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Merck
CN

88810

Sigma-Aldrich

硫脲

puriss. p.a., ACS reagent, ≥99.0%

别名:

Sulfourea, 硫代尿素

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About This Item

线性分子式:
NH2CSNH2
CAS号:
分子量:
76.12
Beilstein:
605327
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:

等级

ACS reagent
puriss. p.a.

方案

≥99.0%

表单

crystals

灼烧残渣

≤0.1% (as SO4)

缺失

≤0.5% loss on drying, 105°C, 2h

mp

170-176 °C (lit.)
174-177 °C

溶解性

water: soluble 137 g/L at 20 °C

痕量阴离子

sulfate (SO42-): ≤100 mg/kg

痕量阳离子

Cd: ≤5 mg/kg
Co: ≤5 mg/kg
Cr: ≤5 mg/kg
Cu: ≤5 mg/kg
Fe: ≤5 mg/kg
K: ≤50 mg/kg
Mg: ≤10 mg/kg
Mn: ≤5 mg/kg
Na: ≤50 mg/kg
Ni: ≤5 mg/kg
Pb: ≤5 mg/kg
Zn: ≤5 mg/kg

SMILES字符串

NC(N)=S

InChI

1S/CH4N2S/c2-1(3)4/h(H4,2,3,4)

InChI key

UMGDCJDMYOKAJW-UHFFFAOYSA-N

基因信息

mouse ... Ephx2(13850)

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应用

离液剂;强变性剂。增加蛋白质的溶解性和回收率
Thiourea may be used in the synthesis of thiobarbiturates and graphitic carbon nitride (g-C3N4).

警示用语:

Warning

危险分类

Acute Tox. 4 Oral - Aquatic Chronic 2 - Carc. 2 - Repr. 2

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

法规信息

危险化学品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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访问文档库

Polycondensation of thiourea into carbon nitride semiconductors as visible light photocatalysts.
Zhang G, et al.
Journal of Materials Chemistry, 22(16), 8083-8091 (2012)
The dissolution of gold in acidic solutions of thiourea.
Groenewald T.
Hydrometallurgy, 1(3), 277-290 (1976)
Eagleson M.
Concise Encyclopedia Chemistry, 115-115 (1994)
Adam R Brown et al.
Journal of the American Chemical Society, 135(18), 6747-6749 (2013-04-20)
Catalysis of Cope-type rearrangements of bis-homoallylic hydroxylamines is demonstrated using chiral thiourea derivatives. This formal intramolecular hydroamination reaction provides access to highly enantioenriched α-substituted pyrrolidine products and represents a complementary approach to metal-catalyzed methods.
Yoshiji Takemoto
Chemical & pharmaceutical bulletin, 58(5), 593-601 (2010-05-13)
We have developed several multifunctional thiourea catalysts bearing a tertiary amine or an 1,2-amino alcohol in expectation of their synchronous activation of a nucleophile and an electrophile through both acid-base and hydrogen-bonding interactions. From these studies, it was revealed that

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