| Identification | More | [Name]
Cyclopentylamine | [CAS]
1003-03-8 | [Synonyms]
AKOS BBS-00003621
AMINOCYCLOPENTANE
CYCLOPENTYLAMINE
cb1689
Cyclopentanamine
Cyclopentylamine, 99+%
AMINOCYCLAOPENTANE
1-Aminocyclopentane
1-Cyclopentanamine
Cyclopentane-1-amine | [EINECS(EC#)]
213-697-3 | [Molecular Formula]
C5H11N | [MDL Number]
MFCD00001380 | [Molecular Weight]
85.15 | [MOL File]
1003-03-8.mol |
| Safety Data | Back Directory | [Hazard Codes ]
F,Xi,T | [Risk Statements ]
R11:Highly Flammable.
R37/38:Irritating to respiratory system and skin .
R43:May cause sensitization by skin contact.
R34:Causes burns.
R25:Toxic if swallowed.
R20:Harmful by inhalation. | [Safety Statements ]
S16:Keep away from sources of ignition-No smoking .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
S25:Avoid contact with eyes .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . | [RIDADR ]
UN 2733 3/PG 2
| [WGK Germany ]
3
| [RTECS ]
GY8452000
| [F ]
8-10-23 | [TSCA ]
Yes | [HazardClass ]
3 | [PackingGroup ]
II | [HS Code ]
29213099 |
| Hazard Information | Back Directory | [Chemical Properties]
clear liquid | [Uses]
Cyclopentylamine acts as an important raw material and intermediate used in organic synthesis and pharmaceuticals. Further, it serves as chemokine receptor 2 antagonists. It acts as a ligand in coordination chemistry and forms cis-dichlorobis(cyclopentylamine)platinum(II) complex. | [Application]
Cyclopentylamine is used in small amounts as an intermediate for the potato and rice fungizide pencycuron (Bayer, Nihon Tokushu, Noyaku Seizo). | [Preparation]
Cyclopentylamine is produced from cyclopentanone and ammonia over nickel catalysts at 20 MPa and 150 – 200℃ in the presence of circulating hydrogen over a fixedbed catalyst. | [Flammability and Explosibility]
Highlyflammable | [Purification Methods]
The amine may contain H2O or CO2 in the form of carbamate salt. Dry it over KOH pellets and then distil it from a few pellets of KOH. Store it in a dark, dry CO2-free atmosphere. It is characterised as the thiocyanate salt m 94.5o. The benzenesulfonyl derivative has m 68.5-69.5o. [Roberts & Chambers J Am Chem Soc 73 5030 1951, Bollinger et al. J Am Chem Soc 75 1729 1953, Beilstein 12 IV 4.] |
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