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Merck

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:
Peso molecular:
300.07
Beilstein/REAXYS Number:
506156
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

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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Journal of inclusion phenomena and macrocyclic chemistry, 83(3-4), 321-334 (2015-11-10)
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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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