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1,7-DIMETHYLXANTHINE

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1,7-DIMETHYLXANTHINE Basic information

Product Name:
1,7-DIMETHYLXANTHINE
Synonyms:
  • 1,7-Dimethyl-1H-purine-2,6-dione, 1,7-Dimethylxanthine, 2,6-Dihydroxy-1,7-dimethylpurine, Paraxanthine
  • 1,7-dimethyl-3H-purine-2,6-dione
  • Caffeine Impurity F(EP)
  • Caffeine Impurity 6(Caffeine EP Impurity F)
  • 1,7-Dimethyl-1H-purine-2,6-dione, 2,6-Dihydroxy-1,7-dimethylpurine, Paraxanthine
  • 1,7-Dimethyl-2,3,6,7-tetrahydro-1H-purine-2,6-dione
  • 1,7-Dimethylxanthine-[13C4,15N3] (para-xanthine)
  • 1,7-Dimethylxanthine-[2H6] (para-xanthine)
CAS:
611-59-6
MF:
C7H8N4O2
MW:
180.16
EINECS:
210-271-9
Product Categories:
  • Isolabel
  • Amines
  • Various Metabolites and Impurities
  • Heterocycles
  • Metabolites & Impurities
  • Phosphorylating and Phosphitylating Agents
  • Metabolites
Mol File:
611-59-6.mol
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1,7-DIMETHYLXANTHINE Chemical Properties

Melting point:
294-296 °C (lit.)
Boiling point:
312.97°C (rough estimate)
Density 
1.3640 (rough estimate)
refractive index 
1.6700 (estimate)
Flash point:
9℃
storage temp. 
room temp
solubility 
ethanol: 0.6mg/mL
form 
solid
pka
pKa 8.5 (Uncertain)
color 
white
BRN 
197907
Stability:
Store tightly sealed at RT
InChI
InChI=1S/C7H8N4O2/c1-10-3-8-5-4(10)6(12)11(2)7(13)9-5/h3H,1-2H3,(H,9,13)
InChIKey
QUNWUDVFRNGTCO-UHFFFAOYSA-N
SMILES
N1(C)C2=C(NC(=O)N(C)C2=O)N=C1
EPA Substance Registry System
1H-Purine-2,6-dione, 3,7-dihydro-1,7-dimethyl- (611-59-6)
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Safety Information

Hazard Codes 
Xn,T,F
Risk Statements 
22-39/23/24/25-23/24/25-11
Safety Statements 
22-24/25-45-36/37-16-7
RIDADR 
UN1230 - class 3 - PG 2 - Methanol, solution
WGK Germany 
3
RTECS 
RV9380000
HS Code 
2933.59.9500
Toxicity
mmo-esc 150 mg/L CSHSAZ 16,337,52

MSDS

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1,7-DIMETHYLXANTHINE Usage And Synthesis

Description

Paraxanthine is an inhibitor of phosphodiesterase 9 (PDE9) and an antagonist of adenosine receptors A1 and A2 (Kis = 35 and 22 μM, respectively in equine forebrain tissues). It is the main metabolite of caffeine in humans, making up 80% of the three dimethylxanthine metabolites produced by caffeine demethylation. Paraxanthine increases locomotor activity and counteracts adenosine receptor agonist-induced motor depression in rats not habituated to caffeine. At a dose of 30 mg/kg, paraxanthine induces a significant increase in striatal cGMP and extracellular striatal dopamine concentrations in vivo. It also promotes wakefulness and increases locomotor activity and core temperature in narcoleptic transgenic mice without increasing behavioral anxiety.

Chemical Properties

Off-White to Pale Yellow Solid

Uses

adenosine receptor agonist, CNS stimulant

Uses

Paraxanthine is an adenosine receptor ligand and a major metabolite of caffeine.This compound is a contaminant of emerging concern (CECs).

Uses

1,7-Dimethylxanthine has been used for the quantification of caffeine by high-performance liquid chromatography (HPLC).

Definition

ChEBI: 1,7-dimethylxanthine is a dimethylxanthine having the two methyl groups located at positions 1 and 7. It is a metabolite of caffeine and theobromine in animals. It has a role as a central nervous system stimulant, a human xenobiotic metabolite, a human blood serum metabolite and a mouse metabolite.

General Description

Paraxanthine is a major plasma and urinary metabolite of caffeine. This xanthine derivative is, along with caffeine, a central nervous system stimulant. This Snap-N-Spike? reference solution is applicable for caffeine quantitation in clinical toxicology or urine drug testing by LC-MS/MS or GC/MS.

Biochem/physiol Actions

Adenosine receptor ligand; major metabolite of caffeine

Safety Profile

An experimental teratogen. Mutation data reported. Whenheated to decomposition it emits toxic fumes of NOx.

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