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Merck

51239

Oxytetra Selective Supplement

suitable for microbiology

Synonym(s):

Oxytetracycline, OGYE Selective Supplement

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About This Item

Empirical Formula (Hill Notation):
C22H24N2O9
CAS Number:
79-57-2
Molecular Weight:
460.43
NACRES:
NA.85
PubChem Substance ID:
329757674
UNSPSC Code:
41171614
EC Number:
201-212-8
MDL number:
MFCD00003700

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InChI

1S/C22H24N2O9/c1-21(32)7-5-4-6-8(25)9(7)15(26)10-12(21)17(28)13-14(24(2)3)16(27)11(20(23)31)19(30)22(13,33)18(10)29/h4-6,12-14,17,25,27-29,32-33H,1-3H3,(H2,23,31)/t12-,13-,14+,17+,21-,22+/m1/s1

InChI key

IWVCMVBTMGNXQD-PXOLEDIWSA-N

SMILES string

CN(C)[C@H]1[C@@H]2[C@@H](O)[C@H]3C(=C(O)[C@]2(O)C(=O)C(C(N)=O)=C1O)C(=O)c4c(O)cccc4[C@@]3(C)O

sterility

sterile

form

powder

shelf life

limited shelf life, expiry date on the label

antibiotic activity spectrum

Gram-negative bacteria, Gram-positive bacteria

application(s)

environmental
food and beverages
pharmaceutical, microbiology

mode of action

protein synthesis | interferes

suitability

molds, yeasts

Quality Level

100

Related Categories

General description

Chemical structure: tetracycline

Application

Oxytetracycline is used as an antibacterial selective agent in microbiology studies . It is a broad spectrum antibiotic that is active against a wide variety of bacteria. When added to OGY-Agar (Cat. No. 75310) Oxytetracycline suppresses the growth of accompanying bacterial flora during culturing yeasts and molds.

Biochem/physiol Actions

Oxytetracycline is a protein synthesis inhibitor .

Features and Benefits

Added to OGY-Agar (Cat. No. 75310) or OGYE ChromoSelect Agar (Cat. No. 66481) Oxytetracycline suppresses the growth of accompanying bacterial flora during culturing yeasts and moulds.

Other Notes

(per vial sufficient for 500 ml medium)
Oxytetracycline 50.0 mg

pictograms

Health hazardEnvironment
GHS08,GHS09

signalword

Warning

Hazard Classifications

Aquatic Chronic 2 - Repr. 2

Storage Class

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
BCCP1484
BCCN4989
BCCN4552
BCCK6006
BCCK3293

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E M MIKOLAJCIK et al.
Applied microbiology, 11, 418-422 (1963-09-01)
Induction of oxytetracycline resistance in a strain of Streptococcus lactis caused this organism to display reduced acid production, salt tolerance, pyruvate synthesis, growth at alkaline pH, and a loss in ability to produce ammonia from arginine. alpha-Ketoglutaric and oxaloacetic acids
Pavel Novy et al.
The Journal of antimicrobial chemotherapy, 66(6), 1298-1300 (2011-03-23)
In this study we examined the in vitro synergistic effect of baicalin, the flavone constituent of Scutellaria spp., in combinations with oxytetracycline and tetracycline on the growth of Staphylococcus aureus. The MICs were determined by the broth microdilution method and
P R Spooner
Parasitology, 101 Pt 3, 387-393 (1990-12-01)
Oxytetracycline (OTC) significantly inhibited cytochrome c oxidase activity in bovine lymphocytes infected with Theileria parva and in uninfected mitogen-stimulated lymphocytes. The inhibitory effect was detected in vitro within 24 h of treatment with drug concentrations as low as 1 micrograms/ml.
A L Stanton et al.
Journal of dairy science, 95(9), 4950-4960 (2012-08-25)
Bovine respiratory disease complex (BRD) is a common disease in weaned dairy calves that incurs economic and welfare costs. This study was an extension of a randomized clinical trial in which a single injection of tulathromycin (TUL) or oxytetracycline (TET)
Getu Kahsay et al.
Journal of pharmaceutical and biomedical analysis, 75, 199-206 (2013-01-02)
A simple, robust and fast high-performance liquid chromatographic method is described for the analysis of oxytetracycline and its related impurities. The principal peak and impurities are all baseline separated in 20 min using an Inertsil C₈ (150 mm × 4.6
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