109169
Benzoato de sodio
99%, ReagentPlus®
Sinónimos:
Ácido benzoico sodium salt
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Acerca de este artículo
Fórmula lineal:
C6H5COONa
Número CAS:
Peso molecular:
144.10
NACRES:
NA.21
PubChem Substance ID:
eCl@ss:
39024301
UNSPSC Code:
12352100
EC Number:
208-534-8
MDL number:
Beilstein/REAXYS Number:
3572467
Assay:
99%
Solubility:
water: soluble(lit.)
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Permítanos ayudarleNombre del producto
Benzoato de sodio, ReagentPlus®, 99%
InChI key
WXMKPNITSTVMEF-UHFFFAOYSA-M
InChI
1S/C7H6O2.Na/c8-7(9)6-4-2-1-3-5-6;/h1-5H,(H,8,9);/q;+1/p-1
SMILES string
[Na+].[O-]C(=O)c1ccccc1
product line
ReagentPlus®
assay
99%
mp
>300 °C (lit.)
solubility
water: soluble(lit.)
functional group
phenyl
Quality Level
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Application
Sodium benzoate may be used in the preparation of various heavy metal benzoates.
General description
Sodium benzoate is the sodium salt of benzoic acid. On dissolution in water it affords weakly basic solution. It has anti-corrosive properties.Its determination in fruit juices, sodas, soy sauce, ketchup, peanut butter, cream cheese and other foods by HPLC method has been proposed. It is a Food and Drug Administration-approved nontoxic drug. It can be obtained via acid-base reaction between benzoic acid and sodium bicarbonate/sodium hydroxide solution.
Sodium benzoate serves as a catalyst in the Knoevenagel condensation reaction to synthesize carbon carbon bond formation.
Sodium benzoate serves as a catalyst in the Knoevenagel condensation reaction to synthesize carbon carbon bond formation.
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2
Clase de almacenamiento
13 - Non Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Eagleson M.
Concise Encyclopedia Chemistry, 121-121 (1994)
Huey-Jen Tsay et al.
Neurotoxicology and teratology, 29(5), 562-569 (2007-07-24)
Sodium benzoate (SB) is a commonly used food preservative and anti-microbial agent in many foods from soup to cereals. However, little is known about the SB-induced toxicity and teratogenicity during early embryonic development. Here, we used zebrafish as a model
Saurav Brahmachari et al.
Journal of immunology (Baltimore, Md. : 1950), 179(1), 275-283 (2007-06-21)
Experimental allergic encephalomyelitis (EAE) is the animal model for multiple sclerosis. This study explores a novel use of sodium benzoate (NaB), a commonly used food additive and a Food and Drug Administration-approved nontoxic drug for urea cycle disorders, in treating
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
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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