laevo-camphor
bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-, (1S)-
Identification
| Name | laevo-camphor |
| IUPAC | (1S)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one |
| CAS Number | 464-48-2 |
| EINECS | 207-354-7 |
| FDA UNII | 213N3S8275 |
| Molecular Formula | C10 H16 O |
| Molecular Weight | 152.23672000 |
| MDL Number | MFCD00064148 |
| Beilstein | 1907612 |
Regulatory
Physical Properties
| Appearance | white crystals (est) |
| Assay | 97.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Optical Rotation | -41.00 to -45.00 |
| Melting Point | 178.00 to 180.00 °C. @ 760.00 mm Hg |
| Boiling Point | 207.42 °C. @ 760.00 mm Hg (est) |
| Vapor Pressure | 0.040000 mmHg @ 20.00 °C. |
| Vapor Density | 5.24 ( Air = 1 ) |
| Flash Point | 149.00 °F. TCC ( 65.00 °C. ) |
| logP (o/w) | 2.089 (est) |
| Soluble in | alcohol |
| Insoluble in | water |
Organoleptic Properties
| Odor Description | at 10.00 % in dipropylene glycol. |
Safety Information
| Preferred SDS | View |
| European information | Most important hazard(s): |
| Oral/Parenteral Toxicity | oral-rat LD50 0.80 mg/kg |
| 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', 'Chemical Systems Laboratory, NIOSH Exchange Chemicals. Vol. NX#02534', 'U.S. Army Armament Research & Development Command, Chemical Systems Laboratory, NIOSH Exchange Chemicals. Vol. NX#02534']
Safety in Use
| Category | flavor and fragrance agents |
| RIFM Fragrance Material Safety Assessment | Search |
| Recommendation for laevo-camphor usage levels up to | 5.0000 % in the fragrance concentrate. |
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Potential Uses
Natural Occurrence
Synonyms
(-)-
alcanfor
bicyclo(2.2.1)heptan-2-one, 1,7,7-trimethyl-, (1S,4S)-
bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-, (1S)-
(-)-
bornan-2-one
(-)-2-
bornanone
(1S,4S)-(-)-
camphor
(1S)-
camphor
(1S)-(-)-
camphor
L-
camphor
laevo-(-)-
camphor
camphor, (1S,4S)-(-)-
camphor, L-, (-)-
(1S,4R)-(-)-1,3,3-
trimethyl bicyclo(2.2.1)heptan-2-one
(1S,4S)-1,7,7-
trimethyl bicyclo(2.2.1)heptan-2-one
(1S)-1,7,7-
trimethyl bicyclo(2.2.1)heptan-2-one
(1S)-1,7,7-
trimethylbicyclo[2.2.1]heptan-2-one
PubMed:
Inhibition of cholinesterase by essential oil from food plant.
PubMed:
Topological and experimental approach to the pressure-temperature-composition phase diagram of the binary enantiomer system d- and l-camphor.
PubMed:
Cocrystallization and configurations of myo-inositol-1,2-L-camphor acetals in two crystal structures.
PubMed:
U.v. absorbers in sun cosmetics 1978.
PubMed:
A transmissible plasmid controlling camphor oxidation in Pseudomonas putida.