Pharmaceutical Intermediates you can trust.
Scientifically verified. Analytically documented. Globally sourced. Veratix Pharma connects U.S. pharmaceutical, biotech, and research organizations with qualified international manufacturing partners — backed by PhD-level analytical verification.
Scientifically Verified
Every product is supplied with a Certificate of Analysis from the manufacturer, reviewed against specification by our PhD-level scientific team. We confirm the documentation covers purity, residual solvents, and heavy metals before release — review is standard, not optional.
Globally Sourced, Locally Supported
We source from qualified manufacturers in India with proven production capabilities, selected through direct evaluation. You get internationally competitive pricing with U.S.-based scientific support and a single accountable point of contact.
Documentation You Can Trust
Every product is supplied with a complete documentation package — Certificate of Analysis, specifications, and supplier qualification records — to support your own regulatory, quality, and audit requirements. LCMS, NMR, and stability data available on request.
A curated portfolio, not a commodity catalog.
We qualify every supplier and review every certificate — focusing on high-demand oncology intermediates, medicinal chemistry building blocks, and specialty fluorinated compounds.
Oncology API Intermediates
Lenalidomide, Pazopanib, Sunitinib, and Nintedanib building blocks and key intermediates — supporting the generic pharmaceutical supply chain with documented, quality-verified materials.
Heterocyclic Building Blocks
Oxindoles, indoles, and aromatic building blocks for medicinal chemistry and drug discovery programs. Kilogram-scale availability with full analytical documentation.
Fluorinated & Specialty Compounds
Trifluoromethyl derivatives and fluorinated building blocks for advanced pharmaceutical synthesis. Premium-grade materials with specialized handling.
New Chemical Entities
Exclusive access to novel heterocyclic structures not available from commodity suppliers. Custom synthesis capability from gram to multi-kilogram scale.
A clear path from inquiry to supply.
A straightforward process designed around what quality and procurement teams actually need.
Inquiry
Send us the compound, CAS number, quantity, and any specification requirements. We confirm availability and lead time.
Quote & CoA
You receive a written quotation with the manufacturer's specification and Certificate of Analysis, reviewed by our scientific team.
Sample
Request a sample for your own evaluation and qualification before committing to a production quantity.
Supply
On approval, we coordinate production, documentation, import logistics, and delivery — with a single U.S. point of contact throughout.
More than a product and a basic certificate.
Our founder holds a PhD in biomedical science with extensive experience in LCMS, HPLC, and analytical method development. Every product we distribute passes through a scientific review process that goes beyond what commodity suppliers offer.
When you source from Veratix Pharma, you're not buying from a broker. You're working with a scientific partner who understands your analytical requirements, speaks your technical language, and delivers documentation that meets the standards your quality team expects.
Industries We Serve
- Generic Pharmaceutical Companies
- Contract Development & Manufacturing Organizations
- Biotech & Translational Research
- Medicinal Chemistry & Drug Discovery
- Research Chemical Distributors
- Academic & Government Research
Scientific credibility,
built into the supply chain.
Veratix Pharma was founded by a PhD scientist to raise the standard of analytical documentation in the pharmaceutical intermediates supply chain.
Veratix Pharma LLC is a pharmaceutical intermediate and specialty chemicals sourcing company based in Irving, Texas. Founded in 2026, we specialize in connecting U.S. pharmaceutical and biotechnology organizations with high-quality, analytically verified intermediates and building blocks from qualified international manufacturing partners.
What sets us apart is our scientific foundation. Unlike traditional chemical brokers, Veratix Pharma was founded by a PhD scientist with deep expertise in analytical chemistry, LCMS, HPLC, and pharmaceutical quality systems. Every product we distribute is evaluated, documented, and verified to standards that go beyond industry norms.
We believe the pharmaceutical supply chain deserves more than commodity brokerage. It deserves scientific credibility, analytical rigor, and documentation that supports your regulatory and audit requirements. That's what Veratix Pharma delivers.
Our Mission
To be the most scientifically credible source of pharmaceutical intermediates and specialty building blocks in the United States — combining global sourcing capability with PhD-level analytical verification and uncompromising quality documentation.
Our Vision
To build a vertically integrated pharmaceutical materials platform that sets new standards for analytical documentation, supplier qualification, and scientific customer support in the intermediates supply chain.
The people behind Veratix.
Bhaskara Chary Arroju
Mr. Arroju brings extensive experience in international sourcing, supply chain management, and business operations. With established manufacturing and sourcing relationships across India's pharmaceutical sector, he oversees capital operations, supplier management, import logistics, and business infrastructure for Veratix Pharma.
Dr. Sivaram Yadav, PhD
Dr. Yadav brings over 15 years of experience in biomedical research, analytical chemistry, and pharmaceutical science, with expertise spanning LCMS, HPLC, proteomics, translational research, and quality systems. His career includes positions at leading academic medical institutions and diagnostic laboratories, with published research in proteomics, cancer biology, and drug development.
At Veratix Pharma, he leads scientific strategy, quality assurance, customer engagement, and technical documentation.
Three principles guide everything.
Source Selectively
We don't list thousands of products from unknown manufacturers. We qualify every supplier, review every certificate against specification, and work only with partners who meet our documentation standards.
Document Thoroughly
Every product ships with comprehensive documentation: Certificate of Analysis with HPLC purity verification, specifications, and storage conditions. LCMS and NMR data available on request — formatted to support your regulatory filings.
Support Scientifically
When you call with a technical question, you talk to a scientist — not a sales rep reading from a script. We understand your synthesis challenges, analytical requirements, and regulatory context.
Products & Catalog
A curated portfolio of pharmaceutical intermediates, heterocyclic building blocks, fluorinated specialty compounds, and new chemical entities — every product sourced from qualified partners and supplied with reviewed analytical documentation.
Pharmaceutical intermediates & building blocks.
Every compound is sourced from qualified manufacturing partners and supplied with a Certificate of Analysis. Filter by category or search by name, CAS, or target drug. Pricing and availability are provided on request.
| Compound | CAS Number | Category / Target | |
|---|---|---|---|
| Methyl 2-(bromomethyl)-3-nitrobenzoate | 98475-07-1 | Lenalidomide | Request Quote |
| 3-(4-Nitro-1-oxoisoindolin-2-yl)piperidine-2,6-dione | 827026-45-9 | Lenalidomide | Request Quote |
| 2-Ethyl-5-nitroaniline | 20191-74-6 | Pazopanib | Request Quote |
| N-(2-Chloropyrimidin-4-yl)-N,2,3-trimethyl-2H-indazol-6-amine | 444731-75-3 | Pazopanib | Request Quote |
| 5-Amino-2-methylbenzenesulfonamide | 6973-09-7 | Pazopanib | Request Quote |
| 5-Fluoroindolin-2-one | 56341-41-4 | Sunitinib | Request Quote |
| Methyl 2-oxoindoline-6-carboxylate | 1027407-75-5 | Nintedanib | Request Quote |
| 5-Nitro-1H-imidazole | 3034-38-6 | Metronidazole | Request Quote |
| Brominated oxindoles (6-Bromo- & 5-Bromo-2-oxindole) | By inquiry | Heterocyclic building block | Request Quote |
| Methoxy-indole derivatives | By inquiry | Heterocyclic building block | Request Quote |
| Nitrovinyl indoles | By inquiry | Heterocyclic building block | Request Quote |
| Brominated aromatic acids | By inquiry | Aromatic building block | Request Quote |
| Trifluoromethyl-substituted aryl compounds | By inquiry | Fluorinated specialty | Request Quote |
| Fluorinated oximes & acetyl derivatives | By inquiry | Fluorinated specialty | Request Quote |
| Fluoroanisole & diazonium specialty reagents | By inquiry | Fluorinated specialty | Request Quote |
| Novel triazole derivatives | Exclusive | New chemical entity | Request Quote |
| Pyrrolopyrimidine scaffolds | Exclusive | New chemical entity | Request Quote |
Building blocks, fluorinated specialties, and new chemical entities are supplied to specification; exact CAS numbers, purity grades, and analytical data are provided with each quotation. Available in research to multi-kilogram quantities.
Our Services
More than products — a complete scientific sourcing experience, from supplier qualification through analytical verification, documentation, and ongoing technical support.
Analytical Review & Documentation
- Certificate of Analysis (COA) review against specification
- HPLC purity data review
- LCMS identity data review
- NMR structural data review (on request)
- Residual solvent data review (ICH Q3C)
- Heavy metals data review (ICH Q3D)
- Independent confirmatory testing arranged on request
Supplier Qualification
- WHO-GMP and ISO certification verification
- FDA establishment registration confirmation
- Drug Master File (DMF) status review
- Analytical capability assessment
- Quality system documentation review
- Sample evaluation prior to qualification
Technical Documentation Packages
- Product specification sheets
- Manufacturer Certificate of Analysis
- Stability and storage data (where available)
- Supplier qualification summary
- Documentation to support regulatory submissions
Custom Synthesis Sourcing
- Gram to multi-kilogram scale
- Heterocyclic and fluorinated chemistry expertise
- Process development and optimization
- Analytical method development for new compounds
- Full documentation package upon delivery
API Sourcing (On Request)
- Active pharmaceutical ingredients sourced to your requirements
- Compound and specification matched to your program
- Manufacturer qualification and documentation review
- Certificate of Analysis and specifications with each supply
- Documentation to support your regulatory and audit needs
Quality Assurance
Quality is not a department at Veratix Pharma — it's the foundation. Our co-founder is a PhD analytical chemist who built this company specifically to raise the standard of quality documentation in the intermediates supply chain.
Documentation you can stake a submission on.
Supplier Qualification
Every manufacturer is qualified through rigorous evaluation covering facility certifications, production capabilities, analytical instrumentation, quality management systems, and regulatory compliance history, with periodic reviews.
Certificate of Analysis
Every product is supplied with a detailed manufacturer's COA covering identity, purity by HPLC, appearance, residual solvents, heavy metals, and water content. We review each COA against specification before release.
Analytical Review
Our PhD scientific team evaluates the supplied analytical data, confirms the methods are appropriate, and verifies results meet specification. Where a customer requires it, independent confirmatory testing can be arranged through accredited third-party laboratories.
Documentation & Traceability
Each product is supplied with a complete documentation package to support your regulatory and audit requirements. Specifications reference relevant pharmacopeial methods (USP, EP, JP), and every lot carries a unique number traceable to its production batch, analytical records, and shipping documentation.
The methods documented on every release.
Each compound is characterized by the manufacturer using validated analytical methods. We review this data against specification before release, and can arrange independent confirmation on request.
HPLC
Purity determination and impurity profiling.
LCMS
Identity confirmation and molecular weight verification.
NMR
Structural confirmation (¹H, ¹³C).
UV-Vis Spectroscopy
Identity and concentration verification.
Melting Point
Physical characterization.
KF Titration
Water content determination.
Industries We Serve
From early-stage drug discovery through commercial generic manufacturing — Veratix Pharma serves organizations across the pharmaceutical and life sciences value chain.
Generic Pharmaceutical Companies
We supply key intermediates for high-demand generic drugs, particularly in oncology — lenalidomide, pazopanib, sunitinib, and nintedanib building blocks — and can source specific APIs on request, matched to your program and supported by full documentation.
CDMOs
Contract development & manufacturing organizations need reliable, qualified raw material sources with consistent quality. We provide the analytical verification and documentation packages CDMO quality teams require.
Biotech & Translational Research
Early-stage biotech and translational programs need specialized compounds in smaller quantities with rapid turnaround. We offer research-scale quantities with the same documentation quality as bulk offerings.
Medicinal Chemistry & Drug Discovery
Our heterocyclic building blocks and fluorinated compounds support medicinal chemistry programs at pharma companies, CROs, and academic labs — the starting materials teams use to build and optimize leads.
Research Chemical Distributors
We serve as a reliable upstream source for distributors who need analytically verified, well-documented materials to resell to their academic and industrial customers.
Academic & Government Research
University chemistry departments, NIH-funded programs, and government laboratories source specialty intermediates and building blocks from Veratix Pharma for synthesis and drug development research.
Get in Touch
Whether you need a product quote, want to discuss custom synthesis, or have a technical question — our scientific team responds to all inquiries within 24 hours.
Veratix Pharma LLC
Specialty pharmaceutical intermediates & sourcing, headquartered in Irving, Texas.
Irving, TX 75038, USA
Frequently Asked Questions
Answers to the questions procurement and quality teams ask most often. Don't see yours? Contact us directly.
What does Veratix Pharma supply?
Pharmaceutical intermediates, heterocyclic building blocks, fluorinated specialty compounds, and select new chemical entities, along with custom synthesis sourcing. Active pharmaceutical ingredients (APIs) can also be sourced on request, matched to your specification. We are a sourcing and distribution company, not a manufacturer — we connect U.S. buyers with qualified manufacturing partners and manage documentation, quality review, and logistics.
Can you source a specific API or compound not in your catalog?
Yes. Beyond our catalog, we source APIs and custom compounds to your requirements through our qualified manufacturing partners. Send us the compound, specification, and quantity, and we will assess feasibility and provide a quotation with supporting documentation.
What documentation do you provide?
Each product is supplied with a complete documentation package — Certificate of Analysis, product specifications, and supplier qualification records — to support your own regulatory, quality, and audit requirements. LCMS, NMR, and stability data are available on request.
Do you provide a Certificate of Analysis?
Yes. Every compound is supplied with the manufacturer's Certificate of Analysis, which our scientific team reviews against specification before release. Independent third-party confirmatory testing can be arranged on request.
Can I request a sample before ordering?
Yes. We encourage sample evaluation and qualification before any production-scale commitment. Request a sample through the contact form or by emailing info@veratixpharma.com.
What quantities are available?
From research quantities through multi-kilogram scale, depending on the compound. Minimum order quantities and lead times are provided with each quotation.
What are your lead times?
Catalog intermediates vary by availability. Custom synthesis is typically 4–8 weeks depending on complexity and scale. We confirm specific timing at the quotation stage.
Are these products for clinical or human use?
No. Our products are intermediates and building blocks supplied to qualified businesses for research, development, and manufacturing use. They are not finished pharmaceutical products and are not intended for direct human or clinical use.
Where is Veratix Pharma located?
Veratix Pharma LLC is based at 1300 W Walnut Hill Ln, Suite 195, Irving, TX 75038, USA, with manufacturing partners internationally.
Privacy Policy
How Veratix Pharma LLC handles the information you share with us.
Effective date: 2026. This policy explains what information we collect and how we use it.
Information we collect. When you submit an inquiry, we collect the information you provide: name, company, title, email, phone, and the details of your request. We do not collect sensitive personal data.
How we use it. We use your information solely to respond to your inquiry, provide quotations and documentation, and communicate with you about your request. We do not sell or rent your information to third parties.
Sharing. We may share necessary details with our manufacturing and logistics partners only to fulfill your request. We may disclose information where required by law.
Data retention & security. We retain inquiry records only as long as needed for business and legal purposes, and take reasonable measures to protect them.
Your choices. To request access to, correction of, or deletion of your information, email info@veratixpharma.com.
This policy may be updated from time to time. Material changes will be reflected on this page.
Terms of Use
The terms governing use of this website and our services.
Use of this website. This website is provided for general information about Veratix Pharma LLC and its products and services. Content is provided as-is, without warranties of any kind.
Products and intended use. All products listed are pharmaceutical intermediates, building blocks, and specialty chemicals supplied to qualified businesses for research, development, and manufacturing use. They are not finished pharmaceutical products and are not intended for direct human or clinical use. Buyers are responsible for determining suitability and for compliance with all applicable laws and regulations.
No specification or pricing guarantee. Product information, availability, and pricing are indicative and confirmed only in a written quotation. Specifications and Certificates of Analysis are provided per shipment.
Limitation of liability. To the fullest extent permitted by law, Veratix Pharma LLC is not liable for indirect or consequential damages arising from use of this website or reliance on its content.
Governing law. These terms are governed by the laws of the State of Texas, USA.
Contact. Questions about these terms: info@veratixpharma.com.