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109169

Sigma-Aldrich

Benzoato sodico

ReagentPlus®, 99%

Sinonimo/i:

Acido benzoico

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About This Item

Formula condensata:
C6H5COONa
Numero CAS:
532-32-1
Peso molecolare:
144.10
Beilstein:
3572467
Numero CE:
208-534-8
Numero MDL:
MFCD00012463
Codice UNSPSC:
12352100
eCl@ss:
39024301
ID PubChem:
57646852
NACRES:
NA.21
Saggio:
99%
Solubilità:
water: soluble(lit.)

Livello qualitativo

200

Nome Commerciale

ReagentPlus®

Saggio

99%

Punto di fusione

>300 °C (lit.)

Solubilità

water: soluble(lit.)

Gruppo funzionale

phenyl

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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Descrizione generale

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.

Applicazioni

Sodium benzoate may be used in the preparation of various heavy metal benzoates.

Note legali

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H319

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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Certificati d'analisi (COA)

Lot/Batch Number
0000293609
0000293609
MKCQ4761
MKCQ1028
MKCN7783

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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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