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Key Documents

28-1830

Sigma-Aldrich

Sodium benzoate

SAJ special grade, ≥99.0%

Synonym(s):

Benzoic acid sodium salt

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About This Item

Linear Formula:
C6H5COONa
CAS Number:
Molecular Weight:
144.10
Beilstein:
3572467
MDL number:
UNSPSC Code:
12352300
PubChem Substance ID:

grade

SAJ special grade

vapor pressure

<0.01 hPa ( 20 °C)

Assay

≥99.0%

form

solid

availability

available only in Japan

pH

7.0-8.5 (25 °C, 144.1 g/L)

mp

>300 °C (lit.)

storage temp.

15-25°C

SMILES string

[Na+].[O-]C(=O)c1ccccc1

InChI

1S/C7H6O2.Na/c8-7(9)6-4-2-1-3-5-6;/h1-5H,(H,8,9);/q;+1/p-1

InChI key

WXMKPNITSTVMEF-UHFFFAOYSA-M

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Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

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Saurabh Khasnavis et al.
Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology, 7(2), 424-435 (2011-06-28)
DJ-1 (PARK7) is a neuroprotective protein that protects cells from oxidative stress. Accordingly, loss-of-function DJ-1 mutations have been linked with a familial form of early onset Parkinson disease. Mechanisms by which DJ-1 level could be enriched in the CNS are
Yumei Dai et al.
Journal of food science, 75(7), M482-M488 (2011-05-04)
Growth of Saccharomyces cerevisiae and Zygosaccharomyces bailii cells was monitored in the presence of sodium benzoate and eugenol alone or combined. The two antimicrobials' concentration, addition order, and timing were varied to determine and quantify any additive inhibitory effect on
Xu Huang et al.
CNS neuroscience & therapeutics, 18(1), 4-13 (2012-01-28)
D-Serine, the endogenous co-agonist of N-methyl-D-aspartate (NMDA) receptors, has been recognized as an important gliotransmitter in the mammalian brain. D-serine has been shown to prevent psychostimulant-induced decrease in hippocampal neurogenesis. However, the mechanism whereby D-serine regulates neurogenesis has not been
Jane Pui Ki Tsang et al.
Pediatric neurology, 47(4), 263-269 (2012-09-12)
In areas without expanded newborn screening, instead of presenting neonatally, patients with arginase deficiency typically present with spastic paraplegia in early childhood. Diagnosis of this rare neurometabolic disease poses the first challenge because it is often misdiagnosed as cerebral palsy
Sandesh C S Nagamani et al.
Genetics in medicine : official journal of the American College of Medical Genetics, 14(5), 501-507 (2012-01-14)
The urea cycle consists of six consecutive enzymatic reactions that convert waste nitrogen into urea. Deficiencies of any of these enzymes of the cycle result in urea cycle disorders (UCDs), a group of inborn errors of hepatic metabolism that often

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