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538-42-1

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538-42-1 Usage

Description

Sodium cinnamate is a chemical compound derived from cinnamic acid, characterized by its white, crystalline powder form and solubility in water. It possesses a slightly sweet, cinnamon-like odor and taste, making it a versatile ingredient in various applications.

Uses

Used in Food Industry:
Sodium cinnamate is used as a food preservative and flavoring agent for its antimicrobial properties, which help inhibit the growth of bacteria and fungi, thereby extending the shelf life of baked goods, beverages, and condiments.
Used in Cosmetics and Personal Care Industry:
Sodium cinnamate is used as a fragrance ingredient in the production of cosmetics and personal care products, enhancing their sensory qualities and providing a pleasant, cinnamon-like scent.

Check Digit Verification of cas no

The CAS Registry Mumber 538-42-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,3 and 8 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 538-42:
(5*5)+(4*3)+(3*8)+(2*4)+(1*2)=71
71 % 10 = 1
So 538-42-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H8O2.Na/c10-9(11)7-6-8-4-2-1-3-5-8;/h1-7H,(H,10,11);/q;+1/p-1/b7-6+;

538-42-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Sodium cinnamate

1.2 Other means of identification

Product number -
Other names sodium,(E)-3-phenylprop-2-enoate

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:538-42-1 SDS

538-42-1Relevant articles and documents

Enhanced Activity and Recyclability of Palladium Complexes in the Catalytic Synthesis of Sodium Acrylate from Carbon Dioxide and Ethylene

Manzini, Simone,Cadu, Alban,Schmidt, Anna-Corina,Huguet, Núria,Trapp, Oliver,Paciello, Rocco,Schaub, Thomas

, p. 2269 - 2274 (2017)

The Pd-catalysed synthesis of sodium acrylate from ethylene and CO2 in the presence of alcoholate bases has been improved significantly. We used amide solvents such as N-cyclohexylpyrrolidone or N,N-dibutylformamide to achieve turnover numbers

Decarboxylative Alkylcarboxylation of α,β-Unsaturated Acids Enabled by Copper-Catalyzed Oxidative Coupling

Gao, Bao,Xie, Yinjun,Shen, Zhiqiang,Yang, Lei,Huang, Hanmin

supporting information, p. 4968 - 4971 (2015/11/03)

A facile and general method for copper-catalyzed decarboxylative alkylcarboxylation of cinnamic acids with dimethyl 2,2′-azobis(2-methylpropionate) has been developed. The scope and versatility of the reaction was demonstrated, and a broad range of substrates bearing electron-donating and -withdrawing groups on the aromatic rings were all compatible with this reaction to provide desired β,γ-unsaturated esters in moderate to good yields. Moreover, α,β-unsaturated acids with a carbonyl group on the γ-position of acrylic acids also smoothly proceeded to furnish the desired products in good yields.

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