538-42-1

Basic information

• Product Name: Sodium cinnamate
• Synonyms: 2-Propenoicacid,3-phenyl-,sodiumsalt;3-phenyl-2-propenoicacisodiumsalt;fortificar;sodium3-phenyl-2-propenoate;SODIUM CINNAMATE;CINNAMIC ACID SODIUM SALT;CINNAMYLIC ACID SODIUM SALT;3-PHENYLACRYLIC ACID SODIUM SALT
• CAS NO: 538-42-1
• Molecular Formula: C₉H₇O₂*Na
• Molecular Weight: 170.14
• EINECS: 208-691-2
• Product Categories: FINE Chemical & INTERMEDIATES;Cinnamic acid
• Mol File: 538-42-1.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 265oC at 760mmHg
• Flash Point: 189.5oC
• Appearance: /
• Vapor Pressure: 0.00471mmHg at 25°C
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: Sodium cinnamate(CAS DataBase Reference)
• NIST Chemistry Reference: Sodium cinnamate(538-42-1)
• EPA Substance Registry System: Sodium cinnamate(538-42-1)

Safety Data

• Hazardous Substances Data: 538-42-1(Hazardous Substances Data)

Usage

General Description

Sodium cinnamate is a chemical compound that is derived from cinnamic acid and is commonly used as a food preservative and flavoring agent. It is a white, crystalline powder that is soluble in water and has a slightly sweet, cinnamon-like odor and taste. Sodium cinnamate is often added to baked goods, beverages, and condiments to extend their shelf life and enhance their flavor. It has antimicrobial properties, which help inhibit the growth of bacteria and fungi, making it a popular choice for food preservation. Additionally, sodium cinnamate is also used in the production of cosmetics and personal care products as a fragrance ingredient. Overall, sodium cinnamate plays a crucial role in extending the shelf life and improving the sensory qualities of various food and personal care products.

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+;

Upstream product

• 621-82-9 Cinnamic acid 
• 100-42-5 styrene 
• 124-38-9 carbon dioxide 

Downstream Products

• 34882-18-3 2-bromo-3-hydroxy-3-phenyl-propanoic acid 
• 6622-79-3 2-bromo-3-chloro-3-phenyl-propionic acid 
• 103-25-3 3-phenylpropanoic acid methyl ester 
• 672-78-6 methyl p-toluene sulfinate 
• 114-84-1 phenylpropionic acid sodium salt 
• 824-79-3 sodium 4-methylbenzenesulfinate 
• 37818-47-6 (E)-3-Phenyl-acrylic acid 3,4,7-trioxo-2,5,6-triphenyl-cyclohepta-1,5-dienyl ester 
• 193750-60-6 C₆H₅C₂H₂COOI 
• 15813-24-8 (Z)-2-bromo-3-phenylacrylic acid 
• 110301-90-1 biscinnamatobis(p-biphenyl)tin(IV) 
• 1469370-28-2 C₃₉H₄₀N₇NiO₂⁽¹⁺⁾*NO₃^(1-)*H₂O 

Relevant articles and documents

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

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

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.