1,3,2-Dioxathiolane 2,2-dioxide supplier

Name
ETHYLENESULFATE
EINECS 600-809-4
CAS No. 1072-53-3
Article Data48
CAS DataBase
Density 1.604 g/cm³
Solubility
Melting Point 95-97 °C(lit.)
Formula C2H4 O4 S
Boiling Point 231.1 °C at 760 mmHg
Molecular Weight 124.117
Flash Point 93.5 °C
Transport Information
Appearance yellowish crystal
Safety Questionable carcinogen with experimental tumorigenic and neoplastigenic data. Mutation data reported. When heated to decomposition it emits toxic fumes of SO_x. See also SULFATES and ESTERS.
Risk Codes 22
Molecular Structure
Hazard Symbols
Synonyms Ethyleneglycol, cyclic sulfate (8CI); Ethylene sulfate (((CH2O)2SO2)) (6CI,7CI);1,2-Ethylene sulfate; Ethylene sulfate; NSC 526594
PSA 60.98000
LogP 0.35880

Synthetic route

: 75-21-8
oxirane

: 1072-53-3
ethyleneglycol sulfate

Conditions

Conditions	Yield
With cerium(IV) oxide; iron(III) chloride; sulfur dioxide; antimony(III) chloride at 140℃; under 45004.5 Torr; for 2h; Pressure; Temperature; Inert atmosphere; Autoclave;	97.8%
With aminosulfonic acid; acetic anhydride at -10 - 20℃; for 24h; Autoclave;	73.22%

: 107-21-1
ethylene glycol

: 1072-53-3
ethyleneglycol sulfate

Conditions

Conditions	Yield
With fluorosulfonyl fluoride; N,N,N,N,-tetramethylethylenediamine In acetonitrile at 60℃; for 36h; Reagent/catalyst; Solvent; Temperature;	96.5%
Stage #1: ethylene glycol With fluorosulfonyl fluoride; sodium sulfate; tetra(n-butyl)ammonium hydrogensulfate; sodium hydroxide In tert-butyl methyl ether at 5 - 10℃; for 1h; Autoclave; Stage #2: With 15-crown-5; 18-crown-6 ether In dichloromethane Solvent; Reagent/catalyst; Temperature;	81.8%
With potassium hydroxide; sulfuryl dichloride; silica gel 1.) reflux; 2.) rt., 3 h; Yield given. Multistep reaction;
Stage #1: ethylene glycol With potassium hydroxide In 5,5-dimethyl-1,3-cyclohexadiene at 130 - 140℃; for 20h; Stage #2: With fluorosulfonyl fluoride In acetonitrile at -15 - -5℃; for 1h; Temperature; Reagent/catalyst; Solvent; Sealed tube; Inert atmosphere;	106.3 g
With sulfuryl dichloride In chloroform at 5 - 60℃; for 3h;	375 g

: 3741-38-6
ethylene sulfite

: 1072-53-3
ethyleneglycol sulfate

Conditions

Conditions	Yield
With manganese(IV) oxide In water at 5℃; for 0.75h; Reagent/catalyst; Temperature;	95.84%
With sodium hydrogencarbonate; iron(II) sulfate In dichloromethane pH=7 - 8; Concentration;	90.66%
With ruthenium trichloride; calcium hypochlorite at 15℃;	83%

: 74-85-1
ethene

: 1072-53-3
ethyleneglycol sulfate

Conditions

Conditions	Yield
With PhI(1+)OSO2O(1-) In dichloromethane at 15℃; for 0.3h;	85%
With μ-oxodiphenyldiiodine(III) sulfate; phenyliodine(III) sulfate Yield given;

: 96-49-1
[1,3]-dioxolan-2-one

: 1072-53-3
ethyleneglycol sulfate

Conditions

Conditions	Yield
With carbon dioxide; sulfur trioxide at 25 - 65℃; for 8h; Inert atmosphere;	76%

: 7719-09-7
thionyl chloride

: 107-21-1
ethylene glycol

: 1072-53-3
ethyleneglycol sulfate

Conditions

Conditions	Yield
Stage #1: thionyl chloride; ethylene glycol at 25 - 30℃; for 3h; Inert atmosphere; Stage #2: With sodium hypochlorite; ruthenium(III) chloride trihydrate at 0 - 10℃; for 3h; pH=7-8; Concentration; Temperature;	74%

: C2H5ClO3S

: 1072-53-3
ethyleneglycol sulfate

Conditions

Conditions	Yield
With sodium periodate; ruthenium(III) chloride trihydrate In water; acetonitrile for 0.25h; Cooling with ice; Inert atmosphere;	70%

: 106-93-4
ethylene dibromide

: 1072-53-3
ethyleneglycol sulfate

Conditions

Conditions	Yield
With silver sulfate; xylene
With silver sulfate In xylene

: 3741-38-6
ethylene sulfite

: ruthenium (IV) oxide dihydrate

: 1072-53-3
ethyleneglycol sulfate

Conditions

Conditions	Yield
With sodium hypochlorite In dichloromethane; isopropyl alcohol

: 23248-21-7, 26982-08-1, 31283-39-3, 53651-66-4, 59733-01-6
potassium ethyleneglycolate

: 1072-53-3
ethyleneglycol sulfate

Conditions

Conditions	Yield
Stage #1: potassium ethyleneglycolate With sulfuryl dichloride In dichloromethane at -10 - 10℃; for 2h; Inert atmosphere; Stage #2: With 18-crown-6 ether In toluene at 20℃; for 1h; Reagent/catalyst; Solvent;	37.9 g

: 74-84-0
ethane

A: 1072-53-3
ethyleneglycol sulfate

B: 6914-91-6
ethane-1,2-diyl bis(hydrogen sulfate)

Conditions

Conditions	Yield
With fuming sulphuric acid; iodine at 90℃; under 22502.3 Torr; for 2h; Catalytic behavior; Reagent/catalyst; Temperature; Autoclave;

: 1072-53-3
ethyleneglycol sulfate

: 14990-09-1
tert-butyl cinnamate

: C12H20NSi(1-)*Li(1+)

: 1394979-11-3
(-)-tert-butyl (2S,3R)-1-benzyl-2-phenylpyrrolidine-3-carboxylate

Conditions

Conditions	Yield
Stage #1: C12H20NSi(1-)*Li(1+) With (1S,2S)-1,2-dimethoxy-1,2-diphenylethane In toluene at -78℃; for 0.583333h; Stage #2: tert-butyl cinnamate In toluene at -78℃; for 1.63h; Stage #3: ethyleneglycol sulfate enantioselective reaction; Further stages;	97%

...Expand

: 1072-53-3
ethyleneglycol sulfate

: 5205-93-6
2-methyl-acrylic acid 3-dimethylamino-propyl amide

: 2-((3-methacrylamidopropyl)dimethylammonio)ethyl sulfate

Conditions

Conditions	Yield
With nitrobenzene In acetonitrile at 50℃; for 24h; Schlenk technique; Inert atmosphere;	95.6%

: 1072-53-3
ethyleneglycol sulfate

: 1535-65-5
difluoromethyl phenyl sulfone

: 3,3-difluoro-3-(phenylsulfonyl)propan-1-ol

Conditions

Conditions	Yield
With N,N,N,N,N,N-hexamethylphosphoric triamide; sulfuric acid; lithium hexamethyldisilazane In tetrahydrofuran; water at 20℃; for 2h;	94%
Stage #1: ethyleneglycol sulfate; difluoromethyl phenyl sulfone With N,N,N,N,N,N-hexamethylphosphoric triamide; lithium hexamethyldisilazane In tetrahydrofuran at -78 - 20℃; for 3.5h; Inert atmosphere; Stage #2: With sulfuric acid In tetrahydrofuran at 60℃;	90%

: 16587-47-6
6-methylbenzo[b]thiophene

: 1072-53-3
ethyleneglycol sulfate

: 873692-99-0
2-(6-methyl-benzo[b]thiophen-2-yl)-ethanol

Conditions

Conditions	Yield
Stage #1: 6-methylbenzo[b]thiophene With n-butyllithium In tetrahydrofuran; hexanes at -60℃; for 0.75h; Stage #2: ethyleneglycol sulfate In tetrahydrofuran; hexanes at -60 - 20℃; Stage #3: With acetyl chloride In methanol at 0 - 20℃; for 4.25h;	89%

: 616-47-7
1-methyl-1H-imidazole

: 1072-53-3
ethyleneglycol sulfate

: 65567-06-8, 4541-02-0
lithium diphenylphosphide

: 2-(2-(diphenylphosphino)ethyl)-1-methyl-1H-imidazol

Conditions

Conditions	Yield
Stage #1: 1-methyl-1H-imidazole With n-butyllithium In tetrahydrofuran; hexane at -78 - 60℃; Inert atmosphere; Stage #2: ethyleneglycol sulfate In tetrahydrofuran; hexane at -78 - 0℃; Inert atmosphere; Stage #3: lithium diphenylphosphide In tetrahydrofuran; hexane at 0℃; Inert atmosphere; Reflux;	89%

...Expand

: 1072-53-3
ethyleneglycol sulfate

: 113975-22-7
2-fluoro-3-iodopyridine

: 1620011-25-7
2-(2-fluoro-4-iodopyridin-3-yl)ethane-1-ol

Conditions

Conditions	Yield
Stage #1: 2-fluoro-3-iodopyridine With lithium diisopropyl amide In tetrahydrofuran; n-heptane at -78℃; for 1.5h; Stage #2: ethyleneglycol sulfate In tetrahydrofuran; n-heptane at -78 - 20℃; for 2.33333h; Stage #3: With hydrogenchloride In tetrahydrofuran; n-heptane; water at 0 - 20℃; for 3h;	87%
Stage #1: 2-fluoro-3-iodopyridine With lithium diisopropyl amide In tetrahydrofuran; n-heptane; ethylbenzene at -78℃; for 1.5h; Stage #2: ethyleneglycol sulfate In tetrahydrofuran; n-heptane; ethylbenzene at -78 - 30℃; for 2.67h; Stage #3: With hydrogenchloride; water In tetrahydrofuran; n-heptane; ethylbenzene at 0 - 30℃; for 3h;	87%

: 1072-53-3
ethyleneglycol sulfate

: 22282-70-8
2-fluoro-4-iodopyridine

: 1620011-25-7
2-(2-fluoro-4-iodopyridin-3-yl)ethane-1-ol

Conditions

Conditions	Yield
Stage #1: 2-fluoro-4-iodopyridine With lithium diisopropyl amide In tetrahydrofuran; n-heptane; ethylbenzene at -78℃; for 1.5h; Stage #2: ethyleneglycol sulfate In tetrahydrofuran; n-heptane; ethylbenzene at -78 - 20℃; for 2.66667h; Stage #3: With hydrogenchloride In tetrahydrofuran; n-heptane; ethylbenzene; water at 0 - 20℃; for 3h;	87%
Stage #1: 2-fluoro-4-iodopyridine With lithium diisopropyl amide In tetrahydrofuran at -65℃; for 1.5h; Inert atmosphere; Stage #2: ethyleneglycol sulfate In tetrahydrofuran at -65 - 20℃; Inert atmosphere;	86.2%
Stage #1: 2-fluoro-4-iodopyridine With lithium diisopropyl amide In tetrahydrofuran; n-heptane; ethylbenzene at -78℃; for 1.5h; Stage #2: ethyleneglycol sulfate In tetrahydrofuran; n-heptane; ethylbenzene at -78 - 20℃; for 2.67h;	1950 mg

: 1072-53-3
ethyleneglycol sulfate

: 1191028-34-8
2,2-bis((decyloxy)methyl)propane-1,3-diol

: disodium 5,5-bis(decyloxymethyl)-3,7-dioxa-1,9-nonadiyl disulfate

Conditions

Conditions	Yield
Stage #1: 2,2-bis((decyloxy)methyl)propane-1,3-diol With sodium hydride In tetrahydrofuran; mineral oil for 0.5h; Cooling with ice; Stage #2: ethyleneglycol sulfate In tetrahydrofuran; mineral oil at 20℃; for 26h;	86%
Stage #1: 2,2-bis((decyloxy)methyl)propane-1,3-diol With sodium hydride In tetrahydrofuran; mineral oil for 0.5h; Cooling with ice; Stage #2: ethyleneglycol sulfate In tetrahydrofuran; mineral oil for 24.33h;

: 1072-53-3
ethyleneglycol sulfate

: 113939-45-0
1-bromo-4-(2-bromo-1,1,2,2-tetrafluoroethoxy)benzene

: 4-(4-bromophenoxy)-3,3,4,4-tetrafluorobutan-1-ol

Conditions

Conditions	Yield
Stage #1: 1-bromo-4-(2-bromo-1,1,2,2-tetrafluoroethoxy)benzene With TurboGrignard In tetrahydrofuran at -78℃; Inert atmosphere; Schlenk technique; Stage #2: ethyleneglycol sulfate In tetrahydrofuran at -78 - 20℃; for 3h; Inert atmosphere; Schlenk technique; Stage #3: With sulfuric acid In water Inert atmosphere; Schlenk technique; Reflux;	86%

: 1072-53-3
ethyleneglycol sulfate

: 8-cyclosporin

: C64H114N11O17S(1-)*Na(1+)

Conditions

Conditions	Yield
With sodium hydride In tetrahydrofuran at 30℃; for 2h;	85%

: 1072-53-3
ethyleneglycol sulfate

: 91631-71-9
1-methyl-2-((trimethylsilyl)methyl)-1H-imidazole

: 65567-06-8, 4541-02-0
lithium diphenylphosphide

: 2-(2-(diphenylphosphino)ethyl)-1-methyl-1H-imidazol

Conditions

Conditions	Yield
Stage #1: ethyleneglycol sulfate; 1-methyl-2-[(trimethylsilyl)methyl]-1H-imidazole In tetrahydrofuran at -78 - 100℃; for 6h; Stage #2: lithium diphenylphosphide at -78℃; Reflux;	85%

...Expand

: 1072-53-3
ethyleneglycol sulfate

: 1333108-98-7
(3S)-4-(4,6-dichloropyrimidin-2-yl)-3-methylmorpholine

: 2-{4,6-dichloro-2-[(3S)-3-methylmorpholin-4-yl]pyrimidin-5-yl}ethanol

Conditions

Conditions	Yield
Stage #1: (3S)-4-(4,6-dichloropyrimidin-2-yl)-3-methylmorpholine With n-butyllithium In tetrahydrofuran at -78℃; for 0.5h; Stage #2: ethyleneglycol sulfate In tetrahydrofuran for 0.5h; Stage #3: With hydrogenchloride In tetrahydrofuran; water at 40℃; for 22h;	85%

: 1072-53-3
ethyleneglycol sulfate

: benzyl N-[2-[2-(cyanomethyl)phenoxy]ethyl]-N-methylcarbamate

: benzyl N-[2-[2-(1-cyanocyclopropyl)phenoxy]ethyl]-N-methylcarbamate

Conditions

Conditions	Yield
Stage #1: benzyl N-[2-[2-(cyanomethyl)phenoxy]ethyl]-N-methylcarbamate With sodium hydroxide In dimethyl sulfoxide at 20 - 25℃; for 0.166667h; Stage #2: ethyleneglycol sulfate In tetrahydrofuran; dimethyl sulfoxide at 20 - 25℃; for 16h;	84.6%

: 10397-13-4
4,6-dichloro-2-(morpholine-4-yl)pyrimidine

: 1072-53-3
ethyleneglycol sulfate

: 2-[4,6-dichloro-2-(morpholin-4-yl)pyrimidin-5-yl]ethanol

Conditions

Conditions	Yield
Stage #1: 4,6-dichloro-2-(morpholine-4-yl)pyrimidine With n-butyllithium In tetrahydrofuran; hexane at -65℃; for 0.5h; Inert atmosphere; Stage #2: ethyleneglycol sulfate In tetrahydrofuran; hexane at -65℃; for 1.5h; Stage #3: With hydrogenchloride In tetrahydrofuran; hexane; water at 20℃; for 18h;	84%
Stage #1: 4,6-dichloro-2-(morpholine-4-yl)pyrimidine With n-butyllithium In tetrahydrofuran at -78℃; for 0.5h; Stage #2: ethyleneglycol sulfate In tetrahydrofuran for 0.666667h; Stage #3: With hydrogenchloride In tetrahydrofuran; water at 20 - 40℃; for 22h;	42%

: 2,2-bis((dodecyloxy)methyl)propane-1,3-diol

: 1072-53-3
ethyleneglycol sulfate

: disodium 5,5-bis(dodecyloxymethyl)-3,7-dioxa-1,9-nonadiyl disulfate

Conditions

Conditions	Yield
Stage #1: 2,2-bis((dodecyloxy)methyl)propane-1,3-diol With sodium hydride In tetrahydrofuran; mineral oil for 0.5h; Cooling with ice; Stage #2: ethyleneglycol sulfate In tetrahydrofuran; mineral oil at 20℃;	83.3%
Stage #1: 2,2-bis((dodecyloxy)methyl)propane-1,3-diol With sodium hydride In tetrahydrofuran; mineral oil for 0.5h; Cooling with ice; Stage #2: ethyleneglycol sulfate In tetrahydrofuran; mineral oil at 20℃; for 21h;	83%

: 1072-53-3
ethyleneglycol sulfate

: 14990-09-1
tert-butyl cinnamate

: 113709-50-5
Lithium N-benzyl-N-(trimethylsilyl)amide

: 1394979-19-1
(-)-tert-butyl (2S,3R)-1-benzyl-2-phenylazetidine-3-carboxylate

Conditions

Conditions	Yield
Stage #1: Lithium N-benzyl-N-(trimethylsilyl)amide With (1S,2S)-1,2-dimethoxy-1,2-diphenylethane In toluene at -78℃; for 0.583333h; Stage #2: tert-butyl cinnamate In toluene at -78℃; for 1.63h; Stage #3: ethyleneglycol sulfate enantioselective reaction; Further stages;	82%

...Expand

: 1072-53-3
ethyleneglycol sulfate

: (μ-1,3-propanedithiolate)Fe2(CO)4[μ-3-(Ph2P)2NC5H4N]

: (μ-1,3-propanedithiolate)Fe2(CO)4[μ-3-(Ph2P)2NC5H4N((CH2)2OSO3)]

Conditions

Conditions	Yield
In acetonitrile for 8h; Inert atmosphere; Schlenk technique; Reflux;	81%

: 1072-53-3
ethyleneglycol sulfate

: 51643-96-0
N,N-dibenzylamino-acetonitrile

: 137360-51-1
1-<(dibenzyl)amino>cyclopropanecarbonitrile

Conditions

Conditions	Yield
With N,N,N,N,N,N-hexamethylphosphoric triamide; lithium diisopropyl amide In tetrahydrofuran at -70℃;	80%
With N,N,N,N,N,N-hexamethylphosphoric triamide; lithium diisopropyl amide In tetrahydrofuran at -70℃; for 1.5h; Product distribution; further dielectophiles; access to cyclopropane aminonitriles;
With N,N,N,N,N,N-hexamethylphosphoric triamide; lithium diisopropyl amide In tetrahydrofuran at -70℃; for 1.5h; Yield given;

: 1072-53-3
ethyleneglycol sulfate

: 22204-53-1
(2S)-2-(6-methoxy(2-naphthyl))propanoic acid

: (S)-naproxen ethyl sulfate potassium salt

Conditions

Conditions	Yield
With potassium tert-butylate In isopropyl alcohol at 45℃; for 0.166667h;	80%

: 1072-53-3
ethyleneglycol sulfate

: bis(2-phenylpyridinato-N,C2)-mono(4-[hydroxymethyl]-2-pyridine carboxylato-N,O)iridium(III)

: 1112-67-0
tetrabutyl-ammonium chloride

: 1119493-11-6
tetra-n-butylammonium bis(2-phenylpyridinato-N,C2)-mono(4-[sulfatoethyloxymethyl]-2-pyridinecarboxylato-N,O)iridium(III)

Conditions

Conditions	Yield
With NaH In N,N-dimethyl-formamide (N2, in the absence of light); a soln. of Ir complex stirred at 0°C for 30 min, NaH added, stirred at room temp. for 16 h, (CH2O)2SO2 added, stirred for 12 h; concd., pptd. in Et2O, dissolved in CH2Cl2, added to an aq. soln. of N(C4H9)4Cl, stirred for 16 h, the org. layer sepd., washed (H2O), dried (MgSO4), concd., pptd. in Et2O; elem. anal.;	80%

...Expand

: 1072-53-3
ethyleneglycol sulfate

: methyl 2-(pyrimidin-5-yl)acetate

: methyl 1-(pyrimidin-5- yl)cyclopropane-1-carboxylate

Conditions

Conditions	Yield
Stage #1: methyl 2-(pyrimidin-5-yl)acetate With lithium hexamethyldisilazane In tetrahydrofuran at -70℃; for 1h; Stage #2: ethyleneglycol sulfate In tetrahydrofuran at -70 - -20℃; for 1.5h; Stage #3: With lithium hexamethyldisilazane In tetrahydrofuran at -72 - 20℃; for 15h;	80%

: 188290-36-0
thiophene

: 1072-53-3
ethyleneglycol sulfate

: 5402-55-1
2-thiophenethanol

Conditions

Conditions	Yield
Stage #1: thiophene With n-butyllithium In tetrahydrofuran; hexane at -78℃; Stage #2: ethyleneglycol sulfate In tetrahydrofuran; hexane at -78 - 20℃; Stage #3: With sulfuric acid In tetrahydrofuran; hexane for 3h; Heating; Further stages.;	79%

: 1072-53-3
ethyleneglycol sulfate

: 95-15-8
Benzo[b]thiophene

: 30962-69-7
2-(β-Hydroxyethyl)-benzothiophene

Conditions

Conditions	Yield
Stage #1: Benzo[b]thiophene In tetrahydrofuran; hexanes at -50 - -40℃; for 0.75h; Stage #2: ethyleneglycol sulfate In tetrahydrofuran; hexanes at -40 - 20℃; Stage #3: With acetyl chloride In methanol at 20℃; for 4.25h;	79%

: 1072-53-3
ethyleneglycol sulfate

: 2723-38-8
cyclopentylacetic acid methyl ester

: 3-cyclopentyldihydrofuran-2(3H)-one

Conditions

Conditions	Yield
Stage #1: cyclopentylacetic acid methyl ester With lithium diisopropyl amide In tetrahydrofuran at -78℃; Stage #2: ethyleneglycol sulfate In tetrahydrofuran at -78 - 20℃; for 5h; Stage #3: With sulfuric acid In toluene Reflux;	79%

: 1072-53-3
ethyleneglycol sulfate

: 20491-53-6
di-isopropylphosphine

: 829-85-6
diphenylphosphane

: 262359-83-1
(CH(CH3)2)2PCH2CH2P(C6H5)2

Conditions

Conditions	Yield
Multistep reaction;	76%

...Expand

1,3,2-Dioxathiolane 2,2-dioxide Chemical Properties

IUPAC Name: 1,3,2-Dioxathiolane 2,2-dioxide
The MF of 1,3,2-Dioxathiolane 2,2-dioxide (CAS NO.1072-53-3) is C₂H₄O₄S.

The MW of 1,3,2-Dioxathiolane 2,2-dioxide (CAS NO.1072-53-3) is 124.12.
Synonyms of 1,3,2-Dioxathiolane 2,2-dioxide (CAS NO.1072-53-3): Ethylene glycol, cyclic sulphate ; 1,3,2-Dioxathiolane 2,2-dioxide ; Sulfuric acid, cyclic ethylene ester
Product Categories: Biphenyl & Diphenyl ether;Heterocyclic Compounds;Heterocyclic Building Blocks;Others;S-Containing
Index of Refraction: 1.469
Density: 1.604 g/ml
Flash Point: 93.5 °C
Boiling Point: 231.1 °C
Melting Point: 95-97 °C
Storage temp: 2-8 °C

1,3,2-Dioxathiolane 2,2-dioxide Production

Raw materials: Xylene-->1,2-Dibromoethane-->Silver sulfate

1,3,2-Dioxathiolane 2,2-dioxide Toxicity Data With Reference

1.		mmo-sat 1 µmol/plate		CBINA8 Chemico-Biological Interactions. 19 (1977),241.
2.		hma-mus/sat 5 mmol/kg		CBINA8 Chemico-Biological Interactions. 19 (1977),241.

1,3,2-Dioxathiolane 2,2-dioxide Consensus Reports

EPA Genetic Toxicology Program.

1,3,2-Dioxathiolane 2,2-dioxide Safety Profile

Questionable carcinogen with experimental tumorigenic and neoplastigenic data. Mutation data reported. When heated to decomposition it emits toxic fumes of SO_x. See also SULFATES and ESTERS.Safety information of 1,3,2-Dioxathiolane 2,2-dioxide (CAS NO.1072-53-3):
WGK Germany 3
RTECS JH4800000

Product Name

ETHYLENESULFATE

Synthetic route

1,3,2-Dioxathiolane 2,2-dioxide Chemical Properties

1,3,2-Dioxathiolane 2,2-dioxide Production

1,3,2-Dioxathiolane 2,2-dioxide Toxicity Data With Reference

1,3,2-Dioxathiolane 2,2-dioxide Consensus Reports

1,3,2-Dioxathiolane 2,2-dioxide Safety Profile

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