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Anhydrodemeclocycline CAS NO 22688-73-9


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CAS No.:22688-73-9

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Anhydrodemeclocycline is a key pharmaceutical intermediate and a derivative of the tetracycline class of antibiotics. This compound is valued for its role in the research and development of novel antimicrobial agents and as a critical reference standard in analytical chemistry. It is primarily utilized by pharmaceutical manufacturers, research institutions, and quality control laboratories engaged in antibiotic development and production. Our supply ensures high purity and batch-to-batch consistency for demanding industrial and research applications.

Application

  • Pharmaceutical Intermediate: A crucial building block in the synthesis of advanced tetracycline-derived antibiotics and novel therapeutic agents.
  • Reference Standard: Used for analytical method development, validation, and quality control testing in pharmaceutical manufacturing to ensure product purity and potency.
  • Biochemical Research: Serves as a tool compound in microbiological and pharmacological studies to investigate antibiotic mechanisms of action and resistance.
  • Active Pharmaceutical Ingredient (API) Development: Employed in the R&D of new antibiotic formulations and combination therapies.
  • Veterinary Medicine: Potential application in the development of antimicrobial treatments for animal health.

Basic Information

Item Detail
Product Name Anhydrodemeclocycline
CAS No. 22688-73-9
Molecular Formula C₂₁H₂₀ClN₂O₇
Molecular Weight 447.85 g/mol
Synonyms Anhydrodemeclocycline; 6-Desoxy-6-demethyltetracycline; 4-(Dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,6,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-2-naphthacenecarboxamide; Demeclocycline Impurity; Demeclocycline Related Compound A; NSC 643093; Antibiotic X 68
EINECS Contact for details

Quality Control

Our Anhydrodemeclocycline is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity, IR for identification, and residual solvent analysis, to ensure it meets stringent specifications for pharmaceutical research and development. A Certificate of Analysis (COA) documenting all test results is provided with every shipment to guarantee traceability and compliance.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive) and must be kept in a desiccated environment to maintain stability and purity.

Specification

Item Specification
Appearance Yellow to light brown powder
Identification (IR) Conforms to reference spectrum
Identification (HPLC) Retention time corresponds to reference standard
Assay (HPLC) ≥ 98.0%
Water Content (KF) ≤ 2.0%
Residue on Ignition ≤ 0.5%
Heavy Metals ≤ 20 ppm
Related Substances (HPLC) Total impurities ≤ 2.0% Any single impurity ≤ 1.0%

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.

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With our own production facilities, we ensure consistent quality, reliable supply, and full traceability.

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Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.

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Our in-house lab drives process innovation, new product development, and tailored synthesis solutions.