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D39800

Sigma-Aldrich

1,10-Dibromodecane

97%

Synonyme(s) :

Decamethylene dibromide

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About This Item

Formule linéaire :
Br(CH2)10Br
Numéro CAS:
4101-68-2
Poids moléculaire :
300.07
Numéro Beilstein :
506156
Numéro CE :
223-871-0
Numéro MDL:
MFCD00000222
Code UNSPSC :
12352100
ID de substance PubChem :
24893803
Nomenclature NACRES :
NA.22

Pureté

97%

Forme

crystals

Indice de réfraction

n20/D 1.4912 (lit.)

Point d'ébullition

160 °C/15 mmHg (lit.)

Pf

25-27 °C (lit.)

Densité

1.335 g/mL at 25 °C (lit.)

Chaîne SMILES 

BrCCCCCCCCCCBr

InChI

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

Clé InChI

GTQHJCOHNAFHRE-UHFFFAOYSA-N

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Catégories apparentées

Description générale

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).

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

233.6 °F - closed cup

Point d'éclair (°C)

112 °C - closed cup

Équipement de protection individuelle

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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