等级
SAJ first grade
蒸汽压
<0.01 hPa ( 20 °C)
方案
≥98.5%
表单
solid
存货情况
available only in Japan
pH值(酸碱度)
7.0-8.5 (25 °C, 144.1 g/L)
mp
>300 °C (lit.)
储存温度
15-25°C
SMILES字符串
[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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警示用语:
Warning
危险声明
危险分类
Eye Irrit. 2
储存分类代码
13 - Non Combustible Solids
WGK
WGK 1
闪点(°F)
Not applicable
闪点(°C)
Not applicable
法规信息
新产品
Matthew J Palframan et al.
Organic letters, 13(12), 3150-3153 (2011-05-20)
(+)-Grandifloracin was synthesized from sodium benzoate by means of a dearomatizing dihydroxylation that proceeds with unusual regioselectivity. Iron diene complexes formed from the arene oxidation product permit the use of otherwise inaccessible transformations. The synthetic material was shown to be
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
Yue Mu et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 83(1), 130-135 (2011-09-06)
The toxicity of sodium benzoate to trypsin was investigated by fluorescence spectroscopy, synchronous fluorescence spectroscopy, UV-visible absorption spectroscopy and circular dichroism (CD) spectroscopy under mimic physiological conditions. Sodium benzoate could unfold trypsin by decreasing the β-sheet structure, which leads to
Trelita de Sousa et al.
Bioresource technology, 123, 256-262 (2012-09-04)
Pseudomonas nitroreducens TSB.MJ10 exhibiting growth and bioemulsifier production with 0.5% sodium benzoate as the sole carbon source was isolated from a mangrove ecosystem in the vicinity of a petroleum pump. The bioemulsifier is a lipopeptide that is stable over a
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
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