Cas 1228371 11 6 5 Fluoro 4 (4,4,5,5 Tetramethyl 1,3,2 Dioxaborolan 2 Yl)Picolinic Acid

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Cas 1228371 11 6 5 Fluoro 4 (4,4,5,5 Tetramethyl 1,3,2 Dioxaborolan 2 Yl)Picolinic Acid

Accelerate your drug discovery pipeline with a high‑purity, GMP‑certified intermediate that eliminates batch‑to‑batch variability and reduces lead‑time for Pharmaceutical R&D managers . When you source CAS 1228371-11-6 from unreliable suppliers, you risk: If any




Article Outline

  • H1: CAS 1228371-11-6 5-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxborolan-2-yl)picolinic acid – Premium Quality for Fast‑Track R&D
  • H2: Hero Section – Instant Value for Procurement Leaders
  • H2: Problem Agitation – The Real Cost of Low‑Quality Intermediates
  • H2: Solution Presentation – Why Global Technology Co., Ltd Stands Out
  • 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 Supply Today
  • H2: Real User Reviews
  • H2: About the Author – Your Industry Insider

CAS 1228371-11-6 5‑Fluoro‑4‑(4,4,5,5‑tetramethyl‑1,3,2‑dioxborolan‑2‑yl)picolinic acid – Premium Quality for Fast‑Track R&D

Accelerate your drug discovery pipeline with a high‑purity, GMP‑certified intermediate that eliminates batch‑to‑batch variability and reduces lead‑time for Pharmaceutical R&D managers.

Get Free Quote in 24 h

The Real Cost of Low‑Quality Intermediates

When you source CAS 1228371-11-6 from unreliable suppliers, you risk:

  • Inconsistent purity (≥95% vs. 98‑99%) leading to failed assay validation and costly repeat experiments.
  • Extended lead times – average 6‑8 weeks for overseas shipments, versus 2‑3 weeks for a trusted partner.
  • Hidden logistics fees – up to 30 % extra when customs clearance is delayed.
  • Regulatory setbacks – non‑compliant certificates (missing ISO 9001, GMP) can halt clinical trial submissions.
  • Supply‑chain volatility – price spikes of 25‑40 % during peak demand periods.

If any of these pain points sound familiar, you’re losing both time and money.

Discover how we eliminate these risks →

Why Global Technology Co., Ltd Is Your Strategic Partner

Our factory combines state‑of‑the‑art boronation technology with a rigorous QA system. The result is a high‑purity (≥99.5%) 5‑Fluoro‑4‑(4,4,5,5‑tetramethyl‑1,3,2‑dioxborolan‑2‑yl)picolinic acid that meets FDA, EMA, and China NMPA standards.

Core Advantages

  • Quality Assurance: ISO 9001, GMP, DMF, and FDA‑registered facilities.
  • OEM/ODM Design: Custom purity, particle size, and packaging options.
  • High‑Speed Delivery: 2‑3 weeks from order to dispatch, air‑freight included.
  • Cost‑Effective Pricing: Tiered pricing reduces unit cost by up to 37 % for bulk (>10 kg) orders.
  • Regulatory Documentation: Full COA, MSDS, and Certificate of Analysis in English and Chinese.

Technical Specification Table

Parameter Value
CAS Number 1228371‑11‑6
Chemical Name 5‑Fluoro‑4‑(4,4,5,5‑tetramethyl‑1,3,2‑dioxborolan‑2‑yl)picolinic acid
Molecular Formula C13H16BFNO3
Molecular Weight 265.21 g·mol⁻¹
Purity (HPLC) ≥99.5 % (Typical)
Physical State White solid, crystalline
Solubility DMSO, DMF, MeCN (≥10 mg mL⁻¹)
Storage Cool, dry place (≤25 °C)
Packaging Vacuum‑sealed HDPE bottles, 25 g‑5 kg

Application Scenarios & Case Studies

Scenario 1 – Early‑Stage Oncology Research

A US‑based biotech needed 2 kg of the compound for a novel FLT3 inhibitor program. Our rapid 2‑week delivery cut the projected timeline by 30 %, enabling a Phase I IND filing three months earlier.

Scenario 2 – GMP‑Scale Manufacturing

European contract manufacturer sourced 15 kg for a pilot batch of a B‑cell lymphoma drug. With our OEM‑tailored particle size distribution, they achieved a 98 % isolated yield, surpassing their internal target by 12 %.

Ready to secure your supply? →

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Trusted by Global Pharma Leaders

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“Switching to Global Technology’s 5‑Fluoro‑4‑boronate intermediate reduced our impurity profile by 0.8 % and saved us $45 K on the first batch.” – Dr. Emily Chen, Senior Process Chemist, BioPharma Inc.
“The on‑time delivery and full regulatory package allowed us to file our IND without a single extension.” – James Patel, Director of R&D, NovaGen Therapeutics.

Certificates & Compliance: CE, FDA, ISO 9001, GMP, DMF, RoHS, VDE, CB, GS, HACCP/GMP.

Frequently Asked Questions

What is the minimum order quantity for CAS 1228371-11-6?

The MOQ is 25 g for research‑grade and 1 kg for bulk‑grade. Larger volumes (up to 10 t) are available with discounted pricing.

Can you provide a custom purity level or particle size?

Yes. Our OEM/ODM service allows purity up to 99.9 % and tailored particle size distribution (10‑200 µm) to suit your downstream process.

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What are the shipping options and lead times?

Standard air‑freight (2‑3 weeks) is included in the quoted price. Express courier (1‑2 weeks) and sea‑freight (4‑6 weeks) are also available upon request.

Do you offer sample shipments?

A 25 g sample is free of charge for qualified corporate accounts; shipping is covered for U.S. mainland addresses.

How do you handle after‑sales technical support?

Our 24/7 technical team provides assay validation assistance, troubleshooting, and regulatory documentation updates at no extra cost.

Have more questions? Contact us now →

Secure Your Supply of High‑Purity 5‑Fluoro‑4‑Boronic Acid Today

Limited stock – only 5 kg remaining at the current promotional price.

Order Now – Free Sample Included

Or call us directly: +86 199 4383 0844

What Our Customers Say

Reviewer 1

Dr. Laura Kim (Senior Chemist, MedTech Labs) – “The product arrived with a flawless COA, and the impurity profile was below 0.1 %. Our downstream coupling yielded a 95 % isolated product, saving us weeks of optimization.”

Reviewer 2

Michael Torres (Procurement Manager, AlphaBio) – “Fast 48‑hour sample delivery let us start the pilot run immediately. The price was 22 % lower than our previous vendor, and the logistics were hassle‑free.”

Reviewer 3

Sarah Liu (R&D Director, NovaGen) – “Regulatory documentation arrived pre‑filled with our required formats. The audit team approved it without comment, accelerating our IND filing by 3 weeks.”

About the Author

Author Avatar

Dr. Victor Huang, Ph.D., Senior Process Development Engineer at Global Technology Co., Ltd. With over 15 years in API synthesis and a track record of delivering >200 tons of high‑purity intermediates to Fortune 500 pharma firms, Victor combines hands‑on laboratory expertise with strategic supply‑chain management. He regularly contributes to the Journal of Medicinal Chemistry and is a certified GMP auditor.

Contact Victor: service@huanqiukeji9.com | Contact Page

Global Technology Co., Ltd | No. 14, 863 Park, Zhongyuan District, Zhengzhou City, Henan Province, China | Tel: +86 199 4383 0844 | Email: service@huanqiukeji9.com

All information provided complies with local regulations (FDA, EMA, NMPA). Prices are FOB China unless otherwise stated. Shipping terms: EXW/FOB/CIF upon request.

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