CAS No.50-71-5,Alloxan Suppliers

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Basic Information

Molecular Structure:
CAS No.:	50-71-5
Name:	Alloxan
Article Data:	2

Formula:	C4H2 N2 O4
Molecular Weight:	142.071
Synonyms:	Alloxan(8CI); 2,4,5,6-Pyrimidinetetrone; 2,4,5,6-Tetraoxohexahydropyrimidine;Alloxane; Mesoxalylcarbamide; Mesoxalylurea; NSC 7169; Pyrimidinetetrone
EINECS:	200-062-0
Density:	1.681g/cm³
Melting Point:	255 C (Decomposes)
Boiling Point:	409.5°C at 760 mmHg
Flash Point:	201.4°C
Solubility:		white crystalline powder
Hazard Symbols:	UN NO.
Risk Codes:	20/21/22-36/37/38
Transport Information:	OTH
PSA:	129.26000
LogP:	-1.67810

Synthetic route

: 67-52-7
BARBITURIC ACID

: 50-71-5
5,5-dihydroxypyrimidine-2,4,6(1H,3H,5H)-trione

Conditions

Conditions	Yield
With chromium(VI) oxide In acetic acid

: 108-73-6
3,5-dihydroxyphenol

: 50-71-5
5,5-dihydroxypyrimidine-2,4,6(1H,3H,5H)-trione

: 5-hydroxy-5-[2,4,6-trihydroxy-3,5-bis(5-hydroxy-2,4,6-trioxo-3,5-dihydro-1H-pyrimidin-5-yl)phenyl]-3,5-dihydro-1H-pyrimidine-2,4,6-trione

Conditions

Conditions	Yield
With acetic acid at 20℃; for 24h;	92%

: 95-54-5
1,2-diamino-benzene

: 50-71-5
5,5-dihydroxypyrimidine-2,4,6(1H,3H,5H)-trione

: 490-59-5
alloxazine

Conditions

Conditions	Yield
With boric acid In acetic acid at 60℃; for 15h; Inert atmosphere;	86%

: benzyl (2-amino-3-(cyclohexylamino)phenyl)carbamate

: 50-71-5
5,5-dihydroxypyrimidine-2,4,6(1H,3H,5H)-trione

: benzyl (10-cyclohexyl-2,4-dioxo-2,3,4,10-tetrahydrobenzo[g]-pteridine-6-yl)carbamate

Conditions

Conditions	Yield
With boron trioxide; acetic acid at 20℃; for 18h;	82%

: dibenzyl ((((1‘‘R,2‘‘R)-cyclohexane-1‘‘,2‘‘-diyl)bis(azanediyl))bis(2-amino-3,1-phenylene))dicarbamate

: 50-71-5
5,5-dihydroxypyrimidine-2,4,6(1H,3H,5H)-trione

: dibenzyl (((1‘‘R,2‘‘R)-cyclohexane-1‘‘,2‘‘-diyl)bis(2,4-dioxo-2,3,4,4a-tetrahydrobenzo[g]pteridine-9a,6-diyl))dicarbamate

Conditions

Conditions	Yield
With boron trioxide; acetic acid at 20℃; for 14h;	78%

: pyrene‐4,5‐diamine

: 50-71-5
5,5-dihydroxypyrimidine-2,4,6(1H,3H,5H)-trione

: pyreno[4,5-g]pteridine-11,13(10H,12H)-dione

Conditions

Conditions	Yield
With boric acid In acetic acid at 60℃; for 15h; Inert atmosphere;	75%

: 771-97-1
2,3-Diaminonaphthalene

: 50-71-5
5,5-dihydroxypyrimidine-2,4,6(1H,3H,5H)-trione

: 4794-65-4
naphtho[2,3-g]pteridine-2,4(1H,3H)-dione

Conditions

Conditions	Yield
With boric acid In acetic acid at 60℃; for 15h; Inert atmosphere;	73%

: copper(II) choride dihydrate

: 50-71-5
5,5-dihydroxypyrimidine-2,4,6(1H,3H,5H)-trione

: Cu(2+)*C4N2O4(2-)*3H2O=Cu(C4N2O4)*3H2O

Conditions

Conditions	Yield
With water In water gradual addn. of an aq. soln. of CuCl2*2H2O to an aq. soln. of alloxane; simultaneous addn. of 10% aq. NaOH (->pH=7.5); pH=5 or pH=6 for a few hours;; ppt.; washing with cold H2O; drying in vac. at ambient temp. over CaCl2;;	72%
With H2O In water gradual addn. of an aq. soln. of CuCl2*2H2O to an aq. soln. of alloxane; simultaneous addn. of 10% aq. NaOH (->pH=7.5); pH=5 or pH=6 for a few hours;; ppt.; washing with cold H2O; drying in vac. at ambient temp. over CaCl2;;	72%

: 50-71-5
5,5-dihydroxypyrimidine-2,4,6(1H,3H,5H)-trione

: 7646-79-9
cobalt(II) chloride

: alloxane, Co-salt * pentahydrate

Conditions

Conditions	Yield
With sodium hydroxide In water addition of CoCl2 in H2O to a solution of alloxane in H2O under addition of NaOH-solution until pH=7.5; then pH=5-6; seperation of the ppt. after some hours;; washing the product with cold H2O; drying in vac. at normal temperature over CaCl2;;	69%
With NaOH In water

: nickel(II) nitrate hexahydrate

: 50-71-5
5,5-dihydroxypyrimidine-2,4,6(1H,3H,5H)-trione

: Ni(2+)*C4N2O4(2-)*5H2O=NiC4N2O4*5H2O

Conditions

Conditions	Yield
With sodium hydroxide In water gradual addn. of equimolar amt. of aq. Ni(NO3)2*6H2O soln. to aq. soln. of alloxan, addn. of 10% NaOH soln. to pH 7.5, then adjusting to pH 5-6;; pptn., sepg. after several hours, washing with cold H2O, drying in vac. at ambient temp. over CaCl2;;	66%

Raw Materials

61066-33-9

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Chemistry

IUPAC Name: 1,3-diazinane-2,4,5,6-tetrone
Molecular Weight: 142.06968 g/mol
Molecular Formula: C₄H₂N₂O₄
Density: 1.681 g/cm³
Melting Point: ~245 °C (dec.)
Boiling Point: 409.5 °C at 760 mmHg
Flash Point: 201.4 °C
Index of Refraction: 1.519
Molar Refractivity: 25.66 cm³
Molar Volume: 84.5 cm³
Polarizability: 10.17*10^-24cm³
Surface Tension: 62.6 dyne/cm
Enthalpy of Vaporization: 76.46 kJ/mol
Vapour Pressure: 2.05E-08 mmHg at 25 °C
XLogP3-AA: -1
H-Bond Donor: 2
H-Bond Acceptor: 4
Tautomer Count: 5
Exact Mass: 142.001457
MonoIsotopic Mass: 142.001457
Topological Polar Surface Area: 92.3
Heavy Atom Count: 10
Complexity: 222
Canonical SMILES: C1(=O)C(=O)NC(=O)NC1=O
InChI: InChI=1S/C4H2N2O4/c7-1-2(8)5-4(10)6-3(1)9/h(H2,5,6,8,9,10)
InChIKey: HIMXGTXNXJYFGB-UHFFFAOYSA-N
EINECS: 200-062-0
Storage temp.: 2-8 °C

History

Alloxan (CAS NO.50-71-5) was originally isolated in 1818 by Brugnatelli and got its name in 1838 by Friedrich Wöhler and Justus von Liebig. The name "Alloxan" emerged from an amalgamation of the words "Allantoin" and "Oxalsäure" (oxaluric acid).

Production

The original preparation for Alloxan (CAS NO.50-71-5) was by oxidation of uric acid by nitric acid. Alloxan is a strong oxidizing agent and it forms a hemiacetal with its reduced reaction product dialuric acid (in which a carbonyl group is reduced to a hydroxyl group) which is called alloxantin.

Toxicity Data With Reference

1.	eye-rbt 500 mg/24H MLD		85JCAE Prehled Prumyslove Toxikologie; Organicke Latky Marhold, J.,Prague, Czechoslovakia.: Avicenum,1986,862.
2.	cyt-mus-ipr 50 mg/kg		JOHEA8 Journal of Heredity. 65 (1974),345.
3.	ipr-mus TDLo:200 mg/kg (female 8D post):TER		JEEMAF Journal of Embryology and Experimental Morphology. 14 (1965),63.
4.	orl-rat LD50:5210 mg/kg		28ZOAH Chemicals in War Prentiss, A.M.,1972,150.
5.	ivn-rat LD50:300 mg/kg		CRSBAW Comptes Rendus des Seances de la Societe de Biologie et de Ses Filiales. 142 (1948),1335.
6.	ipr-mus LDLo:300 mg/kg		PSEBAA Proceedings of the Society for Experimental Biology and Medicine. 67 (1948),154.
7.	scu-mus LDLo:400 mg/kg		PSEBAA Proceedings of the Society for Experimental Biology and Medicine. 67 (1948),154.
8.	ivn-mus LDLo:200 mg/kg		PSEBAA Proceedings of the Society for Experimental Biology and Medicine. 67 (1948),154.
9.	ivn-rbt LDLo:300 mg/kg		AJCPAI American Journal of Clinical Pathology. 16 (1946),257.
10.	rec-rbt LDLo:180 mg/kg	&nbs

Consensus Reports

Reported in EPA TSCA Inventory.

Safety Profile

Poison by intraperitoneal, intravenous, subcutaneous, and rectal routes. Moderately toxic by ingestion. An experimental teratogen. Other experimental reproductive effects. Mutation data reported. Produces diabetes in experimental animals. Decomposes in storage to release CO₂. Do not store in sealed container. Explodes when heated above 170°C. When heated to decomposition it emits toxic fumes of NO_x.
Hazard Codes: Harmful Xn
Risk Statements: 20/21/22-36/37/38
R20/21/22: Harmful by inhalation, in contact with skin and if swallowed
R36/37/38: Irritating to eyes, respiratory system and skin
Safety Statements: 26-36
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice
S36: Wear suitable protective clothing
WGK Germany: 3
F: 8-10-23
Hazardous Substances Data: 50-71-5(Hazardous Substances Data)

Specification

Alloxan (CAS NO.50-71-5) is also called 2,4,5,6(1H,3H)-Pyrimidinetetrone ; Mesoxalylurea ; Mesoxalylcarbamide ; 4,5,6-Pyrimidinetetrone ; 2,4,5,6-Pyrimidintetron ; 2,4,5,6-Tetraoxohexahydropyrimidine . Alloxan (CAS NO.50-71-5) is a kind of pesticides. It's moderate toxic. It will explosive by heating above 170 °C. Alloxan (CAS NO.50-71-5) is also flammable. It will produce toxic nitrogen oxide fumes when buring. And it decomposits of carbon dioxide at room temperature. So the storage environment should be ventilate, low-temperature and dry. Keep Anthramycin (CAS NO.4803-27-4) separate from raw materials of food. Do not store in a sealed tank.