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Di-p-Anisoyl-D-tartaric Acid CAS 191605-10-4

Di-p-Anisoyl-D-tartaric Acid CAS 191605-10-4

Di-p-Anisoyl-D-tartaric Acid (CAS 191605-10-4) is a chiral D-tartaric acid derivative containing two p-methoxybenzoyl groups. Its defined stereochemistry and specific rotation support its use in chiral resolution and the preparation of optically enriched intermediates.

Product Introduction

Di-p-Anisoyl-D-tartaric Acid (CAS 191605-10-4) is a chiral D-tartaric acid derivative containing two p-methoxybenzoyl groups. Its defined stereochemistry and specific rotation support its use in chiral resolution and the preparation of optically enriched intermediates.

 

Chemical Specifications

 

Appearance

White to off-white powder or crystal

Purity

98.0%min

Water

0.5%max

Specific rotation

+165.0- +171.0

Upon request, we can submit the latest specifications and analysis report.

 

Product Specifications

 

Parameter

Specification

Product Name

Di-p-Anisoyl-D-tartaric Acid

CAS No.

191605-10-4

EINECS

471-150-6

Synonyms

(+)-Bis(4-methoxybenzoyl)-D-tartaric Acid; (+)-Di-p-anisoyl-D-tartaric Acid

IUPAC Name

(2S,3S)-2,3-Bis((4-methoxybenzoyl)oxy)succinic acid

Molecular Formula

C20H18O10

Molecular Weight

418.35 g/mol

Appearance

White to off-white powder or crystal

Purity

≥98.0%

Water

≤0.5%

Specific Rotation

+165.0° to +171.0°

 

Key Properties

 

Optical Activity: Exhibits a defined specific rotation range of +165.0° to +171.0°, providing a useful parameter for batch identification and stereochemical quality control.


High Chemical Purity: Available with a purity of ≥98.0%, suitable for chiral synthesis, resolution studies, pharmaceutical intermediate development, and related research applications.


Low Moisture Content: Controlled water content of ≤0.5% helps maintain consistent material quality during storage, handling, and downstream synthetic processes.

 

Applications

 

Active Pharmaceutical Ingredients (APIs): Critical chiral intermediate and resolving agent used in the synthesis of cardiovascular, antiviral, and central nervous system (CNS) therapeutics.


Chiral Synthons: Serves as a foundational precursor for building enantiopure nitrogen-containing heterocycles and complex chiral building blocks.


Agrochemical Intermediates: Utilized in the preparation of specialized enantiomerically enriched agrochemical active ingredients and pyrethroid precursors.


Drug Discovery R&D: Deployed in academic and industrial laboratories for asymmetric synthesis method development and optical resolution screening.

 

Custom Synthesis & Bulk Supply

 

Scale Capabilities: CDMO services managed by an R&D team of 15+ organic chemists, supporting kilogram-scale pilot runs up to multi-ton commercial production.


Reaction Capabilities: Technical capacity covering catalytic hydrogenation, asymmetric synthesis, fluorination, and organometallic reactions.


Supply Arrangements: Tailored bulk supply agreements, scheduled shipments, and dedicated customer account management for B2B procurement partners.


Research Infrastructure: Utilization of laboratory facilities at Zhejiang University and Zhejiang Industry University for route scouting and process optimization.

 

Quality Assurance

 

Analytical Testing: Every production batch undergoes multi-stage inspection and testing using high-performance liquid chromatography (HPLC) and gas chromatography-mass spectrometry (GC-MS) to ensure consistent batch-to-batch quality.


Quality Management: Manufacturing facilities operate under ISO 9001:2015 quality management principles, backed by full batch tracking documentation from raw material input through final QA release.


Technical & Compliance Documents: Batch-specific Certificates of Analysis (COA) containing purity, water content, and specific rotation data are provided prior to shipment alongside comprehensive Safety Data Sheets (SDS).


Regulatory Support: Complete documentation packages include REACH compliance data, origin statements, and non-hazardous transport declarations to support global regulatory audits and customs clearance.

 

Packaging & Storage

 

Standard Packaging: Packed in robust 20 kg/drum industrial fiber or plastic drums designed to prevent moisture ingress and contamination.


Transport Classification: Shipped globally as a non-hazardous chemical via air freight, sea freight, DHL, FedEx, and UPS with full customs support.


Storage Conditions: Store in tightly sealed containers in a cool, dry, well-ventilated area away from direct sunlight, moisture, and incompatible oxidizing agents.


Global Logistics Support: Specialized hazardous/non-hazardous packaging complying with IATA and IMDG standards, backed by real-time shipment tracking and transit insurance.

 

f-2S3S-23-Bis4-methoxybenzoyloxysuccinic acid

s-EINECS-471-150-6

 

Spectrum

 

t-cas-191605-10-4-C20H18O10

manufacturer

certificate

 

FAQ

 

Q: What is the minimum order quantity (MOQ) for routine production orders?

A: Standard order quantities generally start at one 20 kg drum, though trial quantities for laboratory evaluation can be evaluated on a case-by-case basis.

Q: What is the typical lead time for standard delivery orders?

A: In-stock materials typically ship within 3 to 5 business days, while custom or larger volume schedules are established during order confirmation based on active production capacity.

Q: What international payment methods are accepted for commercial transactions?

A: Accepted payment terms include Telegraphic Transfer (T/T), Letter of Credit (L/C) at sight, and PayPal for qualifying small-scale sample transactions.

Q: Can analytical testing methods be customized to align with client-specific pharmacopeial standards?

A: Analytical protocols can be reviewed against specific client compendial requirements during contract setup to determine feasibility and alignment.

Q: Are customized packaging sizes available aside from the standard 20 kg drum?

A: Alternative packaging configurations can be discussed depending on specific handling needs or pilot-scale processing requirements.

Q: How are customs clearance documents coordinated for shipments into regulated regions like the EU or North America?

A: Commercial invoices, packing lists, origin statements, and non-hazardous transport declarations are prepared and included with shipments to support local customs entry.

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