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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
MSDS File:
SDS
Last updated:2026-05-27 23:49:18

pramocaine Properties

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

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P280-P305+P351+P338
Toxicity LD50 in mice (mg/kg): 300 i.p., 900 s.c. (Monash, Gibbs)

pramocaine price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
aablocks AA009DH7 4-(3-(4-Butoxyphenoxy)propyl)morpholine 95% 140-65-8 250mg $130 2026-05-28 Buy
aablocks AA009DH7 4-(3-(4-Butoxyphenoxy)propyl)morpholine 95% 140-65-8 1g $133 2026-05-28 Buy
aablocks AA009DH7 4-(3-(4-Butoxyphenoxy)propyl)morpholine 95% 140-65-8 5g $137 2026-05-28 Buy
American Custom Chemicals Corporation API0008739 PRAMOXINE 95.00% 140-65-8 5MG $500.54 2021-12-16 Buy
Product number Packaging Price Buy
AA009DH7 250mg $130 Buy
AA009DH7 1g $133 Buy
AA009DH7 5g $137 Buy
API0008739 5MG $500.54 Buy

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

Raw materials

Preparation Products

Global Suppliers ( 21)
Supplier Tel Email Country ProdList Advantage
LGM Pharma 1-(800)-881-8210 inquiries@lgmpharma.com United States 2110 70
Beijing HuaMeiHuLiBiological Chemical 010-56205725 waley188@sohu.com China 12323 58
BOC Sciences 16314854226 info@bocsci.com United States 9909 65
Shenzhen Polymeri Biochemical Technology Co., Ltd. +86-400-002-6226 sales@rrkchem.com China 57336 58
Guangzhou Juntang Technology Co., Ltd 020-36607679 13502246435 sales@dmstandards.com China 10922 58
Shanghai Sunway Pharmaceutical Technology Co.,Ltd. 13611835272 13611835272 mmwang@sunwaypharm.com China 44090 58
Shaanxi DIDU pharmaceutical and Chemical Co., Ltd 029-029-81120477 17792793610 1033@dideu.com China 9990 58
Shandong Hydrocarbon Bio-Chemical Co. LTD 13060081947 13060081947 1581910236@qq.com China 1593 58
Shanghai Yaoheping Biopharmaceutical Technology Co., Ltd 57540919 13120888836 lily@yhp-biomedicine.com China 9248 58
TLC Pharmaceutical Standards Ltd. 18012923235 chinasales04@tlcstandards.com.cn China 8143 58
pramocaine 4-(3-(4-BUTOXYPHENOXY)PROPYL)-MORPHOLINE 4-[3-(4-Butoxyphenoxy)propyl]morphorine Proxazocain Tronopthane Tronothane Tronotene Pramoxin p-Butoxyphenyl gamma-morpholinopropyl ether gamma-Morpholinopropyl 4-n-butoxyphenyl ether Morpholine, 4-[3-(4-butoxyphenoxy)propyl]- 140-65-8 research chemical