| Identification | More | [Name]
1-(3-Aminopropyl)piperidine | [CAS]
3529-08-6 | [Synonyms]
3-(1-PIPERIDINO)PROPYLAMINE
3-PIPERIDIN-1-YLPROPAN-1-AMINE
3-PIPERIDIN-1-YL-PROPYLAMINE
3-PIPERIDINOPROPYLAMINE
AKOS MSC-0392
ASINEX-REAG BAS 12433284
N-AMINOPROPYL PIPERIDINE
RARECHEM AL BW 0252
TIMTEC-BB SBB010073
Piperidinopropylamine
piperidine-1-propylamine
3-(Piperidin-1-yl)propylamine 97%
1-(3-Aminopropyl)piperidine
1-Piperidine-1-propanamine | [EINECS(EC#)]
222-557-0 | [Molecular Formula]
C8H18N2 | [MDL Number]
MFCD00023784 | [Molecular Weight]
142.24 | [MOL File]
3529-08-6.mol |
| Safety Data | Back Directory | [Hazard Codes ]
C,Xi | [Risk Statements ]
R10:Flammable.
R34:Causes burns.
R22:Harmful if swallowed. | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) . | [RIDADR ]
2735 | [WGK Germany ]
3 | [Hazard Note ]
Corrosive | [HazardClass ]
IRRITANT | [HS Code ]
2933399990 |
| Hazard Information | Back Directory | [Uses]
Reactant for synthesis of:
- A chemotype that inhibits Botulinum neurotoxin serotype A light chain, P. falciparum Malaria, and Ebola filovirus
- Membrane targeting antibiotics
- 5-HT3A receptor antagonists
- Histamine H3 antagonists
- Berberine derivatives for stabilization of G-quadruplex DNA and down regulation of oncogene c-myc
Reactant for incorporation of basic side chains into cryptolepine scaffold for antimalarial activity |
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