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Key Documents

234451

Sigma-Aldrich

1-Bromohexadecane

97%

Synonym(s):

Cetyl bromide, Hexadecyl bromide

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About This Item

Linear Formula:
CH3(CH2)15Br
CAS Number:
Molecular Weight:
305.34
Beilstein/REAXYS Number:
773989
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

vapor density

10.6 (vs air)

Quality Level

vapor pressure

<1 mmHg ( 20 °C)

assay

97%

refractive index

n20/D 1.461 (lit.)

bp

190 °C/11 mmHg (lit.)

mp

16-18 °C (lit.)

density

0.999 g/mL at 25 °C (lit.)

SMILES string

CCCCCCCCCCCCCCCCBr

InChI

1S/C16H33Br/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17/h2-16H2,1H3

InChI key

HNTGIJLWHDPAFN-UHFFFAOYSA-N

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Application

1-Bromohexadecane has been used:
  • in the preparation of soluble carbon nano-onions by covalent functionalization with hexadecyl chains
  • as extraction solvent in determination of endocrine-disrupting phenols (EDPs) in water samples by ultrasound-assisted emulsification microextraction (MS-USAEME) method
  • in the preparation of [2-(methacryloyloxy)ethyl]dimethylhexadecylammonium bromide monomer, required for the synthesis of novel methacrylate based adsorbents
  • in the synthesis of surfactant, N-hexadecyl ethylenediamine triacetic acid (HED3A)

Pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Skin Irrit. 2

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

350.6 °F - closed cup

flash_point_c

177 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


Certificates of Analysis (COA)

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Ming-Wei Shu et al.
The Analyst, 137(9), 2143-2150 (2012-03-03)
Manual shaking-enhanced, ultrasound-assisted emulsification microextraction (MS-USAEME) combined with ultraperformance liquid chromatography (UPLC) with UV detection has been developed for the determination of five endocrine-disrupting phenols (EDPs) in seawater samples and detergent samples: 4-tert-butylphenol (4-t-BP), 4-cumylphenol (4-CP), 4-tert-octylphenol (4-t-OP), 2,4-di-tert-butylphenol (2,4-di-t-BP)
Agustín Molina-Ontoria et al.
Chemical communications (Cambridge, England), 49(24), 2406-2408 (2013-02-16)
Herein we report the preparation of truly soluble CNOs by covalent functionalization with hexadecyl chains. These compounds are prepared in two steps: first, reduction of CNOs with a Na-K alloy in 1,2-DME under vacuum, followed by nucleophilic substitution employing 1-bromohexadecane.
Xixin Wang et al.
Journal of colloid and interface science, 279(2), 548-551 (2004-10-07)
A new kind of surfactant named N-hexadecyl ethylenediamine triacetic acid (HED3A) was synthesized from anhydrous ethylenediamine, 1-bromohexadecane, and chloroacetic acid. Testing showed stability of HED3A in hard water, wetting power, dispersing power, and surface tension increased along with pH value.
Siti Norain Harun et al.
Pharmaceutics, 13(2) (2021-01-28)
The ruthenium polypyridyl complex [Ru(dppz)2PIP]2+ (dppz: dipyridophenazine, PIP: (2-(phenyl)-imidazo[4,5-f ][1,10]phenanthroline), or Ru-PIP, is a potential anticancer drug that acts by inhibiting DNA replication. Due to the poor dissolution of Ru-PIP in aqueous media, a drug delivery agent would be a
Yansong Ma et al.
Journal of dentistry, 64, 58-67 (2017-06-24)
White spot lesions due to biofilm acid-induced enamel demineralization are prevalent in orthodontic treatments. The aim of this study was to develop a novel bioactive multifunctional cement with protein-repellent, antibacterial and remineralizing capabilities, and investigate the effects on enamel hardness

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