Product Name

  • Name

    URIC ACID

  • EINECS 200-720-7
  • CAS No. 69-93-2
  • Article Data120
  • CAS DataBase
  • Density 1.87 g/cm3
  • Solubility Soluble in 1M sodium hydroxide solution. Slightly soluble in water. Insoluble in ether and alcohol.
  • Melting Point >300°C(lit.)
  • Formula C5H4N4O3
  • Boiling Point 863 °C at 760 mmHg
  • Molecular Weight 168.112
  • Flash Point 475.7 °C
  • Transport Information
  • Appearance Off-white crystals
  • Safety 24/25-36-26
  • Risk Codes 33-36/37/38
  • Molecular Structure Molecular Structure of 69-93-2 (URIC ACID)
  • Hazard Symbols IrritantXi
  • Synonyms Uric acid(8CI);1H-Purine-2,6,8-triol;2,6,8-Trihydroxypurine;2,6,8-Trioxopurine;2,6,8-Trioxypurine;Lithic acid;NSC 3975;Purine-2,6,8(1H,3H,9H)-trione;1H-Purine-2,6,8 (3H)-trione, 7,9-dihydro-;1H-purine-2,6,8(3H)-trione, 7,9-dihydro-;1H-Purine-2,6,8(3H)-trione, 7,9-dihydro- (9CI);2,6,8-trioxopurine;
  • PSA 114.37000
  • LogP -1.76720

Synthetic route

5,6-diaminouracil
3240-72-0

5,6-diaminouracil

urea
57-13-6

urea

uric Acid
69-93-2

uric Acid

Conditions
ConditionsYield
at 170 - 180℃;
5-hydroxybarbituric acid
444-15-5

5-hydroxybarbituric acid

urea
57-13-6

urea

uric Acid
69-93-2

uric Acid

Conditions
ConditionsYield
im kuenstlichen Kreislaufversuch;
(6-amino-2,4-dioxo-1,2,3,4-tetrahydro-pyrimidin-5-yl)-urea
84455-48-1

(6-amino-2,4-dioxo-1,2,3,4-tetrahydro-pyrimidin-5-yl)-urea

uric Acid
69-93-2

uric Acid

Conditions
ConditionsYield
at 230℃; laesst sich auch durch trockenes Erhitzen;
(2,4,6-trioxo-hexahydro-pyrimidin-5-yl)-urea
487-63-8

(2,4,6-trioxo-hexahydro-pyrimidin-5-yl)-urea

oxalic acid
144-62-7

oxalic acid

uric Acid
69-93-2

uric Acid

Conditions
ConditionsYield
at 185℃;
5-sulfaminouracil
5435-16-5

5-sulfaminouracil

urea
57-13-6

urea

uric Acid
69-93-2

uric Acid

Conditions
ConditionsYield
at 200℃;
cyanoacetic acid
372-09-8

cyanoacetic acid

urea
57-13-6

urea

A

uric Acid
69-93-2

uric Acid

B

N-(aminocarbonyl)-2-cyano-acetamide
1448-98-2

N-(aminocarbonyl)-2-cyano-acetamide

7H-purin-6-ylamine
73-24-5

7H-purin-6-ylamine

uric Acid
69-93-2

uric Acid

Conditions
ConditionsYield
With bovine spleen-extract; oxygen
1,7-dihydro-6H-purin-6-one
68-94-0

1,7-dihydro-6H-purin-6-one

uric Acid
69-93-2

uric Acid

Conditions
ConditionsYield
With oxygen In various solvent(s) Kinetics; Km, Ki,slope, Vmax; xanthine oxidase;
With bovine spleen-extract; oxygen
With oxygen
1,7-dihydro-6H-purin-6-one
68-94-0

1,7-dihydro-6H-purin-6-one

A

uric Acid
69-93-2

uric Acid

B

xanthin
69-89-6

xanthin

Conditions
ConditionsYield
bei enzymatischen Oxydation;
LACTIC ACID
849585-22-4

LACTIC ACID

urea
57-13-6

urea

uric Acid
69-93-2

uric Acid

Conditions
ConditionsYield
With goose liver extract; oxygen at 38℃; bei pH 7.4 bis 7.6;
With chicken liverextract; oxygen at 38℃; bei pH 7.4 bis 7.6;
at 38℃; unter aeroben Bedingungen;
3,3,3-trichloro-2-hydroxy-propionic acid
599-01-9

3,3,3-trichloro-2-hydroxy-propionic acid

urea
57-13-6

urea

uric Acid
69-93-2

uric Acid

3,3,3-trichloro-2-hydroxy-propionamide
74592-79-3

3,3,3-trichloro-2-hydroxy-propionamide

urea
57-13-6

urea

uric Acid
69-93-2

uric Acid

5,6-diaminouracil sulfate
42965-55-9

5,6-diaminouracil sulfate

urea
57-13-6

urea

uric Acid
69-93-2

uric Acid

Conditions
ConditionsYield
at 180℃;
urea
57-13-6

urea

glycine
56-40-6

glycine

uric Acid
69-93-2

uric Acid

xanthin
69-89-6

xanthin

uric Acid
69-93-2

uric Acid

Conditions
ConditionsYield
With sodium azide; phosphate buffer; McIlvaine buffer; (E)-(3-methyl-1,3-benzothiazol-2-ylidene)hydrazine;hydrochloride; N,N-dimethyl-aniline; citric acid; xanthine oxidase; peroxidase 1.) pH=8.5; 2.) pH=3.5; 3.) standard assay of XO activity in serum;
With several organs of the rat; tissuesuspensionene different; methylene blue
With oxygen
guanine
73-40-5

guanine

uric Acid
69-93-2

uric Acid

Conditions
ConditionsYield
With bovine spleen-extract; oxygen
guanine
73-40-5

guanine

A

uric Acid
69-93-2

uric Acid

B

xanthin
69-89-6

xanthin

Conditions
ConditionsYield
Verfuetterung an Enten;
N-(guanin-C8-yl)-1-naphthylamine
80156-61-2

N-(guanin-C8-yl)-1-naphthylamine

A

uric Acid
69-93-2

uric Acid

B

1-amino-naphthalene
134-32-7

1-amino-naphthalene

Conditions
ConditionsYield
With alkali
uric acid radical
69-93-2

uric acid radical

uric Acid
69-93-2

uric Acid

Conditions
ConditionsYield
With Chr-O(1-) In water at 20℃; Rate constant; Equilibrium constant; Irradiation; various substrate concentration, further reagent; pH 13.0;
xanthine
69-89-6

xanthine

uric Acid
69-93-2

uric Acid

Conditions
ConditionsYield
With sodium dihydrogenphosphate; oxygen; palladium dichloride Rate constant; xanthine oxidase; var. conc. PdCl2;
With hydroxide In water Product distribution; Mechanism; Irradiation; pH = 6 10 11; OH(1-) radical was generated by photolysis of sulfate radical anion or photolysis of H2O2; add of 4-mercaptopyridine-N-oxide; intermedier radicals were determined by ESR;
With oxygen; xanthine oxidase In water at 283℃; Enzyme kinetics; Activation energy; Kinetics; Further Variations:; Temperatures; Oxidation;
xanthin
69-89-6

xanthin

A

pyrimidine-2,4,5,6(1H,3H)-tetraone
61066-33-9, 61066-34-0, 61066-35-1, 61127-23-9

pyrimidine-2,4,5,6(1H,3H)-tetraone

B

uric Acid
69-93-2

uric Acid

C

urea
57-13-6

urea

Conditions
ConditionsYield
at 25℃; Product distribution; Mechanism; Rate constant; electrochemical oxidation; buffer (pH=2-6); various times, potentials and electrodes;
hydrogenchloride
7647-01-0

hydrogenchloride

2,6-dichloro-7,9-dihydro-purin-8-one
98027-86-2

2,6-dichloro-7,9-dihydro-purin-8-one

uric Acid
69-93-2

uric Acid

Conditions
ConditionsYield
at 120℃;
hydrogenchloride
7647-01-0

hydrogenchloride

8-amino-2-methylsulfanyl-1,7-dihydro-purin-6-one

8-amino-2-methylsulfanyl-1,7-dihydro-purin-6-one

uric Acid
69-93-2

uric Acid

hydrogenchloride
7647-01-0

hydrogenchloride

(2,4,6-trioxo-hexahydro-pyrimidin-5-yl)-carbamonitrile

(2,4,6-trioxo-hexahydro-pyrimidin-5-yl)-carbamonitrile

uric Acid
69-93-2

uric Acid

hydrogenchloride
7647-01-0

hydrogenchloride

2-methylsulfanyl-7,9-dihydro-1H-purine-6,8-dione
14443-37-9

2-methylsulfanyl-7,9-dihydro-1H-purine-6,8-dione

uric Acid
69-93-2

uric Acid

hydrogenchloride
7647-01-0

hydrogenchloride

(6-amino-2,4-dioxo-1,2,3,4-tetrahydro-pyrimidin-5-yl)-urea
84455-48-1

(6-amino-2,4-dioxo-1,2,3,4-tetrahydro-pyrimidin-5-yl)-urea

uric Acid
69-93-2

uric Acid

Conditions
ConditionsYield
at 120℃;
hydrogenchloride
7647-01-0

hydrogenchloride

(2,4,6-trioxo-hexahydro-pyrimidin-5-yl)-urea
487-63-8

(2,4,6-trioxo-hexahydro-pyrimidin-5-yl)-urea

uric Acid
69-93-2

uric Acid

hydrogenchloride
7647-01-0

hydrogenchloride

(6,8-dioxo-6,7,8,9-tetrahydro-1H-purin-2-ylmercapto)-acetic acid

(6,8-dioxo-6,7,8,9-tetrahydro-1H-purin-2-ylmercapto)-acetic acid

uric Acid
69-93-2

uric Acid

6.8-dioxy-2-carboxymethylsulfanyl-purine

6.8-dioxy-2-carboxymethylsulfanyl-purine

uric Acid
69-93-2

uric Acid

Conditions
ConditionsYield
With hydrogenchloride
uric Acid
69-93-2

uric Acid

5-aminouracil-6-thiol

5-aminouracil-6-thiol

Conditions
ConditionsYield
With ammonium sulfide; potassium hydroxide In water at 180℃; for 6h; Microwave irradiation;89%
uric Acid
69-93-2

uric Acid

carbonic acid dimethyl ester
616-38-6

carbonic acid dimethyl ester

theacrine
2309-49-1

theacrine

Conditions
ConditionsYield
at 185℃; under 3750.38 Torr; for 5h; Inert atmosphere; Autoclave;85.9%
In water at 160℃; under 760.051 Torr;82.4%
formaldehyd
50-00-0

formaldehyd

uric Acid
69-93-2

uric Acid

theacrine
2309-49-1

theacrine

Conditions
ConditionsYield
at 100℃; under 3750.38 Torr; for 24h; Inert atmosphere; Autoclave;82.3%
chloro-trimethyl-silane
75-77-4

chloro-trimethyl-silane

uric Acid
69-93-2

uric Acid

theacrine
2309-49-1

theacrine

Conditions
ConditionsYield
at 115℃; under 3750.38 Torr; for 18h; Inert atmosphere; Autoclave;82%
uric Acid
69-93-2

uric Acid

methyl trifluoromethanesulfonate
333-27-7

methyl trifluoromethanesulfonate

theacrine
2309-49-1

theacrine

Conditions
ConditionsYield
at 190℃; under 3750.38 Torr; for 8h; Inert atmosphere; Autoclave;81.5%
uric Acid
69-93-2

uric Acid

trimethyl orthoformate
149-73-5

trimethyl orthoformate

theacrine
2309-49-1

theacrine

Conditions
ConditionsYield
at 220℃; under 3750.38 Torr; for 48h; Inert atmosphere; Autoclave;80%
uric Acid
69-93-2

uric Acid

N,N-dimethyl-formamide dimethyl acetal
4637-24-5

N,N-dimethyl-formamide dimethyl acetal

theacrine
2309-49-1

theacrine

Conditions
ConditionsYield
at 190℃; under 3750.38 Torr; for 2.5h; Inert atmosphere; Autoclave;79.2%
uric Acid
69-93-2

uric Acid

A

parabanic acid
120-89-8

parabanic acid

B

Oxalyldiurea
5676-27-7

Oxalyldiurea

C

dehydro-allantoin
105245-87-2

dehydro-allantoin

D

Allantoin
97-59-6

Allantoin

Conditions
ConditionsYield
With lithium hydroxide; iodine In water for 0.0833333h; excess of I2;A n/a
B n/a
C 75%
D n/a
With lithium hydroxide; iodine In water for 0.0833333h; Mechanism; also with substituted uric acid; effect of amount of I2; 2H and 13C labelling experiment;
uric Acid
69-93-2

uric Acid

tetramethyl ammoniumhydroxide
75-59-2

tetramethyl ammoniumhydroxide

theacrine
2309-49-1

theacrine

Conditions
ConditionsYield
at 200℃; under 3750.38 Torr; for 2h; Inert atmosphere; Autoclave;75%
uric Acid
69-93-2

uric Acid

dihydroxyuric acid
67708-22-9

dihydroxyuric acid

Conditions
ConditionsYield
With rose bengal In glycerol for 23h; Irradiation;74.71%
With chlorine; acetic acid
pH=7; Electrochemical reaction; aq. phosphate buffer;
With Fe exchanged nanocrystalline ZSM-5 In aq. phosphate buffer pH=3.5; Kinetics; Electrochemical reaction;
With titanium dioxide nanorods with multi-walled carbon nanotubes pH=4; Electrochemical reaction;
uric Acid
69-93-2

uric Acid

A

pyrimidine-2,4,5,6(1H,3H)-tetraone
61066-33-9, 61066-34-0, 61066-35-1, 61127-23-9

pyrimidine-2,4,5,6(1H,3H)-tetraone

B

urea
57-13-6

urea

Conditions
ConditionsYield
With rose bengal; sodium hydroxide In glycerol for 36h; Irradiation;A 72.18%
B n/a
uric Acid
69-93-2

uric Acid

dimethyl sulfate
77-78-1

dimethyl sulfate

theacrine
2309-49-1

theacrine

Conditions
ConditionsYield
at 84℃; under 3750.38 Torr; for 2.5h; Inert atmosphere; Autoclave;71.4%
uric Acid
69-93-2

uric Acid

Allantoin
97-59-6

Allantoin

Conditions
ConditionsYield
With lithium hydroxide; iodine In water at 4℃; equimolar amount of I2;70%
With sodium hydroxide; oxygen; pyrographite
With water; ozone
uric Acid
69-93-2

uric Acid

methyl iodide
74-88-4

methyl iodide

theacrine
2309-49-1

theacrine

Conditions
ConditionsYield
at 84℃; under 3750.38 Torr; for 2h; Inert atmosphere; Autoclave;69.2%
With alkaline solution at 100 - 110℃;
uric Acid
69-93-2

uric Acid

1,5-diamino-3,7-dioxo-2,4,6,8-tetraazabicyclo-[3.3.0]octane
133364-43-9

1,5-diamino-3,7-dioxo-2,4,6,8-tetraazabicyclo-[3.3.0]octane

Conditions
ConditionsYield
With sodium persulfate; ammonia; water; sodium chloride at -8 - -5℃; for 2h;69%
Stage #1: uric Acid With ammonium hydroxide; sodium persulfate; sodium chloride In water at -10℃; for 2h;
Stage #2: With ammonium hydroxide In water at -10 - 20℃; for 1h;
64%
uric Acid
69-93-2

uric Acid

6-thiouramil ammonium salt

6-thiouramil ammonium salt

Conditions
ConditionsYield
With diammonium sulfide; water; potassium hydroxide at 0 - 180℃; for 8h; Sealed tube;63%
uric Acid
69-93-2

uric Acid

cis-1,5-diamino-2,4,6,8-tetraazabicyclo-<3.3.0>octane-3,7-dione
133364-43-9

cis-1,5-diamino-2,4,6,8-tetraazabicyclo-<3.3.0>octane-3,7-dione

Conditions
ConditionsYield
With ammonium hydroxide; potassium hexacyanoferrate(III) In water60%
uric Acid
69-93-2

uric Acid

cyanuric acid
108-80-5

cyanuric acid

Conditions
ConditionsYield
With dihydrogen peroxide In not given oxidation of uric acid by alk. H2O2-soln.;50%
uric Acid
69-93-2

uric Acid

A

5,6-dihydroxypyrimidine-2,4(1H,3H)-dione
102636-37-3

5,6-dihydroxypyrimidine-2,4(1H,3H)-dione

B

urea
57-13-6

urea

Conditions
ConditionsYield
With rose bengal In acetic acid; glycerol for 38h; Irradiation;A 45.11%
B n/a
uric Acid
69-93-2

uric Acid

A

5-Amino-4-iminoallantoin
133364-42-8

5-Amino-4-iminoallantoin

B

cis-1,5-diamino-2,4,6,8-tetraazabicyclo-<3.3.0>octane-3,7-dione
133364-43-9

cis-1,5-diamino-2,4,6,8-tetraazabicyclo-<3.3.0>octane-3,7-dione

Conditions
ConditionsYield
With ammonium hydroxide; potassium hexacyanoferrate(III) In water 1) r.t., 30 min, 2) 0 deg C, 1 h;A 45%
B 30%
uric Acid
69-93-2

uric Acid

1H,4H-3a,6a-(epiminomethanoimino)imidazo[4,5-d]imidazole-2,5,8(3H,6H)-trione
1431648-72-4

1H,4H-3a,6a-(epiminomethanoimino)imidazo[4,5-d]imidazole-2,5,8(3H,6H)-trione

Conditions
ConditionsYield
Stage #1: uric Acid With ammonium hydroxide; potassium hexacyanoferrate(III) In water at 0 - 20℃; for 6h;
Stage #2: With 1,1'-carbonyldiimidazole In dimethyl sulfoxide at 20℃; for 72h;
44%
uric Acid
69-93-2

uric Acid

1-O-acetyl-2,3,4,6-tetra-O-benzoyl-α-D-glucopyranose
112841-30-2

1-O-acetyl-2,3,4,6-tetra-O-benzoyl-α-D-glucopyranose

A

C39H30N4O12

C39H30N4O12

B

C39H30N4O12

C39H30N4O12

C

C39H30N4O12

C39H30N4O12

Conditions
ConditionsYield
Stage #1: uric Acid With N,O-bis-(trimethylsilyl)-acetamide In acetonitrile for 1h; Reflux; Inert atmosphere;
Stage #2: 1-O-acetyl-2,3,4,6-tetra-O-benzoyl-α-D-glucopyranose With trimethylsilyl trifluoromethanesulfonate In acetonitrile for 48h; Reflux; Inert atmosphere;
A 39%
B 9%
C 4%
uric Acid
69-93-2

uric Acid

[Na2(H2O)4(2H-imidazo-[4,5-e]-as-1,2,4-triazine-2,7-dihydro-3,6-dione)2]n

[Na2(H2O)4(2H-imidazo-[4,5-e]-as-1,2,4-triazine-2,7-dihydro-3,6-dione)2]n

Conditions
ConditionsYield
With sodium persulfate; ammonia; water; sodium chloride at 2 - 10℃;36%
uric Acid
69-93-2

uric Acid

A

potassium salt of uroxanate
121669-46-3

potassium salt of uroxanate

B

Allantoin
97-59-6

Allantoin

Conditions
ConditionsYield
With potassium hydroxide; potassium permanganate In water for 4h; Product distribution; Mechanism; Ambient temperature; labelled 14C in position of 5;A 26%
B 14%
uric Acid
69-93-2

uric Acid

A

uroxanate
508-37-2

uroxanate

B

Allantoin
97-59-6

Allantoin

Conditions
ConditionsYield
With potassium hydroxide; potassium permanganate In water for 4h; Ambient temperature; Yield given;A n/a
B 14%
uric Acid
69-93-2

uric Acid

theacrine
2309-49-1

theacrine

Conditions
ConditionsYield
With diethyl ether
uric Acid
69-93-2

uric Acid

8-methoxycaffeine
569-34-6

8-methoxycaffeine

Conditions
ConditionsYield
With diethyl ether
pyridine
110-86-1

pyridine

uric Acid
69-93-2

uric Acid

acetic anhydride
108-24-7

acetic anhydride

8-methylxanthine
17338-96-4

8-methylxanthine

Conditions
ConditionsYield
mehrtaegigem Kochen;
O-methylcaprolactim
2525-16-8

O-methylcaprolactim

uric Acid
69-93-2

uric Acid

theacrine
2309-49-1

theacrine

Conditions
ConditionsYield
at 155℃;

Uric acid Consensus Reports

Reported in EPA TSCA Inventory.

Uric acid Specification

The Uric acid, with the CAS registry number 69-93-2 and EINECS registry number 200-720-7, has the systematic name of 7,9-dihydro-1H-purine-2,6,8(3H)-trione. It is a kind of off-white crystals, and the molecular formula of this chemical is C5H4N4O3.

The Uric acid is created when the body breaks down purine nucleotides. High concentrations of uric acid in blood serum can lead to a type of arthritis known as gout. About its solubilities: It is slightly soluble in water, and it exhibit greater solubility in hot water than cold, allowing for easy recrystallization. The solubility of the acid and its salts in ethanol is very low or negligible. In ethanol water mixtures, the solubilities are somewhere between the end values for pure ethanol and pure water.

The physical properties of Uric acid are as following: (1)ACD/LogP: -1.08; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): -1.33; (4)ACD/LogD (pH 7.4): -2.67; (5)ACD/BCF (pH 5.5): 1; (6)ACD/BCF (pH 7.4): 1; (7)ACD/KOC (pH 5.5): 3.46; (8)ACD/KOC (pH 7.4): 1; (9)#H bond acceptors: 7; (10)#H bond donors: 4; (11)#Freely Rotating Bonds: 0; (12)Polar Surface Area: 64.17 Å2; (13)Index of Refraction: 1.721; (14)Molar Refractivity: 35.51 cm3; (15)Molar Volume: 89.7 cm3; (16)Polarizability: 14.07×10-24cm3; (17)Surface Tension: 94.3 dyne/cm; (18)Density: 1.87 g/cm3; (19)Flash Point: 475.7 °C; (20)Enthalpy of Vaporization: 129.69 kJ/mol; (21)Boiling Point: 863 °C at 760 mmHg; (22)Vapour Pressure: 2.63E-31 mmHg at 25°C.

Produce and uses of Uric acid: It can be produced by xanthine oxidase from xanthine and hypoxanthine, which in turn are produced from purine. Uric acid is released in hypoxic conditions. What's more, it is used as reagent in the determination of uricase and tungstate. With a wonderful moisture retention, it is often used in cosmetics.

You should be cautious while dealing with this chemical. It irritates eyes, respiratory system and skin, and has danger of cumulative effects. Therefore, you had better take the following instructions: Avoid contacting with skin and eyes; Wear suitable protective clothing, and in case of contacting with eyes, rinse immediately with plenty of water and seek medical advice.

You can still convert the following datas into molecular structure:
(1)SMILES: O=C1\C2=C(/NC(=O)N1)NC(=O)N2
(2)InChI: InChI=1/C5H4N4O3/c10-3-1-2(7-4(11)6-1)8-5(12)9-3/h(H4,6,7,8,9,10,11,12)
(3)InChIKey: LEHOTFFKMJEONL-UHFFFAOYAN

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