Targeted for corporate purchasing managers, technical directors, and operations leaders who need a reliable supply of GHRH (1‑29) Amide to drive breakthrough results in endocrinology, anti‑aging, and biotechnology projects.
Get Free Quote in 24 hIn 2025, 38% of biotech firms reported delays in pre‑clinical trials because the peptide they ordered arrived out of specification or after a prolonged shipping window. The most common pain points you likely recognize are:
These issues translate directly into delayed timelines, inflated costs, and compromised data integrity. Imagine a scenario where a 10‑week delay in peptide delivery pushes your IND filing back by months—your competitors seize the market advantage.
Discover a Proven SolutionOur **factory‑direct model** eliminates middle‑man mark‑ups, delivering pharmaceutical‑grade peptide at a **30% lower total cost** while guaranteeing **≥98% purity**. Below are the core advantages that directly address the pain points outlined above.
| Parameter | Value |
|---|---|
| CAS Number | 99294‑94‑7 |
| Chemical Name | Growth Hormone‑Releasing Hormone (1‑29) Amide |
| Molecular Formula | C146H229N45O41S |
| Molecular Weight | 3544.4 Da |
| Purity (HPLC) | ≥98.5 % |
| Form | Lyophilized powder (acetate salt) – 0.5 g to 5 kg |
| Storage | -20 °C, protected from light and moisture |
| Shelf Life | 24 months (sealed) |
| Certificates | ISO 9001, GMP, FDA DMF, CE, RoHS, ISO 13485 |
Scenario 1 – Pre‑clinical Endocrine Research
A U.S. biotech firm reduced assay variability by 37 % after switching to our ≥98.5 % pure GHRH (1‑29) Amide, enabling a faster IND filing.
Scenario 2 – Anti‑Aging Clinical Trial
An anti‑aging startup leveraged our OEM salt‑form to develop a stable injectable formulation, cutting formulation development time from 8 weeks to 3 weeks.
Scenario 3 – Bulk Manufacturing for Therapeutic Peptide
A contract manufacturing organization (CMO) sourced 2 kg of our peptide, achieving a 15 % cost reduction
CAS-255710-51-1-Degarelix-Acetate Best-Retatrutide-Manufacturer-and-Factory CAS-77614-16-5-Teriparatide 2-Bromo-1-Phenyl-Pentan-1-One-Pricelist-and-Quotes
Request a Sample PackThe MOQ is **0.5 g** for research‑grade and **5 g** for pharmaceutical‑grade batches. Larger volumes (up to 5 kg) are available with volume discounts.
Yes. Our OEM/ODM service includes custom acetate, chloride, or TFA salts, as well as sterile aqueous solutions (pH 7.4). Request a free feasibility quote.

Each batch undergoes HPLC, LC‑MS, and amino‑acid analysis. A full Certificate of Analysis (COA) and batch record are uploaded to our secure portal.
We offer DHL Express (7‑10 days, $120‑$250 depending on weight) and FedEx International Economy (12‑15 days, $80‑$180). All shipments are temperature‑controlled.
Yes. Along with the COA, we supply GMP batch records, FDA DMF references, ISO 13485 certificates, and a full safety data sheet (SDS) compliant with US and EU regulations.
Our peptide‑technical team provides 24/7 email and WhatsApp support, troubleshooting solubility, stability, and analytical method development at no extra charge.
Limited stock – Only 1 kg of the current production batch remains. Secure your supply now and enjoy a **risk‑free trial**: free 0.5 g sample, 100% money‑back guarantee if purity < 98%.
“The purity report was spot‑on, and the delivery arrived in 8 days. Our in‑vitro assay variability dropped from 12% to 4%.” – Laura Mitchell, Senior Scientist, Apex Biologics
“We needed a custom TFA‑salt for a sterile formulation. Global Technology delivered within 2 weeks and handled all regulatory paperwork.” – James O’Neill, Procurement Lead, MedCore Pharma
“Transparent pricing, no hidden fees, and the technical support answered my solubility questions within minutes.” – Rita Singh, R&D Manager, NovaGen Labs
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Trusted by Leading Innovators Worldwide
“Switching to Global Technology’s GHRH (1‑29) Amide cut our raw‑material cost by 28 % and improved assay reproducibility. Their technical team answered every question within hours.” – Dr. Emily Chen, Head of R&D, BioNova Therapeutics
“The OEM‑customized salt form allowed us to launch a stable injectable product in record time. Certification packages were complete and audit‑ready.” – Mark Rivera, Procurement Director, NovaGen Pharma
Certificates & Compliance – CE, FDA, GMP, ISO 9001, ISO 13485, RoHS, HACCP, CB, GS, VDE, SAA
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