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145785

Sigma-Aldrich

1-Bromodecane

98%

Synonym(s):

Decyl bromide

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About This Item

Linear Formula:
CH3(CH2)9Br
CAS Number:
112-29-8
Molecular Weight:
221.18
Beilstein:
1735227
EC Number:
203-955-3
MDL number:
MFCD00000221
UNSPSC Code:
12352100
PubChem Substance ID:
24848745
NACRES:
NA.22

Assay

98%

form

liquid

refractive index

n20/D 1.456 (lit.)

bp

238 °C (lit.)

density

1.066 g/mL at 25 °C (lit.)

SMILES string

CCCCCCCCCCBr

InChI

1S/C10H21Br/c1-2-3-4-5-6-7-8-9-10-11/h2-10H2,1H3

InChI key

MYMSJFSOOQERIO-UHFFFAOYSA-N

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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.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319

Precautionary Statements

P302 + P352 - P305 + P351 + P338

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

201.2 °F - closed cup

Flash Point(C)

94 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
1,1'-Disubstituted ferrocene containinghexacatenar thermotropic liquid crystals.
Seo JS, et al.
Journal of Materials Chemistry, 11(5), 1332-1338 (2001)
Omar F Hernández-Zepeda et al.
Frontiers in plant science, 9, 1076-1076 (2018-08-09)
Plants in more than 100 families secrete extrafloral nectar (EFN) to establish food-for-protection mutualisms with ants. Facultative ant-plants secrete EFN as a jasmonic acid (JA)-dependent response to attract generalist ants. In contrast, obligate ant-plants like the Central American "Swollen-Thorn Acacias"
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
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