InChI
1S/C7H6O2/c8-7(9)6-4-2-1-3-5-6/h1-5H,(H,8,9)
SMILES string
OC(=O)c1ccccc1
InChI key
WPYMKLBDIGXBTP-UHFFFAOYSA-N
grade
pharmaceutical primary standard
agency
Ph. Eur.
vapor density
4.21 (vs air)
vapor pressure
10 mmHg ( 132 °C)
description
API family: benfluorex
API family
mefenamic acid, benfluorex, metronidazole
autoignition temp.
1061 °F
manufacturer/tradename
EDQM
availability
not available in (Sales restrictions may apply)
bp
249 °C (lit.)
mp
121-125 °C (lit.)
application(s)
pharmaceutical (small molecule)
format
neat
storage temp.
2-8°C
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General description
This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia.For further information and support please go to the website of the issuing Pharmacopoeia.
Application
Benzoic acid EP Reference standard, intended for use in laboratory tests only as specifically prescribed in the European Pharmacopoeia.
Packaging
The product is delivered as supplied by the issuing Pharmacopoeia. For the current unit quantity, please visit the EDQM reference substance catalogue.
Other Notes
Sales restrictions may apply.
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Irrit. 2 - STOT RE 1 Inhalation
target_organs
Lungs
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
flash_point_f
Not applicable
flash_point_c
Not applicable
G C Tremblay et al.
Pharmacology & therapeutics, 60(1), 63-90 (1993-10-01)
Detoxification of sodium benzoate by elimination as a conjugate with glycine, a nonessential amino acid, provides a pathway for the disposal of waste nitrogen. Since 1979, sodium benzoate has been widely used in the therapeutic regimen to combat ammonia toxicity
Benzoic acid intermediates in the anaerobic biodegradation of phenols.
K L Londry et al.
Canadian journal of microbiology, 38(1), 1-11 (1992-01-01)
Bradley S Moore et al.
Journal of natural products, 65(12), 1956-1962 (2002-12-28)
Although phenylpropanoids and flavonoids are common plant natural products, these major classes of biologically active secondary metabolites are largely absent from bacteria. The ubiquitous plant enzymes phenylalanine ammonia-lyase (PAL) and chalcone synthase (CHS) are key biosynthetic catalysts in phenylpropanoid and
Ludger Beerhues et al.
Phytochemistry, 70(15-16), 1719-1727 (2009-08-25)
Type III polyketide synthases (PKSs) generate a diverse array of secondary metabolites by varying the starter substrate, the number of condensation reactions, and the mechanism of ring closure. Among the starter substrates used, benzoyl-CoA is a rare starter molecule. Biphenyl
Nathalie Martin et al.
Molecular cancer, 13, 151-151 (2014-06-16)
Epidemiological data show that the incidence of carcinomas in humans is highly dependent on age. However, the initial steps of the age-related molecular oncogenic processes by which the switch towards the neoplastic state occurs remain poorly understood, mostly due to
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