Prostaglandin G2

Modify Date: 2024-01-06 18:23:26

Prostaglandin G2 Structure
Prostaglandin G2 structure
Common Name Prostaglandin G2
CAS Number 51982-36-6 Molecular Weight 368.465
Density 1.2±0.1 g/cm3 Boiling Point 517.3±50.0 °C at 760 mmHg
Molecular Formula C20H32O6 Melting Point N/A
MSDS USA Flash Point 175.5±23.6 °C
Symbol GHS02 GHS07
GHS02, GHS07
Signal Word Danger

 Names

Name prostaglandin G2
Synonym More Synonyms

 Chemical & Physical Properties

Density 1.2±0.1 g/cm3
Boiling Point 517.3±50.0 °C at 760 mmHg
Molecular Formula C20H32O6
Molecular Weight 368.465
Flash Point 175.5±23.6 °C
Exact Mass 368.219879
PSA 85.22000
LogP 4.39
Vapour Pressure 0.0±3.1 mmHg at 25°C
Index of Refraction 1.545

 Safety Information

Symbol GHS02 GHS07
GHS02, GHS07
Signal Word Danger
Hazard Statements H225-H319-H336
Supplemental HS Repeated exposure may cause skin dryness or cracking.
Precautionary Statements P210-P280-P304 + P340 + P312-P305 + P351 + P338-P337 + P313-P403 + P235
Personal Protective Equipment Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter
Hazard Codes F: Flammable;Xi: Irritant;
Risk Phrases R11
Safety Phrases 9-16-26
RIDADR UN 1090 3

 Precursor & DownStream

Precursor  0

DownStream  2

 Articles27

More Articles
The cyclooxygenase reaction mechanism.

Biochemistry 41(52) , 15451-8, (2002)

Endotoxin priming of thromboxane-related vasoconstrictor responses in perfused rabbit lungs.

J. Appl. Physiol. 83(1) , 18-24, (1997)

In prior studies of perfused lungs, endotoxin priming markedly enhanced thromboxane (Tx) generation and Tx-mediated vasoconstriction in response to secondarily applied bacterial exotoxins. The present...

Comparison of peroxidase reaction mechanisms of prostaglandin H synthase-1 containing heme and mangano protoporphyrin IX.

J. Biol. Chem. 272(14) , 8885-94, (1997)

Prostaglandin H synthase (PGHS) is a heme protein that catalyzes both the cyclooxygenase and peroxidase reactions needed to produce prostaglandins G2 and H2 from arachidonic acid. Replacement of the h...

 Synonyms

Prostaglandin G2
(5Z)-7-{(1R,4S,5R,6R)-6-[(1E,3S)-3-Hydroperoxy-1-octen-1-yl]-2,3-dioxabicyclo[2.2.1]hept-5-yl}-5-heptenoic acid
5-Heptenoic acid, 7-[(1R,4S,5R,6R)-6-[(1E,3S)-3-hydroperoxy-1-octen-1-yl]-2,3-dioxabicyclo[2.2.1]hept-5-yl]-, (5Z)-
MFCD00036971