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demeclocycline

CAS No.
127-33-3
Chemical Name:
demeclocycline
Synonyms
D03680;Deganol;10192 RP;RP 10192;Demeclor;Mexocine;Diuciclin;Sumaclina;Ledermycin;Elkamicina
CBNumber:
CB5918843
Molecular Formula:
C21H21ClN2O8
Molecular Weight:
464.85
MDL Number:
MFCD00864922
MOL File:
127-33-3.mol
MSDS File:
SDS
Last updated:2024-11-15 19:19:13

demeclocycline Properties

Melting point 176°C (rough estimate)
Boiling point 787.1±60.0 °C(Predicted)
Density 1.3118 (rough estimate)
refractive index 1.6000 (estimate)
solubility H2O:1.5(Max Conc. mg/mL);3.23(Max Conc. mM)
form Solid
pka 4.50±1.00(Predicted)
color Green to dark green
Water Solubility 1.4g/L(25 ºC)
FDA UNII 5R5W9ICI6O

SAFETY

Risk and Safety Statements

Hazardous Substances Data 127-33-3(Hazardous Substances Data)

demeclocycline Chemical Properties,Uses,Production

Description

Demethylchlortetracycline was isolated from the culture broth of a mutant of Streptomyces aureofaciens, the chlortetracycline-producing strain, by Lederle Research Laboratories in 1957. It shows one and one-half to two times as much in vitro antimicrobial activity and in vivo protective effect as tetracycline. Its base and hydrochloride have been used orally and by topical application to treat infections caused by Staphylococcus, Streptococcus, Rickettsia, Chlamydiae, Neisseria, Klebsiella, Proteus, Escherichia coli, and Haemophilus influenzae.

Originator

Declomycin,Lederle,US,1959

Uses

Demeclocycline, a chlortetracycline analogue produced by a mutagenised strain of Streptomyces aureofaciens, was first isolated in 1957. Like all tetracyclines, demeclocycline shows broad spectrum antibacterial and antiprotozoan activity and acts by binding to the 30S and 50S ribosomal subunits, blocking protein synthesis. Demeclocycline has been extensively cited in the literature with over 800 references relating almost exclusively to in vivo use.

Definition

ChEBI: Tetracycline which lacks the methyl substituent at position 7 and in which the hydrogen para- to the phenolic hydroxy group is substituted by chlorine. Like tetracycline, it is an antibiotic, but being excreted more slowly, effective blood lev ls are maintained for longer. It is used (mainly as the hydrochloride) for the treatment of Lyme disease, acne and bronchitis, as well as for hyponatraemia (low blood sodium concentration) due to the syndrome of inappropriate antidiuretic hormone (SIADH) w ere fluid restriction alone has been ineffective.

Manufacturing Process

According to US Patent 2,878,289, a suitable medium for the preparation of inocula for the fermentation may be prepared with the following substances.
The pH of the medium thus prepared is about 6.8. An 8 ml portion is measured into an 8 inch Brewer tube and sterilized at 120°C for 20 minutes. The sterilized medium is then inoculated with 0.5 ml of an aqueous spore suspension of a strain of S. aureofaciens capable of producing chlorodemethyltetracycline, such as S-604, containing approximately 40-60 million spores per milliliter. The inoculated medium is incubated for 24 hours at 28°C on a reciprocating shaker operated at 110 cycles per minute.
A suitable fermentation medium contains water and a source of assimilable carbon and nitrogen and essential mineral salts. A typical medium suitable for production of chlorodemethyltetracycline is as follows:
A suitable fermentation medium contains water and a source of assimilable carbon and nitrogen and essential mineral salts. A typical medium suitable for production of chlorodemethyltetracycline is as follows:
Ten percent of the resulting inoculum is then transferred to a 250 ml Erlenmeyer flask containing 50 ml of the medium employed above and the flask agitated a further 72 hours under the same conditions. One ml of the resulting inoculum is then employed for the inoculation of 10 ml of an aqueous medium containing, per 1,000 ml, 30 grams extraction process soybean meal, 1 gram sodium chloride, 50 grams glucose and 7 grams calcium carbonate, in a 1" x 6" test tube.
In addition, 1 mg of sterile S-2-hydroxyethyl-DL-homocysteine is added to the tube and the tube is shaken on a rotary shaker at 280 cycles per minute at 25°C for seven days. The contents of the tube were then acidified to pH 2 by the addition of sulfuric acid and centrifuged. Examination of the supernatant liquid by paper chromatography employing the methods of Bohonos et al, Antibiotics Annual (1953-4, page 49),demonstrates the presence of 7-chloro6-demethyltetracycline,7-chlorotetracycline and tetracycline.

brand name

Declomycin (Lederle).

Therapeutic Function

Antibacterial

Safety Profile

Poison by intravenous and intraperitoneal routes. Human systemic effects by ingestion: diabetes insipidus, urine volume increase, other changes in urine composition, dermatitis, changes in the nails, allergic rhinitis, serum sickness, effects on cyclic nucleotides. Human reproductive effects by an unspecified route: postnatal measures or effects on newborn. An experimental teratogen. Experimental reproductive effects. Human mutation data reported. When heated to decomposition it emits very toxic fumes of Cland NOx.

demeclocycline Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 52)Suppliers
Supplier Tel Email Country ProdList Advantage
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21634 55
SHANDONG ZHI SHANG CHEMICAL CO.LTD
+86 18953170293 sales@sdzschem.com China 2930 58
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000 marketing@targetmol.com United States 32161 58
AFINE CHEMICALS LIMITED
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Dayang Chem (Hangzhou) Co.,Ltd.
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TargetMol Chemicals Inc.
support@targetmol.com United States 38631 58
GIHI CHEMICALS CO.,LIMITED
+8618058761490 info@gihichemicals.com China 49978 58
Wuhan Topule Biopharmaceutical Co., Ltd
+8618327326525 masar@topule.com China 8467 58
LEAPCHEM CO., LTD.
+86-852-30606658 market18@leapchem.com China 43340 58
Shanghai Likang New Materials Co., Limited
+86-16631818819 +86-17736933208 3684455296@qq.com China 9300 58

View Lastest Price from demeclocycline manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Demeclocycline pictures 2024-11-14 Demeclocycline
127-33-3
US $38.00-118.00 / mg 97.46% 10g TargetMol Chemicals Inc.
Demeclocycline pictures 2024-11-14 Demeclocycline
127-33-3
US $38.00-118.00 / mg 97.46% 10g TargetMol Chemicals Inc.
  • Demeclocycline pictures
  • Demeclocycline
    127-33-3
  • US $38.00-118.00 / mg
  • 97.46%
  • TargetMol Chemicals Inc.
  • Demeclocycline pictures
  • Demeclocycline
    127-33-3
  • US $38.00-118.00 / mg
  • 97.46%
  • TargetMol Chemicals Inc.
DEMETHYLCHLOROTETRACYCLINE 10192 RP Bioterciclin Deganol Ledermycin Periciclina RP 10192 D03680 Demeclocycline (usp) Demethylchlortetracycline (jan) 6-DeMethylchlotetracycline, DMCT, 7-Chloro-6-deMethyltetracycline, LederMycin, RP 10192 Demethylchlortetracycline 7-Chloro-6-demethyltetracycline Demeclor Demethylchlortetracyclin Demetraclin Diuciclin Elkamicina Mexocine Novotriclina Perciclina Sumaclina Tri-demethylchlortetracycline Demethyichlortetracycline METHYLCHLOROTETRACYCLINE 2-Naphthacenecarboxamide, 7-chloro-4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,6,10,12,12a-pentahydroxy-1,11-dioxo-, (4S,4aS,5aS,6S,12aS)- Demeclocycline DISCONTINUED. Please offer D230725. Demeclocycline D6 Chlortetracycline Impurity B MW: 464.85 127-33-3