Substance
ID:315702
Names and Identifiers
IUPAC name
1,1,3,3-tetramethylguanidine
IUPAC Traditional name
1,1,3,3-tetramethylguanidine
Synonyms
四甲基胍N,N,N′,N′-Tetramethylguanidine1,1,3,3-四甲基胍1,1,3,3-Tetramethylguanidine
Registration numbers
EC Number
Beilstein Number
CAS Number
PubChem SID
MDL Number
Properties
Safety Information
European Hazard Symbols
Corrosive (C)GHS Pictograms
Corrosive to metals, category 1
Skin corrosion, categories 1A,1B,1C
Serious eye damage, category 1
Flammable gases, category 1
Flammable aerosols, categories 1,2
Flammable liquids, categories 1,2,3
Self-reactive substances and mixtures, Types B,C,D,E,F
Pyrophoric liquids, category 1
Pyrophoric solids, category 1
Self-heating substances and mixtures
Substances and mixtures, which in contact with water, emit flammable gases, categories 1,2,3
Organic peroxides, Types B,C,D,E,F
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
RID/ADR
UN 2920 8/PG 2
GHS Signal Word
Danger
GHS Precautionary statements
P280-P305+P351+P338-P310
Personal Protective Equipment
Faceshields, full-face respirator (US), Gloves, Goggles, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
Safety Statements
26-27-36/37/39-45
Hazard Class
8
GHS Hazard statements
H226-H302-H314
Risk Statements
22-34
UN Number
2920
MSDS Link
Packing Group
2
German water hazard class
1
Physical Property
Density
0.918 g/mL at 25 °C(lit.)
Boiling Point
52-54 °C/11 mmHg(lit.)
Flash Point
60 °C
140 °F
Vapor Pressure
0.2 mmHg ( 20 °C)
Refractive Index
n20/D 1.469(lit.)
Pharmacology Properties
Gene Information
human ... EPHX2(2053)mouse ... Ephx2(13850)
Product Information
Linear Formula
(CH3)2NC(=NH)N(CH3)2
Purity
99%
Molecule Details
Packaging
5, 100, 500 mL in glass bottle
Application
Base employed in the preparation of alkyl nitriles from alkyl halides and 3′-alkylthymidines from 3′-nitrothymidines.
Promotes the pentavalent bismuth oxidation of primary and secondary alchohols to aldehydes and ketones.1
5, 100, 500 mL in glass bottle
Application
Base employed in the preparation of alkyl nitriles from alkyl halides and 3′-alkylthymidines from 3′-nitrothymidines.
Promotes the pentavalent bismuth oxidation of primary and secondary alchohols to aldehydes and ketones.1
Molecular Spectra
No Data Available
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References
No Data Available
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