Views: 0 Author: Site Editor Publish Time: 2025-07-07 Origin: Site
CAS No. 90357-53-2, known as (2R,3S)-3-Phenylisoserine methyl ester hydrochloride, is a highly specialized chiral intermediate used in the synthesis of Docetaxel (Taxotere)—a leading anti-cancer medication used in the treatment of breast cancer, non-small cell lung cancer, prostate cancer, and other solid tumors.
This compound represents the esterified and salt-formed version of 3-phenylisoserine, making it more soluble and reactive in key coupling steps during taxane production. The (2R,3S) configuration ensures the pharmacologically active stereochemistry required for effective microtubule inhibition in cancer cells.
As part of the Docetaxel side chain, this intermediate plays a central role in assembling the final cytotoxic compound with optimal activity.
The methyl ester form facilitates downstream esterification steps, while the hydrochloride salt enhances solubility and stability.
Only the (2R,3S) enantiomer is used in API synthesis due to its alignment with receptor binding and therapeutic effect.
Used in taxane semi-synthesis from natural precursors such as 10-DAB (10-deacetylbaccatin III), it enables high-yield API production.
This intermediate is in consistent demand from contract manufacturers and pharmaceutical companies working on cancer therapeutics.
Location: Basel, Switzerland
Overview: Lonza delivers high-purity chiral intermediates under GMP, including taxane building blocks like CAS 90357-53-2 for oncology APIs.
Specialty: Scalable and compliant synthesis of cytotoxic intermediates.
Location: Bubendorf, Switzerland
Overview: Bachem specializes in the production of stereochemically defined amino acid derivatives and oncology intermediates.
Specialty: Advanced peptide and esterified intermediates with salt forms.
Location: Changzhou City, Jiangsu Province, China
Overview: Eastfine supplies CAS No. 90357-53-2 with high enantiomeric purity, strong batch consistency, and full regulatory documentation for global export.
Specialty: Oncology-grade intermediates for semi-synthetic APIs like Docetaxel.
Location: Plankstadt, Germany
Overview: CordenPharma produces high-potency intermediates and GMP-compliant taxane side chains for clinical and commercial supply.
Specialty: Oncology-focused CDMO with full route development.
Location: Craigavon, Northern Ireland
Overview: Almac offers cGMP synthesis of esterified and protected intermediates for cancer drug development and commercial manufacturing.
Specialty: Route optimization for small- to mid-volume oncology intermediates.
Location: Milan, Italy
Overview: Olon supports taxane production with tailored building blocks like CAS 90357-53-2, manufactured in EU GMP-certified facilities.
Specialty: Consistent intermediate supply for injectable oncology APIs.
Location: Hoddesdon, United Kingdom
Overview: Pharmaron’s UK operations offer contract synthesis of taxane-related intermediates for early- and late-stage development.
Specialty: Flexible manufacturing with emphasis on purity and speed.
Location: Bubendorf, Switzerland
Overview: Carbogen Amcis delivers custom synthesis of cytotoxic intermediates, including esterified chiral acids and their salts.
Specialty: Contained GMP manufacturing of highly potent intermediates.
Location: Düsseldorf, Germany
Overview: Enzymaster uses enzyme-driven processes to produce optically pure chiral intermediates like 90357-53-2 with excellent yield and sustainability.
Specialty: Biocatalytic routes for green and scalable chiral synthesis.
Location: Ecully, France
Overview: Seqens produces Docetaxel intermediates under GMP, with capabilities in crystallization, salt formation, and analytical validation.
Specialty: Custom manufacturing for oncology intermediates in Europe.
Docetaxel remains a frontline treatment for multiple cancers. Intermediate demand continues as new generic and combination formulations emerge globally.
Intermediates like CAS 90357-53-2 are increasingly preferred in hydrochloride salt form for better stability and solubility during synthesis and transport.
New asymmetric synthesis and enzymatic methods are improving yield and reducing waste in taxane intermediate manufacturing.
Oncology intermediates face strict scrutiny from the FDA, EMA, and PMDA, requiring detailed impurity profiling and consistent quality control.
Many pharmaceutical companies are outsourcing the production of intermediates to experienced CDMOs to save time and ensure regulatory compliance.
CAS No. 90357-53-2, or (2R,3S)-3-Phenylisoserine Methyl Ester Hydrochloride, is a highly valuable intermediate in the synthesis of Docetaxel, a globally used cancer treatment. With its Boc-protected ester form and high chiral purity, it supports efficient and reliable oncology drug production.
Manufacturers like Lonza, Bachem, Eastfine, and others continue to play a key role in ensuring the pharmaceutical industry’s access to this critical building block under rigorous international standards.
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