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99% Chlortetracycline Hydrochloride Chlortetracycline Hydrochloride Manufacturer Broad-spectrum Antibiotics
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Chlortetracycline hydrochloride Basic information |
Product Name: | Chlortetracycline hydrochloride |
Synonyms: | 2-Naphthacenecarboxamide,7-chloro-4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,6,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-,monohydrochloride;6,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-ydro-monohydrochloride;Aureociclina;Aureocycline;Auxeomycin;chlortetracyclinehydrochloride’canbeusedassecondarystandard’;clorotetraciclinacloridrato;Isphamycin |
CAS: | 64-72-2 |
MF: | C22H24Cl2N2O8 |
MW: | 515.34 |
EINECS: | 200-591-7 |
Product Categories: | Intermediates & Fine Chemicals;Pharmaceuticals;AUREOMYCIN;Inhibitors |
Mol File: | 64-72-2.mol |
Chlortetracycline hydrochloride Chemical Properties |
Melting point | 210-215 °C (dec.)(lit.) |
alpha | D23 -240° |
storage temp. | 2-8°C |
solubility | 1 M NaOH: soluble50mg/mL |
form | Powder |
color | faint yellow to yellow |
pka | 3.3(at 25℃) |
Water Solubility | Soluble in water |
Sensitive | Light Sensitive |
Merck | 13,2211 |
CAS DataBase Reference | 64-72-2(CAS DataBase Reference) |
EPA Substance Registry System | 2-Naphthacenecarboxamide, 7-chloro-4-(dimethylamino)- 1,4,4a,5,5a,6,11,12a-octahydro- 3,6,10,12,12a-pentahydroxy- 6-methyl-1,11-dioxo-, monohydrochloride, (4S,4aS,5aS,6S,12aS)-(64-72-2) |
Safety Information |
Hazard Codes | Xi |
Risk Statements | 36/37/38 |
Safety Statements | 26-36 |
WGK Germany | 2 |
RTECS | QI7800000 |
HazardClass | 3 |
Chlortetracycline hydrochloride Usage And Synthesis |
Chemical Properties | Yellow Solid |
Uses | antibacterial, antiamebic, Ca chelator, hepatotoxic; inhibits protein synthesis |
Uses | Chlortetracycline is an antibiotic substance isolated from the substrate of Streptomyces aureofaciens. Chlortetracycline is an antimicrobial and antibacterial. |
Uses | Chlortetracycline hydrochloride is a salt prepared from chlortetracycline taking advantage of the basic dimethylamino group which protonates and readily forms the salt in hydrochloric acid solutions. The hydrochloride is the preferred formulation for pharmaceutical applications. Like all tetracyclines, chlortetracycline shows broad spectrum antibacterial and antiprotozoan activity and acts by binding to the 30S and 50S ribosomal sub-units, blocking protein synthesis. |
Uses | An antimicrobial and antibacterial. This compound contains an undetermined amount of epi-chlortetracycline |
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