cis-Butene-1,4-diol is a chemical compound used in the production of endosulfan. It reacts with hexachlorocyclopentadiene to form endosulfan diol. Endosulfan diol then reacts with thionyl chloride to form endosulfan.[1]
Quick Facts Names, Identifiers ...
cis-Butene-1,4-diol
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| Names |
| Preferred IUPAC name
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| Identifiers |
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| ChemSpider |
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| ECHA InfoCard |
100.025.532 |
| EC Number |
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| UNII |
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InChI=1S/C4H8O2/c5-3-1-2-4-6/h1-2,5-6H,3-4H2/b2-1- Key: ORTVZLZNOYNASJ-UPHRSURJSA-N
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| Properties |
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C4H8O2 |
| Molar mass |
88.106 g·mol−1 |
| Density |
1.07 |
| Melting point |
7 °C (45 °F; 280 K) |
| Boiling point |
141–149 °C (286–300 °F; 414–422 K) |
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very soluble |
| Solubility |
ethanol, acetone |
| Hazards |
| GHS labelling: |
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Warning |
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H302, H315, H319, H335 |
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P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P340, P305+P351+P338, P312, P321, P330, P332+P313, P337+P313, P362, P403+P233, P405, P501 |
| Flash point |
128 °C (262 °F; 401 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). |
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