Basic Information |
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Product Name: | 3-(PIPERIDIN-1-YL)PROPAN-1-AMINE |
CAS: | 3529-08-6 |
English Synonyms: | 3-(1-PIPERIDINO)PROPYLAMINE ; 1-(3-AMINOPROP-1-YL)PIPERIDINE ; 3-(N-PIPERIDINO)PROPYLAMINE ; 1-(3-AMINOPROPYL)PIPERIDINE ; 3-PIPERIDIN-1-YL-PROPYLAMINE ; N-AMINOPROPYL PIPERIDINE ; 3-(AMINOPROPYL)PIPERIDINE ; 1-PIPERIDINEPROPANAMINE ; 3-PIPERIDINEPROPYLAMINE ; 3-PIPERIDINOPROPYLAMINE ; 3-(PIPERIDIN-1-YL)PROPAN-1-AMINE ; 1-AMINO-3-(PIPERIDIN-1-YL)PROPANE ; N-(3-AMINOPROPYL)PIPERIDINE |
MDL Number.: | MFCD00023784 |
H bond acceptor: | 2 |
H bond donor: | 1 |
Smile: | C1CCN(CC1)CCCN |
InChi: | InChI=1S/C8H18N2/c9-5-4-8-10-6-2-1-3-7-10/h1-9H2 |
InChiKey: | InChIKey=JMUCXULQKPWSTJ-UHFFFAOYSA-N |
Property |
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Boiling Point: | 84-86 DEG C |
Density: | DENSITY: 0.895 G/ML AT 25 DEG C |
Physical Property: | FLASHPOINT: 179.6 DEG F FLASHPOINT: 82 DEG C REFRACTIVE INDEX: N20/D 1.476 |
Comments: | APPLICATION: 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 RIDADR: UN 2735 8/PG 3 WGK: 3 |
Safety information |
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Symbol: |
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Signal word: | Danger |
Hazard statements: | H302-H314 |
Precautionary statements: | P280-P305 + P351 + P338-P310 |
hazard symbol: | C |
Risk Code: | R:22-34 |
Safe Code: | S:26-36/37/39-45 |
WGK Germany: | 3 |
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