195332
1-Bromotetradecane
97%
Synonym(s):
Myristyl bromide, Tetradecyl bromide
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About This Item
Linear Formula:
CH3(CH2)13Br
CAS Number:
Molecular Weight:
277.28
Beilstein:
1742640
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
97%
form
liquid
refractive index
n20/D 1.460 (lit.)
bp
175-178 °C/20 mmHg (lit.)
mp
5-6 °C (lit.)
density
0.932 g/mL at 25 °C (lit.)
functional group
alkyl halide
bromo
SMILES string
CCCCCCCCCCCCCCBr
InChI
1S/C14H29Br/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15/h2-14H2,1H3
InChI key
KOFZTCSTGIWCQG-UHFFFAOYSA-N
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Application
1-Bromotetradecane was used in the synthesis of:
- tetradecylferrocene
- cationic and zwitterionic gemini surfactants
- metallomesogenic polymers based on bis[η1(N)-3,4-dialkyloxybenzylidene-4′-dodecyloxyaniline]dichloropalladium(II) with octyl, decyl, dodecyl, tetradecyl and hexadecyl alkyl groups
- 9-tetradecylcarbazole
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
235.4 °F - closed cup
Flash Point(C)
113 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Atakilt Abebe et al.
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New organic salts were synthesized by quaternizing 1,10-phenanthroline using 1-bromotetradecane. The first step yielded an organic salt of formula [C26H37N2]Br. Anion exchange reaction using Li[(CF3SO2)2N] resulted in a more stable salt of formula [C26H37N2][(CF3SO2)2N]. The organic salts were investigated by
R Hernández-Bravo et al.
The journal of physical chemistry. B, 122(15), 4325-4335 (2018-03-29)
A combined study for understanding the molecular interactions of asphaltenes with molecular species such as ionic liquids (ILs) comprised experimental measurements and computational numerical simulation calculations, using density-functional theory (DFT) with dispersion corrections, molecular dynamics (MD) calculations, and experimental rheological
Novel Metallomesogenic Polymers Derived from ? 1-Benzylideneaniline Palladium (II) Complex.
Lee M, et al.
Macromolecules, 32(8), 2777-2782 (1999)
Katrin Wedeking et al.
Langmuir : the ACS journal of surfaces and colloids, 22(7), 3161-3165 (2006-03-22)
Tetradecylferrocene (4, Fc-(CH2)13CH3) was synthesized via lithiation of ferrocene by treatment with tert-butyl lithium, followed by alkylation with 1-bromotetradecane. Complex 4 forms a physisorbed ordered molecular monolayer on the surface of highly oriented pyrolytic graphite (HOPG) that was analyzed by
Preparation of a Carbazole-Based Macrocycle Via Precipitation-Driven Alkyne Metathesis.
Zhang W, et al.
Organic Syntheses, 177-191 (2007)
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