Other Industries

Pyridoxine hydrochloride
DISODIUM PYROPHOSPHATE, N° CAS : 7758-16-9 - Pyrophosphate disodique. Origine(s) : Synthétique. Nom INCI : DISODIUM PYROPHOSPHATE. N° EINECS/ELINCS : 231-835-0. Le pyrophosphate disodique se présente sous la forme d'une poudre cristalline blanche. Dans les cosmétiques, on s'en sert d'agent tampon, de chélateur et d'anti-corrosif. Ses fonctions (INCI): Anticorrosif : Empêche la corrosion de l'emballage Régulateur de pH : Stabilise le pH des cosmétiques Agent de chélation : Réagit et forme des complexes avec des ions métalliques qui pourraient affecter la stabilité et / ou l'apparence des produits cosmétiques
PYRİDOXİNE HYDROCHLORİDE
Pyridoxol hydrochloride; Vitamin B6 hydrochloride; Deamine Hydrochloride; 5-Hydroxy-6-methyl-3,4-pyridinedimethanol hydrochloride; Pyridoxinium chloride; Adermine hydrochloride; Hexabione hydrochloride; 2-Methyl-3-hydroxy-4,5-bis(hydroxymethyl)pyridine hydrochloride; 5-Hydroxy-6-methyl-3,4-pyridinedicarbinol hydrochloride; Pyridoxyl hydrochloride; 3-Hydroxy-4,5-dimethylol-a-picoline hydrochloride; Bonasanit; Pyridipea cas no:58-56-0
Pyrogallic Acid
Poly(1-vinylpyrrolidone-co-vinyl acetate); Copovidone; Poly(1-vinylpyrrolidone-co-Vinyl Acetate); Vinyl acetate-vinylpyrrolidone copolymer; PVP/VA Copolymer; Vinyl acetate-vinylpyrrolidinone polymer; Vinylpyrrolidinone-vinyl acetate polymer;
Pyrophosphate disodique
219-574-0 [EINECS]; 2466-09-3 [RN]; Acide diphosphorique [French] [ACD/IUPAC Name]; Diphosphoric acid ; Diphosphorsäure [German] [ACD/IUPAC Name]; hydrogen pyrophosphate; MFCD00011343 [MDL number]; phosphoric anhydride; Pyrophosphic acid; Pyrophosphoric Acid; (phosphonooxy)phosphonic acid [2466-09-3] 03.09.2466 1314-56-3 [RN] 14000-31-8 [RN] 2-(5-Chloro-2-methoxyphenyl)pyrrolidine [ACD/IUPAC Name] 2',3'-Dideoxycytidine 5'-triphosphate 215-236-1 [EINECS] 2'-Deoxyadenosine 5'-triphosphate 33943-49-6 [RN] 3-methylbut-3-enyl trihydrogen diphosphate 69639-93-6 [RN] 7722-88-5 [RN] ADENOSINE-5'-DIPHOSPHATE Adenosine-5'-triphosphate ADP ATP CTP CYTIDINE-5'-TRIPHOSPHATE dCt dimethylallyl diphosphate Diphosphorsaeure DMA DPO DTP IPE MFCD02663458 [MDL number] Oxy-1,1-diphosphonic acid phosphono dihydrogen phosphate Phosphonooxyphosphonic acid Phosphoricanhydride Phosphotex POP PPV Pyrophosphoricacid Pyrophosphorsaeure THYMIDINE-5'-TRIPHOSPHATE TTP μ-oxido-bis(dihydroxidooxidophosphorus) 焦磷酸 [Chinese]
Pyrophosphoric Acid ( Acide diphosphorique)
PYRUVIC ACID, N° CAS : 127-17-3, Nom INCI : PYRUVIC ACID, Nom chimique : Propanoic Acid, 2-oxo, N° EINECS/ELINCS : 204-824-3. Ses fonctions (INCI). Agent masquant : Réduit ou inhibe l'odeur ou le goût de base du produit
Pyrus communis
pyrus communis flower extract; extract of the flowers of the pear, pyrus communis l., rosaceae; european pear flower extract CAS NO:90082-43-2
PYRUVIC ACID
Quartemine; 1-Hexadecanaminium, N,N,N-trimethyl-, chloride cas no: 112-02-7
QUARTAMİN
Yumuşatıcı (%6-10)
Quartemine
Quartemine; 1-Hexadecanaminium, N,N,N-trimethyl-, chloride cas no: 112-02-7
Quartenary Ammonium Compounds
QUARTZ, N° CAS : 14808-60-7 - E551, Nom INCI : QUARTZ, N° EINECS/ELINCS : 238-878-4. Ses fonctions (INCI). Agent Abrasif : Enlève les matières présentes en surface du corps, aide à nettoyer les dents et améliore la brillance.
QUARTZ
Didecyl Dimethyl Ammonium Carbonate; Didecyl Dimethyl Ammonium Bicarbonate; Carboquat™ H;
Quat carbonate
Coco-ethyldimonium ethosulfate; Quaternary ammonium compounds, coco alkyl ethyldimethyl, ethyl sulfates; Cocodimethylammonium diethyl sulfate;Cocodimethylethylammonium ethosulfate; Cocodimethylethylammonium, ethylsulfate; Dimethylcocoethylammonium, ethylsulfate; Ethyldimethylcocoammonium, ethyl sulfate; N,N-Dimethyl-N-ethyl-N-cocoammonium ethylsulfate CAS NO:68308-64-5
Quaternary ammonium ethosulphate
alkyl ethyl benzyl dimethyl ammonium chloride; Dodecyl(ethylbenzyl)dimethylammonium chloride; QUATERNIUM-14, N° CAS : 27479-28-3. Origine(s) : Synthétique. Nom INCI : QUATERNIUM-14. Nom chimique : Dodecyl(ethylbenzyl)dimethylammonium chloride. N° EINECS/ELINCS : 248-486-5, Classification : Ammonium quaternaire. Ses fonctions (INCI). Antimicrobien : Aide à ralentir la croissance de micro-organismes sur la peau et s'oppose au développement des microbes; Antistatique : Réduit l'électricité statique en neutralisant la charge électrique sur une surface; Conditionneur capillaire : Laisse les cheveux faciles à coiffer, souples, doux et brillants et / ou confèrent volume, légèreté et brillance; Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation. Noms français : AMMONIUM, DODECYL(AR-ETHYLBENZYL)DIMETHYL-, CHLORIDE; BENZENEMETHANAMINIUM, N-DODECYL-AR-ETHYL-N,N-DIMETHYL-, CHLORIDE; Chlorure de dodécyldiméthyl(éthylbenzyl)ammonium. Noms anglais : Dodecyldimethyl(ethylbenzyl)ammonium chloride. TETRADECYLDIMETHYL(ETHYLBENZYL)AMMONIUM CHLORIDE; alkyl ethyl benzyl dimethyl ammonium chloride; benzenemethanaminium, N-dodecyl-ar-ethyl-N,N-dimethyl-, chloride; dodecyl (ethyl benzyl) dimethyl ammonium chloride; dodecyl dimethyl ethyl benzyl ammonium chloride; dodecyl dimethyl ethylbenzyl ammonium chloride; dodecyl-[(4-ethylphenyl)methyl]-dimethylazanium chloride; N- dodecyl-ar-ethyl-N,N-dimethylbenzenemethanaminium chloride; dodecyldimethyl(ethylbenzyl)ammonium chloride; quaternary ammonium compounds, C12-14-alkyl[(ethylphenyl)methyl]dimethyl, chloridesUtilisation et sources d'émission: Additif alimentaire, fabrication de cosmétiques. 273-318-2 [EINECS] 68956-79-6 [RN] Benzenemethanaminium, 4-ethyl-N,N-dimethyl-N-tetradecyl-, chloride (1:1) [ACD/Index Name] Chlorure de N-(4-éthylbenzyl)-N,N-diméthyl-1-tétradécanaminium [French] [ACD/IUPAC Name] DIMETHYL ETHYLBENZYL MYRISTYL AMMONIUM CHLORIDE N-(4-Ethylbenzyl)-N,N-dimethyl-1-tetradecanaminium chloride [ACD/IUPAC Name] N-(4-Ethylbenzyl)-N,N-dimethyl-1-tetradecanaminiumchlorid [German] [ACD/IUPAC Name] (4-ethylbenzyl)-dimethyl-myristyl-ammonium chloride (4-ethylbenzyl)-lauryl-dimethyl-ammonium chloride (4-ethylphenyl)methyl-dimethyl-tetradecylammonium chloride (4-ethylphenyl)methyl-dimethyl-tetradecyl-ammonium chloride (4-ethylphenyl)methyl-dimethyl-tetradecylazanium chloride (4-ethylphenyl)methyl-dimethyl-tetradecyl-azanium chloride [(4-ETHYLPHENYL)METHYL]DIMETHYLTETRADECYLAZANIUM CHLORIDE 27479-28-3 [RN] Benzenemethanaminium, N-dodecyl-ar-ethyl-N,N-dimethyl-, chloride Dodecyl dimethyl ethylbenzyl ammonium chloride dodecyl(ethylbenzyl)dimethylammonium chloride dodecyl-[(4-ethylphenyl)methyl]-dimethylammonium chloride dodecyl-[(4-ethylphenyl)methyl]-dimethyl-ammonium chloride dodecyl-[(4-ethylphenyl)methyl]-dimethylazanium chloride dodecyl-[(4-ethylphenyl)methyl]-dimethyl-azanium chloride DODECYLDIMETHYL(ETHYLBENZYL)AMMONIUM CHLORIDE EINECS 248-486-5 N-[(4-Ethylphenyl)methyl]-N,N-dimethyltetradecan-1-aminium chloride N-ALKYL ETHYLBENZYL DIMETHYL AMMONIUM CHLORIDE (C12-C14) N-Dodecyl-ar-ethyl-N,N-dimethylbenzenemethanaminium chloride NOCAS_872364 Quaternary ammonium compounds, C12-18-alkyl[(ethylphenyl)methyl]dimethyl, chlorides QUATERNIUM-14 TETRADECYLDIMETHYL(ETHYLBENZYL)AMMONIUM CHLORIDE alkyl ethyl benzyl dimethyl ammonium chloride benzenemethanaminium, N-dodecyl-ar-ethyl-N,N-dimethyl-, chloride dodecyl (ethyl benzyl) dimethyl ammonium chloride dodecyl dimethyl ethyl benzyl ammonium chloride dodecyl dimethyl ethylbenzyl ammonium chloride dodecyl-[(4-ethylphenyl)methyl]-dimethylazanium chloride N- dodecyl-ar-ethyl-N,N-dimethylbenzenemethanaminium chloride dodecyldimethyl(ethylbenzyl)ammonium chloride quaternary ammonium compounds, C12-14-alkyl[(ethylphenyl)methyl]dimethyl, chlorides
QUATERNIUM-14 ( Dodecyldimethyl(ethylbenzyl)ammonium chloride )
QUATERNIUM-15, N° CAS : 4080-31-3 / 51229-78-8. Origine(s) : Synthétique. Nom INCI : QUATERNIUM-15, Nom chimique : Methenamine 3-chloroallylochloride, N° EINECS/ELINCS : 223-805-0 / 426-020-3. Classification : Ammonium quaternaire, Règlementé, Libérateur de Formaldéhyde, Conservateur. Restriction en Europe : La concentration maximale autorisée dans les préparations cosmétiques prêtes à l'emploi est de 0,2 %. Interdit en Europe à partir du 12 juin 2019. Ses fonctions (INCI): Conservateur : Inhibe le développement des micro-organismes dans les produits cosmétiques.Quaternium-15 (systematic name: hexamethylenetetramine chloroallyl chloride) is a quaternary ammonium salt used as a surfactant and preservative in many cosmetics and industrial substances. It acts as an antimicrobial agent because it acts as a formaldehyde releaser,[2][3] though doing so can also cause contact dermatitis, a symptom of an allergic reaction, especially in those with sensitive skin. Noms français : 1-(3-CHLORO-2-PROPENYL)-3,5,7-TRIAZA-1-AZONIATRICYCLO(3.3.1.1(3,7))DECANE CHLORIDE 1-(3-CHLOROALLYL)-3,5,7-TRIAZA-1-AZONIAADAMANTANE CHLORIDE 3,5,7-TRIAZA-1-AZONIAADAMANTANE, 1-(3-CHLOROALLYL)-, CHLORIDE 3,5,7-TRIAZA-1-AZONIATRICYCLO(3.3.1.1(3,7)DECANE, 1-(3-CHLORO-2-PROPENYL)-, CHLORIDE 3,5,7-TRIAZA-1-AZONIATRICYCLO(3.3.1.13,7)DECANE, 1-(3-CHLORO-2-PROPENYL)-, CHLORIDE 3-Chloroallylochlorure de méthenamine CCTA Chlorure de 1-(3-chloroallyl)-3,5,7-triaza-1-azonia-adamantane Chlorure de N-(chloro-3 allyl) hexaminium Chlorure de N-(chloro-3 allyl) hexaminium (Quaternium 15) N-(3-CHLOROALLYL)HEXAMINIUM CHLORIDE N-(CHLORO-3 ALLYL) HEXAMINIUM, CHLORURE DE Noms anglais :Methenamine 3-chloroallylochloride; Utilisation et sources d'émission : Bactéricide, fabrication de cosmétiques. 1-(3-Chloroallyl)-3,5,7-triaza-1-azoniaadamantane chloride 3,5,7-Triaza-1-azoniaadamantane, 1-(3-chloroallyl)-, chloride 3,5,7-Triaza-1-azoniatricyclo(3.3.1.13,7)decane, 1-(3-chloro-2-propen-1-yl)-, chloride (1:1) 3,5,7-Triaza-1-azoniatricyclo(3.3.1.13,7)decane, 1-(3-chloro-2-propenyl)-, chloride Cinartc 200 Dowco 184 Dowicide Q Dowicil 100 Dowicil 75 Hexamethylenetetramine chloroallyl chloride Methenamine 3-chloroallylochloride N-(3-Chloroallyl)hexaminium chloride Quaternium-15 XD-1840 Translated names 1-(3-chlorallyl)-3,5,7-triaza-1-azoniaadamantan-chlorid (CTAC) (cs) 3-chloroallylochlorure de méthénamine (CTAC) (fr) 3-Cloroalilcloreto de metenamina (CTAC) (pt) 3-Cloroalilocloruro de metenamina (CTAC) (es) 3-cloroallilocloruro di metenamina (CTAC) (it) 3-Kloroalliloklorur tal-metenammina (CTAC) (mt) 3-χλωραλλυλοχλωρίδιο της μεθεναμίνης (CTAC) (el) Chlorek 3-chloroallilometenaminy (CTAC) (pl) Meteenamiin-3-kloroallülokloriid (CTAC) (et) Metenamiini-3-klooriallyylokloridi (CTAC) (fi) Metenamin 3-cloroaliloclorură (CTAC) (ro) Metenamin 3-kloroaliloklorid (CTAC) (hr) Metenamin-3-kloroallylklorid (CTAC) (sv) Metenamino 3-chloralilochloridas (CTAC) (lt) Methenamin-3-chlorallylchlorid (CTAC) (de) methenamin-3-chlorallylochlorid (CTAC) (da) Methenamine 3-chloroallylochloride (CTAC) (no) Methenamine-3-chloorallylchloride (CTAC) (nl) Metén-amin-3-klór-allil-klorid (CTAC) (hu) meténamín-3-chlóralylchlorid (CTAC) (sk) Metēnamīna 3-hloralilhlorīds (CTAC) (lv) Метенаминов 3-хлороалилохлорид (CTAC) (bg) 1-(3-chloroprop-2-en-1-yl)-3,5,7-triaza-1-azoniatricyclo[3.3.1.1~3,7~]decane chloride 3,5,7-Triaza-1-azoniatricyclo[3.3.1.13,7]decane,1-(3-chloro-2-propenyl)-, chloride 3,5,7-Triaza-1-azoniatricyclo[3.3.1.13,7]decane,1-(3-chloro-2-propenyl)-, chloride (9CI) 3,5,7-TRIAZA-1-AZONIATRICYCLODECANE-1-(3-CHLORO-2-PROPENYL)-,CHLORIDE CHLOROALLYLTRIAZAAZONIAADAMANTANE CHLORIDE. 1-(3-Chloro-2-propenyl)-3,5,7-triaza-1-azoniatricyclo[3.3.1.13,7]decane Chloride 1-[(2E)-3-Chlor-2-propen-1-yl]-3,5,7-triaza-1-azoniatricyclo[3.3.1.13,7]decanchlorid [German] [ACD/IUPAC Name] 1-[(2E)-3-Chloro-2-propen-1-yl]-3,5,7-triaza-1-azoniatricyclo[3.3.1.13,7]decane chloride [ACD/IUPAC Name] 1-[(2E)-3-Chloroprop-2-en-1-yl]-3,5,7-triaza-1-azoniatricyclo[3.3.1.13,7]decane chloride 1-[(2E)-3-chloroprop-2-en-1-yl]-3,5,7-triaza-1-azoniatricyclo[3.3.1.13,7]decane chloride 2W5B4VJ152 3,5,7-Triaza-1-azoniaadamantane, 1- (3-chloroallyl)-, chloride 3,5,7-Triaza-1-azoniatricyclo[3.3.1.13,7]decane, 1-[(2E)-3-chloro-2-propen-1-yl]-, chloride (1:1) [ACD/Index Name] 3,5,7-triaza-1-azoniatricyclo[3.3.1.13,7]decane, 1-[(2E)-3-chloro-2-propenyl]-, chloride 3,5,7-Triaza-1-azoniatricyclo[3.3.1.13,7]decane, 1-(3-chloro-2-propenyl)-, chloride 4080-31-3 [RN] Chlorure de 1-[(2E)-3-chloro-2-propén-1-yl]-3,5,7-triaza-1-azoniatricyclo[3.3.1.13,7]décane [French] [ACD/IUPAC Name] Quaternium-15 [Wiki] QUATERNIUM-15 TRANS-FORM 1-(3-Chloroallyl)-1,3,5,7-tetraazaadamantan-1-ium chloride 1-(3-CHLOROALLYL)-3,5,7-TRIAZA-1-AZONIAADAMANTANECHLORIDE 1-(3-Chloroallyl)-3,5,7-triazo-1-azoniaadamantane chloride 3,5,7-Triaza-1-azoniaadamantane, 1-(3-chloroallyl)-, chloride 3,5,7-Triaza-1-azoniatricyclo(3.3.1.13,7)decane, 1-(3-chloro-2-propenyl)-, chloride 51229-78-8 [RN] Chloroallyl methenamine chloride Cinartc 200 DOWICIDE Q Dowicil 100 Dowicil 100[1-(3-chloroallyl)-3,5,7-triazo-1-azoniaadamantane chloride] Dowicil 200 Dowicil 75 Dowicil75 EINECS 223-805-0 Hexamethylenetetramine chloroallyl chloride Methenamine 3-chloroallylochloride N-(3-CHLORALLYL)HEXAMINIUM CHLORIDE N-(3-Chloroallyl)hexaminium chloride quaternium 15
QUATERNIUM-15
QUATERNIUM-16, N° CAS : 64425-88-3 / 35239-12-4, Origine(s) : Synthétique, Nom INCI : QUATERNIUM-16, N° EINECS/ELINCS : 264-890-4 / -. Classification : Ammonium quaternaire: Ses fonctions (INCI). Antistatique : Réduit l'électricité statique en neutralisant la charge électrique sur une surface. Conditionneur capillaire : Laisse les cheveux faciles à coiffer, souples, doux et brillants et / ou confèrent volume, légèreté et brillance. Quaternary ammonium compounds, tris(hydroxyethyl)tallow alkyl, chlorides; 1-Octadecanaminium, N,N,N-tris(2-hydroxyethyl)-, chloride (1:1) [ACD/Index Name] 35239-12-4 [RN] Chlorure de N,N,N-tris(2-hydroxyéthyl)-1-octadécanaminium [French] [ACD/IUPAC Name] N,N,N-Tris(2-hydroxyethyl)-1-octadecanaminium chloride [ACD/IUPAC Name] N,N,N-Tris(2-hydroxyethyl)-1-octadecanaminiumchlorid [German] [ACD/IUPAC Name] QUATERNIUM-16 TRIS(2-HYDROXYETHYL)(OCTADECYL)AZANIUM CHLORIDE
QUATERNIUM-15
Quaternium-15 is also known by other names, such as Dowicil 100, Methenamine 3-chloroallylochloride, and several others listed in the previous response.
Quaternium-15 is commonly used in personal care products such as cosmetics, soaps, and shampoos.
Quaternium-15 releases small amounts of formaldehyde, which can cause skin irritation and allergic reactions in some individuals.

CAS Number: 51229-78-8
Molecular Formula: C9H16Cl2N4
Molecular Weight: 251.16

Synonyms: Quaternium-15, Quaternium-15 trans-form, 4080-31-3, Quaternim-15 trans-form, Methenamine 3-chloroallylochloride, Dowicil 100, UNII-2W5B4VJ152, 194805-30-6, Hexamethylenetetramine chloroallyl chloride, Dowicide Q, Quaternium 15, 2W5B4VJ152, Dowicil 75, Cinartc 200, 1-(3-Chloroallyl)-3,5,7-triaza-1-azoniaadamantane chloride, N-(3-Chloroallyl)hexaminium chloride, Dowco 184, XD-1840, 3,5,7-Triaza-1-azoniatricyclo[3.3.1.13,7]decane, 1-(3-chloro-2-propenyl)-, chloride, Caswell No. 181, CHEBI:59607, UNII-E40U03LEM0, CCRIS 1398, HSDB 6820, 3,5,7-Triaza-1-azoniatricyclo(3.3.1.13,7)decane, 1-(3-chloro-2-propenyl)-, chloride, 1-[(2E)-3-chloroprop-2-en-1-yl]-3,5,7-triaza-1-azoniatricyclo[3.3.1.13,7]decane chloride, EINECS 223-805-0, EPA Pesticide Chemical Code 017901, NSC 172971, E40U03LEM0, 1-(3-chloro-2-propenyl)-3,5,7-triaza-1-azoniatricyclo(3.3.1.13,7)decane chloride, 3,5,7-Triaza-1-azoniaadamantane, 1-(3-chloroallyl)-, chloride, AKOS016009992, n-(3-chloroallyl) hexaminium chloride, LS-13676, EN300-18430961, 3,5,7-triaza-1-azoniatricyclo[3.3.1.13,7]decane, Q27255687, (E)-1-(3-Chloroallyl)-1,3,5,7-tetraazaadamantan-1-ium chloride, 1-(3-chloroprop-2-en-1-yl)-1,3,5,7-tetraazatricyclo[3.3.1.1,3,7]decan-1-ium chloride, 1-[3-chloroprop-2-en-1-yl]-3,5,7-triaza-1-azoniatricyclo[3.3.1.1(3),(7)]decanium chloride, 3,5,7-TRIAZA-1-AZONIATRICYCLO(3.3.1.13,7)DECANE, 1-((2E)-3-CHLORO-2-PROPEN-1-YL)-, CHLORIDE (1:1), 3,5,7-Triaza-1-azoniatricyclo(3.3.1.13,7)decane, 1-(3-chloro-2-propen-1-yl)-, chloride (1:1)

Quaternium-15 has been banned in the EU since 2017 and a bill was introduced in the US in 2017 to require the FDA to investigate its safety.
Its use is regulated in many countries due to its potential health effects, and there are restrictions on the maximum allowable concentration in cosmetic products.
Quaternium-15 commonly found in shampoos, conditioners, lotions, creams, and makeup products.

Quaternium-15 is an allergen, and can cause dermatitis.
Many of those with an allergy to quaternium-15 are also allergic to formaldehyde.
At low pHs, Quaternium-15 would be expected to release significant amounts of formaldehyde due to acid hydrolysis via the Delepine reaction.

Allergic sensitivity to quaternium-15 can be detected using a patch test.
Quaternium-15 is the single most often found cause of allergic contact dermatitis of the hands (16.5% in 959 cases).
In 2005–06, Quaternium-15 was the fourth-most-prevalent allergen in patch tests (10.3%).

Although quaternium-15 releases low amounts of formaldehyde.
Even so, Johnson & Johnson announced plans to phase out its use of quaternium-15 in cosmetic products by 2015 in response to consumer pressure.
Quaternium-15, a known skin toxicant and allergen, may be especially dangerous for hairdressers and janitors, who are sometimes exposed to this formaldehyde-releasing
chemical at regular doses for long periods of time.

Quaternium-15 refers to any polymer that has been modified by a process called quaternization.
This process results in changes to molecules that improve the performance of body care products.
Quaternium-15 may also be referred to as quaternary ammonium compounds (QACs) or simply quats.

Quaternium-15 is a known human skin toxicant and allergen and possible eye irritant.
Quaternium-15 is also a formaldehyde-releasing preservative.
Quaternium-15 is often the culprit of skin irritation and allergic reactions.

Quaternium-15 is used in many cosmetics and pharmaceutical preparations.
Quaternium-15 is also used as a preservative in many commercial and industrial products. The table below shows some of the products that may contain quaternium-15.
Hair conditioners, hair styling products, creams, lotions, cleansers, shaving products, eye drops contact solutions and household cleaning products.

Benzalkonium chloride, Quaternium-15, quaternium-15, centrimonium bromide, polyquaternium – followed by a number (i.e. polyquaternium-7).
Polyquaternium refers to any polymer that has been modified by a process called quaternization.
This process results in changes to molecules that improve the performance of body care products.

Polyquaternium may also be referred to as quaternary ammonium compounds (QACs) or simply quats.
Quaternium-15 is an odorless, colorless, water-soluble, antimicrobial agent that is active against bacteria more so than yeast and molds.
Quaternium-15 is a quaternary ammonium salt used as a surfactant and preservative in many products including cosmetics.

Quaternium-15 is an anti-microbial agent by virtue of being a formaldehyde releaser, however this can also cause contact dermatitis, a symptom of an allergic reaction, especially in those with sensitive skin.
In 2005, Quaternium-15 was named in the top 15 most frequently positive allergens identified in patch tests by the North American Contact Dermatitis Group (NACDG).
Sensitivity to Quaternium-15 may be identified with a clinical patch test.

Quaternium-15 is commonly used in personal care products such as cosmetics, soaps, and shampoos.
Quaternium-15 also is found in industrial polishes, waxes, inks, paints, and metal working fluids.
Quaternium-15 belongs to a group of preservatives known as formaldehyde-releasing agents

Quaternium-15 is a quaternary ammonium salt prepared by reaction of hexamethylenetetramine and 1,3-dichloropropene.
Quaternium-15 is a cream-colored powder with a pungent odor.
In addition to its use in cosmetic products, it is also used in the formulation of metal cutting fluids, paints, adhesives, and glues.

Quaternium-15 tension between two components of the product like two liquids or a liquid and a solid.
Lower the surface tension, better mixing capability of that particular ingredient.
Quaternium-15 contains a water-loving end and fat-loving core in a single molecule.

Quaternium-15 attracts dirt, oil, and other impurities accumulated on the surface of the skin with an oil-loving end which then can be washed off easily with water via a water-loving end.
Quaternium-15 also possesses anti-microbial properties.
Quaternium-15 kills the microorganism and stops them from coming back by stopping reproduction.

Quaternium-15 inhibits the growth of molds and fungus in cosmetic products.
Quaternium-15 is also used as an anti-static agent.
Quaternium-15 prevents the build of static charge in the product because of its special chemical structure.

Quaternium-15 is used in formulations of creams, lotions, gels, make-up products, shampoos, baby products, and other skin and hair care products.
Quaternium-15 is a preservative found in a variety of cosmetics, topical pharmaceutical preparations, and industrial substances.
As a preservative, it has activity against bacteria, fungi, and molds.

Quaternium-15 is most frequently found in hair-care products such as conditioners, rinses, and shampoos as well as several popular moisturizing lotions and a number of cosmetic products.
Quaternium-15 is commonly used in personal care products such as cosmetics, soaps, and shampoos.
Quaternium-15 also is found in industrial polishes, waxes, inks, paints, and metal working fluids.

Quaternium-15 belongs to a group of preservatives known as formaldehyde-releasing agents.
Quaternium-15 is a quaternary ammonium salt derived from hexamethylenetetramine; used as a preservative in many cosmetics and industrial substances.
Also acts as a disinfectant and allergenic agent.

Quaternium-15 has a role as a disinfectant and an antibacterial agent.
Quaternium-15 is a quaternary ammonium salt and an organochlorine compound.
Quaternium-15 uses and applications include: Antimicrobial, preservative in adhesives, latex emulsions, paints, cutting fluids, topical pharmaceuticals; preservative in cosmetics, food packaging adhesives, food-contact PU resins; preservative for pigment slurries and latexes used as pigment binders in food-contact paperpaperboard

Quaternium-15 works by releasing formaldehyde, a potent antimicrobial agent.
The formaldehyde released can penetrate the cell walls of microorganisms and disrupt their function, effectively killing them or inhibiting their growth.
Quaternium-15 found in a variety of products including moisturizers, foundations, sunscreens, shampoos, conditioners, and hair dyes.

Quaternium-15 is used in cleaning products and industrial formulations to prevent microbial contamination.
Helps in maintaining the shelf life and efficacy of these products by preventing microbial growth.
Quaternium-15 is known to release formaldehyde, which can cause allergic reactions, contact dermatitis, and other skin irritations.

Due to these health concerns, its use is regulated.
Different regions have set limits on the permissible concentration of Quaternium-15 in products.
The European Union has set a maximum concentration limit of 0.2% in cosmetic products.

The United States Food and Drug Administration (FDA) also monitors its use, but does not have specific concentration limits.
Products containing Quaternium-15 must be labeled appropriately to inform consumers of its presence.
Evidence presented in animal and human studies show that other quaternary ammonium compounds may lead to contact dermatitis.

Quaternium-15 use of products containing quats may contribute significantly to cases of contact dermatitis.
Studies estimate 13 percent[4] to 34 percent of contact dermatitis cases may be linked to quats.
Concentrated solutions of quats may cause burns to the skin as well.

In rare cases, quat use may elicit more severe health symptoms.
Quaternium-15 a study performed on hairdressers, who are routinely exposed to quaternary ammonium compounds in hair products found hairdressers had almost five times as many antibodies to quats.
Increased levels of this antibody relate to an increased risk of allergic reactions to anesthesia, a serious concern since allergic reactions to anesthesia can lead to life-threatening reactions.

A case study reported that a woman suffered from cutaneous cell death after applying a quat-containing antiseptic.
Yet another case study described a man with a pre-existing skin condition who developed dermatitis due to a quaternary ammonium Quaternium-15 in his deodorant, suggesting that quats have the potential to induce sensitivity, especially on damaged skin.
Quaternium-15 is a quaternary ammonium salt used as a surfactant and preservative in many cosmetics and industrial substances.

Quaternium-15 acts as an antimicrobial agent because it acts as a formaldehyde releaser, though doing so can also cause contact dermatitis, a symptom of an allergic reaction, especially in those with sensitive skin.
Quaternium-15 can be found under a variety of names, most commonly those of the Dow Chemical Company: Dowicil 200 (cis isomer only), Dowicil 75 and Dowicil 100 (both a mix of cis and trans isomers).
Quaternium-15 can be prepared by reacting hexamethylenetetramine with 1,3-dichloropropene to produce the product as a mixture of cis and trans isomers.

The isolated cis-Quaternium-15 is used primarily in cosmetic applications, with a maximum permitted concentration in the EU of 0.2%.
The mixed product (cis- and trans-) is used in a wider range of formulations such as: emulsifiable metal-cutting fluids; latex and emulsion paints; liquid floor polishes and floor waxes; glues and adhesives.
Quaternium-15 is a formaldehyde-releasing preservative.

Quaternium-15 also is found in industrial polishes, waxes, inks, paints, and metal working fluids.
Quaternium-15 belongs to a group of preservatives known as formaldehyde-releasing agents.
It is a derivative of hexamethylenetetramine chloroallyl chloride.

Quaternium-15 acts as an antimicrobial agent because it slowly releases formaldehyde, which is a preservative with biocidal properties.
Both quaternium-15 and formaldehyde release agents have been the subjects of controversy.
They are often banned in US and Europe.

Quaternium-15 can be found under a variety of names, including Dow Chemical Company: Dowicil 200 (cis isomer only), Dowicil 75 and Dowicil 100 (both a mix of cis and trans isomers).
Quaternium-15 can be prepared by treating hexamethylenetetramine with 1,3-dichloropropene.
A mixture of cis and trans isomers are produced.

Quaternium-15 is a quaternary ammonium compound used as a preservative in many cosmetics and personal care products.
Quaternium-15 functions by releasing formaldehyde, which acts as an antimicrobial agent, helping to prevent the growth of bacteria, fungi, and other microorganisms in the products.
Quaternium-15 is a quaternary ammonium salt that has been used as a surfactant and preservative.

storage temp.: under inert gas (nitrogen or Argon) at 2-8°C
solubility: DMSO (Slightly), Methanol (Slightly)
form: Solid
color: White to Pale Yellow
Stability: Stable, but moisture sensitive. Incompatible with strong oxidizing agents.
InChI: InChI=1S/C9H16ClN4.ClH/c10-2-1-3-14-7-11-4-12(8-14)6-13(5-11)9-14;/h1-2H,3-9H2;1H/q+1;/p-1/b2-1-;
InChIKey: UKHVLWKBNNSRRR-ODZAUARKSA-M
SMILES: [N+]12(C/C=C\Cl)CN3CN(CN(C3)C1)C2.[Cl-]

Quaternium-15 belongs to a group of preservatives known as formaldehydereleasing agents.
Quaternium-15 is a cream colored powder with a pungent odor.
1-(cis-3-Chloroallyl)-3,5,7-triaza-1-azoniaadamantane chloride, also known as quaternium-15, is used as a preservative in some cosmetics and other industrial products.

Quaternium-15 is included in cosmetic formulations as an antimicrobial agent.
Quaternium-15 is used as a preservative in adhesives and food packaging materials and is regulated by the FDA as an indirect food additive.
Quaternium-15 is also utilized as an antimicrobial agent in water-based metalworking fluids.

Quaternium-15 is a preservative found in many cosmetics and industrial substances that releases formaldehyde.
Quaternium-15 can be found in numerous sources, including but not limited to: mascara, eyeliner, moisturizer, lotion, shampoo, conditioner, nail polish, personal lubricants, soaps, body wash, baby lotion or shampoo, facial cleanser, tanning oil, self-tanning cream, sunscreen, powder, shaving products, ointments, personal wipes or cleansers, wipes, paper, inks, paints, polishes, waxes and industrial lubricants.

Quaternium-15 can cause contact dermatitis, a symptom of an allergic reaction, especially in those with sensitive skin, on an infant's skin, or on sensitive areas such as the genitals.
Quaternium-15s chemical formula is C9H16Cl2N4.
Quaternium-15 can be found under a variety of names, including: Dowicil 75; Dowicil 100; Dowco 184; Dowicide Q; 1-(3-Chloroallyl)-3,5,7-triaza-1-azoniaadamantane chloride; N-(3-chloroallyl) hexaminium chloride; hexamethylenetetramine chloroallyl chloride; 3,5,7-Triaza-1-azoniaadamantane; 1-(3-chloroallyl)-chloride.

Quaternium-15s CAS number is and its SMILES structure is ClC=C/C[N+]23CN1CN(C3)CN(C2)C1.[Cl-].
Quaternium-15 doesn't occur naturally in the environment.
Quaternium-15 may be used in some self-care products (cosmetics, natural health products, over-the-counter drugs), cleaning products, paints and coatings.

Quaternium-15 's also used in the automotive, aircraft and transportation industry.
Quaternium-15 is a formaldehyde releasing preservative used in personal care products usually cosmetics.
Quaternium-15 is also used as a biocide in household and industrial products.

Quaternium-15 is found in many cosmetics, shampoos and skin care products, as well as in household and industrial products.
Examples of cosmetic products and toiletries are lotions, creams, moisturizers, emollients, foundations, powders, concealers, bronzers, self-tanners, makeup removers, blushes, eye shadows, eyeliners, eyebrow makeup and mascaras and sunscreens as well as shampoos, soaps etc. Adhesives, paper, paperboard, inks, polishes and latex paints may contain Quaternium-15.
Industrial cutting fluid may contain Quaternium-15 as a preservative.

Formaldehyde-releasing preservative used in cosmetics.
Quaternium-15 can aggravate skin, as can all preservatives, although quaternium-15’s ability to do so is very low if the amount in a product is less than 0.2%.
Quaternium-15 is a quaternary ammonium salt used as a surfactant and preservative in many products including cosmetics.

Helps slow the growth of microorganisms on the skin and opposes the growth of microbes
Inhibits the development of microorganisms in cosmetic products.
Quaternium-15 is a broad-spectrum preservative found in many cosmetics and personal care products.

Quaternium-15 is one of the formaldehyde-releasing preservatives that include imidazolidinyl urea, diazolidinyl urea, 2-bromo-2- nitropropane-l,3-diol, DMDM (dimethylolmethyl)hydantoin, and tris (hydroxymethyl) nitromethane.
Although quaternium-l 5 does release small amounts of formaldehyde, not all patients who are allergic to quaternium-15 are allergic to formaldehyde and vice versa.
Quaternium-15 can cause contact dermatitis, a symptom of an allergic reaction, especially in those with sensitive skin, on an infant's skin, or on sensitive areas such as the genitals.

Quaternium-15 releases formaldehyde therefore, repeated use products containing quaternium-15 may cause contact dermatitis.
Can cause skin sensitization leading to allergic contact dermatitis, particularly in individuals with formaldehyde sensitivity.
Inhalation of vapors or dusts containing formaldehyde can cause respiratory irritation and other issues.

Formaldehyde is classified as a human carcinogen by several health organizations, including the International Agency for Research on Cancer (IARC).
Quaternium-15 is not readily biodegradable, and its persistence in the environment can contribute to pollution.
Toxic to aquatic organisms, which can have detrimental effects on aquatic ecosystems.

Due to health and environmental concerns, there is a growing trend to replace Quaternium-15 with safer preservatives.
Quaternium-15 is a commonly used in personal care products such as cosmetics, soaps and shampoos.
Quaternium-15 is readily soluble in water and practically insoluble in mineral oil.

Uses:
Quaternium-15 is used as an antimicrobial preservative in cosmetic, soaps and shampoos. International restrictions 0.1 to 1% - other use; surfactant, hair conditioning, adhesives, binding, lacquers and varnishes.
Commerical use; cutting fluids, lubricants, hydraulic fluids, additives, cleaning, pesticides, bacteriasides, food additives, paper, pharmaceuticals (antiarrhythmic and anticonvulsant agents).

Quaternium-15 is a quaternary ammonium salt derived from hexamethylenetetramine; used as a preservative in many cosmetics and industrial substances. Also acts as a disinfectant and allergenic agent.
Quaternium-15 has a role as a disinfectant, an antibacterial agent, a hapten and an allergen.
Quaternium-15 found in baby shampoos and lotions, although its use in baby products is increasingly scrutinized due to potential sensitization risks.

Included in various household cleaners to prevent bacterial and fungal growth.
Quaternium-15 helps preserve the formulation and effectiveness of the detergent.
Quaternium-15 prevents microbial growth in the product, ensuring it remains effective over time.

Quaternium-15 is used in formulations to enhance antimicrobial efficacy.
Quaternium-15 is used as a preservative to prevent the growth of microbes that can degrade the product.
Prevents microbial contamination, ensuring the adhesive maintains its properties and effectiveness.

Helps preserve the fluid and prevent microbial growth that can cause spoilage and degradation.
Prevents microbial contamination that can affect performance.
Quaternium-15 is used to treat fabrics to prevent microbial growth and odors, enhancing the durability and freshness of the textiles.

Added to paper products to prevent microbial degradation and extend shelf life.
Quaternium-15 is used in formulations to prevent the growth of mold, mildew, and other microorganisms that can damage wood products.
Helps preserve leather products by preventing microbial growth that can cause deterioration.

Quaternium-15 is used as a preservative in some topical pharmaceutical formulations to maintain sterility and efficacy.
Added to food packaging materials to prevent microbial contamination and extend the shelf life of packaged foods.
Quaternium-15 is a quaternary ammonium salt and an organochlorine compound.

Quaternium-15 derives from a hexamethylenetetramine.
Quaternium-15 is an antimicrobial agent used in cosmetics as a cosmetic preservative and antistatic agent.
Formaldehyde-releasing preservative in hand creams, lotions, face creams, shampoos, latex paints, topical medicaments, polishes, metal working fluids, adhesives, inks, etc

Quaternium-15 is used as a preservative and antistatic agent in cosmetics.
Quaternium-15 can be found in a wide variety of products, including eye shadows, foundations, facial powders, body washes, mascaras, shampoos, conditioner, hair colors, facial cleansers, bronzers and nail treatments.
Quaternium-15 is a quaternary ammonium salt used as a preservative in many cosmetics and industrial substances.

Quaternium-15 acts as a formaldehyde releaser.
Quaternium-15 can cause contact dermatitis in sensitive individuals.

Quaternium-15's toxicity is also due to it's ability to react and release formaldehyde and nitrosamines, both of which are believed to be carcinogenic.
Quanternium-15 is a type of preservative which is widely used in many cosmetic and industrial products.

Quaternium-15 may be used as a formaldehyde releaser to investigate the influence of formaldehyde in dermatitis patients with or without contact allergy to formaldehyde through baseline patch test series.
Quaternium-15 is used to preserve water-based formulations against microbial contamination.
Ensures product stability and prevents the growth of bacteria and fungi.

Maintains product efficacy and extends shelf life by preventing microbial growth.
Found in nail polishes and treatments to keep formulations free from microbial contamination.
Quaternium-15 is used in some mouthwashes and toothpastes to prevent bacterial growth, though less common due to oral sensitivity concerns.

Ensures the longevity and effectiveness of cleaning products used on various surfaces.
Preserves the formula to prevent spoilage and maintain cleaning efficacy.
Helps in maintaining the integrity of liquid air fresheners by preventing microbial growth.

Occasionally used in formulations to provide antimicrobial properties.
Quaternium-15 is used in drilling fluids and other formulations to prevent bacterial contamination that can lead to corrosion and other issues.
Found in certain pesticides and fungicides to prevent microbial contamination and enhance stability.

Incorporated into textiles to prevent the growth of odor-causing bacteria and extend the freshness of fabrics used in sportswear, medical garments, and home textiles.
Quaternium-15 is used in the finishing process of textiles to impart antimicrobial properties.
Ensures the integrity of paper-based packaging by preventing microbial growth.

Quaternium-15 is used in the production of specialty papers that require antimicrobial properties, such as medical-grade papers and currency papers.
Applied to wood used in construction to prevent mold and mildew growth, thereby extending the life and durability of the materials.
Used in the preservation of wood furniture to prevent microbial damage and maintain appearance and structural integrity.

Quaternium-15 is used during the tanning process to preserve leather and prevent microbial degradation.
Helps maintain the quality of finished leather goods, including shoes, bags, and jackets, by preventing mold and mildew.
Occasionally used in eye drops to prevent microbial contamination, though alternatives are preferred due to sensitivity concerns.

Used in some topical medications to maintain sterility and efficacy over time.
Quaternium-15 is used in the production of antimicrobial films for food packaging to extend the shelf life of perishable goods by preventing microbial contamination.
Added to plastic and other materials used for food storage to prevent the growth of bacteria and fungi.

Quaternium-15 is used in certain inks and dyes to prevent microbial growth that can affect the quality and consistency of the products.
Helps maintain the integrity of sealants and caulks by preventing microbial degradation.
Found in some automotive cleaning and maintenance products to preserve formulations and prevent microbial growth.

Quaternium-15 is used in cleaning products for electronics to prevent microbial contamination and ensure product efficacy.
Quaternium-15 is a formaldehyde-releasing preservative in hand creams, lotions, face creams, shampoos, latex paints, topical medicaments, polishes, metal-working fluids, adhesives, inks, etc.; quatemium-15.
Prevents microbial contamination and extends the shelf life.

Quaternium-15 acts as a preservative to prevent the growth of bacteria and fungi.
Found in foundations, powders, and eyeliners to maintain product integrity.
Quaternium-15 is used to preserve formulations against microbial growth.

Quaternium-15 is used in a wide variety of cosmetic products as a surfactant and preservative.
As a surfactant, Quaternium-15 lowers the surface.
Quaternium-15 may be used as a formaldehyde releaser to investigate the influence of formaldehyde in dermatitis patients with or without contact allergy to formaldehyde through baseline patch test series.

Quaternium-15 is a quaternary ammonium salt used as a preservative in many cosmetics and industrial substances.
Quaternium-15 acts as a formaldehyde releaser.
Preservative in cosmetics, hair care products, soaps, adhesives.

Safety Profile:
Prolonged exposure to products containing Quaternium-15 can lead to skin irritation, even in individuals who are not formally allergic.
This can manifest as dryness, itching, and rash.
Inhalation of vapors or dust containing Quaternium-15 can irritate the respiratory tract, leading to symptoms such as coughing, sneezing, and throat irritation.

People with asthma or other respiratory conditions may experience exacerbated symptoms upon exposure.
Quaternium-15 can cause allergic contact dermatitis in sensitive individuals.

Symptoms include redness, itching, and inflammation of the skin.
People sensitive to formaldehyde may experience more severe reactions, including hives and blistering.

QUATERNIUM-16
QUATERNIUM-18, N° CAS : 61789-80-8, Origine(s) : Synthétique. Nom INCI : QUATERNIUM-18, N° EINECS/ELINCS : 263-090-2. Classification : Ammonium quaternaire, Libérateur de Formaldéhyde. Ses fonctions (INCI) : Antistatique : Réduit l'électricité statique en neutralisant la charge électrique sur une surface. Conditionneur capillaire : Laisse les cheveux faciles à coiffer, souples, doux et brillants et / ou confèrent volume, légèreté et brillance. Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation. Noms français : DIHYDROGENATEDTALLOW DIMETHYL AMMONIUM CHLORIDE; N,N-DIHYDROGENATEDTALLOW N,N-DIMETHYL AMMONIUM CHLORIDE Noms anglais : BIS(HYDROGENATED TALLOW)DIMETHYLAMMONIUM CHLORIDE; QUATERNARY AMMONIUM COMPOUNDS, BIS(HYDROGENATED TALLOW ALKYL)DIMETHYL, CHLORIDES. Quaternary ammonium compounds, bis(hydrogenated tallow alkyl)dimethyl, chlorides; bis(hydrogenated tallow alkil)dimethyl, chlorides; Bis(hydrogenated tallow alkyl)dimethylammonium chlorides; Distearyldimethylammonium chloride; N,N-Dimethyl-N,N-di-n-alkyl(C16-18)-ammoniumchloride; Quaternary ammonium compounds, bis(hydrogenated tallow alkyl)dimethyl chlorides. 107-64-2 [RN] 1-Octadecanaminium, N,N-dimethyl-N-octadecyl-, chloride (1:1) [ACD/Index Name] 203-508-2 [EINECS] Aliquat 207 Ammonium, dimethyldioctadecyl-, chloride BQ1923000 Chlorure de N,N-diméthyl-N-octadécyl-1-octadécanaminium [French] [ACD/IUPAC Name] Dimethyl dioctadecyl ammonium chloride DIMETHYL DIOCTADECYLAMMONIUM CHLORIDE Dimethyldioctadecylammonium chloride [Wiki] Dimethyldistearylammonium Chloride Di-n-octadecyldimethylammonium chloride dioctadecyl dimethyl ammonium chloride dioctadecyldimethylammonium chloride Distearyl dimethylammonium chloride DISTEARYLDIMETHYLAMMONIUM CHLORIDE Distearyldimonium chloride DODAC MFCD00055540 [MDL number] N,N-Dimethyl-N-octadecyl-1-octadecanaminium chloride [ACD/IUPAC Name] N,N-Dimethyl-N-octadecyl-1-octadecanaminiumchlorid [German] [ACD/IUPAC Name] N,N-Dimethyl-N-octadecyloctadecan-1-aminium chloride OM9573ZX3X [107-64-2] 12677-13-3 [RN] 129119-79-5 [RN] 134191-39-2 [RN] 14357-21-2 [RN] 1-Octadecanaminium, N,N-dimethyl-N-octadecyl-, chloride 263-090-2 [EINECS] 59111-82-9 [RN] 61789-80-8 [RN] 66359-86-2 [RN] 76723-98-3 [RN] Adogen TA 100 Ammonyx 2200P100 Arosurf TA 100 Arosurf TA-100 Arquad 218-100 Arquad 218-100P Arquad R 40 Cation DS Cedequat TD 75 Dehyquart DAM Dimethyl distearylammonium chloride dimethyl(dioctadecyl)azanium and chloride Dimethyldi-n-octadecylammonium chloride dimethyldioctadecylamine, chloride dimethyl-dioctadecylammonium chloride dimethyl-dioctadecyl-ammonium chloride dimethyldioctadecylammoniumchloride dimethyl-dioctadecylazanium chloride dimethyl-dioctadecyl-azanium chloride DIMETHYLDIOCTADECYLAZANIUM CHLORIDE dimethyl-distearyl-ammonium chloride Dioctadecyldimethylammoniumchloride Distearyl dimethyl ammonium chloride DODA(Cl) EINECS 203-508-2 Genamin DSAC Jsp000681 Kemamine Q 9702CLP N,N-dimethyl-dioctadecyl ammonium chloride N,N-Dimethyl-N-octadecyl-1-octadecanaminiumchloride N,N-Dioctadecyl-N,N-dimethylammonium chloride Q-D 86P Quartamin D 86 Quartamin DM 86P Quaternium 5 QUATERNIUM-18 Quaternium-5 Sokalan 9200 Surfroyal DSAC Talofloc Varisoft 100 Varisoft TA 100
QUATERNIUM-18
QUATERNIUM-22, N° CAS : 51812-80-7 / 82970-95-4. Origine(s) : Synthétique. Nom INCI : QUATERNIUM-22. Nom chimique : 3-(D-Gluconoylamino)propyl(2-hydroxyethyl)dimethylammonium chloride. N° EINECS/ELINCS : 257-440-3. Classification : Ammonium quaternaire. Ses fonctions (INCI) : Antistatique : Réduit l'électricité statique en neutralisant la charge électrique sur une surface, Agent filmogène : Produit un film continu sur la peau, les cheveux ou les ongles. Conditionneur capillaire : Laisse les cheveux faciles à coiffer, souples, doux et brillants et / ou confèrent volume, légèreté et brillance. -(D-gluconoylamino)propyl(2-hydroxyethyl)dimethylammonium chloride; (2-hydroxyethyl)dimethyl{3-[(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanamido]propyl}azanium chloride; 1-Propanaminium, 3-(D-gluconoylamino)-N-(2-hydroxyethyl)-N,N-dimethyl-, chloride; CERAPHYL® 60 (ca. 60% substance in water). Jump to main contentJump to site nav Home About us Web APIs Help Sign in ChemSpider Search and share chemistry Search ChemSpider For medical information relating to Covid-19, please consult the World Health Organisation or local healthcare provision. Simple Structure Advanced History Found 1 result Search term: 51812-80-7 (Found by approved synonym) COMMENT ON THIS RECORD ChemSpider 2D Image | QUATERNIUM-22 | C13H29ClN2O7Save3DZoom QUATERNIUM-22 Molecular FormulaC13H29ClN2O7 Average mass360.832 Da Monoisotopic mass360.166321 Da ChemSpider ID36681 defined stereocentres - 4 of 4 defined stereocentres More details: This record has not been tagged. TAG Names Properties Searches Spectra Vendors Articles More Names and SynonymsDatabase ID(s) Validated by Experts, Validated by Users, Non-Validated, Removed by Users 257-440-3 [EINECS] 51812-80-7 [RN] Chlorure de N-(2-hydroxyéthyl)-N,N-diméthyl-3-{[(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanoyl]amino}-1-propanaminium [French] [ACD/IUPAC Name] Chlorure de N-(2-hydroxyéthyl)-N,N-diméthyl-3-{[(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanoyl]amino}-1-propanaminium (non-preferred name) [French] [ACD/IUPAC Name] N-(2-Hydroxyethyl)-N,N-dimethyl-3-{[(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanoyl]amino}-1-propanaminium chloride [ACD/IUPAC Name] N-(2-Hydroxyethyl)-N,N-dimethyl-3-{[(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanoyl]amino}-1-propanaminium chloride (non-preferred name) [ACD/IUPAC Name] N-(2-Hydroxyethyl)-N,N-dimethyl-3-{[(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanoyl]amino}-1-propanaminiumchlorid [German] [ACD/IUPAC Name] N-(2-Hydroxyethyl)-N,N-dimethyl-3-{[(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanoyl]amino}-1-propanaminiumchlorid (non-preferred name) [German] [ACD/IUPAC Name] QUATERNIUM-22 (2-HYDROXYETHYL)DIMETHYL{3-[(2R,3S,4R,5R)-2,3,4,5,6-PENTAHYDROXYHEXANAMIDO]PROPYL}AZANIUM CHLORIDE (α-Gluconamidopropyl)dimethyl-2-hydroxyethylammonium chloride [51812-80-7] 149358-34-9 [RN] 1-Propanaminium, 3-(D-gluconoylamino)-N-(2-hydroxyethyl)-N,N-dimethyl-, chloride 3-(D-Gluconoylamino)-N-(2-hydroxyethyl)-N,N-dimethyl-1-propanamin- ium chloride 3-(D-Gluconoylamino)propyl(2-hydroxyethyl)dimethylammonium chloride 82970-95-4 [RN] N-(2-Hydroxyethyl)-N,N-dimethyl-3-{[(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanoyl]amino}-1-propanaminiumchloride QUATERNIUM 22 γ-Gluconamidopropyl dimethyl 2-hydroxyethyl ammonium chloride
QUATERNIUM-22
Decyldimethyloctylammonium chloride; Decyldimethyloctylammonium chloride; Decyldimethyloctylammonium chloride; Decyldimethyloctylammonium chloride; Octyl decyl dimethyl ammonium chloride; QUATERNIUM-24, N° CAS : 32426-11-2, Origine(s) : Synthétique. Nom INCI : QUATERNIUM-24. Nom chimique : Decyldimethyloctylammonium chloride. N° EINECS/ELINCS : 251-035-5, Classification : Ammonium quaternaire. Ses fonctions (INCI) : Antimicrobien : Aide à ralentir la croissance de micro-organismes sur la peau et s'oppose au développement des microbes, Antistatique : Réduit l'électricité statique en neutralisant la charge électrique sur une surface, Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation. Noms français : 1-DECANAMINIUM, N,N-DIMETHYL-N-OCTYL-, CHLORIDE; Chlorure de décyldiméthyloctylammonium; DECYLOCYTLDIMETHYLAMMONIUM CHLORIDE. OCTYL DECYL DIMETHYL AMMONIUM CHLORIDE. Noms anglais : 1-Decaminium N-octyl-N,N-dimethyl-, chloride; Decyldimethyloctylammonium chloride; Decyldimethyloctylammonium chloride; Decyldimethyloctylammonium chloride; Decyldimethyloctylammonium chloride; Octyl decyl dimethyl ammonium chloride; 1-Decanaminium, N,N-dimethyl-N-octyl-, chloride (1:1) [ACD/Index Name] ; 251-035-5 [EINECS] ; 32426-11-2 [RN]; Chlorure de N,N-diméthyl-N-octyl-1-décanaminium [French] [ACD/IUPAC Name]; Decyloctyldimethylammonium chloride; N,N-Dimethyl-N-octyl-1-decanaminium chloride [ACD/IUPAC Name]; N,N-Dimethyl-N-octyl-1-decanaminiumchlorid [German] [ACD/IUPAC Name]; N,N-Dimethyl-N-octyldecan-1-aminium chloride; Quaternium-24 ; 1-Decaminium, N-octyl-N,N-dimethyl-, chloride; 1-Decanaminium, N,N-dimethyl-N-octyl-, chloride; Ammonium, decyldimethyloctyl, chloride; Decyl dimethyl octyl ammonium chloride; decyl-dimethyl-octylammonium chloride; decyl-dimethyl-octyl-ammonium chloride; DECYLDIMETHYLOCTYLAMMONIUM CHLORIDE; decyl-dimethyl-octylazanium and chloride; decyl-dimethyl-octylazanium chloride; decyl-dimethyl-octyl-azanium chloride; DECYLDIMETHYLOCTYLAZANIUM CHLORIDE; decyl-dimethyl-octylazanium;chloride; Decylocytldimethylammonium chloride ; Di-(Octyl-decyl)dimethylammonium chloride; EINECS 251-035-5; N,N-Dimethyl-N-octyl-1-decanaminiumchloride; N-Octyl-N-decyl-N-dimethylammonium chloride; N-Octyl-N-decyl-N-dimethyl-ammonium chloride; Octyl Decyldimethyl Ammonium Chloride; Quaternium 24
QUATERNIUM-24 ( Chlorure de décyldiméthyloctylammonium ) Decyldimethyloctylammonium chloride
QUATERNIUM-26, N° CAS : 68953-64-0 / 64156-20-3, Origine(s) : Synthétique. Nom INCI : QUATERNIUM-26, N° EINECS/ELINCS : 273-222-0. Classification : Ammonium quaternaire Ses fonctions (INCI). Antistatique : Réduit l'électricité statique en neutralisant la charge électrique sur une surface. Conditionneur capillaire : Laisse les cheveux faciles à coiffer, souples, doux et brillants et / ou confèrent volume, légèreté et brillance. 1-Propanaminium, 3-amino-N-(2-hydroxyethyl)-N,N-dimethyl-, N-mink-oil acyl derivs., chlorides; EC Inventory, ; 1-Propanaminium, 3-amino-N-(2-hydroxyethyl)-N,N-dimethyl-, N-mink-oil acyl derivs, chlorides; CERAPHYL 65 ; Quaternium-26
QUATERNIUM-26
QUATERNIUM-27, N° CAS : 68122-86-1. Origine(s) : Synthétique. Nom INCI : QUATERNIUM-27. N° EINECS/ELINCS : 268-531-2. Classification : Ammonium quaternaire. Ses fonctions (INCI), Antistatique : Réduit l'électricité statique en neutralisant la charge électrique sur une surface. Conditionneur capillaire : Laisse les cheveux faciles à coiffer, souples, doux et brillants et / ou confèrent volume, légèreté et brillance. Noms français : Méthylsulfate de composés imidazolium du dihydro-4,5 méthyl-1 alkyle de suif nor-2 (amidoéthyl-2 de suif)-1 Noms anglais : 1-(2-TALLOW AMIDOETHYL)-1-METHYL-2-NOR(TALLOW ALKYL)-2-IMIDAZOLINIUM METHYL SULFATE 1-(2-TALLOWAMIDOETHYL)-1-METHYL-2-TALLOWALKYLIMIDAZOLINIUM METHYLSULFATE 1-METHYL-1-(2-TALLOWAMIDOETHYL)-2-TALLOWIMIDAZOLINIUM METHYLSULFATE 1-METHYL-1-TALLOWALKYLAMIDOETHYL-2-TALLOWALKYLIMIDAZOLINE METHOSULFATE IMIDAZOLIUM COMPOUNDS, 4,5-DIHYDRO-1-METHYL-2-NORTALLOW ALKYL-1-(2-TALLOW AMIDOETHYL), ME SULFATES; Imidazolium compounds, 4,5-dihydro-1-methyl-2-nortallow alkyl-1-(2-tallow amidoethyl), Me sulfates.
QUATERNIUM-27
QUATERNIUM-33, N° CAS : 72102-40-0 / 86221-07-0, Origine(s) : Synthétique, Nom INCI : QUATERNIUM-33, N° EINECS/ELINCS : 276-339-5. Classification : Ammonium quaternaire: Ses fonctions (INCI). Antistatique : Réduit l'électricité statique en neutralisant la charge électrique sur une surface. Conditionneur capillaire : Laisse les cheveux faciles à coiffer, souples, doux et brillants et / ou confèrent volume, légèreté et brillance. 1-Propanaminium, 3-amino-N-ethyl-N,N-dimethyl-, N-lanolin acyl derivs., Et sulfates; Lanolin acids, APMA amide, di-Et sulfate; Quaternium-33; iso and antiso C10-40 AAP EDM-ES
QUATERNIUM-33
QUATERNIUM-45; N° CAS : 21034-17-3; Origine(s) : Synthétique; Nom INCI : QUATERNIUM-45; Nom chimique : 3,4-Dimethyl-2-[2-(phenylamino)vinyl]oxazolium iodide; N° EINECS/ELINCS : 244-158-0; Classification : Ammonium quaternaire. Ses fonctions (INCI). 3,4-dimethyl-2-[2-(phenylamino)vinyl]oxazolium iodide. : 3,4-dimethyl-2-[(E)-2-(phenylamino)ethenyl]-1,3-oxazol-3-ium iodide. Antistatique : Réduit l'électricité statique en neutralisant la charge électrique sur une surface. 2-[(E)-2-Anilinovinyl]-3,4-dimethyl-1,3-oxazol-3-ium iodide [ACD/IUPAC Name] ; 2-[(E)-2-Anilinovinyl]-3,4-dimethyl-1,3-oxazol-3-iumiodid [German] [ACD/IUPAC Name]; 244-158-0 [EINECS]; Iodure de 2-[(E)-2-anilinovinyl]-3,4-diméthyl-1,3-oxazol-3-ium [French] [ACD/IUPAC Name]; Oxazolium, 3,4-dimethyl-2-[(E)-2-(phenylamino)ethenyl]-, iodide (1:1) [ACD/Index Name]; 21034-17-3 [RN]; 3,4-Dimethyl-2-(2-(phenylamino)vinyl)oxazolium iodide; 3,4-DIMETHYL-2-[2-(PHENYLAMINO)ETHENYL]-1,3-OXAZOL-3-IUM IODIDE; 3,4-dimethyl-2-[2-(phenylamino)vinyl]oxazolium iodide; Kankohso 401; Kankohso 401 [Japanese]; Oxazolium, 2-(2-anilinovinyl)-3,4-dimethyl-, iodide; Oxazolium, 3,4-dimethyl-2-(2-(phenylamino)ethenyl)-, iodide (9CI); Quaternium-45
QUATERNIUM-45
QUATERNIUM-51; N° CAS : 1463-95-2; Origine(s) : Synthétique; Nom INCI : QUATERNIUM-51; N° EINECS/ELINCS : 215-976-5. Classification : Ammonium quaternaire; 2-[2-[(5-bromo-2-pyridyl)amino]vinyl]-1-ethyl-6-methylpyridinium iodide; : 2-[(E)-2-[(5-bromopyridin-2-yl)amino]ethenyl]-1-ethyl-6-methylpyridin-1-ium iodide. Ses fonctions (INCI) : Antistatique : Réduit l'électricité statique en neutralisant la charge électrique sur une surface. 2-{(E)-2-[(5-Brom-2-pyridinyl)amino]vinyl}-1-ethyl-6-methylpyridiniumiodid [German] [ACD/IUPAC Name]; 2-{(E)-2-[(5-Bromo-2-pyridinyl)amino]vinyl}-1-ethyl-6-methylpyridinium iodide [ACD/IUPAC Name]; 2-{(E)-2-[(5-Bromopyridin-2-yl)amino]vinyl}-1-ethyl-6-methylpyridinium iodide ;215-976-5 [EINECS]; Iodure de 2-{(E)-2-[(5-bromo-2-pyridinyl)amino]vinyl}-1-éthyl-6-méthylpyridinium [French] [ACD/IUPAC Name]; Pyridinium, 2-[(E)-2-[(5-bromo-2-pyridinyl)amino]ethenyl]-1-ethyl-6-methyl-, iodide (1:1) [ACD/Index Name]; 1463-95-2 [RN]; 2-(2-((5-Bromo-2-pyridyl)amino)vinyl)-1-ethyl-6-methylpyridinium iodide; 2-[(E)-2-[(5-BROMOPYRIDIN-2-YL)AMINO]ETHENYL]-1-ETHYL-6-METHYLPYRIDIN-1-IUM IODIDE; 2-[2-[(5-bromo-2-pyridyl)amino]vinyl]-1-ethyl-6-methylpyridinium iodide; Pyridinium, 2-(2-((5-bromo-2-pyridinyl)amino)ethenyl)-1-ethyl-6-methyl-, iodide ;Pyridinium,2-[2-[(5-bromo-2-pyridinyl)amino]ethenyl]-1-ethyl-6-methyl-, iodide (1:1); Quaternium-51
QUATERNIUM-51
QUATERNIUM-52, N° CAS : 58069-11-7. Origine(s) : Synthétique. Nom INCI : QUATERNIUM-52. Classification : Ammonium quaternaire. Ses fonctions (INCI) : Antistatique : Réduit l'électricité statique en neutralisant la charge électrique sur une surface, Conditionneur capillaire : Laisse les cheveux faciles à coiffer, souples, doux et brillants et / ou confèrent volume, légèreté et brillance, Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation. Poly(oxy-1,2-ethanediyl), α,α',α''-[(octadecylnitrilio)tri-2,1-ethanediyl]tris[ω-hydroxy-, phosphate (1:1); Talgaminphosphat, ethoxyliert
QUATERNIUM-52
QUATERNIUM-53; N° CAS : 68410-69-5; Origine(s) : Synthétique; Nom INCI : QUATERNIUM-53; N° EINECS/ELINCS : 268-762-9; Classification : Ammonium quaternaire. Ses fonctions (INCI) : Antistatique : Réduit l'électricité statique en neutralisant la charge électrique sur une surface. Conditionneur capillaire : Laisse les cheveux faciles à coiffer, souples, doux et brillants et / ou confèrent volume, légèreté et brillance. Noms français : Méthylsulfate de dérivés méthylés de suif et de diéthylènetriamine,polyéthoxylés. Noms anglais :METHYL TALLOW DIETHYLENETRIAMINE CONDENSATE, POLYETHOXYLATED, METHYL SULFATE; Poly(oxy-1,2-ethanediyl),alpha-(2-(bis(2-aminoethyl)methylammonio- )ethyl)-omega-hydroxy, N,N'-ditallow acyl derivs, methyl sulfates; ; Noms français : Méthylsulfate de dérivés méthylés de suif et de diéthylènetriamine,polyéthoxylés. Noms anglais : METHYL TALLOW DIETHYLENETRIAMINE CONDENSATE, POLYETHOXYLATED, METHYL SULFATE; Poly(oxy-1,2-ethanediyl),alpha-(2-(bis(2-aminoethyl)methylammonio- )ethyl)-omega-hydroxy, N,N'-ditallow acyl derivs, methyl sulfates
QUATERNIUM-53
QUATERNIUM-60 Origine(s) : Synthétique Nom INCI : QUATERNIUM-60 Classification : Ammonium quaternaire Ses fonctions (INCI) Antistatique : Réduit l'électricité statique en neutralisant la charge électrique sur une surface Conditionneur capillaire : Laisse les cheveux faciles à coiffer, souples, doux et brillants et / ou confèrent volume, légèreté et brillance
QUATERNIUM-60
QUATERNIUM-70; N° CAS : 68921-83-5; Origine(s) : Synthétique; Nom INCI : QUATERNIUM-70; Nom chimique : Dimethyl[3-[(1-oxooctadecyl)amino]propyl][2-oxo-2-(tetradecyloxy)ethyl]ammonium chloride; N° EINECS/ELINCS : 272-964-2; Classification : Ammonium quaternaire; Ses fonctions (INCI): Antistatique : Réduit l'électricité statique en neutralisant la charge électrique sur une surface ; Conditionneur capillaire : Laisse les cheveux faciles à coiffer, souples, doux et brillants et / ou confèrent volume, légèreté et brillance. Dimethyl[3-[(1-oxooctadecyl)amino]propyl][2-oxo-2-(tetradecyloxy)ethyl]ammonium chloride; Ceraphyl 70 ; dimethyl(3-octadecanamidopropyl)[2-oxo-2-(tetradecyloxy)ethyl]azanium chloride; 1-Propanaminium, N,N-dimethyl-3-[(1-oxooctadecyl)amino]-; N-[2-oxo-2-(tetradecyloxy)ethyl]-, chloride (1:1) [ACD/Index Name]; 272-964-2 [EINECS]; 68921-83-5 [RN]; Chlorure de N,N-diméthyl-N-[2-oxo-2-(tétradécyloxy)éthyl]-3-(stearoylamino)-1-propanaminium [French] [ACD/IUPAC Name]; N,N-Dimethyl-N-[2-oxo-2-(tetradecyloxy)ethyl]-3-(stearoylamino)-1-propanaminium chloride [ACD/IUPAC Name]; N,N-Dimethyl-N-[2-oxo-2-(tetradecyloxy)ethyl]-3-(stearoylamino)-1-propanaminiumchlorid [German] [ACD/IUPAC Name]; N,N-Dimethyl-N-[2-oxo-2-(tetradecyloxy)ethyl]-3-(stearoylamino)propan-1-aminium chloride; Quaternium-70; (2-keto-2-myristyloxy-ethyl)-dimethyl-(3-stearamidopropyl)ammonium chloride; (3-Stearamidopropyl)dimethylmyristoyloxycarbonylmethylammonium chloride ; 1-Propanaminium, N,N-dimethyl-3-((1-oxooctadecyl)amino)-N-(2-oxo-2-(tetradecenylox- y)ethyl)-, chloride; 1-Propanaminium, N,N-dimethyl-3-((1-oxooctadecyl)amino)-N-(2-oxo-2-(tetradecyloxy)ethyl)-, chloride; Dimethyl(3-((1-oxooctadecyl)amino)propyl)(2-oxo-2-(tetradecyloxy)ethyl)ammonium chloride; DIMETHYL(3-OCTADECANAMIDOPROPYL)[2-OXO-2-(TETRADECYLOXY)ETHYL]AZANIUM CHLORIDE; dimethyl-[3-(1-oxooctadecylamino)propyl]-(2-oxo-2-tetradecoxyethyl)ammonium chloride; dimethyl-[3-(octadecanoylamino)propyl]-(2-oxo-2-; tetradecoxy-ethyl)ammonium chloride; dimethyl-[3-(octadecanoylamino)propyl]-(2-oxo-2-tetradecoxyethyl)azanium chloride; dimethyl-[3-(octadecanoylamino)propyl]-(2-oxo-2-tetradecoxy-ethyl)azanium chloride; dimethyl[3-[(1-oxooctadecyl)amino]propyl][2-oxo-2-(tetradecyloxy)ethyl]ammonium chloride, EINECS 272-964-2; N,N-Dimethyl-3-((1-oxooctadecyl)amino)-N-(2-oxo-2-(tetradecenylox- y)ethyl)-1-propanaminium chloride; Stearamidopropyl dimethyl (myristyl acetate) ammonium chloride
QUATERNIUM-70
QUATERNIUM-73; N° CAS : 15763-48-1; Origine(s) : Synthétique; Nom INCI : QUATERNIUM-73; Nom chimique : 3-Heptyl-2-[(3-heptyl-4-methyl-3H-thiazol-2-ylidene)methyl]-4-methylthiazolium iodide; 3-heptyl-2-[(3-heptyl-4-methyl-3H-thiazol-2-ylidene)methyl]-4-methylthiazolium iodide; 3-heptyl-2-{[(2Z)-3-heptyl-4-methyl-2,3-dihydro-1,3-thiazol-2-ylidene]methyl}-4-methyl-1,3-thiazol-3-ium iodide; N° EINECS/ELINCS : 239-852-5. Classification : Ammonium quaternaire; Ses fonctions (INCI). Antistatique : Réduit l'électricité statique en neutralisant la charge électrique sur une surfa. 239-852-5 [EINECS] 3-Heptyl-2-[(3-heptyl-4-methyl-1,3-thiazol-2(3H)-ylidene)methyl]-4-methyl-1,3-thiazol-3-ium iodide 3-Heptyl-2-[(E)-(3-heptyl-4-methyl-1,3-thiazol-2(3H)-yliden)methyl]-4-methyl-1,3-thiazol-3-iumiodid [German] [ACD/IUPAC Name] 3-Heptyl-2-[(E)-(3-heptyl-4-methyl-1,3-thiazol-2(3H)-ylidene)methyl]-4-methyl-1,3-thiazol-3-ium iodide [ACD/IUPAC Name] Iodure de 3-heptyl-2-[(E)-(3-heptyl-4-méthyl-1,3-thiazol-2(3H)-ylidène)méthyl]-4-méthyl-1,3-thiazol-3-ium [French] [ACD/IUPAC Name] thiazolium, 3-heptyl-2-[(3-heptyl-4-methyl-2(3H)-thiazolylidene)methyl]-4-methyl-, iodide (1:1) Thiazolium, 3-heptyl-2-[(E)-(3-heptyl-4-methyl-2(3H)-thiazolylidene)methyl]-4-methyl-, iodide (1:1) [ACD/Index Name] 15763-48-1 [RN] 3-Heptyl-2-((3-heptyl-4-methyl-3H-thiazol-2-ylidene)methyl)-4-methylthiazolium iodide 3-Heptyl-2-((3-heptyl-4-methyl-4-thiazolin-2-ylidene)methyl)-4-methylthiazolium iodide 3-HEPTYL-2-[(3-HEPTYL-4-METHYL-1,3-THIAZOL-2-YLIDENE)METHYL]-4-METHYL-1,3-THIAZOL-3-IUM IODIDE 3-heptyl-2-[(3-heptyl-4-methyl-3H-thiazol-2-ylidene)methyl]-4-methylthiazolium iodide 3-HEPTYL-2-{[(2E)-3-HEPTYL-4-METHYL-1,3-THIAZOL-2-YLIDENE]METHYL}-4-METHYL-1,3-THIAZOL-3-IUM IODIDE Kankohso 201 MFCD01680792 Pionin Quaternium 73 QUATERNIUM-73 Thiazolium, 3-heptyl-2-((3-heptyl-4-methyl-2(3H)-thiazolylidene)methyl)-4-methyl-, iodide Thiazolium, 3-heptyl-2-((3-heptyl-4-methyl-4-thiazolin-2-ylidene)methyl)-4-methyl-, iodide
QUATERNIUM-73
QUATERNIUM-75 Origine(s) : Synthétique Nom INCI : QUATERNIUM-75 Classification : Ammonium quaternaire Ses fonctions (INCI) Antistatique : Réduit l'électricité statique en neutralisant la charge électrique sur une surface Conditionneur capillaire : Laisse les cheveux faciles à coiffer, souples, doux et brillants et / ou confèrent volume, légèreté et brillance
QUATERNIUM-75
QUATERNIUM-8; Origine(s) : Synthétique; Nom INCI : QUATERNIUM-8. Classification : Ammonium quaternaire. Ses fonctions (INCI); Antimicrobien : Aide à ralentir la croissance de micro-organismes sur la peau et s'oppose au développement des microbes. Antistatique : Réduit l'électricité statique en neutralisant la charge électrique sur une surface Conditionneur capillaire : Laisse les cheveux faciles à coiffer, souples, doux et brillants et / ou confèrent volume, légèreté et brillance; It helps make drying easier, whilst it totally respects hair structure. It protects the hair from the heat damage caused by hairdryer or hair iron, as well from mechanical stress. It has softening, conditioning and antistatic proprieties.
QUATERNIUM-8
QUATERNIUM-80, N° CAS : 134737-05-6. Origine(s) : Synthétique. Nom INCI : QUATERNIUM-80. Classification : Ammonium quaternaire. Ses fonctions (INCI) : Antistatique : Réduit l'électricité statique en neutralisant la charge électrique sur une surface : Conditionneur capillaire : Laisse les cheveux faciles à coiffer, souples, doux et brillants et / ou confèrent volume, légèreté et brillance. Quaternium-80 is the quaternary ammonium salt with the alkyl groups derived from coconut oil; Siloxanes and Silicones, di-Me, 3-[3-[(3-coco amidopropyl)dimethylammonio]-2-hydroxypropoxy]propyl group-terminated, acetates (salts); Siloxanes and silicones, di-Me, 3-{3-[(3-Cocoamidopropyl) -dimethylammonia]-2-hydroxy-propoxy}propyl group terminated, acetates (salts)
QUATERNIUM-80
QUATERNIUM-82, N° CAS : 65059-61-2 / 173833-36-8. Origine(s) : Synthétique. Nom INCI : QUATERNIUM-82. N° EINECS/ELINCS : 265-339-0 / -. Classification : Ammonium quaternaire. Ses fonctions (INCI) : Antistatique : Réduit l'électricité statique en neutralisant la charge électrique sur une surface. Conditionneur capillaire : Laisse les cheveux faciles à coiffer, souples, doux et brillants et / ou confèrent volume, légèreté et brillance. [2-[bis(2-hydroxypropyl)amino]ethyl]bis(2-hydroxypropyl)(methyl)ammonium methyl sulphate, dioleate (ester); (2-hydroxypropyl)({2-[(2-hydroxypropyl)({2-[(9E)-octadec-9-enoyloxy]propyl})amino]ethyl})methyl({2-[(10E)-octadec-10-enoyloxy]propyl})azanium methyl sulfate; 2-Hydroxy-N-{2-[(2-hydroxypropyl){2-[(9E)-9-octadecenoyloxy]propyl}amino]ethyl}-N-methyl-N-{2-[(10E)-10-octadecenoyloxy]propyl}-1-propanaminium methyl sulfate [ACD/IUPAC Name] 2-Hydroxy-N-{2-[(2-hydroxypropyl){2-[(9E)-9-octadecenoyloxy]propyl}amino]ethyl}-N-methyl-N-{2-[(10E)-10-octadecenoyloxy]propyl}-1-propanaminiummethylsulfat [German] [ACD/IUPAC Name] Sulfate de 2-hydroxy-N-{2-[(2-hydroxypropyl){2-[(9E)-9-octadecenoyloxy]propyl}amino]éthyl}-N-méthyl-N-{2-[(10E)-10-octadecenoyloxy]propyl}propane et de méthyle [French] [ACD/IUPAC Name] (2-(Bis(2-hydroxypropyl)amino)ethyl)bis(2-hydroxypropyl)(methyl)ammonium methyl sulphate, dioleate (ester) (2-HYDROXYPROPYL)({2-[(2-HYDROXYPROPYL)({2-[(9E)-OCTADEC-9-ENOYLOXY]PROPYL})AMINO]ETHYL})METHYL({2-[(10E)-OCTADEC-10-ENOYLOXY]PROPYL})AZANIUM METHYL SULFATE(1-) 1-Propanaminium, N-(2-(bis(2-hydroxypropyl)amino)ethyl)-2-hydroxy-N-(2-hydroxypropyl)-N-methyl-, di-(9Z)-9-octadecenoate (ester), methyl sulfate (salt) 265-339-0 [EINECS] 65059-61-2 [RN]
QUATERNIUM-82
QUATERNIUM-83, N° CAS : 91723-55-6. Origine(s) : Synthétique. Nom INCI : QUATERNIUM-83. N° EINECS/ELINCS : 294-563-1. Classification : Ammonium quaternaire. Ses fonctions (INCI): Antistatique : Réduit l'électricité statique en neutralisant la charge électrique sur une surface. Conditionneur capillaire : Laisse les cheveux faciles à coiffer, souples, doux et brillants et / ou confèrent volume, légèreté et brillance
QUATERNIUM-83
QUATERNIUM-87, N° CAS : 92201-88-2. Origine(s) : Synthétique. Nom INCI : QUATERNIUM-87. N° EINECS/ELINCS : 931-745-8. Classification : Ammonium quaternaire. Ses fonctions (INCI): Agent nettoyant : Aide à garder une surface propre. Conditionneur capillaire : Laisse les cheveux faciles à coiffer, souples, doux et brillants et / ou confèrent volume, légèreté et brillance. Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation
QUATERNIUM-87
QUATERNIUM-88, Origine(s) : Synthétique. Nom INCI : QUATERNIUM-88. Classification : Ammonium quaternaire. Ses fonctions (INCI). Antistatique : Réduit l'électricité statique en neutralisant la charge électrique sur une surface. Conditionneur capillaire : Laisse les cheveux faciles à coiffer, souples, doux et brillants et / ou confèrent volume, légèreté et brillance
QUATERNIUM-88
QUATERNIUM-89 Origine(s) : Synthétique Nom INCI : QUATERNIUM-89 Classification : Ammonium quaternaire Ses fonctions (INCI) Antistatique : Réduit l'électricité statique en neutralisant la charge électrique sur une surface Conditionneur capillaire : Laisse les cheveux faciles à coiffer, souples, doux et brillants et / ou confèrent volume, légèreté et brillance
QUATERNIUM-89
QUATERNIUM-90, Origine(s) : Synthétique, Nom INCI : QUATERNIUM-90. Classification : Ammonium quaternaire. Ses fonctions (INCI). Antistatique : Réduit l'électricité statique en neutralisant la charge électrique sur une surface
QUATERNIUM-90
QUATERNIUM-91 Origine(s) : Synthétique Nom INCI : QUATERNIUM-91 Classification : Ammonium quaternaire Ses fonctions (INCI) Conditionneur capillaire : Laisse les cheveux faciles à coiffer, souples, doux et brillants et / ou confèrent volume, légèreté et brillance
QUATERNIUM-91
QUATERNIUM-95; N° CAS : 1030827-59-8; Origine(s) : Synthétique; Nom INCI : QUATERNIUM-95. Classification : Ammonium quaternaire. Ses fonctions (INCI). Conditionneur capillaire : Laisse les cheveux faciles à coiffer, souples, doux et brillants et / ou confèrent volume, légèreté et brillance. Absorbant UV : Protège le produit cosmétique contre les effets de la lumière UV
QUATERNIUM-95
QUATERNIUM-96, Origine(s) : Synthétique. Nom INCI : QUATERNIUM-96. Classification : Ammonium quaternaire. Ses fonctions (INCI). Agent nettoyant : Aide à garder une surface propre. Conditionneur capillaire : Laisse les cheveux faciles à coiffer, souples, doux et brillants et / ou confèrent volume, légèreté et brillance. Tensioactif : Réduit la tension superficielle des cosmétiques et contribue à la répartition uniforme du produit lors de son utilisation
QUATERNIUM-96
SYNONYMS C.I.Acid Yellow 3; C.I. 47005; Quinoline Yellow, water soluble; Food Yellow 13; Sodium 2-(1,3-dioxoindan-2-yl)quinolinedisulfonate; 2-(1,3-Dioxoindan-2-yl) quinolinedisulfonic acid sodium salt; Sodium 2-(2-quinolyl) indan-1,3-dione-disulfonates; Quinoline Yellow;CAS NO 8004-92-0
QUERCETIN

Quercetin is a flavonoid found naturally in many fruits, vegetables, and grains, known for its powerful antioxidant, anti-inflammatory, and immune-boosting properties.
Quercetin is widely recognized for its ability to neutralize free radicals, reduce inflammation, and support cardiovascular health, making it a valuable ingredient in dietary supplements, skincare products, and wellness formulations.
This versatile compound offers numerous health benefits, including enhanced immune defense, reduced allergy symptoms, and protection against oxidative stress.

CAS Number: 117-39-5
EC Number: 204-187-1

Synonyms: Quercetin, Quercetin Dihydrate, Quercetol, Sophoretin, Meletin, Quercetine, Quercetin Bioflavonoid, 3,3',4',5,7-Pentahydroxyflavone, Quercetin Phytocomplex, Quercetin Bioactive, Quercetol Phytocomplex, Flavonoid Quercetin



APPLICATIONS


Quercetin is extensively used in dietary supplements for its antioxidant properties, providing support for neutralizing free radicals and reducing oxidative stress, which contributes to overall health and longevity.
Quercetin is favored in the formulation of immune-boosting supplements, where it enhances the body’s natural defenses and helps reduce the duration and severity of colds and infections.
Quercetin is utilized in allergy-relief supplements, offering natural antihistamine effects that help reduce allergy symptoms such as sneezing, congestion, and itchy eyes.

Quercetin is widely used in cardiovascular health supplements, where it supports healthy blood circulation, reduces blood pressure, and helps to lower LDL cholesterol levels.
Quercetin is employed in the creation of anti-inflammatory supplements, providing relief from chronic inflammation and supporting overall joint health.
Quercetin is essential in the development of sports recovery supplements, where it helps reduce muscle soreness and enhance athletic performance by decreasing oxidative stress in the muscles.

Quercetin is utilized in the production of respiratory health products, offering benefits for reducing asthma symptoms and improving lung function, particularly in individuals with chronic respiratory issues.
Quercetin is a key ingredient in wellness products designed to support healthy aging, where it helps protect cells from oxidative damage and promotes longevity.
Quercetin is used in the development of weight management supplements, where it supports fat metabolism and helps regulate glucose levels, making it a valuable component in managing obesity and metabolic disorders.

Quercetin is applied in the formulation of skincare products for its anti-aging and anti-inflammatory benefits, offering protection against UV-induced skin damage and helping to reduce redness, irritation, and inflammation.
Quercetin is employed in the production of creams and lotions for sensitive skin, providing antioxidant protection while soothing irritation and helping to repair damaged skin.
Quercetin is used in wellness supplements to support brain health, providing neuroprotective benefits and helping to improve cognitive function and memory by reducing oxidative stress in the brain.

Quercetin is widely utilized in the creation of detox products, where it helps to eliminate toxins and support liver function, contributing to overall wellness and vitality.
Quercetin is a key component in supplements designed to support vascular health, helping to strengthen blood vessels, improve circulation, and reduce the risk of cardiovascular diseases.
Quercetin is used in the production of eye health supplements, providing antioxidant support to protect the eyes from oxidative stress and helping to reduce the risk of cataracts and age-related macular degeneration.

Quercetin is employed in the formulation of supplements that support metabolic health, helping to regulate blood sugar levels and improve insulin sensitivity.
Quercetin is applied in natural remedies for reducing the symptoms of prostate inflammation and supporting overall prostate health.
Quercetin is utilized in the creation of anti-aging supplements, where it helps to reduce wrinkles, improve skin elasticity, and promote youthful-looking skin.

Quercetin is found in sports nutrition products, helping to reduce oxidative stress during exercise, enhance recovery, and improve endurance in athletes.
Quercetin is used in the development of natural antihistamines for individuals suffering from seasonal allergies, providing relief from common symptoms like nasal congestion, sneezing, and watery eyes.
Quercetin is a key ingredient in supplements designed to support healthy blood pressure, providing natural benefits for managing hypertension and improving cardiovascular health.



DESCRIPTION


Quercetin is a flavonoid found naturally in many fruits, vegetables, and grains, known for its powerful antioxidant, anti-inflammatory, and immune-boosting properties.
Quercetin is widely recognized for its ability to neutralize free radicals, reduce inflammation, and support cardiovascular health, making it a valuable ingredient in dietary supplements, skincare products, and wellness formulations.

Quercetin offers additional benefits such as supporting respiratory health, improving circulation, and promoting longevity by protecting cells from oxidative damage.
Quercetin is often incorporated into formulations designed to support immune function, improve allergy symptoms, and reduce inflammation, providing a comprehensive approach to wellness.
Quercetin is recognized for its ability to help prevent and manage chronic conditions such as heart disease, diabetes, and neurodegenerative disorders.

Quercetin is commonly used in both traditional and modern wellness formulations, providing a reliable solution for supporting the immune system, improving heart health, and promoting overall vitality.
Quercetin is valued for its ability to reduce oxidative stress, which plays a crucial role in preventing premature aging and promoting healthy skin and overall well-being.
Quercetin is a versatile ingredient that can be used in a variety of products, including supplements, capsules, creams, lotions, and skincare products.

Quercetin is an ideal choice for products targeting immune support, inflammation reduction, and cardiovascular health, providing natural and effective care for these concerns.
Quercetin is known for its compatibility with other antioxidant-rich and anti-inflammatory ingredients, making it easy to integrate into multi-functional formulations.
Quercetin is often chosen for formulations requiring a balance between immune support, inflammation relief, and heart health, ensuring comprehensive wellness benefits.

Quercetin enhances the overall effectiveness of wellness products by providing natural support for immune defense, inflammation reduction, and oxidative stress protection.
Quercetin is a reliable ingredient for creating products that offer noticeable improvements in immune function, allergy relief, and cardiovascular health.
Quercetin is an essential component in innovative wellness and beauty products known for their performance, safety, and ability to support immune health, skin protection, and overall vitality.



PROPERTIES


Chemical Formula: C15H10O7
Common Name: Quercetin
Molecular Structure:
Appearance: Yellow crystalline powder
Density: Approx. 1.8 g/cm³
Melting Point: 316 °C (601 °F)
Solubility: Soluble in ethanol, methanol; slightly soluble in water
Flash Point: Not applicable
Reactivity: Stable under normal conditions; no known reactivity issues
Chemical Stability: Stable under recommended storage conditions
Storage Temperature: Store between 15-25°C in a cool, dry place
Vapor Pressure: Low



FIRST AID


Inhalation:
If Quercetin 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:
Wash the affected area with soap and water.
If skin irritation persists, seek medical attention.

Eye Contact:
In case of 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:
If Quercetin is ingested, 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) such as gloves and safety goggles if handling large quantities.
Use in a well-ventilated area to avoid inhalation of dust.

Ventilation:
Ensure adequate ventilation when handling large amounts of Quercetin to control airborne concentrations below occupational exposure limits.

Avoidance:
Avoid direct contact with eyes and prolonged skin contact.
Do not eat, drink, or smoke while handling Quercetin.
Wash hands thoroughly after handling.

Spill and Leak Procedures:
Contain spills to prevent further release and minimize exposure.
Absorb with inert material (e.g., sand, vermiculite) and collect for disposal.
Dispose of in accordance with local regulations.

Storage:
Store Quercetin in a cool, dry, 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 inhalation of dust and direct contact with skin and eyes.
Use explosion-proof equipment in areas where dust or vapors may be present.

Quercus infectoria (Oak) gall
quercus infectoria fruit extract;oak fruit extract CAS NO:93165-57-2
QUINOLINE YELLOW
ood Yellow 13; Sodium 2-(1,3-dioxoindan-2-yl)quinolinedisulfonate; 2-(1,3-Dioxoindan-2-yl) quinolinedisulfonic acid sodium salt; Sodium 2-(2-quinolyl) indan-1,3-dione-disulfonates CAS:8004-92-0
QUINOLINE YELLOW WS
SYNONYMS C.I.Acid Yellow 3; C.I. 47005; Quinoline Yellow, water soluble; Food Yellow 13; Sodium 2-(1,3-dioxoindan-2-yl)quinolinedisulfonate; 2-(1,3-Dioxoindan-2-yl) quinolinedisulfonic acid sodium salt; Sodium 2-(2-quinolyl) indan-1,3-dione-disulfonates; Quinoline YellowCAS NO 8004-92-0
Quinoline
Quartemine; 1-Hexadecanaminium, N,N,N-trimethyl-, chloride cas no: 112-02-7
Rabeprazole Sodium
SYNONYMS Aciphex;2-[[[4-(3-methoxypropoxy) -3-methyl-2-pyridinyl]-methyl]sulfinyl] -1H–benzimidazole sodium salt; cas no:117976-89-3
RACEMIC ACID
Racemic acid is an organic acid found in many vegetables and fruits such as bananas, and grapes, but also in bananas, citrus, and tamarinds.
Racemic acid is a white, crystalline organic acid that occurs naturally in many fruits, most notably in grapes, but also in tamarinds, bananas, avocados and citrus.
Naturally occurring Racemic acid is a useful raw material in organic chemical synthesis.

CAS Number: 87-69-4
EC Number: 205-695-6
Molecular Formula: C4H6O6
Molecular Weight (g/mol): 150.09

Synonyms: (+)-L-Tartaric acid, (+)-Tartaric acid, 87-69-4, L-(+)-Tartaric acid, L-Tartaric acid, L(+)-Tartaric acid, tartaric acid, (2R,3R)-2,3-dihydroxysuccinic acid, (2R,3R)-2,3-dihydroxybutanedioic acid, (R,R)-Tartaric acid, Threaric acid, L-threaric acid, Dextrotartaric acid, Natural tartaric acid, Acidum tartaricum, DL-Tartaric acid, (2R,3R)-(+)-Tartaric acid, (+)-(R,R)-Tartaric acid, Tartaric acid, L-, Rechtsweinsaeure, Kyselina vinna, (2R,3R)-Tartaric acid, (R,R)-(+)-Tartaric acid, tartrate, Succinic acid, 2,3-dihydroxy, Weinsteinsaeure, L-2,3-Dihydroxybutanedioic acid, 133-37-9, (2R,3R)-rel-2,3-Dihydroxysuccinic acid, 1,2-Dihydroxyethane-1,2-dicarboxylic acid, EINECS 201-766-0, (+)-Weinsaeure, NSC 62778, FEMA No. 3044, INS NO.334, DTXSID8023632, UNII-W4888I119H, CHEBI:15671, Kyselina 2,3-dihydroxybutandiova, AI3-06298, Lamb protein (fungal), INS-334, (+/-)-Tartaric Acid, Butanedioic acid, 2,3-dihydroxy- (2R,3R)-, (R,R)-tartrate, NSC-62778, W4888I119H, Tartaric acid (VAN), Kyselina vinna [Czech], DTXCID203632, E 334, E-334, RR-tartaric acid, (+)-(2R,3R)-Tartaric acid, Tartaric acid, L-(+)-, EC 201-766-0, TARTARIC ACID (L(+)-), Tartaric acid [USAN:JAN], Weinsaeure, BAROS COMPONENT TARTARIC ACID, L-2,3-DIHYDROXYSUCCINIC ACID, MFCD00064207, C4H6O6, L-tartarate, 4J4Z8788N8, 138508-61-9, (2R,3R)-2,3-Dihydroxybernsteinsaeure, TARTARIC ACID COMPONENT OF BAROS, Resolvable tartaric acid, d-alpha,beta-Dihydroxysuccinic acid, TARTARIC ACID (II), TARTARIC ACID [II], 144814-09-5, Kyselina 2,3-dihydroxybutandiova [Czech], REL-(2R,3R)-2,3-DIHYDROXYBUTANEDIOIC ACID, TARTARIC ACID (MART.), TARTARIC ACID [MART.], (1R,2R)-1,2-Dihydroxyethane-1,2-dicarboxylic acid, TARTARIC ACID (USP-RS), TARTARIC ACID [USP-RS], BUTANEDIOIC ACID, 2,3-DIHYDROXY-, (R-(R*,R*))-, Tartaric acid D,L, Butanedioic acid, 2,3-dihydroxy- (R-(R*,R*))-, TARTARIC ACID (EP MONOGRAPH), TARTARIC ACID [EP MONOGRAPH], Tartarate, DL-TARTARICACID, 132517-61-4, L(+) tartaric acid, (2RS,3RS)-Tartaric acid, 2,3-dihydroxy-succinic acid, Traubensaeure, Vogesensaeure, Weinsaure, acide tartrique, acido tartarico, tartaric-acid, para-Weinsaeure, L-Threaric aci, 4ebt, NSC 148314, NSC-148314, (r,r)-tartarate, (+)-tartarate, l(+)tartaric acid, Tartaric acid; L-(+)-Tartaric acid, Tartaric acid (TN), (+-)-Tartaric acid, Butanedioic acid, 2,3-dihydroxy-, (R*,R*)-, L-(+) tartaric acid, (2R,3R)-Tartarate, 1d5r, DL TARTARIC ACID, TARTARICUM ACIDUM, 2,3-dihydroxy-succinate, TARTARIC ACID,DL-, SCHEMBL5762, TARTARIC ACID, DL-, Tartaric acid (JP17/NF), TARTARIC ACID [FCC], TARTARIC ACID [JAN], d-a,b-Dihydroxysuccinic acid, TARTARIC ACID [INCI], MLS001336057, L-TARTARIC ACID [MI], TARTARIC ACID [VANDF], DL-TARTARIC ACID [MI], CCRIS 8978, L-(+)-Tartaric acid, ACS, TARTARIC ACID [WHO-DD], CHEMBL1236315, L-(+)-Tartaric acid, BioXtra, TARTARICUM ACIDUM [HPUS], UNII-4J4Z8788N8, (2R,3R)-2,3-tartaric acid, CHEBI:26849, HMS2270G22, Pharmakon1600-01300044, TARTARIC ACID, DL- [II], TARTARIC ACID, (+/-)-, TARTARIC ACID,DL- [VANDF], HY-Y0293, STR02377, TARTARIC ACID [ORANGE BOOK], EINECS 205-105-7, Tox21_300155, (2R,3R)-2,3-dihydroxysuccinicacid, NSC759609, s6233, AKOS016843282, L-(+)-Tartaric acid, >=99.5%, CS-W020107, DB09459, NSC-759609, (2R,3R)-2,3-dihydroxy-succinic acid, Butanedioic acid, 2,3-dihydroxy-; Butanedioic acid, 2,3-dihydroxy-, (R-(R*,R*))-, CAS-87-69-4, L-(+)-Tartaric acid, AR, >=99%, (R*,R*)-2,3-dihydroxybutanedioic acid, NCGC00247911-01, NCGC00254043-01, BP-31012, SMR000112492, SBI-0207063.P001, (2R,3R)-rel-2,3-dihydroxybutanedioic acid, NS00074184, T0025, EN300-72271, (R*,R*)-(+-)-2,3-dihydroxybutanedioic acid, C00898, D00103, D70248, L-(+)-Tartaric acid, >=99.7%, FCC, FG, L-(+)-Tartaric acid, ACS reagent, >=99.5%, L-(+)-Tartaric acid, BioUltra, >=99.5% (T), J-500964, J-520420, L-(+)-Tartaric acid, ReagentPlus(R), >=99.5%, L-(+)-Tartaric acid, SAJ first grade, >=99.5%, L-(+)-Tartaric acid, tested according to Ph.Eur., Butanedioic acid, 2,3-dihydroxy-, (R*,R*)-(+-)-, L-(+)-Tartaric acid, JIS special grade, >=99.5%, L-(+)-Tartaric acid, natural, >=99.7%, FCC, FG, L-(+)-Tartaric acid, p.a., ACS reagent, 99.0%, L-(+)-Tartaric acid, Vetec(TM) reagent grade, 99%, Q18226455, F8880-9012, Z1147451717, Butanedioic acid, 2,3-dihydroxy-, (theta,theta)-(+-)-, 000189E3-11D0-4B0A-8C7B-31E02A48A51F, L-(+)-Tartaric acid, puriss. p.a., ACS reagent, >=99.5%, L-(+)-Tartaric acid, certified reference material, TraceCERT(R), Tartaric acid, United States Pharmacopeia (USP) Reference Standard, L-(+)-Tartaric acid, anhydrous, free-flowing, Redi-Dri(TM), ACS reagent, >=99.5%, L-(+)-Tartaric acid, p.a., ACS reagent, reag. ISO, reag. Ph. Eur., 99.5%, Tartaric Acid, Pharmaceutical Secondary Standard; Certified Reference Material

Racemic acid is an organic acid found in many vegetables and fruits such as bananas, and grapes, but also in bananas, citrus, and tamarinds.
Racemic acid is also known as 2,3-dihydroxysuccinic acid or Tartaric acid.

Racemic acid is used to generate carbon dioxide.
Racemic acid is a diprotic aldaric acid which is crystalline white.
Baking powder is a mixture of Racemic acid with sodium bicarbonate.

Racemic acid is widely used in the field of pharmaceuticals.
High doses of Racemic acid can lead to paralysis or death.

Racemic acid is one of the least antimicrobial of the organic acids known to inactivate fewer microorganisms and inhibit less microbial growth in comparison with most other organic acids (including acetic, ascorbic, benzoic, citric, formic, fumaric, lactic, levulinic, malic, and propionic acids) in the published scientific literature.

Racemic acid is a tetraric acid, which is butanedioic acid substituted with hydroxy groups at the 2 and 3 positions.
Racemic acid has a role as a human xenobiotic metabolite and a plant metabolite.
Racemic acid is a conjugate acid of 3-carboxy-2,3-dihydroxypropanoate.

Racemic acid is a white, crystalline organic acid that occurs naturally in many fruits, most notably in grapes, but also in tamarinds, bananas, avocados and citrus.
Racemic acid salt, potassium bitartrate, commonly known as cream of tartar, develops naturally in the process of fermentation.

Racemic acid is commonly mixed with sodium bicarbonate and is sold as baking powder used as a leavening agent in food preparation.
Racemic acid itself is added to foods as an antioxidant E334 and to impart Racemic acid distinctive sour taste.

Racemic acid is an organic acid that naturally occurs in many fruits, most notably in grapes but also in bananas and citrus fruits.
Racemic acid is a white, crystalline solid which can easily be dissolved in water.

Approx. 50 % of the produced Racemic acid is subsequently used by the food and pharmaceutical industry, the other half is used in technical applications.
When added to food or beverage products, Racemic acid is denoted by E-number E 334.

Besides that, Racemic acid and its derivatives are often used in the field of pharmaceuticals or as a chelating agent in the farming and metal industry.

Naturally occurring Racemic acid is a useful raw material in organic chemical synthesis.
Racemic acid, an alpha-hydroxy-carboxylic acid, is diprotic and aldaric in acid characteristics, and is a dihydroxyl derivative of succinic acid.

Racemic acid is a white crystalline organic acid that occurs naturally in many plants, most notably in grapes.
2,3-dihydroxybutanedioic is an alpha-hydroxy-carboxylic acid, is diprotic and aldaric in acid characteristics, and is a dihydroxyl derivative of succinic acid.

Racemic acid is a white crystalline organic acid that occurs naturally in many plants, most notably in grapes.
2,3-dihydroxybutanedioic is an alpha-hydroxy-carboxylic acid, is diprotic and aldaric in acid characteristics, and is a dihydroxyl derivative of succinic acid.

Racemic acid is a white crystalline diprotic organic acid.
Racemic acid occurs naturally in many plants, particularly in grapes, bananas, and tamarinds.
Racemic acid is also one of the main acids found in wine.

Racemic acid can be added to food when a sour taste is desired.
Racemic acid is also used as an antioxidant.

Salts of Racemic acid are known as tartarates.
Racemic acid is a dihydroxy derivative of succinic acid.

Racemic acid is found in cream of tartar and baking powder.
Racemic acid is used in silvering mirrors, tanning leather, and in Rochelle Salt.
In medical analysis, Racemic acid is used to make solutions for the determination of glucose.

Racemic acid is a naturally occurring dicarboxylic acid containing two stereocenters.
Racemic acid exists as a pair of enantiomers and an achiral meso compound.

Racemic acid is present in many fruits (fruit acid), and Racemic acid monopotassium salt is found as a deposit during the fermentation of grape juice.

Racemic acid is a historical compound, dating back to when Louis Pasteur separated Racemic acid into two enantiomers with a magnifying lens and a pair of tweezers more than 160 years ago.

Racemic acid has a stronger, sharper taste than citric acid.
Although Racemic acid is renowned for its natural occurrence in grapes, Racemic acid also occurs in apples, cherries, papaya, peach, pear, pineapple, strawberries, mangos, and citrus fruits.

Racemic acid is used preferentially in foods containing cranberries or grapes, notably wines, jellies, and confectioneries.
Commercially, Racemic acid is prepared from the waste products of the wine industry and is more expensive than most acidulants, including citric and malic acids.

Racemic acid is one of the least antimicrobial of the organic acids known to inactivate fewer microorganisms and inhibit less microbial growth in comparison with most other organic acids (including acetic, ascorbic, benzoic, citric, formic, fumaric, lactic, levulinic, malic, and propionic acids) in the published scientific literature.
Furthermore, when dissolved in hard water, undesirable insoluble precipitates of calcium tartrate can form.

Racemic acid is an abundant constituent of many fruits such as grapes and bananas and exhibits a slightly astringent and refreshing sour taste.
Racemic acid is one of the main acids found in wine.

Racemic acid is added to other foods to give a sour taste and is normally used with other acids such as citric acid and malic acid as an additive in soft drinks, candies, and so on.
Racemic acid is produced by acid hydrolysis of calcium tartrate, which is prepared from potassium tartrate obtained as a by-product during wine production.
Optically active Racemic acid is used for the chiral resolution of amines and also as an asymmetric catalyst.

Racemic acid is the most water-soluble of the solid acidulants.
Racemic acid contributes a strong tart taste that enhances fruit flavors, particularly grape and lime.

Racemic acid is often used as an acidulant in grape- and lime-flavored beverages, gelatin desserts, jams, jellies, and hard sour confectionery.

Racemic acid, a dicarboxylic acid, one of the most widely distributed of plant acids, with a number of food and industrial uses.
Along with several of Racemic acid salts, cream of tartar (potassium hydrogen tartrate) and Rochelle salt (potassium sodium tartrate), Racemic acid is obtained from by-products of wine fermentation.

Study of the crystallographic, chemical, and optical properties of the Racemic acids by French chemist and microbiologist Louis Pasteur laid the basis for modern ideas of stereoisomerism.

Racemic acid is widely used as an acidulant in carbonated drinks, effervescent tablets, gelatin desserts, and fruit jellies.
Racemic acid has many industrial applications—e.g., in cleaning and polishing metals, in calico printing, in wool dyeing, and in certain photographic printing and development processes.
Racemic acid is used in silvering mirrors, in processing cheese, and in compounding mild cathartics.

Racemic acid is incorporated into baking powders, hard candies, and taffies; and Racemic acid is employed in the cleaning of brass, the electrolytic tinning of iron and steel, and the coating of other metals with gold and silver.

Racemic acid is an organic acid.
Racemic acid is also known as 2,3-dihydroxysuccinic acid or Tartaric acid.
Racemic acid is in use to generate carbon dioxide.

Racemic acid is a diprotic aldaric acid.
Racemic acid is an alpha-hydroxy-carboxylic acid and is a dihydroxyl derivative of succinic acid.

Racemic acid is widely in use in the field of pharmaceuticals.
A High dose of Racemic acid can affect our body to a great extent.

Racemic acid is a white and crystalline that occurs naturally in many fruits and vegetables and most notably in grapes.
Racemic acid is also present in bananas, tamarinds, and citrus.

Racemic acid is commonly mixed with sodium bicarbonate and is sold as a baking powder that is in use as a leavening agent in food preparation.
The Racemic acid is added to foods being an antioxidant i.e., E334 and to impart Racemic acid distinctive sour taste.

Racemic acid, sometimes called Tartaric acid, is an organic compound that naturally occurs in plants, wine, and many fruits, such as grapes, tamarinds, citrus, and bananas.
The acid is available as a white solid that’s soluble in water.
Racemic acid salt, commonly referred to as cream of tartar, is created naturally through fermentation.

Racemic acid is made from potassium acid tartrate obtained from different by-products of the wine industry, such as lees, argol, and press cakes from fermented grape juice.
This dibasic acid is usually mixed with sodium bicarbonate and is available as baking powder commonly used as a food additive.

Uses of Racemic acid:
Racemic acid is Levo form of dextrorotatory Racemic acid.
Racemic acid is found throughout nature and classified as a fruit acid.

Racemic acid is used in soft drinks and foods, as an acidulant, complexing agent, pharmaceutic aid (buffering agent), in photography, tanning, ceramics, and to make tartrates.
Diethyl and dibutyl ester derivatives are commercially significant for use in lacquers and in textile printing.

Racemic acid is used as an intermediate, in construction and ceramics applications, in cleaning products, cosmetics/personal care products, and metal surface treatments (including galvanic and electroplating products).
Racemic acid is used as a flavoring agent, anticaking agent, drying agent, firming agent, humectant, leavening agent, and pH control agent for foods.

Racemic acid is used to improve the taste of oral medications.
Racemic acid is used to chelate metal ions such as magnesium and calcium.

Racemic acid is used in recipes as a leavening agent along with baking soda.
Racemic acid is used as an antioxidant.

Racemic acid is as one of the important acids in wine.
Racemic acid is used in foods to give a sour taste.

Racemic acid is sometimes used to induce vomiting.
Racemic acid is used to make silver mirrors.

In its ester form, Racemic acid is used in the dyeing of textiles.
Racemic acid is used in the tanning of leather.

Racemic acid is used in candies.
In its cream form, Racemic acid is used as a stabilizer in food.

Food industry:
Racemic acid is used as acidifier and natural preservative for marmalades, ice cream, jellies, juices, preserves, and beverages.
Racemic acid is used as effervescent for carbonated water.
Racemic acid is used as emulsifier and preservative in the bread-making industry and in the preparation of candies and sweets.

Oenology:
Racemic acid is used as an acidifier.
Racemic acid is used in musts and wines to prepare wines that are more balanced from the point of view of taste, the result being an increase in their degree of acidity and a decrease in their pH content.

Pharmaceuticals industry:
Racemic acid is used as an excipient for the preparation of effervescent tablets.

Construction industry:
Racemic acid is used in cement, plaster, and plaster of Paris to retard drying and facilitate the handling of these materials.

Cosmetics industry:
Racemic acid is used as a basic component of many natural body crèmes.

Chemical sector:
Racemic acid is used in galvanic baths.
Racemic acid is used in electronics industry.

Racemic acid is used as mordant in the textile industry.
Racemic acid is used as an anti-oxidant in industrial greases.

Industry Uses:
Processing aids not otherwise specified

Consumer Uses:
Processing aids not otherwise specified

Industrial Processes with risk of exposure:
Electroplating
Painting (Pigments, Binders, and Biocides)
Leather Tanning and Processing
Photographic Processing
Textiles (Printing, Dyeing, or Finishing)

Usage Areas of Racemic acid:
Racemic acid, this crystalline acid, is commonly seen in plants and fruits.
The chemical formula of Racemic acid, an organic acid, is C4H6O6 and its density is 1.788g/cm.

Racemic acid is used in different branches of industry, especially industry.
Racemic acid is generally preferred for the fermentation of wine and is formed as a byproduct of potassium during fermentation.

Racemic acid is frequently used in wool dyeing, polishing, gelatin, desserts and sodas.
Racemic acid, which is mostly found in grape fruits, also occurs in some fruits other than grapes.

Racemic acid, which is formed from the mixture of raceme, is called levo.
Racemic acids are among the water-soluble dicarboxylic acids.

Racemic acid is used to give a sour taste to foods.
Racemic acid, E334, is a good antioxidant.

The most common use of Racemic acid is in soda production.
Racemic acid, which is used to flavor soda, is an indispensable component of soda.

Racemic acid is preferred for dyeing wool.
Racemic acid can be used for polishing, polishing and cleaning metals.

Racemic acid is used to release carbon dioxide in bakery products.
Racemic acid, an indispensable ingredient in gelatin desserts, is generally preferred as a thickener in products such as meringue, Turkish delight and whipped cream.

The form of Racemic acid obtained from grapes is generally preferred in pastry.
Racemic acid can be preferred over baking powder for rising cakes.

Racemic acid, which is frequently found in fruits and has a tart and strong taste, is preferred for winemaking and fermentation of wine.
Racemic acid is used in making marmalade and jams.

Applications of Racemic acid:
Racemic acid and its derivatives have a plethora of uses in the field of pharmaceuticals.
For example, Racemic acid has been used in the production of effervescent salts, in combination with citric acid, to improve the taste of oral medications.

Racemic acid also has several applications for industrial use.

The acid has been observed to chelate metal ions such as calcium and magnesium.
Therefore, the acid has served in the farming and metal industries as a chelating agent for complexing micronutrients in soil fertilizer and for cleaning metal surfaces consisting of aluminium, copper, iron, and alloys of these metals, respectively.

Racemic acid is used in fuels and fuel additives, laboratory chemicals, lubricants and lubricant additives, coating agents and surface treatment agents.
Racemic acid is used in processing aids and petroleum production specific processing aids.

Racemic acid is used in ink, toner and coloring products, laboratory use, lubricants and greases.
Racemic acid is found in cream of tartar, which is used in making candies and frostings for cakes.

Racemic acid is also used in baking powder where Racemic acid serves as the source of acid that reacts with sodium bicarbonate (baking soda).
This reaction produces carbon dioxide gas and lets products “rise,” but Racemic acid does so without the “yeast” taste that can result from using active yeast cultures as a source of the carbon dioxide gas.

Racemic acid is used in silvering mirrors, tanning leather, and in the making of Rochelle Salt, which is sometimes used as a laxative.
Blue prints are made with ferric tartarte as the source of the blue ink.

In medical analysis, Racemic acid is used to make solutions for the determination of glucose.
Common esters of Racemic acid are diethyl tartarate and dibutyl tartrate.
Both are made by reacting Racemic acid with the appropriate alcohol, ethanol or n-butanol.

Racemic acid in wine:
Racemic acid may be most immediately recognizable to wine drinkers as the source of "wine diamonds", the small potassium bitartrate crystals that sometimes form spontaneously on the cork or bottom of the bottle.

Racemic acid plays an important role chemically, lowering the pH of fermenting "must" to a level where many undesirable spoilage bacteria cannot live, and acting as a preservative after fermentation.
In the mouth, Racemic acid provides some of the tartness in the wine, although citric and malic acids also play a role.

Racemic acid in fruits:
Grapes and tamarinds have the highest levels of Racemic acid concentration.
Other fruits with Racemic acid are bananas, avocados, prickly pear fruit, apples, cherries, papayas, peaches, pears, pineapples, strawberries, mangoes and citrus fruits.

Results from a study showed that in citrus (oranges, lemons and mandarins), fruits produced in organic farming contain higher levels of Racemic acid than fruits produced in conventional agriculture.

Trace amounts of Racemic acid have been found in cranberries and other berries.
Racemic acid is also present in the leaves and pods of Pelargonium plants and beans.

Retarding Agent:
Racemic acid is widely used as a retarding agent in oilfield applications as well as in cementitious-based systems.
Racemic acid works by slowing the setting of cement by impeding certain reactions during the hydration of the cement process.
Racemic acid retards various steps, including ettringite formation and C3A hydration.

Food Additive:
Racemic acid also has many uses in the food industry.
As an acidulant, Racemic acid offers a pleasant sour taste and gives food a sharp flavor.

Racemic acid also serves as a preservative food agent and can help set gels.
Racemic acid is usually added to most products, including carbonated beverages, gelatin, fruit jellies, and effervescent tablets.
This acid is also used as an ingredient in candy and various brands of baking powders and leavening systems to make goods rise.

Industrial Applications:
Racemic acid has many industrial applications.
Racemic acid’s used in gold and silver plating, making blue ink for blueprints, tanning leather, and cleaning and polishing metals.
Racemic acid’s also one of the ingredients in Rochelle Salt, which is luxuriant and reacts with silver nitrate to form the silvering in mirrors.

Commercial Application:
The by-products obtained from the fermentation of wine during the production of Racemic acid are heated with calcium hydroxide.
This causes calcium tartrate to develop a residue, which is further treated with sulfuric acid to form a mixture of Racemic acid and calcium sulfate.
Once the mixture is separated, Racemic acid is purified and used for commercial production.

Other Racemic acid uses include pharmaceutical applications to produce effervescent salt that helps enhance the taste of oral medications.
Racemic acid’s also used in the metals and farming industry as a chelating agent for cleaning metal surfaces and adding nutrients to the soil.

Derivatives of Racemic acid:

Important derivatives of Racemic acid include:
Sodium ammonium tartrate, the first material separated into Racemic acid enantiomers
Cream of tartar (potassium bitartrate), used in cooking
Rochelle salt (potassium sodium tartrate), which has unusual optical properties
Tartar emetic (antimony potassium tartrate), a resolving agent.
Diisopropyl tartrate is used as a co-catalyst in asymmetric synthesis.

Racemic acid is a muscle toxin, which works by inhibiting the production of malic acid, and in high doses causes paralysis and death.
As a food additive, Racemic acid is used as an antioxidant with E number E334; Racemic acids are other additives serving as antioxidants or emulsifiers.

Production of Racemic acid:
Racemic acid is industrially produced in the largest amounts.
Racemic acid is obtained from lees, a solid byproduct of fermentations.
The former byproducts mostly consist of potassium bitartrate (KHC4H4O6).

This potassium salt is converted to calcium tartrate (CaC4H4O6) upon treatment with calcium hydroxide "milk of lime" (Ca(OH)2):
KH(C4H4O6) + Ca(OH)2 -> Ca(C4H4O6) + KOH + H2O

In practice, higher yields of calcium tartrate are obtained with the addition of calcium chloride.

Calcium tartrate is then converted to Racemic acid by treating the salt with aqueous sulfuric acid:
Ca(C4H4O6) + H2SO4 -> H2(C4H4O6) + CaSO4

Racemic Racemic acid:
Racemic Racemic acid can be prepared in a multistep reaction from maleic acid.

In the first step, the maleic acid is epoxidized by hydrogen peroxide using potassium tungstate as a catalyst.
HO2CC2H2CO2H + H2O2 → OC2H2(CO2H) 2

In the next step, the epoxide is hydrolyzed.
OC2H2(CO2H)2 + H2O → (HOCH)2(CO2H)2

meso-Racemic acid:
A mixture of racemic acid and meso-Tartaric acid is formed when dextro-Racemic acid is heated in water at 165 °C for about 2 days.

meso-Racemic acid can also be prepared from dibromosuccinic acid using silver hydroxide:
HO2CCHBrCHBrCO2H + 2 AgOH → HO2CCH(OH)CH(OH)CO2H + 2 AgBr

meso-Tartaric acid can be separated from residual racemic acid by crystallization, the racemate being less soluble.

General Manufacturing Information of Racemic acid:

Industry Processing Sectors:
Computer and Electronic Product Manufacturing
Construction
Not Known or Reasonably Ascertainable

Stereochemistry of Racemic acid:
Naturally occurring form of the acid is dextro Racemic acid.
Because Racemic acid is available naturally, Racemic acid is cheaper than its enantiomer and the meso isomer.

Dextro and levo form monoclinic sphenoidal crystals and orthorhombic crystals.
Racemic Racemic acid forms monoclinic and triclinic crystals (space group P1).

Anhydrous meso Racemic acid form two anhydrous polymorphs: triclinic and orthorhombic.
Monohydrated meso Racemic acid crystallizes as monoclinic and triclinic polymorphys depending on the temperature at which crystallization from aqueous solution occurs.
Racemic acid in Fehling's solution binds to copper(II) ions, preventing the formation of insoluble hydroxide salts.

History of Racemic acid:
Racemic acid has been known to winemakers for centuries.
However, the chemical process for extraction was developed in 1769 by the Swedish chemist Carl Wilhelm Scheele.

Racemic acid played an important role in the discovery of chemical chirality.
This property of Racemic acid was first observed in 1832 by Jean Baptiste Biot, who observed Racemic acid ability to rotate polarized light.

Louis Pasteur continued this research in 1847 by investigating the shapes of sodium ammonium tartrate crystals, which he found to be chiral.
By manually sorting the differently shaped crystals, Pasteur was the first to produce a pure sample of levoRacemic acid.

Pharmacology and Biochemistry of Racemic acid:

Pharmacodynamics:
Racemic acid is used to generate carbon dioxide through interaction with sodium bicarbonate following oral administration.
Carbon dioxide extends the stomach and provides a negative contrast medium during double contrast radiography.
In high doses, this agent acts as a muscle toxin by inhibiting the production of malic acid, which could cause paralysis and maybe death.

Route of Elimination:
Only about 15-20% of consumed Racemic acid is secreted in the urine unchanged.

Metabolism / Metabolites:
Most tartarate that is consumed by humans is metabolized by bacteria in the gastrointestinal tract, primarily in the large instestine.

Human Metabolite Information of Racemic acid:

Tissue Locations:
Adipose Tissue
Platelet
Prostate

Cellular Locations:
Cytoplasm

Reactivity of Racemic acid:
Racemic acid, can participate in several reactions.

As shown the reaction scheme below, dihydroxymaleic acid is produced upon treatment of Racemic acid with hydrogen peroxide in the presence of a ferrous salt.
HO2CCH(OH)CH(OH)CO2H + H2O2 → HO2CC(OH)C(OH)CO2H + 2 H2O

Dihydroxymaleic acid can then be oxidized to Racemic acid with nitric acid.

Accidental Release Measures of Racemic acid:

Spillage Disposal:

Personal protection:
Particulate filter respirator adapted to the airborne concentration of Racemic acid.
Sweep spilled substance into covered containers.

If appropriate, moisten first to prevent dusting.
Store and dispose of according to local regulations.

Identifiers of Racemic acid:
CAS Number:
R,R-isomer: 87-69-4
S,S-isomer: 147-71-7
racemic: 133-37-9
meso-isomer: 147-73-9
ChEBI: CHEBI:15674

ChEMBL:
ChEMBL333714
ChEMBL1200861

ChemSpider: 852
DrugBank: DB01694
ECHA InfoCard: 100.121.903
E number: E334 (antioxidants, ...)
KEGG: C00898
MeSH: tartaric+acid
PubChem CID: 875 unspecified isomer
UNII: W4888I119H
CompTox Dashboard (EPA): DTXSID5046986
InChI: InChI=1S/C4H6O6/c5-1(3(7)8)2(6)4(9)10/h1-2,5-6H,(H,7,8)(H,9,10)
Key: FEWJPZIEWOKRBE-UHFFFAOYSA-N
InChI=1/C4H6O6/c5-1(3(7)8)2(6)4(9)10/h1-2,5-6H,(H,7,8)(H,9,10)
Key: FEWJPZIEWOKRBE-UHFFFAOYAZ
SMILES: O=C(O)C(O)C(O)C(=O)O

CAS number: 147-71-7
EC number: 205-695-6
Hill Formula: C₄H₆O₆
Chemical formula: HOOCCH(OH)CH(OH)COOH
Molar Mass: 150.09 g/mol
HS Code: 2918 12 00

CAS: 87-69-4
Molecular Formula: C4H6O6
Molecular Weight (g/mol): 150.09
MDL Number: MFCD00064207
InChI Key: FEWJPZIEWOKRBE-UHFFFAOYNA-N
PubChem CID: 444305
ChEBI: CHEBI:15671
SMILES: OC(C(O)C(O)=O)C(O)=O

Properties of Racemic acid:
Chemical formula:
C4H6O6 (basic formula)
HO2CCH(OH)CH(OH)CO2H (structural formula)

Molar mass: 150.087 g/mol
Appearance: White powder

Density:
1.737 g/cm3 (R,R- and S,S-)
1.79 g/cm3 (racemate)
1.886 g/cm3 (meso)

Melting point:
169, 172 °C (R,R- and S,S-)
206 °C (racemate)
165-6 °C (meso)

Solubility in water:
1.33 kg/L (L or D-tartaric)
0.21 kg/L (DL, racemic)
1.25 kg/L ("meso")

Acidity (pKa): L(+) 25 °C: pKa1= 2.89, pKa2= 4.40
meso 25 °C: pKa1= 3.22, pKa2= 4.85
Conjugate base: Bitartrate
Magnetic susceptibility (χ): −67.5·10−6 cm3/mol

Density: 1.8 g/cm3 (20 °C)
Flash point: 210 °C
Ignition temperature: 425 °C
Melting Point: 172 - 174 °C
Solubility: 1394 g/l

grade: ACS reagent
Quality Level: 200
vapor density: 5.18 (vs air)
Assay: ≥99.5%

form:
crystalline powder
crystals

optical activity: [α]20/D +12.4°, c = 20 in H2O
optical purity: ee: 99% (GLC)
autoignition temp.: 797 °F

impurities:
≤0.002% S compounds
≤0.005% insolubles

ign. residue: ≤0.02%
mp: 170-172 °C (lit.)

anion traces:
chloride (Cl-): ≤0.001%
oxalate (C2O42-): passes test
phosphate (PO43-): ≤0.001%

cation traces:
Fe: ≤5 ppm
heavy metals (as Pb): ≤5 ppm

SMILES string: O[C@H]([C@@H](O)C(O)=O)C(O)=O
InChI: 1S/C4H6O6/c5-1(3(7)8)2(6)4(9)10/h1-2,5-6H,(H,7,8)(H,9,10)/t1-,2-/m1/s1
InChI key: FEWJPZIEWOKRBE-JCYAYHJZSA-N

Molecular Weight: 150.09 g/mol
XLogP3-AA: -1.9
Hydrogen Bond Donor Count: 4
Hydrogen Bond Acceptor Count: 6
Rotatable Bond Count: 3
Exact Mass: 150.01643791 g/mol
Monoisotopic Mass: 150.01643791 g/mol
Topological Polar Surface Area: 115Ų
Heavy Atom Count: 10
Complexity: 134
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 2
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 Racemic acid:
Assay (acidimetric): ≥ 99.0 %
Melting range (lower value): ≥ 166 °C
Melting range (upper value): ≤ 169 °C
Spec. rotation [α²0/D (c=10 in water): -14.0 - -12.0 °
Identity (IR): passes test

Melting Point: 168.0°C to 172.0°C
Color: White or Colorless
Assay Percent Range: 99+%
Linear Formula: HO2CCH(OH)CH(OH)CO2H
Solubility Information: Solubility in water: 1390g/L (20°C).
Other solubilities: soluble in methanol, ethanol, propanol and, glycerol, 4g/L ether, insoluble in chloroform
IUPAC Name: Racemic acid
Formula Weight: 150.09
Percent Purity: ≥99%
Quantity: 500 g
Flash Point: 210°C
Infrared Spectrum: Authentic
Loss on Drying: 0.5% (1g, 105°C) max.
Packaging: Plastic bottle
Physical Form: Crystals or Crystalline Powder
Chemical Name or Material: L(+)-Tartaric acid

Related compounds of Racemic acid:
2,3-Butanediol
Cichoric acid

Other cations:
Monosodium tartrate
Disodium tartrate
Monopotassium tartrate
Dipotassium tartrate

Related carboxylic acids:
Butyric acid
Succinic acid
Dimercaptosuccinic acid
Malic acid
Maleic acid
Fumaric acid

Names of Racemic acid:

Preferred IUPAC name:
Racemic acid

Other names:
Tartaric acid
2,3-Dihydroxysuccinic acid
Threaric acid
Tartaric acid
Uvic acid
Paratartaric acid
Winestone
RADIA 7513
Radia 7513 is the ester obtained from the reaction of tridecyl alcohol combined with stearic acid.


CAS Number: 95912-88-2
EC Number: 306-084-8
Chemical name : isotridecyl stearate
chemical name : Fatty acids, C16-18, isotridecyl esters


In raw material form, Radia 7513 is described as a clear oily liquid that may have a light-yellow hue.
Radia 7513 has been deemed safe by the Cosmetic Ingredient Review Expert Panel.


Radia 7513 contains tridecyl alcohol (1-tridecanol) as alcoholic component.
Stearates are salts or esters of stearic acid (octadecanoic acid).
Radia 7513 is the ester obtained from the reaction of tridecyl alcohol combined with stearic acid.



USES and APPLICATIONS of RADIA 7513:
Radia 7513 is used Ingredients for skincare.
Radia 7513 or 11-methyldodecyl octadecanoate or Octadecanoic acid is isotridecyl ester.
Radia 7513 is used in Skin care products, Raw material for spin finishes and oiling agent for textile, Rubber processing agent, Plastic lubricant, Paint & Ink additive.


Radia 7513 is ester used as a processing additive in polymers.
Radia 7513 is used raw material for spin finishes and oiling agent for textile, Rubber processing agent, Plastic lubricant, Paint & Ink additive.
Radia 7513’s used in cosmetics as a texture-enhancer/thickening agent and emollient and may be animal-derived or synthetic (Paula’s Choice uses the latter).



RADIA 7513 AT A GLANCE:
*The ester obtained from the reaction of tridecyl alcohol combined with stearic acid
*Works as a texture-enhancer/thickening agent and skin-softening emollient
*Touted for its quick absorption and velvety after feel
*Described as a clear oily liquid in raw material form



FUNCTIONS OF RADIA 7513 IN COSMETIC PRODUCTS:
*SKIN CONDITIONING
Radia 7513 maintains the skin in good condition



PHYSICAL and CHEMICAL PROPERTIES of RADIA 7513:
Appearance : light yellow oily liquid
acid value : max 1 mg KOH/g
other : iodine value: max 1 gI2/100 g
viscosity at 40 °C: 14-18 mm²/s
Moisture : max 0,1%
Density : 0,85:
Flashpoint: >210 °C
Molecular Weight: 466.8 g/mol
XLogP3-AA: 14.4
Hydrogen Bond Donor Count: 0
Hydrogen Bond Acceptor Count: 2
Rotatable Bond Count: 28
Exact Mass: 466.47498122 g/mol
Monoisotopic Mass: 466.47498122 g/mol
Topological Polar Surface Area: 26.3Ų
Heavy Atom Count: 33

Formal Charge: 0
Complexity: 377
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
LogP: 14.386 (est)
EWG's Food Scores: 1
Appearance: Clear colorless to light yellow liquid.
Purity: 96% minimum.
Boiling point: 490C.
Flash point: 255C.
Relative density: about 0.9
Acid value: 1.0 maximum.
Saponification value: 120 – 130
Hydroxyl value: 3 maximum.
Color: 50 apha maximum.
Moisture: 0.1% maximum.



FIRST AID MEASURES of RADIA 7513:
-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 RADIA 7513:
-Environmental precautions:
No special environmental precautions required.
-Methods and materials for containment and cleaning up:
Keep in suitable, closed containers for disposal.



FIRE FIGHTING MEASURES of RADIA 7513:
-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 RADIA 7513:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection
*Skin protection:
Handle with gloves.
Wash and dry hands.
Full contact:
Material: Nitrile rubber
Minimum layer thickness: 0,4 mm
Break through time: 480 min
Splash contact:
Material: Nitrile rubber
Minimum layer thickness: 0,4 mm
Break through time: 480 min
*Body Protection:
Impervious clothing.
*Respiratory protection:
Respiratory protection not required.
-Control of environmental exposure:
No special environmental precautions required



HANDLING and STORAGE of RADIA 7513:
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Store in cool place.
Keep container tightly closed in a dry and well-ventilated place.



STABILITY and REACTIVITY of RADIA 7513:
-Reactivity:
No data available
-Chemical stability:
Stable under recommended storage conditions.
-Possibility of hazardous reactions:
No data available
-Conditions to avoid:
No data available



SYNONYMS:
Fettsuren, C16-18-, Isotridecylester
Fatty acids, C16-18, isotridecyl esters
Fatty acids, C16-18, isotridecyl esters
Isotridecyl stearate
31565-37-4
11-methyldodecyl octadecanoate
Octadecanoic acid, isotridecyl ester
Octadecanoic acid,isotridecyl ester
J8793TKA30
Stearic acid, isotridecyl ester
EINECS 250-703-3
UNII-J8793TKA30
EXCEPARL TD-S
SCHEMBL2699239
ISOTRIDECYL STEARATE [INCI]
W-110802
Q27281337
Isotridecylstearat
isotridecyl stearate
11-methyldodecyl octadecanoate
Stearic acid, isotridecyl ester
Octadecanoic acid, isotridecyl ester


RADIACID 0907
RADIACID 0907 is derived from 100% vegetable origin.
Due to their branched structure the RADIACID 0907 has a characteristic emollient feel
RADIACID 0907 has a non-greasy feel


CAS NUMBER: 2724-58-5

EC NUMBER: 250-178-0

MOLECULAR FORMULA: C18H36O2

MOLECULAR WEIGHT: 284.5 g/mol

IUPAC NAME: 16-methylheptadecanoic acid


RADIACID 0907 has a highly substantive lipid film
Soft skin feel and leaves a glossy appearance to the skin

RADIACID 0907 is used in colour cosmetics, deodorants and personal care products, where it provides film-forming and spreading functions.
RADIACID 0907 is an exceptionally good emollient with a pleasant feel, and is used widely in skin and body care products.

RADIACID 0907 is used in the following products:
-washing & cleaning products
-adhesives and sealants
-fuels
-lubricants and greases
-coating products
-fertilisers

RADIACID 0907 is used in biocides (e.g. disinfectants, pest control products)
RADIACID 0907 is also used in pH regulators and water treatment products

RADIACID 0907 can be used in laboratory chemicals, plant protection products, water softeners and water treatment chemicals.
RADIACID 0907 is used in formulation of mixtures
RADIACID 0907 is used for the manufacture of chemicals.

RADIACID 0907 is prepared from soybean oil and tallow.
RADIACID 0907 comes as white to pale yellow, clear oily liquid.

RADIACID 0907 is liquid at room temperature.
RADIACID 0907 is chemically, a carboxyl group attached to alkyl chain, methylated, branched at various carbons makes it much more stable compared to other linear chain fatty acids, including oxidation potential.

RADIACID 0907 is a yellow solution and its chemical formula is C18H36O2.
RADIACID 0907 is a saturated carbon solution.
RADIACID 0907 is found naturally in meat products and vegetable oils.

RADIACID 0907 can be used as a lubricant, that can improve flow of a powder mixture.
RADIACID 0907 has excellent spreadability without oiliness

RADIACID 0907 is a fatty acid molecule with an 18-carbon atom chain backbone.
RADIACID 0907 is an isomer of stearic acid, meaning that they both have a chemical formula of C18H36O2, but differ in the arrangement of their atoms.

RADIACID 0907 is used in personal care products
RADIACID 0907 is also used in cosmetic industry

RADIACID 0907 has lubricating or adhesive properties
RADIACID 0907 is also used in paper products.

While stearic acid has a linear carbon chain with 18 carbon atoms, isosteric acid as a carbon chain with 17 atoms and a single carbon branch at the 16th carbon atom. Its chemical structure can be represented as (CH3)2CH(CH2)14CO2H.
RADIACID 0907 is found naturally in meat products and vegetable oils.

RADIACID 0907 has a wide range of industrial uses.
RADIACID 0907 is mainly used as an additive in adhesives or lubricants for both paints and personal care products.

RADIACID 0907 is an important raw material in the preparation of speciality surfactants for consumer care products.
RADIACID 0907 (RADIACID 0907) is used in the synthesis of methyl-branched poly(hydroxyalkanoate)s, biosurfactants and silver nanoparticles

RADIACID 0907 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, RADIACID 0907 is based 100% on the parent oil or fat.

RADIACID 0907 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 RADIACID 0907 also enhances its dispersing power

RADIACID 0907 has high performance lubricants with excellent cold stability
RADIACID 0907 is used in metal rolling fluids

Being a fatty acid, RADIACID 0907 is also amphiphilic, meaning it is a molecule with a hydrophobic end and a hydrophilic end.
As such, RADIACID 0907 can have favorable interactions with both polar and non-polar molecules, enabling it to act as a surfactant.

RADIACID 0907 is also soluble in many oils, which allows it to be used as an emulsifier or dispersant.
With this set of properties, RADIACID 0907 is a useful additive in a variety of applications, including:

-Adhesives
-Coatings and paints
-Finishing agents
-Lubricants
-Sealants
-Solvents
-Surfactants
-Viscosity adjusters

RADIACID 0907 is used as a cosmetic esters
RADIACID 0907 is used in manufacturing of soaps

RADIACID 0907 is a long-chain fatty acid
RADIACID 0907 is functionally related to a heptadecanoic acid.
RADIACID 0907 is a natural product found in Aristolochia grandiflora, Streptomyces, and other organisms with data available.


PHYSICAL PROPERTIES:

-Molecular Weight: 284.5 g/mol

-XLogP3: 7.2

-Exact Mass: 284.271530387 g/mol

-Monoisotopic Mass: 284.271530387 g/mol

-Topological Polar Surface Area: 37.3Ų

-Physical Description: Colorless Liquid

-Boiling Point: 400 °C

-Melting Point: 69.5 °C

-Solubility: 0.007116 mg/L

-LogP: 7.674

-Refractive Index: 1.4440 (estimate)

-Storage Temperature: 2-8°C

-pka: 4.78


RADIACID 0907 is used in cosmetic and industrial applications for the stabilisation of pigments and mineral particles in oils and solvents.
RADIACID 0907 is used for a cosmetic formulations

RADIACID 0907 can be used in industrial applications for the stabilisation of pigments mineral particles in oils and solvents
RADIACID 0907 differs from other C18 fatty acids of the same category in a number of ways.


CHEMICAL PROPERTIES:

-Hydrogen Bond Donor Count: 1

-Hydrogen Bond Acceptor Count: 2

-Rotatable Bond Count: 15

-Heavy Atom Count: 20

-Formal Charge: 0

-Complexity: 212

-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


RADIACID 0907 is also used in paper products
RADIACID 0907 is a methyl-branched fatty acid that is heptadecanoic acid (margaric acid) substituted by a methyl group at position 16.
RADIACID 0907 is used in the synthesis of methyl-branched poly(hydroxyalkanoate)s, biosurfactants and silver nanoparticles.

RADIACID 0907 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, RADIACID 0907 is based 100% on the parent oil or fat.
RADIACID 0907's is a light yellow liquid

APPLICATIONS:
Synthetic lubricants – RADIACID 0907 has good thermal and oxidative stability

Lubricant additives – RADIACID 0907 is derivatized to isostearyl amide to provide boundary lubrication and detergency

Coatings – RADIACID 0907 imparts flexibility and durability properties to industrial coatings

Metalworking – RADIACID 0907 has good surface activity for protective coatings and thermal stability for rolling and stamping

Personal care products – RADIACID 0907 is derivatized to isostearyl alcohol to impart feel and texture to creams and lotions.

RADIACID 0907 is used in personal care formulations for its function as both an emollient and co-emulsifier.
RADIACID 0907 is a synthetically created fatty acid most often used as a binder in skin and beauty products, although it is also seen in products as a surfactant and emulsifier.

RADIACID 0907 is a unique fatty acid.
RADIACID 0907 combines the best properties of stearic acid with the best properties of oleic acid.

RADIACID 0907 is an 18-carbon branched-chain fatty acid naturally found in plants and animals.
However, RADIACID 0907's a blend of many octadecanoic acids, found in vegetables and animals fat.

RADIACID 0907 is used to thicken most formulas as a binder and emulsifier.
RADIACID 0907 is a lightly-branched, liquid fatty acid produced by the reaction of oleic acid with a natural mineral catalyst.
RADIACID 0907 serves as a smooth, dry feeling emollient able to assist the skin in replenishing its natural moisture.

RADIACID 0907 can be easily used in a cosmetic which not only moisturizes skin but also does not leave any oily feel.
However, in cosmetic formulation RADIACID 0907 is used as a binder to form cake-like compact powder or eye shadow.
RADIACID 0907 is also used in cleansing and emulsifying agent, because of presence of both ionic and nonionic groups.

RADIACID 0907 is used in varieties of cosmetic and personal care products.
RADIACID 0907 is a synthetically created fatty acid
RADIACID 0907 is used as a binder in skin and beauty products

RADIACID 0907 is a clear, oily liquid that is used in a wide variety of cosmetics and personal care products.
RADIACID 0907 (16-Methylheptadecanoic acid) is used in the synthesis of methyl-branched poly(hydroxyalkanoate)s, biosurfactants and silver nanoparticles.
RADIACID 0907 is a fatty acid that is used as an emollient in pharmaceutical preparations.
RADIACID 0907 has been shown to have skin-moisturizing and anti-inflammatory properties, which are due to its ability to inhibit the activity of phospholipase A2.

RADIACID 0907 is a fatty acid molecule with an 18-carbon atom chain backbone.
RADIACID 0907 is an isomer of stearic acid
RADIACID 0907's chemical formula is C18H36O2

RADIACID 0907 is a liquid fatty acid created from oleic acid.
RADIACID 0907'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.

RADIACID 0907's quite popular in foundations.
RADIACID 0907 is our unique, highly branched, saturated fatty acid.

RADIACID 0907 has some features that are transparent and odorless, unlike straight chain fatty acids.
Additionally, RADIACID 0907 has excellent heat stability, oxidation resistance, pigment dispensing ability, defoaming property and is compatible with various organic solvents.

RADIACID 0907 is a fatty acid which contains 18-carbon atom chain.
The IUPAC name of RADIACID 0907 is octadecanoic acid.

RADIACID 0907 is a yellow solution and its chemical formula is C18H36O2.
RADIACID 0907 is a saturated carbon solution.

RADIACID 0907 is found naturally in meat products and vegetable oils.
The molecular mass of RADIACID 0907 is 284.48 g/mol.

RADIACID 0907 is soluble in many oils
RADIACID 0907 is used as an emulsifier or dispersant.

RADIACID 0907 is derived from renewable sources, offering unique characteristics such as high oxidation resistance and excellent cold temperature properties.
Applications include additives or base stock for the fuel and lubricants industry and emollients for personal care.

RADIACID 0907 is a high quality 16-Methylheptadecanoic acid used in synthesis.
This product has been used as molecular tool for various biochemical applications.
RADIACID 0907 has also been used in a wide array of other chemical and immunological applications.


SYNONYMS:

RADIACID 0907
Radiacid 0907
jaric I-18CG
jaric I-18IG
jaric I-18LG
liponate ISA
ISOOCTADECANOIC ACID
isostearic
16-METHYLHEPTADECANOIC ACID
Isostearinsure
ISOSTEARIC ACID
16-methyl-heptadecanoicaci
Heptadedecanoicacid,16-Methyl
ISOSTEARIC ACID MIXED ISOMERS
Heptadecanoic acid, 16-methyl-
heptadecanoic acid, 16-methyl-
jaric I-18CG
jaric I-18IG
jaric I-18LG
liponate ISA
16-methyl heptadecanoic acid
16-methyl margaric acid
16-methylheptadecanoic acid
isooctadecanoic acid
prisorine 3505
prisorine 3515
isostearicacid
ISOSTEARIC ACID
Isooctadecanoic acid
16-METHYLHEPTADECANOIC ACID
2724-58-5
30399-84-9
Prisorine 3509
Heptadecanoic acid, 16-methyl-
16-methyl margaric acid
16-methyl-heptadecanoic acid
LZM5XA0ILL
CHEBI:84896
(+)-Isostearic acid
UNII-LZM5XA0ILL
EINECS 220-336-3
16-methylmargaric acid
EMERSOL 873
SCHEMBL15489
CHEMBL1865303
DTXSID1040790
16-METHYLHEPTADECANOICACID
LMFA01020014
HY-W127433
NCGC00164392-01
NCGC00164392-02
NCGC00255115-01
AS-57253
CAS-30399-84-9
CS-0185665
Isostearic acid
16-Methylheptadecanoic acid
220-336-3
250-178-0
2724-58-5
30399-84-9
Heptadecanoic acid, 16-methyl-
Isooctadecanoic acid
MFCD00044082
MI3875000
X33R8U0062
(+)-isostearic acid
16-methyl margaric acid
16-methyl-heptadecanoic acid
16-methylmargaric acid
2-methyl-heptadecanoic acid
2-Methylheptadecanoic acid
Heptadecanoic acid, 2-methyl-
λ-Isostearic acid
Isostearic acid
16-Methylheptadecanoic acid
220-336-3
250-178-0
2724-58-5
30399-84-9
Acide 16-méthylheptadécanoïque
Heptadecanoic acid, 16-methyl-
Isooctadecanoic acid
MI3875000
X33R8U0062
(+)-isostearic acid
16-methyl margaric acid
16-methyl-heptadecanoic acid
16-methylmargaric acid
2-methyl-heptadecanoic acid
2-Methylheptadecanoic acid
Heptadecanoic acid, 2-methyl-
λ-Isostearic acid

RADIASURF 7403
DESCRIPTION:

Radiasurf 7403 acts as a non-ionic surfactant and emulsifier for o/w emulsions.
Radiasurf 7403 is non-toxic, non-irritating, non-exhaustive, fully biodegradable and environment friendly in nature.
Radiasurf 7403 is an electrolyte tolerant, high molecular weight member and is used as viscosity builder in detergent systems.



CAS NUMBER: 9004-96-0

EC NUMBER: 500-015-7

MOLECULAR FORMULA: C18H33O2.(C2H4O)n.H



DESCRIPTION:

Radiasurf 7403 can also be used for melting point control and is suitable for use in antiperspirants.
Radiasurf 7403 finds application in formulating facial-, body-, baby- and sun-care products.
Radiasurf 7403 is an ingredient commonly used in cosmetic and personal care products.

Radiasurf 7403 is a polyethylene glycol (PEG) derivative of oleic acid, which is a naturally occurring fatty acid found in various vegetable oils.
Radiasurf 7403 is created by reacting oleic acid with ethylene oxide, resulting in a compound that has emulsifying and surfactant properties.
In cosmetic formulations, Radiasurf 7403 functions as an emulsifier, helping to mix oil and water-based ingredients together.

Radiasurf 7403 is often used in skincare products, such as lotions, creams, and cleansers, to create a smooth and stable texture.
Additionally, Radiasurf 7403 can act as a mild cleansing agent and can help improve the spreadability of products on the skin.
It's worth noting that Radiasurf 7403 compounds, have been subject to some controversy due to their potential to be contaminated with impurities called 1,4-dioxane, which is considered a possible human carcinogen.

Radiasurf 7403 is the polyethylene glycol ester of oleic acid.
Radiasurf 7403 is used as an emulsifier for personal care and water treatment and as a processing aid in textile industry.
Radiasurf 7403 is a mid-range HLB, surface active agent suggested for use in animal feed, cosmetics, textile chemicals, lubricant, softener, scouring agent), coatings and industrial degreasers.



USAGE AREAS:

Radiasurf 7403 is used in a variety of cosmetic and personal care products due to its emulsifying, cleansing, and texture-enhancing properties.


-Skincare Products:

Radiasurf 7403 is frequently found in lotions, creams, moisturizers, and serums, where it helps to create smooth and stable formulations.
Radiasurf 7403 contributes to the texture, spreadability, and absorption of these products.


-Cleansing Products:

Radiasurf 7403 can be used in facial cleansers, body washes, and soaps.
Radiasurf 7403 aids in the removal of dirt, oils, and impurities from the skin while providing a mild cleansing action.


-Hair Care Products:

Radiasurf 7403 is sometimes included in hair care formulations such as shampoos, conditioners, and styling products.
Radiasurf 7403 can assist in improving the texture and manageability of the hair.


-Makeup Products:

Radiasurf 7403 can be found in various cosmetic formulations, including foundations, primers, and creams.
Radiasurf 7403 helps to create a smooth and blendable texture and can enhance the spreadability and application of these products.


-Sunscreen and Sun Care Products:

Radiasurf 7403 can be used in sunscreens and sun care products to aid in the dispersion and even distribution of UV filters.
Radiasurf 7403 can contribute to the overall stability and performance of these products.




PHYSICAL AND CHEMICAL PROPERTIES:

-Cloud Point: ≤ 6 °C
-Lovibond 1", Yellow: ≤ 10
-Lovibond 1", Red: ≤ 2.5
-Kinematic viscosity at 100°C: ca. 9.5 mm²/s
-Kinematic viscosity at 40°C: ca. 49 mm²/s
-Flash Point: ca. 260 °C
-Pour point: ca. -3 °C



BENEFITS:


-Emulsifying Agent:

Radiasurf 7403 acts as an emulsifier, helping to blend oil and water-based ingredients together.
This property allows for the creation of stable formulations, ensuring that the product remains well-mixed and consistent.


-Improved Texture:

Radiasurf 7403 helps to enhance the texture and spreadability of skincare products.
Radiasurf 7403 can provide a smooth and silky feel when applied to the skin, contributing to a pleasant sensory experience.


-Mild Cleansing:

Radiasurf 7403 can also function as a mild cleansing agent.
Radiasurf 7403 helps to remove dirt, oils, and impurities from the skin's surface without excessive drying or stripping of natural oils.


-Enhanced Skin Penetration:

Due to its emulsifying properties, Radiasurf 7403 can improve the delivery and penetration of active ingredients into the skin.
This can potentially enhance the effectiveness of other beneficial ingredients in a formulation.


-Compatibility with Various Formulations:

Radiasurf 7403 is compatible with a wide range of cosmetic ingredients, making it suitable for use in various formulations such as lotions, creams, serums, and cleansers.




PHYSICAL AND CHEMICAL PROPERTIES:

-Boiling point: >260 °C(lit.)
-density: 1.034 g/mL at 25 °C
-refractive index: n20/D 1.468
-Fp: 113 °C
-storage temp.: Amber Vial, Refrigerator
-solubility: toluene, ethanol and acetone: soluble (dispersible in water)
-form: Oil
-color: Colourless to Light Beige
-Hydrophilic-Lipophilic Balance (HLB): 15.1
-Stability: Light Sensitive
-LogP: 7.185 (est)




STORAGE:

Radiasurf 7403 should be stored at room temperature, typically between 20°C and 25°C (68°F and 77°F).



SYNONYM:

Polyethylene Glycol 8 Oleate
PEG-8 Esters of Oleic Acid
Polyethylene Glycol 8 Monooleate
Macrogol 8 Oleate
Polyoxyethylene (8) Oleate
crodet
hydroxyethyl (Z)-octadec-9-enoate (peg-8)
pegosperse 400 MO
poly(oxy-1,2-ethanediyl), .alpha.-(1-oxo-9-octadecenyl)-.omega.-hydroxy-, (Z)- (8 mol EO average molar ratio)
polyethylene glycol (8) monooleate
polyethylene glycol (8) oleate
polyoxyethylene (8) monooleate
polyoxyethylene (8) oleate
nonisol200
nopalcol1-0
Poly(oxy-1,2-ethanediyl), .alpha.-[(9Z)-1-oxo-9-octadecen-1-yl]-. omega.-hydroxy-
PEG-8 OLEATE
PEG-9 OLEATE
PEG-10 OLEATE
PEG-11 OLEATE
PEG-12 OLEATE










Rafine Babassu Yağı
BABASSU OIL REFINED ;orbignya oleifera seed oil; babassu nut oil; orbignya oleifera oil; fixed oil obtained from the nuts of the babassu, orbignya oleifera, palmaceae CAS NO: 91078-92-1
Rafine Baladur Ağacı Cevizi Yağı
CASHEW NUT OIL REFINED; cashew nutshell liquid; cashew nut shell oil; acajuba occidentalis nut shell oil; cassuvium pomiferum nut shell oil; fixed oil obtained from the seeds of the cashew, anacardium occidentale l., anacardiaceae CAS NO:8007-24-7
Rafine Buğday Tohumu Yağı
WHEAT GERM OIL REFINED; triticum aestivum l. germ oil; wheat germ oil; triticum vulgare germ oil; wheat husk oil; cropure wheatgerm CAS NO:68917-73-7
Rafine Çuha Çiçeği Yağı
EVENING PRIMROSE OIL REFINED; evening primrose seed oil; cropure evening primrose; oenothera biennis seed oil; primrose seed oil ; evening primrose oil china organic; evening primrose oil organic; evening primrose seed oil; fixed oil derived from the seeds of the evening primrose, oenothera biennis, onagraceae CAS NO:65546-85-2
Rafine Fındık Yağı
HAZELNUT OIL REFINED; hazelnut oil; european hazelnut oil; corylus avellana seed oil; oil expressed from the nuts of the hazelnut, corylus avellana l., betulaceae CAS NO:185630-72-2
Rafine Hodan Yağı
BORAGE OIL REFINED ;borage oil organic; borage seed; fats and glyceridic oils, borage seed; cropure borage; borago officinalis seed oil cas no: 225234-12-8
Rafine Kavun Yağı
MELON OIL REFINED; citrullus vulgaris seed extract;extract of the seeds of the watermelon, citrullus lanatus, cucurbitaceae CAS NO:90244-99-8
Rafine Kenevir Yağı
HEMP OIL REFINED; CANNABIS SATIVA SEED OIL;Cannabis sativa; cannabis indica seed CAS NO:89958-21-4
Rafine Ketencik Otu Yağı
CAMELINA SATIVA OIL REFINED; camelina sativa seed oil ; camelina oil;fixed oil expressed from the seeds of the gold of pleasure, camelina sativa (l.), brassicaceae CAS NO:68956-68-3
Rafine Kiraz Çekirdeği Yağı
CHERRY KERNEL OIL REFINED; prunus avium seed oil; sweet cherry kernel oil; fixed oil obtained from the kernels of the sweet cherry, prunus avium l., rosaceae CAS NO:8022-29-5
Rafine Kukui Oil
KUKUI OIL REFINED; kukui nut oil; candlenut oil; kemiri oil; kendi oil; oil expressed from nuts of the candle nut tree, aleurites moluccana, euphorbiaceae CAS NO:8015-80-3
Rafine Macadamia Cevizi Yağı
MACADAMIA NUT OIL REFINED; macadamia nut oil; floramac macadamia oil; macadamia nut oil; macadamia tetraphylla; fixed oil obtained from the nuts of the bushnut, macadamia ternifolia, proteaceae CAS NO: 129811-19-4
Rafine Organik Katı Shea Yağı
SHEA BUTTER REFINED ORGANIC ;Butyrospermum Parkii (Shea) Butter; Butyrospermum Parkii Butter Extract is an extract obtained from the Shea Tree, Butyrospermum parkii, Sapotaceae; Butyrospermum parkii butter extract; BUTYROSPERMUM PARKII (SHEA BUTTER);Fats and Glyceridic oils, shea butter;BUTYROSPERMUM PARKII (SHEA BUTTER LIQUID);SHEA BUTTER BUTYROSPERMUM PARKII; Shea Butter Powder;Shea Butter SB-I;Shea Liquid; extract obtained from the shea tree, butyrospermum parkii, sapotaceae; shea tree butter extract CAS NO:91080-23-8
Rafine Palm Yağı
PALM OIL REFINED; palm oil; natural oil obtained from the fruits of the palmoil tree, elaeis guineensis, palmaceae; elaeis guineensis fruit oil CAS NO:8002-75-3
Rafine Pirinç Kepeği Yağı
RICE BRAN OIL REFINED; rice bran oil; oryza sativa l. bran oil; edible ricebran oil CAS NO:68553-81-1
Rafine Soya Fasulyesi Yağı
SOYABEAN OIL REFINED (IP AVAILABLE); soybean oil; glycine max seed oil; bionatrol; glycine max oil; lipovol soy; soja hispida oil CAS NO:8001-22-7
Rafine Şeftali Çekirdeği Yağı
PEACH KERNEL OIL REFINED; prunus persica l. kernel oil; amygdalus persica kernel oil; lipobutter peach; persic oil CAS NO: 8023-98-1
Rafine Üzüm Çekirdeği Yağı
GRAPESEED OIL REFINED; grapeseed oil; vitis vinifera seed oil; grape seed oil; fixed oil, consisting primarily of the glycerides of the fatty acids, obtained by pressing the seeds of the grape, vitis vinifera l., vitaceae CAS NO: 8024-22-4
Rafine ve ya Ham Ceviz Yağı
WALNUT OIL REFINED AND UNREFINED; walnut oil ; juglans regia l. seed oil; juglans regia seed oil CAS NO:8024-09-7
Rafine ya da Fraksiyone Hindistan Cevizi Yağı
COCONUT OIL REFINED OR FRACTIONATED; coconut oil; coconut palm oil; cocoanut oil; kokos oil; oils, coconut; fixed oil obtained by expression of the kernels of the seeds of the coconut, cocos nucifera l., palmaceae CAS NO:8001-31-8
Rafine ya da Soğuk Pres Avokado Yağı
AVOCADO OIL REFINED OR COLD PRESSED; persea gratissima oil; nikkol avocado oil; persea americana oil; avocado oil ;cropure avocado;fixed oil obtained by pressing the dehydrated sliced flesh of the avocado pear, persea gratissima, lauraceae CAS NO:8024-32-6
Rafine ya da Soğuk Pres Kolza Tohumu Yağı
RAPESEED OIL REFINED OR COLD PRESSED; rapeseed oil; brassica campestris seed oil; brassica oleifera oil; colza oil; rape seed oil CAS NO:8002-13-9
Rafine ya da Toasted Susam Çekirdeği Yağı
SESAME SEED OIL REFINED OR TOASTED; sesame seed oil; sesamum indicum l. seed oil; sesamum indicum seed oil; teel oil (sesamum indicum); gingelly oil CAS NO: 8008-74-0
Rafine Yer Fıstığı Yağı
PEANUT OIL REFINED; peanut oil; refined fixed oil obtained from the seed kernels of one or more of the cultivated varieties of the peanut, arachis hypogaea l., leguminosae; arachis hypogaea oil; katchung oil; arachis hypogaea oil CAS NO:8002-03-7
Rafine/Extra Virgin/Posa Zeytin Yağı
OLIVE OIL POMACE, REFINED OR EXTRA VIRGIN; olea europaea l. fruit oil; cropure olive; olive oil olifeel organic oil CAS NO:8001-25-0
RAPESEED ACID
RESORCINOL, N° CAS : 108-46-3 - Résorcine. Nom INCI : RESORCINOL. Nom chimique : Resorcinol (CI 76505). N° EINECS/ELINCS : 203-585-2. Ses fonctions (INCI). Agent colorant pour cheveux : Colore les cheveux; Agent masquant : Réduit ou inhibe l'odeur ou le goût de base du produit. Antioxydant : Inhibe les réactions favorisées par l'oxygène, évitant ainsi l'oxydation et la rancidité. Dénaturant : Rend les cosmétiques désagréables. Principalement ajouté aux cosmétiques contenant de l'alcool éthylique. Agent parfumant : Utilisé pour le parfum et les matières premières aromatiques. Noms français : 1,3-BENZENEDIOL; 1,3-DIHYDROXYBENZENE; META-DIHYDROXYBENZENE; RESORCINE; Résorcinol. Noms anglais : Resorcinol: Utilisation et sources d'émission; Fabrication de produits pharmaceutiques, fabrication de résines. 1,3-Benzenediol 1,3-dihydroxybenzene resorcinol; 1,3-benzenediol Translated names 1,3-bencenodiol (es) 1,3-benseendiool (et) 1,3-Bentseenidioli (fi) 1,3-benzeendiol (nl) 1,3-benzen diol (ro) 1,3-benzendiol (da) 1,3-benzendiolis (lt) 1,3-benzenodiol (pt) 1,3-benzodiols (lv) 1,3-benzoldiol (hu) 1,3-benzènediol (fr) 1,3-dihidroksibenzen (sl) 1,3-dihydroksybenzen (pl) 1,3-Dihydroxybenzol (de) 1,3-diidrossibenzene (it) 1,3-diidroxibenzeno (pt) 1,3-διυδροξυβενζόλιο ρεσορκινόλ (el) 1,3-бензендиол (bg) benzene-1,3-diol (cs) benzeno-1,3-diol (pl) benzén-1,3-diol (sk) Resorcin (de) resorcina (it) resorcinol (cs) Resorsinoli (fi) resortsinool (et) rezorcin (hu) rezorcinol (hr) rezorcinolis (lt) rezorcyna (pl) rezorcynol (pl) rezorcīns (lv) résorcinol (fr) резорцинол (bg) 1,3 benzenediol 1,3-dihydroxybenzene ( resorcinol) 1,3-dihydroxybenzene; 1-3-dihydroxybenzene benzene 1,3-diol Resourcinol Trade names 1,3-Benzenediol (9CI) 1,3-BENZENEDIOL 1,3 DIHYDROXYBENZENE 1,3-Benzoldiol; Resorcin 3-Hydroxyphenol C.I. 76505 C.I. Developer 4 C.I. Oxidation Base 31 Developer O Developer RS dihydroxybenzol Durafur Developer G Fouramine RS Fourrine 79 Jarocol RL RES Resorcinol (8CI); 1,3-Benzenediol [ACD/Index Name] 1,3-dihydroxybenzene 108-46-3 [RN] 203-585-2 [EINECS] 906905 [Beilstein] Benzol-1,3-diol Resorcin [German] [ACD/IUPAC Name] Resorcino Resorcinol [ACD/IUPAC Name] [USP] [Wiki] Résorcinol [French] [ACD/IUPAC Name] Resorcinolum 1,3-Dihydroxy-Benzene 1,3-Dihydroxybenzol 26982-54-7 [RN] 3-benzosemiquinone 3-Hydroxycyclohexadien-1-one 3-Hydroxyphenol 40248-84-8 [RN] 4-06-00-05658 (Beilstein Handbook Reference) [Beilstein] 6025-45-2 [RN] 70938-00-0 [RN] 953390-31-3 [RN] Acnomel Benzene, 1,3-dihydroxy- Benzene, m-dihydroxy- benzene-1,3-diol C.I. Developer 4 C.I. Oxidation Base 31 Developer O Developer RS Dihydroxybenzol Durafur developer G Eskamel Fouramine RS Fourrine 79 Fourrine EW m-Benzenediol m-dihydroxybenzene m-Dioxybenzene m-Hydroquinone m-hydroxyphenol m-Hydroxy-Phenol Nako TGG Pelagol Grey RS Pelagol RS Phenol, m-hydroxy- RCO Resorcin (JAN) [JAN] Resorcin (TN) Resorcin;1,3-Benzenediol Resorcine Resorcinol (USP) Resorcinol 10 µg/mL in Methanol Resorzin Rezamid Rezorsine Rodol RS Sulforcin WLN: QR CQ α-Resorcinol 间苯二酚 [Chinese]
RAPESEED OIL FATTY ACID METHYLESTER
cas no 85586-25-0 fatty acids, rape-oil, me esters; Rübfettsuremethylester, erucaarm; Fatty acids, rape-oil Methyl esters;
Rasuvastatin Calcium
SYNONYMS Crestor; (3R,5S,6E)-7-(4-(4-fluorophenyl)-2-(N-methylmethane sulfonamido)- 6-(propan-2-yl) pyrimidin-5-yl)- 3,5-dihydroxyhept-6-enoic acid; (E)-7-[4-(4-Fluorophenyl)-6-isopropyl-2-[methyl(methylsulfonyl)amino]pyrim idin-5-yl]-(3R,5S)-3,5-dihydroxyhept-6-enoic acid, calcium salt (2:1), Rosuvastatin hemicalcium cas no:147098-20-2
RBW Mısır Yağı
MAIZE / CORN OIL RBW; corn oil; zea mays oil; fixed oil obtained from wet milling of the corn, zea mays l., gramineae CAS NO:8001-30-7
REACTIVE SILICONE FLUID EMULSION
Reactive silicone fluid emulsion is a type of silicone-based emulsion that contains reactive groups, such as hydroxyl or epoxy groups, on the silicone polymer chains.
These reactive groups allow the emulsion to crosslink with other materials, leading to improved adhesion, durability, and other enhanced properties.



APPLICATIONS


Reactive silicone fluid emulsion is used as a hydrophobic and water-repellent coating for fabrics, papers, and leather.
Reactive silicone fluid emulsion provides an excellent release and anti-stick properties to molds, metal surfaces, and plastics.

Reactive silicone fluid emulsion enhances the water resistance, oil resistance, and anti-fouling properties of coatings and paints.
Reactive silicone fluid emulsion is used as a lubricant for plastic gears, electronic devices, and automotive parts.

Reactive silicone fluid emulsion acts as a softener and anti-static agent for textiles and plastics.
Reactive silicone fluid emulsion is used as a defoaming agent in various industrial processes such as papermaking, coatings, and adhesives.

Reactive silicone fluid emulsion enhances the stability and durability of emulsions and suspensions.
Reactive silicone fluid emulsion improves the compatibility between different materials, such as pigments and resins.

Reactive silicone fluid emulsion increases the elasticity, durability, and heat resistance of rubber and silicone products.
Reactive silicone fluid emulsion is used as an anti-corrosion agent for metals in various industries such as automotive, aerospace, and marine.

Reactive silicone fluid emulsion provides anti-fogging properties to optical lenses, mirrors, and glass surfaces.
Reactive silicone fluid emulsion is used as a hydrophobic agent for construction materials such as concrete, bricks, and tiles.
Reactive silicone fluid emulsion acts as a water-repellent and moisture barrier for packaging materials.

Reactive silicone fluid emulsion enhances the thermal stability and heat resistance of polymers.
Reactive silicone fluid emulsion is used as a leveling and wetting agent for coatings and inks.
Reactive silicone fluid emulsion provides anti-blocking properties to plastic films and coatings.

Reactive silicone fluid emulsion enhances the water resistance and dimensional stability of paper and cardboard.
Reactive silicone fluid emulsion is used as a slip agent for polyolefin films and sheets.

Reactive silicone fluid emulsion provides anti-graffiti properties to building surfaces.
Reactive silicone fluid emulsion acts as a foam control agent for various industrial processes such as oil and gas drilling, fermentation, and water treatment.

Reactive silicone fluid emulsion is used as a coating and sealant for electronics and electrical components.
Reactive silicone fluid emulsion provides lubrication and protection to metal surfaces in cutting and machining processes.

Reactive silicone fluid emulsion enhances the anti-soiling properties of carpets and fabrics.
Reactive silicone fluid emulsion is used as a hydrophobic agent for wood and wood-based materials.
Reactive silicone fluid emulsion provides anti-blocking and slip properties to printing inks and coatings.


Reactive silicone fluid emulsion has a wide range of applications in various industries.
Here are some of the common applications:

As a coating material for textiles and fabrics to improve water repellency and softness.
As a release agent for molds in the production of rubber and plastic parts.
As a water-resistant and breathable coating for leather products.
As a waterproofing agent for building materials such as concrete, brick, and stone.
As a lubricant in the automotive and industrial sectors, to reduce friction and wear.
As a surfactant and stabilizer in personal care and cosmetic products such as shampoos, lotions, and creams.
As a crosslinker in the production of silicone elastomers, resins, and adhesives.
As a foam control agent in various processes, including paper production, water treatment, and fermentation.
As a coating for electronic components, to protect against moisture and environmental factors.
As a binder and water repellent in the production of mineral-based building materials such as plaster and mortar.


Reactive silicone fluid emulsion can be used in the production of sealants and adhesives for industrial and construction applications.
Reactive silicone fluid emulsion can be used as a lubricant in various mechanical processes.
Reactive silicone fluid emulsion is used in the formulation of mold release agents for the manufacturing of plastic and rubber products.

Reactive silicone fluid emulsion can be used in the formulation of printing inks and coatings for paper and textile substrates.
Reactive silicone fluid emulsion can be used as a surface modifier for various substrates, including glass, metal, and plastic.

Reactive silicone fluid emulsion can be used as a water-repellent agent for textiles and leather products.
Reactive silicone fluid emulsion is used as an anti-foaming agent in various industrial processes, such as fermentation and wastewater treatment.

Reactive silicone fluid emulsion can be used as an additive in personal care products, such as shampoos, conditioners, and lotions, to improve the wetting and conditioning properties.
Reactive silicone fluid emulsion is used in the production of automotive and industrial coatings to improve the scratch and abrasion resistance.

Reactive silicone fluid emulsion can be used as a binder in the formulation of pressure-sensitive adhesives.
Reactive silicone fluid emulsion is used as a release agent for the production of composite materials.
Reactive silicone fluid emulsion can be used as an additive in the formulation of emulsion polymers to improve the stability and performance.

Reactive silicone fluid emulsion can be used as a coating for electronic components to provide insulation and protection from moisture.
Reactive silicone fluid emulsion is used as a surfactant in the formulation of detergent and cleaning products.

Reactive silicone fluid emulsion can be used in the formulation of flame retardants for various substrates, including textiles and plastics.
Reactive silicone fluid emulsion can be used as an additive in the formulation of paints and coatings to improve the weatherability and UV resistance.

Reactive silicone fluid emulsion is used in the production of silicone rubber products, such as gaskets, O-rings, and seals.
Reactive silicone fluid emulsion can be used as a water-repellent agent for masonry and concrete substrates.
Reactive silicone fluid emulsion can be used as a sizing agent in the production of glass fibers.

Reactive silicone fluid emulsion is used in the formulation of high-performance greases and lubricants for various applications, including aerospace and automotive.
Reactive silicone fluid emulsion can be used as a release agent in the production of polyurethane foam products.

Reactive silicone fluid emulsion can be used as a binder in the production of ceramic products, such as tiles and refractories.
Reactive silicone fluid emulsion is used as a surfactant in the formulation of crop protection products, such as herbicides and fungicides.

Reactive silicone fluid emulsion can be used as an additive in the formulation of oil and gas drilling fluids to improve the lubricity and reduce friction.
Reactive silicone fluid emulsion can be used as a water-repellent agent for wood and wood-based products.
Reactive silicone fluid emulsion is used as a coating for optical lenses to improve the scratch resistance and clarity.

Reactive silicone fluid emulsion can be used as an additive in the formulation of concrete admixtures to improve the workability and durability.
Reactive silicone fluid emulsion can be used as a release agent in the production of rubber products, such as tires and conveyor belts.

Reactive silicone fluid emulsion is used in the formulation of thermal interface materials for electronic devices, such as heat sinks and thermal pads.
Reactive silicone fluid emulsion can be used as a water-repellent agent for glass and ceramic substrates.


Some applications of Reactive silicone fluid emulsion:

Textile industry
Paper industry
Paints and coatings
Adhesives and sealants
Personal care and cosmetics
Agriculture
Construction materials
Electronics and electricals
Automotive industry
Leather industry
Packaging materials
Metalworking
Plastic and rubber industry
Petroleum industry
Water treatment
Printing and ink industry
Wood industry
Glass industry
Renewable energy industry
Food processing
Medical devices and implants
Aerospace and defense industry
Marine and offshore industry
Sports and recreation industry
Household cleaning and maintenance
Mining industry
Chemical manufacturing
Ceramics industry
Pharmaceuticals industry
Environmental protection and remediation.



DESCRIPTION


Reactive silicone fluid emulsion is a type of silicone-based emulsion that contains reactive groups, such as hydroxyl or epoxy groups, on the silicone polymer chains.
These reactive groups allow the emulsion to crosslink with other materials, leading to improved adhesion, durability, and other enhanced properties.

Reactive silicone fluid emulsion is used in a wide range of applications, including coatings, adhesives, sealants, and elastomers.
Reactive silicone fluid emulsion is often used as an additive in formulations to improve the properties of the end product.

In coatings, reactive silicone fluid emulsion can be used as a surface modifier to improve the wetting and adhesion of the coating to the substrate.
Reactive silicone fluid emulsion can also improve the scratch resistance, durability, and water repellency of the coating.

In adhesives and sealants, reactive silicone fluid emulsion can be used to improve the bonding strength and flexibility of the adhesive.
Reactive silicone fluid emulsion can also improve the heat resistance and chemical resistance of the adhesive or sealant.

In elastomers, reactive silicone fluid emulsion can be used as a processing aid to improve the flow properties of the elastomer during manufacturing.
Reactive silicone fluid emulsion can also improve the tear resistance, elasticity, and low-temperature properties of the elastomer.
Reactive silicone fluid emulsion is also used in the textile industry as a softener and in the personal care industry as an emollient and conditioning agent.

Overall, reactive silicone fluid emulsion is a versatile material with a wide range of applications in various industries. Its unique properties and crosslinking capabilities make it a valuable additive for improving the performance and properties of many different types of formulations.

Reactive silicone fluid emulsion is a type of silicone emulsion that contains reactive groups, such as epoxy or vinyl groups, that can react with other materials to form crosslinked networks.
Reactive silicone fluid emulsion is commonly used as a coating or adhesive in a variety of industries, including automotive, electronics, and construction.
Reactive silicone fluid emulsions can be formulated to have a range of properties, including low or high viscosity, fast or slow curing times, and different levels of adhesion or flexibility.

Because of their reactive nature, Reactive silicone fluid emulsions require careful handling and storage to prevent premature crosslinking or degradation.
Reactive silicone fluid emulsions are often used to improve the adhesion and durability of coatings and adhesives on a variety of substrates, including metals, plastics, and composites.

Reactive silicone fluid emulsions can also be used as a mold release agent or as a surface treatment to improve the water and oil resistance of materials.
Reactive silicone fluid emulsions can be blended with other polymers or additives to achieve specific properties, such as improved scratch resistance or UV stability.

Reactive silicone fluid emulsions can be applied by a variety of methods, including spray, dip, or brush, depending on the substrate and desired coating thickness.
Reactive silicone fluid emulsions are often used in high-performance applications where durability, flexibility, and adhesion are critical, such as in the aerospace or marine industries.
Proper formulation and application of reactive silicone fluid emulsions can result in coatings and adhesives with excellent weatherability, chemical resistance, and thermal stability.


Here are some more properties of Reactive silicone fluid emulsion:

Good thermal stability
High lubricity
Non-toxic and non-corrosive
Excellent water repellency
Low surface tension
High surface energy
High chemical stability
Good electrical insulation properties
Resistant to oxidation and weathering
Low volatility
Good adhesion to various substrates
Compatible with a wide range of materials
Low foaming tendency
Good wetting properties
High boiling point
High flash point
High viscosity
Non-flammable
Good emulsifying properties
Low toxicity
Resistant to UV radiation
Good release properties
Excellent slip and leveling properties
Good spreading properties
Good compatibility with solvents and other additives
Low pour point
Good film-forming properties
Excellent thermal stability at high temperatures
High refractive index
Good defoaming properties
Excellent dielectric properties



PROPERTIES


Appearance: white or off-white liquid
Odor: odorless
pH: neutral
Solubility: emulsifiable in water
Viscosity: typically low to moderate
Flash point: not applicable
Stability: stable under normal conditions
Density: typically between 1.0-1.2 g/cm3
Boiling point: typically above 100°C
Chemical formula: varies depending on the specific type of reactive silicone fluid emulsion



FIRST AID


It is important to handle Reactive Silicone Fluid Emulsion with care to avoid any potential hazards.
If accidental exposure or ingestion occurs, the following first aid measures should be taken:

Inhalation:

Move the person to fresh air immediately.
If the person is not breathing, perform artificial respiration and seek medical attention immediately.
If the person is breathing, but experiencing difficulty, provide oxygen and seek medical attention.


Skin Contact:

Remove contaminated clothing and wash the affected area with plenty of soap and water for at least 15 minutes.
If skin irritation persists, seek medical attention.


Eye Contact:

Rinse the affected eye with plenty of water for at least 15 minutes while keeping the eyelid open.
If eye irritation persists, seek medical attention.


Ingestion:

Rinse mouth with water immediately.
Do not induce vomiting unless instructed to do so by a medical professional.
Seek medical attention immediately.


It is important to seek immediate medical attention in case of any doubt or serious symptoms.
Always have a copy of the Safety Data Sheet (SDS) available for reference.



HANDLING AND STORAGE


Reactive silicone fluid emulsion should be handled and stored with care to ensure its quality and safety.
Here are some general guidelines for handling and storage:

Handling:

Use appropriate personal protective equipment (PPE), such as gloves and safety goggles, when handling reactive silicone fluid emulsion.
Avoid contact with skin, eyes, and clothing.
In case of contact, immediately flush the affected area with plenty of water for at least 15 minutes and seek medical attention.

Avoid inhaling mist or vapors. Use adequate ventilation and respiratory protection in poorly ventilated areas.
Do not smoke, eat, or drink while handling the emulsion.


Storage:

Store reactive silicone fluid emulsion in a cool, dry, well-ventilated area, away from heat, flames, and other sources of ignition.
Do not store near oxidizing agents, acids, or alkalis.
Keep containers tightly closed and upright to prevent leakage or spills.

Store away from direct sunlight or other sources of ultraviolet light.
Follow the manufacturer's recommendations for storage temperature and shelf life.
Do not reuse empty containers.


Always consult the safety data sheet (SDS) and follow the manufacturer's instructions for safe handling and storage of reactive silicone fluid emulsion.



SYNONYMS


Reactive polysiloxane emulsion
Reactive silicone emulsion
Reactive silicone fluid dispersion
Reactive silicone oil emulsion
Reactive silicone surfactant emulsion
Crosslinkable silicone emulsion
Crosslinkable polysiloxane emulsion
Crosslinkable silicone fluid dispersion
Crosslinkable silicone oil emulsion
Crosslinkable silicone surfactant emulsion
Reactive polydimethylsiloxane emulsion
Reactive methylsilicone emulsion
Crosslinkable polydimethylsiloxane emulsion
Crosslinkable methylsilicone emulsion
Reactive silicone polymer emulsion
Crosslinkable silicone polymer emulsion
Modified silicone emulsion
Modified polysiloxane emulsion
Modified silicone fluid dispersion
Modified silicone oil emulsion
Modified silicone surfactant emulsion
Silanol-functionalized silicone emulsion
Silanol-modified silicone emulsion
Alkoxy-functionalized silicone emulsion
Alkoxy-modified silicone emulsion
Hydroxyl-functionalized silicone emulsion
Hydroxyl-modified silicone emulsion
Epoxy-functionalized silicone emulsion
Epoxy-modified silicone emulsion
Vinyl terminated silicone emulsion
Reactive silicone fluid dispersion
Reactive polydimethylsiloxane emulsion
Reactive silicone polymer emulsion
Reactive silicone copolymer emulsion
Reactive silicone surfactant emulsion
Reactive silicone emulsion
Reactive silicone fluid suspension
Vinyl functionalized silicone emulsion
Vinyl modified silicone emulsion
Vinyl silicone emulsion
Vinyl siloxane emulsion
Vinyl-terminated polydimethylsiloxane emulsion
Vinyl-terminated silicone emulsion
Methacrylate-functionalized silicone emulsion
Methacrylate-modified silicone emulsion
Methacryloxypropyl terminated silicone emulsion
Methacryloxypropyl-functionalized silicone emulsion
Methacryloxypropyl-modified silicone emulsion
Acrylate-functionalized silicone emulsion
Acrylate-modified silicone emulsion
Acryloxypropyl terminated silicone emulsion
Acryloxypropyl-functionalized silicone emulsion
Acryloxypropyl-modified silicone emulsion
Epoxy-functionalized silicone emulsion
Epoxy-modified silicone emulsion
Epoxy-terminated silicone emulsion
Epoxide-functionalized silicone emulsion
Epoxide-modified silicone emulsion
Epoxide-terminated silicone emulsion
RED CLOVER FLOWER EXTRACT

Red Clover Flower Extract, derived from the flowers of Trifolium pratense, is known for its estrogen-like effects, antioxidant, and anti-inflammatory properties.
Red Clover Flower Extract is widely recognized for its ability to support women’s health, alleviate menopausal symptoms, and improve skin health, making it a valuable ingredient in dietary supplements and skincare formulations.
This versatile extract offers both therapeutic and cosmetic benefits, helping to maintain hormonal balance, improve skin elasticity, and provide antioxidant support.

CAS Number: 85085-25-2
EC Number: 285-356-7

Synonyms: Red Clover Extract, Trifolium pratense Flower Extract, Red Clover Bioactive Extract, Trifolium Extract, Trifolium pratense Herbal Extract, Red Clover Phytocomplex, Red Clover Blossom Extract, Red Clover Blossom Phytocomplex, Trifolium pratense Active, Clover Flower Extract



APPLICATIONS


Red Clover Flower Extract is extensively used in women’s health supplements, offering natural relief from menopausal symptoms such as hot flashes, night sweats, and mood swings.
Red Clover Flower Extract is favored in the formulation of hormonal balance supplements, where it helps to regulate estrogen levels, making it a popular ingredient for women experiencing perimenopause and menopause.
Red Clover Flower Extract is utilized in the development of supplements designed to support bone health, providing natural phytoestrogens that help maintain bone density and reduce the risk of osteoporosis.

Red Clover Flower Extract is widely used in skincare products for its antioxidant properties, which help to protect the skin from free radical damage and promote a youthful appearance.
Red Clover Flower Extract is employed in the creation of anti-aging creams, where it helps improve skin elasticity, reduce fine lines, and restore firmness.
Red Clover Flower Extract is essential in the development of lotions designed to soothe and hydrate the skin, providing antioxidant care and improving overall skin texture.

Red Clover Flower Extract is utilized in the production of cardiovascular health supplements, offering benefits for improving blood circulation, reducing cholesterol levels, and supporting heart health.
Red Clover Flower Extract is a key ingredient in detox products, where it helps to cleanse the body, eliminate toxins, and promote healthy skin.
Red Clover Flower Extract is used in the development of respiratory health products, where it helps to reduce inflammation in the respiratory tract and improve lung function.

Red Clover Flower Extract is applied in the formulation of supplements designed to improve hair health, providing phytoestrogen support for reducing hair thinning and promoting hair growth in women.
Red Clover Flower Extract is employed in the production of creams and lotions for sensitive skin, offering soothing and anti-inflammatory benefits, making it suitable for skin conditions such as eczema and rosacea.
Red Clover Flower Extract is used in the development of herbal teas, offering benefits for supporting women’s hormonal health and providing antioxidant protection.

Red Clover Flower Extract is widely utilized in the formulation of natural remedies for skin irritation and redness, helping to calm sensitive skin and improve skin tone.
Red Clover Flower Extract is a key component in wellness supplements that support detoxification, helping to cleanse the liver and promote healthy digestion.
Red Clover Flower Extract is used in the creation of supplements designed to reduce inflammation throughout the body, supporting joint health and providing relief from arthritis symptoms.

Red Clover Flower Extract is employed in the formulation of weight management supplements, where it helps regulate metabolism and improve the body’s fat-burning capabilities.
Red Clover Flower Extract is applied in the development of breast health supplements, offering phytoestrogen support for maintaining breast tissue health and reducing the risk of breast-related conditions.
Red Clover Flower Extract is utilized in the creation of products designed to support prostate health, helping to reduce inflammation and improve overall prostate function in men.

Red Clover Flower Extract is found in the formulation of stress-relief supplements, where it helps reduce anxiety and improve mood by balancing hormone levels.
Red Clover Flower Extract is used in the production of beauty supplements, offering benefits for improving skin texture, hair growth, and overall appearance.
Red Clover Flower Extract is a key ingredient in supplements designed to reduce symptoms of PMS, offering natural support for hormonal balance and mood regulation.

Red Clover Flower Extract is employed in the creation of wellness beverages, providing benefits for hormone regulation, detoxification, and antioxidant protection.
Red Clover Flower Extract is applied in natural remedies for reducing the risk of cardiovascular diseases, offering benefits for improving circulation, lowering blood pressure, and reducing cholesterol levels.
Red Clover Flower Extract is utilized in supplements that promote cognitive function, offering support for reducing memory loss and improving focus and concentration.



DESCRIPTION


Red Clover Flower Extract, derived from the flowers of Trifolium pratense, is known for its estrogen-like effects, antioxidant, and anti-inflammatory properties.
Red Clover Flower Extract is widely recognized for its ability to support women’s health, alleviate menopausal symptoms, and improve skin health, making it a valuable ingredient in dietary supplements and skincare formulations.

Red Clover Flower Extract offers additional benefits such as improving cardiovascular health, enhancing detoxification processes, and reducing inflammation throughout the body.
Red Clover Flower Extract is often incorporated into formulations designed to support bone health, improve skin elasticity, and provide relief from menopausal symptoms such as hot flashes and mood swings.
Red Clover Flower Extract is recognized for its ability to protect the skin from free radical damage, helping to reduce the signs of aging and improve overall skin health.

Red Clover Flower Extract is commonly used in both traditional and modern wellness formulations, providing a reliable solution for maintaining hormonal balance, promoting heart health, and supporting healthy skin.
Red Clover Flower Extract is valued for its ability to provide phytoestrogen support, which helps balance estrogen levels in women and alleviate symptoms related to menopause and hormonal imbalances.
Red Clover Flower Extract is a versatile ingredient that can be used in a variety of products, including supplements, creams, lotions, teas, and detox products.

Red Clover Flower Extract is an ideal choice for products targeting women’s health, anti-aging, and cardiovascular support, providing natural and effective care for these concerns.
Red Clover Flower Extract is known for its compatibility with other phytoestrogen-rich and antioxidant ingredients, making it easy to integrate into multi-functional formulations.
Red Clover Flower Extract is often chosen for formulations requiring a balance between hormone regulation, anti-aging care, and cardiovascular support, ensuring comprehensive wellness benefits.

Red Clover Flower Extract enhances the overall effectiveness of wellness and skincare products by providing natural support for hormonal balance, detoxification, and antioxidant protection.
Red Clover Flower Extract is a reliable ingredient for creating products that offer noticeable improvements in skin health, hormonal balance, and cardiovascular wellness.
Red Clover Flower Extract is an essential component in innovative wellness products known for their performance, safety, and ability to support women’s health, heart function, and overall vitality.



PROPERTIES


Chemical Formula: N/A (Natural extract)
Common Name: Red Clover Flower Extract (Trifolium pratense Flower Extract)
Molecular Structure:
Appearance: Yellow-brown powder or liquid extract
Density: Approx. 1.00-1.05 g/cm³ (for powder)
Melting Point: N/A (powder form)
Solubility: Soluble in water and ethanol; insoluble in oils
Flash Point: >100°C (for powder)
Reactivity: Stable under normal conditions; no known reactivity issues
Chemical Stability: Stable under recommended storage conditions
Storage Temperature: Store between 15-25°C in a cool, dry place
Vapor Pressure: Low (for liquid extract)



FIRST AID


Inhalation:
If Red Clover Flower Extract 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:
Wash the affected area with soap and water.
If skin irritation persists, seek medical attention.

Eye Contact:
In case of 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:
If Red Clover Flower Extract is ingested, 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) such as gloves and safety goggles if handling large quantities.
Use in a well-ventilated area to avoid inhalation of dust.

Ventilation:
Ensure adequate ventilation when handling large amounts of Red Clover Flower Extract to control airborne concentrations below occupational exposure limits.

Avoidance:
Avoid direct contact with eyes and prolonged skin contact.
Do not eat, drink, or smoke while handling Red Clover Flower Extract.
Wash hands thoroughly after handling.

Spill and Leak Procedures:
Contain spills to prevent further release and minimize exposure.
Absorb with inert material (e.g., sand, vermiculite) and collect for disposal.
Dispose of in accordance with local regulations.

Storage:
Store Red Clover Flower Extract in a cool, dry, 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 inhalation of dust and direct contact with skin and eyes.
Use explosion-proof equipment in areas where dust or vapors may be present.





REOFOS 35
DESCRIPTION:
REOFOS 35 is a low viscosity triarylphosphate ester which is recommended for use in PVC plastisols for fabric coating and other applications where its low, stable viscosity offers improved processing.
REOFOS 35 can give a drier finish to coated fabrics than other standard triaryl phosphate esters.
REOFOS 35 has a high plasticizing efficiency that enable formulaters to achieve better flame retardance at lower costs.
REOFOS 35 is also designed for use as a flame retardant in phenolic laminates.

CAS No. 68937-41-7
Molecular formula C18H15R3O4P
Molecular weight 390


SYNONYMS OF REOFOS 35:
Isopropylated Triphenyl Phosphate (IPPP, Reofos 35/50/65), [68937-41-7]; MFCD01705485; SUM OF ISOMERS; TRIS(ISOBUTANE); Triphenyl phosphate; TRIS(2-METHYLPROPANE); Phenolphosphateisopropylated; Triarylphosphatisopropylated; isopropylated phenol phosphate; ISOPROPYLATED TRIPHENYL PHOSPHATE; triisopropylated phenyl phosphate; Phenol,isopropylated,phosphate(3:1); Triphenyl phosphate - isobutane (1:3); TRIS(ISOPROPYLPHENYL)PHOSPHATE-1M ALKYL; Tris(o,m,p-isopropylphenyl) phosphate, tech.; Phosphoric acid, triphenyl ester, compd. with 2-methylpropane (1:3); TRISISOPROPYLTRISPHENYL PHOSPHATE, TIPPP PURIFIED ION M/Z 452 OF TECHNICAL GRADE; tris(4-propan-2-ylphenyl) phosphate


REOFOS 35 is a flame retardant in plastisols.
This synthetic isopropylated triaryl phosphate ester can give a drier finish to coated fabrics than other standard triaryl phosphate esters.

REOFOS 35 has a high plasticizing efficiency that enable to achieve better flame retardance at lower cost.
REOFOS 35 is used in applications where low, stable viscosity offers improved processing.

REOFOS 35 is a low viscosity synthetic isopropylated triaryl phosphate ester which widely used as a flame-retardant plasticizer.


REOFOS 35 is a synthetic isopropylated triaryl phosphate ester flame retardant, which can be used in a wide variety of resins, particularly PVC.

REOFOS 35 is a flame retardant plasticizer used primarily in PVC and phenolic resins.

REOFOS 35 is a synthetic isopropylated triaryl phosphate ester flame retardant, which can be used in a wide variety of resins, particularly PVC.


APPLICATIONS of REOFOS 35:
They are used because of their plasticizing properties mainly in PVC and PUR.
Additionally they are applicable in TPU, in phenolic resins, synthetic rubber, resins and other applications.
Typical end uses are soft PVC, PUR foams, adhesives, sealants and coatings.

We are happy to consult you in choosing and applying phosphorus flame retardants.
Additionally we offer brominated flame retardants, other halogen free flame retardants, synergists and smoke suppressants.


REOFOS 35 improves the characteristics of the coated fabrics (compared to other additives, it gives a drier finish) and has a high plasticizing efficiency combined with flame retardant properties.
REOFOS 35 is also used as a flame retardant additive in phenolic resins.

PVC industry: cable, windows and door, sheet, decorating sheet, agricultural membrane, floor membrane etc.
Other synthetic material industry: used as light-heat stabilizer or oxide-heat stabilizer.
Other industry: complex liquid and ointment compound stabilizer etc.

As a plasticizer or flame retardant added in PVC, PU, PE, PP, PC/ABS, PPO/HIPS, PVAC, PS, fabric coatings, circuit boards, spinning Chemicalbook fabrics, phenolic resin, polyethylene, artificial leather, film, plate, conveyor belt, air pipe, floor material cable, synthetic resin, plastic, rubber and fiber to increase the process performance of the product.


USES OF REOFOS 35:

REOFOS 35 Is Used For Rubber Products
REOFOS 35 Is Used For PVC Plastic Flame Retardant Conveyor Belt
REOFOS 35 Is Used For Cable
REOFOS 35 Is Used For Chloroprene Rubber

REOFOS 35 Is Used For Rubber And Other Synthetic Rubber Flame Retardant Plasticizer
REOFOS 35 Is Used For Fabric Coating
REOFOS 35 Is Used For Circuit Boards

REOFOS 35 Is Used For Flooring
REOFOS 35 Is Used For Textiles
REOFOS 35 Is Used For PVC
REOFOS 35 Is Used For Phenolic Resin


CHEMICAL AND PHYSICAL PROPERTIES OF REOFOS 35:
Basic Elements Of The Product:
Chemical Name: Triary Phosphate Isopropylated(IPPP35)
Product Name: IPPP
Cas Number.: 68937-41-7
Same Name: flame Retardant IPPP
Industrial: Plastic

Application: REOFOS 35 Phosphorus Flame Retardant is a flame retardant plasticizer for PVC applications.
Packaging Details: 200kg drum IBC ISO tank
Production Capacity: 15 tons per day
Hs Code: 29199000902
Reach: Full Registration
Appearance.

Colorless transparent liquid.

Viscosity (25 °C,CP)

42-65

Specific Gravity (20°C)

1.183

Flashing point °C

220 min.

P%

8.60

Acid Value (mg KOH/g)

0.10max.

Chroma (APHA)

50.0 max.

Water content %

0.10 max.

The Isopropylphenyl phosphate,Flame Retardant ippp35,Reofos 35 Quality Description:
Traits: Colorless Or Light Yellow Transparent Liquid
Density Density (D20) :: 1.183
Flash Point Flash Point: 220 ℃ MIN
Viscosity Viscosity (25 ° C, CP): 42-50
Acid Value (MgKOH / G): 0.1 MAX
Refractive Index Refractive Index (N23): 1.546-1.555
Color Value: ≤ 50
Moisture% Water Content: 0.1% MAX
Phosphate Content: BY8.6%
Appearance Colorless or light yellow transparent liquid
Specific gravity(20/20℃) 1.183
Acid value(mgKOH/g) Less than 0.2
Chroma(APAH PT-CO) Less than 80
Viscosity 35-50
Color(Pt-Co): ≤50
Density: 1.183-1.192
Refractive index: 1.585-1.590
Solidification point°C: 19-24
Oxide(Cl- %): ≤0.20
Boiling point 400ºC[at 101 325 Pa]
density 1.168[at 20ºC]
vapor pressure 0Pa at 25ºC
storage temp. Hygroscopic, Refrigerator, under inert atmosphere
solubility Benzene (Slightly), Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly)
form Oil
color Colourless



SAFETY INFORMATION ABOUT REOFOS 35
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.
REOFOS 50
DESCRIPTION:
REOFOS 50 is a low viscosity triarylphosphate ester which is recommended for use in PVC plastisols for fabric coating and other applications where its low, stable viscosity offers improved processing.
REOFOS 50 can give a drier finish to coated fabrics than other standard triaryl phosphate esters.
REOFOS 50 has a high plasticizing efficiency that enable formulaters to achieve better flame retardance at lower costs.
REOFOS 50 is also designed for use as a flame retardant in phenolic laminates.

CAS No. 68937-41-7
Molecular formula C18H15R3O4P
Molecular weight 390


SYNONYMS OF REOFOS 50:
Isopropylated Triphenyl Phosphate (IPPP, REOFOS 50/50/65), [68937-41-7]; MFCD01705485; SUM OF ISOMERS; TRIS(ISOBUTANE); Triphenyl phosphate; TRIS(2-METHYLPROPANE); Phenolphosphateisopropylated; Triarylphosphatisopropylated; isopropylated phenol phosphate; ISOPROPYLATED TRIPHENYL PHOSPHATE; triisopropylated phenyl phosphate; Phenol,isopropylated,phosphate(3:1); Triphenyl phosphate - isobutane (1:3); TRIS(ISOPROPYLPHENYL)PHOSPHATE-1M ALKYL; Tris(o,m,p-isopropylphenyl) phosphate, tech.; Phosphoric acid, triphenyl ester, compd. with 2-methylpropane (1:3); TRISISOPROPYLTRISPHENYL PHOSPHATE, TIPPP PURIFIED ION M/Z 452 OF TECHNICAL GRADE; tris(4-propan-2-ylphenyl) phosphate


REOFOS 50 is a flame retardant in plastisols.
This synthetic isopropylated triaryl phosphate ester can give a drier finish to coated fabrics than other standard triaryl phosphate esters.

REOFOS 50 has a high plasticizing efficiency that enable to achieve better flame retardance at lower cost.
REOFOS 50 is used in applications where low, stable viscosity offers improved processing.

REOFOS 50 is a low viscosity synthetic isopropylated triaryl phosphate ester which widely used as a flame-retardant plasticizer.


REOFOS 50 is a synthetic isopropylated triaryl phosphate ester flame retardant, which can be used in a wide variety of resins, particularly PVC.

REOFOS 50 is a flame retardant plasticizer used primarily in PVC and phenolic resins.

REOFOS 50 is a synthetic isopropylated triaryl phosphate ester flame retardant, which can be used in a wide variety of resins, particularly PVC.


APPLICATIONS of REOFOS 50:
They are used because of their plasticizing properties mainly in PVC and PUR.
Additionally they are applicable in TPU, in phenolic resins, synthetic rubber, resins and other applications.
Typical end uses are soft PVC, PUR foams, adhesives, sealants and coatings.

We are happy to consult you in choosing and applying phosphorus flame retardants.
Additionally we offer brominated flame retardants, other halogen free flame retardants, synergists and smoke suppressants.


REOFOS 50 improves the characteristics of the coated fabrics (compared to other additives, it gives a drier finish) and has a high plasticizing efficiency combined with flame retardant properties.
REOFOS 50 is also used as a flame retardant additive in phenolic resins.

PVC industry: cable, windows and door, sheet, decorating sheet, agricultural membrane, floor membrane etc.
Other synthetic material industry: used as light-heat stabilizer or oxide-heat stabilizer.
Other industry: complex liquid and ointment compound stabilizer etc.

As a plasticizer or flame retardant added in PVC, PU, PE, PP, PC/ABS, PPO/HIPS, PVAC, PS, fabric coatings, circuit boards, spinning Chemicalbook fabrics, phenolic resin, polyethylene, artificial leather, film, plate, conveyor belt, air pipe, floor material cable, synthetic resin, plastic, rubber and fiber to increase the process performance of the product.


USES OF REOFOS 50:

REOFOS 50 Is Used For Rubber Products
REOFOS 50 Is Used For PVC Plastic Flame Retardant Conveyor Belt
REOFOS 50 Is Used For Cable
REOFOS 50 Is Used For Chloroprene Rubber

REOFOS 50 Is Used For Rubber And Other Synthetic Rubber Flame Retardant Plasticizer
REOFOS 50 Is Used For Fabric Coating
REOFOS 50 Is Used For Circuit Boards

REOFOS 50 Is Used For Flooring
REOFOS 50 Is Used For Textiles
REOFOS 50 Is Used For PVC
REOFOS 50 Is Used For Phenolic Resin


CHEMICAL AND PHYSICAL PROPERTIES OF REOFOS 50:
Basic Elements Of The Product:
Chemical Name: Triary Phosphate Isopropylated(IPPP35)
Product Name: IPPP
Cas Number.: 68937-41-7
Same Name: flame Retardant IPPP
Industrial: Plastic

Application: REOFOS 50 Phosphorus Flame Retardant is a flame retardant plasticizer for PVC applications.
Packaging Details: 200kg drum IBC ISO tank
Production Capacity: 15 tons per day
Hs Code: 29199000902
Reach: Full Registration
Appearance.

Colorless transparent liquid.

Viscosity (25 °C,CP)

42-65

Specific Gravity (20°C)

1.183

Flashing point °C

220 min.

P%

8.60

Acid Value (mg KOH/g)

0.10max.

Chroma (APHA)

50.0 max.

Water content %

0.10 max.

The Isopropylphenyl phosphate,Flame Retardant ippp35,REOFOS 50 Quality Description:
Traits: Colorless Or Light Yellow Transparent Liquid
Density Density (D20) :: 1.183
Flash Point Flash Point: 220 ℃ MIN
Viscosity Viscosity (25 ° C, CP): 42-50
Acid Value (MgKOH / G): 0.1 MAX
Refractive Index Refractive Index (N23): 1.546-1.555
Color Value: ≤ 50
Moisture% Water Content: 0.1% MAX
Phosphate Content: BY8.6%
Appearance Colorless or light yellow transparent liquid
Specific gravity(20/20℃) 1.183
Acid value(mgKOH/g) Less than 0.2
Chroma(APAH PT-CO) Less than 80
Viscosity 35-50
Color(Pt-Co): ≤50
Density: 1.183-1.192
Refractive index: 1.585-1.590
Solidification point°C: 19-24
Oxide(Cl- %): ≤0.20
Boiling point 400ºC[at 101 325 Pa]
density 1.168[at 20ºC]
vapor pressure 0Pa at 25ºC
storage temp. Hygroscopic, Refrigerator, under inert atmosphere
solubility Benzene (Slightly), Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly)
form Oil
color Colourless



SAFETY INFORMATION ABOUT REOFOS 50
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.



REOFOS 65
DESCRIPTION:
REOFOS 65 is a low viscosity triarylphosphate ester which is recommended for use in PVC plastisols for fabric coating and other applications where its low, stable viscosity offers improved processing.
REOFOS 65 can give a drier finish to coated fabrics than other standard triaryl phosphate esters.
REOFOS 65 has a high plasticizing efficiency that enable formulaters to achieve better flame retardance at lower costs.
REOFOS 65 is also designed for use as a flame retardant in phenolic laminates.

CAS No. 68937-41-7
Molecular formula C18H15R3O4P
Molecular weight 390


SYNONYMS OF REOFOS 65:
Isopropylated Triphenyl Phosphate (IPPP, REOFOS 65/50/65), [68937-41-7]; MFCD01705485; SUM OF ISOMERS; TRIS(ISOBUTANE); Triphenyl phosphate; TRIS(2-METHYLPROPANE); Phenolphosphateisopropylated; Triarylphosphatisopropylated; isopropylated phenol phosphate; ISOPROPYLATED TRIPHENYL PHOSPHATE; triisopropylated phenyl phosphate; Phenol,isopropylated,phosphate(3:1); Triphenyl phosphate - isobutane (1:3); TRIS(ISOPROPYLPHENYL)PHOSPHATE-1M ALKYL; Tris(o,m,p-isopropylphenyl) phosphate, tech.; Phosphoric acid, triphenyl ester, compd. with 2-methylpropane (1:3); TRISISOPROPYLTRISPHENYL PHOSPHATE, TIPPP PURIFIED ION M/Z 452 OF TECHNICAL GRADE; tris(4-propan-2-ylphenyl) phosphate


REOFOS 65 is a flame retardant in plastisols.
This synthetic isopropylated triaryl phosphate ester can give a drier finish to coated fabrics than other standard triaryl phosphate esters.

REOFOS 65 has a high plasticizing efficiency that enable to achieve better flame retardance at lower cost.
REOFOS 65 is used in applications where low, stable viscosity offers improved processing.

REOFOS 65 is a low viscosity synthetic isopropylated triaryl phosphate ester which widely used as a flame-retardant plasticizer.


REOFOS 65 is a synthetic isopropylated triaryl phosphate ester flame retardant, which can be used in a wide variety of resins, particularly PVC.

REOFOS 65 is a flame retardant plasticizer used primarily in PVC and phenolic resins.

REOFOS 65 is a synthetic isopropylated triaryl phosphate ester flame retardant, which can be used in a wide variety of resins, particularly PVC.


APPLICATIONS of REOFOS 65:
They are used because of their plasticizing properties mainly in PVC and PUR.
Additionally they are applicable in TPU, in phenolic resins, synthetic rubber, resins and other applications.
Typical end uses are soft PVC, PUR foams, adhesives, sealants and coatings.

We are happy to consult you in choosing and applying phosphorus flame retardants.
Additionally we offer brominated flame retardants, other halogen free flame retardants, synergists and smoke suppressants.


REOFOS 65 improves the characteristics of the coated fabrics (compared to other additives, it gives a drier finish) and has a high plasticizing efficiency combined with flame retardant properties.
REOFOS 65 is also used as a flame retardant additive in phenolic resins.

PVC industry: cable, windows and door, sheet, decorating sheet, agricultural membrane, floor membrane etc.
Other synthetic material industry: used as light-heat stabilizer or oxide-heat stabilizer.
Other industry: complex liquid and ointment compound stabilizer etc.

As a plasticizer or flame retardant added in PVC, PU, PE, PP, PC/ABS, PPO/HIPS, PVAC, PS, fabric coatings, circuit boards, spinning Chemicalbook fabrics, phenolic resin, polyethylene, artificial leather, film, plate, conveyor belt, air pipe, floor material cable, synthetic resin, plastic, rubber and fiber to increase the process performance of the product.


USES OF REOFOS 65:

REOFOS 65 Is Used For Rubber Products
REOFOS 65 Is Used For PVC Plastic Flame Retardant Conveyor Belt
REOFOS 65 Is Used For Cable
REOFOS 65 Is Used For Chloroprene Rubber

REOFOS 65 Is Used For Rubber And Other Synthetic Rubber Flame Retardant Plasticizer
REOFOS 65 Is Used For Fabric Coating
REOFOS 65 Is Used For Circuit Boards

REOFOS 65 Is Used For Flooring
REOFOS 65 Is Used For Textiles
REOFOS 65 Is Used For PVC
REOFOS 65 Is Used For Phenolic Resin


CHEMICAL AND PHYSICAL PROPERTIES OF REOFOS 65:
Basic Elements Of The Product:
Chemical Name: Triary Phosphate Isopropylated(IPPP35)
Product Name: IPPP
Cas Number.: 68937-41-7
Same Name: flame Retardant IPPP
Industrial: Plastic

Application: REOFOS 65 Phosphorus Flame Retardant is a flame retardant plasticizer for PVC applications.
Packaging Details: 200kg drum IBC ISO tank
Production Capacity: 15 tons per day
Hs Code: 29199000902
Reach: Full Registration
Appearance.

Colorless transparent liquid.

Viscosity (25 °C,CP)

42-65

Specific Gravity (20°C)

1.183

Flashing point °C

220 min.

P%

8.60

Acid Value (mg KOH/g)

0.10max.

Chroma (APHA)

50.0 max.

Water content %

0.10 max.

The Isopropylphenyl phosphate,Flame Retardant ippp35,REOFOS 65 Quality Description:
Traits: Colorless Or Light Yellow Transparent Liquid
Density Density (D20) :: 1.183
Flash Point Flash Point: 220 ℃ MIN
Viscosity Viscosity (25 ° C, CP): 42-50
Acid Value (MgKOH / G): 0.1 MAX
Refractive Index Refractive Index (N23): 1.546-1.555
Color Value: ≤ 50
Moisture% Water Content: 0.1% MAX
Phosphate Content: BY8.6%
Appearance Colorless or light yellow transparent liquid
Specific gravity(20/20℃) 1.183
Acid value(mgKOH/g) Less than 0.2
Chroma(APAH PT-CO) Less than 80
Viscosity 35-50
Color(Pt-Co): ≤50
Density: 1.183-1.192
Refractive index: 1.585-1.590
Solidification point°C: 19-24
Oxide(Cl- %): ≤0.20
Boiling point 400ºC[at 101 325 Pa]
density 1.168[at 20ºC]
vapor pressure 0Pa at 25ºC
storage temp. Hygroscopic, Refrigerator, under inert atmosphere
solubility Benzene (Slightly), Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly)
form Oil
color Colourless



SAFETY INFORMATION ABOUT REOFOS 65
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.




REOFOS 95
DESCRIPTION:
REOFOS 95 is a low viscosity triarylphosphate ester which is recommended for use in PVC plastisols for fabric coating and other applications where its low, stable viscosity offers improved processing.
REOFOS 95 can give a drier finish to coated fabrics than other standard triaryl phosphate esters.
REOFOS 95 has a high plasticizing efficiency that enable formulaters to achieve better flame retardance at lower costs.
REOFOS 95 is also designed for use as a flame retardant in phenolic laminates.

CAS No. 68937-41-7
Molecular formula C18H15R3O4P
Molecular weight 390


SYNONYMS OF REOFOS 95:
Isopropylated Triphenyl Phosphate (IPPP, REOFOS 95/50/65), [68937-41-7]; MFCD01705485; SUM OF ISOMERS; TRIS(ISOBUTANE); Triphenyl phosphate; TRIS(2-METHYLPROPANE); Phenolphosphateisopropylated; Triarylphosphatisopropylated; isopropylated phenol phosphate; ISOPROPYLATED TRIPHENYL PHOSPHATE; triisopropylated phenyl phosphate; Phenol,isopropylated,phosphate(3:1); Triphenyl phosphate - isobutane (1:3); TRIS(ISOPROPYLPHENYL)PHOSPHATE-1M ALKYL; Tris(o,m,p-isopropylphenyl) phosphate, tech.; Phosphoric acid, triphenyl ester, compd. with 2-methylpropane (1:3); TRISISOPROPYLTRISPHENYL PHOSPHATE, TIPPP PURIFIED ION M/Z 452 OF TECHNICAL GRADE; tris(4-propan-2-ylphenyl) phosphate


REOFOS 95 is a flame retardant in plastisols.
This synthetic isopropylated triaryl phosphate ester can give a drier finish to coated fabrics than other standard triaryl phosphate esters.

REOFOS 95 has a high plasticizing efficiency that enable to achieve better flame retardance at lower cost.
REOFOS 95 is used in applications where low, stable viscosity offers improved processing.

REOFOS 95 is a low viscosity synthetic isopropylated triaryl phosphate ester which widely used as a flame-retardant plasticizer.


REOFOS 95 is a synthetic isopropylated triaryl phosphate ester flame retardant, which can be used in a wide variety of resins, particularly PVC.

REOFOS 95 is a flame retardant plasticizer used primarily in PVC and phenolic resins.

REOFOS 95 is a synthetic isopropylated triaryl phosphate ester flame retardant, which can be used in a wide variety of resins, particularly PVC.


APPLICATIONS of REOFOS 95:
They are used because of their plasticizing properties mainly in PVC and PUR.
Additionally they are applicable in TPU, in phenolic resins, synthetic rubber, resins and other applications.
Typical end uses are soft PVC, PUR foams, adhesives, sealants and coatings.

We are happy to consult you in choosing and applying phosphorus flame retardants.
Additionally we offer brominated flame retardants, other halogen free flame retardants, synergists and smoke suppressants.


REOFOS 95 improves the characteristics of the coated fabrics (compared to other additives, it gives a drier finish) and has a high plasticizing efficiency combined with flame retardant properties.
REOFOS 95 is also used as a flame retardant additive in phenolic resins.

PVC industry: cable, windows and door, sheet, decorating sheet, agricultural membrane, floor membrane etc.
Other synthetic material industry: used as light-heat stabilizer or oxide-heat stabilizer.
Other industry: complex liquid and ointment compound stabilizer etc.

As a plasticizer or flame retardant added in PVC, PU, PE, PP, PC/ABS, PPO/HIPS, PVAC, PS, fabric coatings, circuit boards, spinning Chemicalbook fabrics, phenolic resin, polyethylene, artificial leather, film, plate, conveyor belt, air pipe, floor material cable, synthetic resin, plastic, rubber and fiber to increase the process performance of the product.


USES OF REOFOS 95:

REOFOS 95 Is Used For Rubber Products
REOFOS 95 Is Used For PVC Plastic Flame Retardant Conveyor Belt
REOFOS 95 Is Used For Cable
REOFOS 95 Is Used For Chloroprene Rubber

REOFOS 95 Is Used For Rubber And Other Synthetic Rubber Flame Retardant Plasticizer
REOFOS 95 Is Used For Fabric Coating
REOFOS 95 Is Used For Circuit Boards

REOFOS 95 Is Used For Flooring
REOFOS 95 Is Used For Textiles
REOFOS 95 Is Used For PVC
REOFOS 95 Is Used For Phenolic Resin


CHEMICAL AND PHYSICAL PROPERTIES OF REOFOS 95:
Basic Elements Of The Product:
Chemical Name: Triary Phosphate Isopropylated(IPPP35)
Product Name: IPPP
Cas Number.: 68937-41-7
Same Name: flame Retardant IPPP
Industrial: Plastic

Application: REOFOS 95 Phosphorus Flame Retardant is a flame retardant plasticizer for PVC applications.
Packaging Details: 200kg drum IBC ISO tank
Production Capacity: 15 tons per day
Hs Code: 29199000902
Reach: Full Registration
Appearance.

Colorless transparent liquid.

Viscosity (25 °C,CP)

42-65

Specific Gravity (20°C)

1.183

Flashing point °C

220 min.

P%

8.60

Acid Value (mg KOH/g)

0.10max.

Chroma (APHA)

50.0 max.

Water content %

0.10 max.

The Isopropylphenyl phosphate,Flame Retardant ippp35,REOFOS 95 Quality Description:
Traits: Colorless Or Light Yellow Transparent Liquid
Density Density (D20) :: 1.183
Flash Point Flash Point: 220 ℃ MIN
Viscosity Viscosity (25 ° C, CP): 42-50
Acid Value (MgKOH / G): 0.1 MAX
Refractive Index Refractive Index (N23): 1.546-1.555
Color Value: ≤ 50
Moisture% Water Content: 0.1% MAX
Phosphate Content: BY8.6%
Appearance Colorless or light yellow transparent liquid
Specific gravity(20/20℃) 1.183
Acid value(mgKOH/g) Less than 0.2
Chroma(APAH PT-CO) Less than 80
Viscosity 35-50
Color(Pt-Co): ≤50
Density: 1.183-1.192
Refractive index: 1.585-1.590
Solidification point°C: 19-24
Oxide(Cl- %): ≤0.20
Boiling point 400ºC[at 101 325 Pa]
density 1.168[at 20ºC]
vapor pressure 0Pa at 25ºC
storage temp. Hygroscopic, Refrigerator, under inert atmosphere
solubility Benzene (Slightly), Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly)
form Oil
color Colourless



SAFETY INFORMATION ABOUT REOFOS 95
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.




Repaglinide
SYNONYMS Pioglitazone hydrochloride;5-[4-[2-(5-Ethyl-2-pyridinyl) ethoxy] benzyl] thiazolidine-2,4-dione, Hydrochloride; Actos; 5-(p-(2-(5-Ethyl-2-pyridyl)ethoxy)benzyl)-2,4-thiazolidinedione monohydrochloride; Other CAS RN: 105355-27-9; 198077-89-3; 5-[[4-[2-(5-Ethyl-2-pyridinyl)ethoxy]phenyl]methyl]-2,4-thiazolidinedione monohydrochloride, Pioglitazone hydrochloride cas no:111025-46-8 (Base) 112529-15-4 (HCl)
RESIFLOW FL 2
RESIFLOW FL 2 Resiflow FL 2 is a silicone free, polymeric flow control agent and resin modifier used as an additive to correct imperfections in coatings and printing ink formulations. Craters, pin holes and fisheyes may be eliminated or substantially reduced by incorporating 0.2 - 2.0% of the agent into total formulation. Resiflow FL 2 is designed for powder coatings, solvent based coatings, high solids, coil coatings and UV-coatings. Printing inks based on flexographic or silk screen have also shown improved characteristics. Resiflow FL 2-50 Silicone free acrylic flow control agent for solvent based and solvent free coatings based on alkyd, polyester, acrylic, vinyl, epoxy and polyurethane resin. Resiflow FL 2 Resiflow FL 2 is a silicone free, polymeric flow control agent and resin modifier used as additive to correct imperfections in coatings and printing ink formulations. Craters, pin holes and fisheyes may be eliminated or substantially reduced by incorporating 0.2 - 2.0% of the agent into total formulation. The initial and recoating adhesion is normally not affected by addition of Resiflow FL 2. Resiflow FL 2 is stable to UV-radiation. The unique chemical structure of this product renders it suitable for epoxy, polyester, acrylic, vinyl, alkyd, urethane resins and other systems. Technical Data of Resiflow FL 2: Non volatile content, 1h/125 °C, DIN EN ISO 3251 min. 98% Appearance of Resiflow FL 2 colourless, high viscous liquid Viscosity of Resiflow FL 2, 20 °C, delivery form, DIN 53015, ball 6 30 - 50 Paּs Density of Resiflow FL 2 , 20 °C, DIN EN ISO 2811-1 approx. 1.0 g/cm³ Application and Properties of Resiflow FL 2: Resiflow FL 2 is designed for powder coatings, solvent based coatings, high solids, coil coatings and UV-coatings. Printing inks based on flexographic or silk screen have also shown improved characteristics. A small addition of Resiflow FL 2 into vinyl organosols and polyester gel coats improves their performance. In powder coating applications best results are obtained when the flow control agent is used as master batch consisting of 90 - 95% resin and 5 - 10% Resiflow FL 2. The compatibility of powder coatings containing different flow control agents could be critical. Therefore we recommend corresponding preliminary trials. Durability of Resiflow FL 2: Stored in original containers and at room temperature Resiflow FL 2 has a shelf life of min. 12 months. Resiflow FL 2 Resiflow FL 2 is a silicone free, polymeric flow control agent and resin modifier used as additive to correct imperfections in coatings and printing ink formulations. Craters, pin holes and fisheyes may be eliminated or substantially reduced by incorporating 0.2 - 2.0% of the agent into total formulation. The initial and recoating adhesion is normally not affected by addition of Resiflow FL 2. Resiflow FL 2 is stable to UV-radiation. The unique chemical structure of this product renders it suitable for epoxy, polyester, acrylic, vinyl, alkyd, urethane resins and other systems Resiflow FL 2 is designed for powder coatings, solvent based coatings, high solids, coil coatings and UV-coatings. Printing inks based on flexographic or silk screen have also shown improved characteristics. A small addition of Resiflow FL 2 into vinyl organosols and polyester gel coats improves their performance. In powder coating applications best results are obtained when the flow control agent is used as master batch consisting of 90 - 95% resin and 5 - 10% Resiflow FL 2. The compatibility of powder coatings containing different flow control agents could be critical. Therefore we recommend corresponding preliminary trials. Resiflow FL 2 Addition (calc. on total form.) 0,4 - 4,0 Appearance Farblose Flüssigkeit Chemical Specification Polyacrylat Forms of delivery Article number Sample Liquid 114001-00271 Order
RESORCINOL
RETINYL ACETATE, N° CAS : 127-47-9. Nom INCI : RETINYL ACETATE. Nom chimique : Retinyl acetate. N° EINECS/ELINCS : 204-844-2. Ses fonctions (INCI) : Agent d'entretien de la peau : Maintient la peau en bon état
Resorcinol Bis(diphenyl Phosphate)
SYNONYMS C.I.Acid Yellow 3; C.I. 47005; Quinoline Yellow, water soluble; Food Yellow 13; Sodium 2-(1,3-dioxoindan-2-yl)quinolinedisulfonate; 2-(1,3-Dioxoindan-2-yl) quinolinedisulfonic acid sodium salt; Sodium 2-(2-quinolyl) indan-1,3-dione-disulfonates; Quinoline Yellow;CAS NO 8004-92-0
RETINOL
Retinol, retinal and retinoic acid are the aldehyde, alcohol and acid forms of vitamin A.
Retinol is well-known for its potential benefits in skincare.
Retinol, in the form of retinal, combines with opsin to form rhodopsin which is vital for low-light and color vision.

CAS Number: 68-26-8
Molecular Formula: C20H30O
Molecular Weight: 286.45
EINECS No.: b200-683-7

Retinol is biologically active in a wide range of processes.
Retinol is a group of unsaturated nutritional organic compounds, including vitamin A, retinal, retinoic acid, provitamin A carotenoids, and beta-carotene.
As retinoic acid,Retinol functions as a hormone-like growth factor that supports epithelial cells.

Retinol also shows lipoperoxy radical scavenging activity, and has antioxidant and fluorescent properties.
Retinol is a form of vitamin A, which is a fat-soluble vitamin essential for various bodily functions, including vision, immune system support, and skin health.
Retinol, specifically, is a derivative of vitamin A that is commonly used in skincare products and is known for its beneficial effects on the skin.

Human Retinol is derived from the natural food.
Natural Retinol exists in dif ferent forms.
The human immune system is unable to grow and develop without Retinol.

The retinoids exist as many geometric isomers due to the unsaturated bonds in the aliphatic chain.
Retinol, also called vitamin A1, is a fat-soluble vitamin in the vitamin A family that is found in food and used as a dietary supplement.
Therefore, food is the main source of Retinol.

As early as 1000 years ago, the Qian Jin Yao Fang written by Sun Simiao in Tang Dynasty recorded that animal liver can cure night blindness.
This is the early recognition in vitamin A supplementation.
The traditional Chinese medicine books also recorded that nourishing the liver can improve eyesight.

Researches on the therapy of vitamin A deficient-diseases are mainly related to nourishing the liver and kidney, supplementing essence and blood, and activating qi.
In animal tissues, Retinol is present in the form of retinoids.
Retinol or other forms of vitamin A are needed for vision, cellular development, maintenance of skin and mucous membranes, immune function and reproductive development.

Dietary sources include fish, dairy products, and meat.
As a supplement it is used to treat and prevent Retinol deficiency, especially that which results in xerophthalmia.
High doses may cause enlargement of the liver, dry skin, and hypervitaminosis A.

High doses during pregnancy may harm the fetus.
The body converts retinol to retinal and retinoic acid, through which it acts.
Collagen is a protein that helps maintain skin's elasticity and firmness, making it an effective ingredient for reducing the appearance of wrinkles and fine lines.

Retinol encourages skin cell turnover, which means it helps shed old, damaged skin cells and promotes the growth of new, healthy skin cells.
This can lead to smoother and more youthful-looking skin.
Retinol is used to treat acne by preventing the formation of clogged pores, promoting the shedding of dead skin cells, and reducing inflammation associated with acne breakouts.

Retinol can help fade dark spots and hyperpigmentation, such as age spots and sunspots, by inhibiting the production of melanin in the skin.
Retinol has a mild exfoliating effect, which can help unclog pores and improve skin texture.
Similar results were obtained using as co-solvents (with the liquid ammonia) ethylene diamine and ether; pentane; tetrahydrofuran; diethylamine and hexamethylphosphoramide.

Retinol and its derivatives exhibit anti-aging properties.
Retinol is used for treating wrinkles and signs of aging.
However, due to its photo instability and skin irritation potency, Retinol is hardly used in cosmetic formulations.

Retinol is also used as a therapeutic for dermatoses.
Retinol deficiency leads to xerosis and follicular hyperkeratosis.
Principal dietary sources of Retinol are milk fat (cheese and butter) and eggs.

Since it is stored in the liver, inclusion of liver in the diet also provides Retinol.
A plant pigment, carotene, is a precursor for Retinol and is present in highly pigmented vegetables, such as carrots, rutabaga, and red cabbage.
Retinol can increase the skin's sensitivity to UV radiation, so it is crucial to use sunscreen daily when using products containing retinol.

Sun protection helps prevent sunburn and further sun damage.
Retinol often takes several weeks to months of consistent use to see noticeable improvements in the skin.
Prescription versions, such as tretinoin, are generally more potent but may also be associated with more side effects.

OTC products are milder and are suitable for many people without a prescription.
Retinol can cause skin irritation, redness, dryness, and peeling, especially when first starting to use it.
One group at great risk are children from low-income families, who are likely to lack fresh vegetables (carotene) and dairy products (vitamin A) in the diet.

Retinol or other forms of vitamin A are needed for eyesight, maintenance of the skin, and human development.
Other than for vision, the active compound is all-trans-retinoic acid, synthesized from retinal, in turn synthesized from retinol.
Retinol is part of a family of compounds known as retinoids.

The retinoid family includes various forms of Retinol, such as retinyl palmitate, retinol, retinaldehyde, and prescription-strength retinoids like tretinoin (Retin-A) and isotretinoin (Accutane).
Retinols vary in potency, with prescription-strength options typically being more potent than over-the-counter retinol.
When using a retinol product, a pea-sized amount is often recommended for the entire face.

Retinol using too much can increase the risk of skin irritation.
Retinol is typically applied at night as it can break down in sunlight and may become less effective.
Applying it before bedtime allows for maximum absorption and benefits.

Retinol can be used in combination with other skincare ingredients like hyaluronic acid, niacinamide, and antioxidants to address multiple skin concerns.
For best results, it's important to use retinol consistently over time.
Skipping applications can delay or reduce its effectiveness.

Retinol's advisable to start with a lower concentration product and gradually increase the strength as skin builds tolerance.
This can help minimize initial irritation.

Retinol's a good idea to consult with a dermatologist.
They can provide personalized recommendations and may even prescribe stronger retinoid formulations if needed.
Retinol may not be suitable for everyone, especially those with certain skin conditions or sensitivities.

Pregnant or nursing individuals are typically advised to avoid retinol products due to potential risks to the developing fetus or infant.
Adapalene is another Retinol that is often available over-the-counter and by prescription.
Retinol is known for its effectiveness in treating acne and is typically gentler on the skin compared to some other retinoids.

The efficacy of retinol can vary from person to person, depending on factors like skin type, the concentration of retinol in the product, and the frequency of use.
Retinol is essential to follow product instructions and introduce retinol gradually into your skincare routine to minimize these side effects.
Manufacturing process for Retinol includes these steps as follows: Step A: Synthesis of Preparation of ethyl ether of ethynyl-β-ionol;Step B: Coupling Reaction; Step C:Semi-
Hydrogenation of Coupling Product;Step D:Hydrolysis of Semi-Hydrogenated Coupling Product.

Separation of Retinol from the product obtained was achieved by acetylating the total reaction product using pyridine-acetic anhydride at room temperature and chromatographing on alumina neutralized with acetic acid.
The Retinol acetate fraction was sufficiently pure to become crystallized from pentane at -15°C when seeded with a pure Vitamin A acetate crystal.
When the Retinol acetate was converted to the alcohol form of Vitamin A, the final product showed the characteristic infrared and ultraviolet absorption curves for Retinol.

Retinol is available in various skincare products, including creams, serums, and oils.
The concentration of retinol in these products can vary, so it's essential to choose the right product for your skin type and concerns.
There are both over-the-counter (OTC) and prescription-strength retinol products.

Retinol was discovered in 1909, isolated in 1931, and first made in 1947.
Retinol is on the World Health Organization's List of Essential Medicines.
Retinol is available as a generic medication and over the counter.

Retinol is used to address a range of skin concerns, including fine lines, wrinkles, uneven skin tone, acne, and sun damage.
Retinol stimulates collagen production in the skin.
Retinol is taken by mouth or by injection into a muscle.

As an ingredient in skin-care products, it is used to reduce wrinkles and other effects of skin aging.
Retinol at normal doses is well tolerated.
However, in plants, the form of Retinol called carotenoids is contained in the green, orange, and yellow plant tissue.

Retinol compounds such as vitamin A, reti nal, carotene, and so on from these foods can be converted to vitamin A in the human body.
Beyond addressing specific skin concerns, retinol is often used for anti-aging and as part of a long-term skincare routine to maintain healthy and youthful-looking skin.
This vitamin plays an essential role in vision, particularly night vision, normal bone and tooth development, reproduction, and the health of skin and mucous membranes (the mucus-secreting layer that lines body regions such as the respiratory tract).

Retinol also acts in the body as an antioxidant, a protective chemical that may reduce the risk of certain cancers.
There are two sources of dietary Retinol.
Active forms, which are immediately available to the body are obtained from animal products.

These are known as retinoids and include retinaldehyde and retinol.
Precursors, also known as provitamins, which must be converted to active forms by the body, are obtained from fruits and vegetables containing yellow, orange and dark green pigments, known as carotenoids, the most well-known being β-carotene.

For this reason, amounts of Retinol are measured in Retinol Equivalents (RE).
Approximately 250,000 to 500,000 malnourished children in the developing world go blind each year from a deficiency of Retinol.
Retinol deficiency in expecting mothers increases the mortality rate of children shortly after childbirth.

Night blindness is one of the first signs of vitamin A deficiency.
Retinol deficiency contributes to blindness by making the cornea very dry and damaging the retina and cornea.
Retinol is one of the animal forms of vitamin A.

Retinol is a diterpenoid and an alcohol.
Commercial production of retinol typically requires retinal synthesis through reduction of a pentadiene derivative and subsequent acidification/hydrolysis of the resulting isomer to produce retinol.
Pure retinol is extremely sensitive to oxidization and is prepared and transported at low temperatures and oxygen free atmospheres.

All retinoid forms of vitamin A are used in cosmetic and medical applications applied to the skin.
One RE is equivalent to 0.001 mg of retinol, or 0.006 mg of β-carotene, or 3.3 International Units of vitamin A.
In the intestine, vitamin A is protected from being chemically changed by vitamin E.

Retinol is fat-soluble and can be stored in the body.
Retinol, or Vitamin A, is essential for the proper maintenance of the functional and structural integrity of epithelial cells, and it plays a major role in epithelial differentiation.
Bone development and growth in children have also been linked to adequate vitamin A intake.

Retinol, when reduced to the aldehyde 11-cis-retinal, combines with opsin to produce the visual pigment rhodopsin.
This pigment is present in the rods of the retina and is partly responsible for the process of dark adaptation.

Melting point: 61-63 °C(lit.)
Boiling point: 368.81°C (rough estimate)
Density: 0.9933 (rough estimate)
refractive index: 1.641
Flash point: -26 °C
storage temp.: -20°C
solubility: Chloroform (Slightly), Methanol (Slightly)
pka: 14.09±0.10(Predicted)
form: crystalline
color: yellow to orange
Water Solubility: Practically insoluble inwaterorglycerol; soluble in absolute alcohol,methanol,℃hloroform, ether, fats and oils.
Sensitive: Moisture & Light Sensitive
Merck: 13,10073
BRN: 403040
Stability: Stable, but light and air sensitive. Incompatible with strong acids, strong oxidizing agents.
LogP: 5.680
CAS DataBase Reference: 68-26-8(CAS DataBase Reference)
FDA 21 CFR: 184.1930; 582.5930; 101.9; 104.20; 107.10; 107.100; 310.545
Substances Added to Food (formerly EAFUS): VITAMIN A

Retinol plays an important role in main taining healthy skin.
Retinol deficiency disrupts human keratin cell terminal dif ferentiation and makes the skin rough, dry, scaly, and clogged.
Retinol is reported that vitamin A can degrade malignant melanoma and T-cell lymphoma epidermal transfer, reduce the oil secretion of the common acne and the number of bacteria in the epidermis and capillaries, and inhibit immune response of monocytes and neutrophils.

Retinol plays an important role as an important function material in the body system, such as hematopoietic function, bone development, tumor prevention, and so on.
Therefore, supplement of Retinol is necessary for health requirements.

Acute hypervitaminosis A results in drowsiness, headache, vomiting, papilledema, and a bulging fontanel in infants.
Retinol deficiency can lead to animal death.
Retinol functions in reproduction and embryonic development.

Retinol plays an important role in the reproductive process of sperm production and ovula tion, but its biochemical basis is unclear.
Retinol plays a key role in the develop ment of embryos and organism and maintenance of tissue function. The main organs affected by vitamin A deficiency are the heart, eye tissue, circulatory system, geni tourinary system, and respiratory system. Retinol is necessary for embryonic development.

Retinol functions on immune function.
The lymphoid organs, cell distribu tion, histology, lymphocytes, and other characteristics will change when the ani mals lack Retinol.
Retinol deficiency can lead to immune function decrease, induce inflammation, and exacerbate inflammatory symptoms.

Retinol functions in dermatology.
Intake of vitamin A precursors, such as carotenoids, retinyl esters, retinol, and reti nal, can maintain the epithelial cell differentiation, normal proliferation, and visual function.
All of these substances can be metabolized into retinol, retinal, and reti noic acid.

But unlike retinol and retinal, retinoic acid cannot be reduced to retinol and retinal.
Intake of retinoic acid can only maintain the systemic function of Retinol.
Visual and vitamin A, 11-cis-retinal plays an important role as a photographic group of retinal cones and visual pigments in rod cells.

11-cis-retinal would be transformed into all-trans-retinal form under the light induction.
The symptoms of chronic toxicity include scaly skin, hair loss, brittle nails, and hepatosplenomegaly.
Anorexia, irritability, and swelling of the bones have been seen in children.

Retardation of growth also may occur.
Liver toxicity has been associated with excessive Retinol intake.
Retinol is teratogenic in large amounts, and supplements should not be given during a normal pregnancy.

The IOM has reported the UL of vitamin A to be 3,000 μg/day.
Retinol is an essential compound in the cycle of light-activated chemical reactions called the "visual cycle" that underlies vertebrate vision.
Retinol is converted by the protein RPE65 within the pigment epithelium of the retina into 11-cis-retinal.

This molecule is then transported into the retina's photoreceptor cells (the rod or cone cells in mammals) where it binds to an opsin protein and acts as a light-activated molecular switch.
When 11-cis-retinal absorbs light it isomerizes into all-trans-retinal.
The change in the shape of the molecule in turn changes the configuration of the opsin in a cascade that leads to the neuronal firing, which signals the detection of light.

The opsin then splits into the protein component (such metarhodopsin) and the cofactor all-trans-retinal.
The regeneration of active opsin requires conversion of all-trans-retinal back to 11-cis-retinal via retinol.
The regeneration of 11-cis-retinal occurs in vertebrates via conversion of all-trans-retinol to 11-cis-retinol in a sequence of chemical transformations that occurs primarily in the pigment epithelial cells.

Without adequate amounts of retinol, regeneration of rhodopsin is incomplete and night blindness occurs.
Night blindness, the inability to see well in dim light, is associated with a deficiency of Retinol, a class of compounds that includes retinol and retinal.
In the early stages of vitamin A deficiency, the more light-sensitive and abundant rods, which have rhodopsin, have impaired sensitivity, and the cone cells are less affected.

The cones are less abundant than rods and come in three types, each contains its own type of iodopsin, the opsins of the cones.
The cones mediate color vision, and vision in bright light.
The skin around the eyes is thinner and more delicate, making it more prone to irritation.

Retinol's usually best to avoid applying retinol directly to the eyelids or too close to the eye area. Instead, use a specially formulated eye cream if you want to address concerns in that area.
Retinol using sunscreen daily is crucial when using retinol or any retinoid product.
Retinol can increase the skin's sensitivity to UV radiation, so sunscreen helps protect the skin from sun damage and reduces the risk of skin irritation.

Incorporating a moisturizer into your skincare routine can help combat the dryness and peeling that can occur with retinol use.
Look for a gentle, hydrating moisturizer that works well with your skin type.

Retinol's important to be patient when using retinol.
Results may not be immediately visible, and skin improvement can take several weeks to months.
Start with a lower concentration and gradually increase it as skin becomes more accustomed to the product.

While using retinol, it's advisable to avoid harsh or abrasive skincare products, such as strong exfoliants or scrubs, which can exacerbate skin sensitivity.
Pregnant or nursing individuals should avoid retinol and most other retinoids due to the potential risks to the fetus or infant.
Consult with a healthcare professional for safe skincare alternatives during this time.

Deficiencies in Retinol have been linked to an increased susceptibility to skin infection and inflammation.
Retinol appears to modulate the innate immune response and maintains homeostasis of epithelial tissues and mucosa through its metabolite, retinoic acid (RA).
As part of the innate immune system, toll-like receptors in skin cells respond to pathogens and cell damage by inducing a pro-inflammatory immune response which includes increased RA production.

The epithelium of the skin encounters bacteria, fungi and viruses.
Keratinocytes of the epidermal layer of the skin produce and secrete antimicrobial peptides (AMPs).
The dissociation of all-trans Retinol and opsin was coupled with the nerve stimulation of the brain’s visual center.

By a series of biochemical processes, nerve impulses format in the rod cells at the end of synapse, and then the optic nerve conducts the nerve impulses along.
The visual process is a component renewable cycle, and all-trans-retinal can be enzymatically modified to 11-cis form in dark conditions.
The systemic effects of Retinol.

Retinol not only significantly affects visual function but also has a greater physiological impact than visual function.
Retinol deficiency destroys the visual cycle, leads to dark adaptation damage (night blind ness or nyctalopia), and destroys systemic function which is necessary to maintain life (e.g., corneal injury, infection, and hypoplasia).

History:
The vitamin research is the great achievement in the development of life sciences, while human beings only took half a century to discover and understand vitamins.
However, everything is still very difficult for scientists in the early stage of vitamin discovery.
From 1913 to 1915, Elmer McCollum and Marguerite Davis indicated that the growth rate was maintained by at least two different kinds of growth factors: one can be separated from eggs or butter, and the other one which multiple neuritis of chicks and pigeons can be extracted by water; thus they were named fat-soluble Retinol and water-soluble vitamin B.

In 1919, the researchers demonstrated that fat-soluble Retinol not only sup ported the rate of growth but also prevented eye dryness and night blindness in the process of property study.
In 1920, Dr. J.C. Drummond named this active lipid as vitamin A.
Retinol exists in cod liver oil and prevents the occurrence of eye dryness and night blindness.

Uses:
Retinol can be used in combination with other skincare ingredients like hyaluronic acid, vitamin C, and peptides to address multiple skin concerns and provide a comprehensive skincare routine.
Retinol is often used in combination with other active ingredients to create a well-rounded skincare routine.
For example, combining retinol with antioxidants like vitamin C can provide added protection against environmental damage.

They help prevent clogged pores, reduce inflammation, and encourage the shedding of dead skin cells, which can lead to fewer breakouts and clearer skin.
Retinol can fade hyperpigmentation, including dark spots, sunspots, and melasma.

Retinol inhibits the production of melanin and encourages the turnover of pigmented skin cells, resulting in a more even skin tone.
Retinol can help improve skin texture by reducing roughness and promoting smoother, softer skin.
Retinol is often used to address issues like uneven skin texture and large pores.

Some people use retinol as a preventative measure to maintain healthy and youthful-looking skin and to delay the signs of aging.
Retinol may help improve the appearance of certain types of scars, such as acne scars, by promoting skin cell turnover and collagen production.
Retinol can contribute to overall skin health by promoting a more vibrant and youthful appearance.

Retinol is often incorporated into skincare routines to support healthy and radiant skin.
When compared to retinoic acid, retinol has an increased penetration potential and is less irritating, making it an effective ingredient for anti-aging products.
The anti-aging benefits of topically treating skin with retinol are based on its penetration ability, which allows it to reach the sites in the skin requiring treatment.

When used on sensitive skin for a prolonged period of time or in concentrations that are too high, retinol can cause dermatitis.
Through dietary modification involving the adjustment of menu choices of affected persons from available food sources to optimize Retinol content.
Enriching commonly eaten and affordable foods with Retinol, a process called fortification.

Retinol involves addition of synthetic vitamin A to staple foods like margarine, bread, flours, cereals, and infant formula during processing.
By giving high-doses of Retinol to the targeted deficient population, a method known as supplementation.
In regions where deficiency is common, a single large dose is recommended to those at high risk twice a year.

Retinol is widely recognized for its anti-aging properties.
Retinol helps reduce the appearance of fine lines, wrinkles, and age spots by stimulating collagen production, promoting skin cell turnover, and improving skin texture.
Retinol's generally recommended to apply retinol products in the evening as part of your nighttime skincare routine.

This allows the product to work while you sleep and minimizes potential sun sensitivity during the day.
Reiterating the importance of daily sunscreen use is crucial when using retinol or retinoids.
Sunscreen helps protect the skin from UV damage, which can exacerbate skin issues and increase the risk of sunburn.

While retinol can be effective, it may also lead to dryness or flakiness, especially in the initial stages of use.
Incorporating a hydrating moisturizer into your routine can help combat these side effects and keep the skin barrier healthy.
The frequency of retinol use depends on the product's concentration and your skin's tolerance.

Some individuals start by using retinol products every other night or a few times a week and gradually increase usage as their skin adapts.
Avoid using harsh or abrasive cleansers when using retinol.
Opt for a gentle, hydrating cleanser that won't strip the skin of its natural oils.

Achieving desired results with retinol often requires patience.
Retinol may take several weeks to months before significant improvements are visible, so consistency in use is important.
Some individuals experience a temporary worsening of skin issues, such as increased breakouts or redness, when they first start using retinol.

This is often referred to as the "retinol purge" and can be a normal part of the adjustment period.
Many users find that incorporating retinol into their skincare routine is a long-term commitment for maintaining healthy, youthful-looking skin.
Consistency in use can help sustain results over time.

There are various retinol and retinoid products available, ranging from lower to higher concentrations.
Start with a product that matches your skin type and concerns.
Individuals with sensitive skin may need to be particularly cautious when using retinol.

For those with complex skincare concerns or specific goals, working with a dermatologist to create a customized skincare plan can yield the best results.
They can provide insights on retinol usage as part of a holistic approach to skincare.
Retinol can be particularly effective in smoothing rough skin, such as the skin on the elbows, knees, and heels.

Specialized body creams containing retinol can help improve the texture of these areas.
Some individuals use retinol products to reduce the appearance of stretch marks.
While it may not completely eliminate them, retinol's ability to stimulate collagen production and improve skin texture can contribute to a reduction in the visibility of stretch marks.

Dermatologists often recommend retinol or retinoid products as part of post-procedure skincare routines.
These products can help promote healing, reduce redness, and maintain the results of procedures like chemical peels or laser treatments.
Retinol products can be effective for addressing "bacne" or acne on the back.

They work similarly to their role in treating facial acne by unclogging pores and reducing inflammation.
Retinol can have anti-inflammatory properties, which can be beneficial for individuals with certain skin conditions, such as rosacea.
However, the use of Retinol in these cases should be carefully monitored by a dermatologist.

Retinol and retinoids can contribute to an overall improvement in skin tone and texture.
This includes reducing redness, improving skin elasticity, and providing a smoother, more youthful appearance.
Even after achieving desired results, many people continue to use retinol or retinoid products in their skincare routine to maintain healthy and youthful-looking skin as part of their long-term skincare strategy.

Retinol and retinoid products come in various formulations, including creams, serums, gels, and oils.
Choosing the right formulation depends on individual preferences and skin type.
Some individuals incorporate retinol into their skincare routine at a younger age to prevent the signs of aging from appearing prematurely.

This can be part of a proactive approach to skincare.
For those with specific skin concerns or conditions, consulting with a dermatologist is highly recommended before starting a retinol or Retinol regimen.
Many people incorporate retinol into their skincare routine to maintain a youthful complexion.

Retinol and some retinoid derivatives are effective in treating acne.
Retinol) is the fat-soluble vitamin a which is required for new cell growth and prevention of night blindness.
There is no appreciable loss by heating or freezing, and it is stable in the absence of air.

Sources include liver, fortified margarine, egg, and milk.
Retinol palmitate can be found in frozen egg substitute.
Occurs preformed only in animals; metabolized from carotenoids, such β-carotene, in the intestinal mucosa.

Dietary sources include liver, milk, butter, cheese, eggs and fish liver oils or as carotenoi s from fruits and vegetables.
Stored primarily in the liver in esterified form; transported in the blood by retinol binding protein (RBP).
Retinol is a retinoid considered to be a skin revitalizer.

Retinol is reported to enhance skin radiance and treat conditions associated with chronological aging, such as wrinkles and fine lines, as well as dermatological disorders, including acne, follicular and lesion papules, actinic keratosis, oily skin, and rosacea.
According to clinical dermatologists, retinol is one of the few substances with a demonstrated ability to reduce and prevent fine lines and wrinkles.

Retinol is able to alter the behavior of aged cells so they act in a more youthful manner.
Retinol is considered necessary for normal epidermal cell growth and differentiation and stimulates the production of new blood vessels in the skin, improving skin tone.
In addition, retinol has anti-oxidant capacities and protects dermal fibers by counteracting the increased activity of enzymes that degrade collagen and elastin when the skin is exposed to uV rays.

Retinol can be drying to the skin when used for a prolonged period of time or in concentrations that are too high.
A weaker retinoid than retinoic acid, retinol converts to retinoic acid once on the skin.

Safety Profile:
Retinol ngestions of greater than 1 million IU in adults and greater than 300 000 IU in children have resulted in the development of increased intracranial pressure (symptoms described include headache, dizziness, vomiting, visual changes, and bulging fontanel in infants).
Acute ingestions of greater than 12 000 IU per kilogram are also considered toxic.

Toxicity is more frequently seen with chronic ingestion of high doses of 30 000–50 000 IU per day.
Retinol toxicity in children develops following chronic ingestion of 410 times the recommended daily allowance for weeks to months.
The exact mechanism leading to toxicity is not known.

Both acute and chronic toxicity may occur.
Acute toxicity is uncommon in adults.
Moderately toxic by ingestion.

Hepatic toxicity typically requires months or years of daily high doses of Retinol.
There are no known cases of vitamin A toxicity associated with beta-carotene ingestion.
Human teratogenic effects by ingestion: developmental abnormalities of the craniofacial area and urogenital system.

Synonyms:
retinol
Vitamin A
all-trans-Retinol
68-26-8
Vitamin A1
Alphalin
Chocola A
Alphasterol
Apostavit
Aquasynth
Axerophthol
Epiteliol
Prepalin
Testavol
Veroftal
Afaxin
Agiolan
Agoncal
Anatola
Apexol
Dofsol
Myvpack
Vaflol
Vitpex
Aoral
trans-retinol
Vitamin A alcohol
Disatabs Tabs
Oleovitamin A
Bentavit A
Dohyfral A
Alcovit A
Anatola A
Vogan-Neu
all-trans-Retinyl alcohol
A-Mulsal
Biosterol
Ophthalamin
Plivit A
Vi-Alpha
A-Vitan
All-trans retinol
Atars
Avibon
Avitol
Axerol
Vafol
Vogan
Retrovitamin A
Lard Factor
all-trans-Vitamin A alcohol
Homagenets Aoral
Sehkraft A
Testavol S
Hi-A-Vita
Vitamin A1 alcohol
A-Sol
all-trans-Vitamin A
A-Vi-Pel
ACON
ATAV
Super A
Solu-A
11103-57-4
Nio-A-Let
Vio-A
Vi-Dom-A
Anti-infective vitamin
Antixerophthalmic vitamin
Vitavel A
Del-VI-A
Wachstumsvitamin
Vitamine A
Vitavel-A
Axerophtholum
Retinolo
Retinolum
Thalasphere
beta-Retinol
Vitamin A1, all-trans-
Vitamin A alcohol, all-trans-
Vitaminum A
Hydrovit A
trans-Vitamin A alcohol
Retinolo [DCIT]
Cylasphere
Vi-alpha; Vi-alpha
Retinol, all trans-
Antixerophthalmisches Vitamin
Rovimix A 500
all-trans-Vitamin A1
Retinol [INN:BAN]
Retinolum [INN-Latin]
Vitamin A1 alcohol, all trans
All Trans Retinol
Ro-a-vit
tROL
Vitamin A alcohol (VAN)
Retinol (Vit A)
(2E,4E,6E,8E)-3,7-dimethyl-9-(2,6,6-trimethylcyclohex-1-en-1-yl)nona-2,4,6,8-tetraen-1-ol
Aquasol A Parenteral
CCRIS 5444
HSDB 815
C20H30O
Vitamin-A
UNII-G2SH0XKK91
.beta.-Retinol
(2E,4E,6E,8E)-3,7-dimethyl-9-(2,6,6-trimethylcyclohexen-1-yl)nona-2,4,6,8-tetraen-1-ol
EINECS 200-683-7
G2SH0XKK91
[11,12-3H]-Retinol
NSC 122759
NSC-122759
UNII-81G40H8B0T
BRN 0403040
Vitamin A (USP)
(all-E)-3,7-Dimethyl-9-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2,4,6,8-nonatetraen-1-ol
DTXSID3023556
Vitamin A [Natural]
Vitamin A1 alcohol, all-trans-
ophthalamin (obsolete)
Retin-11,12-t2-ol (9CI)
2,4,6,8-Nonatetraen-1-ol, 3,7-dimethyl-9-(2,6,6-trimethyl-1-cyclohexen-1-yl)-, (all-E)-
EINECS 234-328-2
CHEMBL986
M.V.C. 9+3
3,7-Dimethyl-9-(2,6,6-trimethyl-1-cyclchexen-1-yl)-2,4,6,8-nonatetraen-1-ol
DTXCID203556
trans-Retinol acid (Vitamin A)
CHEBI:17336
EC 200-683-7
all-trans-13,14-Dihydro retinol
4-06-00-04133 (Beilstein Handbook Reference)
VITAMINA
3,7-Dimethyl-9-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2,4,6,8-nonatetraen-1-ol, (all-E)-
LPK
Vitamin A (Natural)
NCGC00017343-07
Retinol-(cellular-retinol-binding-protein)
3,7-Dimethyl-9-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2,4,6,8-nonate-traen-1-ol
3,7-Dimethyl-9-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2,4,6,8-nonatetraen-1-ol
3,7-dimethyl-9-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2,4,6,8-nonatetraen-1-ol, (all-E)-Isomer
Alcohol 9,13-dimethyl-7-(1,1,5-trimethyl-6-cyclohexen-5-yl)-7,9,11,13-nonatetraen-15-ol
Vi-a
ALL-TRANS RETINOL (SEE ALSO RETINOID PROJECT 1)
Homagenets aorl
Vogan-nu
Vitamin A cryst
Zinosan N
CAS-68-26-8
all-trans-Retinol;(2E,4E,6E,8E)-3,7-Dimethyl-9-(2,6,6-trimethylcyclohex-1-en-1-yl)nona-2,4,6,8-tetraen-1-ol
SMR000112036
Vitamin A (Feed)
9-cis,13-cis-Retinol
SR-01000763813
MFCD00001552
CHEBI:50211
Tricyclics
lard-factor
Tegosphere VitA
vitamins A
.alpha.sterol
b-Retinol
Retinol-
.alpha.lin
Retinyl A
1rbp
vitamin A vitamer
Vitamin-A alcohol
Vitamin-A1
vitamin A vitamers
Vi-.alpha.
(9Z)-Retinol
LUTAVIT A
MICROVIT A
VIATMIN A
1gx8
RETINOL [HSDB]
RETINOL [INCI]
RETINOL [INN]
retinolum densatum oleosum
Spectrum5_000993
Spectrum5_001997
VITAMIN A [MI]
RETINOL [WHO-DD]
D0AO6P
D0S7WX
Retinol, 95%, synthetic
all-trans vitamin A alcohol
SCHEMBL3112
VITAMIN A (MART.)
all-trans-3,7-Dimethyl-9-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2,4,6,8-nonatetraen-1-ol
Retinol, all-trans-(8CI)
VITAMIN A CONCENTRATE
BIDD:PXR0102
MLS001066379
MLS001074751
MLS006010008
Retinol, all-trans- (8CI)
SPECTRUM1501203
(ALL-E)-
GTPL4053
HMS501I08
A11CA01
D10AD02
R01AX02
S01XA02
VITAMIN A (EP MONOGRAPH)
3,7-dimethyl-9-(2,6,6-trimethylcyclohex-1-en-1-yl)nona-2,4,6,8-tetraen-1-ol
VITAMIN A (USP MONOGRAPH)
81G40H8B0T
DTXSID301014459
HMS1921B04
HMS2092L13
HMS2270C05
Pharmakon1600-01501203
VITAMIN A, UNSPECIFIED FORM
BCP06593
HY-B1342
Tox21_110818
Tox21_202441
Tox21_300287
BDBM50092056
CCG-38864
LMPR01090001
NSC122759
NSC758150
s5592
3,7-dimethyl-9-(2,6,6-trimethyl-1-cyclohexenyl)-nona-2,4,6,8-tetraen-1-ol
AKOS015902578
DB00162
LS-1578
NSC-758150
SDCCGMLS-0066724.P001
(2E,4E,6E,8E)-3,7-dimethyl-9-(2,6,6-trimethylcyclohex-1-enyl)nona-2,4,6,8-tetr aen-1-ol
IDI1_000486
SMP2_000102
NCGC00017343-02
NCGC00017343-03
NCGC00017343-04
NCGC00017343-05
NCGC00017343-06
NCGC00017343-08
NCGC00017343-09
NCGC00017343-11
NCGC00091784-01
NCGC00091784-02
NCGC00091784-03
NCGC00091784-04
NCGC00091784-05
NCGC00091784-06
NCGC00254024-01
NCGC00259990-01
AC-11701
BS-17906
SBI-0051690.P002
CS-0013091
C00473
C17276
D06543
AB00052248_05
EN300-6733268
A836068
Q424976
Retinol, >=95.0% (HPLC), ~2700 U/mg
Retinol, synthetic, >=95% (HPLC), crystalline
J-014834
J-017515
Q-201926
SR-01000763813-2
SR-01000763813-4
W-104683
BRD-K22429181-001-06-8
BRD-K64634304-001-01-5
WLN: L6UTJ A1 B1U1Y1&U2U1Y1&U2Q C1 C1
Retinol, BioXtra, >=97.5% (HPLC), ~3100 U/mg
Z2315574891
3,6,6-trimethyl-1-cyclohexen-1-yl)-2,4,6,8-nonatetraen-1-ol
2,4,6,8-NONATETRAEN-1-OL, 3,7-DIMETHYL-9-(2,6,6-TRIMETHYL-1-CYCLOHEXEN-1-YL)-
2,6,8-Nonatetraen-1-ol, 3,7-dimethyl-9-(2,6,6-trimethyl-1-cyclohexen-1-yl)-, (all-E)-
3,7-Dimethyl-9-(2,6, 6-trimethyl-1-cyclohexen-1-yl)-2,4,6,8-nonatetraen-1-ol
3,7-Dimethyl-9-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2,4,6,8-nonatetraen-1-ol, all (E)-
3,7-Dimethyl-9-(2,6,6-trimethyl-1-cyclohexenyl)-2,4,6,8-nonatetraen-1-ol
(2E,4E,6E,8E)-3,7-dimethyl-9-(2,6,6-trimethyl-1-cyclohexenyl)-1-nona-2,4,6,8-tetraenol
(2E,4E,6E,8E)-3,7-dimethyl-9-(2,6,6-trimethyl-1-cyclohexenyl)nona-2,4,6,8-tetraen-1-ol
(2E,4E,6E,8E)-3,7-dimethyl-9-(2,6,6-trimethylcyclohex-1-enyl)nona-2,4,6,8-tetraen-1-ol
(2Z,4Z,6Z,8Z)-3,7-Dimethyl-9-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2,4,6,8-nonatetren-1-ol
RETINYL ACETATE
RETINYL LINOLEATE, N° CAS : 631-89-0, Nom INCI : RETINYL LINOLEATE. Nom chimique : Retinol, 9,12-octadecadienoate, (Z,Z)-. N° EINECS/ELINCS : 426-960-4. Ses fonctions (INCI), Agent d'entretien de la peau : Maintient la peau en bon état
RETINYL ACETATE
Retinyl acetate (retinol acetate, vitamin A acetate) is a natural form of vitamin A.
Retinyl acetate consists of yellow crystals which are greasy or sticky.
Retinyl acetate has potential antineoplastic and chemo-preventive activities.

CAS Number: 127-47-9
Molecular Formula: C22H32O2
Molecular Weight: 328.49
EINECS Number: 204-844-2

Retinyl acetate is an acetate ester.
Retinyl acetate is functionally related to an all-trans-retinol.
Retinyl acetate is the acetate ester of retinol.

Retinyl acetate has a mild, characteristic odor.
Retinyl acetate can be used to fortify food with vitamin A.
As vitamin A acetate can induce cell differentiation and inhibit cell proliferation, it is used in skin-conditioning agent.

Retinyl acetate is a synthetic compound that belongs to the family of retinoids, which are chemical derivatives of vitamin A.
Retinyl acetate is often used in dietary supplements, cosmetics, and skin care products.
Retinyl acetate can be converted into retinol (the active form of vitamin A) in the body.

Vitamin A and its derivatives like retinyl acetate are important for various biological processes, including maintaining healthy skin, promoting good vision, and supporting the immune system.
In skin care products, retinyl acetate is sometimes included for its potential benefits in reducing the appearance of wrinkles, fine lines, and other signs of aging, as well as for improving skin texture and tone.
Retinyl acetate is considered a milder form of retinoid compared to stronger derivatives like retinol and retinoic acid, which can be more irritating to the skin.

Retinyl acetate (retinol acetate, vitamin A acetate) is a natural[dubious – discuss] form of vitamin A which is the acetate ester of retinol.
Retinyl acetate has potential antineoplastic and chemopreventive activities.
In the United States, retinyl acetate is classified generally recognized as safe (GRAS) in the amounts used to fortify foods with vitamin A.

Retinyl acetate is suitable for use in the retention identification of the analyte when using HPLC and GC.
Not intended for use as an activity reference standard.
Retinyl acetate has been thoroughly evaluated to ensure the utmost quality.

Retinyl acetate, a natural preform of vitamin A, is classified as generally recognized as safe in the amounts used to fortify foods with vitamin A and is especially recommended for maternal supplementation during pregnancy.
Retinyl Acetate promotes collagen synthesis and can reduce the appearance of fine lines and wrinkles.
Additionally, it helps keep pores clear and remove the oil that can lead to blemishes.

Add Retinyl Acetate to your skincare routine with this ingredient.
Use this powder to include everyday skin cream or any oil-based product to help with oil and blemish control.
Retinyl acetate, a variant of vitamin A, holds multifaceted applications in the realms of medicine, science, and industry.

Retinyl acetate is characteristics include being a colorless, slightly viscous liquid with solubility in most organic solvents.
Naturally occurring, retinyl acetate serves as a precursor to the biologically active form of vitamin A known as retinoic acid.
Its primary uses revolve around dietary supplementation and its longstanding presence in the cosmetics industry.

The precise mechanism of action behind retinyl acetate remains incompletely understood.
However, it is believed to scavenge free radicals.
Retinyl acetate is thought to exert influence over gene expression and affect the activity of specific enzymes and proteins.

Retinyl acetate and derivatives of retinol that play an essential role in metabolic functioning of the retina, the growth of and differentiation of epithelial tissue, the growth of bone, reproduction, and the immune response.
Retinyl acetate is derived from a variety of carotenoids found in plants.
Retinyl acetate is enriched in the liver, egg yolks, and the fat component of dairy products.

Retinyl acetate is the acetate ester of retinol and it is commercially used as a vitamin A supplement.
Retinyl acetate exhibits antibiotic, anti-diabetic, anti-inflammatory, and anticancer chemotherapeutic activities.
Retinyl acetate modulates Ca2+ signaling in vitro and is occasionally used to improve embryo production in livestock.

Retinyl acetate displays antibacterial efficacy against Mycobacterium in vitro.
In vivo, retinyl acetate decreases incidence of diabetes and suppresses LPS-stimulated TNF-α expression.
In animal models of colorectal cancer, retinyl acetate upregulates expression of TRAIL receptors, inhibiting tumor growth and increasing survival rates.

Retinyl acetate is effective for the treatment of Vitamin A deficiency.
Retinyl acetate refers to a group of fat-soluble substances that are structurally related to and possess the biological activity of the parent substance of the group called all-trans retinol or retinol.
Retinyl acetate plays vital roles in vision, epithelial differentiation, growth, reproduction, pattern formation during embryogenesis, bone development, hematopoiesis and brain development.

Retinyl acetate is also important for the maintenance of the proper functioning of the immune system.
Retinyl acetate is converted in the retina to the 11-cis-isomer of retinaldehyde or 11-cis-retinal.
Retinyl acetate functions in the retina in the transduction of light into the neural signals necessary for vision.

Retinyl acetate, while attached to opsin in rhodopsin is isomerized to all-trans-retinal by light.
This is the event that triggers the nerve impulse to the brain which allows for the perception of light.
All-trans-retinal is then released from opsin and reduced to all-trans-retinol.

All-trans-retinol is isomerized to 11-cis-retinol in the dark, and then oxidized to Retinyl acetate.
Retinyl acetate recombines with opsin to re-form rhodopsin.
Night blindness or defective vision at low illumination results from a failure to re-synthesize 11-cis retinal rapidly.

Epithelial differentiation: The role of Retinyl acetate in epithelial differentiation, as well as in other physiological processes, involves the binding of Vitamin A to two families of nuclear retinoid receptors (retinoic acid receptors, RARs; and retinoid-X receptors, RXRs).
These receptors function as ligand-activated transcription factors that modulate gene transcription.
When there is not enough Retinyl acetate to bind these receptors, natural cell differentiation and growth are interrupted.

Retinyl acetate plays an important role as an important function material in the body system, such as hematopoietic function, bone development, tumor prevention, and so on.
Therefore, supplement of Retinol is necessary for health requirements.
Acute hypervitaminosis A results in drowsiness, headache, vomiting, papilledema, and a bulging fontanel in infants.
Retinyl acetate plays an important role in main taining healthy skin.

Retinyl acetate deficiency disrupts human keratin cell terminal dif ferentiation and makes the skin rough, dry, scaly, and clogged.
Retinyl acetate is reported that vitamin A can degrade malignant melanoma and T-cell lymphoma epidermal transfer, reduce the oil secretion of the common acne and the number of bacteria in the epidermis and capillaries, and inhibit immune response of monocytes and neutrophils.
Retinyl acetate deficiency can lead to animal death.

Retinyl acetate functions in reproduction and embryonic development.
Retinyl acetate plays an important role in the reproductive process of sperm production and ovula tion, but its biochemical basis is unclear.
Retinyl acetate plays a key role in the develop ment of embryos and organism and maintenance of tissue function. The main organs affected by vitamin A deficiency are the heart, eye tissue, circulatory system, geni tourinary system, and respiratory system. Retinol is necessary for embryonic development.

Retinyl acetate functions on immune function.
Retinyl acetate's advisable to start with a lower concentration product and gradually increase the strength as skin builds tolerance.
This can help minimize initial irritation.

Retinyl acetate's a good idea to consult with a dermatologist.
They can provide personalized recommendations and may even prescribe stronger retinoid formulations if needed.

Retinyl acetate may not be suitable for everyone, especially those with certain skin conditions or sensitivities.
Pregnant or nursing individuals are typically advised to avoid Retinyl acetate products due to potential risks to the developing fetus or infant.

Melting point: 57-58 °C
Boiling point: 406.22°C (rough estimate)
Density: 1.0474 (rough estimate)
refractive index: 1.547-1.555
Flash point: 14℃
storage temp.: 2-8°C
solubility: absolute ethanol: 25 mg/mL
form: solid or viscous liquid
color: Yellow powder
Odor: Amine like
Water Solubility: soluble
Sensitive: Light & Air Sensitive & Hygroscopic
Merck: 14,10013
BRN: 1915439
Stability: Hygroscopic, Light Sensitive
InChIKey: QGNJRVVDBSJHIZ-QHLGVNSISA-N
LogP: 9.4 at 25℃

Retinyl acetates provide pools of vitamin A that are converted into retinol and other retinoids as required.
Retinyl acetate is used in a wide range of biological applications.
Retinyl acetate acts as a chemopreventive agent.

Retinyl acetate also has antineoplastic property.
Retinyl acetate is an essential compound in the cycle of light-activated chemical reactions called the "visual cycle" that underlies vertebrate vision.
Retinol is converted by the protein RPE65 within the pigment epithelium of the retina into 11-cis-retinal.

This molecule is then transported into the retina's photoreceptor cells (the rod or cone cells in mammals) where it binds to an opsin protein and acts as a light-activated molecular switch.
Retinyl acetate absorbs light it isomerizes into all-trans-retinal.
The change in the shape of the molecule in turn changes the configuration of the opsin in a cascade that leads to the neuronal firing, which signals the detection of light.

The opsin then splits into the protein component (such metarhodopsin) and the cofactor Retinyl acetate.
The regeneration of active opsin requires conversion of all-trans-retinal back to Retinyl acetate.
The regeneration of 11-cis-retinal occurs in vertebrates via conversion of Retinyl acetate in a sequence of chemical transformations that occurs primarily in the pigment epithelial cells.

Without adequate amounts of Retinyl acetate, regeneration of rhodopsin is incomplete and night blindness occurs.
Night blindness, the inability to see well in dim light, is associated with a deficiency of Retinyl acetate, a class of compounds that includes retinol and retinal.
In the early stages of Retinyl acetate deficiency, the more light-sensitive and abundant rods, which have rhodopsin, have impaired sensitivity, and the cone cells are less affected.

The cones are less abundant than rods and come in three types, each contains its own type of iodopsin, the opsins of the cones.
The cones mediate color vision, and vision in bright light.
The skin around the eyes is thinner and more delicate, making it more prone to irritation.

Retinyl acetate's usually best to avoid applying retinol directly to the eyelids or too close to the eye area.
Instead, use a specially formulated eye cream if you want to address concerns in that area.
A plant pigment, carotene, is a precursor for Retinyl acetate and is present in highly pigmented vegetables, such as carrots, rutabaga, and red cabbage.

Retinyl acetate can increase the skin's sensitivity to UV radiation, so it is crucial to use sunscreen daily when using products containing retinol.
Sun protection helps prevent sunburn and further sun damage.
Retinyl acetate often takes several weeks to months of consistent use to see noticeable improvements in the skin.

Prescription versions, such as tretinoin, are generally more potent but may also be associated with more side effects.
Retinyl acetate products are milder and are suitable for many people without a prescription.
Retinyl acetate can cause skin irritation, redness, dryness, and peeling, especially when first starting to use it.

One group at great risk are children from low-income families, who are likely to lack fresh vegetables (carotene) and dairy products (vitamin A) in the diet.
Retinyl acetate or other forms of vitamin A are needed for eyesight, maintenance of the skin, and human development.
Other than for vision, the active compound is Retinyl acetate, synthesized from retinal, in turn synthesized from retinol.

Adapalene is another Retinyl acetate that is often available over-the-counter and by prescription.
Retinyl acetate is known for its effectiveness in treating acne and is typically gentler on the skin compared to some other retinoids.
The efficacy of Retinyl acetate can vary from person to person, depending on factors like skin type, the concentration of retinol in the product, and the frequency of use.

Retinyl acetate is essential to follow product instructions and introduce retinol gradually into your skincare routine to minimize these side effects.
Manufacturing process for Retinyl acetate includes these steps as follows: Step A: Synthesis of Preparation of ethyl ether of ethynyl-β-ionol;Step B: Coupling Reaction; Step C:Semi-Hydrogenation of Coupling Product;Step D:Hydrolysis of Semi-Hydrogenated Coupling Product.

As part of the innate immune system, toll-like receptors in skin cells respond to pathogens and cell damage by inducing a pro-inflammatory immune response which includes increased RA production.
The epithelium of the skin encounters bacteria, fungi and viruses.
Keratinocytes of the epidermal layer of the skin produce and secrete antimicrobial peptides (AMPs).

The dissociation of Retinyl acetate and opsin was coupled with the nerve stimulation of the brain’s visual center.
By a series of biochemical processes, nerve impulses format in the rod cells at the end of synapse, and then the optic nerve conducts the nerve impulses along.
The visual process is a component renewable cycle, and Retinyl acetate can be enzymatically modified to 11-cis form in dark conditions.

Retinyl acetate not only significantly affects visual function but also has a greater physiological impact than visual function.
Retinyl acetate deficiency destroys the visual cycle, leads to dark adaptation damage (night blind ness or nyctalopia), and destroys systemic function which is necessary to maintain life (e.g., corneal injury, infection, and hypoplasia).
Separation of Retinyl acetate from the product obtained was achieved by acetylating the total reaction product using pyridine-acetic anhydride at room temperature and chromatographing on alumina neutralized with acetic acid.

The Retinyl acetate fraction was sufficiently pure to become crystallized from pentane at -15°C when seeded with a pure Vitamin A acetate crystal.
When the Retinyl acetate was converted to the alcohol form of Vitamin A, the final product showed the characteristic infrared and ultraviolet absorption curves for Retinol.
Retinyl acetate is taken by mouth or by injection into a muscle.

As an ingredient in skin-care products, Retinyl acetate is used to reduce wrinkles and other effects of skin aging.
Retinyl acetate at normal doses is well tolerated.

However, in plants, the form of Retinyl acetate called carotenoids is contained in the green, orange, and yellow plant tissue.
Retinyl acetate compounds such as vitamin A, reti nal, carotene, and so on from these foods can be converted to vitamin A in the human body.

Uses:
Retinyl acetate is used control diet to study its effect at different developmental periods in fish larvae to study its inhibitory effects on Mycobacterium avium.
This certified solution standard is suitable for use as an internal standard in chromatographic or MS-based methods in clinical testing applications such as assessment of Retinyl acetate deficiency or in food and nutrition testing applications of Retinyl acetate supplements and fortified foods.

Retinyl acetate can be used in combination with other skincare ingredients like hyaluronic acid, vitamin C, and peptides to address multiple skin concerns and provide a comprehensive skincare routine.
Retinyl acetate is used as a dietary supplement to provide the body with vitamin A.
Retinyl acetate is essential for various bodily functions, including maintaining healthy skin and vision, supporting the immune system, and promoting overall health.

In the realm of cosmetics and skin care, retinyl acetate is often included in various products such as creams, serums, and lotions.
Retinyl acetate may help stimulate collagen production, which can improve skin elasticity and reduce the appearance of wrinkles.
Some acne products contain Retinyl acetate derivatives, including retinyl acetate, to help unclog pores, reduce inflammation, and prevent acne breakouts.

Retinyl acetate can contribute to smoother and more even skin texture by promoting cell turnover.
Retinyl acetate may help fade dark spots and pigmentation irregularities.
Retinyl acetate, including that obtained from retinyl acetate, is crucial for maintaining good vision and eye health.

Retinyl acetate plays a role in the functioning of photoreceptor cells in the retina.
Retinyl acetate can be used to treat vitamin A deficiencies when taken under the guidance of a healthcare professional.
Retinyl acetate supports the health of hair and nails, and retinyl acetate may be found in hair and nail care products.

Retinyl acetate is often used in combination with other active ingredients to create a well-rounded skincare routine.
For example, combining Retinyl acetate with antioxidants like vitamin C can provide added protection against environmental damage.
They help prevent clogged pores, reduce inflammation, and encourage the shedding of dead skin cells, which can lead to fewer breakouts and clearer skin.

Retinyl acetate can fade hyperpigmentation, including dark spots, sunspots, and melasma.
Retinyl acetate inhibits the production of melanin and encourages the turnover of pigmented skin cells, resulting in a more even skin tone.
Retinyl acetate can help improve skin texture by reducing roughness and promoting smoother, softer skin.

Retinyl acetate is often used to address issues like uneven skin texture and large pores.
Some people use Retinyl acetate as a preventative measure to maintain healthy and youthful-looking skin and to delay the signs of aging.
Retinyl acetate may help improve the appearance of certain types of scars, such as acne scars, by promoting skin cell turnover and collagen production.

Retinyl acetate can contribute to overall skin health by promoting a more vibrant and youthful appearance.
Retinyl acetate is often incorporated into skincare routines to support healthy and radiant skin.
When compared to retinoic acid, Retinyl acetate has an increased penetration potential and is less irritating, making it an effective ingredient for anti-aging products.

The anti-aging benefits of topically treating skin with Retinyl acetate are based on its penetration ability, which allows it to reach the sites in the skin requiring treatment.
When used on sensitive skin for a prolonged period of time or in concentrations that are too high, retinol can cause dermatitis.
Through dietary modification involving the adjustment of menu choices of affected persons from available food sources to optimize Retinyl acetate content.

Enriching commonly eaten and affordable foods with Retinyl acetate, a process called fortification.
Retinyl acetate involves addition of synthetic vitamin A to staple foods like margarine, bread, flours, cereals, and infant formula during processing.
Retinyl acetate solution may be used as a certified reference material (CRM) for the determination of the analyte in biological samples, dairy foods and pharmaceutical formulations by chromatography techniques.

Retinyl acetate may take several weeks to months before significant improvements are visible, so consistency in use is important.
Some individuals experience a temporary worsening of skin issues, such as increased breakouts or redness, when they first start using Retinyl acetate.
This is often referred to as the "Retinyl acetate purge" and can be a normal part of the adjustment period.

Many users find that incorporating Retinyl acetate into their skincare routine is a long-term commitment for maintaining healthy, youthful-looking skin.
Consistency in use can help sustain results over time.
There are various Retinyl acetate and retinoid products available, ranging from lower to higher concentrations.

Start with a Retinyl acetate that matches your skin type and concerns.
Individuals with sensitive skin may need to be particularly cautious when using Retinyl acetate.
For those with complex skincare concerns or specific goals, working with a dermatologist to create a customized skincare plan can yield the best results.

They can provide insights on Retinyl acetate usage as part of a holistic approach to skincare.
Retinyl acetate can be particularly effective in smoothing rough skin, such as the skin on the elbows, knees, and heels.
Specialized body creams containing retinol can help improve the texture of these areas.

Some individuals use Retinyl acetate products to reduce the appearance of stretch marks.
While it may not completely eliminate them, Retinyl acetate's ability to stimulate collagen production and improve skin texture can contribute to a reduction in the visibility of stretch marks.
Dermatologists often recommend Retinyl acetate or retinoid products as part of post-procedure skincare routines.

Retinyl acetate and its derivatives, including retinyl acetate, act as antioxidants, helping to protect the skin from damage caused by free radicals.
This can help prevent premature aging and maintain healthy skin.
Retinyl acetate is sometimes used in the treatment of skin conditions like psoriasis and eczema.

Retinyl acetate can help to reduce inflammation and support the healing process of damaged skin.
In addition to preventing and treating acne, Retinyl acetate derivatives like retinyl acetate can also assist in minimizing the appearance of acne scars over time by promoting skin renewal and collagen production.
Retinyl acetate is sometimes included in products designed to address the effects of sun damage on the skin, such as sunspots and photodamage.

Retinyl acetate can help improve the overall health and appearance of the skin.
Retinyl acetate is often combined with other skincare ingredients like hyaluronic acid, vitamin C, and peptides to create comprehensive anti-aging and skin-rejuvenating products.
These combinations can enhance the effectiveness of the product.

When using products containing retinyl acetate, it's advisable to start with a lower concentration and gradually increase the dosage to allow the skin to acclimate and minimize potential irritation.
Retinyl acetate's also recommended to use sunscreen during the day when using retinoids, as they can make the skin more sensitive to UV radiation.
Stronger retinoid formulations, such as those containing Retinyl acetate, are typically available by prescription and may be used to address more severe skin issues.

Retinyl acetate, on the other hand, is often found in OTC products and is generally milder.
These products can help promote healing, reduce redness, and maintain the results of procedures like chemical peels or laser treatments.

Retinyl acetate has anti-oxidant capacities and protects dermal fibers by counteracting the increased activity of enzymes that degrade collagen and elastin when the skin is exposed to uV rays.
Retinyl acetate can be drying to the skin when used for a prolonged period of time or in concentrations that are too high.

Safety Profile:
Moderately toxic by ingestion.
Experimental teratogenic and reproductive effects.
Questionable carcinogen with experimental neoplastigenic data.

When heated to decomposition it emits acrid smoke and irritating fumes.
One of the most common side effects of using products containing retinyl acetate is skin irritation.
This can manifest as redness, peeling, dryness, and sensitivity.

To mitigate this, it's advisable to start with a lower concentration of retinyl acetate and gradually increase its use to allow the skin to adapt.
Retinyl acetate and other retinoids can make the skin more sensitive to UV radiation.
Without adequate sun protection, this can lead to an increased risk of sunburn and sun damage.

Retinyl acetate's essential to use sunscreen daily when using retinoids.
Excessive use of retinyl acetate or other vitamin A derivatives can lead to adverse effects, including allergic reactions and severe skin irritation.
World Health Organization recommendation on Maternal Supplementation During Pregnancy states that "health benefits are expected for the mother and her developing fetus with little risk of detriment to either, from a daily supplement not exceeding 10,000 IU Retinyl acetate (3000mcg RE) at any time during pregnancy.

Synonyms:
RETINYL ACETATE
Vitamin A acetate
Retinol acetate
127-47-9
Retinol, acetate
all-trans-Retinyl acetate
Crystalets
Vitamin A1 acetate
all-trans-Retinol acetate
Vitamin A alcohol acetate
Davitan A 650
Vitamin A ester
all-trans-Vitamin A acetate
Retinol, acetate, all-trans-
O~15~-acetylretinol
NSC 122045
trans-Retinyl acetate
(2E,4E,6E,8E)-3,7-dimethyl-9-(2,6,6-trimethylcyclohex-1-en-1-yl)nona-2,4,6,8-tetraen-1-yl acetate
RO 1-5275
Retinol acetate [JAN]
trans-Vitamin A acetate
[(2E,4E,6E,8E)-3,7-dimethyl-9-(2,6,6-trimethylcyclohexen-1-yl)nona-2,4,6,8-tetraenyl] acetate
Myvak (VAN)
Myvax (VAN)
3LE3D9D6OY
all-trans-Retinylacetate
DTXSID6021240
CHEBI:32095
Vitamin A acetate (VAN)
Acetic acid, retinyl ester
9-cis,13-cis-Retinol15-Acetate
NSC-122045
NSC-122760
NCGC00090756-09
Retinol Acetate/All-trans-retinyl Acetate
VitaminAacetate
Vitamin A acetate (tritiated)
DTXCID701240
Vitamin A, acetate
Retinol, acetate, labeled with tritium
O(15)-acetylretinol
9-cis Retinol Acetate
Retinyl acetate, all-trans-
CAS-127-47-9
CCRIS 1907
trans-Retinol Acetate
SR-05000001431
EINECS 204-844-2
UNII-3LE3D9D6OY
BRN 1915439
Retinol acetate;Vitamin A acetate
retinyl-acetate
WLN: L6UTJ A1 B1U1Y1 & U2U1Y1 & U2OV1 C1 C1
Vitamin A acetat
29444-27-7
MFCD00019413
ORISTAR RA
9-cis-Retinol acetate;9-cis-Vitamin A acetate
Spectrum5_001195
Spectrum5_002001
Retinol acetate (JP17)
Retinyl (Retinol) Acetate
EC 204-844-2
retinol, O~15~-acetyl-
BSPBio_002833
SPECTRUM1503051
RETINYL ACETATE [INCI]
C22H32O2 (retinol acetate)
CHEMBL486193
VITAMIN A ACETATE [MI]
CHEBI:94695
HMS501K04
RETINOL ACETATE [WHO-DD]
RETINYL ACETATE [USP-RS]
VITAMIN A ACETATE [VANDF]
HMS1922A19
HMS2089G20
Pharmakon1600-01503051
AMY13865
HY-N0679
Retinyl acetate, analytical standard
Tox21_113549
Tox21_201423
Tox21_302737
BDBM50442911
CCG-39564
LMPR01090012
NSC122045
NSC122760
NSC758220
s4083
AKOS015914999
Tox21_113549_1
CS-8187
NSC-758220
3,7-dimethyl-9-(2,6,6-trimethylcyclohex-1-en-1-yl)nona-2,4,6,8-tetraen-1-yl acetate
IDI1_000522
NCGC00090756-01
NCGC00090756-02
NCGC00090756-03
NCGC00090756-05
NCGC00090756-06
NCGC00090756-07
NCGC00090756-08
NCGC00090756-10
NCGC00090756-11
NCGC00090756-12
NCGC00256509-01
NCGC00258974-01
VITAMIN A (AS ACETATE) [VANDF]
64536-04-5
AC-19999
ALL-(E)-RETINOL ACETATE [WHO-IP]
SBI-0051756.P002
VITAMIN A ACETATE 1.5 M.I.U./G
RO-1-5275
A16783
D01621
H12041
Vitamin A acetate 10 microg/mL in Acetonitrile
AB00052305-02
AB00052305_03
EN300-18533003
EN300-25359996
Vitamin A acetate in gelatin, 500,000 I.U./g
Q7316808
SR-05000001431-1
SR-05000001431-3
W-108382
BRD-K65331431-001-01-3
Vitamin A (acetate), meets USP testing specifications
VITAMIN A (AS ACETATE & BETA CAROTENE) [VANDF]
Retinol acetate, European Pharmacopoeia (EP) Reference Standard
Retinyl acetate, synthetic, crystalline solid or supercooled liquid
Retinyl acetate, United States Pharmacopeia (USP) Reference Standard
Retinyl acetate, solid or viscous liquid, BioReagent, synthetic, suitable for cell culture
Retinyl acetate, synthetic, matrix dispersion, 475,000-650,000 USP units/g
(2E,4E,6E,8E)-3,7-dimethyl-9-(2,6,6-trimethylcyclohex-1-enyl)nona-2,4,6,8-tetraenyl acetate
3,7-Dimethyl-9-(2,6,6,-trimethyl-1-cyclohexen-1-yl)-2,4,6,8-nonatetraen-1-ol acetate, (all trans)-
InChI=1/C22H32O2/c1-17(9-7-10-18(2)14-16-24-20(4)23)12-13-21-19(3)11-8-15-22(21,5)6/h7,9-10,12-14H,8,11,15-16H2,1-6H3/b10-7+,13-12+,17-9+,18-14
Retinyl Acetate (Vitamin A Acetate), Pharmaceutical Secondary Standard; Certified Reference Material
RETINYL LINOLEATE
SYNONYMS Vitamin A palmitate, all−trans−Retinol palmitate;Optovit A;Palmitate de retinyle;palmitato de retinilo;Palmitic acid, ester with retinol CAS NO:79-81-2
RETINYL PALMITATE
RETINYL PALMITATE N° CAS : 79-81-2 Nom INCI : RETINYL PALMITATE Nom chimique : Retinol, hexadecanoate N° EINECS/ELINCS : 201-228-5 Ses fonctions (INCI) Agent d'entretien de la peau : Maintient la peau en bon état
RETINYL PROPIONATE
RETINYL RETINOATE N° CAS : 15498-86-9 Nom INCI : RETINYL RETINOATE Nom chimique : Retinoic acid, retinyl ester Ses fonctions (INCI) Agent d'entretien de la peau : Maintient la peau en bon état
RETINYL RETINOATE
VITAMIN A; VITAMIN A ALCOHOL; VITAMIN A ALCOHOL; RETINOL, N° CAS : 68-26-8 / 11103-57-4 - Rétinol (Vitamine A). Origine(s) : Synthétique. Autres langues : Vitamin A, Vitamin A., Vitamina A, Vitamina a. Nom INCI : RETINOL. Nom chimique : Retinol; vitamin A, N° EINECS/ELINCS : 200-683-7 / 234-328-2. Le rétinol est produit par synthèse, mais il est présent naturellement dans les graisses animales, dans l'huile de foie de poisson et dans les plantes contenant du bêta-carotène. Le rétinol est une forme naturelle de la vitamine A, qui agit en réduisant l'apparence des rides et en renforçant l'épaisseur et l'élasticité de la peau. Il est interdit en bio.Ses fonctions (INCI) : Agent d'entretien de la peau : Maintient la peau en bon état. Noms français : (ALL-E)-3,7-DIMETHYL-9-(2,6,6-TRIMETHYL-1-CYCLOHEXEN-1-YL)-2,4,6,8-NONATETRAEN-1-OL; 2,4,6,8-NONATETRAEN-OL, 3,7-DIMETHYL-9-(2,6,6,TRIMETHYL-1-CYCLOHEXEN-1-YL)-, (ALL-E)-; 3,7-DIMETHYL-9-(2,6,6-TRIMETHYL-1-CYCLOHEXEN-1-YL)-2,4,6,8-NONATETRAEN-1-OL; DIMETHYL-3,7 (TRIMETHYL-2,6,6 CYCLOHEXEN-1 YL-1)-9NONATETRAEN-2,4,6,8 OL-1, (E); RETINOL; VITAMINE A Noms anglais : ALL-TRANS-RETINOL; ALL-TRANS-RETINYL ALCOHOL; ALL-TRANS-VITAMIN A; ALL-TRANS-VITAMIN A ALCOHOL; ALL-TRANS-VITAMIN A1; RETINOL, ALL-TRANS ; TRANS-RETINOL; TRANS-VITAMIN A ALCOHOL; VITAMIN A; VITAMIN A ALCOHOL; VITAMIN A ALCOHOL, ALL-TRANS-; VITAMIN A1; VITAMIN A1 ALCOHOL; VITAMIN A1 ALCOHOL, ALL-TRANS-; VITAMIN A1; ALL-TRANS-. Utilisation et sources d'émission: Vitamine; 200-683-7 [EINECS]; 203-777-6 [EINECS]; 3,7-Dimethyl-9-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2,4,6,8-nonatetraen-1-ol; 3,7-Dimethyl-9-(2,6,6-trimethyl-1-cyclohexenyl)-2,4,6,8-nonatetraen-1-ol; 403040 [Beilstein]; 68-26-8 [RN]; all-trans-3,7-Dimethyl-9-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2,4,6,8-nonatetraen-1-ol all-trans-retinol; Alphalin; Axerophthol; Lard-factor; MFCD00001552 [MDL number]; Retinol ; Retinol [German] ; Rétinol [French] ; trans-retinol; TRANS-VITAMIN A ALCOHOL ; VI-a; Vitamin A [USP] ; Vitamin A (USP); Vitamin A1; Vitamin A1 alcohol, all-trans-; Vitamine A; Vitaminum A; b-Retinol; β-Retinol (2E,4E,6E,8E)-3,7-dimethyl-9-(2,6,6-trimethyl-1-cyclohexenyl)-1-nona-2,4,6,8-tetraenol (2E,4E,6E,8E)-3,7-dimethyl-9-(2,6,6-trimethyl-1-cyclohexenyl)nona-2,4,6,8-tetraen-1-ol (2E,4E,6E,8E)-3,7-dimethyl-9-(2,6,6-trimethylcyclohex-1-en-1-yl)nona-2,4,6,8-tetraen-1-ol (2E,4E,6E,8E)-3,7-dimethyl-9-(2,6,6-trimethylcyclohex-1-enyl)nona-2,4,6,8-tetr aen-1-ol (2E,4E,6E,8E)-3,7-dimethyl-9-(2,6,6-trimethylcyclohex-1-enyl)nona-2,4,6,8-tetraen-1-ol (4E)-3,7-dimethyl-9-(2,6,6-trimethylcyclohex-1-en-1-yl)nona-2,4,6,8-tetraen-1-ol (6E,8E)-3,7-dimethyl-9-(2,6,6-trimethyl-1-cyclohexenyl)nona-2,4,6,8-tetraen-1-ol (all-E)-3,7-Dimethyl-9-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2,4,6,8-nonatetraen-1-ol [RN] 11103-57-4 [RN] 13123-33-6 secondary RN [RN] 17104-91-5 secondary RN [RN] 2,4,6,8-Nonatetraen-1-ol, 3,7-dimethyl-9-(2,6,6-trimethyl-1-cyclohexen-1-yl)-, (all-E)- 3,7-Dimethyl-9-(2,6, 6-trimethyl-1-cyclohexen-1-yl)-2,4,6,8-nonatetraen-1-ol 3,7-Dimethyl-9-(2,6,6-trimethyl-1-cyclchexen-1-yl)-2,4,6,8-nonatetraen-1-ol 3,7-Dimethyl-9-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2,4,6,8-nonate-traen-1-ol 3,7-Dimethyl-9-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2,4,6,8-nonatetraen-1-ol, (all-E)- 3,7-dimethyl-9-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2,4,6,8-nonatetraen-1-ol, (all-E)-Isomer 3,7-Dimethyl-9-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2,4,6,8-nonatetraen-1-ol, all (E)- 3,7-dimethyl-9-(2,6,6-trimethyl-1-cyclohexenyl)nona-2,4,6,8-tetraen-1-ol 3,7-dimethyl-9-(2,6,6-trimethylcyclohex-1-en-1-yl)nona-2,4,6,8-tetraen-1-ol 3,7-Dimethyl-9-(2,6,6-trimethyl-cyclohex-1-enyl)-nona-2,4,6,8-tetraen-1-ol 4-06-00-04133 [Beilstein] 5979-23-7 secondary RN [RN] 9-cis-Retinol ACON AFAXIN Agiolan Agoncal Alcovit A All Trans Retinol All-trans retinol all-trans retinyl alcohol all-trans-retinyl alcohol all-trans-Vitamin A all-trans-vitamin A alcohol all-trans-Vitamin A1 Alphasterol A-Mulsal Anatola Anatola A Anti-infective vitamin Antixerophthalmic vitamin Antixerophthalmisches Vitamin Aoral Apexol Aphalin Apostavit Aquasol A Aquasynth A-Sol ATAV Avibon A-Vi-Pel Avita A-Vitan Avitol Axerol Axerophtholum Bentavit A Biosterol Chocola A Cylasphere DB00162 DEL-VI-A Disatabs Tabs Dofsol Dohyfral A Epiteliol HI-A-Vita Homagenets Aoral Hydrovit A L6UTJ A1 B1U1Y1&U2U1Y1&U2Q C1 C1 [WLN] Lard factor LPK MFCD16037113 [MDL number] Myvpack Nio-A-let Oleovitamin A Ophthalamin PHENOL,2-(AMINOMETHYL)-5-FLUORO-,HYDROCHLORIDE (1:1) Plivit A Prepalin RET Retinal [ACD/Index Name] [ACD/IUPAC Name] [Wiki] Retinol (Vit A) Retinolum [Latin] Retinyl A Retrovitamin A Ro-a-vit Rovimix A 500 RTL Sehkraft A Solu-A Super A Tegosphere VitA Testavol Testavol S Thalasphere tROL Vaflol Vafol Veroftal VI-DOM-A Vio-A Vitamin A 1 Vitamin A alcohol (VAN) Vitavel A Vitavel-A Vitpex Vi-α VI-α Wachstumsvitamin α-Retinol α-sol 维生素A [Chinese]
Rétinol (Vitamine A)
C.I. Basic Violet 10; C.I. 45170; Tetraethylrhodamine,hydrochloride; 9-(2-carboxyphenyl)-3,6-bis(diethylamino) xanthylium chloride; N-[9-(2-carboxyphenyl)-6-(diethylamino)- 3H-xanthen-3- ylidene]- N-ethyl- Ethanaminium chloride; [9-(o-carboxyphenyl)-6-(diethylamino)- 3H-xanthen-3- ylidene]diethyl-Ammonium chloride; C.I. Food Red 15; (9-(o-Carboxyphenyl)-6-(diethyl amino)-3H- xanthen-3-ylidene) diethylammonium chloride CAS NO:81-88-9
REWOCID SB U 185 KE
REWOCID SB U 185 KE (REWOCİD SB U 185 KE) REWOCID SB U 185 KE (REWOCİD SB U 185 KE) is a mild surfactant recommended for application in anti-dandruff shampoos as presents synergism with anti-dandruff agents like zinc pyrithion. Good skin compatibility. REWOCID SB U 185 KE (REWOCİD SB U 185 KE) is used in anti-dandruff shampoos, foam baths, foot shampoos, body shampoos and shower shampoos. REWOCID SB U 185 KE (REWOCİD SB U 185 KE) offers good skin compatibility. Provides substantivity and mildness to hair and skin. Advantages of REWOCID SB U 185 KE (REWOCİD SB U 185 KE): good skin compatibility, Provides substantivity and mildness to hair and skin Other Application sof REWOCID SB U 185 KE (REWOCİD SB U 185 KE): Toiletries (Shower & Bath, Oral care...) > Foot care Toiletries (Shower & Bath, Oral care...) > Shower & bath > Foam bath Hair care (Shampoos, Conditioners & Styling) > Shampoos Skin care (Facial care, Facial cleansing, Body care, Baby care) > Body care Storage of REWOCID SB U 185 KE (REWOCİD SB U 185 KE) Storage at temperatures below 10 °C may lead to cloudiness which does not mean a loss of quality. This product should be homogenized prior to use. Handling of REWOCID SB U 185 KE (REWOCİD SB U 185 KE) Use Level: 4.0-10% Molecular Weight of REWOCID SB U 185 KE (REWOCİD SB U 185 KE): 451.44732856 Formula of REWOCID SB U 185 KE (REWOCİD SB U 185 KE): C17 H27 N Na2 O8 S Functions of REWOCID SB U 185 KE (REWOCİD SB U 185 KE) Cleansing of REWOCID SB U 185 KE (REWOCİD SB U 185 KE): Helps to keep a clean surface Foam boosting of REWOCID SB U 185 KE (REWOCİD SB U 185 KE): Improves the quality of the foam produced by a system by increasing one or more of the following properties: volume, texture and/or stability Hydrotrope of REWOCID SB U 185 KE (REWOCİD SB U 185 KE): Increases the solubility of a substance that is poorly soluble in water. Surfactant of REWOCID SB U 185 KE (REWOCİD SB U 185 KE): Reduces the surface tension of cosmetics and contributes to the even distribution of the product when it is used Disodium undecylenamido MEA-sulfosuccinate REWOCID SB U 185 KE (REWOCİD SB U 185 KE) is a Disodium salt of a substituted ethanolamide half ester of sulfosuccinic acid REWOCID SB U 185 KE (REWOCİD SB U 185 KE) uses and applications include: Surfactant, detergent, foaming agent, antimicrobial for antidandruff shampoos, pharmaceuticals, medicated treatments; fungicide, detergent, foaming agent for personal care products. APPEARANCE of REWOCID SB U 185 KE (REWOCİD SB U 185 KE) Light to yellow liquid with characteristic odor. DESCRIPTION of REWOCID SB U 185 KE (REWOCİD SB U 185 KE) Mild surfactant recommended for application in anti-dandruff shampoos. Good skin compatibility. FUNCTION of REWOCID SB U 185 KE (REWOCİD SB U 185 KE) Used in anti-dandruff shampoos, foam baths, foot shampoos, body shampoos, and shower shampoos. SYNONYMS of REWOCID SB U 185 KE (REWOCİD SB U 185 KE) Disodium Undecylenamido MEA-Sulfosuccinate; Unimate DMS; Rewocid SB U 185; Butanedioicacid, sulfo-, 4-[2-[(1-oxo-10-undecenyl)amino]ethyl] ester, disodium salt(9CI); Succinic acid, sulfo-, 4-ester with N-(2-hydroxyethyl)-10-undecenamide STORAGE of REWOCID SB U 185 KE (REWOCİD SB U 185 KE) Keep in sealed, unopened, original containers at 60ø – 80ø F. Avoid conditions of high humidity and temperature. Properties Appearance of REWOCID SB U 185 KE (REWOCİD SB U 185 KE): (1), solid; (2), liquid. Solubility of REWOCID SB U 185 KE (REWOCİD SB U 185 KE): soluble in water. Stability of REWOCID SB U 185 KE (REWOCİD SB U 185 KE): stable in weak alkali, weak acid, hard water. Under strong acid or strong alkali, easily hydrolyze. Easily oxidized. Risk of REWOCID SB U 185 KE (REWOCİD SB U 185 KE) Solid form: flammable material; irritation, low irritation to skin, eye. Harmful products of combustion are CO, CO2 and so on. Contact with strong oxidants, can cause to burn. Ecology of REWOCID SB U 185 KE (REWOCİD SB U 185 KE): may be hazardous to environment. Water body should be given special attention. Biodegradability of REWOCID SB U 185 KE (REWOCİD SB U 185 KE): biodegradable. Characteristics of REWOCID SB U 185 KE (REWOCİD SB U 185 KE): excellent emulsifying, dispersing, wetting, cleansing, foaming, solubilizing, permeating abilities. Good lime soap dispersing power. Suitable for neutral formula system. Synthesis of REWOCID SB U 185 KE (REWOCİD SB U 185 KE) (1), Esterification reaction Maleic anhydride reacts with undecylenamido-MEA, obtain undecylenamido-MEA maleate. (2), Sulfonation reaction Undecylenamido-MEA maleate reacts with sodium bisulfite, then obtain this product. Test Methods of REWOCID SB U 185 KE (REWOCİD SB U 185 KE) (1), Heavy metals (as Pb) Safety and Technical Standards for Cosmetics (2015 Edition) GB/T 30799 The test method of food detergents - Determination of heavy metals (2), As Safety and Technical Standards for Cosmetics (2015 Edition) GB/T 30797 The test method of food detergents - Determination of total arsenic Product standards of REWOCID SB U 185 KE (REWOCİD SB U 185 KE) QB/T 4085 Disodium sulfosuccinate Further explanation (a), On physical and chemical indexes: firstly, shall be indicated carbon atom distribution; secondly, shall be indicated average molecular weight. (b), Used in cosmetics, should be test for harmful substances; or furtherly test for microorganisms. Major Uses of REWOCID SB U 185 KE (REWOCİD SB U 185 KE) 1, Typical Applications Use as wetting agent, permeating agent. Use as emulsifying agent, dispersing agent. Use as hydrotrope. 2, Textile, leather Use as wetting agent, permeating agent. 3, Household detergents Use as wetting agent, emulsifying agent. 4, Industrial cleaning agents Use as wetting agent, emulsifying agent, hydrotrope. 5, Personal care products Use as cleansing agent, hydrotrope, foam stabilizing agent. disodium undecylenamido MEA-sulfosuccinate = anti bacterial balancing for mucosal (cleaning, foam-enhancing, hydrotropic, surfactant) REWOCID SB U 185 KE (REWOCİD SB U 185 KE) is an amphoteric surfactant for use in biocidal products for terminal disinfectants, sanitizers and detergent sanitizers for all hard surfaces in household and industry. REWOCID SB U 185 KE (REWOCİD SB U 185 KE) can be used in aqueous and alcoholic formulations, and REWOCID SB U 185 KE (REWOCİD SB U 185 KE) is a special amphoteric compound in aqueous solution. When formulated in biocide products, REWOCID SB U 185 KE (REWOCİD SB U 185 KE) provides full spectrum of efficacy, safe handling, good biodegradability, and good compatibility with hard water and other surfactants. REWOCID SB U 185 KE (REWOCİD SB U 185 KE) is also a good cleaner, and REWOCID SB U 185 KE (REWOCİD SB U 185 KE) dissolves fat, possesses good soil carrying capacity and is well-tolerated by common materials. REWOCID SB U 185 KE (REWOCİD SB U 185 KE) contains no aldehydes, active chlorine or alkali. Properties Properties REWOCID SB U 185 KE (REWOCİD SB U 185 KE) is a quaternary surfactant, which is soluble in water and water/alcohol mixtures. It is easily combined with amphoteric and non-ionic surfactants and with anionic surfactants at low levels. Application Application REWOCID SB U 185 KE (REWOCİD SB U 185 KE) has good mucous membrane compatibility in 1 % solutions. REWOCID SB U 185 KE (REWOCİD SB U 185 KE) is used in the following applications of REWOCID SB U 185 KE (REWOCİD SB U 185 KE): • Conditioning shampoos • Liquid soaps • Hair rinses • Skin creams and lotions Suggested usage concentration Suggested usage concentration of REWOCID SB U 185 KE (REWOCİD SB U 185 KE) 1 - 3 % REWOCID SB U 185 KE (REWOCİD SB U 185 KE) Storage of REWOCID SB U 185 KE (REWOCİD SB U 185 KE) A longer storage time, esp. at low temperatures, may lead to small changes of the appearance. This does not mean a loss of quality. In this case it is recommended to homogenize the product prior to usage under moderate agitation at 25-30°C. In general we recommend to use the complete container. Packaging Packaging 800 kg pallet (4 x 200 kg) Hazardous goods classification Hazardous goods classification Information concerning REWOCID SB U 185 KE (REWOCİD SB U 185 KE) • classification and labelling according to regulations for transport and for dangerous substances • protective measures for storage and handling • measures in accidents and fires • toxicity and ecological effects is given in our material safety data sheets. Description of REWOCID SB U 185 KE (REWOCİD SB U 185 KE) REWOCID SB U 185 KE (REWOCİD SB U 185 KE) is a quaternary surfactant recommended for use in anti-dandruff shampoos and as a conditioning agent in hair care and in special skin cleansing formulations. REWOCID UTM 185 is a quaternary surfactant, which is soluble in water and water/alcohol mixtures. It is easily combined with amphoteric and non-ionic surfactants and with anionic surfactants at low levels. Disodium undecylenamido MEA-sulfosuccinate REWOCID SB U 185 KE (REWOCİD SB U 185 KE) (CAS 26650-05-5) Market Research Report 2020 presents comprehensive data on Disodium undecylenamido MEA-sulfosuccinate markets globally and regionally (Europe, Asia, North America etc.) The report includes Disodium undecylenamido MEA-sulfosuccinate REWOCID SB U 185 KE (REWOCİD SB U 185 KE) description, covers its application areas and related patterns. It overviews Disodium undecylenamido MEA-sulfosuccinate REWOCID SB U 185 KE (REWOCİD SB U 185 KE) market, names Disodium undecylenamido MEA-sulfosuccinate REWOCID SB U 185 KE (REWOCİD SB U 185 KE) producers and indicates its suppliers. In addition to the above the report determines Disodium undecylenamido MEA-sulfosuccinate REWOCID SB U 185 KE (REWOCİD SB U 185 KE) consumers in the market. We can analyze the following elements for each chemical product in any country or region: Disodium undecylenamido MEA-sulfosuccinate REWOCID SB U 185 KE (REWOCİD SB U 185 KE) (CAS 26650-05-5) Market Research Report 2020 can feature: market condition and estimations, market forecast, chemical product ranges, trademarks, analogous products, application areas, regional and global producers, consumers and traders (including contact details). REWOCID SB U 185 KE (REWOCİD SB U 185 KE) is an amphoteric surfactant for use in biocidal products for terminal disinfectants, sanitizers and detergent sanitizers for all hard surfaces in household and industry. It can be used in aqueous and alcoholic formulations, and it is a special amphoteric compound in aqueous solution. When formulated in biocide products, it provides full spectrum of efficacy, safe handling, good biodegradability, and good compatibility with hard water and other surfactants. REWOCID SB U 185 KE (REWOCİD SB U 185 KE) is also a good cleaner, and it dissolves fat, possesses good soil carrying capacity and is well-tolerated by common materials. REWOCID SB U 185 KE (REWOCİD SB U 185 KE) contains no aldehydes, active chlorine or alkali.