CAS 1072-21-5

Hexanedial

Description:

Hexanedial, also known as adipaldehyde, is an organic compound characterized by its linear chain structure consisting of six carbon atoms with aldehyde functional groups at both ends. Its molecular formula is C6H10O2, and it is classified as a dialdehyde. Hexanedial is a colorless to pale yellow liquid with a distinct, pungent odor. It is soluble in water and organic solvents, making it versatile in various chemical applications. The compound is primarily used in the synthesis of polymers, resins, and as an intermediate in the production of other chemicals. Hexanedial can undergo typical aldehyde reactions, such as oxidation and condensation, and is known for its reactivity due to the presence of the aldehyde groups. Safety considerations include its potential irritant effects on the skin and respiratory system, necessitating proper handling and storage protocols. Overall, hexanedial is an important compound in organic chemistry and industrial applications.

Formula: C₆H₁₀O₂

InChI: InChI=1S/C6H10O2/c7-5-3-1-2-4-6-8/h5-6H,1-4H2

InChI key: InChIKey=UMHJEEQLYBKSAN-UHFFFAOYSA-N

SMILES: C(CCC=O)CC=O

Synonyms:

• 1,4-Butane dicarboxaldehyde
• 1,6-Hexanedial
• 214-003-1
• Adipic aldehyde
• Adipic dialdehyde
• Adipindialdehyde
• Adipodialdehyde
• Hexanedial
• Hexanedialdehyde
• Adipaldehyde

Adipaldehyde

CAS: 1072-21-5

Formula: C₆H₁₀O₂

Purity: 95%

Color and Shape: Solid

Molecular weight: 114.1424

Ref: IN-DA008XMM

Adipaldehyde

CAS: 1072-21-5

Adipaldehyde

Purity: 1M in H2O

Molecular weight: 114.14g/mol

Ref: 54-OR1024969

Adipaldehyde - 1M solution in water

CAS: 1072-21-5

Succinaldehyde is a white crystalline solid that is soluble in water and alcohol. Succinaldehyde has been shown to be an effective catalyst for the polymerization of polyvinyl chloride, which is used in the production of plastics. It also functions as a cross-linking agent for insoluble polymers, such as collagen. Succinaldehyde has been shown to inhibit t-cell leukemia in mice by inducing apoptosis. This reaction mechanism involves the formation of aldehyde groups on lysine residues within the protein structure, which then react with hydroxyl groups on other lysines or peptides. This reaction leads to covalent bonding between adjacent amino acids and the formation of a stable cross-linked network that results in apoptosis. The function of succinaldehyde as a solid catalyst for this reaction can be attributed to its low volatility and high boiling point.

Formula: C₆H₁₀O₂

Color and Shape: Brown Powder

Molecular weight: 114.14 g/mol

Ref: 3D-FA150571