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D39800

Sigma-Aldrich

1,10-Dibromodecane

97%

Sinónimos:

Decamethylene dibromide

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About This Item

Fórmula lineal:
Br(CH2)10Br
Número de CAS:
4101-68-2
Peso molecular:
300.07
Beilstein/REAXYS Number:
506156
EC Number:
223-871-0
MDL number:
MFCD00000222
UNSPSC Code:
12352100
PubChem Substance ID:
24893803
NACRES:
NA.22

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

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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_germany

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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Rashid Nazir et al.
ACS applied materials & interfaces, 12(6), 7639-7649 (2020-01-24)
Design and synthesis of nanostructured responsive gels have attracted increasing attention, particularly in the biomedical domain. Polymer chain configurations and nanodomain sizes within the network can be used to steer their functions as drug carriers. Here, a catalyst-free facile one-step
Siyang He et al.
Molecules (Basel, Switzerland), 26(4) (2021-02-11)
Diels-Alder reactions on the surface of nanoparticles allow a thermoreversible functionalization of the nanosized building blocks. We report the synthesis of well-defined magnetite nanoparticles by thermal decomposition reaction and their functionalization with maleimide groups. Attachment of these dienophiles was realized
Elżbieta Luboch et al.
Journal of inclusion phenomena and macrocyclic chemistry, 83(3-4), 321-334 (2015-11-10)
The article presents the synthesis of novel 13- and 16-membered azobenzocrown derivatives with peripheral thiol moieties and preliminary studies assessing their possible application in plasmonic sensors based on gold nanoparticles. The effect of the length of the chain connecting the
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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