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415693

Sigma-Aldrich

8-Chloro-1-octanol

98%

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About This Item

Linear Formula:
Cl(CH2)8OH
CAS Number:
23144-52-7
Molecular Weight:
164.67
EC Number:
245-451-6
MDL number:
MFCD00040005
UNSPSC Code:
12352100
PubChem Substance ID:
24866023
NACRES:
NA.22

Quality Level

100

Assay

98%

refractive index

n20/D 1.458 (lit.)

bp

129-130 °C/11 mmHg (lit.)

density

0.976 g/mL at 25 °C (lit.)

functional group

chloro
hydroxyl

SMILES string

OCCCCCCCCCl

InChI

1S/C8H17ClO/c9-7-5-3-1-2-4-6-8-10/h10H,1-8H2

InChI key

YDFAJMDFCCJZSI-UHFFFAOYSA-N

General description

8-Chloro-1-octanol is a ω-chloro-1-alkanol.

Application

8-Chloro-1-octanol may be employed for the following studies:
  • Biosynthesis of bacteriochlorophyll c derivatives, via esterification.
  • Preparation of new macroporous triisobutylphosphine sulphide functionalized polymers.
  • Synthesis of series of new mesogenic azomethine diols.
  • Synthesis of bis(4-hydroxyoctoxyphenyl)sulfone (HOS).

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCK4422
MKCF7050
MKCB2514V
MKBS8717V
MKBP4173V

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Synthesis and Properties of a Ferrocene-based Metallomesogenic Polymer Containing Bis (4-hydroxyoctoxyphenyl) sulfone.
Amer WA, et al.
Journal of Inorganic and Organometallic Polymers and Materials, 22(6), 1229-1239 (2012)
Issam Ahmed Mohammed et al.
Molecules (Basel, Switzerland), 15(5), 3260-3269 (2010-07-27)
A series of new mesogenic azomethine diols were successfully synthesized by condensation reactions between various chloroalkanols and N,N'-bis(4-hydroxy)-benzylidene-o-toluidine (1). The structures of these compounds were confirmed by CHN, FT-IR, (1)H-NMR, and (13)C-NMR spectrophotometer. Their thermotropic liquid crystalline behavior was studied
New macroporous polymers for the selective adsorption of gold (III) and palladium (II). I. The synthesis, characterization, and effect of spacers on metal adsorption.
Sanchez JM, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 38(2), 269-278 (2000)
Yoshitaka Saga et al.
Journal of bioscience and bioengineering, 118(1), 82-87 (2014-02-06)
The green sulfur photosynthetic bacterium Chlorobaculum tepidum newly produced BChl c derivatives possessing a chlorine or bromine atom at the terminus of the esterifying chain in the 17-propionate residue by cultivation with exogenous ω-halo-1-alkanols. The relative ratios of BChl c
Zachary K Zander et al.
Biomaterials, 178, 339-350 (2018-05-23)
The use of catheters is ubiquitous in medicine and the incidence of infection remains unacceptably high despite numerous advances in functional surfaces and drug elution. Herein we report the use of a thermoplastic polyurethane containing an allyl ether side-chain functionality

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