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pramocaine

Product Name
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
Formula Weight
293.4
MOL File
140-65-8.mol
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pramocaine Property

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
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Safety

Toxicity
LD50 in mice (mg/kg): 300 i.p., 900 s.c. (Monash, Gibbs)
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

American Custom Chemicals Corporation
Product number
API0008739
Product name
PRAMOXINE
Purity
95.00%
Packaging
5MG
Price
$500.54
Updated
2021/12/16
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pramocaine Chemical Properties,Usage,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

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pramocaine Suppliers

LGM Pharma
Tel
1-(800)-881-8210
Fax
615-250-9817
Email
inquiries@lgmpharma.com
Country
United States
ProdList
2123
Advantage
70
BOC Sciences
Tel
1-631-485-4226; 16314854226
Email
info@bocsci.com
Country
United States
ProdList
14055
Advantage
65
Beijing HuaMeiHuLiBiological Chemical
Tel
010-56205725
Fax
010-65763397
Email
waley188@sohu.com
Country
China
ProdList
12335
Advantage
58
BOC Sciences
Tel
16314854226
Email
info@bocsci.com
Country
United States
ProdList
9923
Advantage
65
Shenzhen Polymeri Biochemical Technology Co., Ltd.
Tel
+86-400-002-6226 +86-13028896684;
Email
sales@rrkchem.com
Country
China
ProdList
57412
Advantage
58
Alfa Chemistry
Tel
Fax
1-516-927-0118
Email
Info@alfa-chemistry.com
Country
United States
ProdList
24072
Advantage
58
Hubei Jusheng Technology Co.,Ltd.
Tel
18871490254
Fax
027-59599243
Email
linda@hubeijusheng.com
Country
CHINA
ProdList
28172
Advantage
58
Guangzhou Juntang Technology Co., Ltd
Tel
020-36607679 13502246435
Email
sales@dmstandards.com
Country
China
ProdList
10945
Advantage
58
Shanghai Sunway Pharmaceutical Technology Co.,Ltd.
Tel
021-51816796-820 13611835272
Fax
021-5161 3951
Email
sales2@sunwaypharm.com
Country
China
ProdList
44458
Advantage
58
Shaanxi DIDU pharmaceutical and Chemical Co., Ltd
Tel
15229059051
Email
1027@dideu.com
Country
China
ProdList
9993
Advantage
58

140-65-8, pramocaineRelated Search:


  • 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