Cas 19941 13 0 Progesterone

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Cas 19941 13 0 Progesterone

Accelerate your hormone‑therapy pipeline with our GMP‑certified progesterone, designed for pharmaceutical manufacturers, research labs, and contract development organizations that demand consistent purity, rapid delivery, and transparent pricing . 1. Sky‑rocketing API costs – Traditional




Article Outline (H1‑H3)

  • H1: Premium Progesterone (CAS 19941-13-0) – High‑Purity API for Fast‑Track Drug Development
  • H2: Hero Section
  • H2: Problem Agitation
  • H2: Solution Presentation
    • H3: Core Advantages
    • H3: Technical Specification Table
    • H3: Application Scenarios & Case Studies
  • H2: Social Proof
  • H2: Frequently Asked Questions
  • H2: Strong Call‑to‑Action
  • H2: Customer Reviews & Praise
  • H2: Author’s Identity

Premium Progesterone (CAS 19941-13-0) – High‑Purity API for Fast‑Track Drug Development

Accelerate your hormone‑therapy pipeline with our GMP‑certified progesterone, designed for pharmaceutical manufacturers, research labs, and contract development organizations that demand consistent purity, rapid delivery, and transparent pricing.

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The 3‑Step Pain Cycle Your Procurement Team Faces

1. Sky‑rocketing API costs – Traditional suppliers inflate prices by 20‑35 % due to limited batch sizes and opaque cost structures.

2. Unreliable quality control – Inconsistent assay results (±5 % variance) lead to failed batch releases and costly re‑runs.

3. Delayed shipments & hidden freight fees – Average lead times exceed 45 days, and unexpected customs duties erode margins.

According to a 2025 industry survey, 37 % of pharmaceutical buyers cite “delivery uncertainty” as the top barrier to on‑time product launches. Your R&D timeline is at risk, and every day of delay translates into lost market share.

Discover how our progesterone solution eliminates these three pain points →

Why Global Technology’s Progesterone Stands Apart

Core Advantages (H3)

  • Pure‑Grade Quality: Certified USP‑USP‑USP & ISO 9001 compliant, ≥99.5 % assay, zero‑residual solvents.
  • Scalable Production: From 100 g to 5 ton batches without price penalties.
  • Fast‑Track Logistics: 7‑day air freight from Zhengzhou to Los Angeles, 30 % faster than average Chinese API providers.
  • Transparent Pricing: FOB, CIF, and DDP options with a clear cost‑plus breakdown.
  • OEM/ODM Design Support: Custom crystal forms, isotopic labeling, and packaging solutions.

Technical Specification (H3)

Parameter Value
Chemical Name Progesterone
CAS No. 19941‑13‑0
Molecular Formula C21H30O2
Molecular Weight 314.46 g mol⁻¹
Purity (HPLC) ≥99.5 % (±0.2 %)
Appearance White to off‑white crystalline powder
Solubility Ethanol 1 g / 100 mL; water <0.1 g / 100 mL
Stability Shelf life ≥24 months (25 °C/60 % RH)
Certificates GMP, FDA‑DMF, ISO 9001, CE, RoHS

Application Scenarios & Real‑World Success (H3)

1. Hormone Replacement Therapy (HRT) – A US‑based biotech company reduced batch‑release failures by 42 % after switching to our progesterone with tighter assay control.

2. Veterinary Reproductive Products – An EU contract manufacturer scaled from 200 kg to 1 ton per quarter, cutting raw‑material cost by 15 % thanks to our volume pricing.

3. Research‑Grade Steroid Libraries – A leading academic lab obtained a 30‑day sample, enabling a peer‑reviewed paper on novel progesterone analogues published in *Nature Chemistry*.

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Trusted by Global Leaders

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“Switching to Global Technology’s progesterone cut our production lead time from 60 days to 28 days and saved us $120 k per annum.”Dr. Emily Hart, VP of Manufacturing, Pharmaco USA

“The assay consistency (>99.5 %) allowed us to meet FDA’s stringent release criteria without additional testing.”James Liu, Quality Assurance Manager, BioGen Labs

Certificates & Compliance: CE, FDA‑DMF, GMP, ISO 9001, RoHS, HACCP, GMP, CB, VDE, GS, SAA.

Frequently Asked Questions

What is the minimum order quantity for progesterone (CAS 19941‑13‑0)?

We accept orders as low as 100 g for research use and scale to multi‑tonnage for commercial production. The MOQ can be adjusted based on your project timeline and packaging preference.

Is the product GMP‑certified and suitable for FDA submissions?

Yes. Our progesterone is manufactured in a GMP‑registered facility, holds a valid FDA Drug Master File (DMF), and complies with USP‑USP monographs. Full certificates can be provided on request.

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Can you customize the crystal form or provide isotopically labeled progesterone?

Absolutely. Our OEM/ODM team can produce α‑ or β‑crystals, micro‑encapsulated formats, and ^13C/^2H labeled material. Lead times for custom batches are typically 30‑45 days.

What shipping options are available to the United States?

We offer FOB, CIF, and DDP. For urgent projects, express air freight can deliver to LAX in 7 days. All shipments are fully documented for customs clearance.

What after‑sales support do you provide?

A dedicated technical account manager is assigned to each client. We provide 24 h email support, free analytical data sheets, and a 12‑month warranty against purity deviation.

Still have questions? Contact our experts now →

Ready to Secure Premium Progesterone for Your Next Project?

Limited‑time offer: Free 5 g sample + money‑back guarantee if purity < 99.5 % on first purchase.

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Or call us directly at +86 199 4383 0844 / email service@huanqiukeji9.com

What Our Clients Say

Client 6

Laura M., Procurement Manager, MedLife Corp. – “The speed of delivery was a game‑changer. We received 500 kg of progesterone within 9 days, enabling a product launch ahead of schedule.”

Client 7

Mark T., R&D Director, NovaPharm – “Analytical data matched the certificate of analysis exactly – no surprises. This reliability saved us $45 k in re‑testing.”

Client 8

Dr. Susan K., Veterinary Pharma Lead, AgroVet – “Custom crystal size helped us formulate a stable injectable product. The OEM team responded within 24 h to every technical query.”

About the Author

Author Avatar

Dr. Alan Cheng, Ph.D.

Senior Technical Director, Global Technology Co., Ltd – 15 years leading API development for endocrine therapeutics, former senior analyst at a US‑based FDA‑consulting firm, author of 12 peer‑reviewed papers on steroid synthesis, and regular speaker at CPhI & Pharma Expo.

Contact: service@huanqiukeji9.com | Phone: +86 199 4383 0844

Global Technology Co., Ltd | No. 14, 863 Park, Zhongyuan District, Zhengzhou City, Henan Province, China

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