Apicycline

CAS No.
15599-51-6
Chemical Name:
Apicycline
Synonyms
Apicycline;(-)-N-[[4-(2-Hydroxyethyl)piperazino](carboxy)methyl]tetracycline;1-Piperazineacetic acid, α-[[[4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,6,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-2-naphthacenyl]carbonyl]amino]-4-(2-hydroxyethyl)-
CBNumber:
CB51178046
Molecular Formula:
C30H38N4O11
Molecular Weight:
630.64
MDL Number:
MOL File:
15599-51-6.mol
Last updated:2022-12-21 16:56:50

Apicycline Properties

Melting point 144.5° (dec)
alpha D -123° (c = 0.5 in methanol); D -133° (c = 0.5 in water)
FDA UNII T1Y573BS7H

Apicycline price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
American Custom Chemicals Corporation API0025381 APICYCLINE 95.00% 15599-51-6 5MG $500.02 2021-12-16 Buy
Product number Packaging Price Buy
API0025381 5MG $500.02 Buy

Apicycline Chemical Properties,Uses,Production

Originator

Travert,Baxter

Manufacturing Process

Glyoxylic acid monohydrate (1.96 g, 20 mrnoles) is dissolved in 200 ml of methanol, and a solution of 2.60 g (20 mmoles) of N-(2-hydroxyethyl) piperazine in 50 ml of methanol is slowly added thereto with stirring.
Stirring is maintained for 15 minutes and the medium is cooled to 5°C. There is then added 10.2 g (20 mmoles) of tetracycline base trihydrate and the reaction medium is maintained for 20 hours at 5°C under stirring. After that reaction time, the solution is concentrated up to 50 ml and 0.25 liter of acetone is added for precipitating a yellowish product which is filtered and dried to yield N-[(carboxy)(4-β-hydroxyethylpiperazino)methyl] tetracycline (apicycline).
When tested for antibiotic potency against Bacillus cereus var. mycoides ATCC 9634 (diffusion method), the product is shown to present an antibiotic potency equivalent to 97% of the tetracycline present therein.
Anhydrous tetracycline base (0.90 g, 2 mmoles) is dissolved in 30 ml of nbutanol at about 40°C. There is then added thereto under stirring a solution of 0.26 g (2 mmoles) of N-(2-hydroxyethyl)piperazine in 10 ml of butanol and 0.191 g (2 mmoles) of glyoxylic acid monohydrate. A precipitate appears after a few minutes and the suspension is maintained for six hours under stirring and at room temperature.
After that reaction time, precipitation is completed by addition of 120 ml of ether. The yellowish precipitate is filtered and dried to yield N-[(carboxy)(4-β- hydroxyethylpiperazino)methyl]tetracycline (apicycline). Yellow, amorphous powder with slight amine odor, MP: 144.5°C (dec). Freely solves in water. [α]D =-123° (c = 0.5 in methanol); [α]D =-133° (c = 0.5 in water).
The pH value of a 2% aqueous solution of this product is 6.2. When tested for antibiotic potency against Bacillus cercus var. mycoides ATCC 9634 (diffusion method), the product is shown to present an antibiotic potency equivalent to 95% of the tetracycline present therein.

Therapeutic Function

Antibiotic

Apicycline Preparation Products And Raw materials

Raw materials

Preparation Products

Apicycline Suppliers

Global( 2)Suppliers
Supplier Tel Email Country ProdList Advantage
Lanospharma Laboratories Co.,Ltd -- sales@lanospharma.com China 6343 56
Shanghai New Union Textra Import & Export Co., Ltd -- zhou@pharmchemical.com China 2752 60
Apicycline (-)-N-[[4-(2-Hydroxyethyl)piperazino](carboxy)methyl]tetracycline 1-Piperazineacetic acid, α-[[[4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,6,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-2-naphthacenyl]carbonyl]amino]-4-(2-hydroxyethyl)- 15599-51-6 C30H38N4O11