Online Database of Chemicals from Around the World

Oxytetracycline
[CAS# 79-57-2]

List of Suppliers
Zhuhai Jinyou Import & Export Co., Ltd. China Inquire  
+86 (311) 8383-6631
vita@zjpharma.com
Chemical distributor
chemBlink standard supplier since 2006
Capot Chemical Co., Ltd. China Inquire  
+86 (571) 8558-6718
+86 13336195806
capotchem@gmail.com
sales@capotchem.com
QQ chat
Chemical manufacturer
chemBlink standard supplier since 2006
Simagchem Corporation China Inquire  
+86 13806087780
sale@simagchem.com
Chemical manufacturer since 2002
chemBlink standard supplier since 2008
Arshine Technology Co., Ltd. China Inquire  
+86 (755) 3333-0822
marketing@arshine.com.cn
Chemical manufacturer
chemBlink standard supplier since 2010
Hefei TNJ Chemical Industry Co., Ltd. China Inquire  
+86 (551) 6541-8684
sales@tnjchem.com
Chemical manufacturer since 2001
chemBlink standard supplier since 2010
Rainbow Lab China Inquire  
+86 (311) 8381-3879
vita.hao@rainbowlabs.com
Chemical manufacturer
chemBlink standard supplier since 2010
BOC Sciences USA Inquire  
+1 (631) 485-4226
info@bocsci.com
Chemical manufacturer
chemBlink standard supplier since 2010
Shanghai Hohance Chemical Co., Ltd. China Inquire  
+86 (21) 3111-5312
info@hohance.com
Chemical manufacturer
chemBlink standard supplier since 2011
Complete supplier list of Oxytetracycline
Identification
Classification API >> Antibiotics >> Tetracycline
Name Oxytetracycline
Synonyms Terramycin; 4-(Dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,5,6,10,12,12a-hexahydroxy-6-methyl-1,11-dioxo-2-naphthacenecarboxamide; 5-Hydroxytetracycline
Molecular Structure CAS # 79-57-2, Oxytetracycline, Terramycin, 4-(Dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,5,6,10,12,12a-hexahydroxy-6-methyl-1,11-dioxo-2-naphthacenecarboxamide, 5-Hydroxytetracycline
Molecular Formula C22H24N2O9
Molecular Weight 460.44
CAS Registry Number 79-57-2
EC Number 201-212-8
SMILES C[C@@]1([C@H]2[C@@H]([C@H]3[C@@H](C(=O)C(=C([C@]3(C(=O)C2=C(C4=C1C=CC=C4O)O)O)O)C(=O)N)N(C)C)O)O
Properties
Melting point 183 ºC
alpha -223 º (c=1 0.03N HCl)
Water solubility 0.2 g/L
Density 1.7±0.1 g/cm3, Calc.*
Index of Refraction 1.762, Calc.*
Boiling Point 727.8±60.0 ºC (760 mmHg), Calc.*
Flash Point 394.0±32.9 ºC, Calc.*
* Calculated using Advanced Chemistry Development (ACD/Labs) Software.
Safety Data
Hazard Symbols symbol symbol symbol   GHS07;GHS08;GHS09 Warning    Details
Hazard Statements H315-H319-H335-H361-H361d-H362-H410-H411    Details
Precautionary Statements P203-P260-P261-P263-P264-P264+P265-P270-P271-P273-P280-P302+P352-P304+P340-P305+P351+P338-P318-P319-P321-P332+P317-P337+P317-P362+P364-P391-P403+P233-P405-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Acute toxicityAcute Tox.4H312
Acute toxicityAcute Tox.4H332
Acute toxicityAcute Tox.4H302
Chronic hazardous to the aquatic environmentAquatic Chronic1H410
Skin sensitizationSkin Sens.1H317
Reproductive toxicityRepr.1AH360
Acute hazardous to the aquatic environmentAquatic Acute1H400
Reproductive toxicityRepr.2H361
Eye irritationEye Irrit.2H319
Specific target organ toxicity - single exposureSTOT SE3H335
Skin irritationSkin Irrit.2H315
Reproductive toxicityLact.-H362
Acute toxicityAcute Tox.3H301
SDS Available
up Discovory and Applicatios
Oxytetracycline is a broad-spectrum antibiotic belonging to the tetracycline class. It was first discovered in the 1940s and is derived from the bacterium Streptomyces rimosus. Oxytetracycline has been widely used in both human and veterinary medicine to treat a variety of bacterial infections, although its use has decreased in recent years due to the development of antibiotic resistance and the availability of newer antibiotics.

The mechanism of action of oxytetracycline involves inhibiting bacterial protein synthesis. It achieves this by binding to the 30S ribosomal subunit of the bacterial ribosome, which prevents the attachment of aminoacyl-tRNA to the ribosome, thereby blocking the addition of amino acids to the growing peptide chain. This inhibition of protein synthesis disrupts bacterial growth and replication, ultimately leading to bacterial cell death. Oxytetracycline is considered bacteriostatic, meaning it inhibits bacterial growth rather than directly killing bacteria. However, at higher concentrations, it can exhibit bactericidal effects.

Oxytetracycline is effective against a wide range of Gram-positive and Gram-negative bacteria, as well as some atypical organisms such as rickettsiae, chlamydia, and mycoplasma. It is commonly used in the treatment of infections such as respiratory tract infections, urinary tract infections, and certain types of skin infections. In veterinary medicine, oxytetracycline is frequently used to treat infections in livestock, poultry, and fish, as well as in animal feed additives to prevent disease and promote growth.

Oxytetracycline is typically administered orally, but it can also be given via intramuscular or intravenous injection. Its bioavailability is generally good when taken orally, although its absorption can be impaired by the presence of calcium, magnesium, and other divalent cations, which form insoluble complexes with the antibiotic. This is why antacids or dairy products should be avoided when taking oxytetracycline.

Despite its effectiveness, the use of oxytetracycline is associated with a number of potential side effects. These include gastrointestinal disturbances such as nausea, vomiting, and diarrhea. More serious side effects include liver toxicity, especially with prolonged use, and the development of antibiotic resistance. Additionally, oxytetracycline can cause photosensitivity, leading to an increased risk of sunburn and skin reactions when exposed to sunlight. It may also lead to dental staining, particularly in children under the age of 8, as it can bind to calcium in developing teeth and bones.

Oxytetracycline is contraindicated in pregnant women, especially in the second and third trimesters, as it can cross the placenta and affect the development of the fetus. It is also not recommended for use in children under the age of 8 due to the risk of dental staining and bone development issues. In individuals with renal or hepatic impairment, dosage adjustments may be necessary to avoid toxicity.

Over the years, the widespread use of oxytetracycline has contributed to the development of bacterial resistance. Many bacteria have developed mechanisms to evade the effects of tetracyclines, including efflux pumps that expel the antibiotic from the bacterial cell and enzymes that inactivate the drug. As a result, the use of oxytetracycline has been restricted in some regions, and alternative antibiotics are often preferred for certain infections.

In summary, oxytetracycline is a broad-spectrum antibiotic used to treat a variety of bacterial infections. While it is effective against a wide range of pathogens, its use has decreased due to concerns over antibiotic resistance and side effects, such as gastrointestinal disturbances and dental staining. Its use in both human and veterinary medicine remains important, but it is generally reserved for situations where other antibiotics are less effective or appropriate.

References

1979. Evaluation of a new long-acting oxytetracycline formulation against anaplasmosis in colombian cattle. Tropenmedizin und Parasitology, 30(2).
URL: https://pubmed.ncbi.nlm.nih.gov/483386

2024. Pharmaceuticals in the Environment and Their Removal in Conventional Wastewater Treatment Plants. Pollutants and Recent Trends in Wastewater Treatment.
DOI: 10.1007/978-3-031-62054-6_2

2024. Antibiotics and Antibiotic Resistance Genes in Water. Water Reuse and Unconventional Water Resources.
DOI: 10.1007/978-3-031-67739-7_5
Market Analysis Reports
List of Reports Available for Oxytetracycline
Related Products
Oxyphenbutazone  Oxyphencyclimine  Oxyphenonium bromide  Oxyphyllenone A  Oxyprothepin 5,8-disulfide  2-(1-Oxy-pyridin-2-yl)-1,1,3,3-tetramethylisothiouronium tetrafluoroborate  Oxyresveratrol  Oxyresveratrol 2'-O-beta-D-glucopyranoside  Oxyresveratrol 3-O-glucoside  N-Oxysophocarpine  Oxytetracycline dihydrate  Oxytetracycline hydrochloride  Oxytocin  Oxytocin acetate (salt)  Oxytocin, compd. with citric acid  N-Oxytriacetoneamine glycerol ketal  Oxyvanadium phthalocyanine  cis-Ozagrel  Ozagrel  Ozagrel hydrochloride