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Chemical Structure| 6850-28-8 Chemical Structure| 6850-28-8
Chemical Structure| 6850-28-8

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Trizma acetate is a low-toxicity, biologically inert amino alcohol that buffers carbon dioxide and acids in vivo and in vitro, suitable for pH regulation within the physiological range.

Synonyms: THAM acetate; Tris acetate; Tris(hydroxymethyl)aminomethane acetate

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Product Details of Trizma acetate

CAS No. :6850-28-8
Formula : C6H15NO5
M.W : 181.19
SMILES Code : CC(O)=O.NC(CO)(CO)CO
Synonyms :
THAM acetate; Tris acetate; Tris(hydroxymethyl)aminomethane acetate
MDL No. :MFCD00038951
InChI Key :PIEPQKCYPFFYMG-UHFFFAOYSA-N
Pubchem ID :16218782

Safety of Trizma acetate

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of Trizma acetate

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 6850-28-8 ]

[ 6850-28-8 ] Synthesis Path-Downstream   1~10

  • 1
  • [ 6850-28-8 ]
  • [ 4271-18-5 ]
  • 2
  • [ 6850-28-8 ]
  • tris(bromomethyl)aminomethane hydrobromide [ No CAS ]
  • 4
  • [ 830-03-5 ]
  • [ 77-86-1 ]
  • [ 6850-28-8 ]
  • 4-Nitro-phenol; compound with 2-amino-2-hydroxymethyl-propane-1,3-diol [ No CAS ]
  • 5
  • [ 6850-28-8 ]
  • [ 98278-39-8 ]
  • 6
  • [ 6850-28-8 ]
  • [ 86015-22-7 ]
  • 7
  • [ 6850-28-8 ]
  • [ 19383-02-9 ]
  • 8
  • [ 6850-28-8 ]
  • [ 100139-16-0 ]
  • 9
  • [ 6850-28-8 ]
  • [ 102079-81-2 ]
YieldReaction ConditionsOperation in experiment
89% 2 OUABAIN TRI ACETATE (PROCEDURE A mixture of ouabain hexa-acetate (10.0 g, 12.0 mmoles), and potassium carbonate (0.75 g, 5.4 mmoles) in 250 ml of methanol was stirred at room temperature. After 0.5 hr the reaction mixture was filtered, and dilute aqueous acetic acid was added to the filtrate until a 0.25 ml aliquot dissolved in 2 ml of water gave a neutral pH. Fifty grams of silica gel was then added to the reaction mixture, and the solvent was removed by rotary evaporation. The dry silica gel was then placed on a flash chromatography column and eluted with 15% methanol in methylene chloride. The fractions corresponding to the major product were pooled and the solvent removed to yield 8.5 g of product (89%) as a white solid. Evaluation of the product by NMR and mass spectrometry showed it to be 1,11,19-tris(acetyloxy)-3-[(6-deoxy-alpha-L-mannopyranosyl)oxy]-5,14 dihydroxycard 20(22)-enolide (1beta,3beta,5beta,11alpha). TLC on silica gel (20% methanol/methylene chloride) gave an Rf of 0.49 for ouabain tri-acetate.
841 mg (97%) OUABAIN TRI-ACETATE (PROCEDURE I) A mixture of ouabain hexa acetate (1.02 g, 1.22 mmoles) and potassium cyanide (75 mg, 1.15 mmoles) in 15 ml of methanol was stirred at room temperature. The solid hexa-acetate was only slightly soluble in methanol. However all material was dissolved after about 1.5 hr of stirring. After 6 hours approximately 5 g of silica gel was added to the reaction mixture, and the solvent was removed by rotary evaporation. It is important that the temperature be kept below 45 C. during this step. This silica gel was placed on a flash chromatography column and eluted with 10% methanol in methylene chloride. Fractions corresponding to the major product were pooled and the solvent removed to yield 841 mg (97%) of product as a glassy solid, which yielded a white powder when scraped from the sides of the flask. Evaluation of the product by NMR and mass spectrometry showed it to be 1,11,19 -tris(acetyloxy)-3-[(6-deoxy-alpha-L-mannopyranosyl)oxy]-5,14 dihydroxycard-20(22)-enolide (1beta,3beta,5beta,11alpha). TLC on silica gel (20% methanol/methylene chloride) gave an Rf of 0.49 for ouabain tri-acetate.
In water; at 20.0℃; for 3.0h; General procedure: After reacting 2-amino-1,3-propanediol (2.50 g, 27.44 mmol) and formic acid (1.26 g, 27.44 mmol) in 50 ml of water at room temperature for 3 hours, water was distilled off under reduced pressure, A liquid was obtained. By washing the obtained liquid,An ammonium formate salt (3.76 g, 27.44 mmol) was obtained as a colorless transparent liquid.
 

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