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Camphor
[CAS# 76-22-2]

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Complete supplier list of Camphor
Identification
Classification Organic raw materials >> Hydrocarbon compounds and their derivatives >> Cyclic hydrocarbon
Name Camphor
Synonyms 1,7,7-Trimethylbicyclo[2.2.1]-2-heptanone; 1,7,7-Trimethylbicyclo[2.2.1]heptan-2-one; 1,7,7-Trimethylnorcamphor; 2-Camphanone; Bornan-2-one; Caladryl; Radian B; DL-Camphor
Molecular Structure CAS # 76-22-2, Camphor, 1,7,7-Trimethylbicyclo[2.2.1]-2-heptanone, 1,7,7-Trimethylbicyclo[2.2.1]heptan-2-one, 1,7,7-Trimethylnorcamphor, 2-Camphanone, Bornan-2-one, Caladryl, Radian B, DL-Camphor
Molecular Formula C10H16O
Molecular Weight 152.23
CAS Registry Number 76-22-2
EC Number 200-945-0
SMILES CC1(C2CCC1(C(=O)C2)C)C
Properties
Solubility 0.12 g/100 mL (water, 25 ºC), soluble (alcohols, ether, chloroform, benzene) (Expl.)
Density 0.992 g/mL (25 ºC) (Expl/)
Melting point 179 ºC (Expl.)
ajpha 23 º (Expl.)
Boiling point 204 ºC (Expl.)
Flash point 64 ºC (Expl.)
Safety Data
Hazard Symbols symbol symbol symbol   GHS02;GHS07;GHS08 Danger    Details
Hazard Statements H228-H302-H315-H332-H371-H373    Details
Precautionary Statements P210-P240-P241-P260-P261-P264-P270-P271-P280-P301+P317-P302+P352-P304+P340-P308+P316-P317-P319-P321-P330-P332+P317-P362+P364-P370+P378-P405-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Flammable solidsFlam. Sol.2H228
Acute toxicityAcute Tox.4H332
Specific target organ toxicity - single exposureSTOT SE2H371
Specific target organ toxicity - repeated exposureSTOT RE2H373
Acute toxicityAcute Tox.4H302
Skin irritationSkin Irrit.2H315
Chronic hazardous to the aquatic environmentAquatic Chronic2H411
Serious eye damageEye Dam.1H318
Eye irritationEye Irrit.2H319
Specific target organ toxicity - single exposureSTOT SE3H335
Reproductive toxicityRepr.1AH360
Flammable liquidsFlam. Liq.2H225
Flammable solidsFlam. Sol.1H228
Skin sensitizationSkin Sens.1H317
Acute toxicityAcute Tox.3H301
Acute toxicityAcute Tox.2H330
Eye irritationEye Irrit.2AH319
Germ cell mutagenicityMuta.2H341
Transport Information UN 2717
SDS Available
up Discovory and Applicatios
Camphor is a terpene-based compound that has been used for centuries, with its first documented use dating back to ancient civilizations. It is derived from the wood of the camphor tree, *Cinnamomum camphora*, a tree native to Southeast Asia, particularly China and Japan. Camphor is a white, crystalline substance with a strong odor, and its chemical structure includes a bicyclic monoterpene framework. It is soluble in alcohol, ether, and chloroform but is insoluble in water.

The discovery of camphor as a useful substance can be traced back to its first recorded use in Chinese medicine, where it was utilized for its medicinal properties. By the 10th century, camphor was known in the Middle East, and its use spread to Europe during the Renaissance. The compound was originally obtained through the distillation of the camphor tree, although today it can be synthesized chemically, often from turpentine or through other processes.

Camphor has a broad range of applications, both in medicine and in other industries. One of the earliest and most well-known uses of camphor was in the treatment of ailments like coughs and colds. It has been used in topical ointments and creams for its cooling and soothing effects. Camphor acts as a counterirritant, meaning it causes irritation in the skin, which leads to a feeling of cooling and pain relief. This property makes it a common ingredient in topical analgesics used for muscle and joint pain relief, as well as in products designed to treat minor burns and insect bites.

In addition to its use as an analgesic, camphor is also employed in the treatment of respiratory conditions. It is a common ingredient in cough syrups, inhalants, and chest rubs due to its ability to act as a mild expectorant, helping to loosen mucus and ease breathing. Camphor's aromatic qualities also contribute to its effectiveness in these applications.

In the pharmaceutical industry, camphor has been used in various topical formulations, including balms and ointments, for its ability to relieve pain and inflammation. It is also utilized in products designed to reduce itching, such as those used to treat rashes or other skin conditions.

Beyond its medicinal uses, camphor has applications in other industries. In the plastics industry, it is used as a plasticizer in the production of celluloid, which is one of the first synthetic plastics. Camphor is also used as a solvent in certain lacquers and varnishes. Its strong, characteristic smell makes it useful in mothballs and insect repellents, where it is used to deter pests from infesting stored clothing and fabrics.

Camphor is also utilized in aromatherapy for its purported calming and stress-relieving effects. It is sometimes included in essential oil blends and used in massages or inhaled as part of a therapeutic regimen. Despite these benefits, camphor should be used with caution, especially in children, as excessive amounts can be toxic. Ingesting large amounts can cause symptoms such as nausea, vomiting, and dizziness, and in severe cases, it can lead to convulsions or even death.

In summary, camphor is a versatile compound with a wide array of applications, particularly in medicine and the chemical industry. Its long history of use in traditional and modern medicine highlights its importance as an analgesic, anti-inflammatory, and respiratory aid. Although camphor remains a popular and effective substance, its use requires care to avoid toxicity, especially in higher concentrations.

References

2025. Synthesis of a new camphor-derived carboxylesterase-activated fluorescent probe for sensitive detection of dimethoate residues in agricultural products and its applications in biological systems. Food Chemistry, 667(1).
DOI: 10.1016/j.foodchem.2024.141625

2025. Embryonal exposure to 4-methylbenzylidene camphor induces reproduction impairment in adult zebrafish (Danio rerio). Comparative Biochemistry and Physiology Part C: Toxicology & Pharmacology, 276(1).
DOI: 10.1016/j.cbpc.2024.110051

2024. A review on botany, ethnobotany, phytochemistry, ethnopharmacology and conservation status of Pinus gerardiana Wall. ex D. Don- The �elixir of life�. Genetic Resources and Crop Evolution, 71(8).
DOI: 10.1007/s10722-024-02293-9
Market Analysis Reports
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Related Products
Camostat mesilate  Campasterol  (1S)-(-)-Camphanic acid  (1S)-(-)-Camphanic acid amide  (-)-Camphanoyl chloride  Camphene  Campholenic aldehyde  (-)-Camphor  D(+)-Camphor  DL-Camphor  D-(+)-Camphoric acid  (-)-Camphoric acid  (1S,E)-(-)-Camphorquinone 3-oxime  L(-)-Camphorsulfonic acid  D-Camphorsulfonic acid  D-(+)-10-Camphorsulfonic acid  (+)-10-Camphorsulfonimine  D(+)-10-Camphorsulfonyl chloride  L(-)-10-Camphorsulfonyl chloride  DL-10-Camphorsulfonyl chloride