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18106

Sigma-Aldrich

Benzoato sodico

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

Sinonimo/i:

Acido benzoico

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About This Item

Formula condensata:
C6H5COONa
Numero CAS:
Peso molecolare:
144.10
Beilstein:
3572467
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
eCl@ss:
39024301
ID PubChem:
NACRES:
NA.21

Grado

puriss.

Livello qualitativo

Saggio

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

Forma fisica

powder

Qualità

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

Impurezze

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

Perdita

≤1% loss on drying, 105 °C

Punto di fusione

>300 °C (lit.)

Solubilità

water: soluble 556 g/L

Anioni in tracce

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

Cationi in tracce

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

Compatibilità

complies for appearance of solution

Stringa SMILE

[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
WXMKPNITSTVMEF-UHFFFAOYSA-M

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Applicazioni

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.

Note legali

Pittogrammi

Exclamation mark

Avvertenze

Warning

Indicazioni di pericolo

Classi di pericolo

Eye Irrit. 2

Codice della classe di stoccaggio

13 - Non Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

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
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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