Substance
ID:321162
Names and Identifiers
IUPAC Traditional name
3-(piperidin-1-yl)propan-1-amine
IUPAC name
3-(piperidin-1-yl)propan-1-amine
Synonyms
3-哌啶丙胺3-PiperidinopropylamineN-(3-Aminopropyl)piperidine1-(3-氨丙基)哌啶
Properties
Safety Information
Personal Protective Equipment
Faceshields, full-face respirator (US), Gloves, Goggles, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
GHS Signal Word
Danger
Risk Statements
22-34
GHS Hazard statements
H302-H314
GHS Precautionary statements
P280-P305+P351+P338-P310
GHS Pictograms
Corrosive to metals, category 1
Skin corrosion, categories 1A,1B,1C
Serious eye damage, category 1
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
RID/ADR
UN 2735 8/PG 3
European Hazard Symbols
Corrosive (C)UN Number
2735
German water hazard class
3
Safety Statements
26-36/37/39-45
Hazard Class
8
Packing Group
3
MSDS Link
Product Information
Empirical Formula (Hill Notation)
C8H18N2
Purity
95%
Physical Property
Flash Point
179.6 °F
82 °C
Refractive Index
n20/D 1.476
Density
0.895 g/mL at 25 °C
Molecule Details
Packaging
5 g in glass bottle
Application
Reactant for synthesis of:
• A chemotype that inhibits Botulinum neurotoxin serotype A light chain, P. falciparum Malaria, and Ebola filovirus1
• Membrane targeting antibiotics2
• 5-HT3A receptor antagonists3
• Histamine H3 antagonists4
• Berberine derivatives for stabilization of G-quadruplex DNA and down regulation of oncogene c-myc5Reactant for incorporation of basic side chains into cryptolepine scaffold for antimalarial activity6
5 g in glass bottle
Application
Reactant for synthesis of:
• A chemotype that inhibits Botulinum neurotoxin serotype A light chain, P. falciparum Malaria, and Ebola filovirus1
• Membrane targeting antibiotics2
• 5-HT3A receptor antagonists3
• Histamine H3 antagonists4
• Berberine derivatives for stabilization of G-quadruplex DNA and down regulation of oncogene c-myc5Reactant for incorporation of basic side chains into cryptolepine scaffold for antimalarial activity6
Molecular Spectra
No Data Available
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References
No Data Available
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