234451
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:
773989
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
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.)
functional group
alkyl halide
bromo
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)
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Skin Irrit. 2
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
350.6 °F - closed cup
Flash Point(C)
177 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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.
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A series of bis(4-alkoxyphenyl) viologen bis(triflimide) salts with alkoxy chains of different lengths were synthesized by the metathesis reaction of respective bis(4-alkoxyphenyl) viologen dichloride salts, which were in turn prepared from the reaction of Zincke salt with the corresponding 4-n-alkoxyanilines
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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
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Biofilms at the tooth-restoration bonded interface can produce acids and cause recurrent caries. Recurrent caries is a primary reason for restoration failures. The objectives of this study were to synthesize a novel bioactive dental bonding agent containing dimethylaminohexadecyl methacrylate (DMAHDM)
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