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succinic aldehyde
Sign in to saveAlso known as succindialdehyde, succinaldehyde
Succinaldehyde or Butanedial is an organic compound with the formula . It is a colorless viscous liquid. Typical of some other saturated dialdehydes, succinaldehyde is handled as the hydrates or methanol-derived acetal. It is a precursor to tropinone. Succinaldehyde can be used as a crosslinking agent for proteins, but it is less widely used than the related dialdehyde glutaraldehyde.
Chemical data
- Formula
- C4H6O2
- Molecular weight
- 86.09 g/mol
- IUPAC name
- butanedial
- SMILES
- C(CC=O)C=O
- InChIKey
- PCSMJKASWLYICJ-UHFFFAOYSA-N
- XLogP
- -0.9
- Polar surface area
- 34.1 Ų
- H-bond donors
- 0
- H-bond acceptors
- 2
- Formal charge
- 0
via PubChem
Wikidata facts
- Subclass of
- aldehydes
- Mass
- 86.037
Show 4 more facts
- chemical formula
- C₄H₆O₂
- canonical SMILES
- C(CC=O)C=O
- found in taxon
- Phaseolus vulgaris
- Commons category
- Succindialdehyde
Sources (2)
via Wikidata · CC0
~1 min read
Encyclopedic overview
2 sectionsContents
- Preparation and reactions
- References
Succinaldehyde or Butanedial is an organic compound with the formula . It is a colorless viscous liquid. Typical of some other saturated dialdehydes, succinaldehyde is handled as the hydrates or methanol-derived acetal. It is a precursor to tropinone. Succinaldehyde can be used as a crosslinking agent for proteins, but it is less widely used than the related dialdehyde glutaraldehyde.
==Preparation and reactions== thumb|left|2,5-Dihydroxytetrahydrofuran, the hydrated form of succinaldehyde. Succinaldehyde is generated by the oxidation of tetrahydrofuran with chlorine followed by hydrolysis of the chlorinated product. It can also be prepared by the hydroformylation of acrolein or the acetals thereof. Oxidation of 2,5-dimethoxytetrahydrofuran with hydrogen peroxide is yet another route to succinaldehyde.
Excerpted from Wikipedia’s “succinic aldehyde” article, available under the CC BY-SA 4.0 licence.