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415693

Sigma-Aldrich

8-Chloro-1-octanol

98%

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Linear Formula:
Cl(CH2)8OH
CAS Number:
Molecular Weight:
164.67
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

Quality Level

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.)

SMILES string

OCCCCCCCCCl

InChI

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

InChI key

YDFAJMDFCCJZSI-UHFFFAOYSA-N

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This Item
370533112615297887
8-Chloro-1-octanol 98%

Sigma-Aldrich

415693

8-Chloro-1-octanol

1-Octanol ReagentPlus®, 99%

Sigma-Aldrich

112615

1-Octanol

1-Octanol anhydrous, ≥99%

Sigma-Aldrich

297887

1-Octanol

refractive index

n20/D 1.458 (lit.)

refractive index

n20/D 1.313 (lit.)

refractive index

n20/D 1.429 (lit.)

refractive index

n20/D 1.429 (lit.)

bp

129-130 °C/11 mmHg (lit.)

bp

88-95 °C/28 mmHg (lit.)

bp

196 °C (lit.)

bp

196 °C (lit.)

density

0.976 g/mL at 25 °C (lit.)

density

1.651 g/mL at 25 °C (lit.)

density

0.827 g/mL at 25 °C (lit.)

density

0.827 g/mL at 25 °C (lit.)

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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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
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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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