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T1503

Sigma-Aldrich

Trizma® base

Trizma® Base

≥99.9% (titration), crystalline, primary standard, aminopeptidase substrate

Synonym(s):

2-Amino-2-(hydroxymethyl)-1,3-propanediol, THAM, Tris base, Tris(hydroxymethyl)aminomethane, Trometamol

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25 G
€30.10
100 G
€48.10
250 G
€84.70
500 G
€168.00
1 KG
€249.00
5 KG
€891.00
10 KG
€1,490.00
25 KG
Inquire
25 KG
€3,420.00
50 KG
€5,430.00

About This Item

Linear Formula:
NH2C(CH2OH)3
CAS Number:
Molecular Weight:
121.14
Beilstein:
741883
EC Number:
MDL number:
UNSPSC Code:
12352104
PubChem Substance ID:
NACRES:
NA.25

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Please contact Customer Service for Availability

Request a Bulk Order

Product Name

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

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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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)[1]
  • for washing and saturation of wells in double sandwich ELISA immunoenzymatic technique[2]
  • as an assay buffer for reconstitution of extracted and dried protein samples[3]
  • to prepare Tris-HCl buffer that is used to stabilize proteins[4]
  • as a buffer to extract carotenoid from tubers[5]
  • as a component of sample buffer during protein extraction prior to western blotting[6]
  • as a component of sample buffer for sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE)[7]
  • to prepare simulated body fluid (SBF) for calcium phosphate (CaP) resorption assay[8]
  • as a buffer for polydopamine (PDA) deposition on stainless steel (SS) substrate[9]

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

For additional information on our range of Biochemicals, please complete this form.
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.

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

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Certificates of Analysis (COA)

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Osteoprotective action of low-salt diet requires myeloid cell?derived NFAT5
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.
Journal of Vascular Surgery, 55(4), 1124-1133 (2012)
Effective elimination of chronic lymphocytic leukemia cells in the stromal microenvironment by a novel drug combination strategy using redox-mediated mechanisms
Zhang W, et al.
Molecular Medicine Reports, 7374-7388 (2015)
Biochemical isolation of insoluble tau in transgenic mouse models of tauopathies.
Sigurdsson E.M., Calero M., and Gasset M, (eds.)
Amyloid Proteins: Methods and Protocols, 473-491 (2012)
F Foudrinier et al.
Journal of clinical microbiology, 41(4), 1681-1686 (2003-04-12)
The clinical value of immunoenzymatic (enzyme-linked immunosorbent assay) detection of anti-Toxoplasma immunoglobulin E (IgE) was assessed by studying 2,036 sera from 792 subjects, comprising seronegative controls and subjects with acute, active, reactivated, or congenital toxoplasmosis. Included were nonimmunized adults; pregnant

Protocols

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

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

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Questions

1–9 of 9 Questions  
  1. How can I determine the shelf life / expiration / retest date of this product?

    1 answer
    1. If this product has an expiration or retest date, it will be shown on the Certificate of Analysis (COA, CofA). If there is no retest or expiration date listed on the product's COA, we do not have suitable stability data to determine a shelf life. For these products, the only date on the COA will be the release date; a retest, expiration, or use-by-date will not be displayed.
      For all products, we recommend handling per defined conditions as printed in our product literature and website product descriptions. We recommend that products should be routinely inspected by customers to ensure they perform as expected.
      For products without retest or expiration dates, our standard warranty of 1 year from the date of shipment is applicable.
      For more information, please refer to the Product Dating Information document: https://www.sigmaaldrich.com/deepweb/assets/sigmaaldrich/marketing/global/documents/449/386/product-dating-information-mk.pdf

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  2. How is shipping temperature determined? And how is it related to the product storage temperature?

    1 answer
    1. Products may be shipped at a different temperature than the recommended long-term storage temperature. If the product quality is sensitive to short-term exposure to conditions other than the recommended long-term storage, it will be shipped on wet or dry-ice. If the product quality is NOT affected by short-term exposure to conditions other than the recommended long-term storage, it will be shipped at ambient temperature. As shipping routes are configured for minimum transit times, shipping at ambient temperature helps control shipping costs for our customers. For more information, please refer to the Storage and Transport Conditions document: https://www.sigmaaldrich.com/deepweb/assets/sigmaaldrich/marketing/global/documents/316/622/storage-transport-conditions-mk.pdf

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  3. Is this product explosive in nature?

    1 answer
    1. As per the SDS of T1503: https://www.sigmaaldrich.com/sds/sigma/t1503?userType=anonymous, no GHS pictogram for explosive materials has been listed in Section 2, indicating it is not explosive in nature.

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  4. Can I autoclave solutions that contain Product T1503, Trizma® base?

    1 answer
    1. Yes, Trizma buffered solutions may be autoclaved.

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  5. Can Product T1503, Trizma® base be used as a standard?

    1 answer
    1. Trizma base meets the requirements for a primary basimetric standard.

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  6. What is the pH of Trizma® base, T1503?

    1 answer
    1. The pH of a 0.1 M aqueous solution of Trizma base will have a pH of approximately 10.4.

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  7. What type of electrode should I use to measure the pH of Trizma® base T1503?

    1 answer
    1. We recommend the use of glass-calomel electrodes for use with Trizma base solutions through a pH range of 0-12 and a temperature range of -5 °C to 80 °C. Silver/silver chloride reference electrodes are not recommended for use with Trizma solutions that contain proteins.

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  8. How can I use T1503 to make a Trizma® buffered solution?

    1 answer
    1. Trizma base may be used directly in preparing a buffer by adjusting the pH with a 0.1 to 1.0 M HCl or blended with Trizma hydrochloride.

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  9. What is the Department of Transportation shipping information for this product?

    1 answer
    1. Transportation information can be found in Section 14 of the product's (M)SDS.To access the shipping information for this material, use the link on the product detail page for the product.

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