Oxytetracycline hydrochloride
Manufacturer: Sigma Aldrich
CAS Number: 2058-46-0
Synonym(S): 5-Hydroxytetracycline hydrochloride
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 10 G | O5875-10-G | In Stock | ₹ 8,660.00 |
| 50 G | O5875-50-G | In Stock | ₹ 20,123.68 |
| 100 G | O5875-100-G | In Stock | ₹ 41,297.38 |
O5875 - 10 G
In Stock
Quantity
1
Base Price: ₹ 8,660.00
GST (18%): ₹ 1,558.80
Total Price: ₹ 10,218.80
form
powder or crystals
Quality Level
200
impurities
≤3.5% total of impurities (related substances (HPLC))
color
yellow
solubility
soluble (Freely soluble in water, sparingly soluble in Ethanol (96%). Solution in water becomes turbid on standing owing to the precipitation of chromatograms.)
antibiotic activity spectrum
Gram-negative bacteriaGram-positive bacteria
Mode of action
protein synthesis | interferes
SMILES string
Cl.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
InChI
1S/C22H24N2O9.ClH/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);1H/t12-,13-,14+,17+,21-,22+;/m1./s1
InChI key
UBDNTYUBJLXUNN-IFLJXUKPSA-N
Other Options
Related Products
Description
- General description: Chemical structure: tetracycline
- 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). Oxytetracycline hydrochloride is used to study phagosome-lysosome (P-L) fusion in P388D1 cells[1] and antibiotic susceptibilities of Mycoplasma bovis isolates[2].
- Biochem/physiol Actions: 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.
- Other Notes: 10g,50g,100g
SAFETY INFORMATION
Pictograms
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Repr. 2
WGK
WGK 2
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Compare Similar Items
Show Difference
form: powder or crystals
Quality Level: 200
impurities: ≤3.5% total of impurities (related substances (HPLC))
color: yellow
solubility: soluble (Freely soluble in water, sparingly soluble in Ethanol (96%). Solution in water becomes turbid on standing owing to the precipitation of chromatograms.)
antibiotic activity spectrum: Gram-negative bacteriaGram-positive bacteria
Mode of action: protein synthesis | interferes
SMILES string: Cl.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
InChI: 1S/C22H24N2O9.ClH/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);1H/t12-,13-,14+,17+,21-,22+;/m1./s1
InChI key: UBDNTYUBJLXUNN-IFLJXUKPSA-N
form: __
Quality Level: 200
impurities: __
color: __
solubility: __
antibiotic activity spectrum: __
Mode of action: __
SMILES string: Cc1ncc(n1CC(O)CCl)[N+]([O-])=O
InChI: 1S/C7H10ClN3O3/c1-5-9-3-7(11(13)14)10(5)4-6(12)2-8/h3,6,12H,2,4H2,1H3
InChI key: IPWKIXLWTCNBKN-UHFFFAOYSA-N
form: __
Quality Level: 100
impurities: __
color: __
solubility: __
antibiotic activity spectrum: __
Mode of action: __
SMILES string: CC(C)(C)CC(C)(C)N
InChI: 1S/C8H19N/c1-7(2,3)6-8(4,5)9/h6,9H2,1-5H3
InChI key: QIJIUJYANDSEKG-UHFFFAOYSA-N
