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2486-02-4

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2486-02-4 Usage

Description

GALLIC ACID ISOAMYL ESTER is a derivative of gallic acid, which is a naturally occurring phenolic acid found in various plants. It is known for its antioxidant, antimicrobial, and anti-inflammatory properties.

Uses

Used in Conductive Material Production:
GALLIC ACID ISOAMYL ESTER is used as a precursor in the method for producing conductive materials. It is applied for exposing a silver halide emulsion layer to gallic acid and/or its derivative, which aids in the formation of conductive materials.
Used in Pharmaceutical Industry:
GALLIC ACID ISOAMYL ESTER is used as a pharmaceutical candidate for various applications due to its antioxidant, antimicrobial, and anti-inflammatory properties. It can be employed in the development of new drugs or as an additive to enhance the efficacy of existing medications.
Used in Cosmetics Industry:
GALLIC ACID ISOAMYL ESTER can be used as an ingredient in the cosmetics industry, where its antioxidant and anti-inflammatory properties can contribute to the development of skincare products, promoting skin health and protection against environmental stressors.
Used in Food Industry:
GALLIC ACID ISOAMYL ESTER may also find applications in the food industry as a natural preservative due to its antimicrobial properties. It can help extend the shelf life of perishable products and maintain their quality.
Used in Agricultural Industry:
In the agricultural industry, GALLIC ACID ISOAMYL ESTER can be utilized as a natural pesticide or fungicide, providing protection for crops against various pests and diseases while reducing the reliance on synthetic chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 2486-02-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,8 and 6 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2486-02:
(6*2)+(5*4)+(4*8)+(3*6)+(2*0)+(1*2)=84
84 % 10 = 4
So 2486-02-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H16O5/c1-7(2)3-4-17-12(16)8-5-9(13)11(15)10(14)6-8/h5-7,13-15H,3-4H2,1-2H3

2486-02-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methylbutyl 3,4,5-trihydroxybenzoate

1.2 Other means of identification

Product number -
Other names Gallussaeureisoamylester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food Additives: ANTIOXIDANT
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2486-02-4 SDS

2486-02-4Relevant articles and documents

Design, Synthesis, and Antifungal Activity of Alkyl Gallates Against Plant Pathogenic Fungi In Vitro and In Vivo

Zhao, Xiao-Long,Li, Chun-Qing,Song, Xiao-Mei,Yan, Shuang-Mei,Luo, Du-Qiang

, p. 38 - 43 (2021/02/01)

A series of alkyl gallates was synthesized by reacting gallic acid with the corresponding alcohols. Their structures were determined on the basis of spectroscopic data, including NMR and MS. The antifungal activities of these compounds against plant pathogenic fungi in vitro and in vivo were assessed.

Microwave-assisted esterification of gallic acid

Shi, Zhi-Hao,Li, Nian-Guang,Tang, Yu-Ping,Shi, Qian-Ping,Zhang, Wei,Zhang, Peng-Xuan,Li, Wei,Dong, Ze-Xi,Duan, Jin-Ao

, p. 1351 - 1354 (2016/06/13)

An efficient synthesis of alkyl gallates under microwave irradiation was described. The reaction took place in 6-10 mins, which was much shorter than the traditional synthetic methods, with almost quantitative yields.

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