D42607
1,8-Dibromooctane
98%
Synonym(s):
Octamethylene dibromide
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25 G
$87.00
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$300.00
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About This Item
Linear Formula:
Br(CH2)8Br
CAS Number:
Molecular Weight:
272.02
Beilstein/REAXYS Number:
1698114
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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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
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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. [1]
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_germany
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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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)
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)
Enrico Caruso et al.
Bioorganic & medicinal chemistry, 28(21), 115737-115737 (2020-10-17)
A new class of compounds based on the 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene core, known as BODIPYs, has attracted significant attention as photosensitizers suitable for application in photodynamic therapy (PDT), which is a minimally invasive procedure to treat cancer. In PDT the combination of
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
Enrico Caruso et al.
Journal of photochemistry and photobiology. B, Biology, 197, 111548-111548 (2019-07-10)
The visible light combined with photosensitizers (PSs) is exploited in both antitumoral and antimicrobial fields inducing a photo-oxidative stress within the target cells. Among the different PSs, porphyrins belong to the family of the most promising compounds to be used
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