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D39800

1,10-Dibromodecane

Name: 1,10-Dibromodecane
Brand: ALDRICH

97%

Synonym(s):

Decamethylene dibromide

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About This Item

Linear Formula:

Br(CH₂)₁₀Br

CAS Number:

4101-68-2

Molecular Weight:

300.07

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24893803

EC Number:

223-871-0

Beilstein/REAXYS Number:

506156

MDL number:

MFCD00000222

Assay:

97%

Form:

crystals

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Properties

Quality Level

100

assay

97%

form

crystals

refractive index

n20/D 1.4912 (lit.)

bp

160 °C/15 mmHg (lit.)

mp

25-27 °C (lit.)

density

1.335 g/mL at 25 °C (lit.)

SMILES string

BrCCCCCCCCCCBr

InChI

1S/C10H20Br2/c11-9-7-5-3-1-2-4-6-8-10-12/h1-10H2

InChI key

GTQHJCOHNAFHRE-UHFFFAOYSA-N

Description

General description

1,10-Dibromodecane, also known as Decamethylene dibromide, is an aromatic and aliphatic monomer, often utilized in the polymerization reaction to synthesize high molecular weight polysulfides through polycondensation.

Application

1,10-Dibromodecane is used:

as a reactant in the Wurtz-type reaction during the synthesis of polyethylene

Construction of pillar[4]arene[1]quinone-1,10-dibromodecane pseudorotaxanes in solution and in the solid state.: This research highlights the application of 1,10-Dibromodecane in constructing complex molecular structures known as pseudorotaxanes. The study focuses on the synthesis and stabilization of these structures both in solution and solid states, providing a foundational technique for developing advanced materials in chemical engineering, pharmaceutical synthesis, and high-performance materials within industrial chemical manufacturing sectors. This breakthrough offers potential pathways for new drug delivery systems and smart materials based on the unique properties of these supramolecular assemblies (Sheng et al., 2020).

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

233.6 °F - closed cup

flash_point_c

112 °C - closed cup

ppe

Eyeshields, Gloves, type N95 (US)

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Synthesis of polysulfides containing s-triazine rings from 6-substituted amino-1, 3, 5-triazine-2, 4-dithiols and 1, 10-dibromodecane

Yoshiyuki O, et al.

Macromolecular Rapid Communications, 20, 294-298 (1999)

A "Rigid-Flexible" Approach for Processable Perylene Diimide-Based Polymers: Influence of the Specific Architecture on the Morphological, Dielectric, Optical, and Electronic Properties.

Stefania Aivali et al.

The journal of physical chemistry. B, 124(24), 5079-5090 (2020-05-28)

Conjugation-break flexible spacers in-between π-conjugated segments were utilized herein toward processable perylene diimide (PDI)-based polymers. Aromatic-aliphatic PDI-based polymers were developed via the two-phase polyetherification of a phenol-difunctional PDI monomer and aliphatic dibromides. These polyethers showed excellent solubility and film-forming ability

Chemical structures, properties, and applications of selected crude oil-based and bio-based polymers

Piotr K, et al.

Polymers, 14, 5551-5551 (2022)

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Global Trade Item Number

SKU	GTIN
D39800-100G	04061833563762