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About This Item
Linear Formula:
(CH3)2NCSN(CH3)2
CAS Number:
Molecular Weight:
132.23
Beilstein:
1744916
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
98%
form
solid
bp
245 °C (lit.)
mp
75-77 °C (lit.)
storage temp.
2-8°C
SMILES string
CN(C)C(=S)N(C)C
InChI
1S/C5H12N2S/c1-6(2)5(8)7(3)4/h1-4H3
InChI key
MNOILHPDHOHILI-UHFFFAOYSA-N
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General description
Tetramethylthiourea molecule shows crystallographic two-fold symmetry with weak hydrogen bond packing, which connects the molecules to form layers.
Application
Tetramethylthiourea forms BF3 adduct with tetramethylselenourea.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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The oxidation of tetramethylthiourea (TMTU) at gold electrodes in acetonitrile, leading to dissolution of the electrode, has been studied by electrochemical methods and by an electrochemical quartz crystal microbalance (EQCM). TMTU in acetonitrile readily adsorbs at gold electrodes and an
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A Pauson-Khand type of conversion of enynes to bicyclic cyclopentenones employing the commercially available Co2(CO)8 and tetramethylthiourea (TMTU) as catalysts is described. This method allows a variety of enynes with diverse functional groups to be cyclized into cyclopentenones of interest.
Urea-boron trihalide adducts. IV. Ionic-covalent equilibria in the tetramethylthiourea-BF3 and tetramethylselenourea-BF3 systems and the influence of B2F7-formation.
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Tetramethyl and ethylene thiourea are collected from air using midget impingers containing 15 mL water. Ethylene thiourea may also be collected from air using PVC or cellulose ester membrane filters which are then extracted with water. Pentacyanoamineferrate reagent is added
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