Xanthine
Synonym(s):2,6-Dihydroxypurine;2,6-Dioxopurine;Xanthine - CAS 69-89-6 - Calbiochem
- CAS NO.:69-89-6
- Empirical Formula: C5H4N4O2
- Molecular Weight: 152.11
- MDL number: MFCD00078453
- EINECS: 200-718-6
- SAFETY DATA SHEET (SDS)
- Update Date: 2024-08-19 17:35:41
What is Xanthine?
Description
Xanthine is a two-oxygen cousin of adenine and guanine, the purine bases of DNA. Uric acid is a three-oxygen cousin, and methlyated relatives include key ingredients in coffee and chocolate:?caffeine?and, theobromine. Xanthine combined with its isomer oxypurinol forms an anti-cockroach pesticide that doesn’t harm humans.
Chemical properties
White to off-white crystalline powder
The Uses of Xanthine
2,6-Dihydroxypurine was fund in animal organs, yeast, patatoes, coffee beans, tea. 2,6-Dihydroxypurine can be used to relax and widen certain breathing passages of the lungs. It is also found that a large number of derivatives have adenoside receptor antagonist properties.
The Uses of Xanthine
Xanthine and xanthine oxidase system can be used to produce superoxide radicals.
What are the applications of Application
Xanthine is an adenosine receptor antagonist
Definition
A poisonous colorless crystalline organic compound that occurs in blood, coffee beans, potatoes, and urine. It is used as a chemical intermediate.
Definition
Xanthine: a purine base, C5H4N4O2,found in many organisms.
Origin
Xanthines (1H-purine-2,6(3H,7H)-diones) are purine based natural heterocyclic alkaloids. They were first discovered in 1817 by German chemist Emil Fisher and later the name ‘xanthine’ was coined in 1899[1].
Biological Functions
In fact, xanthine and its derivatives act as intermediate molecules in generation of GMP, GDP and GTP via the salvage pathway inside the cells. In addition, xanthine plays imperative role in catabolism of nucleotides and nucleic acids as xanthine acts as precursor of uric acid. Therefore, xanthine contains similar skeleton as that of purines which forms the building blocks of unit of life i.e. ribonucleotides (RNA) and deoxyribonucleotides (DNA). The structural resemblance with two of the important purine derivatives Adenine and Guanine; makes xanthine a good therapeutic molecule[1].
Synthesis Reference(s)
Chemical and Pharmaceutical Bulletin, 22, p. 1200, 1974 DOI: 10.1248/cpb.22.1200
General Description
Xanthine is a purine that can be produced in the purine metabolic pathway via different precursors:
- Guanine deamination by guanine deaminase
- Hypoxanthine conversion by xanthine oxidoreductase
Biochem/physiol Actions
A high level of xanthine is implicated in metabolic disorders like Lesch-Nyhan syndrome. A xanthine-based biosensor may be useful for detecting xanthine in food and clinical samples. Blood and urine samples of patients with renal failure, gout and xanthinuria show high levels of xanthine.
Purification Methods
The monohydrate separates in a microcrystalline form on slow acidification with acetic acid of a solution of xanthine in dilute NaOH. It is also precipitated by addition of conc NH3 to its solution in hot 2N HCl (charcoal). After washing with H2O and EtOH, it is dehydrated by heating above 125o. Its solubility in H2O is 1 in 14,000parts at 16o and 1 in 1,500parts of boiling H2O, and separates as plates . It has no m, but the perchlorate has m 262-264o [Lister Purines Part II, Fused Pyrimidines Brown Ed, Wiley-Interscience pp252-253 1971, ISBN 0-471-38205-1]. [Beilstein 26 H 447, 26 I 131, 26 II 260, 26 III/IV 2327.]
References
[1] Ahlawat, Jyoti Minakshi Sharma and Chandra S. Pundir. “Advances in xanthine biosensors and sensors: A review.” Enzyme and Microbial Technology 69 1 (2023).
Properties of Xanthine
Melting point: | 300 °C |
Boiling point: | 274.55°C (rough estimate) |
Density | 1.5452 (rough estimate) |
vapor density | 5.3 (vs air) |
refractive index | 1.8500 (estimate) |
storage temp. | Keep in dark place,Sealed in dry,Room Temperature |
solubility | NH4OH: freely soluble |
pka | pKa 9.95 (Uncertain) |
form | Powder |
color | White to slightly yellow |
Odor | Odorless |
Water Solubility | Soluble in water(0.067g/L). |
Merck | 14,10059 |
BRN | 8733 |
CAS DataBase Reference | 69-89-6(CAS DataBase Reference) |
NIST Chemistry Reference | Xanthine(69-89-6) |
EPA Substance Registry System | Xanthine (69-89-6) |
Safety information for Xanthine
Signal word | Warning |
Pictogram(s) |
Exclamation Mark Irritant GHS07 |
GHS Hazard Statements |
H317:Sensitisation, Skin H319:Serious eye damage/eye irritation |
Precautionary Statement Codes |
P280:Wear protective gloves/protective clothing/eye protection/face protection. P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing. |
Computed Descriptors for Xanthine
InChIKey | LRFVTYWOQMYALW-UHFFFAOYSA-N |
Abamectin manufacturer
SS Reagents and Chemicals
New Products
ALUMINIUM IODIDE 100 GM BUFFER CAPSULE PH 7.0 - 10 CAP BUFFER SOLUTION PH 9.5 (BORATE) EZEE BLUE GEL STAINER BORAX CARMINE (GRENACHERS ALCOHOLIC) POTASSIUM IODATE - IODIDE SOLN 0.1 N Dabigatran Acyl-O3-D-Glucuronide Trifluoroacetic Acid Salt Isofolic Acid Dabigatran 2-O-acylglucuronide metabolite Dabigatran Acyl-?-D- glucuronide Trifluroacetic Acid Erythromycin EP Impurity A Desloratidine Related Compound ARelated products of tetrahydrofuran
You may like
-
Xanthine, 99.5% CAS 69-89-6View Details
69-89-6 -
Xanthine CAS 69-89-6View Details
69-89-6 -
Xanthine CASView Details
-
Xanthine CAS 69-89-6View Details
69-89-6 -
XANTHINE For Biochemistry CAS 69-89-6View Details
69-89-6 -
Xanthine CAS 69-89-6View Details
69-89-6 -
Xanthine CAS 69-89-6View Details
69-89-6 -
Xanthine CAS 69-89-6View Details
69-89-6