290009
Potassium benzoate
ReagentPlus®, 99%
Synonym(s):
Benzoic acid potassium salt
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250 G
€44.90
1 KG
€140.00
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250 G
€44.90
1 KG
€140.00
About This Item
Linear Formula:
C6H5COOK
CAS Number:
Molecular Weight:
160.21
Beilstein:
3719165
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.21
grade:
reagent
Recommended Products
grade
reagent
Quality Level
product line
ReagentPlus®
Assay
99%
functional group
phenyl
SMILES string
[K+].[O-]C(=O)c1ccccc1
InChI
1S/C7H6O2.K/c8-7(9)6-4-2-1-3-5-6;/h1-5H,(H,8,9);/q;+1/p-1
InChI key
XAEFZNCEHLXOMS-UHFFFAOYSA-M
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Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1 - Skin Irrit. 2
Storage Class Code
13 - Non Combustible Solids
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Microphase Separation with Small Amphiphilic Molecules: Crystal Structure of Preservatives Sodium Benzoate (E 211) and Potassium Benzoate (E 212).
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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)
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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
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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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