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112-29-8 Usage

Chemical Properties

Colorless to light yellow liqui


Different sources of media describe the Uses of 112-29-8 differently. You can refer to the following data:
1. 1-Bromodecane is used to produce decanal. It is also used in organic synthesis.
2. 1-Bromodecane was used in the synthesis of ferrocene containing hexacatenar metallomesogen.

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.

Purification Methods

Shake the it with H2SO4, wash with H2O, dry with K2CO3, and fractionally distil it. [Beilstein 1 IV 470.]

Check Digit Verification of cas no

The CAS Registry Mumber 112-29-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,1 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 112-29:
28 % 10 = 8
So 112-29-8 is a valid CAS Registry Number.

112-29-8 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (A11340)  1-Bromodecane, 98%   

  • 112-29-8

  • 100g

  • 181.0CNY

  • Detail
  • Alfa Aesar

  • (A11340)  1-Bromodecane, 98%   

  • 112-29-8

  • 500g

  • 499.0CNY

  • Detail
  • Alfa Aesar

  • (A11340)  1-Bromodecane, 98%   

  • 112-29-8

  • 2500g

  • 2135.0CNY

  • Detail
  • Alfa Aesar

  • (A11340)  1-Bromodecane, 98%   

  • 112-29-8

  • 10000g

  • 6887.0CNY

  • Detail
  • Aldrich

  • (145785)  1-Bromodecane  98%

  • 112-29-8

  • 145785-100G

  • 335.79CNY

  • Detail
  • Aldrich

  • (145785)  1-Bromodecane  98%

  • 112-29-8

  • 145785-500G

  • 532.35CNY

  • Detail
  • Aldrich

  • (145785)  1-Bromodecane  98%

  • 112-29-8

  • 145785-2KG

  • 2,292.03CNY

  • Detail



According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017


1.1 GHS Product identifier

Product name Decyl Bromide

1.2 Other means of identification

Product number -
Other names Decylbromide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:112-29-8 SDS

112-29-8Relevant articles and documents

Aliphatic bromination with tetrabromomethane on immobilized copper complexes

Zelikman, Vladimir M.,Tarkhanova, Irina G.,Buryak, Alexey K.

, p. 60 - 66 (2015)

New catalytic systems with supported bromine- and chlorine-containing copper complexes for selective bromination of alkanes with tetrabromomethane have been proposed. Introduction of donor additives (e.g., low-molecular-weight alcohols) into the reaction increases the activity and stability of these catalysts. The kinetic features of the processes have been investigated. It has been shown that the dependences of the yield of bromodecanes on temperature and concentration of donor additives are both nonmonotonic in character.

Regiodivergent Conversion of Alkenes to Branched or Linear Alkylpyridines

Kim, Minseok,Shin, Sanghoon,Koo, Yejin,Jung, Sungwoo,Hong, Sungwoo

supporting information, p. 708 - 713 (2022/01/20)

Herein we report a practical protocol for the visible-light-induced regiodivergent radical hydropyridylation of unactivated alkenes using pyridinium salts. This approach provides a unified synthetic platform to control the regioselectivity of the synthesis of linear or branched C4-alkylated pyridines. A remarkable selectivity switch from the anti-Markovnikov to the Markovnikov product can be achieved by the addition of tetrabutylammonium bromide. The versatility of this protocol is further demonstrated based on the late-stage functionalization in pharmaceuticals.



Paragraph 0178; 0179; 0180; 0181; 0182; 0183, (2019/11/05)

A halide compound having one or more carbon-carbon unsaturated bonds is catalytically reduced with substantially no dehalogenation to produce a reduced halide compound in which at least one of the one or more unsaturated bonds is reduced. Specifically provided is a method for producing a reduced halide compound including steps of: reacting a nickel compound, a zinc compound, and a borohydride compound in a solvent to obtain a reduction catalyst; and subjecting a halide compound having one or more carbon-carbon unsaturated bonds to catalytic reduction in the presence of the reduction catalyst to reduce at least one of the one or more carbon-carbon unsaturated bonds to thereby obtain a reduced halide compound.

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