Succinyl chloride
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| Names | |
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| Preferred IUPAC name Butanedioyl dichloride | |
| Other names Succinic acid dichloride, succinoyl dichloride | |
| Identifiers | |
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| ECHA InfoCard | 100.008.035  |
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InChI
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| Properties | |
Chemical formula | C4H4Cl2O2 |
| Molar mass | 154.97 g·mol−1 |
| Appearance | colorless liquid |
| Density | 1.41 g·ml−1 |
| Melting point | 15–18 °C (59–64 °F; 288–291 K) |
| Boiling point | 190 °C (374 °F; 463 K) |
Solubility in water | Reacts violently with water |
| Hazards | |
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| Danger | |
Hazard statements | H227, H314 |
Precautionary statements | P280, P303+P361+P353, P305+P351+P338, P310, P405 |
| Flash point | 76 °C (169 °F; 349 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references | |
Chemical compound
Succinyl chloride is the organic compound with the formula (CH2)2(COCl)2.[1] It is the acyl chloride derivative of succinic acid and a simple diacid chloride. It is a colorless liquid. It used as a reagent in organic synthesis.
References
- ^ "Butanedioyl dichloride". US National Library of Medicine. Retrieved 13 April 2019.
External links
- Fisher Scientific Data
- MSDS Safety Data
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Diacyl chlorides (-COCl)2
- Oxalyl chloride C2O2Cl2
- Malonyl chloride C3H2Cl2O2
- Succinyl chloride C4H4Cl2O2
- Glutaryl chloride C5H6Cl2O2
- Adipoyl chloride C6H8Cl2O2
- Pimeloyl chloride C7H10Cl2O2
- Suberoyl chloride C8H12Cl2O2
- Azelaoyl chloride C9H14Cl2O2
- Sebacoyl chloride C10H16Cl2O2
Category:Acyl chlorides
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