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Merck
CN

442261

Supelco

1-Chlorooctane

analytical standard

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:
41121813
PubChem Substance ID:
24867763

Key Documents

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grade

analytical standard

vapor pressure

1 mmHg ( 22.2 °C)

packaging

ampule of 1000 mg

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

refractive index

n20/D 1.430 (lit.)

bp

183 °C (lit.)

mp

−61 °C (lit.)

density

0.875 g/mL at 25 °C (lit.)

application(s)

environmental

format

neat

storage temp.

room temp

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

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

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

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Certificates of Analysis (COA)

Lot/Batch Number
LC23980V
LC21958V
LC18458V
LC07778V
LB89240V

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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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