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T1503

Sigma-Aldrich

Trizma® base

Primary Standard and Buffer, ≥99.9% (titration), crystalline

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Synonym(s):
2-Amino-2-(hydroxymethyl)-1,3-propanediol, THAM, Tris base, Tris(hydroxymethyl)aminomethane, Trometamol
Linear Formula:
NH2C(CH2OH)3
CAS Number:
Molecular Weight:
121.14
Beilstein:
741883
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.25

Quality Level

description

aminopeptidase substrate

Assay

≥99.9% (titration)

form

crystalline

storage condition

dry at room temperature

technique(s)

ELISA: suitable
protein extraction: suitable

color

white

pH

10.5-12

useful pH range

7-9

pKa (25 °C)

8.1

bp

219-220 °C/10 mmHg (lit.)

mp

167-172 °C (lit.)

solubility

methanol: soluble 26 mg/mL at 25 °C
ethylene glycol: soluble 79.1 mg/mL at 25 °C
water: soluble (678 g/l at 20 °C)

absorption

≤0.05 at 290 nm at 40%

suitability

suitable for Western blot
suitable for electrophoresis

application(s)

cell analysis
diagnostic assay manufacturing
life science and biopharma

SMILES string

NC(CO)(CO)CO

InChI

1S/C4H11NO3/c5-4(1-6,2-7)3-8/h6-8H,1-3,5H2

InChI key

LENZDBCJOHFCAS-UHFFFAOYSA-N

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1 of 4

This Item
T4661T6066T6791
Trizma® base Primary Standard and Buffer, ≥99.9% (titration), crystalline

T1503

Trizma® base

-
Trizma® base ≥99.9% (titration), crystalline

T4661

Trizma® base

-
Trizma® base BioPerformance Certified, meets EP, USP testing specifications, suitable for cell culture, ≥99.9% (titration)

T6066

Trizma® base

Premium Grade
Trizma® base BioXtra, pH 10.5-12.0 (1 M in H2O), ≥99.9% (titration)

T6791

Trizma® base

Premium Grade
technique(s)

ELISA: suitable, protein extraction: suitable

technique(s)

-

technique(s)

DNA extraction: suitable, cell culture | mammalian: suitable, protein purification: suitable

technique(s)

-

Quality Level

300

Quality Level

400

Quality Level

400

Quality Level

400

application(s)

cell analysis
diagnostic assay manufacturing
life science and biopharma

application(s)

diagnostic assay manufacturing

application(s)

clinical research
clinical testing
diagnostic assay manufacturing

application(s)

diagnostic assay manufacturing
life science and biopharma
sample preparation

form

crystalline

form

crystalline

form

crystalline powder

form

crystalline

pH

10.5-12

pH

10.0-11.5

pH

10.0-11.5

pH

10.5-12.0 (1 M in H2O)

General description

Tris(hydroxymethyl)aminomethane, commonly known as Trometamol, Tris base, or Trizma® base, serves a pivotal role in diverse research applications as a biological buffer. Its optimal pKa of 8.1 makes it a preferred choice for formulating buffers like Tris-acetate-EDTA (TAE) and Tris-borate-EDTA (TBE), ensuring the maintenance of pH within the physiological range (pH 7 - 9), applicable to a wide spectrum of living organisms. Despite its utility, researchers need to exercise caution in protein studies, as Tris has the potential to interfere with the activity of specific enzymes.

Tris base may find application as basimetric standard, independently as a buffer and as a crucial component in mixed buffer formulations, including Tris-EDTA (TE) buffer, TAE buffer, TBE buffer, among others. Its attributes include purity, essential stability, and a relative non-hygroscopic nature, making it a dependable choice in laboratory settings. In these environments, Tris base is indispensable for preparing buffers compatible with biological fluids and serves as a standard pH solution. It facilitates various laboratory procedures such as lactate dehydrogenase assays, in situ hybridization, and protein extraction from cells. The versatility of Tris base extends to cell biology, biochemistry, and protein research contributing significantly to studies involving cell membrane permeability and buffer preparation.

Application

Trizma® base has been used:
  • as a component of H buffer (cell dissociation buffer)
  • for washing and saturation of wells in double sandwich ELISA immunoenzymatic technique
  • as an assay buffer for reconstitution of extracted and dried protein samples
  • to prepare Tris-HCl buffer that is used to stabilize proteins
  • as a buffer to extract carotenoid from tubers
  • as a component of sample buffer during protein extraction prior to western blotting
  • as a component of sample buffer for sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE)
  • to prepare simulated body fluid (SBF) for calcium phosphate (CaP) resorption assay
  • as a buffer for polydopamine (PDA) deposition on stainless steel (SS) substrate

Features and Benefits

  • Efficient buffering within the pH range of 7 - 9 with a pKa of 8.1 (25 °C)
  • Tested to confirm low levels of heavy metal contamination, ensuring suitability for various applications
  • Can be used in Cell Biology, and Biochemical research

Other Notes

The pH values of all buffers are temperature- and concentration-dependent. For Tris buffers, pH increases about 0.03 unit per °C decrease in temperature, and decreases 0.03-0.05 unit per ten-fold dilution.
For precise applications, use a carefully calibrated pH meter with a glass/calomel combination electrode.
For additional information on our range of Biochemicals, please complete this form.

Legal Information

Trizma is a registered trademark of Merck KGaA, Darmstadt, Germany

suggested gloves for splash protection

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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25G
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705578-5MG-PW

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MMYOMAG-74K-13

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Schroder A, et al.
JCI insight, 4(23) (2019)
Expression of cytoskeleton and energetic metabolism-related proteins at human abdominal aortic aneurysm sites.
Modrego J, et al.
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Protocols

To measure achromopeptidase activity, this procedure uses bacterial cells and a turbidimetric rate assay. Turbidity is measured at 600 nm using a spectrophotometer.

Carboxypeptidase A activity measured via continuous spectrophotometric rate determination assay with hippuryl-L-phenylalanine substrate.

To measure chloramphenicol acetyltransferase activity, this procedure uses DTNB and coenzyme A. The reaction of DTNB with the –SH group on CoA results in a colorimetric increase at 412 nm.

Measure luciferase activity using a luminometer assay detecting light emission, with applications in ATP detection and genetic function reporting.

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