76-22-2
76-22-2 structure
- Name: (+/-)-Camphor
- Chemical Name: camphor
- CAS Number: 76-22-2
- Molecular Formula: C10H16O
- Molecular Weight: 152.233
- Catalog: Organic raw materials Hydrocarbon compounds and their derivatives Cyclic hydrocarbon
- Create Date: 2018-07-07 20:09:32
- Modify Date: 2026-06-30 22:14:13
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Camphor ((±)-Camphor) is a topical anti-infective and anti-pruritic and internally as a stimulant and carminative. However, Camphor is poisonous when ingested. Antiviral, antitussive, and anticancer activities[1]. Camphor is a TRPV3 agonist[2].
| Name | camphor |
|---|---|
| Synonyms |
(+)-bornan-2-one
camphanone 1,7,7-trimethyl-bicyclo(2.2.1)htan-2-on 3-Fluor-2,2-dimethyl-bicyclo<2.2.1>heptan component of Campho-phenique 1,7,7-trimethyl-norcampho CAMPHORATEDMETACRESOL component of Campho-phenique cold sore gel (±)-Camphor, 1,7,7-Trimethylbicyclo[2.2.1]htan-2-one 2-Oxo-bornan 2-Bornanone,2-Camphanone,D-Camphor lphanon DL-2-Bornanone D-(+)-Camphor Bornane, 2-oxo Alphanon Synthetic camphor powder 2-Camphanone DL-Camphor Camphor (8CI) Camphen-hydrofluorid CAMPHOR SYNTHETIC FLAKES CAMPHOR . ADE (-)-Camphor (à)-Camphor bicyclo[2.2.1]htan-2-one,1,7,7-trimethyl component of Campho-phenique liquid 1,7,7-Trimethylbicyclo[2.2.1]htan-2-one (+/-)-Camphor meets analytical specification of Ph.Eur., BP, >= , racemic EINECS 200-945-0 Dehydrocamphor (1R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one D(+)-Camphor 2-Bornanone 2-Camphanone camphre Camphor,(±)-Camphor, 1,7,7-Trimethylbicyclo[2.2.1]htan-2-one Bicyclo[2.2.1]htane-2-one, 1,7,7-trimethyl 2-oxo-bornan 2-Keto-1,7,7-trimethylnorcamphane 1,7,7-trimethyl-bicyclo[2.2.1]htan-2-on 1,7,7-Trimethylnorcamphor CAMPHOR SYNTHETIC POWDER camphor-natural camphor,natural (1S,4S)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-one bicyclo[2.2.1]htan-2-one,1,7,7,-trimethyl-,(±) 1,7,7-Trimethylbicyclo[2.2.1]-2-heptanone Bicyclo[2.2.1]htan-2-one, 1,7,7-trimethyl 2-Kamfanon (+/-)-CaMphor , synthetic, >= D-CAMPHOR Camphor 5 (±)-bornan-2-one component of Heet 2-Bornanone Radian B METHYLBENZYLIDENE Bicyclo[2,2,1]htan-2-one,1,7,7-trimethyl 2-Camphanonoe MFCD00676613 L(-)-Camphor refined camphor powder 1,7,7-Trimethylbicyclo[2.2.1]heptan-2-one CAMPHOR SPIRITS Bornan-2-one (1RS,4RS)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one Caladryl 2-Keto-1,7,7-trimethylnolcamphane (−)-Camphor,(1S)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-one 2-CAMPHOR CHINESENASALOIL (±)-Camphor 2-Camphonone 1,7,7-Trimethylbicyclo[2.2.1]-2-htanone Camphor (+)-CaMphor 2-Bornanone,2-Camphanone Kampfer 1,7,7-trimethylbicyclo[2.2.1]-2-htanone (camphor) CAMPHOR SQUES SYNTHETIC (+)-Camphor,(1R)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-one (1S)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-one Ordiny camphor 1,7,7-Trimethyl bicyclo(2,2,1)-2-htanone 2-oxobornane |
| Description | Camphor ((±)-Camphor) is a topical anti-infective and anti-pruritic and internally as a stimulant and carminative. However, Camphor is poisonous when ingested. Antiviral, antitussive, and anticancer activities[1]. Camphor is a TRPV3 agonist[2]. |
|---|---|
| Related Catalog | |
| Target |
TRPV3[2] |
| In Vitro | Camphor induces fibroblast proliferation through the PI3K/AKT and ERK signaling pathways. The MTT assay results show that 32.5, 65, 130, and 260 μM Camphor increase fibroblast viability to 108.9±6.6%, 118.6±2.8%, 127.7±4.2%, and 131.6±7.2%, respectively, compared to 0 μM Camphor treatment. Camphor treatment for 24 h increases the generation of ROS by up to 17.97% compared to 5.04% in the no-treatment control[3]. |
| Cell Assay | Primary dermal fibroblast (2×104 cells/mL) cells are plated in 96-well plates in 200μL of medium containing 10% FBS. After 24 h, the cells are treated with various concentrations of chamomile hydrosol or Camphor (0-260 μM). After treatment, 20 μL of MTT solution (5mg/mL) is added to each well, followed by incubation in a humidified environment for 3-4 h. The supernatant is removed and 150 μL of DMSO is added. Cell viability is determined from the absorbance at 570 nm, measured using a Sunrise microplate reader[3]. |
| References |
| Density | 1.0±0.1 g/cm3 |
|---|---|
| Boiling Point | 207.4±0.0 °C at 760 mmHg |
| Melting Point | 175-177 °C(lit.) |
| 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 |
| Stability | Stable. Combustible. Incompatible with strong oxidizing agents, metallic salts, combustible materials, organics. |
| Water Solubility | 0.12 g/100 mL (25 ºC) |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
MUTATION DATA
|
| Symbol |
GHS02, GHS07, GHS08 |
|---|---|
| Signal Word | Warning |
| Hazard Statements | H228-H302 + H332-H371 |
| Precautionary Statements | P210-P260-P301 + P312 + P330-P370 + P378 |
| Target Organs | Lungs |
| Personal Protective Equipment | dust mask type N95 (US);Eyeshields;full-face particle respirator type N100 (US);Gloves;respirator cartridge type N100 (US);type P1 (EN143) respirator filter;type P3 (EN 143) respirator cartridges |
| Hazard Codes | F:Flammable |
| Risk Phrases | R11;R36/37/38 |
| Safety Phrases | S16-S26-S37/39 |
| RIDADR | UN 2717 4.1/PG 3 |
| WGK Germany | 1 |
| RTECS | EX1225000 |
| Packaging Group | III |
| Hazard Class | 4.1 |
| HS Code | 2914291000 |
| Precursor 9 | |
|---|---|
| DownStream 9 | |
![()-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one oxime structure](https://image.chemsrc.com/caspic/300/18674-50-5.png)
![4',7',7'-trimethylspiro[1,3-dithiolane-2,3'-bicyclo[2.2.1]heptane] structure](https://image.chemsrc.com/caspic/379/6787-91-3.png)
| HS Code | 2914291000 |
|---|