluble (3.3E-6 g/L) (25 ºC), Calc.*
Density 1.529±0.06 g/cm3 (20 ºC 760 Torr), Calc.*
CAS# 26040-51-7
EC Number 247-426-5
Molecular Formula C24H34Br4O4
Molecular Weight 706.14
Melting Point: -27°C (-16.6°F)
Boiling Point: >=300°C (572°F)
Flash Point: 207°C (404.6°F) closed cup
Auto-ignition: 370°C (698°F)
Solubility in Water: Slight


SAFETY INFORMATION ABOUT UNIPLEX FRX 44-94:
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.

Alphadrate; Amide of carbonic acid; Carbamimidic acid; Carbamide resin; Carbamimidic acid; Carbonyl diamide; Carbonyldiamine; Isourea CAS NO:57-13-6

URSOLIC ACID N° CAS : 77-52-1 "Bien" dans toutes les catégories. Nom INCI : URSOLIC ACID Nom chimique : Urs-12-en-28-oic acid, 3-hydroxy-, (3beta)-; 3b-Hydroxyurs-12-en-28-oic Acid; Hydroxyursenoic acid N° EINECS/ELINCS : 201-034-0 Ses fonctions (INCI) Agent masquant : Réduit ou inhibe l'odeur ou le goût de base du produit Agent d'entretien de la peau : Maintient la peau en bon état Agent parfumant : Utilisé pour le parfum et les matières premières aromatiques

VALERIC ACID N° CAS : 109-52-4 "Bien" dans toutes les catégories. Nom INCI : VALERIC ACID Nom chimique : Pentanoic Acid N° EINECS/ELINCS : 203-677-2 Compatible Bio (Référentiel COSMOS) Ses fonctions (INCI) Agent parfumant : Utilisé pour le parfum et les matières premières aromatiques

urtica dioica extract; bichu booti extract; extract of the aerial parts of the nettle, urtica dioica l., urticaceae; nettle wort extract CAS NO:84012-40-8

UV STABILIZER UV stabilizer General name of additives used to prevent degradation of organic coating films exposed to UV light. UV stabilizers are classified into two groups. UV stabilizers (also called as UV absorbers). They convert the absorbed UV energy into heat and this heat is then dissipated through the substrate. Benzophenones and benzotriazole derivatives are commonly used UV stabilizers. The other group is free radical scavengers. They act by trapping the free radicals formed by UV light and decompose these radicals along with themselves hereby suppress the degradation of coating. Hindered amine light stabilizers (HALS) are used as free radical scavengers. UV Stabilizers for Engineering PlasticsEngineering plastics like polyamides, polyesters, polycarbonates are majorly used for applications that demand long time U.V stabilization. This selection guide mainly deals with the query "which UV Stabilizer is ideal for which plastic"? This guide will familiarize you with various UV stabilizers used with these engineering plastics. You would be able to find out the functionalities of different UV stabilizers for different engineering plastics in demand. Also one can find the starting point formulations of polycarbonates, polyacetal polyoxymethylene, polyesters like PET & PBT and polyamides.By Pascal Xanthopoulos UV StabilizersUV Stabilizers for PolycarbonateUV Stabilizers for POMUV Stabilizers for PolyestersUV Stabilizers for Polyamides UV Stabilizers UV stabilizers combat the degradation that plastics can undergo under the effects of sunlight, UV rays, heat and reaction with oxygen. The changes witnessed in a plastic can range from discoloration to formation of cracks. Incorporating a UV stabilizer into the polymer mix, improves the appearance/aesthetics and the overall life of the product. Selection of a UV stabilizer largely depends upon the surface to be protected, envisioned functional life & sensitivity to photodegradation. Several engineering thermoplastics like polyamides being majorly used for outdoor applications require long time U.V stabilization. For e.g.polybutylene terephthalate (PBT) finds uses in pigmented automotive exterior applications. Polyurethane based end products like automotive door trims, instrument panels, steering wheels, window sealants, head and arm rests and shoe soles, degrade when exposed to heat and light. Such degradation causes discoloration and formation of cracks. In this selection guide you will come across different UV Stabilizers that are added to impart typical functionalities to the plastic. For e.g. Hindered amine light stabilizers are derivatives of 2, 2, 6, 6-tetramethyl piperidine. They are extremely efficient stabilizers against light-induced degradation of most polymers. HALS do not absorb UV radiation, but act as antioxidants to inhibit or slow down the photochemical degradation of the polymer. Significant levels of UV stabilization are achieved at relatively low concentrations as during the stabilization process HALS get generated rather than being consumed. Others like benzotriazoles and benzophenones are cost effective and provide better performance than other types of UV stabilizers. Benzotriazoles are widely used in high temperature resins like acrylics and polycarbonates. While benzophenones find applications in polyolefins, PVC, etc. uv stabilizer are used individually or together to achieve the synergic effect. Click to check our UV stabilizers selection guide. Any further questions, chat with our online sales or mail at info@linchemical.com Linsorb UV Stabilizers Portfolio Related posts UV Stabilizer additives for polyolefins UV Stabilizer additives for special polymers UV Stabilizer additives for special coating UV Stabilizer additives for special adhesives If you are experiencing issues regarding your polymers or current additives, or sourcing additives or polymers additive solution？ this maybe the ending of your sourcing. Chat with our online engineer, or file the form below. We’ll back to you in 12hous, guaranteed. UV Stabilizers To prevent degradation when exposed to heat, cold and uv-light, plastics require stabilization. Specially designed plastic UV Stabilizers protect the polymer during processing and ensure that plastic end products retain their physical properties during use, prolonging their life. SONGWON offers as a leading manufacturer of polymer UV Stabilizers a comprehensive range of processing, heat and uv-light UV Stabilizers as additives for plastics in a variety of blends and physical forms that facilitate handling and application. Information on the available physical forms is provided in the Technical Datasheets. Manufacturer of Polymer UV Stabilizers / UV Stabilizer Solutions for Plastics Antioxidants, Binary Blends & Thioesters SONGNOX® antioxidants prolong the life of plastics Phenolic antioxidants (AOs), also known as primary antioxidants, are highly effective, non-discoloring UV Stabilizers for organic substrates that are prone to oxidation, e.g., plastics, synthetic fibers, elastomers and waxes. They act as free radical scavengers, and are primarily used to protect the finished product. Phosphite antioxidants, also known as secondary antioxidants, act as peroxide decomposers, protecting the polymer and ensuring color retention of oxidation-prone organic polymers, especially during processing. Thioester antioxidants decompose and neutralize hydroperoxides formed through polymer oxidation. Thioesters are used to provide heat aging protection and to preserve color. Aminic antioxidants help to preserve physical and surface properties, including color, and scorch and heat resistance. Binary blends are a combination of a primary (phenolic) antioxidant and a secondary (phosphite) antioxidant for optimum stabilization during processing and service life. UV Stabilizer Solutions SONGXTEND® stabilization excellence & tailor-made solutions Our SONGXTEND® range of innovative stabilization packages solves a number of the key issues our customers face during processing, conversion and end-use life cycles. SONGXTEND® UV Stabilizer Solutions provide: processing stabilization solutions for PP high heat stabilization in PP based automotive applications solutions for PP fiber & thin wall injection molded grades Our highly advanced production processes and technology enable us to tailor our UV Stabilizer solution products to specification. Hindered Amine Light UV Stabilizers (HALS) SABO®STAB hindered amine light UV Stabilizers (HALS) neutralize harmful UV radiation Hindered amine light UV Stabilizers (HALS) protect polymers from degradation due to UV exposure by neutralizing them. HALS regenerate during neutralization and continue to provide protection throughout the life of the end product. They also act as primary antioxidants with low color generation. Monomeric HALS provide effective surface protection, while polymeric HALS protect the core of the material. SONGWON has a long-term global distribution agreement for distribution of SABO HALS light UV Stabilizers. UV Stabilizer Photo-oxidation is the result of the combined action of light and oxygen, with the action of sunlight in the presence of the air’s oxygen being the most important example. Photo-oxidation of polymers and other materials leads to degradation, discoloration and product failure unless it is prevented or significantly retarded. Mayzo supplies products from three general classes of UV stabilizers: UV Absorbers (which include benzotriazoles and benzophenones) HALS (hindered amine light UV stabilizers) UV Stabilizers – UV Absorber & Hindered Amine Light Stabilizers (HALS) UV stabilizer range contains two types of light stabilizers: Ultraviolet Light Absorbers (UVA) and Hindered-Amine Light Stabilizers (HALS), used individually or as blends. UVA filter harmful UV light and help prevent color change and delamination of coatings, adhesives, and sealants. HALS trap free radicals once they are formed and are effective in retaining surface properties such as gloss and prevent cracking and chalking of paints. The combination of these two families is highly synergistic. UV stabilizer product list UV Absorber BP-3, BP-6, P, 1130, 1164, 1157, 234, 326, 329, 360, 3638, 384-2,400, 531, 928, 99-2, 5050, 5060. Hindered Amine Light Stabilizers 119, 292, 622, 765, 770, 783, 791, 944, 2020, 3808PP5, 3853PP5 UV Stabilizers for Polymers, Plastics, Coatings, Rubber BASF, Songwon, Addivant and Baoxu Chemical UV Stabilizer Compare Baoxu chemical UV stabilizers are min99% similar according to IR, over half of our domestic customers use our UV stabilizers as replacement of imports to have a competitive edge. We control batch to batch quality consistency, to further protect our buyers interests. We use Paypal, Escrow which now known as Alibaba Secure Payment for samples express fees (samples are free to offer). UV stabilizer General name of additives used to prevent degradation of organic coating films exposed to UV light. UV stabilizers are classified into two groups. UV stabilizers (also called as UV absorbers). They convert the absorbed UV energy into heat and this heat is then dissipated through the substrate. Benzophenones and benzotriazole derivatives are commonly used UV stabilizers. The other group is free radical scavengers. They act by trapping the free radicals formed by UV light and decompose these radicals along with themselves hereby suppress the degradation of coating. Hindered amine light stabilizers (HALS) are used as free radical scavengers. UV Stabilizers for Engineering PlasticsEngineering plastics like polyamides, polyesters, polycarbonates are majorly used for applications that demand long time U.V stabilization. This selection guide mainly deals with the query "which UV Stabilizer is ideal for which plastic"? This guide will familiarize you with various UV stabilizers used with these engineering plastics. You would be able to find out the functionalities of different UV stabilizers for different engineering plastics in demand. Also one can find the starting point formulations of polycarbonates, polyacetal polyoxymethylene, polyesters like PET & PBT and polyamides.By Pascal Xanthopoulos UV StabilizersUV Stabilizers for PolycarbonateUV Stabilizers for POMUV Stabilizers for PolyestersUV Stabilizers for Polyamides UV Stabilizers UV stabilizers combat the degradation that plastics can undergo under the effects of sunlight, UV rays, heat and reaction with oxygen. The changes witnessed in a plastic can range from discoloration to formation of cracks. Incorporating a UV stabilizer into the polymer mix, improves the appearance/aesthetics and the overall life of the product. Selection of a UV stabilizer largely depends upon the surface to be protected, envisioned functional life & sensitivity to photodegradation. Several engineering thermoplastics like polyamides being majorly used for outdoor applications require long time U.V stabilization. For e.g.polybutylene terephthalate (PBT) finds uses in pigmented automotive exterior applications. Polyurethane based end products like automotive door trims, instrument panels, steering wheels, window sealants, head and arm rests and shoe soles, degrade when exposed to heat and light. Such degradation causes discoloration and formation of cracks. In this selection guide you will come across different UV Stabilizers that are added to impart typical functionalities to the plastic. For e.g. Hindered amine light stabilizers are derivatives of 2, 2, 6, 6-tetramethyl piperidine. They are extremely efficient stabilizers against light-induced degradation of most polymers. HALS do not absorb UV radiation, but act as antioxidants to inhibit or slow down the photochemical degradation of the polymer. Significant levels of UV stabilization are achieved at relatively low concentrations as during the stabilization process HALS get generated rather than being consumed. Others like benzotriazoles and benzophenones are cost effective and provide better performance than other types of UV stabilizers. Benzotriazoles are widely used in high temperature resins like acrylics and polycarbonates. While benzophenones find applications in polyolefins, PVC, etc. uv stabilizer are used individually or together to achieve the synergic effect. Click to check our UV stabilizers selection guide. Any further questions, chat with our online sales or mail at info@linchemical.com Linsorb UV Stabilizers Portfolio Related posts UV Stabilizer additives for polyolefins UV Stabilizer additives for special polymers UV Stabilizer additives for special coating UV Stabilizer additives for special adhesives If you are experiencing issues regarding your polymers or current additives, or sourcing additives or polymers additive solution？ this maybe the ending of your sourcing. Chat with our online engineer, or file the form below. We’ll back to you in 12hous, guaranteed. UV Stabilizers To prevent degradation when exposed to heat, cold and uv-light, plastics require stabilization. Specially designed plastic UV Stabilizers protect the polymer during processing and ensure that plastic end products retain their physical properties during use, prolonging their life. SONGWON offers as a leading manufacturer of polymer UV Stabilizers a comprehensive range of processing, heat and uv-light UV Stabilizers as additives for plastics in a variety of blends and physical forms that facilitate handling and application. Information on the available physical forms is provided in the Technical Datasheets. Manufacturer of Polymer UV Stabilizers / UV Stabilizer Solutions for Plastics Antioxidants, Binary Blends & Thioesters SONGNOX® antioxidants prolong the life of plastics Phenolic antioxidants (AOs), also known as primary antioxidants, are highly effective, non-discoloring UV Stabilizers for organic substrates that are prone to oxidation, e.g., plastics, synthetic fibers, elastomers and waxes. They act as free radical scavengers, and are primarily used to protect the finished product. Phosphite antioxidants, also known as secondary antioxidants, act as peroxide decomposers, protecting the polymer and ensuring color retention of oxidation-prone organic polymers, especially during processing. Thioester antioxidants decompose and neutralize hydroperoxides formed through polymer oxidation. Thioesters are used to provide heat aging protection and to preserve color. Aminic antioxidants help to preserve physical and surface properties, including color, and scorch and heat resistance. Binary blends are a combination of a primary (phenolic) antioxidant and a secondary (phosphite) antioxidant for optimum stabilization during processing and service life. UV Stabilizer Solutions SONGXTEND® stabilization excellence & tailor-made solutions Our SONGXTEND® range of innovative stabilization packages solves a number of the key issues our customers face during processing, conversion and end-use life cycles. SONGXTEND® UV Stabilizer Solutions provide: processing stabilization solutions for PP high heat stabilization in PP based automotive applications solutions for PP fiber & thin wall injection molded grades Our highly advanced production processes and technology enable us to tailor our UV Stabilizer solution products to specification. Hindered Amine Light UV Stabilizers (HALS) SABO®STAB hindered amine light UV Stabilizers (HALS) neutralize harmful UV radiation Hindered amine light UV Stabilizers (HALS) protect polymers from degradation due to UV exposure by neutralizing them. HALS regenerate during neutralization and continue to provide protection throughout the life of the end product. They also act as primary antioxidants with low color generation. Monomeric HALS provide effective surface protection, while polymeric HALS protect the core of the material. SONGWON has a long-term global distribution agreement for distribution of SABO HALS light UV Stabilizers. UV Stabilizer Photo-oxidation is the result of the combined action of light and oxygen, with the action of sunlight in the presence of the air’s oxygen being the most important example. Photo-oxidation of polymers and other materials leads to degradation, discoloration and product failure unless it is prevented or significantly retarded. Mayzo supplies products from three general classes of UV stabilizers: UV Absorbers (which include benzotriazoles and benzophenones) HALS (hindered amine light UV stabilizers) UV Stabilizers – UV Absorber & Hindered Amine Light Stabilizers (HALS) UV stabilizer range contains two types of light stabilizers: Ultraviolet Light Absorbers (UVA) and Hindered-Amine Light Stabilizers (HALS), used individually or as blends. UVA filter harmful UV light and help prevent color change and delamination of coatings, adhesives, and sealants. HALS trap free radicals once they are formed and are effective in retaining surface properties such as gloss and prevent cracking and chalking of paints. The combination of these two families is highly synergistic. UV stabilizer product list UV Absorber BP-3, BP-6, P, 1130, 1164, 1157, 234, 326, 329, 360, 3638, 384-2,400, 531, 928, 99-2, 5050, 5060. Hindered Amine Light Stabilizers 119, 292, 622, 765, 770, 783, 791, 944, 2020, 3808PP5, 3853PP5 UV Stabilizers for Polymers, Plastics, Coatings, Rubber BASF, Songwon, Addivant and Baoxu Chemical UV Stabilizer Compare Baoxu chemical UV stabilizers are min99% similar according to IR, over half of our domestic customers use our UV stabilizers as replacement of imports to have a competitive edge. We control batch to batch quality consistency, to further protect our buyers interests. We use Paypal, Escrow which now known as Alibaba Secure Payment for samples express fees (samples are free to offer).

Uvinul A plus B refers to a combination of two chemical compounds used in sunscreens and other personal care products to provide UV protection.
The two components are "Uvinul A Plus" and "Uvinul B."
These compounds are organic UV filters that absorb or block certain wavelengths of ultraviolet (UV) radiation from the sun, helping to protect the skin from sunburn and potential damage caused by UV exposure.
Uvinul A plus B is a synergistic combination of UV filters offering comprehensive protection against UVA and UVB rays.



APPLICATIONS


Uvinul A plus B finds its primary application in sunscreens, where it serves as a crucial component for providing effective UV protection.
This combination of UV filters is formulated into a range of sun protection products, including lotions, creams, sprays, and sticks.

Uvinul A plus B is widely used in daily skincare routines as a preventive measure against the harmful effects of sun exposure.
Uvinul A plus B is essential in beach and sport sunscreens, catering to individuals engaged in outdoor activities.
Its inclusion in facial moisturizers with SPF enhances daily protection against photoaging caused by UV rays.

Uvinul A plus B is commonly used in makeup products, offering sun protection without compromising cosmetic elegance.
Uvinul A plus B is also utilized in lip balms with SPF, ensuring UV protection for the delicate skin of the lips.
Uvinul A plus B is a key component in body lotions and creams formulated to provide all-over sun protection during daily application.
Skincare brands often incorporate Uvinul A plus B into products aimed at maintaining the skin's health and appearance.
Its application extends to specialty sunscreens, such as those designed for sensitive skin or specific outdoor activities.
Uvinul A plus B is suitable for year-round use, as UV exposure can occur even on cloudy days or during winter months.

Uvinul A plus B is often found in children's sunscreens, offering parents peace of mind when protecting their children's delicate skin.
Uvinul A plus B is used in anti-aging skincare lines to counteract the premature aging effects of UV radiation.
Uvinul A plus B's compatibility with various formulations makes it a versatile choice for different sunscreen product types.

Uvinul A plus B contributes to the formulation of sunscreens with various SPF levels, allowing users to choose the appropriate protection.
Uvinul A plus B is vital for preventing sunburn, reducing the risk of skin cancer, and maintaining healthy skin.
Uvinul A plus B's broad-spectrum coverage addresses both short-term effects like sunburn and long-term photoaging concerns.
Uvinul A plus B is an integral ingredient in sun protection products that aim to meet regulatory and safety standards.

Brands often highlight the presence of Uvinul A plus B on product labels to emphasize their commitment to UV protection.
Uvinul A plus B is chosen for its ability to provide stable and effective UV protection in various environmental conditions.
Uvinul A plus B's popularity lies in its ability to deliver sun protection without leaving a heavy or greasy residue.
Uvinul A plus B is utilized in skincare products that cater to individuals seeking multifunctional benefits, including hydration and protection.
Uvinul A plus B enables consumers to incorporate sun protection seamlessly into their skincare routines.

Its use is not limited to specific skin types, making it accessible and beneficial for a wide range of users.
Whether for daily wear, outdoor activities, or specific skin concerns, Uvinul A plus B remains a trusted choice for reliable sun protection.

Uvinul A plus B serves as a fundamental component in sunscreens intended for use on both the face and body.
Uvinul A plus B is integrated into tinted sunscreens, providing both sun protection and light coverage.

Brands often incorporate Uvinul A plus B into after-sun products, offering soothing care for skin exposed to UV radiation.
Its inclusion in facial serums with SPF combines skincare benefits with essential sun protection.
Uvinul A plus B is frequently found in makeup primers, acting as a base that shields the skin from UV damage.

Uvinul A plus B is used in daily moisturizers with SPF, making sun protection an integral part of everyday skincare routines.
Uvinul A plus B is essential in body sunscreens designed for outdoor enthusiasts and those spending extended time in the sun.
Uvinul A plus B is featured in sun protection products tailored to specific skin concerns, such as oil control or hydration.

Uvinul A plus B plays a role in setting sprays with SPF, allowing users to refresh their sun protection throughout the day.
Uvinul A plus B's application extends to skincare products formulated to counteract the effects of photoaging.
Uvinul A plus B is an essential ingredient in skincare products designed to minimize the appearance of hyperpigmentation caused by sun exposure.

Brands often integrate Uvinul A plus B into facial mists with SPF, offering on-the-go sun protection and refreshment.
Uvinul A plus B is featured in cosmetic products that prioritize both aesthetics and skin health.

Uvinul A plus B enables the formulation of sunscreens suitable for individuals with different skin tones and types.
Uvinul A plus B contributes to the creation of sun protection products for sensitive skin, offering gentle care without causing irritation.
Uvinul A plus B is a key component in skincare lines that focus on maintaining youthful and healthy-looking skin.
Brands highlight the presence of Uvinul A plus B in products intended for outdoor activities like hiking, sports, and beach outings.
Uvinul A plus B supports the formulation of lightweight and breathable sunscreens, promoting user comfort during wear.
Uvinul A plus B is integral to sun protection products designed to be worn under makeup without compromising its finish.
Uvinul A plus B's application in lip products with SPF ensures UV protection for the often overlooked skin of the lips.

Uvinul A plus B is used in skincare products aiming to address the negative effects of environmental factors, including UV radiation.
Brands emphasize Uvinul A plus B in products that align with the evolving consumer preference for skincare with added benefits.
Its integration in beauty products underscores the commitment to holistic skin health, encompassing both appearance and protection.
Uvinul A plus B supports the creation of sun protection products that cater to the preferences of individuals seeking specific textures and application methods.
Its use in a wide array of sun protection and skincare products demonstrates its role as a foundational ingredient in promoting skin well-being.

Uvinul A plus B is found in sunscreens formulated for various skin types, ensuring accessible sun protection for everyone.
Uvinul A plus B is a key ingredient in sunscreens for individuals with active lifestyles, offering dependable protection during workouts and outdoor activities.
Uvinul A plus B's use in lightweight sunscreen formulations addresses the demand for products that feel comfortable on the skin.

Uvinul A plus B supports the creation of sunscreens suitable for daily urban life, guarding against UV radiation in city environments.
Its application in foundation products with SPF underscores the integration of sun protection into everyday makeup routines.
Brands often integrate Uvinul A plus B into sunscreens that cater to specific climates, adapting to varying UV levels.
Uvinul A plus B is a vital component in sunscreens recommended by dermatologists to prevent the exacerbation of skin conditions triggered by UV exposure.

Uvinul A plus B contributes to the formulation of sunscreens suitable for those with outdoor professions or hobbies.
Uvinul A plus B is chosen for its ability to provide UV protection without leaving a white cast on the skin.
Its inclusion in primer products with SPF primes the skin for makeup while creating a barrier against UV rays.
Uvinul A plus B is used in sunscreens that prioritize the balance between protection and allowing the skin to breathe.
Uvinul A plus B supports the development of sun protection products tailored to specific age groups, including children, adults, and seniors.

Uvinul A plus B's integration in facial mists with SPF offers a refreshing and convenient way to reapply sun protection throughout the day.
Uvinul A plus B is included in skincare products formulated to address the concerns of individuals with sensitive or reactive skin.
Uvinul A plus B is an essential ingredient in sunscreens with a transparent finish, suitable for individuals with various skin tones.
Uvinul A plus B's application in BB creams with SPF combines makeup coverage with essential sun protection.
Uvinul A plus B contributes to the creation of sunscreens recommended for individuals undergoing specific skincare treatments that increase sun sensitivity.

Brands highlight Uvinul A plus B in products that align with the trend of customizable skincare routines, where protection is tailored to individual needs.
Its presence in sun protection products reinforces a holistic approach to skincare that encompasses prevention and preservation.
Uvinul A plus B is a building block in sunscreens designed for the delicate eye area, protecting against UV-induced fine lines and wrinkles.
Uvinul A plus B supports the formulation of sunscreens with antioxidant-rich ingredients, amplifying their protective benefits.
Uvinul A plus B is used in products that cater to those seeking sun protection that complements their minimalist skincare philosophy.

Brands emphasize Uvinul A plus B in sunscreens promoted as travel essentials, essential for maintaining skin health during trips.
Uvinul A plus B's integration in facial sunscreen products with skin-enhancing ingredients supports a comprehensive skincare approach.
Uvinul A plus B serves as a cornerstone of sun protection, driving innovation in skincare products that prioritize both health and beauty.



DESCRIPTION


Uvinul A plus B refers to a combination of two chemical compounds used in sunscreens and other personal care products to provide UV protection.
The two components are "Uvinul A Plus" and "Uvinul B."
These compounds are organic UV filters that absorb or block certain wavelengths of ultraviolet (UV) radiation from the sun, helping to protect the skin from sunburn and potential damage caused by UV exposure.
Uvinul A plus B is a synergistic combination of UV filters offering comprehensive protection against UVA and UVB rays.

Uvinul A plus B harnesses diethylamino hydroxybenzoyl hexyl benzoate (Uvinul A Plus) and ethylhexyl triazone (Uvinul B) for optimal defense.
Its effectiveness lies in its ability to absorb and block UVA and UVB rays, shielding the skin from their damaging effects.

Uvinul A plus B provides advanced sun protection suitable for various outdoor activities and extended sun exposure.
The photo-stable nature of its components ensures its reliability even during prolonged periods under the sun.
Uvinul A plus B is designed with skin compatibility in mind, minimizing the risk of irritation often associated with UV filters.
Upon application, products containing Uvinul A plus B offer a transparent and non-greasy finish for a comfortable experience.
The broad-spectrum coverage of this combination guards against sunburn, skin aging, and potential damage.

Uvinul A plus B forms a protective barrier on the skin, acting as a shield against the harmful effects of UV radiation.
Dermatologists often recommend sunscreens with Uvinul A plus B due to its reliable protection and compatibility.
By incorporating Uvinul A plus B into daily skincare routines, individuals can minimize the effects of sun exposure on their skin.
Uvinul A plus B is suitable for outdoor enthusiasts, providing reliable protection during activities such as swimming and hiking.
The combination's effectiveness aligns with efforts to promote sun safety and minimize the risks of UV-induced damage.

Uvinul A plus B aids in reducing the appearance of fine lines and wrinkles, contributing to a more youthful appearance.
The fusion of diethylamino hydroxybenzoyl hexyl benzoate (Uvinul A Plus) and ethylhexyl triazone (Uvinul B) marks a skincare milestone.
Confidence in outdoor activities is enhanced by the knowledge that Uvinul A plus B is safeguarding the skin from UV harm.
Scientifically tested and formulated, Uvinul A plus B reflects the skincare industry's commitment to effective sun protection.
Its international standards ensure individuals worldwide can access reliable sun protection.

Uvinul A plus B's formulation is based on rigorous research and testing, reinforcing its role in skincare routines.
Incorporating Uvinul A plus B into daily life contributes to long-term skin health and youthful vibrancy.

Uvinul A plus B defends against UV-induced aging, maintaining the skin's vitality and appearance.
Its dual filters revolutionize skincare by offering both UVA and UVB protection in a single solution.
Whether for hiking, swimming, or everyday activities, Uvinul A plus B is a trusted shield against UV exposure.

Daily application provides a shield against sun-induced skin damage, offering both confidence and comfort.
With Uvinul A Plus B, skin protection becomes an investment in overall well-being and lasting skin health.



FIRST AID


Inhalation:

If Uvinul A plus B is inhaled and respiratory irritation occurs, move the affected person to fresh air immediately.
If breathing difficulties persist, seek medical attention.


Skin Contact:

In case of skin contact, remove contaminated clothing and rinse the affected area thoroughly with plenty of water.
If irritation or redness develops, seek medical advice.
Wash contaminated clothing before reuse.


Eye Contact:

In case of eye contact, rinse the affected eye gently with water for at least 15 minutes, while keeping the eyelid open.
Seek medical attention if irritation, redness, or discomfort persists.


Ingestion:

If Uvinul A plus B is ingested accidentally, do not induce vomiting unless directed to do so by medical personnel.
Rinse the mouth with water if the person is conscious and seek medical attention.



HANDLING AND STORAGE


Handling:

Avoid Direct Contact:
When handling "Uvinul A Plus B," avoid direct skin and eye contact to prevent potential irritation.

Personal Protective Equipment:
Wear appropriate personal protective equipment (PPE) such as gloves, safety goggles, and lab coats when handling the product.

Ventilation:
Use in a well-ventilated area to minimize inhalation exposure.
If working in an enclosed space, consider using local exhaust ventilation.

Avoid Inhalation:
Avoid inhaling dust, vapors, or mists generated during handling.
If dust is generated, wear a mask designed to filter particulates.

Prevent Ingestion:
Do not eat, drink, or smoke while handling Uvinul A Plus B.
Wash hands thoroughly after handling and before eating or touching the face.

Spill Response:
In case of spills, carefully sweep or vacuum up the material, taking precautions to minimize the generation of dust.
Dispose of waste according to regulations.


Storage:

Cool, Dry Place:
Store Uvinul A plus B in a cool, dry place away from direct sunlight, heat sources, and open flames.

Temperature Control:
Maintain storage temperatures within the range specified on the product's safety data sheet (SDS) to ensure stability and performance.

Original Containers:
Keep the product in its original container, tightly closed, and properly labeled.

Compatibility:
Store Uvinul A plus B away from incompatible materials, including strong oxidizers, reducing agents, and reactive chemicals.

Segregation:
Separate Uvinul A plus B from food, beverages, and animal feed to prevent cross-contamination.

Moisture Control:
Protect the product from moisture to avoid degradation and clumping.

Childproofing:
Store in a location inaccessible to children and unauthorized personnel.



SYNONYMS


UV Protection Blend
Sunscreen Ingredient Combination
Broad-Spectrum UV Filters
Sun Protection Complex
UV Defense Mixture
Sunblock Formulation
Photoprotective Blend
Sunscreen Component Mix
Solar Radiation Shield
UV Absorption Combination
Radiation Barrier Formula
Sunscreen Additive Mix
Solar Defense Blend
UV Ray Blocking Compound
Photoprotection Matrix
Sunscreen Agent Fusion
Sunblock Ingredient Blend
Solar Radiation Screen
UV-Absorbing Compound Pair
UV Ray Filter Blend
Sunscreen Actives Mixture
Radiation Absorption Duo
Sun Guarding Mixture
Photoprotectant Combination
Sunscreen Defense Cocktail
Solar Shield Formula
Sunscreen Active Duo
Radiation Absorption Blend
UV Defense Cocktail
Photoprotection Pairing
Sunscreen Component Fusion
Sunblock Filter Mixture

GRAPESEED WAX ; Vitis Vinifera (Grape) Seed Oil; GSW; vitis vinifera seed/skin/stem extract; extract of the seeds, skin and stems of vitis vinifera CAS NO:85594-37-2

vaccinium macrocarpon fruit; cranberry fruit; fruit of the cranberry, vaccinium macrocarpon, ericaceae CAS NO:91770-88-6

vaccinium myrtillus fruit extract; bilberry fruit extract; extract of the fruit of the myrtle, vaccinium myrtillus l., ericaceae; vaccinium myrtillus subsp. oreophilum fruit extract; vaccinium myrtillus var. oreophilum fruit extract; vaccinium oreophilum fruit extract; whortleberry extract CAS NO:84082-34-8

vaccinium macrocarpon fruit extract; actipone cranberry (Symrise); fruitapone cranberry (Symrise); cranberry 4:1 extract; fruitapone cranberry B (Symrise); actiphyte of cranberry extract; cranberry extract exocyan cran 10G; cranberry fruit extract; fruitapone cranberry GT (Symrise); extract of the fruit of the cranberry, vaccinium macrocarpon, ericaceae CAS NO:91770-88-6

VANILLIC ACID N° CAS : 121-34-6 "Bien" dans toutes les catégories. Nom INCI : VANILLIC ACID Nom chimique : Benzoic acid, 4-hydroxy-3-methoxy- N° EINECS/ELINCS : 204-466-8 Ses fonctions (INCI) Non classé : Non classé

VALERIC ACID = PENTANOIC ACID = n-VALERIC ACID


CAS Number: 109-52-4
EC Number: 203-677-2
MDL number: MFCD00004413
Molecular Formula: C5H10O2 or CH3(CH2)3COOH


Valeric acid (pentanoic acid, C5H10O2) is a straight, saturated chain, alkyl carboxylic acid.
Valeric acid or pentanoic acid is a straight-chain alkyl carboxylic acid with the chemical formula CH3(CH2)3COOH.
Like other low-molecular-weight carboxylic acids, Valeric acid has an unpleasant odor.
Valeric acid is found in the perennial flowering plant Valeriana officinalis, from which it gets its name.
Valeric acid's primary use is in the synthesis of its esters.


Salts and esters of valeric acid are known as valerates or pentanoates.
Valeric acid is a straight-chain saturated fatty acid containing five carbon atoms.
Valeric acid has a role as a plant metabolite.
Valeric acid is a short-chain fatty acid and a straight-chain saturated fatty acid.
Valeric acid is a conjugate acid of a valerate.


Valeric acid is a natural product found in Rhododendron mucronulatum, Hansenia forbesii, and other organisms with data available.
Valeric acid appears as a colorless liquid with a penetrating unpleasant odor.
Valeric acid's Density is 0.94 g / cm3.
Valeric acid's freezing point is -93.2 °F (-34 °C).
Valeric acid's boiling point is 365.7 °F (185.4 °C).


Valeric acid's flash point is 192 °F (88.9 °C).
Valeric acid (pentanoic acid, C5H10O2) is a straight, saturated chain, alkyl carboxylic acid.
Valeric acid is a colorless, oily liquid with a very unpleasant odor of stale cheese.
Valeric acid exists in four isomeric forms, one of which contains an asymmetric carbon atom and consequently occurs in two optically active modifications and one optically inactive modification.


Valeric acid is found naturally as free or as esters in the vegetable and animal kingdoms.
Valeric acid belongs to the class of organic compounds known as straight chain fatty acids.
These are fatty acids with a straight aliphatic chain.
Valeric acid is a straight-chain alkyl carboxylic acid and saturated fatty acid with the chemical formula CH3(CH2)3COOH.
Valeric acid is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 10 to < 100 tonnes per annum.


Valeric acid is a colorless, oily liquid with an unpleasant odor.
Valeric acid can be extracted by boiling water or soda from the roots of Angelica archangelica and Valeriana officinalis (from which valeric acid gets the name).
The acid can also be obtained by oxidizing fermentation amyl alcohol with chromic acid.
The acid can be formed by microorganisms during the anaerobic fermentation of CO2 and H2 (discussed above) and by the fermentation of other carbon sources, such as wastewater solids.


Valeric acid is a straight-chain saturated fatty acid containing five carbon atoms.
Valeric acid, or pentanoic acid, is a straight chain alkyl carboxylic acid with the chemical formula CH3(CH2)3COOH.
Like other low molecular weight carboxylic acids, it has a very unpleasant odor.
Valeric acid is commonly found in human feces, with an average concentration of 2.4 umol/g feces (range of 0.6-3.8 umol/g) (PMID:6740214 ).
Valeric acid is produced by the gut microbiota, typically Clostridia species and other gut bacterial species such as Megasphaera massiliensis MRx0029 (PMID:30052654 ) via the condensation of ethanol with propionic acid (PMID:18116989 ).


Valeric acid is largely considered as a gut microbial metabolite.
Recently, valeric acid has been found to exert strong gut protective effects.
Valeric acid is also found in certain plants, specifically in the perennial flowering plant valerian (Valeriana officinalis), from which it gets its name.
Valeric acid is considered safe as a food additive by the World Health Organization.
Valeric acid is also known as pentanoic acid.


Valeric acid is a straight-chain alkyl carboxylic acid.
Valeric acid 's chemical formula is C5H10O2.
Valeric acid has a very unpleasant odor like the carboxylic acids with low molecular weight.
Valeric acid can be found in the perennial flowering plant valerian naturally, which is also known as valeriana officinalis.
The most important function of valeric acid is in the synthesis of its esters.


Volatile esters synthesized from valeric acid have more pleasant odors compared with valeric acid.
Valeric acid has similar chemical structure with gamma-Hydroxybutyric acid, which is a naturally occurring neurotransmitter and a psychoactive drug.
Valeric acid also has similar structure with neurotransmitter gamma-Aminobutyric acid, which is the chief inhibitory neurotransmitter in the mammalian central nervous system.
Valeric acid lacks the alcohol and amine functional groups, which contribute to the biological activities of GHB and GABA.


Valeric acid is methylated and results in the formation of mevalonic acid.
Valeric acid, also known as pentanoic acid or valerate, belongs to the class of organic compounds known as straight chain fatty acids.
These are fatty acids with a straight aliphatic chain.
Valeric acid is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral.


Valeric acid, or pentanoic acid, is a straight-chain alkyl carboxylic acid with the chemical formula C5H10O2.
Like other low-molecular-weight carboxylic acids, it has a very unpleasant odor.
Valeric acid is found naturally in the perennial flowering plant valerian (Valeriana officinalis), from which it gets its name.
Valeric acid 's primary use is in the synthesis of its esters.


Valeric acid has a similar structure to both GHB and the neurotransmitter GABA.
Valeric acid differs from valproic acid simply by lacking a 3-carbon side chain.
Valeric acid is an inert ingredient in controlling pest.
Valeric acid is an organic chemical compound with the chemical formula C5H10O2.
The primal use of Valeric acid is in the syntesis of ester.



USES and APPLICATIONS of VALERIC ACID:
Valeric acid is used Stabilizers, Plasticizers, Coatings additives, Lubricants, Pharmaceuticals, Pesticides, Perfumes, Food additives, Chemical intermediates, and perfuming agents.
Several, including ethyl valerate and pentyl valerate are used as food additives because of their fruity flavors.
Valeric acid occurs naturally in some foods but is also used as a food additive.


Valeric acid is used for the preparation of derivatives, notably its volatile esters which, unlike the parent acid, have pleasant odors and fruity flavors and hence find applications in perfumes, cosmetics and foodstuffs.
Typical examples are the methyl valerates, ethyl valerates, and pentyl valerates.
Valeric acid, and its esters, is mainly used in perfumes and cosmetics, as food additives because of the fruity flavor of the esters, and as plasticizers and pharmaceuticals.


Industrially valeric acid is primarily used in the synthesis of its esters.
Volatile esters of valeric acid tend to have pleasant odors and are used in perfumes and cosmetics.
Ethyl valerate and pentyl valerate are used as food additives because of their fruity flavours.
Hydrolysis of these valerate-containing food additives in the gut can also lead to the appearance of valerate in blood, urine and stool samples.
Valeric acid is predominantly used in the synthesis of esters.


Valeric Acid is a reagent that is used in the biological studies of (D)-b-hydroxybutyrate which inhibits adipocyte lipolysis via the nicotinic acid receptor PUMA-G.
Valeric acid is used by consumers, by professional workers (widespread uses), in formulation or re-packing, at industrial sites and in manufacturing.
Valeric acid is used in the following products: perfumes and fragrances and cosmetics and personal care products.


Other release to the environment of Valeric acid is likely to occur from: indoor use as processing aid.
Valeric acid is mainly used as a chemical intermediate to manufacture flavors and perfumes, synthetic lubricants, agricultural chemicals, and pharmaceuticals.
Valeric acid is also used as a flavoring aid in foods.
Valeric acid is can be used in perfumes and cosmetics.


Volatile esters of valeric acid tend to have pleasant odors and are used in perfumes and cosmetics.
Ethyl valerate and pentyl valerate are used as food additives because of their fruity flavors.
Valeric acid, is used as a sex attractant of the sugar beet wireworm, Limonius californicus.
Valeric acid is used predominantly as an intermediate in the manufacture of flavors and perfumes, ester type lubricants, plasticizers and vinyl stabilizers.


Valeric acid is a food additive used as a synthetic flavoring substance dan adjuvant.
Valeric acid tends to have pleasant odors and are used in perfumes and cosmetics.
Some of these esters are used as food additives because of their fruity flavors.
Volatile esters of valeric acid tend to have pleasant odors and are used in perfumes and cosmetics.



HISTORY of VALERIC ACID:
Valeric acid is a minor constituent of the perennial flowering plant valerian (Valeriana officinalis), from which it gets its name.
The dried root of this plant has been used medicinally since antiquity.
The related isovaleric acid shares its unpleasant odor and their chemical identity was investigated by oxidation of the components of fusel alcohol, which includes the five-carbon amyl alcohols.
Valeric acid is one volatile component in swine manure.
Other components include other carboxylic acids, skatole, trimethyl amine, and isovaleric acid.
Valeric acid is also a flavor component in some foods.



MANUFACTURE of VALERIC ACID:
In industry, valeric acid is produced by the oxo process from 1-butene and syngas, forming valeraldehyde, which is oxidised to the final product.
H2 + CO + CH3CH2CH=CH2 → CH3CH2CH2CH2CHO → valeric acid
Valeric acid can also be produced from biomass-derived sugars via levulinic acid and this alternative has received considerable attention as a way to produce biofuels.



REACTIONS of VALERIC ACID:
Valeric acid reacts as a typical carboxylic acid: it can form amide, ester, anhydride, and chloride derivatives.
The latter, valeryl chloride is commonly used as the intermediate to obtain the others.


BENEFITS of VALERIC ACID:
*Low molecular weight
*World's largest portfolio of solvents



ALTERNATIVE PARENTS of VALERIC ACID:
*Monocarboxylic acids and derivatives
*Carboxylic acids
*Organic oxides
*Hydrocarbon derivatives
*Carbonyl compounds



SUBSTITUENTS of VALERIC ACID:
*Straight chain fatty acid
*Monocarboxylic acid or derivatives
*Carboxylic acid
*Carboxylic acid derivative
*Organic oxygen compound
*Organic oxide
*Hydrocarbon derivative
*Organooxygen compound
*Carbonyl group
*Aliphatic acyclic compound



BIOLOGY:
In humans, valeric acid is a minor product of the gut microbiome and can also be produced by metabolism of its esters found in food.
The restoration of levels of this acid in the gut has been suggested as the mechanism that results in control of Clostridioides difficile infection after fecal microbiota transplant.



VALERATE SALTS AND ESTERS:
The valerate, or pentanoate, ion is C4H9COO−, the conjugate base of valeric acid.
Valeric acid is the form found in biological systems at physiological pH.
A valerate, or pentanoate, compound is a carboxylate salt or ester of valeric acid.
Many steroid-based pharmaceuticals, for example ones based on betamethasone or hydrocortisone, include the steroid as the valerate ester.



PHYSICAL and CHEMICAL PROPERTIES of VALERIC ACID:
Chemical formula: C5H10O2
Molar mass: 102.133 g·mol−1
Appearance: Colorless liquid
Density: 0.930 g/cm3
Melting point: −34.5 °C (−30.1 °F; 238.7 K)
Boiling point: 185 °C (365 °F; 458 K)
Solubility in water: 4.97 g/100 mL
Acidity (pKa): 4.82
Magnetic susceptibility (χ): -66.85·10−6 cm3/mol
Molecular Weight: 102.13
XLogP3: 1.4
Hydrogen Bond Donor Count: 1
Hydrogen Bond Acceptor Count: 2
Rotatable Bond Count: 3


Exact Mass: 102.068079557
Monoisotopic Mass: 102.068079557
Topological Polar Surface Area: 37.3 Ų
Heavy Atom Count: 7
Formal Charge: 0
Complexity: 59.1
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


Physical state: clear, liquid
Color: colorless
Odor: Stench.
Melting point/freezing point:
Melting point/range: -20 - -18 °C - lit.
Initial boiling point and boiling range: 110 - 111 °C at 13 hPa - lit. 185 °C - lit.
Flammability (solid, gas): No data available
Upper/lower flammability or explosive limits:
Upper explosion limit: 7,6 %(V)
Lower explosion limit: 1,6 %(V)
Flash point: 89 °C - closed cup
Autoignition temperature: No data available
Decomposition temperature: No data available
pH: 2,7 at 40 g/l at 20 °C


Viscosity
Viscosity, kinematic: No data available
Viscosity, dynamic: 2,3 mPa.s at 20 °C
Water solubility: ca.40 g/l at 20 °C - soluble
Partition coefficient: n-octanol/water:
log Pow: 1,8 at 25 °C
Vapor pressure: 0,19 hPa at 20 °C
Density: 0,939 g/cm3 at 25 °C - lit.
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:
Surface tension: 51,6 mN/m at 1g/l at 20 °C
Dissociation constant: 4,8 at 22,5 °C
Relative vapor density: 3,53 - (Air = 1.0)


Appearance: colorless to pale yellow clear liquid (est)
Assay: 99.00 to 100.00
Food Chemicals Codex Listed: Yes
Specific Gravity: 0.93900 to 0.94200 @ 20.00 °C.
Pounds per Gallon - (est).: 7.823 to 7.848
Refractive Index: 1.40700 to 1.41100 @ 20.00 °C.
Melting Point: -35.00 to -34.00 °C. @ 760.00 mm Hg
Boiling Point: 184.00 to 186.00 °C. @ 760.00 mm Hg
Boiling Point: 112.00 to 113.00 °C. @ 50.00 mm Hg
Vapor Pressure: 0.452000 mmHg @ 25.00 °C. (est)
Vapor Density: 3.5 ( Air = 1 )
Flash Point: 192.00 °F. TCC ( 88.89 °C. )
logP (o/w): 1.390
Soluble in: alcohol, ether, water, 1.86e+004 mg/L @ 25 °C (est)
Insoluble in: water


Molecular Formula / Molecular Weight: C5H10O2 = 102.13
Physical State (20 deg.C): Liquid
CAS RN: 109-52-4
Reaxys Registry Number: 969454
PubChem Substance ID: 87577803
SDBS (AIST Spectral DB): 3381
Merck Index (14): 9904
Appearance (Clarity): Clear
Appearance (Colour): Colourless
Appearance (Form): Liquid
Assay (GC): min. 99%
Density (g/ml) @ 20°C: 0.937-0.939
Refractive Index (20°C): 1.407-1.408
Boiling Range: 184-186°C



FIRST AID MEASURES of VALERIC ACID:
-Description of first-aid measures:
*General advice:
Show this material safety data sheet to the doctor in attendance.
*If inhaled:
After inhalation:
Fresh air.
Call in physician.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with water/ shower.
Call a physician immediately.
*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:
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 VALERIC ACID:
-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 with liquid-absorbent and neutralising material.
Dispose of properly.



FIRE FIGHTING MEASURES of VALERIC ACID:
-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 VALERIC ACID:
-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: butyl-rubber
Minimum layer thickness: 0,3 mm
Break through time: 480 min
Splash contact:
Material: Nature latex/chloroprene
Minimum layer thickness: 0,6 mm
Break through time: 30 min
-Control of environmental exposure:
Do not let product enter drains.



HANDLING and STORAGE of VALERIC ACID:
-Precautions for safe handling:
*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.



STABILITY and REACTIVITY of VALERIC ACID:
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .



SYNONYMS:
Valeric acid
PENTANOIC ACID
n-Valeric acid
109-52-4
n-Pentanoic acid
Valerianic acid
1-Butanecarboxylic acid
Propylacetic acid
Butanecarboxylic acid
pentoic acid
Kyselina valerova
VALERIC ACID, N-
Valeric acid, normal
n-Pentanoate
Valerate
FEMA No. 3101
Valeriansaeure
n-Valerate
1-pentanoic acid
NSC 406833
n-C4H9COOH
GZK92PJM7B
CH3-[CH2]3-COOH
CHEBI:17418
NSC-406833
64118-37-2
NCGC00183281-01
C5:0
DSSTox_CID_1655
DSSTox_RID_76267
DSSTox_GSID_21655
VALERICACID
CAS-109-52-4
SHF
HSDB 5390
Butane-1-carboxylic acid
EINECS 203-677-2
UNII-GZK92PJM7B
MFCD00004413
BRN 0969454
pentoate
Propylacetate
Valerianate
Valeriansaure
AI3-08657
Butanecarboxylate
1-pentanoate
1ylv
1-Butanecarboxylate
Valeric acid normal
n-BuCOOH
1173023-05-6
Valeric acid, 99%
Valeric acid, >=99%
bmse000345
EC 203-677-2
Pentanoic acid
Valeric acid
SCHEMBL5886
WLN: QV4
4-02-00-00868
MLS001066335
PENTANOIC ACID
VALERIC ACID
Pentanoic Acid (Valeric Acid)
CHEMBL268736
GTPL1061
DTXSID7021655
Valeric acid ( Pentanoic acid )
Valeric acid, analytical standard
HMS2267A03
Valeric acid-[3,4,5-13C3]
HY-N6056
Tox21_113414
Tox21_201561
Tox21_303030
LMFA01010005
NSC406833
STL169350
Valeric acid, >=99%, FCC, FG
ZINC31500905
AKOS000118960
DB02406
NCGC00183281-02
NCGC00183281-03
NCGC00256597-01
NCGC00259110-01
BS-42203
SMR000471834
CS-0032261
FT-0651620
FT-0694066
V0003
Valeric acid, pharmaceutical impurity standard
C00803
Q407796
J-002298
F2191-0105
Z955123768
1-Butanecarboxylic acid
CH3-[CH2]3-COOH
N-BuCOOH
N-Pentanoate
N-Pentanoic acid
N-Valeric acid
Pentanoate
Pentanoic acid
Pentoic acid
Propylacetic acid
Valerate
Valerianic acid
Valeriansaeure
Valeric acid, normal
1-Butanecarboxylate
N-Valerate
Pentoate
Propylacetate
Valerianate
Valerate, normal
1-Pentanoate
1-Pentanoic acid
Butanecarboxylate
Butanecarboxylic acid
Kyselina valerova
N-C4H9COOH
Valeriansaure
Valeric acid normal
N-Pentanoic acid, ammonium salt
N-Pentanoic acid, potassium salt
N-Pentanoic acid, sodium salt
N-Pentanoic acid, zinc salt
N-Pentanoic acid, maganese (+2) salt
N-Pentanoic acid, 11C-labeled
Lithium pentanoate
N-Pentanoic acid, 11C-labeled sodium salt
Valeric acid
1-Butanecarboxylate
1-Butanecarboxylic acid
1-pentanoate
1-pentanoic acid
Butanecarboxylate
Butanecarboxylic acid
CH3-[CH2]3-COOH
Kyselina valerova
n-BuCOOH
n-C4H9COOH
n-Pentanoate
n-Pentanoic acid
n-Valerate
n-valeric acid
Pentanoate
Pentanoic acid
pentoate
pentoic acid
Propylacetate
Propylacetic acid
Valerate
Valerianate
Valerianic acid
Valeriansaeure
Valeriansaure
Valeric acid
Valeric acid normal
Valeric acid, n-
Valeric acid, normal
Valerate, normal
N-Pentanoic acid, ammonium salt
N-Pentanoic acid, potassium salt
N-Pentanoic acid, sodium salt
N-Pentanoic acid, zinc salt
N-Pentanoic acid, maganese (+2) salt
N-Pentanoic acid, 11C-labeled
Lithium pentanoate
N-Pentanoic acid, 11C-labeled sodium salt

valeriana officinalis collina root extract; valerian collina root extract CAS NO:97927-02-1

SYNONYMS Diovan;N-(1-Oxopentyl)-N-[[2'-(1H-tetrazol-5-yl) [1,1'-biphenyl]-4-yl] methyl]-L-valine; N-(1-Oxopentyl)-N-[[2′-(2H-tetrazol-5-yl)[1,1′-biphenyl]-4-yl]methyl]-L-valine, Valsartan cas no:137862-53-4

Vanillin is an organic compound with the molecular formula C8H8O3.
Vanillin is the primary component of the extract of the vanilla bean, giving it its distinctive aroma and flavor.
Vanillin is commonly used as a flavoring agent in foods, beverages, and pharmaceuticals, as well as in perfumes and fragrances.

CAS Number: 121-33-5
Molecular Formula: C8H8O3
Molecular Weight: 152.15
EINECS Number: 204-465-2

Synonyms: vanillin, 4-Hydroxy-3-methoxybenzaldehyde, 121-33-5, Vanillaldehyde, Vanillic aldehyde, p-Vanillin, Lioxin, Vanilline, Vanilla, 3-Methoxy-4-hydroxybenzaldehyde, 4-Hydroxy-m-anisaldehyde, 2-Methoxy-4-formylphenol, Benzaldehyde, 4-hydroxy-3-methoxy-, Zimco, p-Hydroxy-m-methoxybenzaldehyde, 4-Hydroxy-3-methoxy-benzaldehyde, Methylprotocatechuic aldehyde, 4-Formyl-2-methoxyphenol, Vanilin, Vanillin (natural), 4-Hydroxy-5-methoxybenzaldehyde, m-Anisaldehyde, 4-hydroxy-, Protocatechualdehyde, methyl-, FEMA No. 3107, vaniline, Rhovanil, Protocatechualdehyde 3-methyl ether, Vanillin (NF), NSC 15351, CCRIS 2687, Vanillin Melting Point Standard, HSDB 1027, Vanillin, natural, EINECS 204-465-2, NSC-15351, NSC-48383, Vanillin [NF], NSC-403658, UNII-CHI530446X, BRN 0472792, m-Methoxy-p-hydroxybenzaldehyde, Vanillin (Standard), CHEBI:18346, 4-hydroxy-3-methoxy-benzyldehyde, AI3-00093, NPLC-0145, CHI530446X, MFCD00006942, CHEMBL13883, DTXSID0021969, EC 204-465-2, H-0264, 4-08-00-01763 (Beilstein Handbook Reference), NSC15351, 4-HYDROXY,3-METHOXY-BENZALDEHYDE, NCGC00091645-03, 4-hydroxy-3-methoxybenzaldehyde (vanillin), VANILLIN (II), VANILLIN [II], VANILLIN (MART.), VANILLIN [MART.], WLN: VHR DQ CO1, Vanillin [USAN], DTXCID301969, VANILLIN (EP MONOGRAPH), VANILLIN [EP MONOGRAPH], Vanillinum, VANILLIN (METHOXY-13C), Oleoresin vanilla, Vanilla oleoresin, CAS-121-33-5, 3-methoxy-4-hydroxy-benzaldehyde, oleo-Resins vanilla, V55, Vanillin sodium salt, VANILLIN [FHFI], VANILLIN [HSDB], FEMA Number 3107, oleo-Resins vanilla-bean, VANILLIN [FCC], 4-Hydroxy-3-methoxybenzaldehyde(Vanilline), VANILLIN [MI], VANILLIN [VANDF], methyl-Protocatechualdehyde, bmse000343, bmse000597, bmse010006, Methylprotcatechuic aldehyde, VANILLIN [USP-RS], VANILLIN [WHO-DD], SCHEMBL1213, MLS002303069, BIDD
, Vanillin, puriss., 99.5%, GTPL6412, SGCUT00016, 4-hydroxy 3-methoxybenzaldehyde, METHYLPROTOCATECHUALDEHYDE, HY-N0098R, Vanilla oleoresin (vanilla SPP), 3-methoxy-4-hydroxy benzaldehyde, 4-hydroxy-3-methoxy benzaldehyde, VANILLIN, NATURAL [FHFI], 3-methoxy-4-hydroxy benzoaldehyde, Vanillin, ReagentPlus(R), 99%, 4-hydroxy-3-(methoxy)benzaldehyde, HMS3651D20, HMS3885K07, Vanillin, >=97%, FCC, FG, 4-hydoxy-3-(methyloxy)benzaldehyde, BCP29943, HY-N0098, NSC48383, STR01001, to_000089, Tox21_113534, Tox21_201925, Tox21_300352, 4-hydoxy-3-(methyloxy)benz aldehyde, BBL011956, BDBM50177405, MFCD08702848, NSC403658, s3071, STK199262, AKOS000118929, Tox21_113534_1, CCG-266230, CS-W020052, Vanillin, tested according to Ph.Eur., NCGC00091645-01, NCGC00091645-02, NCGC00091645-04, NCGC00091645-05, NCGC00091645-07, NCGC00254468-01, NCGC00259474-01, Vanillin, natural, >=97%, FCC, FG, AC-10370, BP-10602, NCI60_001085, SMR000156285, SY224451, Vanillin 1000 microg/mL in Acetonitrile, Vanillin, JIS special grade, >=98.0%, Vanillin, Vetec(TM) reagent grade, 98%, 3-Methoxy-4-hydroxybenzaldehyde (vanillin), DB-003805, AM20060497, CS-0694801, H0264, NS00009754, SW219190-1, V0080, EN300-18281, vanillin (3-methoxy-4-hydroxy- benzaldehyde), A19444, C00755, D00091, Q33495, 4-Hydroxy-3-methoxybenzaldehyde inclusion complex, Vanillin (83 degrees C) Melting Point Standard, 4-hydroxy-3-methoxy-Benzaldehyde-5-chlorovanillin, 4-hydroxy-3-methoxybenzaldehyde (ACD/Name 4.0), AC-907/21098004, Q-100102, Vanillin, TraceCERT(R), certified reference material, Z57772449, F2190-0587, Vanillin, European Pharmacopoeia (EP) Reference Standard, Mettler-Toledo Calibration substance ME 51143093, Vanillin, Vanillin, United States Pharmacopeia (USP) Reference Standard, NSC 15351;NSC-15351; NSC15351 pound>>4-Hydroxy-3-methoxybenzaldehyde, Vanillin, Pharmaceutical Secondary Standard; Certified Reference Material, InChI=1/C8H8O3/c1-11-8-4-6(5-9)2-3-7(8)10/h2-5,10H,1H, Vanillin Melting Point Standard, United States Pharmacopeia (USP) Reference Standard, Mettler-Toledo Calibration substance ME 51143093, Vanillin, traceable to primary standards (LGC), Vanillin melting point standard, Pharmaceutical Secondary Standard; Certified Reference Material.

Vanillin also has applications in the synthesis of other chemicals.
Vanillin is an organic compound with the molecular formula C8H8O3.
Vanillin is a phenolic aldehyde. Its functional groups include aldehyde, hydroxyl, and ether.

Vanillin is the primary component of the extract of the vanilla bean.
Synthetic vanillin is now used more often than natural vanilla extract as a flavoring in foods, beverages, and pharmaceuticals.
Vanillin and ethylvanillin are used by the food industry; ethylvanillin is more expensive, but has a stronger note.

Vanillin differs from vanillin by having an ethoxy group (−O−CH2CH3) instead of a methoxy group (−O−CH3).
Natural vanilla extract is a mixture of several hundred different compounds in addition to vanillin.
Artificial vanilla flavoring is often a solution of pure vanillin, usually of synthetic origin.

Because of the scarcity and expense of natural vanilla extract, synthetic preparation of its predominant component has long been of interest.
The first commercial synthesis of vanillin began with the more readily available natural compound eugenol (4-allyl-2-methoxyphenol).
Today, artificial vanillin is made either from guaiacol or lignin.

Lignin-based artificial vanilla flavoring is alleged to have a richer flavor profile than that from guiacol-based artificial vanilla; the difference is due to the presence of acetovanillone, a minor component in the lignin-derived product that is not found in vanillin synthesized from guaiacol.
The primary natural source of vanillin is the seed pods of the vanilla orchid (Vanilla planifolia). The beans undergo a curing process to develop the characteristic vanilla flavor.
Vanilla Extract: Made by macerating and percolating vanilla beans in a solution of ethanol and water.

Historically, vanillin was synthesized from lignin, a complex organic polymer found in wood, as a byproduct of the paper industry.
Currently, most synthetic vanillin is produced from guaiacol, a compound derived from petrochemicals.
Advances in biotechnology have enabled the production of vanillin through microbial fermentation.

Microorganisms such as bacteria and fungi are engineered to convert natural precursors like ferulic acid (found in rice bran and corn) into vanillin.
Vanillin is the artificial synthesis of the first kind of flavor, synthesized by the German M. Harman, and G-Dr.
Usually It is divided into methyl vanillin and ethyl vanillin.

White or slightly yellow crystalline, with vanilla aroma and rich milk fragrance, is the largest varieties of perfume industry, is the main ingredients of universal favorite creamy vanilla flavor.
Its use is very extensive, such as in food, chemical, tobacco industry as spices, flavoring agent or a flavor enhancer, which is the majority in food consumption of drinks, candy, cakes, biscuits, bread and roasted seeds.
There are no relevant reports that vanillin was harmful to the human body.

Similar to vanilla beans, aroma than methyl vanillin thicker.
Vanillin is a broad-spectrum flavors, which is one of the world's most important synthetic spice, is an important and indispensable raw material for food additives industry.
The aroma is 3-4 times than the vanillin, with aromas of vanilla bean aroma and long-lasting fragrance.

Widely used in food, chocolate, ice cream, drinks and cosmetics play aroma and flavour.
Also ethyl vanillin also is feed additives, electroplating industry of brightening agent, the pharmaceutical industry of intermediates.
Vanillin route By using guaiacol and glyoxylic acid as raw material then by condensation, oxidation and decarboxylation made to vanillin.

This method is mainly composed of French Rhone-Poulenc company research and development, and production in large scale.
The use of glyoxylic acid from maleic acid methyl ester was prepared by two ozone decomposition.
The synthetic route has the advantages of wide material source, less reaction steps, low cost, less three wastes pollution.

Therefore, Vanillin is considered to be the most appropriate method.
Vanillin is a member of the orchid family, a sprawling conglomeration of some 25,000 different species.
Vanillin is a native of South and Central America and the Caribbean; and the first people to have cultivated it seem to have been the Totonacs of Mexico’s east coast.

The Aztecs acquired vanilla when they conquered the Totonacs in the 15th Century; the Spanish, in turn, got it when they conquered the Aztecs.
Vanillin is a complex blend of flavour and fragrance ingredients extracted from the seed pods of the vanilla orchid, containing at a guess somewhere between 250 and 500 different flavor and fragrance components.
The most important ingredient in this blend is vanillin.

However, because of the cost and supply chain variability of natural Vanillin, most products that want to impart the aroma of vanilla do not in fact use vanilla but rather synthetic vanillin (99% of all vanillin consumed worldwide) made primarily from petrochemicals or chemically derived from lignin.
Vanillin is mainly used as a flavouring agent, primarily in foods and beverages such as chocolate and dairy products, but also to mask unpleasant tastes in medicines or livestock fodder.
Vanillin is also an intermediate in the manufacture of certain pharmaceuticals and agrochemicals.

Vanillin and vanilla extracts have an estimated annual total volume of 16,000 metric tonnes, worth some USD 650 million in total.
Natural vanilla extract represents less than 1% by volume, though it is more important in terms of value.
Sales prices range from about USD 1,500 per kg for natural vanilla extract to USD 10-20 per kg for synthetic vanillin.

The primary market opportunity is in providing a competitively priced product, with good aroma properties, made from a natural and sustainable source.
Evolva believes such properties will allow fermentation-derived vanillin to be used in a wide variety of food and other products.
Evolva does not believe that such a product will significantly replace vanilla obtained from the orchid.

Vanillin is commonly known as vanilla powder, cloud Nepal with powder, vanilla extract, is extracted from the Rutaceae vanilla bean, is a kind of important spices, is one of synthetic fragrances yield the largest varieties, mixing chocolate, ice cream, chewing gum, pastry and tobacco essence of important raw materials.
Naturally occurring in pods of vanilla planifolia, and clove oil, oakmoss oil, balsam of Peru, tolu balsam storax.
Vanillin has strong and unique vanilla bean aroma, aroma stability, under the high temperature, less volatile.

Vanillin is vulnerable to light, and gradually oxidized in the air, easy to change color at encountering alkali or alkaline material.
Aqueous solution reacts with ferric chloride to produce blue purple solution.
Can be used for many fragrance formulas, but mainly used for edible essence.

Especially widely used in the candy, chocolate, soft drinks, ice cream, wine, and in the smoke flavor.
There is no restrictions imposed on the use of IFRA.
But because of easy cause discoloration, should pay attention to use in white fragrant product.

Vanillin is also an important foundation for edible spices, spices, almost all flavors, most used in food industry.
Food flavors are widely used in bread, butter, cream and brandy etc.
The addition amount of cakes, biscuits is 0.01~0.04%, candy is 0.02~0.08%, which is one of the most the baked food with spices, can be used for chocolate, biscuit, cake, ice cream and Boudin.

Before use, Vanillin is dissolved in warm water, the effect is much better.
The highest amount of baked food is 220mg/kg, chocolate is 970mg/kg.
As fixative agent, coordination agent and modifier are widely used in cosmetics, also is the important flavoring agent for food and drink.

Vanillin is used in medicine.
Also used for nickel, chrome metal plating brightener.
Vanillin has strong and unique vanilla beans, naturally found in vanilla and clove oil, oil, oakmoss, balsam of Peru, and the rest of tolu balsam.

Sulfite solution or red pulp softwood lignin sulfonate, under the alkaline conditions, reacted by high-pressure oxidation hydrolysis precipitation to get white to light yellow crystalline powder or acicular crystal.
From petroleum ether precipitation can also generate tetragonal crystal.
Vanillin has Aroma, Bitter sweet.

In the air, Vanillin is gradually oxidized.
In case of light, Vanillin generated decomposition.
In case of alkali, it generated discoloration.

The relative molecular mass is 152.15.
The relative density is 1.056.
Vanillin can generate sublimation without decomposition.

Slightly soluble in cold water, soluble in hot water, soluble in ethanol, ethyl ether, propylene Ketone, benzene, chloroform, carbon disulfide, glacial acetic acid, pyridine and volatile oil.
Water and FeCl3 generate blue purple solution.
For rats, by oral LD 50 1580mg/kg, mice is by percutaneous LD 50 1500mg/kg.
Industrial production method is that eugenol in the presence of potassium hydroxide, produce to ISO eugenol, then reacted with acetic anhydride formation of isoeugenol acetate, followed by oxidation and hydrolysis reaction to produce.

Vanillin is an important raw material for mixing chocolate, ice cream, chewing gum the pastry and tobacco flavor.
Vanillin can also be used as cosmetics fragrance coordination agent and a flavor enhancer.
Vanillin is also the pharmaceutical raw materials of industry.

In recent years, Vanillin appeared a new fashion in the commodity of vanillin.
Use oil of clove or basil oil provided out of eugenol as raw material, vanillin obtained by isomerization and oxidation, as it can be regarded as a natural equivalent quality, therefore it is called natural vanillin and into the spice market, its price is about 5 times that of the synthetic product.
Vanillin is found in many essential oils and foods but is often not essential for their odor or aroma.

However, it does determine the odor of essential oils and extracts from Vanilla planifolia and Vanilla tahitensis pods, in which it is formed during ripening by enzymatic cleavage of glycosides.
Vanillin is a colorless, crystalline solid (mp 82–83°C) with a typical vanilla odor.
Because it possesses aldehyde and hydroxy substituents, it undergoes many reactions.

Additional reactions are possible due to the reactivity of the aromatic nucleus.
Vanillin alcohol and 2-methoxy-4-methylphenol are obtained by catalytic hydrogenation; vanillic acid derivatives are formed after oxidation and protection of the phenolic hydroxy group.
Since vanillin is a phenol aldehyde, it is stable to autoxidation and does not undergo the Cannizzaro reaction.

Numerous derivatives can be prepared by etherification or esterification of the hydroxy group and by aldol condensation at the aldehyde group.
Several of these derivatives are intermediates, for example, in the synthesis of pharmaceuticals.
White or light yellow needle crystal or crystal powder, with a strong aroma.

Vanillin is not only soluble in ethanol, chloroform, ether, carbon disulfide, glacial acetic acid, and pyridine but also in oil, propylene glycol, and hydrogen peroxide in alkaline solution.
Vanillin can slowly oxidize in the air, can be unstable under illumination, and should be stored in a dark condition.
Vanillin occurs widely in nature; it has been reported in the essential oil of Java citronella (Cymbopogon nardus Rendl.), in benzoin, Peru balsam, clove bud oil and chiefly vanilla pods (Vanilla planifolia, V. tahitensis, V. pompona); more that 40 vanilla varieties are cultivated; vanillin is also present in the plants as glucose and vanillin.

Reported found in guava, feyoa fruit, many berries, asparagus, chive, cinnamon, ginger, Scotch spearmint oil, nutmeg, crisp and rye bread, butter, milk, lean and fatty fish, cured pork, beer, cognac, whiskies, sherry, grape wines, rum, cocoa, coffee, tea, roast barley, popcorn, oatmeal, cloudberry, passion fruit, beans, tamarind, dill herb and seed, sake, corn oil, malt, wort, elderberry, loquat, Bourbon and Tahiti vanilla and chicory root.
Vanillin is known as one of the first synthetic spices.
In the perfume industry, it is known as vanillic aldehyde.

As early as 1858, French chemist Gby (NicolasTheodore Gobley) obtained pure vanillin for the first time by the method of rectification.
Due to less production yield of natural vanillin, it spurred the search for a chemical synthesis method of vanillin production.
In 1874, German scientist M.Haarman and co-workers deduced the chemical structure of vanillin and discovered a new way to produce vanillin with abietene as the raw material .

In 1965, Chinese scientists found that vanillin has antiepileptic effect and accomplished a study on the pharmacology and toxicology of vanillin from edible to officinal.
They also found that vanillin has certain antibacterial activity, making it a suitable drug formulation for the treatment of skin disease.
Vanillin can be used as intermediate for synthesis of a variety of drugs, such as berberine and antihypertensive drug L-methyldopa, methoxy-pyrimidine, and heart disease drug papaverine .

Commercial vanillin is obtained by processing waste sulfite liquors or is synthesized from guaiacol.
Preparation by oxidation of isoeugenol is of historical interest only.
The starting material for vanillin production is the lignin present in sulfite wastes from the cellulose industry.

The concentrated mother liquors are treated with alkali at elevated temperature and pressure in the presence of oxidants.
The vanillin formed is separated from the by-products, particularly acetovanillone (4-hydroxy-3- methoxyacetophenone), by extraction, distillation, and crystallization.
A large number of patents describe various procedures for the (mainly) continuous hydrolysis and oxidation processes, as well as for the purification steps required to obtain high-grade vanillin .

Lignin is degraded either with sodium hydroxide or with calcium hydroxide solution and simultaneously oxidized in air in the presence of catalysts.
When the reaction is completed, the solid wastes are removed.
Vanillin is extracted from the acidified solutionwith a solvent (e.g., butanol or benzene) and reextractedwith sodium hydrogen sulfite solution.

Reacidification with sulfuric acid followed by vacuum distillation yields technical-grade vanillin, which must be recrystallized several times to obtain food-grade vanillin.
Water, to which some ethanol may be added, is used as the solvent in the last crystallization step.
Severalmethods can be used to introduce an aldehyde group into an aromatic ring.

Condensation of guaiacol with glyoxylic acid followed by oxidation of the resulting mandelic acid to the corresponding phenylglyoxylic acid and, finally, decarboxylation continues to be a competitive industrial process for vanillin synthesis.
Vanillin from guaiacol and glyoxylic acid: Currently, guaiacol is synthesized from catechol, which is mainly prepared by acid-catalyzed hydroxylation of phenol with hydrogen peroxide.
In China, a guaiacol prepared from o-nitrochlorobenzene via o-anisidine is also used.

Vanillin is obtained as a by-product in the synthesis of glyoxal from acetaldehyde and can also be produced by oxidation of glyoxal with nitric acid.
Condensation of guaiacol with glyoxylic acid proceeds smoothly at room temperature and in weakly alkaline media.
A slight excess of guaiacol is maintained to avoid formation of disubstituted products; excess guaiacol is recovered.

The alkaline solution containing Vanillin is then oxidized in air in the presence of a catalyst until the calculated amount of oxygen is consumed.
Crude vanillin is obtained by acidification and simultaneous decarboxylation of the (4-hydroxy-3-methoxyphenyl)glyoxylic acid solution.
This process has the advantage that, under the reaction conditions, the glyoxyl radical enters the aromatic guaiacol ring almost exclusively para to the phenolic hydroxy group.

Tedious separation procedures are thus avoided. b. Vanillin from guaiacol and formaldehyde: An older process that is still in use consists of the reaction of guaiacolwith formaldehyde or formaldehyde precursors such as urotropine, N,N-dimethyl-aniline, and sodium nitrite .
Vanillin occurs naturally in many essential oils and particularly in the pods of Vanilla planifolia and Vanilla tahitensis.
Industrially, vanillin is prepared from lignin, which is obtained from the sulfite wastes produced during paper manufacture.

Lignin is treated with alkali at elevated temperature and pressure, in the presence of a catalyst, to form a complex mixture of products from which vanillin is isolated.
Vanillin is then purified by successive recrystallizations.
Vanillin may also be prepared synthetically by condensation, in weak alkali, of a slight excess of guaiacol with glyoxylic acid at room temperature.

The resultant alkaline solution, containing 4- hydroxy-3-methoxymandelic acid is oxidized in air, in the presence of a catalyst, and vanillin is obtained by acidification and simultaneous decarboxylation.
Vanillin is then purified by successive recrystallizations.
Vanillin is an indispensable assistant for dessert and cake recipes with its distinguished aroma.

Melting point: 81-83 °C(lit.)
Boiling point: 170 °C15 mm Hg(lit.)
Density: 1.06
vapor density: 5.3 (vs air)
vapor pressure: >0.01 mm Hg ( 25 °C)
refractive index: 1.4850 (estimate)
FEMA: 3107 | VANILLIN
Flash point: 147 °C
storage temp.: 2-8°C
solubility: methanol: 0.1 g/mL, clear
pka: pKa 7.396±0.004(H2O I = 0.00 t = 25.0±1.0) (Reliable)
form: Crystalline Powder
color: White to pale yellow
PH: 4.3 (10g/l, H2O, 20℃)
Odor: at 100.00 %. vanilla
Odor Type: vanilla
Water Solubility: 10 g/L (25 ºC)
Sensitive: Air & Light Sensitive
JECFA Number: 889
Merck: 14,9932
BRN: 472792
Stability: Stable. May discolour on exposure to light. Moisture-sensitive. Incompatible with strong oxidizing agents, perchloric acid.
LogP: 1.17 at 25℃

Vanillin is edible flavouring agent, with vanilla bean aroma and strong desire for milk fragrance, is an important and indispensable raw material for food additives industry, widely used in all need to increase milk fragrance flavor flavoring in food, such as cake, cold drinks, chocolate, candy, biscuits, instant noodles, bread and tobacco, flavoring liquor, toothpaste, soap, cosmetics, perfume, ice cream, drinks and cosmetics play aroma and flavour.
Also Vanillin can be used for soap, toothpaste, perfume, rubber, plastic, pharmaceutical products.
Vanillin Accord with FCCIV standard.

Vanitrope has a strong and enduring clove and vanilla aroma, the aroma intensity is from 16 to 25 times of vanillin. Vanitrope was early developed.
Early synthetic route is that safrole oil as raw material, the alcohol solution of potassium hydroxide reacted hot pressing enable to open ring, and then used sodium ethyl sulfate to make the hydroxy ethylation, finally in the ethanol solution with sulfuric acid hydrolysis to obtain the vanitrope.
But due to the lack purity of aroma of the product, so it is very little actual application.

In the fifties of the 20th century, Vanillin developed from eugenol preparation of vanitrope synthetic route, only then can realize the industrial production.
Catechol flavor chemists,successfully developed by more cheap raw materials of pyrocatechol in the Soviet Union in 1960s.
First with allyl chloride to catechol mono alkylation, and the yield is 75%; followed by rearrangement reaction and yield is 35%~38%; then by using ethyl sodium sulfate for single ethylation, yield is 82%.

Finally with potassium hydroxide isomerization will get vanitrope, yield is 84%, after recrystallization of the crude product melting point 85.5 to 86℃.
Vanillin applied in candy, beverage, ice cream and other food flavoring formulations, the FEMA number is 2922.
Vanillin also can be used in cosmetics and soap fragrance formula.

Vanillin not only can used as a spice, but also can be used as a synergistic agent and antioxidant.
Former Soviet Union perfumers hold different views of vanitrope aroma properties.
They added it to the chocolate and other food flavor.

Vanillin is found that the goods are not vanillin aroma, so that it cannot in the flavor of food as a substitute for vanillin.
But when used for flavoring test of scented soap, found that soap has strong clove and vanilla aroma like it.
The differences with vanillin and isoeugenol, vanitrope to alkali, light, oxidation is very stable, soap like storage does not change color.

Therefore Vanillin should be used in fragrance formulations, particularly appropriate for fantasy flavor.
A great variety of Vanillin plants bearing the vanilla pods, or siliques, exist.
Those mentioned above are the most important species.

Of special value are those cultivated in Mexico, Madagascar, Java, Tahiti, the Comoro Islands and Réunion.
The cultivation of vanilla beans is very long and laborious.
The plant is a perennial herbaceous vine that grows up to 25 m in height and needs suitable supports in order to grow.

Fecundation of flowers is performed (November to December) by perforating the membrane that separates the pollen from the pistil.
This is an exacting task requiring skilled hand labor.
Natural fecundation occurs when a similar operation is carried out by birds or insects that perforate the membrane in search of food.

After a few months, clusters of hanging pods (siliques) are formed; these start to yellow at the lower tip from August to September.
At this point, the siliques are harvested and undergo special treatment that develops the aroma.
The Vanillins are placed in straw baskets and dipped into hot water to rupture the inner cell wall.

After a few months, the aroma starts developing.
Then the siliques are exuded by intermittent exposure to sunlight (by alternately covering and uncovering the siliques with wool blankets).
When exudation is complete, the Vanillins are oiled with cocoa oil to avoid chapping during drying and are finally dried to a suitable residual moisture content.

In the final stage of the preparation, the best quality siliques form a Vanillin “brine” that crystallizes on the surface of the bean.
Generally, the processing of vanilla bean takes more than a year.
The most important commercial qualities are brined vanilla, bastard vanilla and vanilla pompona.

The bean is the only part used. Vanilla has a sweet, ethereal odor and characteristic flavor.
In addition to vanillin (approximately 3%), vanilla contains other aromatic principles: vanillin, piperonal, eugenol, glucovanillin, vanillic acid, anisic acid and anisaldehyde.
Although vanillin is associated with the characteristic fragrance of the plant, the quality of vanilla bean is not associated with the vanillin content.

Bourbon beans contain a high amount of vanillin compared to Mexican and Tahiti beans.
In addition to vanillin (approximately 3%), vanilla contains other aromatic principles: vanillin, piperonal, eugenol, glucovanillin, vanillic acid, anisic acid and anisaldehyde.
Although vanillin is associated with the characteristic fragrance of the plant, the quality of vanilla bean is not associated with the vanillin content.

Bourbon beans contain a high amount of vanillin compared to Mexican and Tahiti beans.
Vanillin is most prominent as the principal flavor and aroma compound in vanilla.
Cured vanilla pods contain about 2% by dry weight vanillin.

On cured pods of high quality, relatively pure vanillin may be visible as a white dust or "frost" on the exterior of the pod.
Vanillin is also found in Leptotes bicolor, a species of orchid native to Paraguay and southern Brazil, and the Southern Chinese red pine.
At lower concentrations, vanillin contributes to the flavor and aroma profiles of foodstuffs as diverse as olive oil, butter, raspberry, and lychee fruits.

Aging in oak barrels imparts vanillin to some wines, vinegar, and spirits.
In other foods, heat treatment generates vanillin from other compounds.
In this way, vanillin contributes to the flavor and aroma of coffee, maple syrup, and whole-grain products, including corn tortillas and oatmeal.

Vanillin can trigger migraine headaches in a small fraction of the people who experience migraines.
Some people have allergic reactions to Vanillin.
They may be allergic to synthetically produced vanilla but not to natural vanilla, or the other way around, or to both.

Vanillin orchid plants can trigger contact dermatitis, especially among people working in the vanilla trade if they come into contact with the plant's sap.
An allergic contact dermatitis called vanillism produces swelling and redness, and sometimes other symptoms.
The sap of most species of vanilla orchid which exudes from cut stems or where beans are harvested can cause moderate to severe dermatitis if it comes in contact with bare skin.

The sap of vanilla orchids contains calcium oxalate crystals, which are thought to be the main causative agent of contact dermatitis in vanilla plantation workers.
Vanillin is widely used to impart vanilla flavor to a variety of products including ice cream, chocolate, baked goods, and beverages.
Enhances the sweetness perception and complexity of flavors in foods.

Vanillin utilized as a key note in many fragrances, providing a warm, sweet, and creamy scent.
Incorporated in lotions, creams, and other personal care products for its pleasant aroma.
Vanillin is used to mask unpleasant tastes in oral medications and supplements.

Acts as a precursor or intermediate in the synthesis of various pharmaceutical compounds.
Vanillin is used as a starting material in the synthesis of other organic compounds, including pharmaceuticals and agrochemicals.
Employed as a reference material for calibrating instruments in analytical chemistry due to its well-defined properties.

Some research indicates potential use in insect repellent formulations.
Valued in aromatherapy for its calming and soothing properties.
Vanillin is listed as GRAS by the U.S. Food and Drug Administration (FDA), meaning it is considered safe for consumption in regulated amounts.

Although rare, some individuals may have allergies to vanillin or natural vanilla extracts.
Efforts are ongoing to develop more sustainable and eco-friendly methods of producing vanillin, such as utilizing renewable resources and minimizing waste in the production process.
The use of genetically engineered microorganisms to produce vanillin is seen as a promising sustainable alternative to traditional synthetic methods.

History:
Although Vanillin is generally accepted that vanilla was domesticated in Mesoamerica and subsequently spread to the Old World in the 16th century, in 2019, researchers published a paper stating that vanillin residue had been discovered inside jars within a tomb in Israel dating to the 2nd millennium BCE, suggesting the possible cultivation of an unidentified, Old World-endemic Vanilla species in Canaan since the Middle Bronze Age.
Traces of vanillin were also found in wine jars in Jerusalem, which were used by the Judahite elite before the city was destroyed in 586 BCE.

Vanillin beans, called tlilxochitl, were discovered and cultivated as a flavoring for beverages by native Mesoamerican peoples, most famously the Totonacs of modern-day Veracruz, Mexico. Since at least the early 15th century, the Aztecs used vanilla as a flavoring for chocolate in drinks called xocohotl.
Vanillin was first isolated as a relatively pure substance in 1858 by Théodore Nicolas Gobley, who obtained it by evaporating a vanilla extract to dryness and recrystallizing the resulting solids from hot water.

In 1874, the German scientists Ferdinand Tiemann and Wilhelm Haarmann deduced its chemical structure, at the same time finding a synthesis for vanillin from coniferin, a glucoside of isoeugenol found in pine bark.
Tiemann and Haarmann founded a company Haarmann and Reimer (now part of Symrise) and started the first industrial production of vanillin using their process (now known as the Reimer–Tiemann reaction) in Holzminden, Germany.
In 1876, Karl Reimer synthesized vanillin (2) from guaiacol (1).

By the late 19th century, semisynthetic vanillin derived from the eugenol found in clove oil was commercially available.
Synthetic vanillin became significantly more available in the 1930s, when production from clove oil was supplanted by production from the lignin-containing waste produced by the sulfite pulping process for preparing wood pulp for the paper industry.
By 1981, a single pulp and paper mill in Thorold, Ontario, supplied 60% of the world market for synthetic vanillin.

However, subsequent developments in the wood pulp industry have made its lignin wastes less attractive as a raw material for vanillin synthesis.
Today, approximately 15% of the world's production of vanillin is still made from lignin wastes, while approximately 85% synthesized in a two-step process from the petrochemical precursors guaiacol and glyoxylic acid.

Beginning in 2000, Rhodia began marketing biosynthetic vanillin prepared by the action of microorganisms on ferulic acid extracted from rice bran.
At USD$700/kg, this product, sold under the trademarked name Rhovanil Natural, is not cost-competitive with petrochemical vanillin, which sells for around US$15/kg.
However, unlike vanillin synthesized from lignin or guaiacol, it can be labeled as a natural flavoring.

Uses:
Vanillin is used as a flavor, fragrance, pharmaceutical intermediates.
Vanillin is to obtain the incense powder, bean fragrant spices. Often used in the fragrance foundation with.
Vanillin is widely used in almost all the flavor that doubles as a combination of such as violet, Cymbidium, sunflower, Oriental flavor.

In edible, smoke flavor as well as wide application, but the amount is larger.
In Vanillin bean type, cream, chocolate, too Princess flavor are need to use spices.
Vanillin is China's regulations allow the use of edible spices, as a fixative agent, is the preparation of the main raw material of vanilla flavor.

Vanillin can also be directly used in biscuits, cakes, candy, drinks and other food flavoring.
Dosage according to the normal production needs, generally in the chocolate 970mg/kg; 270mg/kg in chewing gum; 220mg/kg in pastry, biscuit; 200mg/kg in candy; 150mg/kg in condiment~95mg/kg in cold drinks.
Widely used in the preparation of vanilla, chocolate, butter flavor, the amount is up to 25%~30%, or directly used in biscuits, pastries, dosage is 0.1%~0.4%, cold drink is 0.01%~0.3%, candy is 0.2%~0.8%, especially containing dairy products.

An important synthetic fragrance, widely used in daily life activities.
Vanillin is used as food, tobacco and wine with a fine wisely.
In the food industry usage amount is large for the preparation of the vanilla, chocolate, butter flavor, the amount is up to 25-30%, directly on a cookie, cake, dosage is 0.1-0.4%, cold is 0.01-0.3%, candy is 0.2-0.8, especially is containing dairy products.

Vanillin is used for chemical analysis, tests for protein nitrogen heterocyclic indene, phloroglucinol and tannic acid.
In the pharmaceutical industry, it is used for production of antihypertensive drug methyldopa, catechols L-dopa medication, and Catalin and diaveridine.
Vanillin is used as a reagent in organic analysis standard.

Tests for protein, nitrogen heterocyclic indene, pyrogallol, tannic acid, iron ions.
From benzoic acid in the determination of chloride, spices, organic trace analysis determination of methoxy standard.
Vanillin is a flavorant made from synthetic or artificial vanilla which can be derived from lignin of whey sulfite liquors and is syntheti- cally processed from guaiacol and eugenol.

The related product, ethyl vanillin, has three and one-half times the flavoring power of vanillin.
Vanillin also refers to the primary flavor ingredient in vanilla, which is obtained by extraction from the vanilla bean.
Vanillin is used as a substitute for vanilla extract, with application in ice cream, desserts, baked goods, and beverages at 60–220 ppm.

Occurs naturally in a wide variety of foods and plants such as orchids; major commercial source of natural vanillin is from vanilla bean extract.
Synthetically produced in-bulk fro m lignin-based byproduct of paper processes or from guaicol.
Vanillin is widely used as a flavor in pharmaceuticals, foods, beverages, and confectionery products, to which it imparts a characteristic taste and odor of natural vanilla.

Vanillin is also used in perfumes, as an analytical reagent and as an intermediate in the synthesis of a number of pharmaceuticals, particularly methyldopa.
Additionally, Vanillin has been investigated as a potential therapeutic agent in sickle cell anemia and is claimed to have some antifungal properties.
In food applications, vanillin has been investigated as a preservative.

As a pharmaceutical excipient, vanillin is used in tablets, solutions (0.01–0.02% w/v), syrups, and powders to mask the unpleasant taste and odor characteristics of certain formulations, such as caffeine tablets and polythiazide tablets.
Vanillin is similarly used in film coatings to mask the taste and odor of vitamin tablets.
Vanillin has also been investigated as a photostabilizer in furosemide 1% w/v injection, haloperidol 0.5% w/v injection, and thiothixene 0.2% w/v injection.

The largest use of vanillin is as a flavoring, usually in sweet foods.
The ice cream and chocolate industries together comprise 75% of the market for vanillin as a flavoring, with smaller amounts being used in confections and baked goods.
Vanillin is also used in the fragrance industry, in perfumes, and to mask unpleasant odors or tastes in medicines, livestock fodder, and cleaning products.

Vanillin is also used in the flavor industry, as a very important key note for many different flavors, especially creamy profiles such as cream soda.
Additionally, vanillin can be used as a general-purpose stain for visualizing spots on thin-layer chromatography plates.
This stain yields a range of colors for these different components.

Vanillin–HCl staining can be used to visualize the localisation of tannins in cells.
Vanillin is becoming a popular choice for the development of bio-based plastics.
Vanillin has been used as a chemical intermediate in the production of pharmaceuticals, cosmetics, and other fine chemicals.

In 1970, more than half the world's vanillin production was used in the synthesis of other chemicals.
As of 2016, vanillin uses have expanded to include perfumes, flavoring and aromatic masking in medicines, various consumer and cleaning products, and livestock foods.
Vanillin is used as a vanilla substitute in ice cream, baked goods, beverages, chocolate, confectionery, gelatinous desserts, and many food products.

Vanillin enhances the overall flavor profile and sweetness perception in food products.
Vanillin is used as a base note in many fragrances, providing a warm, sweet, and creamy scent.
It is included in lotions, creams, shampoos, and other personal care products for its pleasant aroma.

Vanillin helps mask unpleasant tastes in oral medications, making them more palatable.
In some cases, vanillin itself may have therapeutic properties, including antioxidant and anti-inflammatory effects.
Vanillin serves as a precursor in the synthesis of certain pharmaceuticals.

Vanillin is a starting material for the synthesis of various chemicals, including:
Vanillin is used as a standard for calibrating analytical instruments due to its well-defined melting point and chemical properties.
Some formulations may include vanillin or its derivatives as active ingredients due to potential insect-repellent properties.

Vanillin is added to cleaning products to provide a pleasant scent.
Vanillin is used in air fresheners and scented candles to create a vanilla aroma.
Vanillin derivatives are used in the production of certain polymers and resins.

Utilized in biotechnological processes for the production of bio-based chemicals.
Vanillin is used in aromatherapy for its calming and soothing effects.
Vanillin has been studied for its potential to act as a natural preservative due to its antioxidant activity.

Vanillin is used in various research applications, including studies on its potential health benefits and its role in food chemistry.
Vanillin is used to improve the taste of dietary supplements and nutraceutical products, making them more palatable for consumers.
Vanillin is added to animal feed to enhance the palatability, encouraging consumption by livestock and pets.

Emerging research suggests that vanillin may have antimicrobial properties, which can help in extending the shelf life of food products.
Vanillin derivatives can be used as fixatives in textile dyeing processes to improve color fastness.
Vanillin is used as a substrate in biocatalysis for the production of other valuable chemicals.

Enzymes that convert vanillin are studied for applications in green chemistry.
Vanillin is used in skin care formulations for its potential antioxidant properties, which can help in protecting the skin from oxidative damage.
Added for flavoring and potential antibacterial effects.

Vanillin-based polymers are being researched for use in environmentally friendly packaging materials.
Vanillin and its derivatives are being studied for their potential use in bioremediation to break down pollutants and toxic substances in the environment.
Research is ongoing into vanillin’s potential health benefits, including its role as an anti-inflammatory and antioxidant agent.

Vanillin-based compounds are being explored for use in drug delivery systems due to their biocompatibility and bioactive properties.
Vanillin is widely used in educational settings as a reagent for chemistry experiments and demonstrations, particularly in organic synthesis labs.
Vanillin is used to flavor tobacco products, including cigarettes and e-cigarettes, to enhance the sensory experience.

Vanillin can be used in the preservation and restoration of artworks, particularly in maintaining the quality of natural resins and varnishes.
Vanillin is a key component in both pure vanilla extract and imitation vanilla flavoring, widely used in home baking and commercial food production.
Vanillin is a popular fragrance used in homemade candles.

Added to soaps and bath products for its fragrance and potential skin benefits.
Vanillin is used as a certified reference material (CRM) for ensuring the quality and accuracy of analytical measurements in laboratories.
Vanillin is included in household cleaning products to provide a pleasant vanilla scent.

Vanillin is used in laundry detergents and fabric softeners to impart a fresh, vanilla fragrance.
Research is exploring vanillin’s potential as a natural pesticide or as a synergist to enhance the effectiveness of other pesticide compounds.

Vanillin is used to flavor protein powders and nutritional shakes, making them more appealing to consumers.
Vanillin is added to fortified foods to improve taste while delivering additional nutrients or health benefits.

Storage:
Vanillin oxidizes slowly in moist air and is affected by light.
Solutions of vanillin in ethanol decompose rapidly in light to give a yellow-colored, slightly bitter tasting solution of 6,6’-dihydroxy- 5,5’-dimethoxy-1,1’-biphenyl-3,3’-dicarbaldehyde.
Alkaline solutions also decompose rapidly to give a brown-colored solution.

However, solutions stable for several months may be produced by adding sodium metabisulfite 0.2% w/v as an antioxidant.
The bulk material should be stored in a well-closed container, protected from light, in a cool, dry place.

Safety Profile
Moderately toxic by ingestion, intraperitoneal, subcutaneous, and intravenous routes.
Experimental reproductive effects.
Human mutation data reported. Can react violently with Br2, HClO4, potassium-tert-butoxide, tert- chlorobenzene + NaOH, formic acid + thallium nitrate.

When heated to decomposition it emits acrid smoke and irritating fumes.
There have been few reports of adverse reactions to vanillin, although it has been speculated that cross-sensitization with other structurally similar molecules, such as benzoic acid, may occur.
Adverse reactions that have been reported include contact dermatitis and bronchospasm caused by hypersensitivity.

Vanilin is an organic compound with the molecular formula C8H8O3.
Vanilin is an intermediate and analytical reagent.
Vanilin is a phenolic aldehyde.


CAS Number: 121-33-5
EC Number: 204-465-2
MDL Number: MFCD00006942
Chemical formula: C8H8O3



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CHI530446X, MFCD00006942, CHEMBL13883, DTXSID0021969, VANILIN (METHOXY-13C), EC 204-465-2, H-0264, 4-08-00-01763 (Beilstein Handbook Reference), NSC15351, 4-HYDROXY,3-METHOXY-BENZALDEHYDE, NCGC00091645-03, 4-hydroxy-3-methoxybenzaldehyde (Vanilin), 86884-84-6, VANILIN (II), VANILIN [II], VANILIN (MART.), VANILIN [MART.], WLN: VHR DQ CO1, Vanilin [USAN], DTXCID301969, VANILIN (EP MONOGRAPH), VANILIN [EP MONOGRAPH], Oleoresin vanilla, Vanilla oleoresin, MFCD08702848, CAS-121-33-5, 3-methoxy-4-hydroxy-benzaldehyde, oleo Resins vanilla, V55, Vanilin sodium salt, VANILIN [FHFI], VANILIN [HSDB], VANILIN [INCI], FEMA Number 3107, oleo-Resins vanilla-bean, VANILIN [FCC], 4-Hydroxy-3-methoxybenzaldehyde(Vaniline), VANILIN [MI], VANILIN [VANDF], methyl-Protocatechualdehyde, bmse000343, bmse000597, bmse010006, Methylprotcatechuic aldehyde, VANILIN [USP-RS], VANILIN [WHO-DD], SCHEMBL1213, MLS002303069, BIDD:ER0330, Vanilin, puriss., 99.5%, GTPL6412, SGCUT00016, 4-hydroxy 3-methoxybenzaldehyde, 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Vanilin (3-methoxy-4-hydroxy- benzaldehyde), 3-Methoxy-4-hydroxybenzaldehyde (Vanilin)



Vanilin appears as a white, crystalline powder.
Vanilin dissolves well in some organic solvents, especially ethyl alcohol.
Vanilin is an organic compound that carries a pleasant vanilla odor and taste.


Vanilin is an indispensable ingredient for all kinds of cakes, cookies, sweet buns, milk and pastries.
Vanilin adds aroma and flavor to your desserts.
Vanilin is a sugary substance.


Vanilin has a pleasant smell.
Vanilin is frequently used by pastry chefs.
Vanilin is often confused with vanilla .


Vanilin is a fragrant and delicious substance used in cakes, cakes, donuts, ice cream, chocolate and desserts.
Vanilin is a chemical product.
Vanilin is obtained by chemical means and a by-product obtained from trees.


Vanilin is a kind of sweet flavoring.
Vanilin appears as white or very slightly yellow needles.
Vanilin is a member of the class of benzaldehydes carrying methoxy and hydroxy substituents at positions 3 and 4 respectively.


Vanilin has a role as a plant metabolite, an anti-inflammatory agent, a flavouring agent, an antioxidant and an anticonvulsant.
Vanilin is a member of phenols, a monomethoxybenzene and a member of benzaldehydes.
Vanilin is a natural product found in Ficus erecta var beecheyana, Pandanus utilis, and other organisms with data available.


Vanilin is a metabolite found in or produced by Saccharomyces cerevisiae.
As harvested, the green seed pods contain Vanilin in the form of its β-d-glucoside; the green pods do not have the flavor or odor of vanilla.
Vanilin is an organic compound with the molecular formula C8H8O3.


Vanilin is a phenolic aldehyde.
Vanilin's functional groups include aldehyde, hydroxyl, and ether.
Vanilin is the primary component of the extract of the vanilla bean.


Vanilin and ethylVanilin are used by the food industry; ethylVanilin is more expensive, but has a stronger note.
Vanilin differs from Vanilin by having an ethoxy group (−O−CH2CH3) instead of a methoxy group (−O−CH3).
Vanilin is a mixture of several hundred different compounds in addition to Vanilin.


Vanilin flavoring is often a solution of pure Vanilin, usually of synthetic origin.
Because of the scarcity and expense of Vanilin, synthetic preparation of its predominant component has long been of interest.
The first commercial synthesis of Vanilin began with the more readily available natural compound eugenol (4-allyl-2-methoxyphenol).


Today, Vanilin is made either from guaiacol or lignin.
Vanilin crystals extracted from vanilla extract
Lignin-based artificial vanilla flavoring is alleged to have a richer flavor profile than oil-based flavoring; the difference is due to the presence of acetovanillone, a minor component in the lignin-derived product that is not found in Vanilin synthesized from guaiacol.


Vanilin is a white, crystalline needles; sweetish smell.
Vanilin is soluble in 125 parts water, 20 parts glycerol, and 2 parts 95% alcohol; soluble in chloroform and ether.
Vanilin is a white needle-like crystals. Aromatic odor.


Vanilin (p-Vanilin) is a single molecule extracted from vanilla beans and also a popular odor used widely in perfume, food and medicine.
Vanilin is a white crystals or slightly yellow needles with vanilla, sweet, balsamic and pleasant odor
Vanilin is a phenolic aldehyde, which is an organic compound with the molecular formula C8H8O3.


Vanilin's functional groups include aldehyde, hydroxyl, and ether.
Vanilin is the primary component of the extract of the vanilla bean.
anillin and ethylVanilin are used by the food industry; ethylVanilin is more expensive, but has a stronger note.


It differs from Vanilin by having an ethoxy group (–O–CH2CH3) instead of a methoxy group (–O–CH3).
Natural "vanilla extract" is a mixture of several hundred different compounds in addition to Vanilin.
Artificial vanilla flavoring is often a solution of pure Vanilin, usually of synthetic origin.


Because of the scarcity and expense of natural vanilla extract, synthetic preparation of Vanilin's predominant component has long been of interest.
The first commercial synthesis of Vanilin began with the more readily available natural compound eugenol.
Today, artificial Vanilin is made either from guaiacol or lignin.


Lignin-based artificial vanilla flavoring is alleged to have a richer flavor profile than oil-based flavoring; the difference is due to the presence of acetovanillone, a minor component in the lignin-derived product that is not found in Vanilin synthesized from guaiacol.
Vanilin is a white to slightly yellow crystals, usually needelike


Vanilin is a single molecule extracted from vanilla beans and also a popular odor used widely in perfume, food and medicine.
Vanilin is a phenolic aldehyde, which is an organic compound with the molecular formula C8H8O3.
Vanilin's functional groups include aldehyde, hydroxyl, and ether.


Vanilin is the primary component of the extract of the vanilla bean.
Vanilin is a phenolic aldehyde, which is an organic compound with the molecular formula C8H8O3.
Vanilin's functional groups include aldehyde, hydroxyl, and ether.


Vanilla is a flavor derived from orchids of the genus Vanilla, and has a strong vanilla and milk flavor.
Vanilin is a white to pale yellow crystal; melting 76.5 C; having 3.5 times stronger flavor and more stable in organic solvents and in storage than Vanilin but does not have the true flavor.
Vanilin is widely used in various flavored foods that need to increase the flavor of milk.



USES and APPLICATIONS of VANILIN:
Vanilin is now used more often than natural vanilla extract as a flavoring in foods, beverages, and pharmaceuticals.
The largest use of Vanilin is as a flavoring, usually in sweet foods. The ice cream and chocolate industries together comprise 75% of the market for Vanilin as a flavoring, with smaller amounts being used in confections and baked goods.


Vanilin is also used in the fragrance industry, in perfumes, and to mask unpleasant odors or tastes in medicines, livestock fodder, and cleaning products.
Vanilin is also used in the flavor industry, as a very important key note for many different flavors, especially creamy profiles such as cream soda.
Vanilin is the primary component of the extract of the vanilla bean. Synthetic Vanilin, instead of natural vanilla extract, is sometimes used as a flavouring agent in foods, beverages, and pharmaceuticals.


Vanilin is used by the food industry as well as ethylVanilin.
Artificial vanilla flavoring is a solution of pure Vanilin, usually of synthetic origin.
Because of the scarcity and expense of natural vanilla extract, there has long been interest in the synthetic preparation of its predominant component.


The first commercial synthesis of Vanilin began with the more readily available natural compound eugenol.
Today, artificial Vanilin is made from either guaiacol or from lignin, a constituent of wood which is a byproduct of the paper industry.
Vanilin is used as food flavor, daily chemical flavor, pharmaceutical intermediate, also can be used as the standard reagent for organic analysis.


Vanilin is used as a standard reagent for organic analysis
Vanilin is now used more often than natural vanilla extract as a flavoring agent in foods, beverages, and pharmaceuticals.
Vanilin is used as a food flavor, daily flavor, and pharmaceutical intermediates.


The largest use of Vanilin is as a flavoring, usually in sweet foods. The ice cream and chocolate industries together comprise 75% of the market for Vanilin as a flavoring, with smaller amounts being used in confections and baked goods.
Vanilin is also used in the flavor industry, as a very important key note for many different flavors, especially creamy profiles.


Vanilin has been used as a chemical intermediate in the production of pharmaceuticals and other fine chemicals.
The aroma, Vanilin, is stable and not volatile at high temperatures.
Vanilin is easy to oxidize in air and change color when exposed to alkaline substances.


Vanilin has vanilla bean fragrance and strong milk fragrance.
Vanilin is widely used in cosmetics, tobacco, pastries, candy and baked food industries.
Vanilin is one of the most productive synthetic fragrance varieties in the world.


The industrial production of Vanilin has a history of more than 100 years.
According to the regulations of the Ministry of Health, Vanilin can be used in larger infants, infant formula foods and infant cereals (except infant formula cereal powder), with the maximum usage of 5 mg/ml and 7 mg/100 g, respectively.


Vanilin can also be used as plant growth promoter, bactericide, lubricant defoamer, etc.
Vanilin is also an important intermediate of synthetic drugs and other spices.
In addition, Vanilin can also be used as polishing agent in electroplating industry, ripening agent in agriculture, deodorant in rubber products, anti-hardening agent in plastic products and pharmaceutical intermediates.


Vanilin is the primary component of the extract of the vanilla bean.
Synthetic Vanilin is now used more often than natural vanilla extract as a flavoring agent in foods, beverages, and pharmaceuticals.
Vanilin can be used to an important synthetic fragrance widely used in daily chemical products for food, tobacco and alcohol.


Vanilla Extract Powder is the most popular way that vanilla is used by home bakers.
Vanilla Extract Powder is produced by steeping the vanilla beans in an alcohol and water solution for several months, sometimes with sugar added, thereby producing a clear dark liquid with a rich flavor that is highly aromatic.


There are two fold and three fold extracts, called essences, but these are very strong and are mainly used by professionals.
Do not add vanilla extract powder to hot liquids as the alcohol evaporates, along with some of the vanilla flavor.
Vanilin is an edible flavoring agent.


It has a vanilla bean aroma and a strong milky aroma.
Vanilin is an indispensable and important raw material in the food additive industry.
Vanilin is soluble in hot water, glycerol and alcohol, insoluble in cold water and vegetable oil.



ANTIOXIDANT FUNCTION OF VANILIN:
The mechanism of action of antioxidants with similar structure is different.
Vanilin accelerates the scavenging of free radicals mainly by vanillic acid, an oxidation product.
Vanilin has antioxidant effect, which can significantly prolong the shelf life of oily foods and conceal their rancidity.
The isomer of Vanilin, o-Vanilin (2-hydroxy-3-methoxybenzaldehyde), has been proved to have the effect of scavenging peroxynitrite anion, but it is not a good free radical scavenger.



VANILIN, STABILIZE OTHER INGREDIENTS IN FOOD:
It has been proved that the reaction products of Vanilin can stabilize other ingredients in food: resveratrol is a natural functional component.
In order to improve its stability and give full play to its functional role, resveratrol is coated with reticular chitosan microspheres formed by the reaction of Vanilin and chitosan, which helps to control the release of resveratrol.
The condensation products of Vanilin and amino group have good ability to complex with metal ions, which can effectively improve the stability of the inclusion substances.



HISTORY OF VANILIN:
Although Vanilin is generally accepted that vanilla was domesticated in Mesoamerica and subsequently spread to the Old World in the 16th century, in 2019, researchers published a paper stating that Vanilin residue had been discovered inside jars within a tomb in Israel dating to the 2nd millennium BCE, suggesting the cultivation of an unidentified, Old World-endemic Vanilla species in Canaan since the Middle Bronze Age.
Traces of Vanilin were also found in wine jars in Jerusalem, which were used by the Judahite elite before the city was destroyed in 586 BCE.

Vanilla beans, called tlilxochitl, were discovered and cultivated as a flavoring for beverages by native Mesoamerican peoples, most famously the Totonacs of modern-day Veracruz, Mexico.
Since at least the early 15th century, the Aztecs used vanilla as a flavoring for chocolate in drinks called xocohotl.

Vanilin was first isolated as a relatively pure substance in 1858 by Théodore Nicolas Gobley, who obtained it by evaporating a vanilla extract to dryness and recrystallizing the resulting solids from hot water.
In 1874, the German scientists Ferdinand Tiemann and Wilhelm Haarmann deduced its chemical structure, at the same time finding a synthesis for Vanilin from coniferin, a glucoside of isoeugenol found in pine bark.

Tiemann and Haarmann founded a company Haarmann and Reimer (now part of Symrise) and started the first industrial production of Vanilin using their process in Holzminden, Germany.
In 1876, Karl Reimer synthesized Vanilin (2) from guaiacol (1).

By the late 19th century, semisynthetic Vanilin derived from the eugenol found in clove oil was commercially available.
Synthetic Vanilin became significantly more available in the 1930s, when production from clove oil was supplanted by production from the lignin-containing waste produced by the sulfite pulping process for preparing wood pulp for the paper industry.

By 1981, a single pulp and paper mill in Thorold, Ontario, supplied 60% of the world market for synthetic Vanilin.
However, subsequent developments in the wood pulp industry have made its lignin wastes less attractive as a raw material for Vanilin synthesis.
Today, approximately 15% of the world's production of Vanilin is still made from lignin wastes, while approximately 85% synthesized in a two-step process from the petrochemical precursors guaiacol and glyoxylic acid.

Beginning in 2000, Rhodia began marketing biosynthetic Vanilin prepared by the action of microorganisms on ferulic acid extracted from rice bran.
Vanilin is used as a flavoring agent for perfumery, cosmetics and pharmaceutical products.
Additionally, Vanilin can be used as a general-purpose stain for visualizing spots on thin-layer chromatography plates.
This stain yields a range of colors for these different components.

Vanilin–HCl staining can be used to visualize the localisation of tannins in cells.
Vanilin is becoming a popular choice for the development of bio-based plastics.
Vanilin is mostly used for flavoring foods.
The usage rate of Vanilin varies between 0.1% and 1% depending on the effect of the product and its interaction with other substances.



ARE VANILIN AND VANILLA THE SAME THING?
Even though Vanilin and vanilla are used for the same purpose, they are not the same product.
Vanilla is a natural aroma obtained from plants.
On the contrary, Vanilin is a chemically structured product.

Only 2% of Vanilin comes from vanilla.
Vanilin is a flavoring substance produced by the vanilla beetle.
Naturally, the Vanilin produced by the vanilla beetle is of higher quality than other Vanilin substances in terms of taste and aroma.

Vanilin is used as a variety of sweeteners in foods, beverages, perfumes, cosmetics and other products.
Vanilin is also used in pharmaceutical products.
The key difference between Vanilin and pure Vanilin is that pure Vanilin is produced naturally while Vanilin is usually produced synthetically.

Pure Vanilin contains vanilla beetle bean produced by the vanilla beetle, so it provides a higher quality aroma and taste.
Vanilin, on the other hand, is produced synthetically, usually without vanilla beetle bean, and provides a less high-quality aroma and taste.
Pure Vanilin is more expensive because it is harder to produce and much less efficient.



β-d-GLUCOSIDE OF VANILIN:
After being harvested, their flavor is developed by a months-long curing process, the details of which vary among vanilla-producing regions, but in broad terms Vanilin proceeds as follows:

First, the seed pods are blanched in hot water, to arrest the processes of the living plant tissues.
Then, for 1–2 weeks, the pods are alternately sunned and sweated: during the day they are laid out in the sun, and each night wrapped in cloth and packed in airtight boxes to sweat.

During this process, the pods become dark brown, and enzymes in the pod release Vanilin as the free molecule.
Finally, the pods are dried and further aged for several months, during which time their flavors further develop.
Several methods have been described for curing vanilla in days rather than months, although they have not been widely developed in the natural vanilla industry, with its focus on producing a premium product by established methods, rather than on innovations that might alter the product's flavor profile.



BIOSYNTHESIS OF VANILIN:
Although the exact route of Vanilin biosynthesis in V. planifolia is currently unknown, several pathways are proposed for its biosynthesis.
Vanilin biosynthesis is generally agreed to be part of the phenylpropanoid pathway starting with l-phenylalanine, which is deaminated by phenylalanine ammonia lyase (PAL) to form t-cinnamic acid.

The para position of the ring is then hydroxylated by the cytochrome P450 enzyme cinnamate 4-hydroxylase (C4H/P450) to create p-coumaric acid.
Then, in the proposed ferulate pathway, 4-hydroxycinnamoyl-CoA ligase (4CL) attaches p-coumaric acid to coenzyme A (CoA) to create p-coumaroyl CoA.
Hydroxycinnamoyl transferase (HCT) then converts p-coumaroyl CoA to 4-coumaroyl shikimate/quinate.

This subsequently undergoes oxidation by the P450 enzyme coumaroyl ester 3’-hydroxylase (C3’H/P450) to give caffeoyl shikimate/quinate.
HCT then exchanges the shikimate/quinate for CoA to create caffeoyl CoA, and 4CL removes CoA to afford caffeic acid.
Caffeic acid then undergoes methylation by caffeic acid O-methyltransferase (COMT) to give ferulic acid.

Finally, Vanilin synthase hydratase/lyase (vp/VAN) catalyzes hydration of the double bond in ferulic acid followed by a retro-aldol elimination to afford Vanilin.
Vanilin can also be produced from vanilla glycoside with the additional final step of deglycosylation.

In the past p-hydroxybenzaldehyde was speculated to be a precursor for Vanilin biosynthesis.
However, a 2014 study using radiolabelled precursor indicated that p-hydroxybenzaldehyde is not used to synthesise Vanilin or Vanilin glucoside in the vanilla orchids.



CHEMICAL SYNTHESIS OF VANILIN:
The demand for vanilla flavoring has long exceeded the supply of vanilla beans.
As of 2001, the annual demand for Vanilin was 12,000 tons, but only 1,800 tons of natural Vanilin were produced.
The remainder was produced by chemical synthesis.

Vanilin was first synthesized from eugenol (found in oil of clove) in 1874–75, less than 20 years after it was first identified and isolated. Vanilin was commercially produced from eugenol until the 1920s.
Later it was synthesized from lignin-containing "brown liquor", a byproduct of the sulfite process for making wood pulp.

Counterintuitively, though it uses waste materials, the lignin process is no longer popular because of environmental concerns, and today most Vanilin is produced from the petrochemical raw material guaiacol.
Several routes exist for synthesizing Vanilin from guaiacol.

At present, the most significant of these is the two-step process practiced by Rhodia since the 1970s, in which guaiacol (1) reacts with glyoxylic acid by electrophilic aromatic substitution.
The resulting vanillylmandelic acid (2) is then converted by 4-Hydroxy-3-methoxyphenylglyoxylic acid (3) to Vanilin (4) by oxidative decarboxylation.



WOOD-BASED VANILIN:
15% of the world's production of Vanilin is produced from lignosulfonates, a byproduct from the manufacture of cellulose via the sulfite process.
The sole producer of wood-based Vanilin is the company Borregaard located in Sarpsborg, Norway.
Wood-based Vanilin is produced by copper-catalyzed oxidation of the lignin structures in lignosulfonates under alkaline conditions and is claimed by the manufacturing company to be preferred by their customers due to, among other reasons, its much lower carbon footprint than petrochemically synthesized Vanilin.



FERMENTATION OF VANILIN:
The company Evolva has developed a genetically modified microorganism which can produce Vanilin.
Because the microbe is a processing aid, the resulting Vanilin would not fall under U.S. GMO labeling requirements, and because the production is nonpetrochemical, food using the ingredient can claim to contain "no artificial ingredients".
Using ferulic acid as an input and a specific non GMO species of Amycolatopsis bacteria, natural Vanilin can be produced.



BIOCHEMISTRY OF VANILIN:
Several studies have suggested that Vanilin can affect the performance of antibiotics in laboratory conditions.



MANUFACTURING OF VANILIN:
Vanilin has been used as a chemical intermediate in the production of pharmaceuticals, cosmetics, and other fine chemicals.
In 1970, more than half the world's Vanilin production was used in the synthesis of other chemicals.
As of 2016, Vanilin uses have expanded to include perfumes, flavoring and aromatic masking in medicines, various consumer and cleaning products, and livestock foods.



ANTIBACTERIAL ACTIVITY OF VANILIN:
VanilinCAS 121-33-5 is a kind of natural bacteriostatic agent.
Vanilin is often combined with other bacteriostatic methods in the field of food.
Vanilin has different bacteriostatic effects on different strains of bacteria.

The bacteriostatic effect of Vanilin is related to its concentration and pH value.
Higher Vanilin concentration and lower pH value are beneficial to improve the bacteriostatic effect of Vanilin.
Vanilin has different bacteriostatic effect on different strains. Compared with other strains, Vanilin has better bacteriostatic effect on Escherichia coli.

Vanilin can inhibit many kinds of yeasts.
High concentration of Vanilin can improve its bacteriostatic effect, but high concentration of Vanilin can not kill yeasts immediately.
Compound preservation achieves synergistic effect between preservatives (or preservation methods).

Vanilin CAS 121-33-5 is a widely accepted preservation method for fruits and vegetables.
The antimicrobial effect of spices is often synergistic and the dosage is smaller than that of single use.
For example, for the prevention of Aspergillus Niger pollution, the effective sterilization dose of Vanilin alone is 0.5%.

The mixture of 0.05% Vanilin and 0.0025% cinnamaldehyde can play a bactericidal role.
Vanilin also plays an important role in assisting bacteriostasis and sterilization.

In the current production process, thermal sterilization is still the most common way of sterilization in juice processing, which is generally pasteurization and instantaneous sterilization at high temperature.
Traditional sterilization methods often lead to the destruction of nutrients and browning of fruit juice.



PHYSICAL and CHEMICAL PROPERTIES of VANILIN:
Chemical formula: C8H8O3
Molar mass: 152.149 g•mol−1
Appearance: White crystals
Odor: Vanilla, sweet, balsamic, pleasant
Density: 1.056 g/cm3
Melting point: 81 °C (178 °F; 354 K)
Boiling point: 285 °C (545 °F; 558 K)
Solubility in water: 10 g/L
log P: 1.208
Vapor pressure: >1 Pa
Acidity (pKa): 7.781
Basicity (pKb): 6.216
Structure:
Crystal structure: Monoclinic
Thermochemistry:
Std enthalpy of combustion (ΔcH⦵298): −3.828 MJ/mol

Synonyms: 4-hydroxy-3-methoxybenzaldehyde
IUPAC Name: 4-hydroxy-3-methoxybenzaldehyde
Molecular Weight: 152.15
Molecular Formula: C8H8O3
Canonical SMILES: COC1=C(C=CC(=C1)C=O)O
InChI: InChI=1S/C8H8O3/c1-11-8-4-6(5-9)2-3-7(8)10/h2-5,10H,1H3
InChIKey: MWOOGOJBHIARFG-UHFFFAOYSA-N
Boiling Point: 170 °C at 15 mmHg
Melting Point: 81-83 °C
Flash Point: 147ºC
Purity: > 98%
Density: 1.06 g/cm3
Solubility: Soluble in chloroform (slightly), ethyl acetate (slightly), methanol (slightly).

Appearance: White to pale yellow crystalline or powder
Storage Keep container tightly closed in a dry and well-ventilated place.
EINECS: 204-465-2
Hazard Codes: Xn
HS Code: 2912410000
Log P: 1.21330
MDL: MFCD00006942
pH: Solutions are acid to litmus
PSA: 46.53
Quality Standard: Enterprise Standard
Refractive Index: 1.555
Risk Statements: R22
RTECS: YW5775000
Safety Statements: S22-S24/25
Stability: Stable.
May discolour on exposure to light.
Moisture-sensitive.

Incompatible with strong oxidizing agents, perchloric acid.
Vapor Pressure: 1 mmHg at 225 °F
Molecular Weight: 152.15 g/mol
XLogP3: 1.2
Hydrogen Bond Donor Count: 1
Hydrogen Bond Acceptor Count: 3
Rotatable Bond Count: 2
Exact Mass: 152.047344113 g/mol
Monoisotopic Mass: 152.047344113 g/mol
Topological Polar Surface Area: 46.5Ų
Heavy Atom Count: 11
Formal Charge: 0
Complexity: 135
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

Beilstein Number: 0472792
MDL: MFCD00006942
CoE Number: 107
XlogP3: 1.20 (est)
Molecular Weight: 152.14936000
Formula: C8 H8 O3
Appearance: white to off white crystalline powder (est)
Assay: 99.00 to 100.00
Food Chemicals Codex Listed: Yes
Melting Point: 81.00 to 84.00 °C. @ 760.00 mm Hg
Boiling Point: 285.00 to 286.00 °C. @ 760.00 mm Hg
Boiling Point: 170.00 to 171.00 °C. @ 15.00 mm Hg
Vapor Pressure: 0.002000 mmHg @ 25.00 °C. (est)
Vapor Density: 5.3 ( Air = 1 )
Flash Point: 307.00 °F. TCC ( 153.00 °C. )
logP (o/w): 1.210
Shelf Life: 24.00 month(s) or longer if stored properly.
Storage: store in cool, dry place in tightly sealed containers, protected from heat and light.

Soluble in:
chloroform
dipropylene glycol
ether
ethyl alcohol, 1:2 in 95% alcohol
ethyl alcohol, 1:3 in 70% alcohol
ethyl alcohol, 4 parts in 50% alcohol
glycerol
glycerol, 1:20
hot ligroin
isopropyl myristate
water, 1:125 in water
water, 1gm in 100ml
water, 6875 mg/L @ 25 °C (est)
Insoluble in:
paraffin oil
Stability:
cream
hair spray
lotion
powder

CAS number: 121-33-5
EC number: 204-465-2
Grade: Ph Eur,BP,NF
Hill Formula: C₈H₈O₃
Chemical formula: (CH₃O)(OH)C₆H₃CHO
Molar Mass: 152.15 g/mol
HS Code: 2912 41 00
Density: 1.06 g/cm3 (20 °C)
Flash point: 159.8 - 160.8 °C
Ignition temperature: >400 °C
Melting Point: 81 - 83 °C
pH value: 4.3 (10 g/l, H₂O, 20 °C)
Vapor pressure: 0.0029 hPa (25 °C)
Bulk density: 600 kg/m3
Solubility: 9 g/l
Molecular Formula / Molecular Weight: C8H8O3 = 152.15

Physical State (20 deg.C): Solid
Store Under Inert Gas: Store under inert gas
Condition to Avoid: Light Sensitive,Air Sensitive,Moisture Sensitive
CAS RN: 121-33-5
Reaxys Registry Number: 472792
PubChem Substance ID: 87570691
SDBS (AIST Spectral DB): 726
Merck Index (14): 9932
MDL Number: MFCD00006942
Physical state: crystalline, powder
Color: light yellow
Odor: characteristic
Melting point/freezing point:
Melting point/range: 81 - 83 °C - lit.
Initial boiling point and boiling range: 170 °C at 20 hPa - lit.
Flammability (solid, gas): No data available
Upper/lower flammability or explosive limits: No data available
Flash point: 159,8 - 160,8 °C - closed cup
Autoignition temperature: No data available
Decomposition temperature: No data available
pH: 4,3 at 10 g/l at 20 °C

Viscosity
Viscosity, kinematic: Not applicable
Viscosity, dynamic: Not applicable
Water solubility: 9 g/l at 25 °C
Partition coefficient: n-octanol/water:
log Pow: 1,21 at 25 °C - Bioaccumulation is not expected.
Vapor pressure: < 0,01 hPa at 25 °C
Density: 1,056 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: none
Relative vapor density: 5,3 at 25 °C
CAS: 121-33-5
EINECS: 204-465-2
InChI: InChI:1S/C8H8O3/c1-11-8-4-6(5-9)2-3-7(8)10/h2-5,10H,1H3
Molecular Formula: C8H8O3
Molar Mass: 152.15

Density: 1.06
Melting Point: 81-83°C(lit.)
Boling Point: 170°C15mm Hg(lit.)
Flash Point: 147 °C
JECFA Number: 889
Water Solubility: 10 g/L (25 ºC)
Solubility: Soluble in 125 times water, 20 times ethylene glycol and 2 times 95% ethanol, soluble in chloroform.
Vapor Presure: >0.01 mm Hg ( 25 °C)
Vapor Density: 5.3 (vs air)
Appearance: White needle crystal.
Color: White to pale yellow
Merck: 14,9932
BRN: 472792
pKa: pKa 7.396±0.004(H2OI = 0.00t = 25.0±1.0) (Reliable)
PH: 4.3 (10g/l, H2O, 20℃)
Storage Condition: 2-8°C
Stability: Stable.
May discolour on exposure to light.
Moisture-sensitive.
Incompatible with strong oxidizing agents, perchloric acid.

Sensitive: Air & Light Sensitive
Refractive Index: 1.4850 (estimate)
MDL: MFCD00006942
Chemical Name: Vanilin
CAS Registry Number: 121-33-5
PubChemID: 1183
Molecular Weight: 152.14732
PSA: 46.53000
LogP: 1.21330
EINECS: 204-465-2
Molecular Formula: C8H8O3
Density: 1.06
Boiling Point: 170℃ (15 mmHg)
Flash Point: 147℃
Melting Point: 81-84℃
Vapour: 0.00194mmHg at 25°C
Refractive Index: 1.555
HS Code: 29124100



FIRST AID MEASURES of VANILIN:
-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 VANILIN:
-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 VANILIN:
-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 VANILIN:
-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 VANILIN:
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
Dry.
Air, light, and moisture sensitive.



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

SYNONYMS 4-Hydroxy-3-methoxybenzaldehyde; 3-Methoxy-4-hydroxybenzaldehyde; p-Hydroxy-m-methoxybenzaldehyde; Vanillic aldehyde; 2-Methoxy-4-formylphenol; 4-Formyl-2-methoxyphenol; 4-Hydroxy-5-methoxybenzaldehyde; Vanilla; 4-Hydroxy-m-anisaldehyde; Methyl protocatechualdehyde; p-Vanillin; 4-Hydroxy-m-anisaldehyde; Vanillaldehyde; m-Methoxy-p-hydroxybenzaldehyde; Protocatechualdehyde 3-methyl ether; 2-Methoxy-4-formylphenol;CAS NO. 121-33-5; 52447-63-9; 8014-42-4

Vanilline; VANILLIN, N° CAS : 121-33-5 - Vanilline, Origine(s) : Végétale, Synthétique, Autres langues : Vaniglia, Vanilina, vanilin, Nom INCI : VANILLIN, Nom chimique : Vanillin. N° EINECS/ELINCS : 204-465-2. Compatible Bio (Référentiel COSMOS) : Ses fonctions (INCI): Agent masquant : Réduit ou inhibe l'odeur ou le goût de base du produit. Noms français : 2-METHOXY-4-FORMYLPHENOL; 3-METHOXY-4-HYDROXYBENZALDEHYDE; 4-FORMYL-2-METHOXYPHENOL; 4-HYDROXY-3-METHOXY BENZALDEHYDE; 4-HYDROXY-3-METHOXYBENZALDEHYDE; 4-HYDROXY-5-METHOXYBENZALDEHYDE; 4-HYDROXY-M-ANISALDEHYDE; BENZALDEHYDE, 4-HYDROXY-3-METHOXY-; HYDROXY-4 METHOXY-3 BENZALDEHYDE;M-ANISALDEHYDE, 4-HYDROXY M-ANISALDEHYDE, 4-HYDROXY-; METHYLPROTOCATECHUIC ALDEHYDE; P-HYDROXY-M-METHOXYBENZALDEHYDE; PROTOCATECHUALDEHYDE 3-METHYL ETHER; PROTOCATECHUALDEHYDE, METHYL-; Vanilline. Utilisation et sources d'émission: Agent de saveur; Vanillin. CAS names : Benzaldehyde, 4-hydroxy-3-methoxy-; IUPAC names: 1-butoxypropan-2-ol; 3-hydroxy-4-methoxybenzaldehyde; 3-Methoxy-4-hydroxy benzaldehyde; 4-hydroksy-3-metoksybenzaldehyd, ; 4-Hydroxy-3-methoxy-benzaldehyde; 4-Hydroxy-3-methoxybenzaldehyd; 4-Hydroxy-3-methoxybenzaldehyde; 4-Hydroxy-3-methoxybenzaldehyde, Vanillic aldehyde; 4-hydroxy-3-méthoxybenzaldéhyde; Ester; vanilin; vanilla; Vanillin (4-hydroxy-3-methoxybenzaldehyde); wanilina; 121-33-5 [RN], vanilya; 204-465-2 [EINECS]; 2-Methoxy-4-formylphenol ; 3-methoxy-4-hydroxybenzaldehyde; 4-08-00-01763 [Beilstein]; 472792 [Beilstein]; 4-formyl-2-methoxyphenol; 4-Hydroxy-3-methoxybenzaldehyd [German] [ACD/IUPAC Name] ; 4-hydroxy-3-methoxy-benzaldehyde; 4-Hydroxy-3-methoxybenzaldehyde [ACD/IUPAC Name]; 4-Hydroxy-3-méthoxybenzaldéhyde [French] [ACD/IUPAC Name]; 4-Hydroxy-5-methoxybenzaldehyde 4-hydroxy-m-anisaldehyde; Benzaldehyde, 4-hydroxy-3-methoxy- [ACD/Index Name]; m-Anisaldehyde, 4-hydroxy-; MFCD00006942 [MDL number]; p-hydroxy-m-methoxybenzaldehyde ; Vanilin [Turkish]; Vanilina [Portuguese]; Vanilina [Spanish]; Vanillic aldehyde; Vanillin; Vanillin [German]; Vanillin Melting Point Standard; Vanillina [Italian]; Vanilline [French]; Βανιλίνη [Modern Greek (1453-)]; Ванилин [Russian]; バニリン [Japanese]; 香草醛 [Chinese]; 4-hydroxy 3-methoxybenzaldehyde; Acetovanillone; apocynine; Lioxin; m-Methoxy-p-hydroxybenzaldehyde; para-Hydroxy-meta-methoxybenzaldehyde; p-vanillin; Vanilin; vaniline; Vanilla; vanillaldehyde; Vanillin|4-Hydroxy-3-methoxybenzaldehyde; VHR DQ CO1 [WLN]; Zimco

SYNONYMS 4-Hydroxy-3-methoxybenzaldehyde;4-Hydroxy-3-methoxybenzaldehyde, Vanillic aldehyde CAS NO:121-33-5

SYNONYMS 2-Ethoxy-4-formylphenol;3-Ethoxy-4-hydroxybenzaldehyd;3-Ethoxy-4-hydroxybenzaldehyde;3-etoxi-4-hidroxibenzaldehido;4-HYDROXY-3-ETHOXYBENZALDEHYDE;AETHYLVANILLIN;Arovanillon;Benzaldehyde, 3-ethoxy-4-hydroxy-;Bourbonal;Ethavan;Ethovan;ETHYL VANILLIN;ETHYL VANILLIN/ BOURBONAL;Ethylprotal CAS NO:121-32-4

VANTOCIL IB VANTOCIL IB Antimicrobial VANTOCIL IB Antimicrobial is a broad spectrum, fast acting bactericide for the formulation of disinfectants and sanitisers. This product is a 20% aqueous solution of poly (hexamethylene biguanide) hydrochloride (PHMB). VANTOCIL IB Antimicrobial is produced for use in industrial, institutional, agricultural, food, beverage, and domestic disinfection applications, primarily as a solid surface disinfectant, specifically for hospitals, veterinary establishments, dairies, milking parlors, breweries, air-conditioning units, and pasteurizers in canned food & beverage bottling plants. Vantocil Product Overview Vantocil IB and Vantocil TG are aqueous solutions of the powerful antibacterial preservative poly(hexamethylene biguanide) hydrochloride [PHMB], an active offering broad pH tolerance, low foam and good heat stability. Applications are varied, and include surface care, fabric care and automotive care. PROPERTIES Vantocil IB and Vantocil TG are aqueous solutions of the powerful antibacterial preservative poly(hexamethylene biguanide) hydrochloride [PHMB], an active offering broad pH tolerance, low foam and good heat stability. Applications are varied, and include surface care, fabric care and automotive care. Vantocil IB Antimicrobial is a broad spectrum, fast acting bactericide for disinfectants and sanitizers in industrial, institutional, agricultural, food, beverage and domestic disinfection applications. It is effective in a wide range of industrial disinfection applications, primarily as a solid surface dispersant. Application areas include hospitals, institutions, veterinary establishments, dairies, milking parlors, and other food processing plants. VANTOCIL IB has been shown to be very effective against Mycobacterium smegmatis and Mycobacterium intracellularis responsible for tuberculosis in pigs. VANTOCIL IB has also been shown to be effective at eradicating Salmonella pullorum, Salmonella typhimurium, Heamophilus gallinarum, Mycoplasma synoviae and pathogenic E.coli, which are responsible for white diarrhoea, respiratory disease and colibacillosis in chickens. Features VANTOCIL IB is based on Arch's highly active biocide poly(hexamethylene biguanide) hydrochloride, also known as PHMB. •Fast acting bactericide, effective at low concentrations •Extensive toxicity studies suggest acceptable use •Retains activity in the presence of organic matter such as •Active against enveloped RNA, enveloped DNA, naked •Readily dilutable in hot and cold water •Provides stable formulations with both acids and alkalis •Low corrosion, and compatible with common materials of •Active in both soft and hard water •Effective and stable over a pH range of 1 - 11 VANTOCIL IB is a highly effective, fast-acting biocide for the formulation of disinfectants and sanitizers, and is a 20%aqueous solution of poly(hexamethylene biguanide) hydrochloride, also known as PHMB. VANTOCIL FHC is anaqueous formulation of PHMB and quaternary ammonium compound. PARA-GENE Poly BiQuinide Disinfectant Vantocil IB concentrate formula isdesigned for use as a powerful surface and terminal non-tainting sanitiser which has a broad spectrum of activity against micro-organisms. VANTOCIL IB is a broad spectrum, fast acting bactericide for the formulation of disinfectants and sanitizers, for use in industrial, institutional, agricultural, food, beverage and domestic disinfection applications. VANTOCIL IB is a 20% aqueous solution of poly(hexamethylene biguanide) hydrochloride also known as PHMB. Poly (hexamethylene biguanide)hydrochloride (PHMB),Vantocıl IB, An effective preservative for formulations containing non-ionic or cationic ingredients, such as PVA & VAEemulsion polymers, silicone emulsions, PVA & starch based adhesives, and certain types of rheology modifiers Rapid, non-formaldehdye mechanism. Vantocil IB by Lonza is an aqueous solution. It is highly effective preservative for use in a wide variety of applications including oil-inwater and water-in-oil emulsions, industrial reagents, silicone systems, cellulose solutions and oil recovery systems. Can also be used to preserve aqueous based adhesives (such as animal glues, latex adhesives based on polyvinyl acetate, PVA, starch, dextrin, casein and other glues, and latex adhesives intended for food packaging applications). Recommended usage level of Vantocil IB is 500-5000 ppm. This product can be used alone or in combination with other biocides to create products for a wide range of disinfection applications. It is a broad-spectrum, fast-acting bactericide that can be used in various formulations for disinfectants and sanitizers. The Vantocil IB product can be used for industrial, institutional, agricultural, food and beverage, and pool and spa water treatment applications as well as domestic disinfection applications. This product is a 20% aqueous solution of poly (hexamethylene biguanide) hydrochloride, also known as PHMB. The combination of the different modes of biocidal action reduces the risk of bacterial resistance, and the product is effective in a wide range of industrial disinfection applications. Disinfection by fumigation or fogging is commonly practiced in areas, which require a high degree of hygiene control. This disinfection encompasses control of microorganisms in air as well as on surface. The process of disinfection involves the use of antimicrobial chemicals or biocides to kill viable microorganisms. In the present study, the efficacy of biocide Vantocil-IB as an aerial and surface disinfectant was determined. Solution of Vantocil-IB was fogged in to a room with help of mechanical fogger and the aerial and surface microbial load was determined before and after fogging. Vantocil-IB at 0.2 gm% concentration showed significant reduction in the number of viable microorganisms in air and on the surface of the room. A contact time of 1hour and a fogging time of 20-25 minutes proved effective in reducing the number of microorganisms to safe level. Study of a biocide [Vantocil-IB] for aerial and surface disinfection. Immersion of freshly processed poultry carcasses in solutions of poly(hexamethylenebiguanide hydrochloride), PHMB,VANTOCIL IB, retarded bacterial growth and markedly improved the shelf-life during storage at 2 C.Birds treated with 200, 300, and 400 ppm PHMB had average shelf-livesof 22.9, 25.9, and 26.0 days, respectively, compared to the 10.5 days ofshelf-life for water-treated controls. Duncan's multiple range testrevealed that the shelf-life differences among PHMB-treated birds were not statistically significant. VANTOCIL IB is a 20% aqueous solution of poly (hexamethylene biguanide) hydrochloride, also known as PHMB. The combination of the different modes of biocidal action reduces the risk of bacterial resistance, and the products are effective in a wide range of industrial disinfection applications. The levels of VANTOCIL IB Antimicrobial to prevent thegrowth of problem micro-organisms are listed in Table 1.MICs do not represent effective use levels but do indicatethe intrinsic broad spectrum of activity of VANTOCIL IB Antimicrobial.VANTOCIL IB Antimicrobial has a non-specific mode ofbiocidal action which means that bacterial resistance is veryunlikely to occur. Detailed information on the mode ofaction of VANTOCIL IB Antimicrobial is available onrequest. VANTOCIL IB Antimicrobial can be used alone or incombination with other biocides to create products for awide range of disinfection applications. Considerable data exists which provides a measure of theintrinsic anti-microbial activity of VANTOCIL IBAntimicrobial, generated via European suspension testprotocols relevant to application in Food, Industrial,Domestic and Institutional Hygiene.Its activity has been further demonstrated under conditionsrepresentative of practical use, and a range of useconcentrations is provided in Table 3. However, it isrecommended that field tests under practical conditions beundertaken to determine the most cost-effective dose foryour application.This data and information on the compatibility of VANTOCIL IB Antimicrobial with a range of formulating chemicals is available on request. VANTOCIL IB is a liquid antimicrobial agent. Used in conjunction with Proxel GXL to prevent bacterial attack during brine curing; and for short term preservation of fresh hides. As a quick kill bactericide Vantocil quickly lowers the bacterial count in the raceway and on the hides, and results in a more bacteria free hide which then can be treated with a longer term bactericide such as Proxel GXL. Vantocil ib polymeric biguanide; a preservative for coatings raw materials including silicone emulsions, polyvinyl alcohol and polyvinyl acetate; quick kill, broad spectrum antimicrobial activity; pale yellow liquid; odorless. The polychaete Platynereis dumerilii (Polychaeta: Nereidae) has been evaluated as a candidate bioassay species for marine ecotoxicity testing. The species conforms with many of the requirements of an ideal bioassay organism in that (i) it is amenable to laboratory culture, (ii) its relatively small size makes it convenient for handling and laboratory exposure studies, (iii) its diet is defined and can be controlled, (iv) it reproduces throughout the year and, using photoperiod manipulation, can be induced to spawn as required, and (v) it has a short life cycle (approximately 3 months at 20°C) making it feasible to study the effects of xenobiotics on chronic endpoints such as reproduction. The components of the life history which have been examined to date include fertilization rate, embryo-larval development, and larval survival. These life stages were evaluated using the reference materials used in the 1991 International Paris Commission (PARCOM) Ring Test (namely, the biocides, Bioban P-1487 and Vantocil IB, and the widely used reference toxicant, 3,5-dichlorophenol). For fertilization rate, the median effect concentrations (1-h EC50 values) were 0.32 mg · liter−1 for Bioban P-1487, 1.99 mg · liter−1 for 3,5-dichlorophenol, and 9.66 mg · liter−1 for Vantocil IB. For embryo-larval development, the median effect concentrations (48-h EC50 values) were 0.29 mg · liter−1 for Bioban P-1487, 2.13 mg · liter−1 for 3,5-dichlorophenol, and 4.81 mg · liter−1 for Vantocil IB. For larval survival, the median lethal concentrations (48-h LC50 values) were 0.32 mg · liter−1 for Bioban P-1487, 3.64 mg · liter−1 for 3,5-dichlorophenol, and 10.9 mg · liter−1 for Vantocil IB. These results (all based on nominal values) suggest that, for these reference materials, the early life stages of P. dumerilii are of similar sensitivity to other marine invertebrate species. Together with the amenability of this species to laboratory culture, these data suggest that P. dumerilii has significant potential for use in marine ecotoxicity testing. PHMB (Vantocil) acts as disinfectant and preservative. It typically exhibits goodbactericidal activity but slower fungicidal and acanthamoebicide activity and provides long term storage capability for the lens. The usual disinfection time is 4-6 hours. The multipurpose solution containing Polyhexanide or PHMB (Vantocil) meets FDA and ISO primary standards. The effects of chlorhexidine diacetate and vantocil IB on the viability of Providencia stuartii strains are described. Exposure of Prov. stuartii strains to different concentrations of chlorhexidine in broth culture resulted in a decrease in viability over the first 6 h, followed by regrowth. During incubation, bacteria adhered to the surface of the culture vessel and multiplied despite the presence of a bactericidal concentration of the drug in the medium. It is concluded that the phenomenon of ‘regrowth’ results from adhesion to glass containers and the subsequent dispersal of some of these cells into the culture medium. With the objective of characterizing the occurrence of red leg in Minas Gerais, young and adult frogs with foot and finger ulcers, hemorrhagic effusion on the skin of the ventral region, motor incoordination, high mortality rates in adults and abscesses to necropsy. In the culture of fragments of damaged skin and abscesses, Aeromonas hydrophila was isolated and identified . The bactericidal effect of VANTOCIL IB was higher than potassium permanganate, determined by the minimum inhibitory concentration for isolated colonies. The actions of chlorhexidine, cetrimide and Vantocil (the hydrochloride of a polymeric biguanide) on bacteria and spheroplasts or protoplasts derived therefrom have been compared. Lysis of Escherichia coli spheroplasts by chlorhexidine or cetrimide is due to rupture of the cytoplasmic membrane. Membranes ruptured with cetrimide can reform to give small, empty envelopes. With increasing concentrations of cetrimide or chlorhexidine more and more granules appear in the cytoplasm, increasing in size with increasing concentration, until the structure becomes transformed to a granular body similar in size to the original spheroplast. With chlorhexidine or Vantocil this now electron‐dense body is rigid, but with cetrimide it collapses to a flat disc which does not lyse. The granules appear to consist of coagulated cytoplasm. This effect of excess of these antiseptics not only prevents osmotic lysis of the spheroplast or the collapsed disc but renders them immune to lysis by a variety of chemical agents. In isolated cytoplasm, chlorhexidine or cetrimide causes precipitation over a narrow range of concentrations but greater than those required for lysis. With Vantocil precipitation occurs gradually over a wide range of concentrations, starting at concentrations equal to those which cause a limited amount of lysis of the spheroplast or a relatively small increase in permeability of intact bacteria. Lanthanous and uranyl ions also precipitate cell contents but do not lyse spheroplasts; spheroplasts treated with these ions are protected from lysis by other agents. VANTOCIL IB Antimicrobial is a bactericide manufactured by Excel Industries Limited. PROPERTIES: VANTOCIL IB is a broad spectrum, fast acting bactericide for the formulation disinfectants and sanitisers, for use in industrial, institution , agriculture, food beverage and domestic disinfection applications. VANTOCIL IB is a 20% aqueous solution of poly (hexamethylene biguanide) hydrocloride, also known as PHMB. Composition: An aqueous solution of PHMB. Physical form: It is a slighty opalesscent colorless to pale yellow liquid of pH 4.0-4.5 and density (at 25øC) 1.14 Application: VANTOCIL IB is effective in a wide range of industrial disinfection applications , primarily as a solid surface disinfectant. application areas include: ? Hospitals ? Institutions ?Veterynary Establishment ? Dairies ? Milking parlours ? Poultry hatcheries ? Food processing plants ? Breweries ? Pasteurisers in canned food & beverage bottling plants ? Yoghurt fermentation ? Air-Conditioning units ? Cheese moulds ? Beer glass cleaner VANTOCIL IB Antimicrobial manufacturer is Excel Industries Limited but there can be plenty of supplier for supplying or exporting of VANTOCIL IB Antimicrobial substitute or equivalent. Such substitute chemicals are usually of same chemistry types and can benefit the user in economical aspects. APPLICATIONS •Hospitals •Institutions •Veterinary establishments •Diaries •Milking parlors •Poultry hatcheries •Food processing plants •Breweries •Pasteurizes in canned food & beverage bottling plants •Yoghurt fermentation •Air-conditioning units •Cheese molds •Beer glass cleaners BENEFITS: • Rapid bactericidal action, in low concentrations, effective against gram positive and negative bacteria. In higher dosage, effective against fungi and yeasts; • Low toxicity to humans; • Maintains activity in the presence of organic matter; • Low foam, suitable for CIP systems and pasteurization processes; • Soluble in hot or cold water; • Active against viruses; • Compatible with acid formulations or alkaline detergents; • Low corrosivity, and can be used on surfaces of different materials; • Stable in the presence of hard water and high temperatures; • Stable and effective in the pH range from 1 to 11. The active ingredient, PHMB, is thermally stable and non-volatile, with bactericidal, virucidal and fungicidal activity. It does not leave spots on the surfaces, it has low formation of foam, of easy rinsing, besides not changing the organoleptic properties

Vantocil P is best known for its broad-spectrum antimicrobial and antifungal activity.
Vantocil P is the standard of care for treatment of Acanthamoeba keratitis and an ingredient in multipurpose contact lens solutions, such as Renu (Bauch & Lomb, Rochester, NY).
Vantocil P is a cationic disinfectant that is effective against Gram-negative and Gram-positive bacteria through its electrostatic interaction with negative sites on the lipopolysaccharide component of bacterial cell membranes.

CAS Number: 32289-58-0
Molecular Formula: C10H23N5
Molecular Weight: 213.32312
EINECS Number: 1308068-626-2

32289-58-0, N'-[6-[(N'-methylcarbamimidoyl)amino]hexyl]ethanimidamide, SCHEMBL24018755, Polyhexamethylene Biguanidine HCl, BCP13780, AKOS015919499, N-(6-(3-Methylguanidino)hexyl)acetimidamide, 1824322-57-7, Poly(iminoimidocarbonyliminoimidocarbonyliminohexamethylene) hydrochloride, Vantocil IB, Vantocil TG,
Poly(iminoimidocarbonyliminoimidocarbonylimino hexamethylene monohydrochloride), Guanidine,Poly(hexamethylene Diguanide)
Hydrochloride,Poly(hexamethylenebicyanoguanide-Hexamethylenediamine) Hydrochloride, Reputex20, Vantocil 100, Vantocil Ib, Vantocil P, Vantocil Tg, A-Breeze, Baquacil, Baquacil Ultra, Caswell No. 676, Chlorhexidine complex, Cosmoquil QC, PHMB, Polyhexanide, Vantocil 1B, Vantocil P (20% w/w polihexanide), Baquacil, Clorhidrato de poli(imino imido) biguanidina, Cosmoquil CQ, Vantocil 1B, Vandocil P, Baquacil, cosmocil, Lavasept, PHMB polymer, polihexanide, polihexanidehydrochloride, poly(hexamethylene biguanide), poly(hexamethylenebiguanide) hydrochloride, polyhexamethylenbiguanide, polyhexamethylenbiguanid,
polyhexamethylenbiguanide ,polyhexamethylene biguanide, Vantocil P,polyhexanide,Vantocil,Vantocil IB of Vantocil

Vantocil P Antimicrobial is a broad spectrum, fast acting antimicrobial for the formulation of disinfectants and sanitizers for use in commercial, industrial, and domestic disinfection applications.
Vantocil P may be used to formulate sanitizers and disinfectants for use in food handling and storage establishments, premises, and equipment.
Vantocil P is a chemical compound that belongs to the biguanide class of chemicals.

Vantocil P is a polymer, meaning it is made up of repeating units of smaller molecules.
Vantocil P is known for its antimicrobial properties, which make it effective against a broad spectrum of microorganisms, including bacteria, fungi, and some viruses.
Vantocil P and Vantocil TG are aqueous solutions of the powerful antibacterial preservative poly(hexamethylene biguanide) hydrochloride [PHMB], an active offering broad pH tolerance, low foam and good heat stability.

Vantocil P applications are varied, and include surface care, fabric care and automotive care.
Vantocil P is a cationic disinfectant that is effective against Gram-negative and Gram-positive bacteria through its electrostatic interaction with negative sites on the lipopolysaccharide component of bacterial cell membranes.
Vantocil P may be used to formulate sanitizers and disinfectants for use in food handling/storage establishments, premises and equipment, including food contact surfaces in public eating places, dairy processing equipment, and food processing equipment and utensils.

Vantocil P is best known for its broad-spectrum antimicrobial and antifungal activity.
Vantocil P is the standard of care for treatment of Acanthamoeba keratitis and an ingredient in multipurpose contact lens solutions, such as Renu (Bauch & Lomb, Rochester, NY).

Vantocil P is a polymer used as a disinfectant and antiseptic.
In dermatological use,Vantocil P is spelled polihexanide (INN) and sold under the names Lavasept, Serasept, Prontosan, and Omnicide.
Vantocil P has been shown to be effective against Pseudomonas aeruginosa, Staphylococcus aureus, Escherichia coli, Candida albicans, Aspergillus brasiliensis, enterococci, and Klebsiella pneumoniae.

Vantocil Ps are used for inter-operative irrigation, pre- and post-surgery skin and mucous membrane disinfection, post-operative dressings, surgical and non-surgical wound dressings, surgical bath/hydrotherapy, chronic wounds like diabetic foot ulcer and burn wound management, routine antisepsis during minor incisions, catheterization, first aid, surface disinfection, and linen disinfection.
Vantocil P eye drops have been used as a treatment for eyes affected by Acanthamoeba keratitis.
Vantocil P is an antiseptic with antiviral and antibacterial properties used in a variety of products including wound care dressings, contact lens cleaning solutions, perioperative cleansing products, and swimming pool cleaners.

Vantocil P is a cationic polymer with antimicrobial and antiviral properties.
Vantocil P Antimicrobial is a broad spectrum, fast acting bactericide for the formulation of disinfectants and sanitisers.
Vantocil P is a 20% aqueous solution of poly (hexamethylene biguanide) hydrochloride (PHMB).

Vantocil P Antimicrobial is produced for use in industrial, institutional, agricultural, food, beverage, and domestic disinfection applications, primarily as a solid surface disinfectant, specifically for hospitals, veterinary establishments, dairies, milking parlors, breweries, air-conditioning units, and pasteurizers in canned food & beverage bottling plants.
Vantocil P is a new environment-friendly cationic water-soluble polymer.
Vantocil P is a water solution that can be used as a broad spectrum and high efficient disinfectant.

Vantocil P is low toxic, steady, non-flammable, non-explosive, and basically non-corrosive to stainless steel, copper, carbon steel, wood, and plastic.
Because of its special bactericidal mechanisms, almost all kinds of bacteria shall be killed efficiently and will not develop resistance action.
Vantocil P is often used in products such as hand sanitizers, antiseptic creams, wound care products, and contact lens solutions for its antimicrobial and preservative properties.

Vantocil P can be used in textiles to impart antimicrobial properties, helping to prevent the growth of bacteria and fungi on fabrics.
Vantocil P is used in swimming pools and hot tubs as a disinfectant to control microbial growth in the water.
Some medical devices and equipment may be treated with Vantocil P to reduce the risk of microbial contamination.

Vantocil P is a cationic polymer with antimicrobial and antiviral properties.
Vantocil P has been commonly accepted that the antimicrobial activity is due to the ability of Vantocil P to perforate the bacterial phospholipid membrane leading ultimately to its death.
Vantocil P is sold as a swimming pool and spa disinfectant in place of chlorine or bromine based products under the name Baquacil.

Vantocil P has been commonly accepted that the antimicrobial activity is due to the ability of Vantocil P to perforate the bacterial phospholipid membrane leading ultimately to its death.
Vantocil P is a new environment-friendly cationic water-soluble polymer.
Vantocil P is low toxic, steady, non-flammable, non-explosive, and basically non-corrosive to stainless steel, copper, carbon steel, wood, and plastic.

Because of its special bactericidal mechanisms, almost all kinds of bacteria shall be killed efficiently and will not develop resistance action.
Vantocil P and Vantocil TG are aqueous solutions of the powerful antibacterial preservative poly(hexamethylene biguanide) hydrochloride [PHMB], an active offering broad pH tolerance, low foam and good heat stability.
Applications are varied, and include surface care, fabric care and automotive care.

Vantocil P Antimicrobial is a broad spectrum, fast acting bactericide for disinfectants and sanitizers in industrial, institutional, agricultural, food, beverage and domestic disinfection applications.
Vantocil P is effective in a wide range of industrial disinfection applications, primarily as a solid surface dispersant.
Application areas include hospitals, institutions, veterinary establishments, dairies, milking parlors, and other food processing plants.

Vantocil P has been shown to be very effective against Mycobacterium smegmatis and Mycobacterium intracellularis responsible for tuberculosis in pigs.
Vantocil P has also been shown to be effective at eradicating Salmonella pullorum, Salmonella typhimurium, Heamophilus gallinarum, Mycoplasma synoviae and pathogenic E.coli, which are responsible for white diarrhoea, respiratory disease and colibacillosis in chickens.
Vantocil P is based on Arch's highly active biocide poly(hexamethylene biguanide) hydrochloride, also known as PHMB.

Vantocil P is also used as an ingredient in some contact lens cleaning products, cosmetics, personal deodorants and some veterinary products.
Vantocil P is also used to treat clothing (Purista), purportedly to prevent the development of unpleasant odors.
Vantocil P hydrochloride salt (solution) is used in the majority of formulations.

Vantocil P is a chemical compound that belongs to the biguanide class of disinfectants and antiseptics.
Vantocil P is commonly used for its antimicrobial properties in various applications, ranging from healthcare and personal care to industrial settings.
Vantocil P has broad-spectrum antimicrobial activity against bacteria, fungi, and some viruses.

Vantocil P is also used as a surface disinfectant and is alleged to be suitable for skin disinfection.
Vantocil P, also known as PHMB, polyhexanide or polihexanide, is a highly water soluble and hydrolytically stable polymeric material.
The presence of multiple hydrogen bond and chelation sites within Vantocil P renders it of potential interest in the field of supramolecular chemistry.

Vantocil P Antimicrobial is a bactericide manufactured by Excel Industries Limited.
Vantocil P is a broad spectrum, fast acting bactericide for the formulation disinfectants and sanitisers, for use in industrial, institution , agriculture, food beverage and domestic disinfection applications.
Vantocil P is a 20% aqueous solution of poly (hexamethylene biguanide) hydrocloride, also known as PHMB.

Composition: An aqueous solution of Vantocil P. Physical form:
Vantocil P is a slighty opalesscent colorless to pale yellow liquid of pH 4.0- 4.5 and density (at 25øC) 1.14.
Vantocil P is effective in a wide range of industrial disinfection applications , primarily as a solid surface disinfectant.

Vantocil P Antimicrobial manufacturer is Excel Industries Limited but there can be plenty of supplier for supplying or exporting of Vantocil P Antimicrobial substitute or equivalent.
Such substitute chemicals are usually of same chemistry types and can benefit the user in economical aspects.
Vantocil P shows activity against both Gram-positive and Gram-negative bacteria and is widely used across several sectors, typically as the hydrochloride salt, in a variety of disinfectant solutions and antiseptics.

Vantocil P is available also as a solid.
Vantocil P is a new environment-friendly cationic water-soluble polymer.
Vantocil P is non-corrosive to skin, and can not be easily absorbed by human organs.

Vitro studies show that Vantocil P is non-toxic to human cells.
Skin irritancy test of rabbits and human hands shows that Vantocil P is non-irritant to animal and human skin.
Vantocil P has a slow effectand does not meet the practical requirementsfor prophylactic antiseptics in this respect.

Vantocil P is a water solution that can be used as a broad-spectrum and high-efficiency disinfectant.
Vantocil P biocide is low toxic, steady, non-flammable, non-explosive, and basically non-corrosive to stainless steel, copper, carbon steel, wood, and plastic.
Because of its special bactericidal mechanisms, almost all kinds of bacteria shall be killed efficiently and will not develop resistance action.

Vantocil P is a 20% aqueous solution of poly (hexamethylene biguanide) hydrochloride, also known as PHMB.
The combination of the different modes of biocidal action reduces the risk of bacterial resistance, and the product is effective in a wide range of industrial disinfection applications.
Vantocil P disinfectant is a high molecular polymer, which is easy to be washed away.

Vantocil P has a chemical structure characterized by a repeating unit of hexamethylene biguanide.
The polymer consists of a chain of repeating biguanide groups, which are positively charged.
This positive charge contributes to its antimicrobial properties by interacting with the negatively charged components of microorganisms.

storage temp.: Inert atmosphere,Room Temperature
solubility: Water
CAS DataBase Reference: 32289-58-0(CAS DataBase Reference)
FDA UNII: 4XI6112496

Vantocil P has a chemical structure characterized by a repeating unit of hexamethylene biguanide.
The polymer consists of a chain of repeating biguanide groups, which are positively charged.
This positive charge contributes to its antimicrobial properties by interacting with the negatively charged components of microorganisms.

Vantocil P is also used as a surface disinfectant and is alleged to be suitable for skin disinfection.
Vantocil P is very effective against Pseudomonas aeruginosa, Staphylococcus aureus (also the methicillin-resistant type, MRSA), Escherichia coli, Candida albicans (yeast), Aspergillus brasiliensis (mold), vancomycin-resistant enterococci, and Klebsiella pneumoniae (carbapenem-resistant enterobacteriaceae).
Some products containing Vantocil P (PHMB) CAS 32289-58-0 Poly(hexamethylenebiguanide) Hcl are applied for inter-operative irrigation, both before and after surgery skin and mucous membrane disinfection, post-operative dressings, surgical and non-surgical wound dressings, surgical bath/hydrotherapy, chronic wounds like diabetic foot ulcer and burn wound management, routine antisepsis during minor incisions, catheterization, scopy, first aid, surface disinfection, and linen disinfection.

Vantocil P Hcl eye drops have been used as a treatment for eyes affected by Acanthamoeba keratitis.
Another good application of Vantocil P Hcl is that it is widely used as a swimming-pool and spa water sanitizer instead of chlorine- or bromine-based commodities.
Vantocil P Antimicrobial can be used alone or incombination with other biocides to create products for awide range of disinfection applications.

Considerable data exists which provides a measure of theintrinsic anti-microbial activity of Vantocil P Antimicrobial, generated via European suspension testprotocols relevant to application in Food, Industrial,Domestic and Institutional Hygiene.Its activity has been further demonstrated under conditionsrepresentative of practical use, and a range of useconcentrations.
However, Vantocil P isrecommended that field tests under practical conditions beundertaken to determine the most cost-effective dose foryour application.

Vantocil P is used as a biocidal agent in various products, including disinfectants, antiseptics, wound care products, contact lens solutions, and preservatives for textiles.
In the medical field, Vantocil P is employed in wound care products to prevent infections in cuts, abrasions, and surgical wounds.
Vantocil P is used in solutions, gels, or impregnated dressings.

Vantocil P Poly(hexamethylenebiguanide) Hcl is also utilized as an ingredient in some contact lens cleaning products, cosmetics, personal deodorants and some veterinary products.
Vantocil P is known for its strong antimicrobial activity.
Vantocil P acts as disinfectant and preservative.

Vantocil P typically exhibits goodbactericidal activity but slower fungicidal and acanthamoebicide activity and provides long term storage capability for the lens.
The usual disinfection time is 4-6 hours. The multipurpose solution containing Polyhexanide or Vantocil P meets FDA and ISO primary standards.
The effects of chlorhexidine diacetate and Vantocil P on the viability of Providencia stuartii strains are described.

Vantocil P is concluded that the phenomenon of ‘regrowth’ results from adhesion to glass containers and the subsequent dispersal of some of these cells into the culture medium.
With the objective of characterizing the occurrence of red leg in Minas Gerais, young and adult frogs with foot and finger ulcers, hemorrhagic effusion on the skin of the ventral region, motor incoordination, high mortality rates in adults and abscesses to necropsy.
In the culture of fragments of damaged skin and abscesses, Aeromonas hydrophila was isolated and identified .

The bactericidal effect of Vantocil P was higher than potassium permanganate, determined by the minimum inhibitory concentration for isolated colonies.
Vantocil P disrupts the cell membranes of microorganisms, leading to their destruction.
This makes Vantocil P effective against a wide range of pathogens.

Vantocil P has a slow effectand does not meet the practical requirementsfor prophylactic antiseptics in this respect.
Although Vantocil P is somewhat less effective than benzalkonium chloride, it is sometimes used instead of benzalkonium because it is less foamproducing under use conditions.
The preparation method of Vantocil P:By a certain proportion of 1, the own bisguanides of 6-and catalyst join in reaction vessel, under nitrogen protection, said mixture is heated to 80-200 DEGC and reacts, react 2-24 hour, reaction terminates, cooling blowing, obtains poly hexamethylene biguanide, poly hexamethylene biguanide aqueous acid is neutralized to pH value 5-9, and performing filtering so as to obtain a polyhexamethylene biguanidine salt.

Vantocil P has demonstrated efficacy against some resilient microorganisms, making it valuable in situations where standard antiseptics may be less effective.
Vantocil P is generally compatible with a variety of materials, including plastics, textiles, and metals, making it suitable for use in different product formulations.
Vantocil P is known for having a low likelihood of inducing resistance in microorganisms.

This property is important in maintaining the effectiveness of the compound over time.
Vantocil P may be used in aquaculture to control bacterial and fungal infections in fish or other aquatic organisms.
Vantocil P may be found in consumer antiseptic products, such as hand sanitizers, providing an additional option for individuals seeking effective antimicrobial solutions.

Vantocil P is incorporated into certain wound dressings to provide an antimicrobial barrier and aid in the healing process.
Vantocil Ps are subject to regulatory oversight, and compliance with relevant regulations ensures the safety and efficacy of the products.
Vantocil P is often used in water-based formulations due to its solubility in water, making it applicable in a variety of liquid products

Vantocil P may be used in veterinary wound care products to manage infections in animals.
Vantocil P is used in some formulations for mold and mildew control, particularly in products designed for damp or humid environments.
Vantocil P may be used in sanitizing solutions for food contact surfaces, helping to control microbial contamination in food processing and preparation areas.

Vantocil P is considered biocompatible, which is an important factor in its use in healthcare and personal care products.
A hydrochloride salt of polyhexamethylene biguanide.
Vantocil P is a high molecular polymer, which is easy to be washed away.

Vantocil P is non-corrosive to the skin, and can not be easily absorbed by human organs.
Vitro studies show that Vantocil P is non-toxic to human cells.
Skin irritancy test of rabbits and human hands shows that Vantocil P is non-irritant to animal and human skin.

Vantocil P is a polymer used as a sanitizer or preservative to kill bacteria.
Vantocil P is a broad spectrum and fast acting bactericide which is used for the formulation of disinfectants and sanitisers.

Vantocil P is a new environment-friendly cationic water-soluble polymer.
Vantocil P is a water solution that can be used as a broad-spectrum and high efficiency disinfectant.
Vantocil P is low toxic, steady, non-flammable, non-explosive, and basically non-corrosive to stainless steel, copper, carbon steel, wood, and plastic.

Uses:
Vantocil P is a polymer used as a disinfectant and antiseptic.
Vantocil P may be included in foot care products, such as creams or powders, to provide antimicrobial protection and address issues related to foot hygiene.
Vantocil P is used in some disposable medical products, such as wound dressings and bandages, to help prevent microbial contamination.

In public spaces, such as gyms, swimming pools, and public restrooms, Vantocil P may be used in cleaning solutions and disinfectants to control the spread of infections.
Vantocil P can be incorporated into the manufacturing of hospital bed linens and textiles to provide an additional layer of protection against microbial contamination.
Vantocil P may be used in the preservation of hemodialysis fluids, helping to maintain the sterility of these solutions used in renal replacement therapy.

Vantocil P is commonly used in personal care and cosmetic products, including hand sanitizers, soaps, shampoos, and skin cleansers.
Vantocil P helps in preventing the growth of bacteria and fungi on the skin and in the products themselves.
In addition to wound care products, Vantocil P is sometimes used in medical settings for skin disinfection and as a coating for certain medical devices.

Vantocil P is found in some household items like disinfectant wipes and cleaning solutions.
Vantocil P is used in swimming pools, hot tubs, and other water systems as a disinfectant to control the growth of algae, bacteria, and other microorganisms.
Vantocil P-treated textiles, such as clothing and bedding, may offer antimicrobial properties, reducing the risk of bacterial and fungal growth.

Long-term care facilities may use products containing Vantocil P as part of infection control measures to reduce the risk of healthcare-associated infections among residents.
Vantocil P is sometimes included in insect repellent formulations for its antimicrobial properties, providing additional protection against microbial contamination.
Vantocil P may be found in household disinfectants and cleaning products, contributing to their antimicrobial efficacy.

Vantocil P may be used in agricultural and horticultural settings to control microbial contamination in soil, plant care products, or agricultural equipment.
Vantocil P has been explored for potential use in biodegradable plastics, providing a way to control microbial degradation in certain plastic materials.
Vantocil P may be included in wound irrigation solutions to prevent infections during the cleaning of wounds.

Vantocil P may be used in the preservation of construction materials, such as coatings and sealants, to inhibit microbial growth.
Vantocil P can be applied in the preservation of wood and timber products to protect against decay caused by fungi and bacteria.
In healthcare settings, Vantocil P may be used for the disinfection of respiratory equipment to prevent the growth of harmful microorganisms.

Vantocil P is included in some preventive skin care products, such as barrier creams, to protect the skin from microbial contamination.
Vantocil P can be used in swimming pool water treatment to control bacteria and other microorganisms, contributing to water hygiene.
Vantocil P is used in cosmetics, personal care products, fabric softeners, contact lens solutions and more.

Vantocil P can completely kill escherichia coli, staphylococcus aureus, candida Albicans, gonococcus, salmonella, pseudomonas aeruginosa, listeria, dysentery, aspergillus niger, brucella, vibrio parahaemolyticus, vibrio algolyticus, vibrio eels, Aeromonas hydrophilic, sulfate-reducing bacteria, iron bacteria, and saprophytic bacteria.
In dermatological use, it is spelled polihexanide (INN) and sold under names such as Lavasept, Serasept, Prontosan and Omnicide.
Vantocil P has been shown to be effective against Pseudomonas aeruginosa, Staphylococcus aureus (also the methicillin-resistant type, MRSA), Escherichia coli, Candida albicans (yeast), Aspergillus brasiliensis (mold), vancomycin-resistant enterococci, and Klebsiella pneumoniae (carbapenem-resistant enterobacteriaceae).

Designed to be used for regular sanitizing of contaminated linen, garments & fabrics as part of the laundering process.
Vantocil P can be used in home-type or commercial laundering machines.
Ideal for use in health care laundry applications.

Vantocil P Antimicrobial is not compatible with high levels of chlorine.
Articles treated with Vantocil P Antimicrobial should not be subsequently bleached with chlorine.
Vantocil P Antimicrobial is not compatible with common soap and anionic detergents.

Vantocil P is suitable to care solutions for contact lenses, cosmetics, medical, pharmaceutical, skin, mucosa, vegetable, fruit, air, drinking water, swimming pool, paper making, tissue, sanitary pads, clothes, etc.
Vantocil P is used to control bacterial and fungal infections in fish or other aquatic organisms.
Vantocil P contributes to the preservation of cosmetic and personal care products, preventing microbial growth and ensuring product stability over time.

Vantocil P may be used in disinfection protocols in hospitality settings, such as hotels and leisure facilities, to control the spread of infections.
Vantocil P is used in some residential cleaning products to provide effective antimicrobial action.
Vantocil P may be incorporated into formulations for sports equipment to prevent microbial contamination and odors.

Vantocil P may be used in air fresheners to inhibit the growth of bacteria and fungi in the product.
Vantocil P is used in the stabilization of fabric linings in shoes.
Biguanide solution used in cleaning contact lenses.

Vantocil P is used in dermatological formulations for the treatment of various skin conditions, including infections or inflammatory skin disorders.
Vantocil P is included in mouthwashes and oral care products for its antimicrobial properties.
Vantocil P helps control bacteria in the oral cavity, contributing to oral hygiene.

Vantocil P is investigated for potential biomedical applications, including drug delivery systems and tissue engineering, due to its biocompatibility and antimicrobial properties.
Vantocil P is employed in healthcare settings to help prevent infections in wounds, surgical sites, and catheter-related applications.
PHMB is often included in waterless hand sanitizers due to its antimicrobial properties.

These sanitizers are convenient for situations where traditional handwashing is not possible.
Some foot care products, such as foot creams and powders, may incorporate Vantocil P to help prevent the growth of bacteria and fungi that can contribute to foot odor and infections.
Vantocil P can be used in agriculture as a disinfectant for equipment, tools, and surfaces to control microbial contamination.

Certain consumer products, such as antimicrobial wipes, household cleaners, and deodorants, may include PHMB to provide protection against microbes.
Vantocil P is sometimes used in veterinary products, including shampoos and wound care solutions for animals.
Vantocil P can be incorporated into various industrial processes to control microbial contamination in water systems, manufacturing equipment, and other settings where microbial growth can be problematic.

In addition to contact lens solutions, Vantocil P may be used in ophthalmic solutions for eye care.
Vantocil P can serve as a preservative in cosmetic formulations, helping to prevent the growth of microorganisms in products like lotions and creams.
Vantocil P is sometimes incorporated into wound dressings and bandages to help prevent infections in cuts and abrasions.

In some formulations, Vantocil P may be included in mouthwashes for its antimicrobial properties.
Vantocil P may be used in veterinary wound care products to manage infections in animals.
Vantocil P is used in some formulations for mold and mildew control, particularly in products designed for damp or humid environments.

Vantocil P may be used in sanitizing solutions for food contact surfaces, helping to control microbial contamination in food processing and preparation areas.
Vantocil P can be found in consumer antiseptic products, such as hand sanitizers, providing an additional option for individuals seeking effective antimicrobial solutions.

Safety Profile:
On the 20th of April 2018, the european commission decided to ban preservative uses of Vantocil P PT9 (Fibre, leather, rubber and polymerised materials preservatives).
Vantocil P’s still allowed for uses as disinfectants PT2 (Disinfectants and algaecides not intended for direct application to humans or animals).
Vantocil P was classified as category 2 carcinogen by the European Chemical Agency, but it is still allowed in cosmetics in small quantities if exposure by inhalation is impossible.

Vantocil P is widely used in environmental disinfection including hospitals, schools, hotels, and public places.
Concentrated solutions of Vantocil P may cause irritation to the skin and eyes.
Furthermore, Vantocil P has been declared as a candidate for substitution by the ECHA.

While Vantocil P is generally considered safe for use in approved concentrations in various products, it's important to follow product instructions and guidelines.
Concentrations and formulations may vary, and excessive use or exposure can lead to irritation or other adverse effects.
As with any chemical, it's crucial to use products containing Vantocil P responsibly and as directed.

VANTOCIL TG Antimicrobial is effective in a wide range of industrial disinfection applications, primarily as a solid surface disinfectant.
VANTOCIL TG is a cationic disinfectant that is effective against Gram-negative and Gram-positive bacteria through its electrostatic interaction with negative sites on the lipopolysaccharide component of bacterial cell membranes.

CAS Number: 32289-58-0
Molecular Formula: C10H23N5
Molecular Weight: 213.32312
EINECS No: 1308068-626-2

VANTOCIL TG is best known for its broad-spectrum antimicrobial and antifungal activity.
It is the standard of care for treatment of Acanthamoeba keratitis and an ingredient in multipurpose contact lens solutions, such as Renu.

VANTOCIL TG, often abbreviated as VANTOCIL TG HCl, is a specific form of the antimicrobial polymer Poly(hexamethylenebiguanide).
It is a cationic polymer that contains positively charged biguanide groups.

The hydrochloride form refers to the presence of chloride ions associated with the polymer, which contribute to its water solubility and effectiveness as an antimicrobial agent.
VANTOCIL TG Antimicrobial is a broad spectrum, fast acting bactericide for the formulation of disinfectants and sanitisers.
It is a 20% aqueous solution of VANTOCIL TG, also known as PHMB.

VANTOCIL TG Antimicrobial is used in industrial, institutional, agricultural, food, beverage and domestic disinfection applications, primarily as a solid surface disinfectant, specifically for hospitals, veterinary establishments, dairies, milking parlors, breweries, air-conditioning units, and pasteurizers in canned food & beverage bottling plants.

VANTOCIL TG is a polymer composed of repeating units of hexamethylenebiguanide.
Each repeating unit contains positively charged guanidine groups.
VANTOCIL TG antimicrobial in bath wipes for all pets Thai Hygienic, Thailand, recently introduced their 'Spets'™ Bath Tub wipes containing Arch's VANTOCIL TG antimicrobial.

VANTOCIL TG, the active ingredient in VANTOCIL TG antimicrobial range is a fast-acting and broad spectrum bactericide with a wide formulation latitude.
Consequently, by careful selection of appropriate co-formulants, a wide range of professional and domestic products can be formulated which meet the stringent demands of today's disinfection and hygiene industries.

VANTOCIL TG, like other forms of PHMB, exhibits potent antimicrobial properties due to its ability to disrupt microbial cell membranes.
The positively charged biguanide groups interact with negatively charged components of microbial membranes, leading to membrane disruption and cell death.

storage temp.: Inert atmosphere,Room Temperature
solubility: Water
Assay: 97%
Composition: An aqueous solution of PHMB
Active Agent: 20% w/w
Physical Form: Slightly opalescent colourless to pale yellow liquid
Viscosity at 25°C: 5 mPa s.
pH at 25°C: 5.0-6.0
Boiling Point: 102°C
Storage Stability: Stable under normal conditions of storage down to 0°C.
Flash Point: Boils without flashing
Density at 25°C: 1.04

VANTOCIL TG is a kind of cationic surfactant, belonging to nonoxidizing boicide.
It can efficiently withhold algae propagation and sludge reproduction.
VANTOCIL TG also has dispersing and penetrating properties, can penetrate and remove sludge and algae, has advantages of low toxicity, no toxicity accumulation, soluble in water, convenient in use, unaffected by water hardness.

VANTOCIL TG can be also used as anti-mildew agent, antistatic agent, emulsifying agent and amendment agent in woven and dyeing fields.
VANTOCIL TG form enhances its water solubility, making it suitable for various aqueous formulations.
This solubility allows VANTOCIL TG to be easily incorporated into liquids, gels, and other water-based products.

VANTOCIL TG antimicrobial action is based on its interaction with microbial cell membranes.
The positively charged biguanide groups are attracted to the negatively charged components of microbial membranes.
The disruption of cell membranes leads to cell death and prevents microbial growth.

In healthcare settings, VANTOCIL TG products are used for; Disinfection of surfaces, medical equipment, and instruments.
Wound care to prevent infection and promote healing, especially in chronic wounds.

VANTOCIL TG is a common ingredient in personal care products like: Antibacterial soaps and body washes for everyday hygiene.
VANTOCIL TG textiles serve multiple purposes, including: Antimicrobial fabrics in healthcare settings to reduce microbial contamination on textiles.
Odor reduction in sportswear and activewear through inhibition of bacteria causing bad odors.

VANTOCIL TG application in water treatment extends to: Swimming pools and spas, where it controls bacterial and algal growth to maintain water hygiene.

In cosmetic and toiletry products, VANTOCIL TG serves as a preservative by preventing the growth of potentially harmful microorganisms.
This helps extend the shelf life of products and ensures their safety for consumer use.

As with all antimicrobial agents, considerations about VANTOCIL TG's potential impact on the environment are important.
Research and regulatory measures aim to address any potential ecological consequences.

VANTOCIL TG-containing products are subject to regulations and guidelines set by health and safety authorities in various regions.
Proper use and adherence to recommended concentrations are essential to ensure product safety.

Preparation
The preparation method of VANTOCIL TG:By a certain proportion of 1; the own bisguanides of 6-and catalyst join in reaction vessel; under nitrogen protection, said mixture is heated to 80-200 DEGC and reacts, react 2-24 hour; reaction terminates; cooling blowing, obtains poly hexamethylene biguanide, poly hexamethylene biguanide aqueous acid is neutralized to pH value 5-9; and performing filtering so as to obtain a VANTOCIL TG salt.

Uses
VANTOCIL TG is a polymer used as a disinfectant and antiseptic.
In dermatological use, it is spelled polihexanide (INN) and sold under names such as Lavasept, Serasept, Prontosan and Omnicide.
VANTOCIL TG has been shown to be effective against Pseudomonas aeruginosa, Staphylococcus aureus (also the methicillin-resistant type, MRSA), Escherichia coli, Candida albicans (yeast), Aspergillus brasiliensis (mold), vancomycin-resistant enterococci, and Klebsiella pneumoniae (carbapenem-resistant enterobacteriaceae).

VANTOCIL TG is also used as a surface disinfectant and is alleged to be suitable for skin disinfection.
VANTOCIL TG has a slow effectand does not meet the practical requirementsfor prophylactic antiseptics in this respect.
Although VANTOCIL TG is somewhat less effective than benzalkonium chloride, it is sometimes used instead of benzalkonium because it is less foamproducing under use conditions.

VANTOCIL TG is also used to preserve wet wipes; to control odor in textiles; to prevent microbial contamination in wound irrigation, sterile dressings; to deodorize vacuums and toilets; to disinfect medical/dental utensil and trays, farm equipment,
animal drinking water and hard surfaces for food handling institutions and hospitals.

VANTOCIL TG can sometimes be used in combination with other antimicrobial agents to create synergistic effects, enhancing overall antimicrobial activity.
VANTOCIL TG has been explored for use in drug delivery systems, where its antimicrobial properties could be harnessed to prevent infections at the site of drug delivery, such as in medical implants.

VANTOCIL TG has found applications in dental and oral care products, such as mouthwashes and toothpaste, as an antimicrobial agent to maintain oral hygiene.
VANTOCIL TG can be used as a surface disinfectant in the food industry to prevent bacterial contamination on equipment and food contact surfaces.

VANTOCIL TG has been investigated for its potential use in aquaculture to control bacterial infections in fish and shrimp farming.
VANTOCIL TG has been used in veterinary medicine for wound care in animals and to prevent infections in pet care products.

VANTOCIL TG's efficacy against various pathogens and its potential to combat emerging microbial resistance.
The stability of VANTOCIL TG in different formulations and under varying conditions is an important consideration for product development and shelf life.

The use of VANTOCIL TG varies by region and industry due to regulatory standards, consumer preferences, and application-specific requirements.
Proper education and training for professionals using VANTOCIL TG-containing products are important to ensure effective and safe application.

As with any antimicrobial agent, the potential environmental impact of VANTOCIL TG must be carefully considered, and efforts toward sustainable practices should be promoted.
Consumer awareness and perception of antimicrobial agents in products are factors that can influence market adoption and acceptance.

Industry collaboration, research initiatives, and regulatory agencies work together to ensure the responsible use of VANTOCIL TG and its derivatives.
VANTOCIL TG is used for surface disinfection, medical equipment sanitation, and wound care to prevent infections and promote healing.

VANTOCIL TG is found in products like antibacterial soaps, shampoos, body washes, and hand sanitizers for personal hygiene and protection against harmful microorganisms.
VANTOCIL TG is applied to textiles to create antimicrobial fabrics used in healthcare, sportswear, and everyday clothing to reduce microbial growth and odors.

In swimming pools and spas, VANTOCIL TG helps control bacterial and algal growth, maintaining water hygiene.
VANTOCIL TG-based formulations are used in cleaning products for effective antimicrobial cleaning.
VANTOCIL TG serves as a preservative in cosmetics and toiletries, ensuring product safety and extending shelf life.

Health and Safety
The VANTOCIL TG Antimicrobial Safety Data Sheet may be supplied upon request.
VANTOCIL TG should be read and understood by all supervisory personnel and employees before using this product.

On the 20th of April 2018, the european commission decided to ban preservative uses of VANTOCIL TG (Fibre, leather, rubber and polymerised materials preservatives).
VANTOCIL TG’s still allowed for uses as disinfectants PT2 (Disinfectants and algaecides not intended for direct application to humans or animals).
As with all antimicrobial agents, the safe and effective use of VANTOCIL TG relies on adherence to recommended concentrations, guidelines, and regulatory standards.

Synonyms
32289-58-0
polyhexamethylene biguanide hydrochloride
polihexanide hydrochloride
polihexanide HCl
poly(hexamethylenebiguanide) hydrochloride
hexamethylenediamine polymer hydrochloride
Cosmoquil CQ
Cosmocil
PHMB hydrochloride
poly(iminoimidocarbonyl-iminoimidocarbonyl-iminohexamethylene) hydrochloride
Prontosan
poly(hexamethylene) biguanide hydrochloride
Prontoderm
TriGene
Reputex 20
Vantocil 1B
Vantocil TG
Vantosan
PHMB-HCl
CHEBI:149534

pétrolatum, gelée de pétrole, No CAS: 8009-03-8, La vaseline officinale est un médicament ; il s'agit d'une pommade employée comme traitement d'appoint des lésions d'irritation, de brûlure et de sécheresse cutanée. Son utilisation la plus célèbre est la forme utilisée pour le soin des lèvres et pour le traitement de la chéilite ou de la perlèche. En effet, elle est pratiquement inerte à la peau et n'entre dans aucune réaction chimique. Elle favorise la cicatrisation des lésions par sa propriété à ne pas laisser l'eau s'évaporer ni à y entrer comme dans le cas d'une plaie endo-nasale qui est en permanence humide et donc difficilement cicatrisable ou dans le traitement d'une épistaxis. Elle agit comme barrière mécanique contre la pullulation des germes, et la présence de phénols, même à quantité minime, agit comme bactéricide. Elle entre aussi dans la composition de la majorité des lotions en cosmétique, utilisée comme excipient. À cause de ses propriétés moléculaires, la vaseline est utilisée comme écran solaire qui filtre certains ultraviolets.(Keerulise koostisega süsivesinike segu, mis saadakse pooltahke massina parafiinse jääkõli deparafiinimisel. Koosneb peamiselt küllastunud kristalsetest ja vedelatest süsivesinikest, mille süsiniku aatomite arv on valdavalt üle C25.) (et) (Složeni sastav ugljikovodika dobiven kao polukruta tvar kod odvoštavanja parafinskog ostatnog ulja. Sastoji se pretežito od zasićenih kristaličnih i tekućih ugljikovodika koji imaju broj ugljikovih atoma pretežito viši od C25.) (hr) [Kompleks blanding av hydrokarboner dannet som halvfast stoff fra avvoksing av parafinrestolje. Består for det meste av mettede, krystallinske og flytende hydrokarboner hovedsakelig større enn C25.] (no) [Komplekss ogļūdeņražu savienojums, ko iegūst kā biezu masu, atdalot vaskus no parafīnu atlikuma eļļas. Pārsvarā tajā ir piesātināti kristāliski un šķidri ogļūdeņraži, kuros oglekļa atomu skaits galvenokārt ir lielāks nekā C25.] (lv) [Komplexe Kombination von Kohlenwasserstoffen, die als Semifeststoff beim Entwachsen von paraffinhaltigem Rückstandsöl erhalten wird. Besteht vorherrschend aus gesättigten kristallinen und flüssigen Kohlenwasserstoffen mit Kohlenstoffzahlen vorherrschend größer als C25.] (de) [Komplexná zmes uhľovodíkov získavaná v podobe polotuhej látky odvoskovaním alkánového zvyškového oleja. Pozostáva predovšetkým z nasýtených kryštalických a kvapalných uhľovodíkov, s počtom atómov uhlíka prevažne väčším ako C25.] (sk) [O combinaţie complexă de hidrocarburi, obţinuta ca semisolid prin deparafinarea uleiurilor reziduale parafinice. Se compune în principal din hidrocarburi saturate cristaline şi lichide cu număr de atomi de carbon mai mare de C25.] (ro) [Paraffinos maradék olajból viaszmentesítéssel, félig szilárd anyagként előállított, bonyolult összetételű szénhidrogén elegy. Főleg C25 fölötti szénatomszámú, telített, kristályos és folyékony szénhidrogéneket tartalmaz.] (hu) [Složitá směs uhlovodíků získaná jako polotuhá látka z odparafinování zbytkového oleje z parafinické ropy. Je složena převážně z nasycených krystalických a kapalných uhlovodíků s počtem uhlíkových atomů převážně větším než C12.] (cs) [sudėtingas angliavandenilių mišinys, gautas kaip pusiau kieta medžiaga deparafinuojant parafino alyvos likutį. Jo svarbiausi komponentai yra sotieji kristaliniai ir skystieji angliavandeniliai, turintys daugiausiai daugiau negu C25 anglies atomus.] (lt) [Комплексна комбинация от въглеводороди, получена като полутвърдо вещество от депарафинизирането на остатъчен суров парафин. Състои се основно от наситени кристални и течни въглеводороди с брой на въглеродните атоми преобладаващо по-голям от С25.] (bg) Amorfni parafin (hr) Combinación compleja de hidrocarburos obtenidos como un semisólido de la desparafinación del aceite residual paraf��nico. Compuesta fundamentalmente de hidrocarburos saturados líquidos y cristalinos con un número de carbonos en su mayor parte superior a C25. (es) Combinaison complexe d'hydrocarbures obtenue sous forme semi-solide lors du déparaffinage d'huile résiduelle paraffinique. Se compose principalement d'hydrocarbures saturés cristallins et liquides dont le nombre de carbones est en majorité supérieur à C25. (fr) Combinazione complessa di idrocarburi, ottenuta in forma semisolida dalla deparaffinazione di olio residuo paraffinico. AE costituito in prevalenza da indrocarburi liquidi e cristallini saturi con numero di atomi di carbonio prevalentemente superiore a C25. (it) Een complexe verzameling van koolwaterstoffen, verkregen als een halfvaste stof bv het van was ontdoen van paraffinische residu-olie. Het bestaat voornamelvk uit verzadigde kristallvne en vloeibare koolwaterstoffen, overwegend groter dan C25. (nl) En sammensat blanding af carbonhydrider udvundet som et halvfast stof fra afvoksning af paraffinrestolie. Den består overvejende af mættede krystallinske og flydende carbonhydrider, overvejende større end C25. (da) Kompleksna kombinacija poltrdih ogljikovodikov dobljenihpri deparafinizaciji parafinskih rezidualnih olj. Sestavljenaje predvsem iz nasičenih kristalnih in tekočihogljikovodikov, ki imajo število ogljikov pretežno večjekot C25. (sl) Petrolaatum (et) Petrolato (it) Petrolatos (pt) Petrolatum (cs) Petrolátum (hu) pretolato (pt) Pétrolatum (fr) Uma combinação complexa de hidrocarbonetos obtida como um semi-sólido na desparafinagem de óleo residual parafínico. BE constituída predominantemente por hidrocarbonetos saturados cristalinos e líquidos com números de átomos de carbono predominantemente superiores a C25. (pt) vaezlin (sl) Vaseliini (fi) Vaselin (da) Vaselina (es) vazelin (sl) vazelinas (lt) vazelīns (lv) Wazelina (pl) Złożona mieszanina węglowodorów otrzymywana jako substancja półpłynna przez odparafinowanie parafinowego oleju pozostałościowego. Składa się przede wszystkim z nasyconych krystalicznych i ciekłych węglowodorów o liczbie atomów węgla głównie powyżej C25. (pl) Ββαζελίνη (el) Петролатум (bg) Петролатум (вазелин) (bg)

Vantocil IB, also known as PHMB or polihexanide, is a highly water soluble and hydrolytically stable polymeric material.
Vantocil IB is a polymer used as an antiseptic.
The presence of multiple hydrogen bond and chelation sites within Vantocil IB renders it of potential interest in the field of supramolecular chemistry.

CAS Number: 28757-47-3
Molecular Formula: C8H19N5.ClH
Molecular Weight: 221.734
EC Number: 923-111-4

Vantocil IB shows activity against both Gram-positive and Gram-negative bacteria and is widely used across several sectors, typically as the hydrochloride salt, in a variety of disinfectant solutions and antiseptics.
Vantocil IB is available also as a solid.

Vantocil IB is a substance used in industrial, institutional, agricultural, food, beverage and home disinfection applications.
Vantocil IB is a broad spectrum, fast acting bactericide for disinfectant and disinfectant formulation.

Vantocil IB, often abbreviated as PHMB, is a polymer with antimicrobial properties.
It belongs to a class of antimicrobial agents known as biguanides.
Vantocil IB is used in various applications, primarily as a disinfectant, preservative, and biocide.

Vantocil IB has gained attention for its effectiveness against a wide range of microorganisms, including bacteria, viruses, and fungi.
Vantocil IB is composed of repeating units of hexamethylenebiguanide, which is a biguanide compound with multiple guanidine functional groups.

Vantocil IB the specific chemical structure can vary based on the degree of polymerization.
Vantocil IB is a structure that is also found in dermatological use.
Vantocil IB is an effective polymer against some ailments.

Vantocil IB (polyhexamethylene biguanide, PHMB) is a polymer used as a disinfectant and antiseptic.
In dermatological use, it is spelled Vantocil IB (INN) and sold under the names Lavasept, Serasept, Prontosan, and Omnicide.
Vantocil IB has been shown to be effective against Pseudomonas aeruginosa, Staphylococcus aureus, Escherichia coli, Candida albicans, Aspergillus brasiliensis, enterococci, and Klebsiella pneumoniae.

Products containing Vantocil IB are used for inter-operative irrigation, pre- and post-surgery skin and mucous membrane disinfection, post-operative dressings, surgical and non-surgical wound dressings, surgical bath/hydrotherapy, chronic wounds like diabetic foot ulcer and burn wound management, routine antisepsis during minor incisions, catheterization, first aid, surface disinfection, and linen disinfection.

Vantocil IB eye drops have been used as a treatment for eyes affected by Acanthamoeba keratitis.
Stakeholders, including manufacturers, regulators, and consumers, play a role in ensuring the responsible use of Vantocil IB-based products and mitigating potential environmental impact.

Molecular Weight: 185.27
XLogP3-AA: 0.5
Exact Mass: 185.16404563
Monoisotopic Mass: 185.16404563
Topological Polar Surface Area: 103 Ų
Heavy Atom Count: 13
Color: white powder or colorless liquid
Form: liquid
Appearance: Colorless or light-yellow solid
Active ingredient: ≥99%
Water soluble: 100% soluble
Odor: Light ammonia smell
Moisture content: ≤0.5%
Water insoluble matter: ≤0.1%
PH in 1% aqueous solution: >1

Vantocil IB by Arxada is an aqueous solution.
Vantocil IB is a highly effective preservative for use in a wide variety of applications including oil-in-water and water-in-oil emulsions, industrial reagents, silicone systems, cellulose solutions and oil recovery systems.
Can also be used to preserve aqueous-based adhesives (such as animal glues, latex adhesives based on polyvinyl acetate, PVA, starch, dextrin, casein and other glues, and latex adhesives intended for food packaging applications).

Recommended usage level of Vantocil IB is 500-5000 ppm.
Vantocil IB is included in products used for disinfection of skin and mucous membranes before and after surgery.
Vantocil IB is a medically viable compound used for post-operative dressings, surgical and non-surgical wound dressings.

Vantocil IB is an important substance used for chronic wounds such as foot ulcers and burns.
Vantocil IB's antimicrobial activity stems from its ability to disrupt the integrity of microbial cell membranes, leading to cell lysis and death.
It is effective against both gram-positive and gram-negative bacteria, as well as viruses and fungi.

Vantocil IB Antimicrobial is a broad spectrum, fast acting bactericide for the formulation of disinfectants and sanitisers.
Vantocil IB is a 20% aqueous solution of poly (hexamethylene biguanide) hydrochloride (PHMB).
Vantocil IB Antimicrobial is produced for use in industrial, institutional, agricultural, food, beverage, and domestic disinfection applications, primarily as a solid surface disinfectant, specifically for hospitals, veterinary establishments, dairies, milking parlors, breweries, air-conditioning units, and pasteurizers in canned food & beverage bottling plants.

Vantocil IB's antimicrobial activity is broad-spectrum, making it effective against a wide range of microorganisms.
It has a relatively low toxicity profile when used at appropriate concentrations.
Vantocil IB can have a long-lasting effect, providing extended protection against microbial growth.

Vantocil IB's antimicrobial mechanism involves its interaction with microbial cell membranes.
The positively charged guanidine groups in the Vantocil IB molecules are attracted to the negatively charged components of microbial cell membranes.

This interaction disrupts the integrity of the cell membrane, leading to leakage of cellular contents, disruption of cellular processes, and ultimately, cell death.
Vantocil IB has demonstrated efficacy against a broad spectrum of microorganisms, including; Gram-positive and gram-negative bacteria, enveloped and non-enveloped viruses, fungi and yeasts.
This broad-spectrum activity contributes to its usefulness in a variety of applications where protection against multiple types of microorganisms is desired.

In healthcare settings, Vantocil IB-based solutions are used for; surface disinfection in hospitals, clinics, and laboratories, disinfection of medical equipment and devices, wound care and prevention of infection in chronic wounds.
Vantocil IB is available in various formulations, including aqueous solutions, gels, creams, and powders.
These formulations are tailored to specific applications, such as wound care, surface disinfection, and textile treatment.

The concentration of Vantocil IB in products can vary depending on the intended use.
For example, wound care products might have higher concentrations to ensure effective antimicrobial activity, while consumer products may have lower concentrations for skin compatibility.
Vantocil IB's mechanism of action, which targets the cell membrane, is different from many traditional antibiotics.

Vantocil IB unique mode of action makes it less likely to contribute to antibiotic resistance.
Vantocil IB's potential in combating antibiotic-resistant bacteria has attracted attention as a valuable alternative in infection control.
Vantocil IB has been used in wound care products, including dressings, gels, and solutions.

Vantocil IB helps prevent infections in both acute and chronic wounds, promoting healing and reducing the risk of complications.
Vantocil IBs broad-spectrum antimicrobial activity makes it effective against various microorganisms commonly found in wounds.

Vantocil IB-treated textiles have found applications in a range of industries, from healthcare to sportswear.
In healthcare settings, Vantocil IB-treated fabrics contribute to infection control by reducing the risk of bacterial contamination and biofilm formation on textiles used in hospitals and clinics.

Uses
Vantocil IB is an environmental-friendly Cationic Polymer.
Vantocil IB is water soluble and the aqueous solution is colorless and odorless, broad-spectrum, high-efficiency,low toxicity, good stability, non-flammable and non-explosive.
Normally non-corrosive to stainless steel, stainless copper, carbon steel, wood, plastic, etc.

Vantocil IB is a high molecular polymer, which is not easily absorbed by tissues, has no corrosive effect, has good stability and is easy to rinse, good biocompatibility.
Vantocil IB is used in healthcare settings as a disinfectant for surfaces, medical equipment, and wound care products.
Wound dressings containing Vantocil IB are used to prevent infection and promote healing in chronic wounds.

Vantocil IB is found in some personal care products, such as antibacterial soaps, shampoos, and body washes.
Vantocil IB is used as a preservative in cosmetics and toiletries to prevent the growth of harmful microorganisms.
Vantocil IB is used to disinfect surfaces, equipment, and instruments in healthcare facilities to reduce the risk of healthcare-associated infections.

Vantocil IB-containing wound dressings and solutions are used to prevent infections in chronic and acute wounds, promoting healing.
Vantocil IBis found in antibacterial soaps, body washes, and hand sanitizers for personal hygiene.
Vantocil IB serves as a preservative in cosmetics and toiletries, preventing the growth of harmful microorganisms and extending product shelf life.

Vantocil IB-treated textiles, including clothing, bedding, and healthcare fabrics, help control microbial growth, reduce odors, and enhance fabric hygiene.
Sportswear and activewear treated with Vantocil IB resist odor-causing bacteria, making them ideal for athletic activities.

Vantocil IB is used to control bacterial and algal growth in swimming pools and spas, contributing to water hygiene and safety.
Vantocil IB-based formulations are used in cleaning products for surfaces, equipment, and areas where antimicrobial protection is necessary.
Vantocil IB is sometimes used in veterinary settings for wound care and hygiene in animals.

Vantocil IB may be found in various consumer products like household disinfectants, cleaning wipes, and fabric sprays.
Vantocil IB can be incorporated into water-based products to provide antimicrobial properties.
This includes various liquid formulations and aqueous solutions.

Vantocil IB is used as an antimicrobial treatment for textiles, including clothing, bedding, and healthcare fabrics.
It helps prevent the growth of odor-causing bacteria and microbes that can lead to fabric degradation.

Vantocil IB is used in swimming pools, spas, and water treatment systems to control the growth of bacteria and algae.
Vantocil IB-based formulations are used in cleaning products to provide antimicrobial protection on various surfaces.

Safety Considerations:
While Vantocil IB is generally considered safe when used according to guidelines, it's important to follow recommended concentrations and safety precautions to avoid any potential adverse effects.
Vantocil IB is considered safe for various applications when used within recommended concentrations and guidelines.

Vantocil IB has a relatively low potential for causing skin irritation when used as directed.
Regulatory agencies in different regions provide guidelines for the use of Vantocil IB in various applications, ensuring safety for consumers and the environment.

Environmental Considerations:
The environmental impact of Vantocil IB depends on factors such as its persistence, potential for bioaccumulation, and biodegradability.
There have been discussions about its potential environmental consequences, particularly when used in high concentrations or when released into the environment.

Synonyms
polihexanide
28757-47-3
Baquacil
cosmocil
Lavasept
PHMB
PHMB polymer
polihexanide hydrochloride
polyhexamethylenbiguanid
polyhexamethylen-biguanide
polyhexamethylenbiguanide
poly(hexamethylene biguanide)
polyhexamethylene biguanide
Vantocil IB hydrochloride
polyhexamethylene biguanide hydrochloride
Vantocil IB
Poly(iminocarbonimidoyliminocarbonimidoylimino-1,6-hexanediyl)
poly(iminocarbonimidoyliminocarbonimidoylimino-1,6-hexanediyl) hydrochloride
Vantocil
Vantocil IB of Vantocil
C031233

SYNONYMS VARDENAFIL(SUBJECTTOPATENTFREE);VARDENAFILHYDROCHLORIDETRIHYDRATE(SUBJECTTOPATENTFREE);2-(2-Ethoxy-5-(4-ethylpiperazin-1-yl-1-sulfonyl)phenyl)-5-methyl-7-propyl-3H-imidazo(5,1-f)(1,2,4)triazin-4-one;Vardenafil hydrochloride trihydrate 99%;Vardenafil Hydrochloride Trihydrate Cas# 224785-90-4 For Sale;Manufacturers Supply best quality Vardenafil hydrochloride trihydrate 224785-90-4 cas no:224785-90-4

DESCRIPTION:


Varonic K 202 is an ethoxylated amine used in household and I&I cleaners, textile, agriculture, leather, metal working, paint, resin and petroleum.
Varonic K 202 is 2 mole propoxylate of primary coco amine.
Varonic K 202 is an excellent emulsifier and wetting agent.



CAS NUMBER: 68516-06-3



DESCRIPTION:

Varonic K 202 provides alkalinity to formulations.
Varonic K 202 works well in acidic and alkaline formulas.

Varonic K 202 has excellent hard water tolerance, acid and alkaly stability, quat compatibility and tend to inhibit corrosion in some applications.
Due to the presence of Varonic K 202 chains and a positive nitrogen, propoxylated amines show an excellent combination of nonionic and cationic behavior.



USAGE:

-household
-I&I cleaners
-textile
-agriculture
-leather
-metal working
-paint
-resin
-petroleum.



APPLICATION:

-Oil/water emulsifiers
-Dye leveling
-Surface tension reduction
-Anticorrosives
-Latex viscosity agents
-Dispersing agents
-Hard surface cleaner
-Chemical itermediate




PROPERTIES:

-Appearance at 25 C: slight yellow to clear liquid
-Tertiary amine wt. %: 99 min.
-Color: 10 max.
-Water, wt. %: 0.2 max.
-Flash point: > 212
-pH: 9-11
-Density: 0.92




SYNONYM:

Genamin C 050
Genamin C 200
K 215
Kostat P 650/5
Lutensol FA 12K
Lutensol FA 5K
Mazeen C 2
Mazeen C 5
Nissan Nymeen F 215
Noramox C
Noramox C 11
Noramox C 2
Nymeen F 202
Nymeen F 215
Optamine PC 5
PPEM 239
Rhodameen C 5
Rofamin KD 3
Sinopol 412
Surfonic C 2
Variquat 1215
Varonic K 202
Varonic K 205
Varonic K 205LC
Varonic K 209
Varonic K 210
Varonic K 210LC
Varonic K 215
Varonic K 215LC
Witcamine 302
Witcamine 305