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About This Item
Linear Formula:
CH3(CH2)9Br
CAS Number:
Molecular Weight:
221.18
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-955-3
Beilstein/REAXYS Number:
1735227
MDL number:
Assay:
98%
Form:
liquid
InChI key
MYMSJFSOOQERIO-UHFFFAOYSA-N
InChI
1S/C10H21Br/c1-2-3-4-5-6-7-8-9-10-11/h2-10H2,1H3
SMILES string
CCCCCCCCCCBr
assay
98%
form
liquid
Quality Level
bp
238 °C (lit.)
density
1.066 g/mL at 25 °C (lit.)
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General description
1-Bromodecane participates in alkylation of pentaerythritol and introduces two lipophilic groups in pentaerythritol. It reacts with 1,2-dimethylimidazole to yield 1-decyl-2,3-dimethylimidazolium bromide.
Application
1-Bromodecane was used in the synthesis of ferrocene containing hexacatenar metallomesogen.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
201.2 °F - closed cup
flash_point_c
94 °C - closed cup
ppe
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
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Xuejing Song et al.
Materials (Basel, Switzerland), 11(10) (2018-10-27)
Pyrazine derivatives quinoxaline and pyridopyrazine were selected as the acceptors, and benzocarbazole was used as the donor to synthesize four different D⁻A⁻D compounds. The results showed that 2,3-bis(decyloxy)pyridine[3,4-b]pyrazine (DPP) exhibited stronger electron-withdrawing ability than that of 2,3-bis(decyloxy)quinoxaline (DPx), because DPP
Andrei Filippov et al.
Magnetic resonance in chemistry : MRC, 56(2), 113-119 (2017-07-29)
We used
Nusrat Jahan et al.
The Journal of organic chemistry, 74(20), 7762-7773 (2009-09-18)
Simple strategies for the synthesis of five series of cationic gemini surfactants and one series of zwitterionic gemini surfactants from pentaerythritol have been developed. Two lipophilic groups were introduced onto pentaerythritol by alkylation of the known compound, O-benzylidenepentaerythritol, with 1-bromooctane
Ibrahim Bou Malham et al.
Journal of colloid and interface science, 328(1), 166-171 (2008-10-07)
1-Decyl-2,3-dimethylimidazolium bromide (ddmimBr) has been synthesized by the reaction of 1,2-dimethylimidazole and 1-bromodecane. Micellization of ddmimBr surfactant in water (W) and water-ethanolamine (W-EA) with the weight percent of EA changing within the range 0-39.79%, has been investigated at 298.15 K.
Isao Kanesaka
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 60(1-2), 297-302 (2003-12-13)
A change in an infrared intensity in dielectric media is treated by an electrostatic model. The basic model is originally formalized for a dipolar liquid. The model is satisfactorily applied to the infrared intensity of the C-H stretching of chloroform
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