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18106

Sigma-Aldrich

Sodium benzoate

puriss., meets analytical specification of Ph. Eur., BP, FCC, E211, 99.0-100.5% (calc. to the dried substance), powder

Synonyme(s) :

BENZOTRON, Benzoic acid sodium salt

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About This Item

Formule linéaire :
C6H5COONa
Numéro CAS:
Poids moléculaire :
144.10
Numéro Beilstein :
3572467
Numéro CE :
Numéro MDL:
Code UNSPSC :
12352100
eCl@ss :
39024301
ID de substance PubChem :
Nomenclature NACRES :
NA.21

Qualité

puriss.
meets analytical specification of Ph. Eur., BP, FCC, E211

Niveau de qualité

Pureté

99.0-100.5% (calc. to the dried substance)

Forme

powder

Impuretés

acidity or alkalinity, complies
oxidizable impurities, complies
residual solvents, complies
≤0.001% heavy metals (as Pb)
≤0.03% halogenated compounds (as Cl)

Perte

≤1% loss on drying, 105 °C

Pf

>300 °C (lit.)

Solubilité

water: soluble 556 g/L

Traces d'anions

chloride (Cl-): ≤100 mg/kg
sulfate (SO42-): ≤100 mg/kg

Traces de cations

As: ≤2 mg/kg
Cu: ≤10 mg/kg
Hg: ≤1 mg/kg
Pb: ≤2 mg/kg
Zn: ≤10 mg/kg

Adéquation

complies for appearance of solution

Chaîne SMILES 

[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

Clé InChI

WXMKPNITSTVMEF-UHFFFAOYSA-M

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Application

Sodium benzoate can be used as areactant to synthesize:
  • 2-Phenoxyethyl benzoate via phase-transfercatalyzed esterification with 2-phenoxyethyl bromide.
  • Ynones by Pd free coupling reactionwith terminal alkynes in the presence of cyanuric chloride and magnesiumchloride.
It can also be used as a catalyst to synthesize:
  • 3-Methyl-4-arylmethylene-isoxazol-5(4H)-onesby reacting ethyl acetoacetate, hydroxylamine hydrochloride, and aromaticaldehydes.
  • 4-Pyrazolylmethylene-3-phenylisoxazol-5(4H)-onesvia three-component cyclocondensation of pyrazole-4-carbaxaldehyde withβ-ketoesters and hydroxylamine hydrochloride.

Informations légales

Pictogrammes

Exclamation mark

Mention d'avertissement

Warning

Mentions de danger

Classification des risques

Eye Irrit. 2

Code de la classe de stockage

13 - Non Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, type N95 (US)


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Les clients ont également consulté

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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
H M Pylypiw et al.
Journal of chromatography. A, 883(1-2), 299-304 (2000-07-26)
A rapid and reliable method is presented for the determination of the preservatives sodium benzoate and potassium sorbate in fruit juices, sodas, soy sauce, ketchup, peanut butter, cream cheese, and other foods. The procedure utilizes high-performance liquid chromatography (HPLC) followed
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

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