CAS 64001-06-5

1-Butanol, 4-[(tetrahydro-2-furanyl)oxy]-

Description:

1-Butanol, 4-[(tetrahydro-2-furanyl)oxy]- is an organic compound characterized by its structure, which features a butanol backbone with a tetrahydro-2-furanyl ether group. This compound is typically a colorless liquid with a moderate boiling point and is soluble in organic solvents. Its molecular structure suggests it may exhibit properties typical of both alcohols and ethers, including potential hydrogen bonding due to the hydroxyl group and ether linkages. The presence of the tetrahydrofuran ring can influence its reactivity and stability, making it of interest in various chemical applications, including as a solvent or intermediate in organic synthesis. Additionally, the compound may have specific applications in the fragrance and flavor industry due to its potential pleasant odor profile. Safety data should be consulted for handling and storage, as with any chemical substance, to ensure proper precautions are taken. Overall, 1-Butanol, 4-[(tetrahydro-2-furanyl)oxy]- represents a unique combination of functional groups that can impart distinctive chemical behavior.

Formula: C₈H₁₆O₃

4-((Tetrahydrofuran-2-yl)oxy)butan-1-ol

CAS: 64001-06-5

Formula: C₈H₁₆O₃

Purity: 96%

Color and Shape: Liquid

Molecular weight: 160.2108

Ref: IN-DA0038KK

4-((Tetrahydrofuran-2-Yl)Oxy)Butan-1-Ol

CAS: 64001-06-5

4-((Tetrahydrofuran-2-Yl)Oxy)Butan-1-Ol

Purity: 95%

Molecular weight: 160.21g/mol

Ref: 54-OR1011093

2-(4-Hydroxybutoxy)tetrahydrofuran

Controlled Product

CAS: 64001-06-5

Applications 2-(4-Hydroxybutoxy)tetrahydrofuran is an impurity of Poly(butylene terephthalate) and a by-product of 1,4-Butanediol.
References Rafler, G., et al.: Acta Polymerica, 39, 661 (1988);

Formula: C₈H₁₆O₃

Color and Shape: Colourless Liquid

Molecular weight: 160.211

Ref: TR-H819500

2-(4-Hydroxybutoxy)tetrahydrofuran

Controlled Product

CAS: 64001-06-5

2-(4-Hydroxybutoxy)tetrahydrofuran is a cyclic ether that is synthesized by the cyclodehydration of 2-butyrolactone. The reaction vessel used for this process must be inert and have an opening with a diameter of 1/8 inch to allow atomization. A catalyst such as sulfuric acid or phosphoric acid is used to promote the reaction and the desired product is obtained in high yield. The liquid phase is then removed from the reaction vessel and the product precipitates out as a white solid, which can then be washed with ether and dried under vacuum. This compound has been shown to have viscosity properties similar to those of tetrahydrofuran, but with a lower vapor pressure and higher boiling point. It also has been shown to react with amines, forming amides.

Formula: C₈H₁₆O₃

Purity: Min. 95%

Molecular weight: 160.21 g/mol

Ref: 3D-PCA00106