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Merck
CN

D42607

1,8-Dibromooctane

98%

Synonym(s):

Octamethylene dibromide

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About This Item

Linear Formula:
Br(CH2)8Br
CAS Number:
Molecular Weight:
272.02
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
224-912-5
Beilstein/REAXYS Number:
1698114
MDL number:
Assay:
98%
Form:
liquid
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Quality Level

assay

98%

form

liquid

refractive index

n20/D 1.498 (lit.)

bp

270-272 °C (lit.)

mp

12-16 °C (lit.)

density

1.477 g/mL at 25 °C (lit.)

SMILES string

BrCCCCCCCCBr

InChI

1S/C8H16Br2/c9-7-5-3-1-2-4-6-8-10/h1-8H2

InChI key

DKEGCUDAFWNSSO-UHFFFAOYSA-N

General description

1,8-Dibromooctane is primarily used in organic synthesis as a building block for the preparationof various chemical intermediates.It is used as an alkylating reagent in one-pot synthesis for the production of paraffin-like oligomers and it is used to enhance crystallization and film formation of perovskite.

Application


  • Efficient manual Fmoc solid-phase synthesis of the N-terminal segment of surfactant protein B (SP-B(1-25)).: This study highlights the application of Fmoc-Gly-Wang resin in the synthesis of peptide segments, specifically demonstrating its utility in constructing the N-terminal segment of surfactant protein B (SP-B). The research underscores the resin′s effectiveness in peptide synthesis, emphasizing its role in generating biochemically significant peptides (Ramli et al., 2009).




Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter



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From N-vinylpyrrolidone anions to modified paraffin-like oligomers via double alkylation with 1, 8-dibromooctane: access to covalent networks and oligomeric amines for dye attachment
Obels, Daniela and Lievenbr{"u}ck, et, al.
Beilstein Journal of Organic Chemistry, 12, 1395-1400 (2016)
Efficiency enhancement in planar CH3NH3PbI3- xClx perovskite solar cells by processing with bidentate halogenated additives
Fu, Guangsheng and Hou, et al.
Solar Energy Materials and Solar Cells, 165, 36-44 (2017)
Kenji Tajima et al.
Biomacromolecules, 21(2), 581-588 (2019-11-22)
Nanofibrillated bacterial cellulose (NFBC) is produced by culturing a cellulose-producing bacterium under agitated aerobic conditions in a carboxymethylcellulose (CMC)-supplemented medium. Detailed structural analyses revealed that NFBC fiber widths varied with the degree of substitution of the CMC used, and zeta



Global Trade Item Number

SKUGTIN
D42607-100G04061833564189
D42607-25G04061833564196