T3383

Tetracycline hydrochloride

≥95% (European Pharmacopoeia HPLC assay)

Manufacturer: Sigma Aldrich

CAS Number: 64-75-5

Synonym(S): 4-Epitetracycline hydrochloride, Achromycin hydrochloride

Select a Size

Pack Size SKU Availability Price
25 G T3383-25-G In Stock ₹ 5,055.28
100 G T3383-100-G In Stock ₹ 11,506.98

T3383 - 25 G

₹ 5,055.28

In Stock

Quantity

1

Base Price: ₹ 5,055.28

GST (18%): ₹ 909.95

Total Price: ₹ 5,965.23

Quality Level

200

Assay

≥95% (European Pharmacopoeia HPLC assay)

form

powder

storage condition

(Keep container tightly closed in a dry and well-ventilated place.)

color

yellow

mp

220-223 °C (lit.)

antibiotic activity spectrum

Gram-negative bacteriaGram-positive bacteria

Mode of action

protein synthesis | interferes

storage temp.

−20°C

SMILES string

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

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Description

  • General description: Chemical structure: tetracycline
  • Application: Tetracycline is a broad spectrum polyketide antibiotic with clinical uses in treating bacterial infections such as Rocky Mountain spotted fever, typush fever, tick fevers, Q fever, and Brill-Zinsser disease and to treat upper respiratory infections and acne. It has been used in studies of multidrug resistance and potential side effects including acute pancreatitis. It is recommended for use in cell culture applications at 10 mg/L.
  • Biochem/physiol Actions: Mode of Action: Tetracycline passively diffuses through proin channels in the cell membrane, binding to 30S ribosomes and inhibits protein synthesis by preventing access of aminoacyl tRNA to the acceptor site on the mRNA-ribosome complex. It also binds to the bacterial 50S ribosomal subunit, altering the membrane and causing intracellular components to leak from bacterial cells. The inhibitory effects can be reversed by washing, suggesting that it is the reversibly bound antibiotic, and not the irreversibly bound drug, that is responsible for antibacterial action.Mode of Resistance: The effects are inactivated via a loss of cell wall permeability.Antimicrobial spectrum: Includes a wide range of antimicrobial activity against gram-positive and gram-negative bacteria.
  • Caution: This product should be frozen below 0°C and protected from light and moisture. In these conditions, the product has been shown to retain activity for 4 years. Stock solutions should be stored at -20°C and are stable at 37°C for 4 days.
  • Preparation Note: The product is freely soluble in water, soluble in methanol and ethanol but is insoluble in ether and hydrocarbons. In water, the product yields a clear, yellow-orange solution with heating and in 95% ethanol, 50 mg dissolved in 4 mL with heating yields a clear, yellow-green solution. Tetracycline is rapidly destroyed by alkali hydroxide solutions and standing water solutions become turbid due to hydrolysis and precipitation. The potency of tetracycline is reduced in solutions with pH below 2.
  • Other Notes: Keep container tightly closed in a dry and well-ventilated place.

SAFETY INFORMATION

Pictograms

GHS08,GHS07,GHS09

Signal Word

Warning

Hazard Statements

H315,H319,H335,H361fd,H410

Precautionary Statements

P202 - P261 - P273 - P302 + P352 - P305 + P351 + P338 - P308 + P313

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 2 - Eye Irrit. 2 - Repr. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

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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Quality Level:
200

Assay:
≥95% (European Pharmacopoeia HPLC assay)

form:
powder

storage condition:
(Keep container tightly closed in a dry and well-ventilated place.)

color:
yellow

mp:
220-223 °C (lit.)

antibiotic activity spectrum:
Gram-negative bacteriaGram-positive bacteria

Mode of action:
protein synthesis | interferes

storage temp.:
−20°C

SMILES string:
Cl.CN(C)[C@H]1[C@@H]2C[C@H]3C(=C(O)[C@]2(O)C(=O)C(C(N)=O)=C1O)C(=O)c4c(O)cccc4[C@@]3(C)O

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Mode of action:
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storage temp.:
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N[C@@H](Cc1ccc(O)cc1)C(=O)Nc2ccc3ccccc3c2

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SMILES string:
CCCCCCCCOCCOCCOCCOCCO