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Merck
CN

34150

Sigma-Aldrich

1,12-二溴十二烷

purum, ≥97.0% (GC)

别名:

十二亚甲基二溴

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线性分子式:
Br(CH2)12Br
化学文摘社编号:
分子量:
328.13
Beilstein:
1742763
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
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等级

purum

方案

≥97.0% (GC)

沸点

215 °C/15 mmHg (lit.)

mp

38-42 °C (lit.)
38-42 °C

溶解性

dioxane: soluble 0.5 g/5mL, clear, colorless

SMILES字符串

BrCCCCCCCCCCCCBr

InChI

1S/C12H24Br2/c13-11-9-7-5-3-1-2-4-6-8-10-12-14/h1-12H2

InChI key

ZJJATABWMGVVRZ-UHFFFAOYSA-N

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一般描述

1,12-Dibromododecane is an α,ω-dihaloalkane and its crystal structure has been described.

应用

1,12-Dibromododecane was used in synthesis of azobenzene isothiouronium salts of different alkyl chains (dodecyl) via reaction with 4-((4-methylphenyl)azo)phenol. It was also used in preparation of novel tboc-protected ionenes with molecular weight exceeding 30kDa.

储存分类代码

13 - Non Combustible Solids

WGK

WGK 3

闪点(°F)

235.4 °F - closed cup

闪点(°C)

113 °C - closed cup

个人防护装备

Eyeshields, Gloves, type N95 (US)

法规信息

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分析证书(COA)

Lot/Batch Number

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The crystal and molecular structure of 1, 12-dibromododecane, C12H24Br2.
Kulpe S, et al.
Kristall und Technik, 16(3), 349-356 (1981)
A M Badawi et al.
Bioorganic & medicinal chemistry, 14(24), 8661-8665 (2006-09-16)
A novel series of azobenzene isothiouronium salts of different alkyl chains (propyl, hexyl and dodecyl) were synthesized by reaction of 4-((4-methylphenyl)azo)phenol with 1,3-dibromopropane, 1,6-dibromohexane and 1,12-dibromododecane, respectively. These salts were reacted with copper (II) halide to give their corresponding metallo
Sean M Ramirez et al.
Macromolecular bioscience, 9(11), 1127-1134 (2009-07-29)
Novel tboc-protected ionenes with M(w) exceeding 30 kDa were prepared from the step-growth polymerization of tert-butyl bis[3-(dimethylamino)propyl]carbamate and 1,12-dibromododecane. The protected ionenes yielded pH-sensitive, protonatable ionenes with pK(a) approximately 6.6 for the conjugate acid of the protonated secondary amine. Polyplexes
Xin Jiang et al.
Cell, 183(1), 258-268 (2020-08-30)
Plasmodium species, the causative agent of malaria, rely on glucose for energy supply during blood stage. Inhibition of glucose uptake thus represents a potential strategy for the development of antimalarial drugs. Here, we present the crystal structures of PfHT1, the

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