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Merck

13929

Sigma-Aldrich

Benzyl thiocyanate

≥95.0% (GC)

Sinónimos:

Benzyl rhodanide

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About This Item

Fórmula lineal:
C6H5CH2SCN
Número de CAS:
Peso molecular:
149.21
Beilstein:
1859726
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de la sustancia en PubChem:
NACRES:
NA.22

Nivel de calidad

Ensayo

≥95.0% (GC)

Formulario

solid

bp

230-235 °C (lit.)

mp

39-41 °C (lit.)
39-41 °C

solubilidad

diethyl ether: soluble 0.5 g/10 mL, clear to very faintly turbid, colorless to almost colorless

grupo funcional

phenyl
thiocyanate
thioether

temp. de almacenamiento

2-8°C

cadena SMILES

N#CSCc1ccccc1

InChI

1S/C8H7NS/c9-7-10-6-8-4-2-1-3-5-8/h1-5H,6H2

Clave InChI

ABNDFSOIUFLJAH-UHFFFAOYSA-N

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Descripción general

Benzyl thiocyanate undergoes regioselective bond dissociation during its electrochemical reduction in acetonitrile at an inert electrode. It is added to stimulate the chlortetracycline biosynthesis during industrial fermentations. It undergoes biotransformation into dibenzyl disulphide by Streptomyces aureofaciens.

Aplicación

Benzyl thiocyanate was used to study the effects of various dietary compounds on the α-hydroxylation of N-nitrosopyrrolidine in male F344 rats in vitro.

Pictogramas

Exclamation mark

Palabra de señalización

Warning

Frases de peligro

Clasificaciones de peligro

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3

Riesgos supl.

Código de clase de almacenamiento

8A - Combustible corrosive hazardous materials

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

230.0 °F

Punto de inflamabilidad (°C)

110 °C

Equipo de protección personal

dust mask type N95 (US), Eyeshields, Gloves


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V Bĕhal et al.
Folia microbiologica, 27(2), 102-106 (1982-01-01)
The level of anhydrotetracyline oxygenase (an enzyme catalyzing the penultimate reaction in the biosynthesis of tetracyline) in Streptomyces aureofaciens was substantially influenced by the amount of inorganic phosphate and by the presence of benzyl thiocyanate in the cultivation medium. Phosphate
S Sugie et al.
Carcinogenesis, 14(2), 281-283 (1993-02-01)
The effects of benzyl isothiocyanate (BITC) and benzyl thiocyanate (BTC) on two types of DNA synthesis were examined in hepatocyte primary cultures (HPC). Male F344 rats were fed BITC- or BTC-containing diets at a concentration of 400 p.p.m. Using hepatocytes
V Erban et al.
Folia microbiologica, 32(5), 411-416 (1987-01-01)
The localization of anhydrotetracycline oxygenase and glucose-6-phosphate dehydrogenase (EC 1.1.1.49) was studied by determining the enzyme activities in subcellular fractions obtained by differential centrifugation of the mycelia of Streptomyces aureofaciens after lysozyme treatment. Glucose-6-phosphate dehydrogenase was a typical cytoplasmic enzyme
L V Trilisenko et al.
Folia microbiologica, 32(5), 402-410 (1987-01-01)
Mycelia of a low- and a high-production strain of Streptomyces aureofaciens were converted into protoplasts and divided into five subcellular fractions in order to localize exopolyphosphatases (EC 3.6.1.11), triphosphatase (EC 3.6.1.25), inorganic diphosphatase (EC 3.6.1.1), apyrase (EC 3.6.1.5) and glucokinase
J Nayini et al.
Carcinogenesis, 10(3), 509-512 (1989-03-01)
The effect of the dietary organoselenium compound, benzylselenocyanate (BSC) along with its sulphur analogue, benzylthiocynanate (BTC) and sodium selenite (Na2SeO3), on 7,12-dimethylbenz[a]anthracene (DMBA)-induced mammary carcinogenesis was examined in female Sprague-Dawley rats during the initiation phase of carcinogenesis. Semipurified diets containing

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