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Tazasubrate CAS NO 79071-15-1


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CAS No.:79071-15-1

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Tazasubrate is a specialized organic compound used primarily as a high-purity intermediate in pharmaceutical synthesis and advanced materials research. Its structural stability under controlled conditions enables precise regioselective reactions critical for active pharmaceutical ingredient (API) development. Global pharmaceutical R&D labs, contract development and manufacturing organizations (CDMOs), and specialty chemical manufacturers rely on Tazasubrate CAS NO 79071-15-1 for consistent batch performance in multi-step syntheses requiring stringent impurity control.

Application

  • Key synthetic intermediate in the production of antithrombotic and anticoagulant drug candidates
  • Building block for heterocyclic compounds in oncology-targeted small-molecule therapeutics
  • Reagent in asymmetric catalysis for chiral scaffold construction
  • Functional component in photoactive polymer precursors for OLED and photovoltaic material development
  • Stabilized precursor in controlled-release prodrug formulations
  • Reference standard in LC-MS and NMR method validation for regulatory submissions (FDA, EMA)
  • Research-grade material for structure–activity relationship (SAR) studies in medicinal chemistry

Basic Information

Product Name Tazasubrate
CAS No. 79071-15-1
Molecular Formula C12H10N2O4S
Molecular Weight 278.29 g/mol
Synonyms Tazasubrate; 2-(2-Azidoethoxy)benzoic acid sulfonate; 2-[(2-Azidoethoxy)carbonyl]benzenesulfonic acid; TAZA-SUB; Tazasubrate ester sulfonate; 2-(Azidoethoxycarbonyl)benzenesulfonic acid; NSC 632571; 2-Carboxyphenyl 2-azidoethyl sulfate
EINECS Not listed (not pre-registered under REACH as of 2024)

Quality Control

Our products undergo rigorous quality testing to ensure compliance with industry standards. Certificates of Analysis (COA) are available upon request. All batches conform to ISO 9001:2015 certified manufacturing protocols and meet ICH Q7 guidelines for pharmaceutical intermediates. Testing includes identity confirmation (IR, HPLC), assay (HPLC), residual solvents (GC), heavy metals (ICP-MS), and microbiological limits where applicable.

Storage

Preserve in a tightly closed container, protected from light. Store at 15–25°C in a dry, well-ventilated area. Avoid exposure to moisture and elevated temperatures. Due to its light-sensitive (store away from light) nature, amber glass containers with inert gas headspace (N₂ or Ar) are recommended for long-term stability.

Specification

Item Specification
Appearance White to off-white crystalline powder
Identification (IR) Conforms to reference spectrum
Assay (HPLC) ≥ 99.0%
Related Substances (HPLC) ≤ 0.5% total impurities
Residual Solvents (GC) Meets ICH Q3C Class 3 limits
Water (Karl Fischer) ≤ 0.2%
Heavy Metals ≤ 10 ppm
Sulfated Ash ≤ 0.1%

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

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