Cyclopropanamine
Suppliers
Names
[ CAS No. ]:
765-30-0
[ Name ]:
Cyclopropanamine
[Synonym ]:
Cyclopropylamine
1,2-Ethanediamine,N-cyclopropyl
N-Cyclopropyl-aethylendiamin
c-propyl amine
cyclopropylNH2
N-cyclopropylethane-1,2-diamine
cyclopropyl-amine
Cyclopropanamine
cyclopropylethylenediamine
MFCD00001301
EINECS 212-142-2
1-aminocyclopropane
Aminocyclopropane
Chemical & Physical Properties
[ Density]:
0.9±0.1 g/cm3
[ Boiling Point ]:
49.3±8.0 °C at 760 mmHg
[ Melting Point ]:
-50 °C
[ Molecular Formula ]:
C3H7N
[ Molecular Weight ]:
57.094
[ Flash Point ]:
-25.6±0.0 °C
[ Exact Mass ]:
57.057850
[ PSA ]:
26.02000
[ LogP ]:
-0.30
[ Vapour Pressure ]:
299.8±0.1 mmHg at 25°C
[ Index of Refraction ]:
1.484
[ Storage condition ]:
Flammables area
MSDS
Safety Information
[ Symbol ]:
GHS02, GHS05, GHS07
[ Signal Word ]:
Danger
[ Hazard Statements ]:
H225-H302-H314
[ Precautionary Statements ]:
P210-P280-P305 + P351 + P338-P310
[ Personal Protective Equipment ]:
Faceshields;full-face respirator (US);Gloves;Goggles;multi-purpose combination respirator cartridge (US)
[ Hazard Codes ]:
C:Corrosive
[ Risk Phrases ]:
R11;R22;R34
[ Safety Phrases ]:
S16-S26-S36/37/39-S45
[ RIDADR ]:
UN 2733 3/PG 2
[ WGK Germany ]:
2
[ RTECS ]:
GZ0685500
[ Packaging Group ]:
II
[ Hazard Class ]:
3
[ HS Code ]:
2921300090
Synthetic Route
Precursor & DownStream
Precursor
DownStream
Customs
[ HS Code ]: 2921300090
[ Summary ]:
2921300090 other cyclanic, cyclenic or cyclotherpenic mono- or polyamines, and their derivatives; salts thereof。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:6.5%。General tariff:30.0%
Articles
Arch. Pharm. (Weinheim) 347(11) , 861-72, (2014)
A series of substituted 4-oxopyrido[2,3-a]phenothiazine-3-carboxylic acids (6a-d) were prepared via cyclization of the corresponding ethyl 7-(arylthioxy)-8-nitro(or azido)-4-oxoquinoline-3-carboxylate...
Chemistry 16 , 13862-13875, (2010)
Thirty-three different N,N-dialkyl- and N-alkyl-N-phosphorylalkyl-substituted carboxamides 9-17 were treated with unsubstituted as well as with 2-alkyl-, 2,2-dialkyl-, and 3-alkenyl-substituted ethylm...
Arch. Biochem. Biophys. 436(2) , 265-75, (2005)
The inactivation of cytochrome P450 enzymes by cyclopropylamines has been attributed to a mechanism involving initial one-electron oxidation at nitrogen followed by scission of the cyclopropane ring l...