Cas 1048377 78 1 Larotrectinib Intermediate

Cas 1239011 60 9 Larotrectinib Intermediate

Cas 1048377 78 1 Larotrectinib Intermediate

Accelerate your clinical pipeline with a chemically pure, GMP‑compatible Larotrectinib intermediate, engineered for pharmaceutical manufacturers and CROs seeking reliable, on‑time delivery at a competitive price. In 2025‑2026, more than 68% of corporate purchasing managers




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CAS 1048377‑78‑1 Larotrectinib Intermediate – Premium Quality for Fast‑Track Oncology R&D

Accelerate your clinical pipeline with a chemically pure, GMP‑compatible Larotrectinib intermediate, engineered for pharmaceutical manufacturers and CROs seeking reliable, on‑time delivery at a competitive price.

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Problem Agitation – Why Procurement Teams Struggle Today

In 2025‑2026, more than 68% of corporate purchasing managers reported at least one of the following bottlenecks when sourcing oncology APIs:

  • High Unit Price: Traditional suppliers inflate costs by 20‑35% due to limited scale and opaque pricing structures.
  • Inconsistent Purity: Batch‑to‑batch variance >0.5% leads to failed stability studies and costly re‑runs.
  • Slow Lead Times: Average delivery exceeds 45 days, jeopardizing clinical trial timelines.
  • Expensive Shipping: Air‑freight fees surged by 28% after 2024, especially for regulated chemicals.
  • Regulatory Gaps: Missing certificates (e.g., FDA, GMP) cause compliance delays in the US and EU.

Consider this scenario: A mid‑size biotech firm needed 2 kg of Larotrectinib intermediate for a Phase II trial. Their legacy supplier quoted $1,850 /kg, required a 60‑day lead time, and could not provide a COA with ≤99.8% purity. The result? A 3‑month trial delay and an additional $150,000 in contingency costs.

Solution‑oriented decision makers cannot afford such risks. The next section shows how Global Technology Co., Ltd. eliminates each of these pain points.

Discover the Solution

Solution Presentation – What Sets Global Technology Apart

3.1 Core Advantages (5‑Point Value Matrix)

  1. Powerful Factory Network: Our partner GMP‑certified plants in Zhengzhou and Shanghai collectively produce >10 MT/month of high‑purity kinase inhibitors.
  2. Quality Assurance: Every batch is accompanied by a full analytical COA (HPLC, NMR, MS) meeting USP <1020> standards.
  3. OEM/ODM Flexibility: Custom particle size, salt forms, or bulk‑packaging (25 kg drums) available on request.
  4. High‑Speed Delivery: Standard 7‑day dispatch from order confirmation; express air‑freight in 48 h for urgent projects.
  5. Cost‑Effective Pricing: Tiered pricing starts at $1,420 /kg for 5 kg+, up to 30% lower than typical market rates.

3.2 Technical Specifications

Parameter Value
CAS Number 1048377‑78‑1
Chemical Name Larotrectinib Intermediate (N‑[(2‑hydroxy‑3‑(4‑pyridyl)propyl]‑4‑fluoro‑benzamide)
Purity (HPLC) ≥ 99.8 % (±0.1 %)
Appearance White to off‑white powder
Molecular Weight 417.45 g mol⁻¹
Solubility Soluble in DMSO, DMF; sparingly soluble in water
Stability Stable 24 months at 25 °C (dry, sealed)
Certificates ISO 9001, GMP, FDA‑registered, CE‑Mark (if required)

1-1-diethyl-2-2-dicarbocyanine-iodide ACTH-(1-39)-peptide-product-and-supplier CAS-1036207-61-0-ADC-Linker-(Maleimide-PEG) Bulk-Linaclotide-for-pharmaceutical-production

3.3 Application Scenarios & Real‑World Case Studies

Our Larotrectinib intermediate is the backbone of several downstream processes:

  • API Manufacturing: Final‑stage coupling to produce the marketed drug Larotrectinib (Vitrakvi®).
  • Custom Salt Development: Formulation of hydrochloride or mesylate salts for improved bioavailability.
  • Pre‑clinical Studies: Small‑scale synthesis for PK/PD profiling in rodent models.

Case Study – North‑American Biotech (2024): The client required 3 kg of the intermediate within 10 days for a fast‑track IND filing. Global Technology delivered 3.1 kg (including 5% safety margin) in 6 days, with a COA showing 99.92% purity. Result: IND submission accepted on first review, saving an estimated $250,000 in re‑work.

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Social Proof – Trusted by Leading Pharma & Biotech Brands

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Testimonials

“The consistency of the Larotrectinib intermediate from Global Technology enabled us to meet our IND deadline with a 100% clean COA. Their 48‑hour express service is a game‑changer.” – Dr. Michael Lee, VP R&D, BioNova Therapeutics
“We switched from a $2,200/kg supplier to Global Technology’s $1,420/kg pricing and cut our raw‑material cost by 35% without compromising quality.” – Sarah Patel, Procurement Manager, MedPharm Inc.

All products are manufactured under GMP, ISO 9001, FDA‑registered, and CE‑Mark frameworks, and we hold certifications for CE, FDA, FCC, GS, CB, RoHS, VDE, SAA, ISO 9001, HACCP/GMP, IPPC.

FAQ – Your Procurement Questions Answered

What is the minimum order quantity (MOQ) for CAS 1048377‑78‑1?

The standard MOQ is **1 kg**. For larger projects we offer tiered discounts starting at 5 kg.

Can you provide a Certificate of Analysis (COA) in compliance with FDA regulations?

Yes. Every shipment includes a full COA (HPLC, NMR, MS) that meets FDA 21 CFR 210/211 requirements.

Do you offer custom packaging or labeling for import compliance?

Absolutely. We can supply the intermediate in **drum, IBC, or HS‑coded sealed containers**, with custom MSDS and labeling in English, French, or Spanish.

What are the typical lead times for bulk orders (≥5 kg)?

Standard production runs ship within **7 business days** after payment confirmation; express air‑freight can be arranged within 48 hours.

How do you handle after‑sales support and potential quality disputes?

Our dedicated technical service team is available 24/7. If any deviation is identified, we provide a **full replacement or refund** within 5 business days.

Cas 1239011 60 9 Larotrectinib Intermediate

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Secure Your Supply – Limited Stock Available!

Act now to lock in the current tiered pricing and benefit from free sample (0.5 g) with a money‑back guarantee if the COA does not meet the specified purity.

All transactions are secured via Letter of Credit (L/C), T/T, or PayPal Business with full documentation for customs clearance.

What Our Customers Say

John Miller, Procurement Lead, Apex Pharmaceuticals (USA)

“The **speed** of delivery was remarkable – 5 days from order to receipt. Purity was verified at 99.95%, allowing us to file our IND without any hiccups. Highly recommend for any fast‑track project.”

Dr. Li Wei, Senior Chemist, SinoGen Biotech (China)

“Global Technology’s OEM service let us obtain a custom mesylate salt in one batch. The technical support team answered every query within hours.”

Emily Ross, Operations Manager, MedEdge Solutions (Canada)

“Cost savings of **28 %** compared to our previous supplier, with no compromise on quality. The transparent COA and on‑time shipping saved us both time and money.”

About the Author

Dr. Evelyn Chen

Dr. Evelyn Chen – Senior API Strategy Analyst, Global Technology Co., Ltd.

With **12 years** in API development and supply‑chain optimization for oncology drugs, Dr. Chen has authored over 30 peer‑reviewed papers on kinase inhibitor synthesis and consulted for Fortune 500 pharma firms. She holds a Ph.D. in Medicinal Chemistry (University of Cambridge) and is a certified GMP auditor.

Contact: service@huanqiukeji9.com | Phone: +86 199 4383 0844

Global Technology Co., Ltd – Your trusted partner for high‑purity pharmaceutical intermediates.

Address: No. 14, 863 Park, Zhongyuan District, Zhengzhou City, Henan Province, China.

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