B79803
3-Bromopropylamine hydrobromide
98%
Synonym(s):
3-Aminopropyl bromide hydrobromide
Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
Linear Formula:
BrCH2CH2CH2NH2 · HBr
CAS Number:
Molecular Weight:
218.92
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
225-675-0
Beilstein/REAXYS Number:
3906418
MDL number:
Assay:
98%
Form:
crystals
Quality Level
assay
98%
form
crystals
mp
171-172 °C (lit.)
SMILES string
Br.NCCCBr
InChI
1S/C3H8BrN.BrH/c4-2-1-3-5;/h1-3,5H2;1H
InChI key
PQIYSSSTRHVOBW-UHFFFAOYSA-N
Application
3-Bromopropylamine hydrobromide is commonly used as a reagent to introduce propylamine group to the molecular skeleton. Some of the other reported applications include:
- Synthesis of photochemically and thermally reactive azobenzene rotaxane and indolocarbazole-containing [2]rotaxane.
- Synthesis of indenoisoquinoline based active topoisomerase I inhibitors as anticancer agents.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Christina Gladkova et al.
Nature, 559(7714), 410-414 (2018-07-12)
Mutations in the E3 ubiquitin ligase parkin (PARK2, also known as PRKN) and the protein kinase PINK1 (also known as PARK6) are linked to autosomal-recessive juvenile parkinsonism (AR-JP)1,2; at the cellular level, these mutations cause defects in mitophagy, the process
A multi-mode-driven molecular shuttle: photochemically and thermally reactive azobenzene rotaxanes.
Murakami H, et al.
Journal of the American Chemical Society, 127(45), 15891-15899 (2005)
Antagonist analogue of 6-[3 `-(1-adamantyl)-4 `-hydroxyphenyl]-2-naphthalenecarboxylic acid (AHPN) family of apoptosis inducers that effectively blocks AHPN-induced apoptosis but not cell-cycle arrest.
Dawson M I, et al.
Journal of Medicinal Chemistry, 47(14), 3518-3536 (2004)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| B79803-100G | 04061833442289 |
| B79803-25G | 04061833442296 |