Cyanocobalamin - Impurity E

Pharmaffiliates offers a wide range of products which includes (?e)-?-[[2-butyl-1-[[4-(methoxycarbonyl)phenyl]methyl]-1h-imidazol-5-yl] methylene]-2-thiophenepropanoic acid ethyl ester. It belongs to eprosartan category. Contact us for more information.

Pharmaffiliates offers a wide range of products which includes (?r,?r)-6-amino-?,?-dihydroxy-9h-purine-9-butanoic acid. It belongs to adenosine category. Contact us for more information.

CAS No. 767625-11-6 ;  Edoxaban M1 Impurity. It is also known as  2-(((1S,2R,4S)-4-(Dimethylcarbamoyl)-2-(5-methyl-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridine-2-carboxamido)cyclohexyl)amino)-2-oxoacetic Acid; 

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CAS No. 767625-11-6 ;  Edoxaban M1 Impurity 2-(((1S,2R,4S)-4-(Dimethylcarbamoyl)-2-(5-methyl-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridine-2-carboxamido)cyclohexyl)amino)-2-oxoacetic Acid;

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CAS No. 767625-11-6 ;  Edoxaban M1 Impurity 2-(((1S,2R,4S)-4-(Dimethylcarbamoyl)-2-(5-methyl-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridine-2-carboxamido)cyclohexyl)amino)-2-oxoacetic Acid;

Cyanocobalamin Impurity E is a related compound of Cyanocobalamin (Vitamin B12) used as a reference standard for pharmaceutical research and analytical testing. It supports laboratories in impurity profiling, method development, quality control, and analytical assessment of Cyanocobalamin.

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Cyanocobalamin Impurity F, also identified as Cyanocobalamin Isomer, is a Cyanocobalamin-related impurity offered by Pharmaffiliates for pharmaceutical and analytical research. It is listed as a pharmaceutical standard and chiral standard, making it suitable for research involving impurity analysis and ana...

Pharmaffiliates is providing all the Analytical Services (i.e. Method Development, Method Validation & Transfer, Stability Studies, Contract Analysis, etc)

Pharmaffiliates is Supplying all the Pharmacopoeial Reference Standards (i.e. USP, EP, BP, IP, JP).Apart from this we offer Pesticide Standards, Phyto-chemical Standards, Food & Environmental Standards, etc.
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Pharmaffiliates Analytics & Synthetics (P) Ltd, is an integrated CRO (Contract Reserach Organisition) established in year 2001. Presently our group consists of more than 130 Scientists with 3 R&D Centres offering its expertise in Custom Synthesis, Impurity synthesis, Isotoped lebelled compound...

Pharmaffiliates providing the full support for the Regulatory Services (i.e. DMF Filling, Dossier Preparations, etc)

Range of Columns

Explore the Pharmaffiliates Catalogue Brochure, featuring our extensive range of pharmaceutical reference standards, impurities, nitrosamines, peptides, stable isotope-labeled compounds, APIs, intermediates, and fine chemicals.

The catalogue provides detailed product information to help pharmaceutical, biotechnology, and research laboratories find suitable materials for analytical research, impurity profiling, quality control, method development, and pharmaceutical development.

Discover our product portfolio and find the right reference materials for your research needs.

Pharmaffiliates offers a range of HPLC columns designed to support reliable and consistent chromatographic analysis in pharmaceutical and research laboratories. Our columns are suitable for applications such as method development, impurity profiling, assay testing, quality control, and routine analysis.

With different column chemistries and configurations available, Pharmaffiliates helps laboratories select suitable HPLC columns based on their specific analytical requirements. Our HPLC columns support pharmaceutical, analytical, and research applications where good separation, reproducible results, and dependable performance are essential.

CRDMO – Contract Research, Development & Manufacturing Pharmaffiliates provides CRDMO services that support pharmaceutical and biotechnology companies across different stages of research, development, and manufacturing. Our team works closely with clients to provide practical solutions tailored to their project requirements.

Our capabilities cover discovery chemistry, custom synthesis, process development, analytical research, API development, impurity synthesis, scale-up, and manufacturing support. With strong scientific expertise and modern facilities, we help customers move projects forward efficiently while maintaining quality and regulatory requirements.

From early-stage research to commercial development, Pharmaffiliates offers flexible support designed to meet the changing needs of pharmaceutical and life science companies.

Nitrosamine Impurities – Description Pharmaffiliates offers a wide range of nitrosamine impurities and reference standards to support pharmaceutical research, impurity testing, and analytical method development. Our portfolio covers API-related nitrosamines, nitrosamine drug substance-related impurities (NDSRIs), and other nitrosamine compounds relevant to pharmaceutical analysis.

These standards help pharmaceutical companies and analytical laboratories with nitrosamine risk assessment, impurity profiling, method development, validation, and regulatory testing. Pharmaffiliates continues to expand its portfolio to support the evolving analytical and quality requirements of the pharmaceutical industry.

Certified Reference Materials (CRM) – Description Pharmaffiliates offers a wide range of Certified Reference Materials (CRMs) to support accurate and reliable pharmaceutical analysis. Our CRMs are suitable for method development, validation, quality control, analytical testing, and research applications.

Our portfolio covers various APIs, impurities, related substances, and other pharmaceutical compounds, helping laboratories maintain consistency and confidence in their analytical results. Pharmaffiliates provides quality reference materials to support the analytical needs of pharmaceutical and research organizations.

GC Traceable GC Traceable Reference Standards – Description Pharmaffiliates offers GC-traceable reference standards designed to support accurate and reliable gas chromatography (GC) analysis. These standards help laboratories with method development, calibration, validation, quality control, and routine analytical testing.

Our GC-traceable products support pharmaceutical and analytical laboratories in achieving consistent results and maintaining confidence in their testing processes.

Formulation Development & Analytical Research and Development (ARD) Pharmaffiliates provides Formulation Development and Analytical Research and Development (ARD) services to support pharmaceutical projects from early development through testing and optimization.

Our formulation expertise includes developing and improving pharmaceutical dosage forms, while our ARD team supports method development, method validation, method transfer, impurity testing, assay, related substances, residual solvents, elemental impurities, and stability studies.

With experienced teams and modern analytical capabilities, Pharmaffiliates helps customers develop reliable formulations and generate accurate analytical data to support their pharmaceutical development needs.

API – Active Pharmaceutical Ingredient.Pharmaffiliates provides API development and research support for pharmaceutical companies at different stages of product development. Our capabilities cover API research, process development, analytical support, impurity profiling, scale-up, and manufacturing support.

We work with a range of pharmaceutical compounds and provide solutions tailored to specific project requirements. Our experienced team and analytical capabilities help customers develop,

Analytical Research & Development (ARD) – Description Pharmaffiliates provides Analytical Research & Development (ARD) services to support pharmaceutical companies throughout their product development journey. Our team works on analytical method development, method validation, method transfer, assay, related substance testing, impurity analysis, residual solvent testing, elemental impurity testing, and stability studies.

With advanced analytical instruments and experienced professionals, we generate reliable data to help customers understand product quality, meet testing requirements, and support pharmaceutical development projects.

Formulation & Development (F&D) – Pharmaffiliates provides Formulation & Development (F&D) services to support pharmaceutical products from early-stage development to final formulation. Our team works on developing and improving formulations based on specific product requirements.

Our capabilities include formulation development, dosage form development, formulation optimization, and analytical support. We work closely with customers to develop formulations that meet their requirements for quality, stability, performance, and consistency.