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Merck

108804

Sigma-Aldrich

N-Allylthioharnstoff

98%

Synonym(e):

1-Allyl-2-thioharnstoff, Thiosinamin

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About This Item

Lineare Formel:
CH2=CHCH2NHCSNH2
CAS-Nummer:
Molekulargewicht:
116.18
Beilstein:
1071470
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22

Agentur

suitable for SM 5210

Qualitätsniveau

Assay

98%

Form

solid

mp (Schmelzpunkt)

70-72 °C (lit.)

Löslichkeit

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

Dichte

1.11 g/mL at 25 °C (lit.)

Funktionelle Gruppe

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)

InChIKey

HTKFORQRBXIQHD-UHFFFAOYSA-N

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Anwendung

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. Wirkung

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

Piktogramme

Skull and crossbones

Signalwort

Danger

H-Sätze

Gefahreneinstufungen

Acute Tox. 3 Oral

Lagerklassenschlüssel

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

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

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


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Die Dokumentenbibliothek aufrufen

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
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
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
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

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