694134
N-(3-Aminopropyl)piperidine
95%
Synonym(s):
3-Piperidinopropylamine
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All Photos(2)
About This Item
Empirical Formula (Hill Notation):
C8H18N2
CAS Number:
Molecular Weight:
142.24
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
95%
form
liquid
refractive index
n20/D 1.476
density
0.895 g/mL at 25 °C
SMILES string
NCCCN1CCCCC1
InChI
1S/C8H18N2/c9-5-4-8-10-6-2-1-3-7-10/h1-9H2
InChI key
JMUCXULQKPWSTJ-UHFFFAOYSA-N
Application
Reactant for synthesis of:
Reactant for incorporation of basic side chains into cryptolepine scaffold for antimalarial activity
- 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
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
180.0 °F
Flash Point(C)
82.2 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Mary E Gagou et al.
Oncotarget, 5(22), 11381-11398 (2014-11-02)
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W Guo et al.
Cell death & disease, 5, e1409-e1409 (2014-09-05)
Btk and Etk/BMX are Tec-family non-receptor tyrosine kinases. Btk has previously been reported to be expressed primarily in B cells and has an important role in immune responses and B-cell malignancies. Etk has been shown previously to provide a strong
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