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Oxytetracycline dihydrate_Molecular_structure_CAS_6153-64-6)
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Oxytetracycline dihydrate

Catalog No. O4636 Name Sigma Aldrich
CAS Number 6153-64-6 Website http://www.sigmaaldrich.com
M. F. C22H26N2O10 Telephone 1-800-521-8956
M. W. 478.44924 Fax
Purity ≥99% (TLC) Email
Storage Chembase ID: 153449

SYNONYMS

Title
土霉素 二水合物
IUPAC name
(4S,4aR,5S,5aR,6S,12aS)-4-(dimethylamino)-3,5,6,10,12,12a-hexahydroxy-6-methyl-1,11-dioxo-1,4,4a,5,5a,6,11,12a-octahydrotetracene-2-carboxamide hydrate
IUPAC Traditional name
oxytetracycline hydrate

DATABASE IDS

MDL Number MFCD00151234
PubChem SID 24898000
EC Number 201-212-8
CAS Number 6153-64-6

PROPERTIES

Antion Traces chloride (Cl-): ≤0.05%
Antion Traces sulfate (SO42-): ≤0.05%
Cation Traces Al: ≤0.001%
Cation Traces Ca: ≤0.2%
Cation Traces Cu: ≤0.0005%
Cation Traces Fe: ≤0.002%
Cation Traces K: ≤0.005%
Cation Traces Mg: ≤0.005%
Cation Traces Na: ≤0.01%
Cation Traces Pb: ≤0.001%
Cation Traces Zn: ≤0.0005%
Empirical Formula (Hill Notation) C22H24N2O9 · 2H2O
Ignition Residue ≤1.0%
Impurities ≤0.001% Phosphorus (P)
Impurities ≤0.1% Insoluble matter
Product Line BioXtra
Purity ≥99% (TLC)
Solubility 1 M HCl: soluble0.1 M, clear (yellow to yellow-orange)
MSDS Link Download
Personal Protective Equipment Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
German water hazard class 3

DETAILS

Description (English)
Biochem/physiol Actions
Antibiotic produced by Streptomyces rimosus.Mode of Action: Inhibits protein synthesis (elongation) by preventing binding of aminoacyl-tRNA to the 30S subunit.Antimicrobial spectrum: Gram-negative and Gram-positive bacteria.Mode of Resistance: Active efflux, ribosome protection, tetracycline inactivation.
Oxytetracycline inhibits translation, which results in cell death. It binds to the 30S ribosomal subunit and prevents the amino-acyl Trna from binding to the A site of the ribosome. The binding is reversible in nature. Oxytetracycline is lipophilic so it can easily pass through a cell membrane and passively diffuses through channels in the bacterial membrane.
Application
Oxytetracycline is a tetracycline analog isolated from the actinomycete Streptomyces rimosus. Oxytetracycline is an antibiotic indicated for treatment of infections caused by Gram positive and Gram negative microorganisms such as Mycoplasma pneumoniae, Pasteurella pestis, Escherichia coli, Haemophilus influenzae, and Diplococcus pneumoniae. It is used in studies on the oxytetracycline-resistance gene (otrA). It is used for fluorescence measurements of hepatocytes1.
Description (简体中文)
Biochem/physiol Actions
Antibiotic produced by Streptomyces rimosus.Mode of Action: Inhibits protein synthesis (elongation) by preventing binding of aminoacyl-tRNA to the 30S subunit.Antimicrobial spectrum: Gram-negative and Gram-positive bacteria.Mode of Resistance: Active efflux, ribosome protection, tetracycline inactivation.
Oxytetracycline inhibits translation, which results in cell death. It binds to the 30S ribosomal subunit and prevents the amino-acyl Trna from binding to the A site of the ribosome. The binding is reversible in nature. Oxytetracycline is lipophilic so it can easily pass through a cell membrane and passively diffuses through channels in the bacterial membrane.
Application
Oxytetracycline is a tetracycline analog isolated from the actinomycete Streptomyces rimosus. Oxytetracycline is an antibiotic indicated for treatment of infections caused by Gram positive and Gram negative microorganisms such as Mycoplasma pneumoniae, Pasteurella pestis, Escherichia coli, Haemophilus influenzae, and Diplococcus pneumoniae. It is used in studies on the oxytetracycline-resistance gene (otrA). It is used for fluorescence measurements of hepatocytes1.

REFERENCES