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Camphor Powder Synthetic
Camphor is said to have been first used as a drug in the Arabian Peninsula around AD 600, and, eventually came to be used as a sacred panacea in Greece and Egypt.
In those days, camphor was obtained only from camphor wood (this product is known as natural camphor). In the 1920's, however, a mass-production synthesis method was developed in which camphor is obtained from rosin-derived turpentine oil. Currently, virtually all camphor is produced by this synthesis process.
Therefore, camphor is categorized into natural camphor and synthetic camphor.
| Synthetic camphor Turpentine oil originating from rosin is synthesized and processed into camphor. |
Natural camphor Camphor wood is subjected to a steam distillation process to obtain camphor. |
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Typical applications of camphor according to properties
1. Chemical properties : Celluloid
2. Sublimation: Insect repellent
3. Tackiness: Binder of metal powder sintering
4. Pharmacodinamic effect: Plaster, cardiotonic
5. Other properties: Raw material for perfume, fragrant pouch
If any enquiry on this product, please feel free to contact us via info@asiaron.com
Item Index Chemical Name (DL)-Camphor; Camphor; Camphor Synthetic; (+-)-Camphor; Camphor, synthetic; 2-Bornanone; 2-Camphonone; 2-Camphanone; 2-Bornanone;
Bicyclo(2,2,1)heptan-2-one, 1,7,7-trimethyl-; Gum Camphor; 1,7,7-Trimethylbicyclo[2,2,1]heptan-2-one; 1,7,7-Trimethylbicyclo[2.2.1]-2-heptanone; 1,7,7-Trimethylbicyclo[2.2.1]heptan-2-one; Caladryl; 2-Kamfanon; 2-Keto-1,7,7-trimethylnorcamphane; 2-Oxobornane; Huile de camphre (French); Kampfer ([German); 1,7,7-Trimethylnorcamphor;Molecular Formula C 10 H 16 O CAS No. 76-22-2 Chemical Formula Molecular Weight 152.24 RTECS EX1225000 TSCA TSCA 8(b) inventory: Camphor (DL) Appearance white powder crystals
Item Index Appearance white powder crystals Water content its 10% (W/V) petroleum spirit solution is clear Involatile substance 0.05% max. alcohol unsolvable substance 0.01% max. Melting point 168 °C min. Purity 96% min. sulfuric acid color not heavier than 1/600 ??? ???
| Item | Index |
| Appearance | white powder crystals |
| Identification | up to the test |
| Melting point | 170 °C min. |
| Specific optical rotation | [α°]D -2° - +5° |
| Chlorinity | 355 ppm max. |
| Purity | 96% max. |
| ??? | ??? |
| Item | Index |
| Appearance | white powder crystals |
| Identification | up to the test |
| Melting point | 174-179 °C |
| Purity | 96.0%-101.0% |
| Water content | the solution (1g/20Ml anhydrous ether) is clear |
| Acidity or alkalinnity | up to the test |
| Involatile substance | 0.1% max. |
| ??? | ??? |
| Item | Index |
| Appearance | white powder crystals |
| Identification | up to the test |
| Melting point | 174-180 °C |
| Solubility | 2.5g sample is soluble in 10Ml alcohol and diluted to 25Ml with solvent clear |
| Purity | 96.0% min. |
| Water content | the solution (1g/10Ml petroleum spirit) is clear |
| Acidity or alkalinnity | up to the test |
| Addition material | up to the test |
| Halogens | 100 ppm max. |
| Evaporate residue | 0.05% max. |
| ??? | ??? |
| Item | Index |
| Appearance | colorless or white crystalline powder |
| Identification | up to the test |
| Melting point | 175-180 °C |
| Purity | 96.0% min. |
| Specific optical rotation | [a]D20-1.5°- +1.5° |
| ??? | ??? |
| Item | Index |
| Appearance | colorless transparent crystals |
| Identification | up to the test |
| Melting point | 174-181 °C |
| Solubility | sample is soluble in water (1/700) or 96% alcohol (1/1) or chloroform (1/0.25) |
| Specific optical rotation | [a]D20-1.5°- +1.5° |
| Purity | 96.0% min. |
| Water content | the solution (1g/10Ml petroleum spirit) is clear during boiling range, 40-60 °C |
| Involatile substance | 0.1% max. |
| ??? | ??? |
| Item | Index |
| Appearance | white powder crystals |
| Melting point | 174-179 °C |
| Specific optical rotation | optically inactive, racemic form |
| Purity | 96.0% min. |
| Water content | the solution (1g/10Ml Hexane) is clear |
| Halogens | 0.035% max. |
| Involatile substance | 0.05% max. |
| ??? | ??? |
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