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Merck
CN

125156

1-Chlorooctane

99%

Synonym(s):

Octyl chloride

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About This Item

Linear Formula:
CH3(CH2)7Cl
CAS Number:
111-85-3
Molecular Weight:
148.67
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24847650
EC Number:
203-915-5
Beilstein/REAXYS Number:
1697464
MDL number:
MFCD00001022

Key Documents

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Product Name

1-Chlorooctane, 99%

InChI key

CNDHHGUSRIZDSL-UHFFFAOYSA-N

InChI

1S/C8H17Cl/c1-2-3-4-5-6-7-8-9/h2-8H2,1H3

SMILES string

CCCCCCCCCl

vapor pressure

1 mmHg ( 22.2 °C)

assay

99%

form

liquid

refractive index

n20/D 1.430 (lit.)

bp

183 °C (lit.)

mp

−61 °C (lit.)

density

0.875 g/mL at 25 °C (lit.)

functional group

alkyl halide
chloro

Quality Level

100

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Application

1-Chlorooctane has been used to determine the excess molar enthalpies of binary mixtures composed by 2-alkanone and 1-chloroalkane. It has been used in hydrophobic modification of ω-carrageenans polymers.

pictograms

Health hazardEnvironment
GHS08,GHS09

signalword

Danger

hcodes

H304,H410

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Asp. Tox. 1

Storage Class

10 - Combustible liquids

wgk

WGK 2

flash_point_f

141.8 °F - closed cup

flash_point_c

61 °C - closed cup

ppe

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)

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Certificates of Analysis (COA)

Lot/Batch Number
WXBF7792V
WXBF5618V
WXBF3759V
MKCS9803
MKCR3771

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Excess enthalpies of some 2-alkanone+ 1-chloroalkane binary mixtures at 25 and 35? C.
Pico JM, et al.
Journal of Solution Chemistry, 20(1), 115-124 (1991)
Hydrophobically modified calcium-induced ?-carrageenan gels.
Jacquier JC, et al.
Prog. Coll. Polym. Sci., 118, 127-131 (2001)
Biosynthesis and characterization of a new bacterial copolyester of 3-hydroxyalkanoates and 3-hydroxy-omega-chloroalkanoates.
Doi Y and Abe C.
Macromolecules, 23(15), 3705-3707 (1990)
Susann Wegner et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 23(26), 6330-6340 (2017-02-15)
The microwave-induced decomposition of bis{N,N'-diisopropylacetamidinate}nickel(II) [Ni{MeC(NiPr)
A R King et al.
British journal of pharmacology, 157(6), 974-983 (2009-06-03)
Monoacylglycerol lipase (MGL) is a presynaptic serine hydrolase that inactivates the endocannabinoid neurotransmitter, 2-arachidonoyl-sn-glycerol. Recent studies suggest that cysteine residues proximal to the enzyme active site are important for MGL function. In the present study, we characterize the role of
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