Skip to Content
MilliporeSigma
All Photos(1)

Documents

T4146

Sigma-Aldrich

1,3,9-Trimethylxanthine

≥98% (HPLC), solid

Synonym(s):

2,6-Dihydroxy-1,3,9-trimethylpurine, Isocaffeine

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C8H10N4O2
CAS Number:
Molecular Weight:
194.19
Beilstein/REAXYS Number:
196140
EC Number:
MDL number:
UNSPSC Code:
41106305
PubChem Substance ID:

biological source

synthetic (organic)

assay

≥98% (HPLC)

form

solid

solubility

H2O: >20 mg/mL

storage temp.

room temp

SMILES string

CN1C(=O)N(C)c2c(ncn2C)C1=O

InChI

1S/C8H10N4O2/c1-10-4-9-5-6(10)11(2)8(14)12(3)7(5)13/h4H,1-3H3

InChI key

LPHGQDQBBGAPDZ-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

1,3,9-Trimethylxanthine (Isocaffeine) may be used to study the mechanism of inositol-trisphosphate (Ins-P3) induced calcium release. 1,3,9-Trimethylxanthine may be used as an internal standard for measuring metabolites of caffeine in urine and other fluids by HPLC or capillary electrophoresis. 1,3,9-Trimethylxanthine may be used in studies on the binding of caffeine analogues to adenosine receptors.

Biochem/physiol Actions

1,3,9-Trimethylxanthine is an adenosine receptor antagonist.

Storage Class

13 - Non Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

L Missiaen et al.
The Biochemical journal, 300 ( Pt 1), 81-84 (1994-05-15)
We have investigated the effect of various methylxanthines on the basal and InsP3-stimulated unidirectional 45Ca2+ efflux from permeabilized A7r5 cells under different experimental conditions. We report that caffeine and theophylline inhibit the InsP3-induced Ca2+ release, whereas the basal Ca2+ leak
Yuli Liu et al.
The journal of physical chemistry. B, 115(47), 13880-13890 (2011-10-06)
Using the recently solved crystal structure of the human adenosine A(2A) receptor, we applied MM/PBSA to compare the binding modes of caffeine with those of the high-affinity selective antagonist ZM241385. MD simulations were performed in the environment of the lipid
N Rodopoulos et al.
Scandinavian journal of clinical and laboratory investigation, 54(4), 305-315 (1994-07-01)
Caffeine (CA) and its 14 main metabolites were determined in urine by reversed-phase high-performance liquid chromatography (RP-HPLC) and capillary electrophoresis (CE). After addition of 1,3,9-trimethylxanthine, uracil and beta-hydroxyethyltheophylline as internal standards, samples were separated by RP-HPLC into three fractions; A

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service