CAS 2051-49-2

Hexanoic anhydride

Description:

Hexanoic anhydride, with the CAS number 2051-49-2, is an organic compound that serves as a derivative of hexanoic acid. It is characterized by its anhydride functional group, which is formed by the dehydration of two hexanoic acid molecules. This compound typically appears as a colorless to pale yellow liquid with a distinctive fatty odor. Hexanoic anhydride is soluble in organic solvents but has limited solubility in water due to its hydrophobic nature. It is primarily used in the synthesis of various esters and as an intermediate in the production of surfactants, lubricants, and plasticizers. The compound is reactive, particularly with water, leading to the formation of hexanoic acid upon hydrolysis. Safety precautions are necessary when handling hexanoic anhydride, as it can be irritating to the skin, eyes, and respiratory system. Proper storage in a cool, dry place away from moisture is essential to maintain its stability and prevent unwanted reactions.

Formula: C₁₂H₂₂O₃

InChI: InChI=1S/C12H22O3/c1-3-5-7-9-11(13)15-12(14)10-8-6-4-2/h3-10H2,1-2H3

InChI key: InChIKey=PKHMTIRCAFTBDS-UHFFFAOYSA-N

SMILES: O(C(CCCCC)=O)C(CCCCC)=O

Synonyms:

• Caproic acid anhydride
• Caproic anhydride
• Capronic acid anhydride
• Capronic anhydride
• Hexanoic Acid Anhydride
• Hexanoic acid, 1,1′-anhydride
• Hexanoyl anhydride
• N-hexanoic anhydride
• n-Hexanoic acid anhydride
• Hexanoic anhydride

Hexanoic Anhydride

CAS: 2051-49-2

Formula: C₁₂H₂₂O₃

Purity: >96.0%(GC)

Color and Shape: Colorless to Almost colorless clear liquid

Molecular weight: 214.31

Ref: 3B-C0021

Hexanoic anhydride, 98%

CAS: 2051-49-2

It is used as a reactant in the synthesis of acremomannolipin A. It is used in green synthesis of esters of acyclovir (acyclovir prodrugs), in the preparation of hexanoyl-modified chitosan nanoparticles, chitosan-based polymeric surfactants via N-acylation of chitosans. This Thermo Scientific Chemi

Formula: C₁₂H₂₂O₃

Purity: 98%

Color and Shape: Clear colorless to pale yellow, Liquid

Molecular weight: 214.31

Ref: 02-B23756

Hexanoic acid, 1,1'-anhydride

CAS: 2051-49-2

Formula: C₁₂H₂₂O₃

Purity: 98%

Color and Shape: Liquid

Molecular weight: 214.3013

Ref: IN-DA0029V2

Caproic anhydride

CAS: 2051-49-2

Formula: C₁₂H₂₂O₃

Molecular weight: 214.31

Ref: 7W-GK3260

Hexanoic Anhydride

CAS: 2051-49-2

Purity: 98%(GC-MS);RG

Color and Shape: Liquid, Clear

Molecular weight: 214.3049927

Ref: 10-F875773

Hexanoic Anhydride

Controlled Product

CAS: 2051-49-2

Applications Hexanoic Anhydride, is used as a reactant in the total synthesis of acremomannolipin A via steroselective β-mannosylation of 4,6,-O-benzylidene-protected mannosyl sulfoxide with a D-mannitol derivative.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Tsutsui, N., et al.: Tetrahedron Lett. 54, 451(2013)

Formula: C₁₂H₂₂O₃

Color and Shape: Neat

Molecular weight: 214.3

Ref: TR-H294335

Hexanoic anhydride

CAS: 2051-49-2

Hexanoic anhydride is a reactive chemical that is used to synthesize esters and amides. It has been shown to have strong antibiotic resistance against most strains of bacteria, including methicillin-resistant Staphylococcus aureus (MRSA). Hexanoic anhydride has also been found to have antioxidative properties and antimicrobial activity. The optimum concentration for the reaction with hexanoic acid is 1.5 Molar (M) in order to produce caproic acid and alkanoic acid as products. Hexanoic anhydride reacts with hexanoic acid at its hydroxyl group, forming an acetate extract as a byproduct. This reaction mechanism may be due to ionotropic gelation or electrophilic addition of the hydroxyl group.

Formula: C₁₂H₂₂O₃

Purity: Min. 95%

Color and Shape: Colorless Clear Liquid

Molecular weight: 214.3 g/mol

Ref: 3D-FH35913