1,3-Dipropyl-7-methylxanthine
Names
[ CAS No. ]:
31542-63-9
[ Name ]:
1,3-Dipropyl-7-methylxanthine
[Synonym ]:
1H-Purine-2,6-dione, 3,7-dihydro-7-methyl-1,3-dipropyl-
Lopac-D-108
1,3-Dipropyl-7-methylxanthine
1,3-di-n-propyl-7-methylxanthine
7-Methyl-1,3-dipropyl-1H-purine-2,6(3H,7H)-dione
MFCD00055219
1,3-dipropyl-7-methyl-xanthine
7-Methyl-1,3-dipropyl-3,7-dihydro-1H-purine-2,6-dione
7-methyl-1,3-dipropyl-3,7-dihydro-1h-purin-2,6-dion
Chemical & Physical Properties
[ Density]:
1.3±0.1 g/cm3
[ Boiling Point ]:
443.5±37.0 °C at 760 mmHg
[ Melting Point ]:
114-117ºC
[ Molecular Formula ]:
C12H18N4O2
[ Molecular Weight ]:
250.297
[ Flash Point ]:
222.0±26.5 °C
[ Exact Mass ]:
250.142975
[ PSA ]:
61.82000
[ LogP ]:
1.99
[ Vapour Pressure ]:
0.0±1.1 mmHg at 25°C
[ Index of Refraction ]:
1.612
[ Stability ]:
Store tightly sealed at RT
[ Water Solubility ]:
0.1 M NaOH: soluble
MSDS
Safety Information
[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
[ RIDADR ]:
NONH for all modes of transport
[ WGK Germany ]:
3
[ HS Code ]:
2933990090
Precursor & DownStream
Precursor
DownStream
Customs
[ HS Code ]: 2933990090
[ Summary ]:
2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%
Articles
J. Pharmacol. Exp. Ther. 242 , 882, (1987)
Caffeine, a nonselective adenosine receptor antagonist, 7-methyl-1,3-dipropylxanthine, a purported A2 selective antagonist and a 1,3-dipropyl-8-phenylxanthine amine congener (XAC), an A1 selective ant...
Caffeine and theophylline analogues: correlation of behavioral effects with activity as adenosine receptor antagonists and as phosphodiesterase inhibitors.Life Sci. 43 , 387-398, (1988)
The behavioral stimulant effects of xanthines, such as caffeine and theophylline, appear to involve blockade of central adenosine receptors. However, 3-isobutyl-1-methylxanthine (IBMX), a potent phosp...
Analogs of caffeine: antagonists with selectivity for A2 adenosine receptors.Life Sci. 39 , 743-750, (1986)
Several analogs of caffeine have been investigated as antagonists at A2 adenosine receptors stimulatory to adenylate cyclase in membranes from rat pheochromocytoma PC12 cells and human platelets and a...