X7375

Xanthine

≥99%

Manufacturer: Sigma Aldrich

CAS Number: 69-89-6

Synonym(S): 2,6-Dihydroxypurine

Select a Size

Pack Size SKU Availability Price
10 G X7375-10-G In Stock ₹ 8,091.90
25 G X7375-25-G In Stock ₹ 17,782.20
100 G X7375-100-G In Stock ₹ 48,840.00

X7375 - 10 G

₹ 8,091.90

In Stock

Quantity

1

Base Price: ₹ 8,091.90

GST (18%): ₹ 1,456.542

Total Price: ₹ 9,548.442

biological source

synthetic (organic)

Quality Level

300

Assay

≥99%

form

powder

solubility

1 M NaOH: soluble 50 mg/mL, clear to slightly hazyNH4OH: freely solubleNaOH: freely soluble

SMILES string

O=C1NC(=O)c2nc[nH]c2N1

InChI

1S/C5H4N4O2/c10-4-2-3(7-1-6-2)8-5(11)9-4/h1H,(H3,6,7,8,9,10,11)

InChI key

LRFVTYWOQMYALW-UHFFFAOYSA-N

Other Options

Image Product Name Manufacturer Price Range
68-205-GM
MilliporeSigma™ Calbiochem™ Xanthine
MilliporeSigma™ --
50-491-312
Chem-Impex International, Inc. Xanthine | 69-89-6 | MFCD00078453 | 5G
Chem-Impex International, Inc. ₹ 3,171.71
501786718
Sigma Aldrich Fine Chemicals Biosciences Xanthine >=99.5% (HPLC), purified by recrystallization | 69-89-6 | MFCD00078453 | 5G
Sigma Aldrich Fine Chemicals Biosciences ₹ 10,209.02
50-491-313
Chem-Impex International, Inc. Xanthine | 69-89-6 | MFCD00078453 | 25G
Chem-Impex International, Inc. ₹ 6,128.66
NC2057097
eMolecules​ Xanthine | 69-89-6 | MFCD00078453 | 100g
eMolecules​ ₹ 7,556.66
50-193-4630
Medchemexpress LLC HY-W017389 1g Medchemexpress, Xanthine CAS:69-89-6 Purity:>98%
Medchemexpress LLC ₹ 4,491.90
50-242-0629
eMolecules​ Ambeed / 1H-Purine-26(3H7H)-dione / 5g / 552699818 / A303257 / / 69-89-6 / [null] / 152.113 / C5H4N4O2
eMolecules​ ₹ 2,251.94
X4002
Xanthine
Sigma Aldrich ₹ 9,590.40 - ₹ 52,869.30
X0626
Xanthine
Sigma Aldrich ₹ 14,152.50 - ₹ 41,547.30
CS-W018105
Xanthine
ChemScene ₹ 855.60 - ₹ 18,480.96

Description

  • General description: Xanthine is synthesized from guanine in the presence of guanine deaminase. Xanthine oxidase catalyzes the production of xanthine from hypoxanthine and its subsequent breakdown to uric acid.[1] Xanthine derivatives are present in coffee, tea and cocoa seeds. Xanthine has been proposed as a lead for the generation of pharmacologically active compounds.[2]
  • Application: Xanthine has been used in a nonradiolabled substrate mix in an Aspergillus nidulans transport assay.[3] It has also been used as a substrate for xanthine oxidase for superoxide anion generation in gill cells[4] and algal cells.[5]
  • 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.[1] Blood and urine samples of patients with renal failure, gout and xanthinuria show high levels of xanthine.[6]

SAFETY INFORMATION

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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1 M NaOH: soluble 50 mg/mL, clear to slightly hazyNH4OH: freely solubleNaOH: freely soluble

SMILES string:
O=C1NC(=O)c2nc[nH]c2N1

InChI:
1S/C5H4N4O2/c10-4-2-3(7-1-6-2)8-5(11)9-4/h1H,(H3,6,7,8,9,10,11)

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LRFVTYWOQMYALW-UHFFFAOYSA-N

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