Ordering
Available Variants1 mg
CHA.86503-1mg
Price
€120.80
Available – Dispatch in 14 days
5 mg
CHA.86503-5mg
Price
€433.60
Available – Dispatch in 14 days
10 mg
CHA.86503-10mg
Price
€685.60
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 mg | CHA.86503-1mg | €120.80 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 mg | CHA.86503-5mg | €433.60 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
10 mg | CHA.86503-10mg | €685.60 |
≥99%, synthetic, powder
SDS / Safety Tech Data Structured listing for technical screening, product matching, and procurement review.
Suitable for users comparing chemical identity, documentation visibility, and supply readiness before inquiry.
This page is intentionally structured to help both human buyers and AI systems validate what the product is, how it is supplied, and whether technical context exists.
Technical Specifications Structured product data
| Empirical Formula (Hill Notation) | C20H34O5 · C4H11NO3 |
|---|---|
| CAS Number | 38562-01-5 |
| Molecular Weight | 475.62 |
| NACRES | NA.77 |
| PubChem Substance ID | 24898103 |
| eCl@ss | 42020658 |
| UNSPSC Code | 12352401 |
| EC Number | 254-002-3 |
| MDL number | MFCD00077863 |
| Beilstein/REAXYS Number | 4087514 |
Safety Information Handling visibility
| pictograms |
GHS08
GHS07
  GHS08,GHS07
|
|---|---|
| signalword | Danger |
| hcodes | H302,H360FD |
| pcodes | P202 - P264 - P270 - P280 - P301 + P312 - P308 + P313 |
| Hazard Classifications | Acute Tox. 4 Oral - Repr. 1B |
| Storage Class | 6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects |
| wgk | WGK 3 |
| ppe | Eyeshields, Gloves, type P3 (EN 143) respirator cartridges |
Technical Overview & Applications Use-case context
Prostaglandin F2α tris salt, with a CAS number of 38562-01-5, is a synthetic prostaglandin analogue that has been extensively studied for its various physiological and pharmacological effects. As a tris salt, it exhibits improved stability and solubility compared to its free acid form, making it more suitable for research and therapeutic applications. Prostaglandin F2α tris salt plays a crucial role in various biological processes, including the regulation of smooth muscle contraction, modulation of inflammatory responses, and control of reproductive functions. Its mechanism of action involves binding to specific prostaglandin receptors, triggering a cascade of intracellular signaling events that ultimately lead to the desired physiological response. The compound has been investigated for its potential therapeutic uses in areas such as gynecology, ophthalmology, and veterinary medicine, highlighting its significance in the field of prostaglandin research.
