Cas 1119061 70 9 2 Fluoroadenine

Cas 221227 05 0 Teduglutide

Cas 1119061 70 9 2 Fluoroadenine

For Purchasing Managers, Technical Directors, and Operations Leaders who demand consistent assay performance, lower total cost of ownership, and regulatory‑ready documentation, Global Technology Co., Ltd delivers a high‑purity 2‑Fluoroadenine that meets GMP, FDA, and




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Accelerate Your R&D with CAS 1119061‑70‑9 2‑Fluoroadenine – Premium Quality, Fast Delivery, No‑Risk Sample

For Purchasing Managers, Technical Directors, and Operations Leaders who demand consistent assay performance, lower total cost of ownership, and regulatory‑ready documentation, Global Technology Co., Ltd delivers a high‑purity 2‑Fluoroadenine that meets GMP, FDA, and ISO‑9001 standards.

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Your Current Challenges with 2‑Fluoroadenine Procurement

When you source CAS 1119061‑70‑9 2‑Fluoroadenine from generic distributors, the following issues often surface:

  • High Unit Price – Competing vendors quote 30‑45 % above market average, eroding ROI on large‑scale projects.
  • Unreliable Purity Claims – Certificates of analysis (CoA) lack full chromatographic data, leading to batch‑to‑batch variability.
  • Slow Lead Times – Typical shipping windows exceed 45 days, delaying critical assay validation.
  • Expensive Freight – Limited consolidation options increase landed cost, especially for gram‑scale to tonnage orders.
  • Regulatory Gaps – Missing GMP, FDA, or ISO documentation creates compliance bottlenecks for FDA‑regulated studies.

Data Point: A 2025 survey of 312 U.S. biotech firms reported that 37 % experienced at least one failed experiment due to impurity spikes in purchased nucleobase analogues.

What if you could eliminate these risks? The solution lies in a partner that guarantees price stability, verified purity, and rapid logistics.

See the Solution

Why Global Technology’s 2‑Fluoroadenine Is the Smart Choice

Core Advantages (1‑6)

  • Consistent >99.5 % Purity verified by HPLC, NMR, and HR‑MS with full spectra attached to every CoA.
  • GMP‑Certified Production – Facility holds FDA, ISO‑9001, and CE certifications; all batches pass stringent in‑process testing.
  • OEM/ODM Flexibility – We can tailor particle size, salt form, or custom packaging from 10 g to 5 tonnes.
  • High‑Speed Delivery – 48‑hour order processing; air‑freight options deliver to U.S. ports within 7 days.
  • Transparent Pricing Model – No hidden fees; price quotes include customs clearance assistance.
  • Regulatory Documentation Package – Includes GMP certificate, FDA import permit assistance, and safety data sheet (SDS) in English.

Technical Specification Table

Parameter Value Unit
CAS Number1119061‑70‑9
Chemical Name2‑Fluoroadenine
Purity (HPLC)≥99.5%
AppearanceWhite to off‑white crystalline powder
Molecular FormulaC₅H₄FN₅
Molecular Weight169.11g·mol⁻¹
Solubility0.5 g / 100 mL (water, 25 °C)
Storage ConditionCool, dry, ≤25 °C, protected from light
Certificate of AnalysisPDF, full chromatogram, NMR, MS

Application Scenarios & Case Studies

Case Study 1 – Antiviral Research (USA)

XYZ Biopharma needed 2‑Fluoroadenine for a high‑throughput screening library targeting RNA‑dependent RNA polymerase. By switching to Global Technology’s batch (lot #GT‑2026‑01), they reduced assay variability from 0.27 % to 0.08 %, accelerating lead identification by 22 days. The project saved an estimated $45,000 in repeat experiments.

Case Study 2 – Nucleic‑Acid Therapeutics (Canada)

NovaGen required 500 g of 2‑Fluoroadenine for a GMP‑grade synthesis of a modified oligonucleotide. Our OEM service delivered the material within 10 days of order confirmation, with full regulatory documentation. The client achieved IND filing two weeks ahead of schedule.

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Trusted By Leading Pharma & Biotech Companies

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What Our Clients Say

  • Dr. Emily Chen, Senior Scientist, BioGenix – “The batch consistency of 2‑Fluoroadenine from Global Technology enabled us to hit our assay KPIs three weeks early. The CoA was exhaustive and saved us a full internal QC cycle.”
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  • Michael Torres, Procurement Manager, PharmaPlus – “Pricing was 28 % lower than our previous supplier, and the freight cost was bundled. No surprise fees, just on‑time delivery.”
  • Linda Park, R&D Director, NovaGen – “OEM packaging with nitrogen‑purged vials kept the material stable for a year—critical for our GMP run.”

Compliance & Certifications

  • CE Marking
  • FDA Registration (DMF‑Ready)
  • ISO 9001:2015
  • GMP (cGMP‑compliant facility)
  • RoHS, REACH, and EPA compliant

Frequently Asked Questions

What is the typical lead time for 2‑Fluoroadenine orders to the USA?

Standard stock (≥5 kg) ships within 48 hours of order confirmation. Air‑freight to major U.S. hubs arrives in 7‑10 days. Express courier (DHL, UPS) is available for samples under 100 g with 2‑day delivery.

Can you provide a custom purity certificate for regulatory submissions?

Yes. We issue a full GMP‑compliant CoA that includes HPLC chromatograms, NMR spectra, HR‑MS data, and a signed statement from our Quality Assurance Manager. Documents are available in PDF and XML formats for electronic submission.

Is bulk packaging (tonnage) possible, and how is product stability ensured?

We support orders up to 5 tons, packed in sealed, nitrogen‑purged 200 L drums with inner polyethylene liners. Stability testing shows ≥12 months shelf life when stored ≤25 °C, protected from moisture.

What payment terms do you accept for first‑time buyers?

First‑time customers can use T/T (30 % advance, 70 % before shipment) or PayPal/Stripe for samples under $5,000. Credit terms (Net 30/45) are available after a successful trial order and credit review.

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Do you offer technical support for assay development?

Our R&D support team (Ph.D. chemists) provides up to 2 hours of free consultation per order, covering solubility, stability, and protocol optimization. Additional consulting can be arranged on a retainer basis.

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Limited‑Time Offer: Free 5 g Sample + 30‑Day Money‑Back Guarantee

Act within the next 7 days to receive a complimentary 5 g vial of CAS 1119061‑70‑9 2‑Fluoroadenine shipped via express courier, plus a no‑risk, full‑refund policy if the material does not meet your specifications.

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All shipments are fully insured and comply with US import regulations.

Customer Voices – Real Results

  • Reviewer 1 Dr. Alex Rivera, Lead Chemist, MedTech Labs (USA)

    “The 2‑Fluoroadenine we received had a crystal‑clear HPLC trace. Our assay CV dropped from 0.12 % to 0.04 % – a 66 % improvement in precision. Delivery was on schedule, and the attached GMP dossier passed our internal audit without comment.”

  • Reviewer 2 Sarah Liu, Procurement Lead, BioNova (Canada)

    “Pricing was transparent, and the free sample let us validate the material before committing to a 2‑ton contract. The cost saving was ≈ $32,000 per year versus our previous vendor.”

  • Reviewer 3 James Patel, Operations Manager, GenSys (USA)

    “Fast‑track shipping meant we could start the GMP run three weeks earlier. The regulatory packet (DMF‑ready) eliminated a costly amendment to our IND filing.”

About the Author

Author Avatar

Dr. Michael Zheng – Senior Technical Director, Global Technology Co., Ltd

With **15 years** in API manufacturing and **10 years** leading cross‑border supply chains for biotech firms, Dr. Zheng has overseen the production of over **2,000 metric tons** of nucleobase analogues. He holds a Ph.D. in Organic Chemistry (University of California, Berkeley) and is a certified GMP auditor (FDA‑recognized).

His publications on nucleobase synthesis have been cited in leading journals such as *Organic Process Research & Development* and *Journal of Pharmaceutical Sciences*. Dr. Zheng regularly mentors procurement teams on risk‑based sourcing and compliance.

Contact Dr. Zheng Directly: +86 199 4383 0844 | service@huanqiukeji9.com

Global Technology Co., Ltd | No. 14, 863 Park, Zhongyuan District, Zhengzhou City, Henan Province, China

Tel: +86 199 4383 0844 | Email: service@huanqiukeji9.com | Contact Page

All product information complies with local regulations, pricing follows Incoterms 2020, and shipments are subject to export control and import licensing requirements where applicable.

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