1-piperidine carboxaldehyde
N-formylpiperidine
Identification
| Name | 1-piperidine carboxaldehyde |
| IUPAC | piperidine-1-carbaldehyde |
| CAS Number | 2591-86-8 |
| EINECS | 219-986-0 |
| FDA UNII | ZIQ29H6CZG |
| Molecular Formula | C6 H11 N O |
| Molecular Weight | 113.15987000 |
| Nikkaji Number | J77.422G |
Regulatory
Physical Properties
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Soluble in | water, 4.582e+004 mg/L @ 25 °C (est) |
No sensory data available
Safety Information
| Oral/Parenteral Toxicity | oral-rat LD50 870 uL/kg |
| Dermal Toxicity | skin-rabbit LD50 840 uL/kg |
| 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 | natural substances and extractives |
| Recommendation for 1-piperidine carboxaldehyde usage levels up to | not for fragrance use. |
| Recommendation for 1-piperidine carboxaldehyde flavor usage levels up to | not for flavor use. |
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Potential Uses
Natural Occurrence
Synonyms
N-
formylpiperidine
piperidine, 1-formyl-
piperidine-1-carbaldehyde
piperidine-N-carbaldehyde
1-
piperidinecarboxaldehyde
PubMed:
Control of the composition of Pt-Ni electrocatalysts in surfactant-free synthesis using neat N-formylpiperidine.
PubMed:
1,3-Diiodocalix[4]arene: synthesis by Ullmann-type iodination of 1,3-bistriflate ester of calix[4]arene, conformational analysis, and transformation into 1,3-dicarboxy-, diformyl-, and dialkylcalix[4]arenes.
PubMed:
Formylation of single-walled carbon nanotubes.
PubMed:
Highly stereoselective asymmetric Pummerer reactions that incorporate intermolecular and intramolecular nonbonded S...O interactions.
PubMed:
Uncompetitive inhibitors of alcohol dehydrogenases.
PubMed:
Binding of formamides to liver alcohol dehydrogenase.
PubMed:
Evaluation of teratogenic potential of N-formylpiperidine in rats.