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Sigma-Aldrich

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
Beilstein:
1697464
EC Number:
203-915-5
MDL number:
MFCD00001022
UNSPSC Code:
12352100
PubChem Substance ID:
24847650
NACRES:
NA.22

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.)

SMILES string

CCCCCCCCCl

InChI

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

InChI key

CNDHHGUSRIZDSL-UHFFFAOYSA-N

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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

Signal Word

Danger

Hazard Statements

H304,H410

Hazard Classifications

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

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

141.8 °F - closed cup

Flash Point(C)

61 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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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