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270997

Dichloromethane

anhydrous, ≥99.8%, contains 40-150 ppm amylene as stabilizer

Synonym(s):

DCM, Methylene chloride

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About This Item

Empirical Formula (Hill Notation):
CH2Cl2
CAS Number:
75-09-2
Molecular Weight:
84.93
UNSPSC Code:
12352101
NACRES:
NA.21
PubChem Substance ID:
57648216
EC Number:
200-838-9
Beilstein/REAXYS Number:
1730800
MDL number:
MFCD00000881
Assay:
≥99.8%
Grade:
anhydrous
Technique(s):
gas chromatography (GC): suitable
Bp:
39.8-40 °C (lit.)
Vapor pressure:
24.45 psi ( 55 °C), 6.83 psi ( 20 °C), 6.86 psi ( 20 °C)
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grade

anhydrous

Quality Level

200

agency

suitable for EPA 1613

vapor density

2.9 (vs air)

vapor pressure

24.45 psi ( 55 °C), 6.83 psi ( 20 °C), 6.86 psi ( 20 °C)

assay

≥99.8%

form

liquid

autoignition temp.

1223 °F

contains

40-150 ppm amylene as stabilizer

expl. lim.

22 %

technique(s)

gas chromatography (GC): suitable

impurities

≤0.001% water, ≤0.005% water (100 mL pkg)

evapn. residue

<0.0005%

refractive index

n20/D 1.424 (lit.)

bp

39.8-40 °C (lit.)

mp

−95 °C (lit.)

density

1.325 g/mL at 25 °C (lit.)

SMILES string

ClCCl

InChI

1S/CH2Cl2/c2-1-3/h1H2

InChI key

YMWUJEATGCHHMB-UHFFFAOYSA-N

General description

Dichloromethane is a chlorinated organic solvent that is susceptible to degradation with time. This can be suppressed by adding amylene as a stabilizer.
Dichloromethane has been tested as a solvent medium for the dipyridine-chromium(VI) oxide. Solubility was reported to be 12.5g/100ml. Role of quantity of TiO2 loading on activated carbon support employed in the photodecomposition of dichloromethane has been investigated.

Application

Dichloromethane has been used for the quantification of herbivore (gypsy moth) induced blueberry volatiles by gas chromatography (GC).
Dichloromethane may be used as a solvent for the oxidation of primary and secondary alcohols using dipyridine-chromium(VI) oxide. Lithium perchlorate suspended in DCM is an effective medium for Mukaiyama aldol reactions of aldehydes with silyl ketene acetal. DCM may also be used as solvent for the synthesis of 2-bromo-6-lithiopyridine from 2,6-dibromopyridine via lithium-bromine exchange reaction.

Packaging

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Other Notes

2024 CiteAb Award Winner for Supplier Succeeding in Parkinson′s Research

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pictograms

Health hazardExclamation mark
GHS08,GHS07

signalword

Warning

Hazard Classifications

Carc. 2 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Central nervous system

wgk

WGK 2

ppe

Eyeshields, Faceshields, Gloves

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

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Certificates of Analysis (COA)

Lot/Batch Number
STBF2595V
04896CK
S78197
16097MJ
66496AK

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Articles

Tabella di miscibilità dei solventi

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Solvent Miscibility Table

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Environmental Methods Consumables Look Up Tool

This page is intended to make it easier to find the consumables you need based on the analytical method you’re using. Methods included on this page come from the EPA, Standard Methods and ASTM.

Efficient Preparation of 2-Bromo-6-lithiopyridine via Lithium? Bromine Exchange in Dichloromethane
Peterson MA & Mitchell JR
The Journal of Organic Chemistry, 62(23), 8237-8239 (1997)
Carbon-carbon bond formation catalyzed by lithium perchlorate in dichloromethane
Reetz MT & Fox DN
Tetrahedron Letters, 34(7), 1119-1122 (1993)
Cesar R Rodriguez-Saona
Journal of visualized experiments : JoVE, (58)(58), doi:10-doi:10 (2012-01-05)
Herbivore-induced plant volatiles (HIPVs) are commonly emitted from plants after herbivore attack. These HIPVs are mainly regulated by the defensive plant hormone jasmonic acid (JA) and its volatile derivative methyl jasmonate (MeJA). Over the past 3 decades researchers have documented
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Global Trade Item Number

SKUGTIN
270997-12X100ML04061826143537
270997-1L04061837532047
270997-2L04061837532054
270997-4X2L04061837532061
270997-6X1L04061826143568
270997-100ML04061837532030
270997-200L04061838151773
270997-250ML04061837536045
270997-PZ04061823900690