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B79803

Sigma-Aldrich

3-Bromopropylamine hydrobromide

98%

Synonym(s):

3-Aminopropyl bromide hydrobromide

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About This Item

Linear Formula:
BrCH2CH2CH2NH2 · HBr
CAS Number:
5003-71-4
Molecular Weight:
218.92
Beilstein:
3906418
EC Number:
225-675-0
MDL number:
MFCD00012912
UNSPSC Code:
12352100
PubChem Substance ID:
24892034
NACRES:
NA.22

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

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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.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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)
Christina Gladkova et al.
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Synthesis and anticancer activity of simplified indenoisoquinoline topoisomerase I inhibitors lacking substituents on the aromatic rings.
Nagarajan M, et al.
Journal of Medicinal Chemistry, 47(23), 5651-5661 (2004)
Interlocked host anion recognition by an indolocarbazole-containing [2] rotaxane.
Brown A, et al.
Journal of the American Chemical Society, 131(13), 4937-4952 (2009)
Maya Juenet et al.
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