Product Name: |
Natural Camphor |
CAS: |
76-22-2 |
MF: |
C10H16O |
MW: |
152.23 |
EINECS: |
200-945-0 |
Mol File: |
76-22-2.mol |
|
Melting point |
175-177 °C(lit.) |
Boiling point |
204 °C(lit.) |
density |
0.992 |
vapor density |
5.2 (vs air) |
vapor pressure |
4 mm Hg ( 70 °C) |
FEMA |
4513 | dl-CAMPHOR |
refractive index |
1.5462 (estimate) |
Fp |
148 °F |
storage temp. |
Store below +30°C. |
solubility |
Soluble in acetone, ethanol, diethylether, chloroform and acetic acid. |
form |
neat |
explosive limit |
0.6-4.5%(V) |
optical activity |
[α]20/D +0.15 to -0.15°, c = 10% in ethanol |
Water Solubility |
0.12 g/100 mL (25 ºC) |
JECFA Number |
2199 |
Merck |
14,1732 |
BRN |
1907611 |
Henry's Law Constant |
(x 10-5 atm?m3/mol): 3.00 at 20 °C (approximate - calculated from water solubility and vapor pressure) |
Exposure limits |
TLV-TWA 12 mg/m3 (2 ppm), STEL 18 mg/m3 (3 ppm) (ACGIH); IDLH 200 mg/m3 (NIOSH). . |
Stability: |
Stable. Combustible. Incompatible with strong oxidizing agents, metallic salts, combustible materials, organics. |
InChIKey |
DSSYKIVIOFKYAU-MHPPCMCBSA-N |
CAS DataBase Reference |
76-22-2(CAS DataBase Reference) |
NIST Chemistry Reference |
Camphor(76-22-2) |
EPA Substance Registry System |
Camphor (76-22-2) |
Hazard Codes |
F,Xn,Xi |
Risk Statements |
11-22-36/37/38-20/21/22 |
Safety Statements |
16-26-37/39 |
RIDADR |
UN 2717 4.1/PG 3 |
WGK Germany |
1 |
RTECS |
EX1225000 |
Autoignition Temperature |
870 °F |
TSCA |
Yes |
HazardClass |
4.1 |
PackingGroup |
III |
HS Code |
29142910 |
Hazardous Substances Data |
76-22-2(Hazardous Substances Data) |
Toxicity |
LD50 orally in mice: 1.3 g/kg (PB293505) |
Interactions |
There are no known mild, moderate or severe drug interactions associated with Camphor. However, if a doctor or pharmacist suggests that one can use camphor while on certain medications, then they are aware of potential drug interactions and they could be putting the patient on observation. One should always notify their doctor or pharmacist if they have health concerns or questions related to camphor. |
Side Effects |
Common side effects associated with Camphor include skin irritation and
redness, burning sensation in the throat and mouth, vomiting, nausea, Lip
dryness, rashes, eczema, seizures, respiratory issues, toxicity, scalp issues
and chest problems. |
Warning |
Cinnamomum camphora, Lodine and cemphire should not be prescribed to a
person who is allergic to camphor or its constituent ingredients. |
Chemical Properties |
Both optical isomers are found widely in nature, with (+)-camphor being
the more abundant. It is, for example, the main component of oils obtained
from the camphor tree C. camphora. Camphor is produced by fractional
distillation and crystallization of camphor oil or, synthetically, by
dehydrogenation of isoborneol over a copper catalyst. |
Chemical Properties |
Camphor, C1oH160, also known as d-2-camphanone, Japan camphor, laurel camphor,Formosa camphor,and gumcamphor,is a terpene ketone. It is colourless solid with a characteristic odour that is obtained from the wood and bark of the camphor tree and is soluble in water and alcohol. It has two optically active forms (dextro and levo) and an optically inactive mixture (racemic) of these two forms. Camphor is used in pharmaceuticals,in disinfectants, in explosives,and to harden nitrocellulose plastics. |
Chemical Properties |
Camphor is a colorless glassy solid. Penetrating, characteristic odor. |
Physical properties |
Colorless to white, flammable granules, crystals or waxy semi-solid with a strong, penetrating, fragrant or aromatic odor. Odor threshold concentration is 0.27 ppm (quoted, Amoore and Hautala, 1983). |
Uses |
dl-Camphor is used as a plasticizer for celluloseesters and ethers; in the manufacture ofplastics and cymene; in cosmetics, lacquers,medicine, explosives, and pyrotechnics; andas a moth repellent. |
Uses |
Antipruritic. |
Uses |
camphor (Cinnamomum camphora) is credited with anesthetic, antiinflammatory, antiseptic, astringent, cooling, and refreshing properties, and thought to be slightly stimulating to blood circulation and function. once absorbed by the subcutaneous tissue, it combines in the body with glucoronic acid and is released through the urine. Camphor is effective for oily and acne skin treatment, and has a scent similar to eucalyptus. In high concentrations, it can be an irritant and numb the peripheral sensory nerves. natural camphor is derived from an evergreen tree indigenous to Asia, although now its synthetic substitute is often used. |
Definition |
A ketone occurring naturally in the wood of the cam- phor tree (Cinnamomum camphora). |
Definition |
A naturally- occurring white organic compound with a characteristic penetrating odor. It is a cyclic compound and a ketone, formerly obtained from the wood of the camphor tree but now made synthetically. Camphor is used as a platicizer for celluloid and as an insecticide against clothes moths. |
Definition |
camphor: A white crystalline cyclicketone, C10H16O; r.d. 0.99; m.p.179°C; b.p. 204°C. It was formerly obtainedfrom the wood of the Formosancamphor tree, but can now besynthesized. The compound has acharacteristic odour associated withits use in mothballs. It is a plasticizerin celluloid. |
Brand name |
Anbesol;Cresophene;Dasin;Ddd;Endrine;Makatussin;Mentol sedans sulfamidad;Nasello;Resol;Root bark oil;Spirit of camphor;Tcp;Tetesept;Topic. |
World Health Organization (WHO) |
Camphor, an aromatic crystalline substance with mild local anaesthetic activity, is available in preparations for both external application and inhalation. The use of such preparations has precipitated convulsions in susceptible infants. This has led several regulatory authorities to require the inclusion of appropriate warnings on labelling. |
General Description |
A colorless or white colored crystalline powder with a strong mothball-like odor. About the same density as water. Emits flammable vapors above 150°F. Used to make moth proofings, pharmaceuticals, and flavorings. |
Air & Water Reactions |
Highly flammable. Slightly soluble in water. |
Reactivity Profile |
Naphthalene, Camphor, glycerol, or turpentine will react violently with chromic anhydride [Haz. Chem. Data 1967 p. 68]. |
Hazard |
Evolves flammable and explosive vapors when heated. Eye and upper respiratory tract irri- tant, and anosmia. Questionable carcinogen. |
Health Hazard |
Vapors of camphor can irritate the eyes, nose,and throat. In humans, such
irritation may be felt at >3 ppm concentration. Prolongedexposure can
cause headache, dizziness, andloss of sense of smell. Ingestion can
causeheadache, nausea, vomiting, and diarrhea,and at high dosages can lead to
convulsion,dyspnea, and coma. High dosages can beharmful to gastrointestinal
tracts, kidney,and brain. |
Health Hazard |
Fire may produce irritating and/or toxic gases. Contact may cause burns to skin and eyes. Contact with molten substance may cause severe burns to skin and eyes. Runoff from fire control may cause pollution. |
Fire Hazard |
Flammable/combustible material. May be ignited by friction, heat, sparks or flames. Some may burn rapidly with flare burning effect. Powders, dusts, shavings, borings, turnings or cuttings may explode or burn with explosive violence. Substance may be transported in a molten form at a temperature that may be above its flash point. May re-ignite after fire is extinguished. |
Safety Profile |
A human poison by ingestion and possibly other routes. An experimental poison by inhalation, subcutaneous, and intraperitoneal routes. A local irritant. Ingestion causes nausea, vomiting, dizziness, excitation, and convulsions. Mutation data reported. Used |
Potential Exposure |
Camphor, a natural product, is used as a plasticizer for cellulose esters and ethers; it is used in lacquers and varnishes; and in explosives and pyrotechnics formulations. It is used as a moth repellent and as a medicinal. |
Source |
Major component in pine oil (quoted, Verschueren, 1983). Also present in a variety of rosemary shoots (330–3,290 ppm) (Soriano-Cano et al., 1993), anise-scented basil leaves (1,785 ppm) (Brophy et al., 1993), Iberian savory leaves (2,660 ppm) (Arrebola et al., 1994), African blue basil shoots (7,000 ppm), Greek sage (160–5,040 ppm), Montane Mountain mint (3,395–3,880 ppm), yarrow leaves (45–1,780 ppm), and coriander (100–1,300 ppm) (Duke, 1992). |
Shipping |
UN2717 Camphor, synthetic, Hazard Class: 4.1; Labels: 4.1-Flammable solid. UN1130 camphor oil, Hazard Class: 3; Labels: 3-Flammable liquid |
Incompatibilities |
May form explosive mixture with air. Violent, possibly explosive, reaction with strong oxidizers, especially chromic anhydride, potassium permanganate. May accumulate static electrical charges, and may cause ignition of its vapors. |
Waste Disposal |
ncineration of a solution in a flammable solven. |