CAS 765-30-0|Cyclopropanamine
| Common Name | Cyclopropanamine | ||
|---|---|---|---|
| CAS Number | 765-30-0 | Molecular Weight | 57.094 |
| Density | 0.9±0.1 g/cm3 | Boiling Point | 49.3±8.0 °C at 760 mmHg |
| Molecular Formula | C3H7N | Melting Point | -50 °C |
| MSDS | ChineseUSA | Flash Point | -25.6±0.0 °C |
| Symbol | GHS02, GHS05, GHS07 | Signal Word | Danger |
Names
| Name | cyclopropylamine |
|---|---|
| Synonym | More Synonyms |
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 |
| InChIKey | HTJDQJBWANPRPF-UHFFFAOYSA-N |
| SMILES | NC1CC1 |
| Storage condition | Flammables area |
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 |
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% |
Articles29
More Articles| 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... |
Synonyms
| 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 |
