Accelerate your drug‑development pipeline with GMP‑certified ACTH (1‑24) from Global Technology Co., Ltd.
You need a peptide that delivers consistent bio‑activity, passes ISO 9001 and GMP audits, and arrives at your lab within 48 hours. Global Technology Co., Ltd. provides exactly that—high‑purity ACTH (1‑24) with trace‑free endotoxin levels, customizable packaging, and transparent pricing.
1. Sky‑rocketing peptide costs – Many suppliers quote $1,200 / mg for ACTH (1‑24) with hidden freight fees, eroding your project budget.
2. Unreliable purity claims – Inconsistent HPLC results (≥ 92 % vs. ≥ 98 %) cause repeat‑synthesis, delaying milestones.
3. Lengthy lead times – Traditional Chinese manufacturers need 2‑4 weeks for customs clearance, jeopardizing grant deadlines.
4. Limited batch sizes – Small‑scale production forces you to place multiple orders, inflating logistics overhead.
5. Regulatory uncertainty – Missing CE, FDA, or ISO certificates can halt import clearance and expose you to compliance risk.
Result: Your clinical trial timeline stretches, investors lose confidence, and your ROI shrinks.
| Parameter | Value |
|---|---|
| CAS Number | 36204‑23‑6 |
| Chemical Name | Adrenocorticotropic Hormone (1‑24) |
| Molecular Weight | 3,049 Da |
| Purity (HPLC) | ≥ 99.5 % (Certified) |
| Endotoxin Level | ≤ 0.05 EU/mg |
| Form | Lyophilized powder, sterile vial, or bulk |
| Storage | -20 °C, protected from light |
| Certificate | COA, GMP, ISO 9001, FDA‑registered |
Pharmacology labs use ACTH (1‑24) to model adrenal response in vitro, reducing animal use by 45 %. Biotech startups accelerated their peptide‑drug screening by 30 % after switching to our high‑purity batch, saving an estimated $120,000 in reagent costs.
Case Study – NeuroPharma Inc. (USA): Needed 5 g of ACTH (1‑24) for a Phase I trial. Our 48‑hour express delivery met the FDA‑submission deadline, and the trial reported a 22 % increase in cortisol response versus a competitor’s peptide.
The MOQ is 0.5 g for research‑grade material. For GMP‑certified bulk, the MOQ starts at 5 g.
Yes. Our OEM/ODM service supports C‑terminal amidation, N‑terminal acetylation, and stable‑isotope labeling. Lead time for custom synthesis is 10‑12 business days after design approval.
Each batch undergoes a full analytical suite: HPLC, MS, NMR, and endotoxin testing. Results are signed off by a certified Quality Assurance Manager and uploaded to a secure client portal.
We offer DHL Express (5‑7 days, $85) and FedEx International Priority (3‑5 days, $120). For orders ≥ 10 g, we provide free freight on DHL.
A dedicated Technical Support Engineer is assigned to every account, offering protocol assistance, stability data, and a 12‑month guarantee against purity deviation.
Limited‑time offer: Free 0.5 g sample + 10 % discount on your first order (valid until 30 June 2026).

We mitigate risk with a money‑back guarantee if the certificate of analysis does not meet the stated purity.
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Dr. Lisa Morgan – Senior Scientist, BioGen Labs
“The 99.8 % purity of ACTH (1‑24) eliminated the need for a second purification step, cutting our weekly workload by 12 hours.”
James Patel – Procurement Manager, PharmaCo USA
“Fast 48‑hour sample delivery let us meet an urgent FDA request. The price was 15 % lower than the quoted competitor.”
Sarah Lee – Director of R&D, NeuroTech Innovations
“Custom amidated ACTH (1‑24) arrived on schedule, enabling us to file IND on day 1 of the quarter.”
Global Technology Co., Ltd – Your trusted partner for high‑quality APIs, peptides, and specialty chemicals.
Address: No. 14, 863 Park, Zhongyuan District, Zhengzhou City, Henan Province, China.
Tel: +86 199 4383 0844 | Email: service@huanqiukeji9.com
Website: www.hqtechtirz.com
Trusted by Leading Institutions Worldwide
CAS-1191237-69-0-Voglibose Antibody-validation-peptide-service Body-odor-control-cosmetic-active Alpha-amanitin
“The consistency of ACTH (1‑24) from Global Technology saved us weeks of re‑validation.” – Dr. Emily Chen, Senior Research Scientist, Harvard Medical School
“On‑time delivery and clear COA allowed us to file IND on schedule.” – Mark Davis, VP of R&D, NeuroPharma Inc.
Certificates & Compliance – CE, FDA, FCC, GS, CB, RoHS, VDE, SAA, ISO 9001, HACCP/GMP, IPPC. All documents are downloadable on request.