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Atorvastatin 3-Deoxy-Hept-2-Enoic Acid Sodium Salt CAS NO 1659317-56-2


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CAS No.:1659317-56-2

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Atorvastatin 3-Deoxy-Hept-2-Enoic Acid Sodium Salt is a key pharmaceutical intermediate in the synthesis of atorvastatin, the active ingredient in leading cholesterol-lowering medications. This high-purity compound is critical for ensuring the efficacy and safety of the final active pharmaceutical ingredient (API). It is primarily required by manufacturers in the pharmaceutical and fine chemical industries engaged in the production of cardiovascular drugs.

Application

  • Primary Intermediate in the synthesis of Atorvastatin Calcium (API).
  • Research & Development for novel statin-based therapeutics and metabolic disorder treatments.
  • Process Chemistry for scaling up and optimizing atorvastatin manufacturing routes.
  • Reference Standard for analytical method development and quality control in API production.
  • Generic Drug Manufacturing for producing cost-effective cholesterol management medications.

Basic Information

Product Name Atorvastatin 3-Deoxy-Hept-2-Enoic Acid Sodium Salt
CAS No. 1659317-56-2
Molecular Formula C33H33FN2NaO5
Molecular Weight 579.62 g/mol
Synonyms Atorvastatin Sodium Salt (3-Deoxy-Hept-2-Enoic Acid); Atorvastatin 3-Deoxy-Hept-2-Enoic Acid Sodium; Sodium (3R,5R)-7-[2-(4-Fluorophenyl)-3-phenyl-4-(phenylcarbamoyl)-5-(propan-2-yl)-1H-pyrrol-1-yl]-3,5-dihydroxyheptanoate; Atorvastatin 3-Deoxy-Hept-2-Enoic Acid Na Salt; Atorvastatin Sodium Salt Intermediate; Atorvastatin 3-Deoxy Hept 2 Enoic Acid Sodium Salt; Atorvastatin 3-Deoxy Hept 2 Enoic Acid Na Salt
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Quality Control

Our Atorvastatin 3-Deoxy-Hept-2-Enoic Acid Sodium Salt is manufactured under strict quality management systems, with a focus on high purity and consistency suitable for pharmaceutical synthesis. We provide comprehensive Certificates of Analysis (COA) for each batch, detailing key parameters such as assay, related substances, and residual solvents. Our quality commitment aligns with GMP principles and relevant ICH guidelines to support our global clientele in regulated markets.

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 material is hygroscopic (moisture-sensitive) and must be kept in a dry environment to prevent degradation. For long-term storage, consider using desiccants.

Specification

Item Specification
Appearance White to off-white powder
Identification (IR) Conforms to reference spectrum
Identification (HPLC) Retention time matches reference standard
Assay (HPLC) ≥ 98.0%
Related Substances (HPLC) Total impurities ≤ 2.0% Any single impurity ≤ 1.0%
Water Content (KF) ≤ 5.0%
Residual Solvents (GC) Complies with ICH Q3C guidelines

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.