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238333

Sigma-Aldrich

1-Bromopentadecane

97%

Synonym(s):

Pentadecyl bromide

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About This Item

Linear Formula:
CH3(CH2)14Br
CAS Number:
629-72-1
Molecular Weight:
291.31
Beilstein/REAXYS Number:
1744553
EC Number:
211-104-2
MDL number:
MFCD00000229
UNSPSC Code:
12352100
PubChem Substance ID:
24854296
NACRES:
NA.22

vapor density

10.1 (vs air)

Quality Level

100

vapor pressure

<1 mmHg ( 20 °C)

assay

97%

form

liquid

refractive index

n20/D 1.461 (lit.)

bp

159-160 °C/5 mmHg (lit.)

mp

17-19 °C (lit.)

density

1.005 g/mL at 25 °C (lit.)

SMILES string

CCCCCCCCCCCCCCCBr

InChI

1S/C15H31Br/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16/h2-15H2,1H3

InChI key

JKOTZBXSNOGCIF-UHFFFAOYSA-N

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General description

Incorporation of 1-bromopentadecane into mixed monolayers of deuterated palmitic acid (dPA) and deuterated stearic acid (dSA) at the air-water interface has been investigated.

Application

1-Bromopentadecane has been used as regent in the synthesis of (S)-eicos-(4E)-en-1-yn-3-ol, a bioactive component of the marine sponge Cribrochalina vasculum.

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

230.0 °F - closed cup

flash_point_c

110 °C - closed cup

ppe

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)

Certificates of Analysis (COA)

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M Roxana Sierra-Hernández et al.
Langmuir : the ACS journal of surfaces and colloids, 26(24), 18806-18816 (2010-12-02)
Mixed monolayers of deuterated palmitic acid C(15)D(31)COOH (dPA) and deuterated stearic acid C(17)D(35)COOH (dSA) with 1-bromoalkanes of different alkyl chain length (C(4) to C(16)) at the air-water interface were investigated. Alkanes and 1-chlorohexadecane ClC(16)H(33) (ClHex) were also studied to compare
Syntheses of two enantiomers of eicos-(4E)-en-1-yn-3-ol, a bioactive component of the marine sponge Cribrochalina vasculum.
Lu W, et al.
Tetrahedron, 55(15), 4649-4654 (1999)
Fabien Lacaille et al.
PloS one, 2(7), e661-e661 (2007-08-22)
Sexual behavior requires animals to distinguish between the sexes and to respond appropriately to each of them. In Drosophila melanogaster, as in many insects, cuticular hydrocarbons are thought to be involved in sex recognition and in mating behavior, but there

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