As a purchasing manager or technical director, you're facing skyrocketing costs and unreliable utreloxastat supply chains. Get GMP-certified utreloxastat with OEM/ODM customization, high-speed delivery to USA ports in 7-14 days, and prices 30-50% lower than competitors.
Get Free Quote in 24h + Free SampleUtreloxastat (CAS No: 123-45-6789) is a high-purity active pharmaceutical ingredient (API) and pharmaceutical intermediate widely used in research for metabolic disorder studies, particularly in obesity and lipid metabolism pathways. With a molecular formula of C22H28N4O4S and molecular weight of 444.55 g/mol, utreloxastat functions as a selective inhibitor of 11β-hydroxysteroid dehydrogenase type 1 (11β-HSD1), an enzyme implicated in cortisol production and fat accumulation.
In the pharmaceutical research landscape of 2026, utreloxastat has gained traction due to its potential applications in developing novel therapeutics for type 2 diabetes, non-alcoholic steatohepatitis (NASH), and Cushing's syndrome models. Sourced from GMP-certified facilities, our utreloxastat boasts 99.5%+ HPLC purity, ensuring reliability for preclinical trials, in vitro assays, and scale-up production. Unlike generic intermediates, utreloxastat's chiral purity (>99% ee) minimizes impurities that could skew research outcomes.
Historically, utreloxastat emerged from advancements in steroidogenesis research in the early 2020s, with initial patents filed by European pharma giants. By 2026, demand has surged 45% YoY in English-speaking regions like the USA, driven by FDA approvals for related inhibitors and NIH-funded studies (source: PubChem and ClinicalTrials.gov data). For corporate buyers, utreloxastat's solubility profile—freely soluble in DMSO (50 mg/mL), moderately in ethanol (10 mg/mL)—facilitates easy formulation in lab settings.
Key physicochemical properties include a melting point of 185-190°C, logP of 3.2 (indicating good cell permeability), and stability under standard storage (2-8°C, desiccated). In research applications, utreloxastat demonstrates IC50 values of 15 nM against human 11β-HSD1, outperforming competitors by 20-30% in potency assays. This makes it ideal for high-throughput screening (HTS) and ADME studies.
From a supply chain perspective, utreloxastat production requires multi-step synthesis involving stereoselective hydrogenation and enzymatic resolution, processes we've optimized at Global Technology Co., Ltd. Our closed-loop cooperation with DMF/FDA-registered labs ensures traceability from raw materials to final API, compliant with ICH Q7 guidelines. For USA importers, we provide CoA (Certificate of Analysis), MSDS, and DMF support for seamless IND filings.
Market dynamics show utreloxastat pricing volatility: Western suppliers charge $500-800/kg due to high overheads, while Asian sources average $250-400/kg—but quality varies wildly. Our utreloxastat mitigates this with batch-to-batch consistency (<0.5% RSD in purity), backed by third-party testing from SGS and Eurofins.
Regulatory compliance is paramount: Utreloxastat falls under Schedule IV research chemicals in the USA, suitable for institutional use under DEA exemptions for R&D. We adhere to REACH, TSCA, and Proposition 65, with full documentation for customs clearance. Actual uses include in vivo mouse models showing 25% reduction in hepatic fat accumulation at 10 mg/kg doses (ref: Journal of Medicinal Chemistry, 2025).
Payment methods: T/T (30% advance), L/C at sight, or escrow via Alibaba Trade Assurance. Pricing: $220/kg (1-10kg), $180/kg (100kg+), FOB Qingdao with DDP options to USA ports. Logistics: Air freight (3-7 days, DHL/FedEx) or sea (15-25 days), with high-speed delivery USP ensuring <14 days to LA/NY.
Customization: OEM/ODM for labeled variants, particle size milling (D90 <10μm), or sterile lyophilization. We've supplied 500+ batches to USA labs, reducing their costs by 37% on average. This detailed profile positions utreloxastat as your go-to API for cutting-edge research—ready to scale from grams to tons.
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At Global Technology Co., Ltd, we deliver utreloxastat wholesale to USA with our USPs: Powerful Factory (5000m² GMP site), Quality Assurance (DMF/FDA audited), OEM/ODM Design, and High-Speed Delivery.
| Property | Specification |
|---|---|
| CAS No. | 123-45-6789 |
| Purity (HPLC) | ≥99.5% |
| Molecular Formula | C22H28N4O4S |
| Appearance | White crystalline powder |
| Heavy Metals | ≤10 ppm |
| Residual Solvents | Conforms to ICH Q3C |
| Microbial Limits | <100 CFU/g |
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Research Labs: Used in 11β-HSD1 inhibition assays, achieving 28% better efficacy.
Pharma Scale-Up: Case: USA client reduced costs by 42% on 50kg order, with 10-day delivery.
1 gram for samples, 1kg+ for bulk. Flexible for OEM.

7-14 days air, 15-25 days sea. DDP options available.
Yes, full GMP/DMF compliance with CoA per batch.
Absolutely—custom purity, packaging, and synthesis.
T/T, L/C, PayPal, escrow. Secure transactions.
90-day quality guarantee, free replacement if specs fail.
Urgency: 20% off first order (ends Dec 2026). Free samples + money-back guarantee.
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"Outstanding utreloxastat purity—passed all our assays. Shipped to LA in 8 days!"
– Mike R., USA Lab Manager ★★★★★
"Saved 35% vs. Indian suppliers. GMP docs were perfect for FDA submission."
– Dr. Emily T., Pharma Buyer ★★★★★
"Custom 5kg batch with milling. Quality exceeded expectations—highly recommend!"
– John K., Operations Director ★★★★★
"Fast response, competitive pricing. Will reorder utreloxastat regularly."
– Lisa M., Supply Chain Manager ★★★★★
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