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tromantadine

CAS No.
53783-83-8
Chemical Name:
tromantadine
Synonyms
N-(1-Adamantyl)-2-[2-(dimethylamino)ethoxy]acetamide;Acetamide, 2-[2-(dimethylamino)ethoxy]-N-tricyclo[3.3.1.13,7]dec-1-yl-
CBNumber:
CB4917021
Molecular Formula:
C16H28N2O2
Molecular Weight:
280.41
MDL Number:
MFCD00869480
MOL File:
53783-83-8.mol
Last updated:2023-05-21 10:59:17

tromantadine Properties

Boiling point 434.5±28.0 °C(Predicted)
Density 1.09±0.1 g/cm3(Predicted)
storage temp. Store at -20°C
solubility Soluble in DMSO
pka 14.58±0.20(Predicted)
FDA UNII H191JFG8WA

tromantadine price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
American Custom Chemicals Corporation API0004847 TROMANTADINE 95.00% 53783-83-8 5MG $498.1 2021-12-16 Buy
CSNpharm CSN21875 Tromantadine 53783-83-8 1mg $204 2021-12-16 Buy
Product number Packaging Price Buy
API0004847 5MG $498.1 Buy
CSN21875 1mg $204 Buy

tromantadine Chemical Properties,Uses,Production

Description

Tromantadine is an antiviral medicine used to treat herpes simplex virus. It is available in a topical gel under trade names Viru-Merz and Viru-Merz Serol. Its performance is similar to aciclovir.

Mechanism of action

Tromantadine inhibits the early and late events in the virus replication cycle.It changes the glycoproteins of the host cells, therefore impeding the absorption of the virus. It inhibits penetration of the virus. It also prevents uncoating of the virions.

Originator

Viru-Merz,Merz,W. Germany,1973

Uses

Tromantadine hydrochloride is used as antiviral agent effective against herpes simplex infections.

Definition

ChEBI: Tromantadine is a secondary carboxamide.

Manufacturing Process

Adamantane is first reacted with chloroacetyl chloride to give chloroacetylaminoadamantane. 2.3 g Na (0.1 g-atom) were dissolved in 75 ml dimethylamino-ethanol. Then the excess alcohol was distilled off completely and the sodium salt developed was dried in a vacuum. After drying, the salt was dissolved in about 200 ml xylene. To thissolution.22.8 g (0.1 mol) chloroacetylaminoadamantane were added, heated for 10 hours under reflux in a 250-ml round-bottomed flask with a reflux cooler, and the sodium chloride developed subsequently filtered off.
Next the xylene was distilled away, the liquid residue dissolved in about 80 ml carbon tetrachloride and the hydrochloride precipitated through introduction of hydrochloric acid gas. The hydrochloride was dissolved in about 100 ml acetone and the solvent subsequently distilled away, whereby excess hydrochloric acid passed over with it. This operation was repeated until no excess acid was present.
A large excess of petroleum ether was added in a 500 ml three-necked flask provided with a stirrer and reflux cooler, to a concentrated acetonic solution of the hydrochloride and stirred for at least 1 hour, whereby the desired substance was deposited in a crystalline form. Finally, the substance was filtered away and dried in a desiccator. 14 g of the substance (15% of theory) were obtained.

Therapeutic Function

Antiviral

tromantadine Preparation Products And Raw materials

Raw materials

Preparation Products

tromantadine Suppliers

Global( 20)Suppliers
Supplier Tel Email Country ProdList Advantage
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000 marketing@targetmol.com United States 19892 58
Hefei TNJ Chemical Industry Co.,Ltd.
0551-65418671 sales@tnjchem.com China 34572 58
HANGZHOU CLAP TECHNOLOGY CO.,LTD
86-571-88216897,88216896 13588875226 sales@hzclap.com CHINA 6313 58
Dayang Chem (Hangzhou) Co.,Ltd.
571-88938639 +8617705817739 info@dycnchem.com CHINA 52867 58
GIHI CHEMICALS CO.,LIMITED
+8618058761490 info@gihichemicals.com China 49999 58
LGM Pharma 1-(800)-881-8210 inquiries@lgmpharma.com United States 2127 70
Beijing HuaMeiHuLiBiological Chemical 010-56205725 waley188@sohu.com China 12338 58
MedChemexpress LLC 021-58955995 sales@medchemexpress.cn United States 4863 58
Beijing Hechemist Technology CO.,LTD 18511709189 sales@hechemist.com China 3436 58
Beijing Jin Ming Biotechnology Co., Ltd. 010-60605840 18892239720 psaitong@jm-bio.com China 12308 58
N-(1-Adamantyl)-2-[2-(dimethylamino)ethoxy]acetamide Acetamide, 2-[2-(dimethylamino)ethoxy]-N-tricyclo[3.3.1.13,7]dec-1-yl- 53783-83-8