Keywords

• 68334-00-9

• Tristearin

• Trometamol

Quick Details

• ProName:China Factory Supply CAS 68334-00-9 Tr...

• CasNo:68334-00-9

• Molecular Formula:C57H110O6

• Application:Ambutatriol is widely used in the prep...

• ProductionCapacity:Metric Ton/Day

• Purity:98%

• LimitNum:0 Metric Ton

Superiority

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Details

PubChem CID	6503
Structure	Find Similar Structures
Chemical Safety	Laboratory Chemical Safety Summary (LCSS) Datasheet
Molecular Formula	C4H11NO3
Synonyms	Trometamol TROMETHAMINE 77-86-1 Tris(Hydroxymethyl)aminomethane Tris More...
Molecular Weight	121.14
Dates	Modify 2022-11-05 Create 2005-03-26
An organic amine proton acceptor. It is used in the synthesis of surface-active agents and pharmaceuticals; as an emulsifying agent for cosmetic creams and lotions, mineral oil and paraffin wax emulsions, as a biological buffer, and used as an alkalizer. (From Merck, 11th ed; Martindale, The Extra Pharmacopoeia, 30th ed, p1424) 3.1Computed Properties Help New Window Property Name Property Value Reference Molecular Weight 121.14 Computed by PubChem 2.2 (PubChem release 2021.10.14) XLogP3-AA -2.9 Computed by XLogP3 3.0 (PubChem release 2021.10.14) Hydrogen Bond Donor Count 4 Computed by Cactvs 3.4.8.18 (PubChem release 2021.10.14) Hydrogen Bond Acceptor Count 4 Computed by Cactvs 3.4.8.18 (PubChem release 2021.10.14) Rotatable Bond Count 3 Computed by Cactvs 3.4.8.18 (PubChem release 2021.10.14) Exact Mass 121.07389321 Computed by PubChem 2.2 (PubChem release 2021.10.14) Monoisotopic Mass 121.07389321 Computed by PubChem 2.2 (PubChem release 2021.10.14) Topological Polar Surface Area 86.7 ?² Computed by Cactvs 3.4.8.18 (PubChem release 2021.10.14) Heavy Atom Count 8 Computed by PubChem Formal Charge 0 Computed by PubChem Complexity 54 Computed by Cactvs 3.4.8.18 (PubChem release 2021.10.14) Isotope Atom Count 0 Computed by PubChem Defined Atom Stereocenter Count 0 Computed by PubChem Undefined Atom Stereocenter Count 0 Computed by PubChem Defined Bond Stereocenter Count 0 Computed by PubChem Undefined Bond Stereocenter Count 0 Computed by PubChem Covalently-Bonded Unit Count 1 Computed by PubChem Compound Is Canonicalized Yes Computed by PubChem (release 2021.10.14)

Therapeutic Uses

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Buffers; Excipients

National Library of Medicine's Medical Subject Headings online file (MeSH, 1999)

Hazardous Substances Data Bank (HSDB)

/Tromethamine is indicated/ for the prevention and correction of metabolic acidosis. /Included in US product label/

Novak, K.M. (ed.). Drug Facts and Comparisons 59th Edition 2005. Wolters Kluwer Health. St. Louis, Missouri 2005., p. 130

Hazardous Substances Data Bank (HSDB)

Metabolic Acidosis Associated with Cardiac Bypass Surgery. Tromethamine solution has been found to be primarily beneficial in correcting metabolic acidosis which may occur during or immediately following cardiac bypass surgical procedures. /Included in US product label/

Medical Economics Co; Physicians Desk Reference: Generics 2nd ed p.3033 (1996)

Hazardous Substances Data Bank (HSDB)

Correction of Acidity of ACD Blood in Cardiac Bypass Surgery. It is well known that ACD blood is acidic and becomes more acidic on storage. Tromethamine effectively corrects this acidity. Tromethamine solution may be added directly to the blood used to prime the pump-oxygenator. When ACD blood is brought to a normal pH range the patient is spared an initial acid load. Additional tromethamine may be indicated during cardiac bypass surgery should metabolic acidosis appear. /Included in US product label/

Medical Economics Co; Physicians Desk Reference: Generics 2nd ed p.3033 (1996)

Hazardous Substances Data Bank (HSDB)

For more Therapeutic Uses (Complete) data for TROMETHAMINE (6 total), please visit the HSDB record page.

Hazardous Substances Data Bank (HSDB)