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Merck
CN

167169

3-Bromo-1-propanol

97%

Synonym(s):

Trimethylene bromohydrin

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About This Item

Linear Formula:
Br(CH2)3OH
CAS Number:
627-18-9
Molecular Weight:
138.99
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24850196
EC Number:
210-986-6
Beilstein/REAXYS Number:
969160
MDL number:
MFCD00002942

Key Documents

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Product Name

3-Bromo-1-propanol, 97%

InChI key

RQFUZUMFPRMVDX-UHFFFAOYSA-N

InChI

1S/C3H7BrO/c4-2-1-3-5/h5H,1-3H2

SMILES string

OCCCBr

assay

97%

form

liquid

refractive index

n20/D 1.488 (lit.)

bp

62 °C/5 mmHg (lit.)

density

1.537 g/mL at 25 °C (lit.)

functional group

bromo
hydroxyl

storage temp.

2-8°C

Quality Level

100

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Application

3-Bromo-1-propanol was used in the synthesis of fluorescent halide-sensitive quinolinium dyes and molten salt-polymers. It was used in the synthesis of chiral, quaternary prolines via cyclization of quaternary amino acids.
Recently used as a grafting agent in the synthesis of recyclable reagents for Swern oxidation

General description

Reaction between 3-bromo-1-propanol, phenol and a series of phenols having substituents in 4-position has been studied in micellar media and in microemulsions based on cationic or a nonionic surfactant.

3-Bromo-1-propanol is an electrophile used as a substrate in nucleophilic substitution reactions and in the redox polymerization.

pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

hcodes

H302,H318

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

149.0 °F - closed cup

flash_point_c

65 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
SHBQ7733
SHBL9166
SHBJ1434
SHBG2565V
SHBF3280V

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Fredrik Currie
Journal of colloid and interface science, 277(1), 230-234 (2004-07-28)
The reaction between 3-bromo-1-propanol and phenol and a series of phenols carrying substituents in 4-position was studied in micellar media and in microemulsions based on either a cationic or a nonionic surfactant. The reactivity and the yield were evaluated and
Takeo Kawabata et al.
Journal of the American Chemical Society, 128(48), 15394-15395 (2006-11-30)
An enantiodivergent asymmetric cyclization of N-Boc-N-omega-bromoalkyl-alpha-amino acid derivatives has been developed. With potassium amide bases in DMF, cyclization proceeds with retention of configuration, while inversion of configuration was observed with lithium amide bases in THF. Chirality of the parent amino
Wei Song et al.
Molecules (Basel, Switzerland), 25(17) (2020-08-23)
Azobenzene (AB) units were successfully introduced into poly(1,6-heptadiyne)s in order to ensure smooth synthesis of double- and single-stranded poly(1,6-heptadiyne)s (P1 and P2) and simultaneously realize the self-assembly by Grubbs-III catalyst-mediated metathesis cyclopolymerization (CP) of AB-functionalized bis(1,6-heptadiyne) and 1,6-heptadiyne monomers (M1
Use of self-assembled surfactant systems as media for a substitution reaction
Fredrik and Currie
Journal of Colloid and Interface Science, 277, 230-234 (2004)
Synthesis and characterization of various block copolymers using PMMA-Br macroinitiator
Melahat and Goktacs et al.
Chemical Papers, 73, 2329-2339 (2019)
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