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125156

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.)

functional group

alkyl halide

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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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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