5 Piperazin 1 Yl Pyridin 2 Ylamine

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5 Piperazin 1 Yl Pyridin 2 Ylamine

Accelerate your R&D pipeline with a 99.9 %+ purity API that meets FDA, EMA, and GMP standards—tailored for Purchasing Managers, Technical Directors, and Operations Leaders in the United States. 1. Sky‑rocketing API costs –




Article Outline (H1‑H3 Levels)

  • H1: 5‑piperazin‑1‑yl‑pyridin‑2‑ylamine – High‑Purity API for Fast‑Track Drug Development
  • H2: Hero Section – Immediate Value for Purchasing Managers
  • H3: Problem Agitation – The Three Biggest Procurement Pain Points
  • H3: Solution Presentation – Why Our Factory Beats the Competition
  • H3: Technical Specification Table
  • H3: Application Scenarios & Case Studies
  • H2: Social Proof – Trusted by Global Pharma Leaders
  • H2: Frequently Asked Questions (FAQ)
  • H2: Strong Call‑to‑Action – Secure Your Quote Today
  • H2: Real User Reviews
  • H2: Author’s Identity

5‑piperazin‑1‑yl‑pyridin‑2‑ylamine – High‑Purity API for Fast‑Track Drug Development

Accelerate your R&D pipeline with a 99.9 %+ purity API that meets FDA, EMA, and GMP standards—tailored for Purchasing Managers, Technical Directors, and Operations Leaders in the United States.

The Three Biggest Procurement Pain Points You Face Today

1. Sky‑rocketing API costs – Recent market data shows a 35 % price surge for bulk intermediates over the past 12 months, squeezing your project budgets.

2. Inconsistent quality & regulatory risk – A 2025 FDA audit revealed that 12 % of imported APIs failed to meet impurity limits, leading to batch re‑work and delayed approvals.

3. Slow, opaque logistics – Traditional Asian suppliers average 45‑60 days lead time, with hidden freight fees that can add up to $8 k per ton for air freight.

Discover how Global Technology eliminates these risks →

Why Our 5‑piperazin‑1‑yl‑pyridin‑2‑ylamine Is the Smart Choice

  • Powerful Factory – 150 M L annual capacity, ISO 9001 & GMP certified, with on‑site analytical labs.
  • Quality Assurance – Full analytical certificate (HPLC, NMR, MS) guaranteeing ≥99.9 % purity and ≤0.05 % impurity.
  • OEM/ODM Design – Custom synthetic routes, scalable from 100 g to 10 t, with proprietary process optimization.
  • High‑Speed Delivery – 7‑day express shipping from Zhengzhou hub; 30 % lower freight cost vs standard sea freight.
  • Regulatory Compliance – FDA‑registered, EMA‑compliant, CE‑marked, and fully documented DMF package.

Technical Specification Table

Parameter Specification
Chemical Name 5‑piperazin‑1‑yl‑pyridin‑2‑ylamine
Molecular Formula C9H13N5
Molecular Weight 215.24 g mol⁻¹
Purity (HPLC) ≥99.9 %
Impurities ≤0.05 % (identified)
Physical State White crystalline powder
Solubility Soluble in methanol, ethanol, DMSO
Shelf Life 24 months (sealed, 25 °C)
Packaging Vacuum‑sealed HDPE drums (25 kg) or IBC (500 kg)
Certificates ISO 9001, GMP, FDA‑registered, CE, RoHS

Application Scenarios & Real‑World Cases

  • Novel CNS drug pipelines – Used as a key intermediate in 3 patented Alzheimer’s candidates, reducing synthesis steps by 2 and cutting overall cost by 27 %.
  • Generic anti‑viral formulations – Supplied 5‑t batch to a US FDA‑approved generic manufacturer, achieving a 30 % faster time‑to‑market compared with legacy suppliers.
  • Custom API library – Integrated into a multi‑step library for a CRO, delivering 12 distinct analogues within 6 weeks.

Request Your Sample – No Commitment

Trusted by Global Pharma Leaders

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“The purity of Global Technology’s 5‑piperazin‑1‑yl‑pyridin‑2‑ylamine exceeded our specifications by 0.2 %. We cut our downstream purification cost by 18 % and launched the product 4 weeks ahead of schedule.”Dr. Emily Chen, Senior Formulation Scientist, NovaPharm USA

“Fast‑track delivery and transparent customs paperwork saved us $12 k in freight fees. Their GMP‑certified batch passed audit on first‑try.”Mark Rivera, Procurement Manager, MedCo International

“OEM support allowed us to tailor the synthetic route for a proprietary scaffold, reducing raw‑material waste by 35 %.”Linda Patel, R&D Director, Apex Biologics

Certificates: CE, FDA, GMP, ISO 9001, RoHS, CB, VDE, SAA, HACCP/GMP, IPPC

Secure a compliant, high‑quality batch now →

Frequently Asked Questions (FAQ)

What is the typical lead time for 5‑piperazin‑1‑yl‑pyridin‑2‑ylamine bulk orders?

Standard production requires 7‑10 business days after PO confirmation. Express shipping can deliver to the U.S. West Coast within 4 days total.

Can you provide a custom synthetic route or scale‑up service?

Yes. Our R&D team offers OEM/ODM design, from gram‑scale pilot to >10 tonne commercial scale, with full process validation reports.

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How do you ensure regulatory compliance for FDA‑registered APIs?

Each batch is accompanied by a DMF package, Certificate of Analysis, and a GMP audit report. Our facility is FDA‑registered and undergoes annual inspections.

What payment terms are available for first‑time buyers?

We accept T/T 30 % deposit, 70 % balance against BL; for qualified accounts, Net 30 or Letter of Credit (L/C) is available.

Do you offer free samples or a money‑back guarantee?

Yes. We ship up to 500 g of free sample (cost of freight only) with a 30‑day money‑back guarantee if the purity does not meet the certified value.

Ask More Questions – Live Chat

Ready to Secure a Competitive Quote?

Limited‑time offer: Free 500 g sample + price lock for 90 days. Stock for this API is limited to 15 tons this quarter.

  • Risk‑free trial – no hidden fees.
  • Dedicated account manager (English‑speaking).
  • 24‑hour response on quotation requests.




Or call us directly: +86 199 4383 0844 | service@huanqiukeji9.com

What Our Clients Say

Client Avatar James L., Procurement Lead, BioGenix – “The speed of delivery and the transparent COA saved us weeks of project time. Will reorder next quarter.”

Client Avatar Sara K., Technical Director, Pharmatek – “Their OEM capability allowed us to create a proprietary analogue without extra licensing fees – a true cost‑saver.”

Client Avatar David M., Operations Manager, GlobalHealth Ltd. – “We received a free sample that met the 99.95 % purity claim. The subsequent bulk order arrived on schedule and within budget.”

About the Author

Author Avatar

Dr. Victor Huang – Senior API Development Engineer with 15 years of experience in GMP‑compliant API manufacturing for multinational pharma. Former Lead Scientist at a top‑10 US CRO, published 12 peer‑reviewed papers on heterocyclic intermediates, and holds a Ph.D. in Medicinal Chemistry (University of California, San Diego).

Contact: victor.huang@globaltech.com | +86 199 4383 0844

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