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ChemicalBook--->CAS DataBase List--->3529-08-6

3529-08-6

3529-08-6 Structure

3529-08-6 Structure
IdentificationMore
[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
Chemical PropertiesBack Directory
[Boiling point ]

84-86°C 15mm
[density ]

0.895
[refractive index ]

1.476
[Fp ]

82 ºC
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[form ]

solid
[pka]

10.44±0.10(Predicted)
[color ]

Colourless to light yellow
[CAS DataBase Reference]

3529-08-6(CAS DataBase Reference)
Safety DataBack 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
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Acetonitrile-->Hydrazinium hydroxide solution-->Potassium iodide-->Piperidine-->Tetrabutylammonium bromide-->Potassium phthalimide-->1,3-Dibromopropane-->1-Piperidineacetonitrile, a-methyl--->1H-ISOINDOLE-1,3(2H)-DIONE, 2-[3-(1-PIPERIDINYL)PROPYL]-(WXG02628)-->1-Piperidinepropionitrile-->1-(3-Chloropropyl)piperidine HCl-->1-Butanol-->N-(3-BROMOPROPYL)PHTHALIMIDE-->Acrylonitrile
Hazard InformationBack 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
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

3529-08-6(sigmaaldrich)
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