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
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
204-008-7
Beilstein/REAXYS Number:
773989
MDL number:
Assay:
97%
InChI key
HNTGIJLWHDPAFN-UHFFFAOYSA-N
InChI
1S/C16H33Br/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17/h2-16H2,1H3
SMILES string
CCCCCCCCCCCCCCCCBr
vapor density
10.6 (vs air)
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
Quality Level
Related Categories
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)
signalword
Warning
hcodes
Hazard Classifications
Skin Irrit. 2
Storage Class
10 - Combustible liquids
wgk
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
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Ning Zhang et al.
International journal of oral science, 10(2), 18-18 (2018-06-22)
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)
Andreas Håkansson et al.
Journal of colloid and interface science, 374(1), 25-33 (2012-03-01)
The Oil Transfer Technique (OTT) was developed by Taisne et al. [1] to measure coalescence during emulsification and has been applied since in several studies. One of the main drawbacks of this technique is that it only gives a qualitative
Pradip K Bhowmik et al.
Molecules (Basel, Switzerland), 25(10) (2020-05-28)
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
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.
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)
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