Tris

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Tris
Chemical structure of tris
General
Systematic name 2-Amino-2-(hydroxymethyl)propane-1,3-diol
Other names TRIS, Tris, Tris base, Tris buffer,
Trizma(TM), Trisamine, THAM,
Tromethamine, Trometamol, Tromethane
Molecular formula C4H11NO3
SMILES C(C(CO)(CO)N)O
Molar mass 121.135 g/mol
Appearance White crystalline powder
CAS number [77-86-1]
Properties
Density and phase  ? g/l, solid (25°C)
Solubility in water 67 g/100 ml (20°C)
Melting point >170°C (443 K)
Boiling point 219°C (492 K)
Acidity (pKa) 8.3
Hazards
MSDS External MSDS
Main hazards Irritant
NFPA 704

0
2
0
 
Flash point Non-flammable
R/S statement R: R36, R37, R38.
S: S26, S36.
RTECS number TY2900000
Except where noted otherwise, data are given for
materials in their standard state (at 25°C, 100 kPa)
Infobox disclaimer and references

Tris is an abbreviation of the trivial name (trishydroxymethylaminomethane) for 2-amino-2-hydroxymethyl-1,3-propanediol. It is widely used as a component of buffer solutions, such as in TAE and TBE buffers used in biochemistry, with an effective pH range between 6.5 and 9.7. Tris has labile protons with a pKa of 8.30 (at 20 °C; this declines approximately 0.03 units per degree Celsius rise in temperature). Tris is often used when working with nucleic acids. Tris is an effective buffer for slightly basic solutions, which keeps DNA deprotonated and soluble in water. EDTA binds to divalent cations, particularly magnesium (Mg2+). These ions are necessary co-factors for many enzymes; Magnesium is a co-factor for many DNA-modifying enzymes.

Tris is toxic to mammalian cells, and reacts strongly with pH electrodes. It can react with primary amines.

Tris is used as an intermediate for the preparation of surface active agents, vulcanization accelerators, and pharmaceuticals, and used as a titrimetric standard.

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