O5875

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

₹ 8,660.00

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

Image Product Name Manufacturer Price Range
46598
Oxytetracycline hydrochloride
Supelco ₹ 5,813.03
PHR1325
Oxytetracycline Hydrochloride
Supelco ₹ 11,864.20
1491015
Oxytetracycline hydrochloride
Sigma Aldrich ₹ 40,756.13
BP275
Oxytetracycline hydrochloride
Sigma Aldrich ₹ 21,401.03
O0500000
Oxytetracycline hydrochloride
Sigma Aldrich ₹ 14,267.35

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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

GHS08

Signal Word

Warning

Hazard Statements

H361fd

Precautionary Statements

P201 - P202 - P280 - P308 + P313 - P405 - P501

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

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Show Difference

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Sigma Aldrich

O5875

--


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

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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

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Quality Level:
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impurities:
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color:
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solubility:
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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

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solubility:
1% acetic acid: 1.00-1.04 mg/mL, clear, colorlesswater: 1.00-1.04 mg/mL, clear, colorless

antibiotic activity spectrum:
__

Mode of action:
__

SMILES string:
__

InChI:
1S/C152H243N47O44S4/c1-20-76(14)118(146(239)188-96(51-74(10)11)138(231)197-119(80(18)201)147(240)180-92(121(156)214)47-70(2)3)195-115(209)62-166-123(216)78(16)171-124(217)79(17)172-131(224)99(55-84-59-162-69-169-84)186-136(229)100(56-111(155)205)174-114(208)61-165-122(215)77(15)170-113(207)60-167-125(218)98(54-83-58-161-68-168-83)185-134(227)95(50-73(8)9)183-132(225)93(48-71(4)5)182-129(222)90(38-41-116(210)211)179-135(228)97(53-82-32-34-85(203)35-33-82)184-133(226)94(49-72(6)7)181-127(220)88(29-24-44-164-152(159)160)177-140(233)104-64-244-245-65-105-141(234)176-87(28-23-43-163-151(157)158)126(219)178-89(36-39-110(154)204)128(221)175-86(27-21-22-42-153)130(223)196-120(81(19)202)148(241)194-107(142(235)190-103(63-200)139(232)192-104)67-247-246-66-106(143(236)193-105)191-137(230)101(57-117(212)213)187-144(237)108-30-26-46-199(108)150(243)102(52-75(12)13)189-145(238)109-31-25-45-198(109)149(242)91-37-40-112(206)173-91/h32-35,58-59,68-81,86-109,118-120,200-203H,20-31,36-57,60-67,153H2,1-19H3,(H2,154,204)(H2,155,205)(H2,156,214)(H,161,168)(H,162,169)(H,165,215)(H,166,216)(H,167,218)(H,170,207)(H,171,217)(H,172,224)(H,173,206)(H,174,208)(H,175,221)(H,176,234)(H,177,233)(H,178,219)(H,179,228)(H,180,240)(H,181,220)(H,182,222)(H,183,225)(H,184,226)(H,185,227)(H,186,229)(H,187,237)(H,188,239)(H,189,238)(H,190,235)(H,191,230)(H,192,232)(H,193,236)(H,194,241)(H,195,209)(H,196,223)(H,197,231)(H,210,211)(H,212,213)(H4,157,158,163)(H4,159,160,164)/t76-,77-,78-,79-,80+,81+,86-,87-,88-,89-,90-,91-,92-,93-,94-,95-,96-,97-,98-,99-,100-,101-,102-,103-,104-,105-,106-,107-,108-,109-,118-,119-,120-/m0/s1

InChI key:
OFNHNCAUVYOTPM-IIIOAANCSA-N