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108804

Sigma-Aldrich

N-Allylthiourea

98%

Sinonimo/i:

1-Allyl-2-thiourea, Thiosinamine

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About This Item

Formula condensata:
CH2=CHCH2NHCSNH2
Numero CAS:
109-57-9
Peso molecolare:
116.18
Beilstein:
1071470
Numero CE:
203-683-5
Numero MDL:
MFCD00004940
Codice UNSPSC:
12352100
ID PubChem:
24846829
NACRES:
NA.22

agenzia

suitable for SM 5210

Livello qualitativo

100

Saggio

98%

Stato

solid

Punto di fusione

70-72 °C (lit.)

Solubilità

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

Densità

1.11 g/mL at 25 °C (lit.)

Gruppo funzionale

amine
thiourea

Stringa SMILE

NC(=S)NCC=C

InChI

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

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Categorie correlate

Applicazioni

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.

Azioni biochim/fisiol

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

Pittogrammi

Skull and crossbones
GHS06

Avvertenze

Danger

Indicazioni di pericolo

H301

Classi di pericolo

Acute Tox. 3 Oral

Codice della classe di stoccaggio

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

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

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

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Certificati d'analisi (COA)

Lot/Batch Number
STBK7956
STBK4755
STBK2778
STBJ9270
STBJ1121

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Marja Lahti et al.
Archives of environmental contamination and toxicology, 61(2), 202-210 (2010-11-18)
Although biotransformation is generally considered to be the main process by which to remove pharmaceuticals, both in sewage treatment plants and in aquatic environments, quantitative information on specific compounds is scarce. In this study, the transformations of diclofenac (DCF), naproxen
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)
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
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
Wei Zheng et al.
Environmental toxicology and chemistry, 24(8), 1867-1874 (2005-09-13)
Halogenated fumigants have been used extensively in production agriculture to control soilborne pests. These types of pesticides are highly volatile and are prone to affect air quality and imperil public health. In the present study, a chemical tarp approach, termed
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