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About This Item
Linear Formula:
Cl(CH2)8Cl
CAS Number:
Molecular Weight:
183.12
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Assay
98%
form
liquid
refractive index
n20/D 1.459 (lit.)
bp
115-116 °C/11 mmHg (lit.)
density
1.025 g/mL at 25 °C (lit.)
SMILES string
ClCCCCCCCCCl
InChI
1S/C8H16Cl2/c9-7-5-3-1-2-4-6-8-10/h1-8H2
InChI key
WXYMNDFVLNUAIA-UHFFFAOYSA-N
Related Categories
General description
1,8-Dichlorooctane is a chloroparaffin. The non-exponentiality of proton spin-lattice relaxation in polycrystalline 1,8-dichlorooctane in Zeeman-quadrupole level-crossing experiments at various frequencies is reported. It has important synthetic applications in food, pharmaceutical, biomedical, electrical and electronic sectors.
Application
1,8-Dichlorooctane may be used:
- as adsorbate to investigate the performance of carbonaceous materials for the adsorption of emerging pollutants
- to prepare the C20-backbone of 1,20-substituted eicosanes carrying phosphate headgroups and readily derivatizable thiol, maleimido, and activated carboxylic ester moieties
- in the synthesis of planar-chiral imidazolium salt
- in the preparation of biosensors
- in the fabrication of strong polymeric membranes for concentrating amino acids, having applications in food and pharmaceutical industry
- in the synthesis of perfluorocarbons having biomedical applications
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Skin Irrit. 2
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
244.4 °F
Flash Point(C)
118 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Limited spin diffusion towards quadrupolar relaxation centers in 1, 8-dichlorooctane
Kozak A, et al.
Chemical Physics Letters, 74(1), 173-175 (1980)
Vibrational analysis of 1, 8-dichlorooctane.
Singh D, et al.
Indian Journal of Pure and Applied Physics, 47(10), 696-696 (2009)
Synthesis and properties of a diastereopure ionic liquid with planar chirality.
Ishida Y, et al.
Tetrahedron Letters, 47(45), 7973-7976 (2006)
Yolanda Patiño et al.
Chemosphere, 119 Suppl, S124-S130 (2014-06-09)
The adsorption of three representative emerging pollutants over different kinds of carbonaceous adsorbents has been studied in this work. The adsorbates were nalidixic acid (NAL, representative of a pharmaceutical), 1,8-dichlorooctane (DCO, a chloroparaffin) and methyl-phenoxy-ethanol (MPET, a surfactant). Activated carbons
Istvan Jablonkai et al.
Chemistry and physics of lipids, 133(1), 103-112 (2004-12-14)
New 1,20-substituted eicosanes carrying phosphate headgroups and readily derivatizable thiol, maleimido, and activated carboxylic ester moieties were prepared. The C20-backbone of these molecules was assembled by a halopolycarbon homologation from 1,8-dichlorooctane and 1,6-dibromohexane. 20-Mercapto- and 20-maleimido-icosylphosphates were synthesized via omega-bromo
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