44601-24-3

Basic information

• Product Name: 4-hydroxypentanal
• Synonyms: 4-Hydroxypentanal
• CAS NO: 44601-24-3
• Molecular Formula: C₅H₁₀O₂
• Molecular Weight: 102.1317
• Mol File: 44601-24-3.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 193.6°C at 760 mmHg
• Flash Point: 75°C
• Density: 0.961g/cm³
• Vapor Pressure: 0.121mmHg at 25°C
• Refractive Index: 1.42
• CAS DataBase Reference: 4-hydroxypentanal(CAS DataBase Reference)
• NIST Chemistry Reference: 4-hydroxypentanal(44601-24-3)
• EPA Substance Registry System: 4-hydroxypentanal(44601-24-3)

Safety Data

• Hazardous Substances Data: 44601-24-3(Hazardous Substances Data)

Usage

Description

4-hydroxypentanal, also known as 4-hydroxyvaleraldehyde, is a chemical compound with the molecular formula C5H10O2. It is a derivative of pentanal with a hydroxyl group attached to the fourth carbon atom. This aldehyde is known for its slight sweet and fruity odor, commonly found in natural sources such as fruits and honey.

Uses

Used in Flavor and Fragrance Industry:
4-hydroxypentanal is used as a flavoring agent and fragrance component for its pleasant aroma, contributing to the creation of various scents and tastes in products like perfumes, food, and beverages.
Used in Organic Synthesis:
In the field of organic synthesis, 4-hydroxypentanal is utilized as a chemical intermediate for the production of a wide range of other compounds, showcasing its versatility in chemical reactions.
Used in Pharmaceutical Industry:
4-hydroxypentanal has potential applications in the pharmaceutical industry, where it may be employed in the development of new drugs or as a component in existing medications, thanks to its unique chemical structure.
Used in Material Development:
Additionally, 4-hydroxypentanal is involved in the development of new materials, where its properties can be leveraged to create innovative products with specific characteristics and applications.

Upstream product

• 626-95-9 1,4-Pentanediol 
• 13311-76-7 5-Hepten-2-ol 

Downstream Products

• 108-29-2 5-methyl-dihydro-furan-2-one 
• 63088-78-8 (2S,5R)-5-hydroxypiperidine-2-carboxylic acid 
• 117836-26-7 cis-5(S)-hydroxy-2(S)-N₁-benzyloxycarbonylpipecolic acid methyl ester 
• 917507-80-3 (2S,5S)-N-[(benzyloxy)carbonyl]-5-hydroxy-2-piperidinecarboxylic acid 
• 117836-13-2 (S)-5-Oxo-piperidine-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester 
• 824943-45-5 (2S,5R)-5-hydroxy-6-methoxy-piperidine-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester 
• 227758-97-6 (2S)-3,4-dihydro-2H-pyridine-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester 
• 154061-64-0 (2S)-2-<(Benzyloxycarbonyl)amino>-6-hydroxyhexanoic acid methyl ester 
• 448957-53-7 N-benzyl-4-hydroxypentylamine 
• 1311159-06-4 C₂₈H₃₇NOSi 

Relevant articles and documents

Fe(III)-porphyrin heterogenized on MCM-41: Matrix effects on the oxidation of 1,4-pentanediol

The metal complex iron meso-tetrakis (2,6-dichlorophenyl)porphyrin (Fe IIIP) has been covalently linked on the surface of the mesoporous material MCM-41 and of amorphous SiO2 to give the photocatalysts FeIIIP/MCM-41 and FeIIIP/SiO2 respectively. The effect of porphyrin addition on specific surface area and porosity of these materials has been evaluated by means of BET and BJH model applied to N 2 adsorption/desorption isotherms. It is seen that the MCM-41 sample presents the largest modification due to the presence of porphyrin: the pore size changes in average value and distribution, the pores formed in the presence of porphyrin being smaller and presenting a larger distribution. The photochemical characterization of FeIIIP/MCM-41 reveals that this is a robust photocatalyst able to induce the O2-assisted oxidation of 1,4-pentanediol. In particular, photoexcitation of FeIIIP/MCM-41 causes the conversion of 1,4-pentanediol to the aldehyde derivative compound with 70% regioselectivity. It is noteworthy that this product can be accumulated with no formation of further oxidized compounds. Due to its high specific surface area, which guarantees a good dispersion of the active centres, Fe IIIP/MCM-41 is about four times more efficient than Fe IIIP/SiO2. Moreover, the nature of the support controls the regioselectivity of the photocatalytic process: this is due to both uptake phenomena and steric effects, which can control the approach of the diol to the photoactive iron porphyrin.

Regioselectivity in the Semiconductor-Mediated Photooxidation of 1,4-Pentanediol

Optimum conditions have been established for the selective semiconductor-photocatalyzed oxidation by long-wavelength ultraviolet light of the primary alcohol functionality in 1,4-pentanediol.On platinized (2percent) TiO2 powder suspended in oxygenated aqueous (4 vol percent) acetonitrile, the initial rate ratio for oxidation of the primary/secondary alcohol site was > 7.Analysis of further oxidation products allowed for mechanistic delineation of the course of the semiconductor-mediated reaction.The selectivity is attributed to the essential role of adsorption, with the criticalphotoinduced electron transfer occurring at the surface of the irradiated particle.ZrO2 and SnO2 samples were much less active than TiO2 as photocatalysts.The effects of oxygen pressure, metal cocatalyst loading, and water content of acetonitrile are discussed.