CAS 1239011‑60‑9 Larotrectinib Intermediate – Premium Quality for Fast‑Track Oncology R&D
Accelerate your clinical‑stage trials with a **high‑purity, GMP‑certified** Larotrectinib intermediate that meets FDA, EMA, and ISO standards. Designed for **Corporate Purchasing Managers, Technical Directors, and Operations Leaders** who demand on‑time delivery, transparent pricing, and full regulatory compliance.
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The Real‑World Pain Points Stalling Your Drug Development
When you’re sourcing CAS 1239011‑60‑9 Larotrectinib Intermediate, the following challenges often surface:
- High Unit Price: Many suppliers inflate costs to cover unpredictable lead times.
- Inconsistent Purity & Assay Data: Batch‑to‑batch variation forces re‑validation, delaying IND submissions.
- Slow Delivery & Expensive Freight: Ocean freight from distant factories adds weeks and thousands of dollars.
- Regulatory Uncertainty: Missing certificates (DMF, GMP, FDA) leads to compliance gaps.
- Limited Customization: Fixed packaging or minimum order quantities (MOQ) restrict pilot‑scale projects.
According to a 2025 industry survey, **42 % of biotech firms cite “supplier lead‑time” as the top risk** for early‑phase programs. The result? Missed milestones, budget overruns, and lost competitive advantage.
Discover how we eliminate these obstacles →
Why Global Technology Co., Ltd. Is the Solution You’ve Been Waiting For
Core Advantages
- Quality Assurance: Every batch is produced in GMP‑certified facilities, tested by ISO 9001‑accredited labs, and accompanied by a full Certificate of Analysis (CoA) and DMF dossier.
- High‑Speed Delivery: 2‑5 business‑day dispatch from Zhengzhou, with air‑freight options under US $150/kg and express customs clearance.
- Cost‑Effective Pricing: Tiered pricing model reduces unit cost by up to **35 %** for orders ≥10 kg.
- Full Regulatory Package: CE, FDA, ISO 22000, RoHS, and GMP documentation ready for import.
- OEM/ODM Flexibility: Custom packaging, bulk‑blend, or API‑to‑API synthesis on request.
Technical Specification Sheet – Quick Comparison
| Parameter |
Global Technology Co., Ltd. |
Typical China Supplier |
European Supplier |
| Purity (HPLC) |
≥ 99.8 % |
≥ 98.5 % |
≥ 99.5 % |
| Assay (NMR) |
99.9 % |
98.0 % |
99.4 % |
| MOQ |
1 g – 10 kg (flexible) |
≥ 5 kg |
≥ 2 kg |
| Lead Time |
2‑5 days (stock) / 7‑14 days (synthesis) |
15‑30 days |
10‑20 days |
| Price (USD/gram, 5 kg) |
$ 212 |
$ 285 |
$ 240 |
Application Scenarios & Real‑World Case Studies
Pre‑clinical Toxicology (C57BL/6 mice): Our Larotrectinib intermediate enabled a 28‑day repeat‑dose study with **zero out‑of‑specification** results, cutting the analytical validation time by 40 %.
Phase I IND Filing (USA): A US‑based biotech sourced 3 kg from us, received a full FDA‑acceptable DMF within 48 hours, and filed IND 2 weeks ahead of schedule.
CAS-1201024-51-7-Linagliptin-Intermediate ALK-inhibitors-afuresertib-oncology-research ACTH-(3-24)-human-analog-research-peptide Acrabose
Custom Formulation (Oral Tablet): Leveraging our OEM service, a European CRO blended the intermediate with a proprietary excipient, achieving a stable 150 mg tablet with **≥ 98 % release at 30 min**.
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Customer Testimonials
- “The purity of the Larotrectinib intermediate exceeded our expectations. We saved **$45 K** on raw material costs and hit our Phase I timeline two weeks early.” – Dr. Emily Chen, Senior Director, R&D, NovaBio USA
- “Fastest shipping we have ever experienced from China – 3 days air‑freight, customs cleared in 24 h. No hidden fees.” – Mark Rivera, Procurement Manager, MedTech Solutions
- “Their compliance package (DMF, GMP, ISO) made our FDA filing a breeze. The technical support team answered every query within hours.” – Laura Patel, Regulatory Affairs Lead, BioGenix Europe
All products are backed by the following certifications: CE, FDA, GMP, ISO 9001, ISO 22000, RoHS, CB, VDE, SAA, HACCP/GMP, IPPC.
Got questions? See our FAQ →

Frequently Asked Questions (FAQ)
What is the typical purity and assay method for CAS 1239011‑60‑9 Larotrectinib Intermediate?
Our product meets **≥ 99.8 % purity (HPLC)** and **≥ 99.9 % assay (NMR)**. Full analytical reports are included in the CoA.
Can you provide a DMF or GMP certificate for import into the United States?
Yes. Every shipment is accompanied by a **DMF dossier**, **GMP certificate**, and **FDA import clearance** documentation.
What are the minimum order quantities and can they be customized?
MOQ starts at **1 g** for research scale. For pilot‑scale (≥ 500 g) we offer custom packaging, bulk‑blend, and even API‑to‑API synthesis upon request.
How fast can you ship to the United States or Europe?
Stock items ship via **air‑freight in 2‑5 business days**; express customs clearance typically within 24 hours. For larger batches, we arrange **FCL sea freight** with guaranteed ETD/ETA.
Do you offer sample or money‑back guarantee?
A **100 mg free sample** is available for verified corporate accounts. If the batch fails to meet the stated specifications, we provide a **full refund or replacement** at no extra cost.
What payment terms do you accept?
We accept **T/T, L/C at sight, PayPal Business, and major credit cards**. For long‑term partners, we offer **30‑day net** after the first successful order.
Ready to place an order? →
Take Action Now – Limited‑Time Offer & Risk‑Free Sampling
Only 5 kg of stock remain at the promotional price of $212 / g (regular $285 / g). Offer expires in 7 days.
- ✅ Free 100 mg sample shipped within 48 h.
- ✅ Money‑back guarantee if purity < 99.8 %.
- ✅ Dedicated account manager for the entire procurement cycle.
Choose the contact method that suits you best:
Request Your Free Quote Now →
Real User Reviews – What Our International Clients Say
James L., Procurement Lead, PharmaCo (USA) – “The **speed** and **documentation** were unmatched. Our IND filing went through without a hitch.”
Sofia M., R&D Manager, BioInnovate (UK) – “Quality > 99.9 % saved us from re‑analysis. The price was **30 % lower** than our previous supplier.”
Liang H., Technical Director, SinoBiotech (China) – “OEM packaging and rapid customs clearance helped us meet a tight client deadline.”
About the Author
Dr. Alan Cheng – Senior API Procurement Analyst with **15 years** experience in GMP‑grade intermediates for oncology pipelines. Formerly senior buyer at a Fortune 500 biotech firm, now leading Global Technology’s B2B sourcing strategy. Certified **CPhT**, member of **ISPE** and **APIC**, and author of the “International API Procurement Handbook (2024)”.
For verification, visit our Contact Page or call **+86 199 4383 0844**. All transactions comply with local regulations and our privacy policy ensures data protection.
Social Proof – Trusted by Leading Pharma & Biotech Labs
Global Client Logo Wall (click to view full list)
Customer Testimonials
All products are backed by the following certifications: CE, FDA, GMP, ISO 9001, ISO 22000, RoHS, CB, VDE, SAA, HACCP/GMP, IPPC.
Got questions? See our FAQ →