pramocaine
- CAS No.
- 140-65-8
- Chemical Name:
- pramocaine
- Synonyms
- Pramoxin;Tronotene;pramocaine;Tronothane;Tronopthane;Proxazocain;4-[3-(4-Butoxyphenoxy)propyl]morphorine;4-(3-(4-BUTOXYPHENOXY)PROPYL)-MORPHOLINE;Morpholine, 4-[3-(4-butoxyphenoxy)propyl]-;p-Butoxyphenyl gamma-morpholinopropyl ether
- CBNumber:
- CB1895935
- Molecular Formula:
- C17H27NO3
- Molecular Weight:
- 293.4
- MDL Number:
- MFCD00864456
- MOL File:
- 140-65-8.mol
| Boiling point | bp6 196°; bp2.8 183-184° |
|---|---|
| Density | 1.0112 (rough estimate) |
| refractive index | 1.5420 (estimate) |
| pka | 7.18±0.10(Predicted) |
| Water Solubility | 3.574mg/L(22.5 ºC) |
| CAS DataBase Reference | 140-65-8 |
| FDA UNII | 068X84E056 |
| ATC code | C05AD07,D04AB07 |
pramocaine Chemical Properties,Uses,Production
Originator
Tronothane, Abbott, US ,1954
Uses
Anesthetic (topical).
Definition
ChEBI: A member of the class of morpholines that is morpholine substituted at the nitrogen atom by a 3-(4-butoxyphenoxy)propyl group.
Manufacturing Process
About 5.6 g of potassium hydroxide is dissolved in about 150 cc of refluxing ethanol, and then about 16.6 g of hydroquinone monobutyl ether is added to the alcoholic solution. When the hydroquinone is dissolved, about 16.3 g of γmorpholinopropyl chloride (dissolved in a small amount of ethanol) is added to the refluxing solution. The solution is refluxed for about 24 hours and then cooled. The product is recovered by filtering the reaction mixture and then removing the solvent by vacuum distillation. The oily residue is acidified and shaken with ether. The acidic phase is made strongly alkaline with 40% sodium hydroxide, and the oil which separates is extracted into ether. The ethereal phase is dried, and the solvent removed by vacuum distillation. The product distills at 183° to 184°C at a pressure of 2.8 mm. The hydrochloride salt of the foregoing base is prepared by dissolving the base in ether and acidifying with hydrochloric acid and is found to have a MP of 181° to 183°C.
brand name
Tronolane (Ross); Tronothane (Abbott).
Therapeutic Function
Local anesthetic
pramocaine Preparation Products And Raw materials
| Supplier | Tel | Country | ProdList | Advantage | |
|---|---|---|---|---|---|
| Hubei Jusheng Technology Co.,Ltd. | 18871490254 | linda@hubeijusheng.com | CHINA | 28180 | 58 |
| Alfa Chemistry | +1-5166625404 | Info@alfa-chemistry.com | United States | 21317 | 58 |
| Shaanxi Didu New Materials Co. Ltd | +86-89586680 +86-13289823923 | 1026@dideu.com | China | 9165 | 58 |
| LGM Pharma | 1-(800)-881-8210 | inquiries@lgmpharma.com | United States | 2127 | 70 |
| BOC Sciences | 1-631-485-4226; 16314854226 | info@bocsci.com | United States | 14059 | 65 |
| Beijing HuaMeiHuLiBiological Chemical | 010-56205725 | waley188@sohu.com | China | 12338 | 58 |
| BOC Sciences | 16314854226 | info@bocsci.com | United States | 9926 | 65 |
| Shenzhen Polymeri Biochemical Technology Co., Ltd. | +86-400-002-6226 13028896684 | sales@rrkchem.com | China | 55717 | 58 |
| Guangzhou Juntang Technology Co., Ltd | 020-36607679 13502246435 | sales@dmstandards.com | China | 10951 | 58 |
| Shanghai Sunway Pharmaceutical Technology Co.,Ltd. | 021-51816796-820 13611835272 | sales2@sunwaypharm.com | China | 44498 | 58 |