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108804

Sigma-Aldrich

N-Allylthiourea

98%

Synonyme(s) :

1-Allyl-2-thiourea, Thiosinamine

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About This Item

Formule linéaire :
CH2=CHCH2NHCSNH2
Numéro CAS:
109-57-9
Poids moléculaire :
116.18
Numéro Beilstein :
1071470
Numéro CE :
203-683-5
Numéro MDL:
MFCD00004940
Code UNSPSC :
12352100
ID de substance PubChem :
24846829
Nomenclature NACRES :
NA.22

Agence

suitable for SM 5210

Niveau de qualité

100

Pureté

98%

Forme

solid

Pf

70-72 °C (lit.)

Solubilité

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

Densité

1.11 g/mL at 25 °C (lit.)

Groupe fonctionnel

amine
thiourea

Chaîne SMILES 

NC(=S)NCC=C

InChI

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

Clé InChI

HTKFORQRBXIQHD-UHFFFAOYSA-N

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Catégories apparentées

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.

Actions biochimiques/physiologiques

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

Pictogrammes

Skull and crossbones
GHS06

Mention d'avertissement

Danger

Mentions de danger

H301

Classification des risques

Acute Tox. 3 Oral

Code de la classe de stockage

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

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

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

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Certificats d'analyse (COA)

Lot/Batch Number
STBL3818
STBL0134
STBL1522
STBL2294
STBK7956

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Consulter la Bibliothèque de documents

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)
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
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
P Falås et al.
Environmental technology, 33(7-9), 865-872 (2012-06-23)
Removal of five acidic pharmaceuticals (ibuprofen, ketoprofen, naproxen, diclofenac and clofibric acid) by activated sludge from five municipal activated sludge treatment processes, with various sludge ages and nitrification capacities, was assessed through batch experiments. The increase in aerobic sludge age
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
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