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ChemicalBook--->CAS DataBase List--->1072-53-3

1072-53-3

1072-53-3 Structure

1072-53-3 Structure
IdentificationBack Directory
[Name]

ETHYLENESULFATE
[CAS]

1072-53-3
[Synonyms]

DTD
NSC 526594
glycolsulfate
Vinyl sulfate
GLYCOLSULPHATE
ETHYLENESULFATE
ETHYLENESULPHATE
1,2-ETHYLENE SULFATE
Ethylenesulfate ,98%
Ethylenesulfate≥ 99% (GC)
Ethylene sulfate 1072-53-3
ethyleneglycol,cyclicsulfate
1,3,2-Dioxathiolan-2,2-oxide
2,2-dioxido-1,3,2-dioxathiolane
1,3,2-DIOXATHIOLANE 2,2-DIOXIDE
1,3,2-Dioxathiolane,2,2-dioxides
sulfuricacid,cyclicethyleneester
1,3,2-Dioxathiolane2,2-Dioxide>
1,2-Ethylene Sulfate DTD 1072-53-3
1,3,2-Dioxathiolan-2,2-oxide (DTD)
1,3,2-Dioxathiolane 2,2-dioxide 98%
ETHYLENESULFATE ISO 9001:2015 REACH
3,2-Dioxathiolane 2,2-dioxide, 97%+
1,3,2-Dioxathiolane 2,2-Dioxide,>98%
1,3,2-Dioxathiolane 2,2-dioxide 1072-53-3
1,3,2-DIOXATHIOLANE2,2-DIOXIDE/ETHYLENESULFATE
[EINECS(EC#)]

600-809-4
[Molecular Formula]

C2H4O4S
[MDL Number]

MFCD00221769
[MOL File]

1072-53-3.mol
[Molecular Weight]

124.12
Chemical PropertiesBack Directory
[Melting point ]

95-97 °C(lit.)
[Boiling point ]

231.1±7.0℃ (760 Torr)
[density ]

1.604±0.06 g/cm3 (20 ºC 760 Torr)
[vapor pressure ]

0.91-1.7Pa at 20-25℃
[refractive index ]

1.5090 (estimate)
[Fp ]

93.5±18.2℃
[storage temp. ]

2-8°C
[solubility ]

Chloroform, Methanol
[form ]

solid
[color ]

White to Off-White
[InChI]

InChI=1S/C2H4O4S/c3-7(4)5-1-2-6-7/h1-2H2
[InChIKey]

ZPFAVCIQZKRBGF-UHFFFAOYSA-N
[SMILES]

C1OS(=O)(=O)OC1
[LogP]

-0.45 at 23℃ and pH1.4-1.7
[Surface tension]

66.8mN/m at 1g/L and 20℃
Safety DataBack Directory
[Risk Statements ]

22
[WGK Germany ]

3
[RTECS ]

JH4800000
[HS Code ]

29209085
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Xylene-->1,2-Dibromoethane-->Silver sulfate
[Preparation Products]

2-Iodoethanol-->1H-Pyrazole-5-ethanol, 1-phenyl--->10:2 FTOH Sulfate PotassiuM Salt-->2-cyclobutoxyethanol-->3-ethyloxolan-2-one
Hazard InformationBack Directory
[Chemical Properties]

White Solid
[Uses]

1,3,2-Dioxathiolane 2,2-Dioxide is an alkylating agent with carcinogenic activty.
[Synthesis]

Cyclic sulfates of 1,2-diols (1,3,2-dioxathiolane 2,2-dioxides) are most easily prepared in a two-step procedure (eq 1). The reaction of a 1,2-diol with Thionyl Chloride leads to a cyclic sulfite, which is then oxidized to the corresponding cyclic sulfate (1). Direct conversion of a 1,2-diol to a cyclic sulfate using Sulfuryl Chloride is generally less efficient.
ETHYLENESULFATE
[Toxics Screening Level]

The initial threshold screening level (ITSL) for 1,3,2-dioxathiolane,2,2-dioxide (CAS #1072-53-3) is 0.1 μg/m3 annual averaging time.
[Precautions]

The structural similarity between cyclic sulfates and Dimethyl Sulfate must be recognized. Dimethyl sulfate, and to a lesser extent, ethylene sulfate, are carcinogenic and potent alkylating agents that are toxic by inhalation and ingestion. Cyclic sulfates must, as a result, be treated with extreme care.
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