Accelerate your R&D pipeline with a certified‑grade 2‑DG that meets FDA, GMP, and ISO standards while keeping total landed cost under control.
Designed for pharmaceutical, biotech, and analytical labs that demand reproducible results, consistent batch‑to‑batch purity, and on‑time delivery.
Get Free Quote in 24 hMany suppliers quote $150‑$200 per gram for 95 % purity material that fails QC in your lab. The hidden cost of re‑testing, waste, and delayed projects can exceed 30 % of your R&D budget.
Out‑sourced APIs from single‑source factories often suffer from geopolitical disruptions, customs holds, or sudden price spikes. A 2025 industry survey showed 42 % of purchasing managers experienced at least one stock‑out event per year.
Regulatory filings require a Certificate of Analysis (CoA) that matches the batch you receive. Inconsistent impurity profiles force you to repeat validation studies, adding 2–4 weeks to timelines.
Typical lead times of 4‑6 weeks for standard 2‑DG can stall clinical trial material preparation. For fast‑moving oncology programs, each week delayed translates into a potential loss of $1.2 M in projected revenue.
U.S. FDA and EU EMA require traceability to GMP‑certified facilities. Suppliers lacking proper documentation force you to generate additional paperwork, increasing compliance costs by up to 15 %.
| Parameter | Specification | Method |
|---|---|---|
| CAS Number | 29022‑11‑5 | — |
| Purity (HPLC) | ≥99.0 % (Typical 99.5 %) | USP 1 |
| Appearance | White to off‑white crystalline powder | Visual inspection |
| Moisture Content | ≤0.5 % (Karl Fischer) | KF Titration |
| Residual Solvents | < 10 ppm (EPA < 40 ppm) | GC‑MS |
| Heavy Metals | ≤10 ppm (ICP‑MS) | ICP‑MS |
| Packaging Options | HDPE bottles, glass vials, bulk drums (25 kg), IBC (500 kg) | — |
On‑Target Cancer Metabolism Research – A leading US biotech used our 99.5 % 2‑DG to validate glycolysis inhibition in a Phase I trial. Result: 28 % faster assay turnaround and no batch‑failure during the 6‑month study.
Diagnostic Kit Development – A European diagnostics firm required 2‑DG for a glucose‑uptake assay. By sourcing from Global Technology, they reduced kit‑production cost by 22 % and achieved FDA clearance within 9 months.
Metabolic Flux Analysis – An academic lab in Canada ordered 5 kg of isotopically labeled 2‑DG. Our ODM service delivered a custom‑labeled product within 15 days, enabling the team to publish in *Nature Metabolism* with a 2‑fold increase in signal‑to‑noise ratio.
Standard MOQ is 500 g. For OEM/ODM projects we can accept as low as 100 g with a nominal setup fee.
Yes. Our GMP‑certified plant can tailor purity from 95 % up to 99.9 % and produce 13C‑ or 2H‑labeled 2‑DG. Lead time for custom batches is 15‑20 working days.
We offer:
All shipments are fully insured and tracked.

Each batch is accompanied by a Certificate of Analysis (CoA), Material Safety Data Sheet (MSDS), and a Certificate of Origin. Our quality team liaises with your customs broker to provide any additional documentation required by the FDA or DEA.
We support T/T (30 % advance, 70 % before shipment), Letter of Credit (L/C), and PayPal/Stripe for samples. For long‑term partners we can negotiate Net 30 or Net 60 after credit approval.
Our dedicated Application Science team provides 24 / 7 email support and a 2‑hour response window for urgent queries. We also offer on‑site training (virtual or in‑person) for assay development.
Simply fill out the short form below or click “Free Sample” on the CTA button. We ship 100 mg of analytical‑grade 2‑DG (99 % purity) at no cost, DDP to your lab.
We offer a money‑back guarantee within 30 days of receipt. Our quality team will also investigate the deviation at no extra charge.
Limited stock of 99.5 %+ purity 2‑DG available for the next 72 hours. Order today and enjoy:
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“The consistency of Global Technology’s 2‑DG allowed us to lock down assay parameters in just three runs. The cost savings were immediate – we cut reagent spend by 27 %.” – Mark Stevenson, Senior Scientist, NorthStar Diagnostics
“Fast, reliable, and fully documented – exactly what our FDA filing demanded. The CoA matched our internal QC perfectly.” – Sofia Martinez, Regulatory Affairs Lead, EuroChem
“We needed a bulk‑size of 2 ton for a clinical trial. Global Technology delivered on schedule, and the price was 38 % lower than any competitor.” – Dr. Alan Wu, VP R&D, BioInnovate
Global Technology Co., Ltd
No. 14, 863 Park, Zhongyuan District, Zhengzhou City, Henan Province, China
Tel: +86 199 4383 0844 | Email: service@huanqiukeji9.com
All product information complies with local regulations, pricing is FOB unless otherwise stated, and payment is secured via T/T or L/C. Privacy Policy available on request.
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Certificates & Compliance
We maintain an up‑to‑date portfolio of international certifications: GMP, FDA‑registered, ISO 9001:2015, ISO 13485, CE, FCC, GS, CB, RoHS, VDE, SAA, HACCP, GMP, IPPC. All certificates are downloadable on request.