6-Amino-1-methyluracil

Names

[ Name ]:
6-Amino-1-methyluracil

[Synonym ]:
6-Amino-1-methyl-1H-pyrimidine-2,4-dione
EINECS 219-422-3
6-Amino-4-hydroxy-1-methyl-2(1H)-pyrimidinone
6-Amino-1-methylpyrimidine-2,4(1H,3H)-dione
2,4(1H,3H)-Pyrimidinedione,6-amino-1-methyl
6-Amino-1-methyl-2,4(1H,3H)-pyrimidinedione
2(1H)-Pyrimidinone, 6-amino-4-hydroxy-1-methyl-
1-methyl-6-aminouracil
6-Amino-1-methyluracil
2,4(1H,3H)-Pyrimidinedione, 6-amino-1-methyl-
MFCD00075366
6-Amino-1-methyluracil
6-amino-1-methyl-1,3-dihydropyrimidine-2,4-dione

Chemical & Physical Properties

[ Density]:
1.6±0.1 g/cm3

[ Boiling Point ]:
294.9±43.0 °C at 760 mmHg

[ Melting Point ]:
300 °C

[ Molecular Formula ]:
C₅H₇N₃O₂

[ Molecular Weight ]:
141.128

[ Flash Point ]:
132.1±28.2 °C

[ Exact Mass ]:
141.053833

[ PSA ]:
80.88000

[ LogP ]:
-1.80

[ Vapour Pressure ]:
0.0±1.4 mmHg at 25°C

[ Index of Refraction ]:
1.663

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H302-H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xn:Harmful;

[ Risk Phrases ]:
R22;R36/37/38

[ Safety Phrases ]:
S26

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2933599090

Synthetic Route

Click to get detail synthetic route

Customs

[ HS Code ]: 2933599090

[ Summary ]:
2933599090. other compounds containing a pyrimidine ring (whether or not hydrogenated) or piperazine ring in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

Experimental study on the thermochemistry of some amino derivatives of uracil. Ribeiro da Silva MAV, et al.

J. Chem. Thermodyn. 43(11) , 1763-67, (2011)

A novel reaction of 6-amino-uracils and isatins. Dabiri M, et al.

Tetrahedron 64(30) , 7307-11, (2008)

Complexation of tetrapropoxycalix [4] arene with uracil and adenine derivatives in water-containing solution. Kalchenko O, et al.

J. Phys. Org. Chem. 16(4) , 246-52, (2003)