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Merck

M84607

Sigma-Aldrich

N-Methylthiourea

97%

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About This Item

Fórmula lineal:
NH2CSNHCH3
Número de CAS:
Peso molecular:
90.15
Beilstein/REAXYS Number:
506162
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

97%

form

crystals

mp

118-121 °C (lit.)

SMILES string

CNC(N)=S

InChI

1S/C2H6N2S/c1-4-2(3)5/h1H3,(H3,3,4,5)

InChI key

KQJQICVXLJTWQD-UHFFFAOYSA-N

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pictograms

Skull and crossbonesEnvironment

signalword

Danger

hcodes

Hazard Classifications

Acute Tox. 2 Oral - Aquatic Chronic 2

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

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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Shruti Sharma et al.
International journal of molecular sciences, 14(1), 255-272 (2013-01-25)
Congenital heart defects with increased pulmonary blood flow (PBF) result in pulmonary endothelial dysfunction that is dependent, at least in part, on decreases in nitric oxide (NO) signaling. Utilizing a lamb model with left-to-right shunting of blood and increased PBF
T S Plantinga et al.
Clinical pharmacology and therapeutics, 102(6), 1017-1024 (2017-05-10)
Agranulocytosis is a rare and serious adverse effect of antithyroid drugs, with unknown etiology. The present study aimed to uncover genetic susceptibility and underlying mechanisms of antithyroid drug-induced agranulocytosis (ATDAC). We studied two independent families with familial Graves' disease, of
[Proper use of noxythiolin: an experimental rat study on interaction with lactic acid].
J Maldonado et al.
Therapie, 35(3), 409-412 (1980-05-01)
S P Gorman et al.
The Journal of applied bacteriology, 60(4), 319-325 (1986-04-01)
The cidal activity of the antimicrobial agent, noxythiolin, was investigated against a laboratory strain and a fresh isolate of Candida albicans. The order of resistance to noxythiolin was hyphal form (isolate) greater than or equal to 25 degrees C-grown blastospores
M Yabuki et al.
European journal of drug metabolism and pharmacokinetics, 22(1), 25-33 (1997-01-01)
Metabolism of 4-[1-(2-fluoro-4-biphenylyl)ethyl]-2-methylaminothiazole (SM-8849), a novel immunomodulatory agent, in rats was investigated. By co-chromatography with authentic samples, desmethylated (SM-8800) p-hydroxylated (SL-5512) and desmethylated-p-hydroxylated SM-8849 (SL-5515) were detected in the bile. Thermospray mass spectrometry (TSP-MS) analysis of five metabolites isolated from

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