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线性分子式:
C6H5COOK
化学文摘社编号:
分子量:
160.21
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
209-481-3
MDL number:
Beilstein/REAXYS Number:
3719165
Assay:
99%
产品名称
苯甲酸钾, ReagentPlus®, 99%
InChI key
XAEFZNCEHLXOMS-UHFFFAOYSA-M
InChI
1S/C7H6O2.K/c8-7(9)6-4-2-1-3-5-6;/h1-5H,(H,8,9);/q;+1/p-1
SMILES string
[K+].[O-]C(=O)c1ccccc1
product line
ReagentPlus®
assay
99%
functional group
phenyl
Quality Level
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Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Irrit. 2
存储类别
13 - Non Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Microphase Separation with Small Amphiphilic Molecules: Crystal Structure of Preservatives Sodium Benzoate (E 211) and Potassium Benzoate (E 212).
Butterhof C, et al.
Zeitschrift fur Anorganische und Allgemeine Chemie, 639(15), 2816-2821 (2013)
N Zengin et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 49(4), 763-769 (2010-12-07)
In this study, the genotoxic effects of sodium benzoate (SB) and potassium benzoate (PB) were investigated in cultured human peripheral lymphocytes using chromosomal aberrations (CA), sister chromatid exchange (SCE), and micronuclei (MN). The level of nuclear DNA damage of SB
Polylactones, 19. Anionic polymerization of L-lactide in solution.
Kricheldorf HR and Kreiser-Saunders I.
Makromol. Chem., 191(5), 1057-1066 (1990)
Ali Kakanejadifard et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 106, 80-85 (2013-02-05)
The new Schiff base 4,4'-(1E,1'E)-(3,3'-(1E,1'E)-(pyridine-2,6-diylbis(azan-1-yl-1-ylid ene))bis(methan-1-yl-1-ylidene)bis(4-hydroxy-3,1-phenylene))bis(diazene-2,1-diyl)dibenzoic acid (1) was prepared from the condensation reaction of 2,6-diaminopyridine with 4-((3-formyl-4-hydroxyphenyl)diazenyl)benzoic acid in methanol. The compound 1 is potentially an N, O multidentate chelating ligand which could form stable complexes with metal ions
Chunhua Liu et al.
European journal of pharmacology, 700(1-3), 118-126 (2013-01-12)
Leonurine possesses cardioprotective effects in myocardial ischemia due to its anti-apoptotic properties. However, the process to isolate and purify leonurine is difficult, because of its low content in the Herb Leonuri and its impurity. Moreover, the high dosage used indicates
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