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Key Documents

900637

Sigma-Aldrich

1,2-Dichloroethane

anhydrous, ZerO2®, 99.8%

Synonym(s):

1,2-Dichloroethane ZerO2®, Degassed and low oxygen 1,2-dichloroethane, Ethylene chloride, Ethylene dichloride

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About This Item

Linear Formula:
ClCH2CH2Cl
CAS Number:
Molecular Weight:
98.96
Beilstein:
605264
EC Number:
MDL number:
UNSPSC Code:
12191502
NACRES:
NA.21

grade

ZerO2®

Quality Level

vapor density

3.4 (20 °C, vs air)

vapor pressure

87 mmHg ( 25 °C)

Assay

99.8%

form

liquid

autoignition temp.

775 °F

quality

anhydrous

expl. lim.

15.6 %

impurities

≤0.003% water
water

refractive index

n20/D 1.444 (lit.)

bp

83 °C (lit.)

mp

−35 °C (lit.)

density

1.256 g/mL at 25 °C (lit.)

SMILES string

ClCCCl

InChI

1S/C2H4Cl2/c3-1-2-4/h1-2H2

InChI key

WSLDOOZREJYCGB-UHFFFAOYSA-N

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Application

ZerO2 products are rigorously degassed with highly pure inert gas providing solvents and solutions (anhydrous if specified) with very low residual oxygen content.

Legal Information

ZerO2 is a registered trademark of Sigma-Aldrich Co. LLC

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Asp. Tox. 1 - Carc. 1B - Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

55.4 °F - closed cup

Flash Point(C)

13 °C - closed cup


Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

EU REACH SVHC Candidate List

CAS No.

EU REACH Annex XVII (Restriction List)

CAS No.

EU REACH Annex XIV (Authorisation List)

CAS No.

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Jana Hammoud et al.
Carbohydrate research, 486, 107834-107834 (2019-11-07)
Herein, a C-H bond functionalization approach is reported as a new route towards non-natural glycosides having a quaternary position 5. The development of this transformation furthermore reveals that insertion of Rh(II)-carbenes into the C5-H bond is controlled by remote stereoelectronic

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