(±)-Camphor
Modify Date: 2026-07-01 11:34:43
(±)-Camphor structure
|
Common Name | (±)-Camphor | ||
|---|---|---|---|---|
| CAS Number | 21368-68-3 | Molecular Weight | 152.233 | |
| Density | 1.0±0.1 g/cm3 | Boiling Point | 207.4±0.0 °C at 760 mmHg | |
| Molecular Formula | C10H16O | Melting Point | 175ºC | |
| MSDS | N/A | Flash Point | 64.4±0.0 °C | |
Use of (±)-Camphor |
| Name | DL-Camphor |
|---|---|
| Synonym | More Synonyms |
| Density | 1.0±0.1 g/cm3 |
|---|---|
| Boiling Point | 207.4±0.0 °C at 760 mmHg |
| Melting Point | 175ºC |
| Molecular Formula | C10H16O |
| Molecular Weight | 152.233 |
| Flash Point | 64.4±0.0 °C |
| Exact Mass | 152.120117 |
| PSA | 17.07000 |
| LogP | 2.13 |
| Vapour density | 5.2 (vs air) |
| Vapour Pressure | 0.2±0.4 mmHg at 25°C |
| Index of Refraction | 1.485 |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
|
| Hazard Codes | Xn |
|---|---|
| Risk Phrases | R22 |
| Safety Phrases | S26-S37/39 |
| RIDADR | UN 2717 4.1/PG 3 |
| WGK Germany | 1 |
| RTECS | EX1225000 |
| Packaging Group | II |
| Hazard Class | 6.1 |
| HS Code | 2914291000 |
| HS Code | 2914291000 |
|---|
|
Name: Fluorescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id: CHRM1_AG_FLUO8_1536_1X%ACT PRUN
|
|
Name: Cytochrome P450 Family 1 Subfamily A Member 2 (CYP1A2) small molecule antagonists: lu...
Source: 824
External Id: CYP273
|
|
Name: Mouse TRPA1 (Transient Receptor Potential channels)
Source: IUPHAR-DB
Target: TRPA1 (Transient Receptor Potential channels) [Mus musculus]
External Id: 485_Mouse
|
|
Name: Fluorescence-based cell-based primary high throughput screening assay to identify pos...
Source: The Scripps Research Institute Molecular Screening Center
Target: muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id: CHRM1_PAM_FLUO8_1536_1X%ACT PRUN
|
|
Name: Hedgehog Measured in Biochemical System Using Plate Reader - 2070-01_Inhibitor_Single...
Source: Broad Institute
Target: hedgehog, isoform A [Drosophila melanogaster]
External Id: 2070-01_Inhibitor_SinglePoint_HTS_Activity
|
|
Name: qHTS Assay for Small Molecule Inhibitors of the Human hERG Channel Activity
Source: NCGC
External Id: HERG01
|
|
Name: Human TRPV1 (Transient Receptor Potential channels)
Source: IUPHAR-DB
Target: TRPV1 (Transient Receptor Potential channels) [Homo sapiens]
External Id: 507_Human
|
|
Name: qHTS for Inhibitors of TGF-b: Cytotox Counterscreen
Source: NCGC
Target: N/A
External Id: SMAD3201
|
|
Name: Antioxidant activity assessed as DPPH radical scavenging activity
Source: ChEMBL
Target: N/A
External Id: CHEMBL1005721
|
|
Name: uHTS identification of cystic fibrosis induced NFkb Inhibitors in a fluoresence assay
Source: Burnham Center for Chemical Genomics
Target: cystic fibrosis transmembrane conductance regulator [Homo sapiens]
External Id: SBCCG-A764-CF-PAF-Primary-Assay
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| MFCD00074738 |
| 1,7,7-Trimethylbicyclo[2.2.1]heptan-2-one |
| DL-Camphor |
| Camphen-hydrofluorid |
| 3-Fluor-2,2-dimethyl-bicyclo<2.2.1>heptan |
| 2-Keto-1,7,7-trimethylnolcamphane |
| EINECS 200-945-0 |
| 2-Oxo-bornan |
| (±)-Camphor |
| 2-Camphonone |
| Dehydrocamphor |
| Camphor |
| DL-2-Bornanone |