(+/-)-Camphor structure
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Common Name | (+/-)-Camphor | ||
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CAS Number | 76-22-2 | 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 | 175-177 °C(lit.) | |
MSDS | Chinese USA | Flash Point | 64.4±0.0 °C | |
Symbol |
GHS02, GHS07, GHS08 |
Signal Word | Warning |
Use of (+/-)-CamphorCamphor ((±)-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 |
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Synonym | More Synonyms |
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]. |
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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 |
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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 |
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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 | |
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DownStream 9 | |
HS Code | 2914291000 |
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(+)-bornan-2-one |
Bicyclo(2.2.1)heptan-2-one, 1,7,7-trimethyl- |
camphanone |
3-Fluor-2,2-dimethyl-bicyclo<2.2.1>heptan |
(1S,4S)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-one |
1,7,7-Trimethylbicyclo[2.2.1]-2-heptanone |
2-Kamfanon |
D-CAMPHOR |
(±)-bornan-2-one |
2-Oxo-bornan |
2-Bornanone,2-Camphanone,D-Camphor |
Radian B |
lphanon |
DL-2-Bornanone |
D-(+)-Camphor |
MFCD00676613 |
Alphanon |
L(-)-Camphor |
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-one |
DL-Camphor |
Camphen-hydrofluorid |
(1RS,4RS)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one |
Caladryl |
(-)-Camphor |
2-Keto-1,7,7-trimethylnolcamphane |
Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl- |
(−)-Camphor,(1S)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-one |
2-CAMPHOR |
EINECS 200-945-0 |
(±)-Camphor |
2-Camphonone |
Dehydrocamphor |
Camphor |
(+)-CaMphor |
(1R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one |
2-Bornanone,2-Camphanone |
D(+)-Camphor |
2-Bornanone 2-Camphanone |
Kampfer |
(+)-Camphor,(1R)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-one |
camphre |
(1S)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-one |