5-hydroxypentanal
pentanal, 5-hydroxy-
Identification
| Name | 5-hydroxypentanal |
| CAS Number | 4221-03-8 |
| EINECS | 224-165-5 |
| FDA UNII | Search |
| Molecular Formula | C5 H10 O2 |
| Molecular Weight | 102.13310000 |
| MDL Number | MFCD00044411 |
| Nikkaji Number | J205.645C |
Regulatory
Physical Properties
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Boiling Point | 187.70 °C. @ 760.00 mm Hg (est) |
| Vapor Pressure | 0.200000 mmHg @ 25.00 °C. (est) |
| Flash Point | 162.00 °F. TCC ( 72.00 °C. ) (est) |
| logP (o/w) | -0.600 (est) |
| Soluble in | water, 5.082e+005 mg/L @ 25 °C (est) |
No sensory data available
Safety Information
| Preferred SDS | View |
| Oral/Parenteral Toxicity | Not determined |
| Dermal Toxicity | Not determined |
| Inhalation Toxicity | Not determined |
GHS Classification
['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']
Safety in Use
| Category | information only not used for fragrances or flavors |
| Recommendation for 5-hydroxypentanal usage levels up to | not for fragrance use. |
| Recommendation for 5-hydroxypentanal flavor usage levels up to | not for flavor use. |
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Potential Uses
Natural Occurrence
Synonyms
5-
hydroxyvaleraldehyde
pentanal, 5-hydroxy-
PubMed:
Aerobic and anaerobic metabolism of glutaraldehyde in a river water-sediment system.
PubMed:
Reaction of alpha-acetoxy-N-nitrosopiperidine with deoxyguanosine: oxygen-dependent formation of 4-oxo-2-pentenal and a 1,N2-ethenodeoxyguanosine adduct.
PubMed:
Effect of ascorbic acid and some reducing agents on N-nitrosopiperidine metabolism by liver microsomes.
PubMed:
Synthesis of pseudo cofactor analogues as potential inhibitors of the folate enzymes.
PubMed:
Alpha-hydroxylation in the metabolism of N-nitrosopiperidine by rat liver microsomes: formation of 5-hydroxypentanal.
PubMed:
Preparation of dihydropyran delta-hydroxyvaleraldehyde and 1,5-pentanediol from tetrahydrofurfuryl alcohol.