Skip to the beginning of the images gallery

Carboprost tromethamine - ≥98%(HPLC), high purity , Prostanoid FP receptor agonist, CAS No.58551-69-2, Prostanoid FP receptor agonist

COA

Grade & Purity:

≥98%(HPLC)

Cas Number: 58551-69-2
Molecular Weight: 489.64
PubChem CID: 5281074

In stock

Item Number

C288595

Grouped product items
SKU	Size	Availability	Price
C288595-5mg	5mg	3	$48.90
C288595-10mg	10mg	3	$78.90
C288595-25mg	25mg	3	$177.90
C288595-50mg	50mg	2	$276.90
C288595-100mg	100mg	2	$414.90
C288595-250mg	250mg	2	$933.90

SyntheticProstaglandin F2α analog

View related series

Class A GPCR (4138) GPCR/G Protein (3172) Prostaglandin Receptor (169)

Basic Description

Synonyms	(15S)-15-METHYLPROSTAGLANDIN F(SUB 2.ALPHA.) TROMETHAMINE \| 2-Amino-2-(hydroxymethyl)propane-1,3-diol (Z)-7-((1R,2R,3R,5S)-3,5-dihydroxy-2-((S,E)-3-hydroxy-3-methyloct-1-en-1-yl)cyclopentyl)hept-5-enoic acid \| carboprost trometamol \| Prostinfenem \| 15-Met
Specifications & Purity	≥98%(HPLC)
Biochemical and Physiological Mechanisms	Synthetic analog ofprostaglandin F2α(PGF2α). Increases uterine contractility in the 14-day pregnant hamster.Carboprost tromethamine is a metabolically stable synthetic analog of prostaglandin F2α. It is used clinically to treat severe postpartum bleeding
Storage Temp	Store at -20°C,Argon charged
Shipped In	Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available.
Action Type	AGONIST
Mechanism of action	Prostanoid FP receptor agonist

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Lipids and lipid-like molecules
  - Class Fatty Acyls
    - Subclass Eicosanoids

Kingdom	Organic compounds
Superclass	Lipids and lipid-like molecules
Class	Fatty Acyls
Subclass	Eicosanoids
Intermediate Tree Nodes	Not available
Direct Parent	Prostaglandins and related compounds
Alternative Parents	Long-chain fatty acids Hydroxy fatty acids Branched fatty acids Unsaturated fatty acids Cyclopentanols Tertiary alcohols Cyclic alcohols and derivatives Monocarboxylic acids and derivatives Carboxylic acids Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework	Not available
Substituents	Prostaglandin skeleton - Long-chain fatty acid - Branched fatty acid - Hydroxy fatty acid - Cyclopentanol - Fatty acid - Unsaturated fatty acid - Cyclic alcohol - Tertiary alcohol - Secondary alcohol - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Organic oxide - Alcohol - Carbonyl group - Hydrocarbon derivative - Organooxygen compound - Organic oxygen compound - Aliphatic homomonocyclic compound
Description	This compound belongs to the class of organic compounds known as prostaglandins and related compounds. These are unsaturated carboxylic acids consisting of a 20 carbon skeleton that also contains a five member ring, and are based upon the fatty acid arachidonic acid.
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

IUPAC Name	2-amino-2-(hydroxymethyl)propane-1,3-diol;(Z)-7-[(1R,2R,3R,5S)-3,5-dihydroxy-2-[(E,3S)-3-hydroxy-3-methyloct-1-enyl]cyclopentyl]hept-5-enoic acid
INCHI	InChI=1S/C21H36O5.C4H11NO3/c1-3-4-9-13-21(2,26)14-12-17-16(18(22)15-19(17)23)10-7-5-6-8-11-20(24)25;5-4(1-6,2-7)3-8/h5,7,12,14,16-19,22-23,26H,3-4,6,8-11,13,15H2,1-2H3,(H,24,25);6-8H,1-3,5H2/b7-5-,14-12+;/t16-,17-,18+,19-,21+;/m1./s1
InChIKey	UMMADZJLZAPZAW-XOWPVRJPSA-N
Smiles	CCCCCC(C)(C=CC1C(CC(C1CC=CCCCC(=O)O)O)O)O.C(C(CO)(CO)N)O
Isomeric SMILES	CCCCC[C@@](C)(/C=C/[C@H]1[C@@H](C[C@@H]([C@@H]1C/C=C\CCCC(=O)O)O)O)O.C(C(CO)(CO)N)O
PubChem CID	5281074
Molecular Weight	489.64

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

6 results found

Lot Number	Certificate Type	Date	Item
F2204280	Certificate of Analysis	Mar 04, 2025	C288595
F2204313	Certificate of Analysis	Mar 04, 2025	C288595
F2204314	Certificate of Analysis	Mar 04, 2025	C288595
F2204315	Certificate of Analysis	Mar 04, 2025	C288595
F2204261	Certificate of Analysis	Mar 04, 2025	C288595
F2204316	Certificate of Analysis	Mar 04, 2025	C288595

Chemical and Physical Properties

Solubility	Solvent:water, Max Conc. mg/mL: 48.96, Max Conc. mM: 100
Sensitivity	Moisture sensitive
Molecular Weight	489.600 g/mol
XLogP3
Hydrogen Bond Donor Count	8
Hydrogen Bond Acceptor Count	9
Rotatable Bond Count	15
Exact Mass	489.33 Da
Monoisotopic Mass	489.33 Da
Topological Polar Surface Area	185.000 Å²
Heavy Atom Count	34
Formal Charge	0
Complexity	527.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	5
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	2
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	2
Covalently-Bonded Unit Count	2

Solution Calculators

Molarity Calculator

Determine the necessary mass, volume, or concentration for preparing a solution.

Mass

Concentration

Volume

M. Wt*

g/mol

*When preparing stock solutions, always use the batch-specific molecular weight of the product found on the vial label and the Certificate of Analysis (available online).

Dilution Calculator

Determine the dilution needed to prepare a stock solution.

Concentration 1 (C1)

Volume 1 (V1)

Concentration 2 (C2)

Volume 2 (V2)

Reconstitution Calculator

The reconstitution calculator enables you to quickly determine the volume of a reagent needed to reconstitute your vial. Just enter the mass of the reagent and the target concentration, and the calculator will do the rest.

Volume (to add to vial)

Mass (in vial)

Desired Reconstitution Concentration