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Merck
CN

108804

N-烯丙基硫脲

98%

别名:

1-烯丙基-2-硫脲, 硫代芥子胺

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线性分子式:
CH2=CHCH2NHCSNH2
化学文摘社编号:
109-57-9
分子量:
116.18
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24846829
EC Number:
203-683-5
Beilstein/REAXYS Number:
1071470
MDL number:
MFCD00004940
Assay:
98%
Form:
solid

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InChI key

HTKFORQRBXIQHD-UHFFFAOYSA-N

InChI

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

SMILES string

NC(=S)NCC=C

agency

suitable for SM 5210

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

Quality Level

100

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相关类别

Application

N-烯丙基硫脲作为硝化抑制剂，被用于研究双氯芬酸、萘普生和比索洛尔在有氧和厌氧条件下的转化。它已可用于医学中，以最大限度减小瘢痕组织并对抗一种皮炎。

Biochem/physiol Actions

N-烯丙基硫脲可抑制小鼠移植瘤的生长。

pictograms

Skull and crossbones
GHS06

signalword

Danger

hcodes

H301

Hazard Classifications

Acute Tox. 3 Oral

存储类别

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

ppe

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

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
SDBB6766
SDBB2298
STBL3818
STBL0134
STBL1522

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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
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
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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