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93778-15-5

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93778-15-5 Usage

Abbreviation

DHHPH

Primary Use

Preservative and antioxidant in food and cosmetic products

Derivative

Derived from hydroxybenzoate

Antioxidant Properties

Derived from its hydroxybenzoate structure

Microbial Growth Inhibition

Capable of inhibiting the growth of bacteria and fungi

Shelf Life Extension

Extends the shelf life of various products

Applications

Personal care products: lotions, shampoos, skincare formulations
Food products: dressings, sauces, processed meats

Safety

Deemed safe for use by regulatory bodies such as the FDA

Check Digit Verification of cas no

The CAS Registry Mumber 93778-15-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,7,7 and 8 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 93778-15:
(7*9)+(6*3)+(5*7)+(4*7)+(3*8)+(2*1)+(1*5)=175
175 % 10 = 5
So 93778-15-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H12O5/c11-5-9(13)6-15-10(14)7-1-3-8(12)4-2-7/h1-4,9,11-13H,5-6H2

93778-15-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-dihydroxypropyl 4-hydroxybenzoate

1.2 Other means of identification

Product number -
Other names EINECS 298-149-1

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
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:93778-15-5 SDS

93778-15-5Relevant articles and documents

Synthesis of α-monoglycerides of aromatic acids

Artamonov,Nigmatullina,Aldabergenova,Dzhiembaev

, p. 404 - 408 (2007/10/03)

The synthesis of α-monoglycerides of aromatic acids has been performed by the transesterification of the methyl esters of the corresponding acids with glycerol. The structures of the compounds obtained have been confirmed by their IR, UV, and 1H and 13C NMR spectra.

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