Epoprostenol structure, CAS 61849-14-7

Epoprostenol

CAS Number61849-14-7

SynonymsMFCD00135629; PGI2; Flolan; Prostacyclin sodium; EINECS 234-237-8; Prosta-5,13-dien-1-oic acid, 6,9-epoxy-11,15-dihydroxy-, sodium salt, (9α,11α,13E,15S)- (1:1); PG12-NA; (5Z,9a,11a,13E,15S)-6,9-Epoxy-11,15-dihydroxyprosta-5,13-dien-1-oic Acid Sodium Salt; U 53217A; PGI2,SODIUM SALT; Sodium PGI2; PGI2-NA; PROSTAGLANDIN I2; Prostaglandin 12; PGI2 sodium; Epoprostenol sodium; Sodium (9α,11α,13E,15S)-11,15-dihydroxy-6,9-epoxyprosta-5,13-dien-1-oate

Molecular FormulaC20H31NaO5

Molecular Weight374.45

Purity≥96 (HPLC)%

Density

Boiling Point530.2ºC at 760mmHg

Melting Point168-170 °C

Flash Point

Appearancepowder

EINECS263-273-7

MSDSChineseEnglish

SymbolTransport

Signal WordWarning

Cat. No.: 2A-9010352 Purity: ≥96 (HPLC)%
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Quality Control of [ 61849-14-7 ] Purity: ≥96 (HPLC)% SDS Specification MoL

Chemical & Physical Properties
CAS Number61849-14-7
Catalog No.2A-9010352
Chinese Name前列腺素 I2 钠盐
SynonymsMFCD00135629; PGI2; Flolan; Prostacyclin sodium; EINECS 234-237-8; Prosta-5,13-dien-1-oic acid, 6,9-epoxy-11,15-dihydroxy-, sodium salt, (9α,11α,13E,15S)- (1:1); PG12-NA; (5Z,9a,11a,13E,15S)-6,9-Epoxy-11,15-dihydroxyprosta-5,13-dien-1-oic Acid Sodium Salt; U 53217A; PGI2,SODIUM SALT; Sodium PGI2; PGI2-NA; PROSTAGLANDIN I2; Prostaglandin 12; PGI2 sodium; Epoprostenol sodium; Sodium (9α,11α,13E,15S)-11,15-dihydroxy-6,9-epoxyprosta-5,13-dien-1-oate
Molecular FormulaC20H31NaO5
Molecular Weight374.45
Purity≥96 (HPLC)
Boiling Point530.2ºC at 760mmHg
Melting Point168-170 °C
Appearancepowder
Water SolubilityH2O: 1 mg/mL Hydrolyzes to 6-ketoprostaglandin F1α
Storage ConditionStore in an airtight container in a cool, dry plac
ApplicationEpoprostenol sodium (Prostaglandin I2 (sodium salt)) is a synthetic form of the natural prostaglandin derivative prostacyclin (prostaglandin I2), used worldwide to treat pulmonary arterial hypertensio
EINECS263-273-7
PubChem ID24898653
SMILESCCCCC[C@H](O)/C=C/[C@H]1[C@H](O)C[C@@](O/2)([H])[C@]1([H])CC2=C\CCCC(O)=O.[Na]
InChI1S/C20H32O5.Na/c1-2-3-4-8-15(21)10-11-16-17(22)12-18-20(16)14(13-25-18)7-5-6-9-19(23)24;/h7,10-11,15-18,20-22H,2-6,8-9,12-13H2,1H3,(H,23,24);/q;+1/p-1/b11-10+,14-7-;/t15-,16-,17+,18-,20+;/m0./s1
InChI KeyOURCVRVJQMLUNA-QFDVFERUSA-M
Beilstein/REAXYS6472195
NACRES CodeNA.77
eCl@ss42020658
UNSPSC12352401
Hazard SymbolsTransport
MSDSmsds/10352_1_61849_14_7.pdf
BioactivityEpoprostenol sodium (Prostaglandin I2 (sodium salt)), the synthetic form of the natural prostaglandin derivative prostacyclin (prostaglandin I2), is registered worldwide for the treatment of Pulmonary arterial hypertension (PAH)[1]. Epoprostenol sodium is used in pulmonary hypertension and transplantation as a potent inhibitor of platelet aggregation[2]. Related Catalog Research Areas >> Cardiovascular Disease Signaling Pathways >> Others >> Others References [1]. Provencher S, et al.Quality of life, safety and efficacy profile of thermostable flolan in pulmonary arterialhypertension. PLoS One. 2015 Mar 20;10(3):e0120657. Chemical & Physical Properties Boiling Point 530.2ºC at 760mmHg Melting Point 168-170 °C Molecular Formula C20H31NaO5 Molecular Weight 374.447 Flash Point 182.1ºC Exact Mass 374.206909 PSA 89.82000 LogP 2.07380 InChIKey LMHIPJMTZHDKEW-HIHHSTLZSA-M SMILES CCCCCC(O)C=CC1C(O)CC2OC(=CCCCC(=O)[O-])CC21.[Na+] Storage condition −20°C Water Solubility H2O: 1 mg/mL Hydrolyzes to 6-ketoprostaglandin F1α in aqueous solution.
Use ofEpoprostenol sodium (Prostaglandin I2 (sodium salt)), the synthetic form of the natural prostaglandin derivative prostacyclin (prostaglandin I2), is registered worldwide for the treatment of Pulmonary arterial hypertension (PAH)[1]. Epoprostenol sodium is used in pulmonary hypertension and transplantation as a potent inhibitor of platelet aggregation[2]. Properties Articles36 Name prostacyclin sodium salt Synonym More Synonyms Epoprostenol sodium Biological Activity Description Epoprostenol sodium (Prostaglandin I2 (sodium salt)), the synthetic form of the natural prostaglandin derivative prostacyclin (prostaglandin I2), is registered worldwide for the treatment of Pulmonary arterial hypertension (PAH)[1]. Epoprostenol sodium is used in pulmonary hypertension and transplantation as a potent inhibitor of platelet aggregation[2]. Related Catalog Research Areas >> Cardiovascular Disease Signaling Pathways >> Others >> Others References [1]. Provencher S, et al.Quality of life, safety and efficacy profile of thermostable flolan in pulmonary arterialhypertension. PLoS One. 2015 Mar 20;10(3):e0120657. Chemical & Physical Properties Molecular Formula C20H31NaO5 Exact Mass 374.206909 PSA 89.82000 LogP 2.07380 InChIKey LMHIPJMTZHDKEW-HIHHSTLZSA-M
Transport InfoProduct name: Purity: 96.0%
MSDS Transport InfoModule 14. Shipping information 14.1 UN dangerous goods number European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.2 Names specified by the United Nations (UN) European Land Transport Dangerous Regulations: Non-dangerous goods IMDG Code: Non-dangerous goods International air transport dangerous goods regulations: non-dangerous goods 14.3 Transport hazard categories European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.4 Package group European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.5 Environmental hazards European Land Transport Dangerous Regulations: No International Maritime Transport Dangerous Regulations Maritime Pollutants: No International Air Transport Risk Regulations: No 14.6 Special reminder to users No data available
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