| Identification | More | [Name]
Tetramethylthiourea | [CAS]
2782-91-4 | [Synonyms]
1,1,3,3-TETRAMETHYL-2-THIOUREA
1,1,3,3-TETRAMETHYLTHIOUREA
TETRAMETHYLTHIOUREA
((CH3)2N)2CS
1,1,3,3-tetramethyl-2-thio-ure
Basthioryl
N,N,N',N'-Tetramethylthiourea
N,N,N’,N’-Tetramethylthioharnstoff
NA-101
Tetramethyl-2-thiourea
tetramethyl-thioure
Thiourea,tetramethyl-
TMTU
Urea, 1,1,3,3-tetramethyl-2-thio-
Urea, thio-, tetramethyl-
N,N,N',N'-Tetramethylthioure | [EINECS(EC#)]
220-488-0 | [Molecular Formula]
C5H12N2S | [MDL Number]
MFCD00008324 | [Molecular Weight]
132.23 | [MOL File]
2782-91-4.mol |
| Safety Data | Back Directory | [Symbol(GHS) ]
GHS07 | [Signal word ]
Warning | [Hazard statements ]
H302 | [Precautionary statements ]
P301+P312+P330 | [Hazard Codes ]
Xn | [Risk Statements ]
R22:Harmful if swallowed.
R20/21/22:Harmful by inhalation, in contact with skin and if swallowed . | [Safety Statements ]
S22:Do not breathe dust .
S24/25:Avoid contact with skin and eyes .
S36:Wear suitable protective clothing . | [WGK Germany ]
3
| [RTECS ]
YU2750000
| [TSCA ]
Yes | [HS Code ]
29309070 | [Safety Profile]
Moderately toxic by ingestion. Questionable carcinogen with experimental carcinogenic and teratogenic data. Human mutation data reported. When heated to decomposition it emits very toxic fumes of NOx and SOx. See also SULFIDES. | [Hazardous Substances Data]
2782-91-4(Hazardous Substances Data) |
| Hazard Information | Back Directory | [General Description]
White crystals. | [Reactivity Profile]
An organosulfide amide. Organosulfides are incompatible with acids, diazo and azo compounds, halocarbons, isocyanates, aldehydes, alkali metals, nitrides, hydrides, and other strong reducing agents. Reactions with these materials generate heat and in many cases hydrogen gas. Many of these compounds may liberate hydrogen sulfide upon decomposition or reaction with an acid. Organic amides/imides react with azo and diazo compounds to generate toxic gases. Flammable gases are formed by the reaction of organic amides/imides with strong reducing agents. Amides are very weak bases (weaker than water). Imides are less basic yet and in fact react with strong bases to form salts. That is, they can react as acids. Mixing amides with dehydrating agents such as P2O5 or SOCl2 generates the corresponding nitrile. The combustion of these compounds generates mixed oxides of nitrogen (NOx). | [Air & Water Reactions]
Water soluble. | [Fire Hazard]
Flash point data for this chemical are not available, but 1,1,3,3-TETRAMETHYL-2-THIOUREA is probably combustible. | [Chemical Properties]
COLORLESS TO YELLOW CRYSTALLINE CHUNKS | [Definition]
ChEBI: Tetramethylthiourea is a member of thioureas. | [Hazard]
Moderately toxic by ingestion. |
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