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108804

Sigma-Aldrich

N-Allylthiourea

98%

Sinónimos:

1-Allyl-2-thiourea, Thiosinamine

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About This Item

Fórmula lineal:
CH2=CHCH2NHCSNH2
Número de CAS:
109-57-9
Peso molecular:
116.18
Beilstein:
1071470
Número CE:
203-683-5
Número MDL:
MFCD00004940
Código UNSPSC:
12352100
ID de la sustancia en PubChem:
24846829
NACRES:
NA.22

Agency

suitable for SM 5210

Nivel de calidad

100

Ensayo

98%

Formulario

solid

mp

70-72 °C (lit.)

solubilidad

H2O: soluble 30 parts
alcohol: soluble
benzene: insoluble
diethyl ether: slightly soluble

densidad

1.11 g/mL at 25 °C (lit.)

grupo funcional

amine
thiourea

cadena SMILES

NC(=S)NCC=C

InChI

1S/C4H8N2S/c1-2-3-6-4(5)7/h2H,1,3H2,(H3,5,6,7)

Clave InChI

HTKFORQRBXIQHD-UHFFFAOYSA-N

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Aplicación

N-Allylthiourea was used as nitrification inhibitor in a study on transformation of diclofenac, naproxen and bisoprolol under aerobic and anaerobic conditions. It has been used in medicine to minimize scar tissue and to fight against a type of dermatitis.

Acciones bioquímicas o fisiológicas

N-Allylthiourea inhibits the growth of transplanted tumours in mice.

Pictogramas

Skull and crossbones
GHS06

Palabra de señalización

Danger

Frases de peligro

H301

Clasificaciones de peligro

Acute Tox. 3 Oral

Código de clase de almacenamiento

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

Equipo de protección personal

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

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Certificados de análisis (COA)

Lot/Batch Number
SDBB2298
STBL3818
STBL0134
STBL1522
STBL2294

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Radiation synthesis and characterization of N-vinyl-2-pyrrolidone/N-allylthiourea hydrogels and their use in the adsorption of invertase.
Sen M, et al.
Angew. Makromol. Chem., 257(1), 1-6 (1998)
Amy J Pogue et al.
Canadian journal of microbiology, 53(5), 559-571 (2007-08-02)
In activated sludge, protozoa feed on free-swimming bacteria and suspended particles, inducing flocculation and increasing the turnover rate of nutrients. In this study, the effect of protozoan grazing on nitrification rates under various conditions in municipal activated sludge batch reactors
Marlene Mark Jensen et al.
Applied and environmental microbiology, 73(10), 3151-3158 (2007-03-21)
The effects of three metabolic inhibitors (acetylene, methanol, and allylthiourea [ATU]) on the pathways of N2 production were investigated by using short anoxic incubations of marine sediment with a 15N isotope technique. Acetylene inhibited ammonium oxidation through the anammox pathway
C D Silva et al.
Chemosphere, 75(10), 1387-1391 (2009-04-04)
The oxidizing ability of a nitrifying consortium exposed to p-cresol (25 mg CL(-1)) was evaluated in batch cultures. Biotransformation of the phenolic compound was investigated by identifying the different intermediates formed. p-Cresol inhibited the ammonia-oxidizing process with a decrease of
Andrew K Shiemke et al.
Journal of bacteriology, 186(4), 928-937 (2004-02-06)
Diphenyliodonium (DPI) is known to irreversibly inactivate flavoproteins. We have found that DPI inhibits both membrane-bound methane monooxygenase (pMMO) from Methylococcus capsulatus and ammonia monooxygenase (AMO) of Nitrosomonas europaea. The effect of DPI on NADH-dependent pMMO activity in vitro is
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