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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
Assay:
99%
Form:
liquid

Key Documents

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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

Quality Level

100

bp

183 °C (lit.)

mp

−61 °C (lit.)

density

0.875 g/mL at 25 °C (lit.)

functional group

alkyl halide, chloro

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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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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)
Hydrophobically modified calcium-induced ?-carrageenan gels.
Jacquier JC, et al.
Prog. Coll. Polym. Sci., 118, 127-131 (2001)
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)
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
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)
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