Propyl-3,4,5-trihydroxybenzoat

Bezeichnung:Propyl-3,4,5-trihydroxybenzoat

CAS-Nr121-79-9

Englisch Name:Propyl gallate

CBNumberCB1465703

SummenformelC10H12O5

Molgewicht212.2

MOL-Datei121-79-9.mol

Synonyma

Propyl-3,4,5-trihydroxybenzoat

Propyl-3,4,5-trihydroxybenzoat physikalisch-chemischer Eigenschaften

Schmelzpunkt	146-149 °C(lit.)
Siedepunkt	312.03°C (rough estimate)
Dichte	1.210
Dampfdruck	0Pa at 20℃
Brechungsindex	1.5140 (estimate)
FEMA	2947 \| PROPYL GALLATE
Flammpunkt	187℃
storage temp.	Store below +30°C.
Löslichkeit	ethanol: 50 mg/mL
Aggregatzustand	powder
pka	8.11(at 25℃)
Farbe	White to light beige
Geruch (Odor)	bland
Wasserlöslichkeit	0.35 g/100 mL (25 ºC)
Merck	14,7859
BRN	1877976
InChIKey	ZTHYODDOHIVTJV-UHFFFAOYSA-N
LogP	1.8
CAS Datenbank	121-79-9(CAS DataBase Reference)
NIST chemische Informationen	Benzoic acid, 3,4,5-trihydroxy-, propyl ester(121-79-9)
EPA chemische Informationen	Propyl gallate (121-79-9)

Sicherheit

Kennzeichnung gefährlicher	Xn
R-Sätze:	22-43-36/37/38
S-Sätze:	24-37-36-26
WGK Germany	2
RTECS-Nr.	LW8400000
TSCA	Yes
HS Code	29182950
Giftige Stoffe Daten	121-79-9(Hazardous Substances Data)
Toxizität	LD50 in mice, rats, hamsters, rabbits (g/kg): 1.70-3.50, 2.1-7, 2.48, 2.75 orally; LD50 i.p. in rats: 0.38 g/kg (J. Am. Coll. Toxicol.)

Gefahreninformationscode (GHS)

Propyl gallate Chemische Eigenschaften,Einsatz,Produktion Methoden

R-Sätze Betriebsanweisung:
R22:Gesundheitsschädlich beim Verschlucken.
R43:Sensibilisierung durch Hautkontakt möglich.
R36/37/38:Reizt die Augen, die Atmungsorgane und die Haut.
S-Sätze Betriebsanweisung:
S24:Berührung mit der Haut vermeiden.
S37:Geeignete Schutzhandschuhe tragen.
S36:DE: Bei der Arbeit geeignete Schutzkleidung tragen.
S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren.
Beschreibung
Propyl gallate is an antioxidant with antimicrobial activity. It is hepatoprotective in vitro and in vivo, preventing CCl₄ induced lipoperoxidation and reduction in polysomes in rat liver. Propyl gallate (100 mg/kg, i.p.) increases expression of HIF-1α, EPO, and VEGF mRNA levels and the number of normal neurons in rat brains after 8 minutes of forebrain ischemia. Propyl gallate in combination with potassium sorbate is bactericidal and bacteriostatic against S. aureus strains known to produce enterotoxins in food. Propyl gallate is commonly added to foods to prevent autoxidation and microbial growth.
Beschreibung
It caused contact dermatitis in a baker and in a female confectioner who fried doughnuts, primarily sensitized by her night cream; the margarine probably contained gallates.
Chemische Eigenschaften
Propyl gallate is an odorless powder having a slightly bitter taste. It functions particularly well in stabilizing animal fats and vegetable oils. With a melting point of 148°C, propyl gallate loses its effectiveness during heat processing and is therefore not suitable in frying applications that involve temperatures exceeding 190°C. Propyl gallate chelates iron ions and forms an unappealing, blue–black complex. Hence, it is always used with chelators such as citric acid to eliminate the pro-oxidative iron and copper catalysts. Good synergism is obtained with BHA and BHT; however, application with TBHQ is not permitted. For additional details, refer to Burdock (1997).
Chemische Eigenschaften
white to light beige crystalline powder
Verwenden
Propyl Gallate is an antioxidant that is the n-propylester of 3,4,5-tri- hydroxybenzoic acid. natural occurrence of propyl gallate has not been reported. it is commercially prepared by esterification of gallic acid with propyl alcohol followed by distillation to remove excess alcohol.
Verwenden
Propyl Gallate is a known inhibitor of Tyrosinase, a polyphenol oxidase, which is an important enzyme in pigment biosynthesis in various organisms. It has also recently been seen to boost biodiesel li pid biosynthesis in cultures.
Verwenden
Antioxidant for cosmetics, foods, fats, oils, ethers, emulsions, waxes, transformer oils.
Definition
ChEBI: N-propyl gallate is a trihydroxybenzoic acid.
Vorbereitung Methode
The preparation process of propyl gallate incldues the following steps: under the action of toluene-p-sulfonic acid as catalyst making gallic acid and n-propyl alcohol produce reaction at high temp., reflux and dehydration for 4-7 hr., distilling to recover excess solvent, dissolving residue by adding water, cooling, centrifuging (or filtering) to obtain crude product, decolouring and drying to obtain finished product. Its product propyl gallate yield rate can be up to 98%, and its cost is low.
synthetische
Produced commercially by the esterification of gallic acid with propyl alcohol followed by distillation to remove the excess alcohol.
Allgemeine Beschreibung
Fine white to creamy-white crystalline powder. Odorless or with a faint odor. Melting point 150°C. Insoluble in water. Slightly bitter taste.
Air & Water Reaktionen
Insoluble in water.
Reaktivität anzeigen
Propyl gallate can react with oxidizing agents. Incompatible with strong acids, strong bases and strong reducing agents. Darkens in the presence of iron and iron salts. Contact with metals should be avoided .
Hazard
Use in foods restricted to 0.02% of fat con- tent.
Brandgefahr
Propyl gallate is combustible.
Flammability and Explosibility
Not classified
Biochem/physiol Actions
An antioxidant that exhibits antimicrobial activity. Propyl gallate has been reported to be an effective antioxidant-based hepatoprotector, both in vitro and in vivo. It has also been shown to prevent neuronal apoptosis and block the death of neurons exposed to FeSO4/GA as well as partially protect endothelial cells against TNF-induced apoptosis.
Kontakt-Allergie
This gallate ester (E 311) is an antioxidant frequently used in the food, cosmetic, and pharmaceutical industries to prevent the oxidation of unsaturated fatty acids into rancid-smelling compounds. It causes cosmetic dermatitis mainly from lipsticks and induced contact dermatitis in a baker, and in a female confectioner, primarily sensitized by her night cream, who fried doughnuts the margarine probably containing gallates.
Toxikologie
Propyl gallate (n-propyl-3,4,5-trihydroxybenzoate) is used in vegetable oils and butter. When 1.2 or 2.3% propyl gallate was added to feed for rats, loss of weight was observed. This may be due to the rats reluctance to eat food that was contaminated with the bitter taste of propyl gallate. When it was given for 10 to 16 months at the 2 to 3% level, 40% of the rats died within the first month and the remainder showed severe growth inhibition. Autopsies of rats indicated kidney damage resulting from the ingestion of propyl gallate. However, no other animal studies show serious problems and further studies indicated that propyl gallate does not cause serious chronic toxicities.
Sicherheitsprofil
Poison by ingestion and intraperitoneal routes. Experimental teratogenic and reproductive effects. Questionable carcinogen with experimental tumorigenic data. Mutation data reported. Combustible when exposed to heat or flame; can react with oxidizing materials. When heated to decomposition it emits acrid smoke and irritating fumes.
Sicherheit(Safety)
Propyl Gallate currently is used as an antioxidant in a reported 167 cosmetic products at maximum concentrations of 0.1%. Propyl Gallate is a generally recognized as safe (GRAS) antioxidant to protect fats, oils, and fat-containing food from rancidity that results from the formation of peroxides.
läuterung methode
Crystallise the ester from aqueous EtOH or *C6H6 (m 146-146.5o). [Beilstein 10 III 2078, 10 IV 2003.]

Propyl gallate Upstream-Materialien And Downstream Produkte

Propyl-3,4,5-trihydroxybenzoat Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

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