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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/REAXYS Number:
1071470
EC Number:
203-683-5
MDL number:
MFCD00004940
UNSPSC Code:
12352100
PubChem Substance ID:
24846829
NACRES:
NA.22

agency

suitable for SM 5210

Quality Level

100

assay

98%

form

solid

mp

70-72 °C (lit.)

solubility

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

density

1.11 g/mL at 25 °C (lit.)

functional group

amine
thiourea

SMILES string

NC(=S)NCC=C

InChI

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

InChI key

HTKFORQRBXIQHD-UHFFFAOYSA-N

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Application

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.

Biochem/physiol Actions

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

pictograms

Skull and crossbones
GHS06

signalword

Danger

hcodes

H301

Hazard Classifications

Acute Tox. 3 Oral

Storage Class

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

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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

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Certificados de análisis (COA)

Lot/Batch Number
STBL3818
STBL0134
STBL1522
STBL2294
STBK7956

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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)
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
I Popiel et al.
Transactions of the Royal Society of Tropical Medicine and Hygiene, 75(2), 287-291 (1981-01-01)
It has been found that treatment of mice infected with Schistosoma mansoni with thiosinamine for five days had a significant effect on the formation of normal egg-shells within the ootype of female worms. The protein material, not organized into complete
Guobin Cai et al.
Parasitology research, 104(3), 601-609 (2008-10-31)
Tyrosinase (TYR) was thought to play a critical role during trematode egg production. In this study, we analyzed two genes (SjTYR1 and SjTYR2), derived from Schistosoma japonicum genome databases, which encode proteins with significant homologies to mammalian TYR. They exhibited
P Stief
Water research, 35(12), 2811-2818 (2001-07-27)
Anaerobic nitrate consumption was accompanied by the accumulation of nitrite in the range of 3-52 micromoll(-1) in laboratory sediment cores continuously perfused with nitrate from below. Highest interstitial nitrite concentrations were observed in organically poor sediment cores with a low
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