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n-Propyl Gallate

CAS 56274-95-4C10H12O5MW 212.20

n-Propyl Gallate (CAS 56274-95-4) — formula C10H12O5, molecular weight 212.20; category organic chemicals.

Product Overview

CAS Number56274-95-4
Molecular FormulaC10H12O5
Molecular Weight212.20
Melting Point302 °F (NTP, 1992)
LogPlog Kow = 1.80
ApplicationsUses: CIR ingredient: Propyl Gallate, Used as antioxidant to prevent rancidity in fats, oils, and other food products, Also used as a laboratory reagent and stabilizer for synthetic vitamin A, [HSDB] Used as an antioxidant for cosmetics, ethers, emulsions, waxes, and transformer oils, [Merck Index] Contact dermatitis documented in a baker and confectioner, [Kanerva, p. 1830], Reported uses (ppm):, Table: Reported uses (ppm): (Flavor and Extract Manufacturers' Association, 1994) [Table#1691], It is used as an antioxidant for foods and cosmetics, especially fats, and waxes. It is also used in transformer oils and as a stabilizer for synthetic vitamin A., Reactive peroxides in povidone often lead to degradation of oxidation-labile drugs. ... The antioxidants ascorbic acid, propyl gallate, and sodium sulfite reduced the peroxide concentration in povidone ... ., Synthetic antioxidants commonly used in food include butylated hydroxyanisole (BHA), butylated hydroxytoluene (BHT), propyl gallate (PG), and tert-butylhydroquinone (TBHQ)., MEDICATION, Use Classification: Food additives, Fragrance Ingredients, Food Additives -> ANTIOXIDANT -> JECFA Functional Classes, Cosmetics -> Antioxidant, Household Products: Information on 8 consumer products that contain Propyl gallate in the following categories is provided:, • Personal Care, Methods of Manufacturing: Propyl gallate is manufactured via a reaction of n-propanol with 3, 4, 5-trihydroxybenzoic acid., Produced commercially by the esterification of gallic acid with propyl alcohol followed by distillation to remove the excess alcohol., REACTION OF N-PROPYL ALCOHOL WITH 3, 5-TRIHYDROXYBENZOIC ACID, Formulations, Preparations: Trade Names: NIPA 49, Nipagallin P, Progallin P, and Tenox PG., The antioxidant formulations most commonly used in edible products contain various combinations of BHA, BHT, and, or propyl gallate together with citric acid in a suitable solvent., U.S. Production: (1975) PROBABLY GREATER THAN 9.08X10+5 GRAMS, Non-confidential 2012 Chemical Data Reporting (CDR) information on the production and use of chemicals manufactured or imported into the United States. Chemical: Benzoic acid, 3, 5-trihydroxy-, propyl ester. National Production Volume: 232, 076 lb, yr., General Manufacturing Information: Benzoic acid, propyl ester: ACTIVE, The Panel on Food Additives and Nutrient Sources added to Food (ANS), European Food Safety Authority (EFSA), concluded in a 2014 report, that the use of propyl gallate as food additive at the current uses and use levels is not of safety concern., Propyl gallate is used as an antioxidant in pesticide formulations at typical concentrations of 0.25% or less., Used in foods restricted to 0.02% of fat content., or propyl gallate together with citric acid in suitable solvent., Tocopherols, gum guaiac, and similar natural antioxidants usually lack potency in most products compared to combinations of BHA, butylated hydroxyanisole, butylated hydroxytoluene, and propyl gallate.
CategoryOrganic Chemicals

Applications

Documented applications: Uses: CIR ingredient: Propyl Gallate, Used as antioxidant to prevent rancidity in fats, oils, and other food products, Also used as a laboratory reagent and stabilizer for synthetic vitamin A, [HSDB] Used as an antioxidant for cosmetics, ethers, emulsions, waxes, and transformer oils, [Merck Index] Contact dermatitis documented in a baker and confectioner, [Kanerva, p. 1830], Reported uses (ppm):, Table: Reported uses (ppm): (Flavor and Extract Manufacturers' Association, 1994) [Table#1691], It is used as an antioxidant for foods and cosmetics, especially fats, and waxes. It is also used in transformer oils and as a stabilizer for synthetic vitamin A., Reactive peroxides in povidone often lead to degradation of oxidation-labile drugs. ... The antioxidants ascorbic acid, propyl gallate, and sodium sulfite reduced the peroxide concentration in povidone ... ., Synthetic antioxidants commonly used in food include butylated hydroxyanisole (BHA), butylated hydroxytoluene (BHT), propyl gallate (PG), and tert-butylhydroquinone (TBHQ)., MEDICATION, Use Classification: Food additives, Fragrance Ingredients, Food Additives -> ANTIOXIDANT -> JECFA Functional Classes, Cosmetics -> Antioxidant, Household Products: Information on 8 consumer products that contain Propyl gallate in the following categories is provided:, • Personal Care, Methods of Manufacturing: Propyl gallate is manufactured via a reaction of n-propanol with 3, 4, 5-trihydroxybenzoic acid., Produced commercially by the esterification of gallic acid with propyl alcohol followed by distillation to remove the excess alcohol., REACTION OF N-PROPYL ALCOHOL WITH 3, 5-TRIHYDROXYBENZOIC ACID, Formulations, Preparations: Trade Names: NIPA 49, Nipagallin P, Progallin P, and Tenox PG., The antioxidant formulations most commonly used in edible products contain various combinations of BHA, BHT, and, or propyl gallate together with citric acid in a suitable solvent., U.S. Production: (1975) PROBABLY GREATER THAN 9.08X10+5 GRAMS, Non-confidential 2012 Chemical Data Reporting (CDR) information on the production and use of chemicals manufactured or imported into the United States. Chemical: Benzoic acid, 3, 5-trihydroxy-, propyl ester. National Production Volume: 232, 076 lb, yr., General Manufacturing Information: Benzoic acid, propyl ester: ACTIVE, The Panel on Food Additives and Nutrient Sources added to Food (ANS), European Food Safety Authority (EFSA), concluded in a 2014 report, that the use of propyl gallate as food additive at the current uses and use levels is not of safety concern., Propyl gallate is used as an antioxidant in pesticide formulations at typical concentrations of 0.25% or less., Used in foods restricted to 0.02% of fat content., or propyl gallate together with citric acid in suitable solvent., Tocopherols, gum guaiac, and similar natural antioxidants usually lack potency in most products compared to combinations of BHA, butylated hydroxyanisole, butylated hydroxytoluene, and propyl gallate..

Technical Profile

What this product is

n-Propyl Gallate is a carbon-based organic compound with CAS registry number 56274-95-4 and molecular formula C10H12O5 (molecular weight 212.20), belonging to the organic chemicals segment of chemical raw materials.

Identification

CAS number: 56274-95-4

Its molecular formula C10H12O5 comprises 10 C, 12 H, 5 O atoms.

Also known as: n-Propyl Gallate · 没食子酸正丙酯

Category: organic chemicals

Frequently Asked Questions

What is the CAS number of n-Propyl Gallate?

The CAS registry number of n-Propyl Gallate is 56274-95-4.

What is the molecular formula and molecular weight of n-Propyl Gallate?

Molecular formula C10H12O5, molecular weight 212.20.

What other names is n-Propyl Gallate known by?

It is also registered under: n-Propyl Gallate, 没食子酸正丙酯.

What are the documented applications of n-Propyl Gallate?

Recorded applications: Uses: CIR ingredient: Propyl Gallate, Used as antioxidant to prevent rancidity in fats, oils, and other food products, Also used as a laboratory reagent and stabilizer for synthetic vitamin A, [HSDB] Used as an antioxidant for cosmetics, ethers, emulsions, waxes, and transformer oils, [Merck Index] Contact dermatitis documented in a baker and confectioner, [Kanerva, p. 1830], Reported uses (ppm):, Table: Reported uses (ppm): (Flavor and Extract Manufacturers' Association, 1994) [Table#1691], It is used as an antioxidant for foods and cosmetics, especially fats, and waxes. It is also used in transformer oils and as a stabilizer for synthetic vitamin A., Reactive peroxides in povidone often lead to degradation of oxidation-labile drugs. ... The antioxidants ascorbic acid, propyl gallate, and sodium sulfite reduced the peroxide concentration in povidone ... ., Synthetic antioxidants commonly used in food include butylated hydroxyanisole (BHA), butylated hydroxytoluene (BHT), propyl gallate (PG), and tert-butylhydroquinone (TBHQ)., MEDICATION, Use Classification: Food additives, Fragrance Ingredients, Food Additives -> ANTIOXIDANT -> JECFA Functional Classes, Cosmetics -> Antioxidant, Household Products: Information on 8 consumer products that contain Propyl gallate in the following categories is provided:, • Personal Care, Methods of Manufacturing: Propyl gallate is manufactured via a reaction of n-propanol with 3, 4, 5-trihydroxybenzoic acid., Produced commercially by the esterification of gallic acid with propyl alcohol followed by distillation to remove the excess alcohol., REACTION OF N-PROPYL ALCOHOL WITH 3, 5-TRIHYDROXYBENZOIC ACID, Formulations, Preparations: Trade Names: NIPA 49, Nipagallin P, Progallin P, and Tenox PG., The antioxidant formulations most commonly used in edible products contain various combinations of BHA, BHT, and, or propyl gallate together with citric acid in a suitable solvent., U.S. Production: (1975) PROBABLY GREATER THAN 9.08X10+5 GRAMS, Non-confidential 2012 Chemical Data Reporting (CDR) information on the production and use of chemicals manufactured or imported into the United States. Chemical: Benzoic acid, 3, 5-trihydroxy-, propyl ester. National Production Volume: 232, 076 lb, yr., General Manufacturing Information: Benzoic acid, propyl ester: ACTIVE, The Panel on Food Additives and Nutrient Sources added to Food (ANS), European Food Safety Authority (EFSA), concluded in a 2014 report, that the use of propyl gallate as food additive at the current uses and use levels is not of safety concern., Propyl gallate is used as an antioxidant in pesticide formulations at typical concentrations of 0.25% or less., Used in foods restricted to 0.02% of fat content., or propyl gallate together with citric acid in suitable solvent., Tocopherols, gum guaiac, and similar natural antioxidants usually lack potency in most products compared to combinations of BHA, butylated hydroxyanisole, butylated hydroxytoluene, and propyl gallate..

Which category does n-Propyl Gallate belong to?

Category: Organic Chemicals.

PubChem Public Data

Independent reference data for n-Propyl Gallate (CAS 56274-95-4), compiled from public chemistry databases.

Registry identifiers across databases

CAS Registry Number56274-95-4
PubChem CID4947
Molecular formulaC10H12O5
IUPAC namepropyl 3,4,5-trihydroxybenzoate
UNII (FDA)8D4SNN7V92
FEMA number2947

Computed descriptors

Molecular Weight212.20
XLogP31.8
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count5
Rotatable Bond Count4
Exact Mass212.06847348
Monoisotopic Mass212.06847348
Topological Polar Surface Area87
Heavy Atom Count15

Physicochemical values on record

Melting Point302 °F (NTP, 1992)
Melting Point147-149 °C
Melting Point150 °C
Flash Point368 °F (NTP, 1992)
Flash Point187 °C (369 °F) - closed cup
Solubility3.5 mg/mL at 25 °C
Density1.21
LogPlog Kow = 1.80
LogP1.80
LogP1.8

Documented uses on record

    Used as antioxidant to prevent rancidity in fats, oils, and other food products; Also used as a laboratory reagent and stabilizer for synthetic vitamin A; [HSDB] Used as an antioxidant for cosmetics, ethers, emulsions, waxes, and transformer oils; [Merck Index] Contact dermatitis documented in a baker and confectioner; [Kanerva, p. 1830]Table: Reported uses (ppm): (Flavor and Extract Manufacturers' Association, 1994) [Table#1691]

    Synonyms and trade names

    propyl gallate; 121-79-9; Propyl 3,4,5-trihydroxybenzoate; N-Propyl gallate; Progallin P; Gallic acid, propyl ester; Tenox PG; Nipagallin P; Gallic acid propyl ester; NIPA 49; Propylester kyseliny gallove; Benzoic acid, 3,4,5-trihydroxy-, propyl ester; FEMA No. 2947; n-Propyl 3,4,5-trihydroxybenzoate; 3,4,5-Trihydroxybenzene-1-propylcarboxylate; Gallate, Propyl

    Regulatory listings held on file

    Regulatory & Food ContactFDA Substance added to food: ANTIOXIDANT, FLAVORING AGENT OR ADJUVANT
    FDA Inventory of Food Contact Substances Listed in 21 CFR: FCS
    ANTIOXIDANT: Food Additives
    JECFA ADI: 0-1.4 mg/kg bw (1993)
    The 1993 ADI was maintained at the forty-sixth meeting (1996)
    TRS 868-JECFA 46/15

    GHS hazard classification

    Reported hazard statementsH302, H317, H400, H410, H318, H411, H334

    H302: Harmful if swallowed [Warning Acute toxicity, oral]

    H317: May cause an allergic skin reaction [Warning Sensitization, Skin]

    What the public record says

    n-Propyl Gallate · CAS 56274-95-4 · C10H12O5. UNII 8D4SNN7V92. Melting Point: 302 °F (NTP, 1992); Melting Point: 147-149 °C; Melting Point: 150 °C.

    Physical description and handling notes

    Source: PubChem / Wikidata; the batch COA governs where values differ.

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