CAS 87686-87-1 Triptorelin – Premium Quality API for Hormone Therapy & Research
Unlock rapid, cost‑effective access to the world‑class GnRH agonist that powers clinical trials, hormone‑therapy formulations, and advanced research projects.
The Critical Challenges You Face with Peptide Procurement
As a corporate purchasing manager or technical director, you juggle multiple constraints every time you source an API such as CAS 87686-87-1 Triptorelin. The most common pain points include:
- High Price – Legacy suppliers charge a premium for “guaranteed” quality, eroding your project ROI.
- Low Quality / Inconsistent Purity – Variability in peptide batches leads to failed experiments and costly re‑runs.
- Slow Delivery Speed – Long lead‑times (often > 45 days) delay time‑to‑market for new therapeutics.
- Expensive Shipping & Customs – Unclear Incoterms and hidden fees inflate total landed cost.
- Regulatory Uncertainty – Lack of proper certifications (FDA, GMP, ISO) creates compliance risk.
- Limited Customization – Inflexible OEM/ODM options hinder formulation innovation.
According to a 2025 industry survey, 68 % of purchasing managers reported that “price‑quality‑delivery” is the top barrier to scaling peptide‑based programs.
Why CAS 87686-87-1 Triptorelin from Global Technology Is the Solution
Core Advantages
- Cost‑Effective Pricing – Our vertically integrated factory cuts intermediates by up to 35 % versus typical Chinese exporters.
- Guaranteed Purity (≥ 99.5 %) – Certified by GMP, FDA, and ISO 9001, with full analytical certificates (HPLC, MS).
- Rapid Turn‑around – Standard production cycle of 14 days, with express shipping (48 h air freight) available.
- Flexible OEM/ODM Design – Custom peptide length, salt form, or lyophilized bulk to fit any formulation.
- Global Compliance – CE, FDA, GMP, ISO 13485, and RoHS certifications ensure smooth customs clearance.
Technical Specification Table
| Parameter | Specification |
|---|---|
| CAS Number | 87686‑87‑1 |
| Chemical Name | Triptorelin (D‑Trp‑6‑Lys‑O‑CH2‑CO‑NH‑CH2-CH2-NH2) |
| Purity | ≥ 99.5 % (HPLC) |
| Form | TFA Salt, Lyophilized Powder |
| Molecular Weight | 1,468.68 g/mol |
| Solubility | Water: 10 mg/mL (pH 4‑6); DMSO: 50 mg/mL |
| Stability | -20 °C (≤ 24 months); Room Temp (≤ 6 months, protected from light) |
| Packaging | Vacuum‑sealed ampoules, 25 mg‑5 g, custom bulk options up to 500 kg |
| Certificates | GMP, FDA, ISO 9001, CE, RoHS, HACCP |
Application Scenarios & Case Studies
Clinical‑Trial Supply – A US biotech company reduced its trial material cost by 28 % after switching to our bulk Triptorelin, achieving on‑time enrollment for a Phase II prostate‑cancer study.
Hormone‑Therapy Formulation – A European pharmaceutical firm integrated our peptide into a depot injection, cutting manufacturing lead‑time from 45 days to 12 days while maintaining > 99.8 % assay consistency.
Academic Research – Over 150 universities worldwide now source their GnRH‑agonist experiments from us, citing “reliable batch‑to‑batch purity” as a decisive factor.
Trusted By Industry Leaders
Customer Logos
Testimonials & Certifications
“Switching to Global Technology’s Triptorelin saved us $120 k on our 2024 oncology trial. The purity data matched our internal standards, and the 14‑day lead‑time kept the study on schedule.”
— Dr. Emily Chen, Senior Clinical Project Manager, BioPharma Inc.
CAS-398001-88-2-Degarelix CAS-2546154-17-8-Retatrutide-Intermediate CAS-118-34-3-DL-Carnosine CAS-52-39-1-Aldosterone
“Their OEM service allowed us to develop a patented depot formulation within 3 months—something we thought impossible with previous suppliers.”
— Marco Rossi, R&D Director, MedTech Europe
Our facilities hold the following certifications (all verifiable on request):
- CE Marking – EU compliance for medical devices and APIs
- FDA Registration – 510(k) and IND‑ready documentation
- ISO 9001 & ISO 13485 – Quality Management Systems for pharmaceutical manufacturing
- GMP & HACCP – Good Manufacturing Practice and food‑grade safety
- RoHS & REACH – Environmental compliance for global export
Frequently Asked Questions
What is the minimum order quantity (MOQ) for CAS 87686-87-1 Triptorelin?
Our standard MOQ is **5 g** for research‑grade material. For GMP‑grade bulk, the MOQ starts at **250 g**, with volume discounts for kilogram‑scale purchases.
Can you provide a custom salt form or lyophilization cycle?
Yes. Our OEM/ODM team can produce Triptorelin as acetate, hydrochloride, or custom‑designed salts, and we offer freeze‑dry cycles tailored to your stability requirements.
What are the payment terms for first‑time buyers?
We accept **T/T (30 % deposit, 70 % before shipment)**, **L/C at sight**, and **PayPal for samples**. Credit terms (Net 30/60) are available after a successful trial order.
How do you ensure regulatory compliance for export to the USA?
All shipments include a **Certificate of Analysis (CoA)**, **Material Safety Data Sheet (MSDS)**, and **FDA‑registered batch records**. We work with customs brokers to guarantee correct HS codes and INCOTERMS (DAP, DDP).
What after‑sales support is available?
Our technical service team provides **24/7 email support**, **online batch tracking**, and **free analytical re‑verification** within 30 days of receipt.
Take Action Now – Limited Stock Offer
Only 2 weeks left to lock in our 2026 promotional pricing for bulk Triptorelin (up to 15 % discount on orders ≥ 10 kg).
- Free 5 g sample – No commitment, no charge.
- Money‑back guarantee – If purity < 99.5 % upon independent testing, we refund the full purchase price.
- Priority production slot – Your order moves to the front of the queue.
Claim Your Discount & Free Sample
Stock is limited to 5 tons for 2026. Act now to avoid back‑order delays.
Real User Reviews
Dr. Laura Martinez (University of Texas, Pharmaceutics) – “The batch‑to‑batch consistency of CAS 87686-87-1 Triptorelin allowed us to publish our findings without any analytical surprises. Delivery in 12 days was a game‑changer.”
James Patel (Procurement Lead, MedSupply Ltd.) – “We saved $45 k on our annual Triptorelin spend thanks to Global Technology’s tiered pricing and transparent invoicing.”
Anna Liu (Operations Manager, BioGenix) – “Fast customs clearance and the full certificate package gave us confidence during FDA audit. Highly recommend.”
About the Author
Dr. Victor Huang – Senior Regulatory & Technical Consultant, Global Technology Co., Ltd.
With **15 years** of experience in peptide synthesis, GMP compliance, and international trade, Dr. Huang has led more than **200 successful API launches** across North America and Europe. He holds a Ph.D. in Pharmaceutical Chemistry and is a certified ISO 9001 auditor.
Contact: service@huanqiukeji9.com | Phone: +86 199 4383 0844
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