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108804

Sigma-Aldrich

N-Allylthiourea

98%

Synonym(s):

1-Allyl-2-thiourea, Thiosinamine

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About This Item

Linear Formula:
CH2=CHCH2NHCSNH2
CAS Number:
109-57-9
Molecular Weight:
116.18
Beilstein:
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.)

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

Signal Word

Danger

Hazard Statements

H301

Hazard Classifications

Acute Tox. 3 Oral

Storage Class Code

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

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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)
Yinghao Yu et al.
Applied microbiology and biotechnology, 82(2), 333-339 (2008-12-25)
Methanotrophs expressing soluble methane monooxygenase (sMMO) may find use in a variety of industrial applications. However, sMMO expression is strongly inhibited by copper, and the growth rate may be limited by the aqueous solubility of methane. In this study, addition
Schistosoma japonicum: establishment of a mouse model that demonstrates concomitant immunity.
Li He et al.
Chinese medical journal, 117(6), 947-949 (2004-06-17)
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
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