Cyclopropanamine

[ 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

Click to get detail MSDS

[ 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

Click to get detail synthetic route

Precursor

DownStream

[ 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%

Synthesis and antibacterial activity of some novel 4-oxopyrido[2,3-a]phenothiazines.

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...

Cyclopropylamines from N,N-dialkylcarboxamides and Grignard reagents in the presence of titanium tetraisopropoxide or methyltitanium triisopropoxide.

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...

Cyclopropylamine inactivation of cytochromes P450: role of metabolic intermediate complexes.

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...

More Articles