1,3-Dipropyl-7-methylxanthine structure
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Common Name | 1,3-Dipropyl-7-methylxanthine | ||
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CAS Number | 31542-63-9 | Molecular Weight | 250.297 | |
Density | 1.3±0.1 g/cm3 | Boiling Point | 443.5±37.0 °C at 760 mmHg | |
Molecular Formula | C12H18N4O2 | Melting Point | 114-117ºC | |
MSDS | USA | Flash Point | 222.0±26.5 °C |
Name | 7-methyl-1,3-dipropylpurine-2,6-dione |
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Synonym | More Synonyms |
Density | 1.3±0.1 g/cm3 |
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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 |
Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
HS Code | 2933990090 |
HS Code | 2933990090 |
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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% |
A1- and A2-selective adenosine antagonists: in vivo characterization of cardiovascular effects.
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... |
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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... |
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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... |
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 |