33012-75-8 Usage
Uses
Used in Organic Synthesis:
2-[(CARBOXYMETHYL)AMINO]PROPANOIC ACID HYDROCHLORIDE is used as a chemical intermediate for the synthesis of various organic compounds, facilitating the creation of a range of products through its reactivity and functional groups.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-[(CARBOXYMETHYL)AMINO]PROPANOIC ACID HYDROCHLORIDE is used as a pharmaceutical intermediate, playing a crucial role in the development of medications for different medical conditions.
Used in Medical Treatments:
2-[(CARBOXYMETHYL)AMINO]PROPANOIC ACID HYDROCHLORIDE is used as an active pharmaceutical ingredient for treating conditions such as cardiac arrhythmia, angina pectoris, and hypertension, due to its ability to interact with biological systems and provide therapeutic effects.
Used as a Chelating Agent:
2-[(CARBOXYMETHYL)AMINO]PROPANOIC ACID HYDROCHLORIDE is utilized as a chelating agent in various chemical processes, where it binds to metal ions, which can be essential for the stability, synthesis, or purification of other compounds.
Used as a Buffering Agent in Pharmaceuticals:
2-[(CARBOXYMETHYL)AMINO]PROPANOIC ACID HYDROCHLORIDE is used as a buffering agent in pharmaceutical formulations to maintain a stable pH, ensuring the optimal conditions for drug efficacy and stability.
Used as a Stabilizer for Medications:
2-[(CARBOXYMETHYL)AMINO]PROPANOIC ACID HYDROCHLORIDE also serves as a stabilizer for certain types of medication, helping to preserve the integrity and potency of drugs during storage and use.
Check Digit Verification of cas no
The CAS Registry Mumber 33012-75-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,0,1 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 33012-75:
(7*3)+(6*3)+(5*0)+(4*1)+(3*2)+(2*7)+(1*5)=68
68 % 10 = 8
So 33012-75-8 is a valid CAS Registry Number.
InChI:InChI=1/C5H9NO4/c1-3(5(9)10)6-2-4(7)8/h3,6H,2H2,1H3,(H,7,8)(H,9,10)/p-1/t3-/m1/s1
33012-75-8Relevant academic research and scientific papers
A mild and efficient method for the one-pot monocarboxymethylation of primary amines
Gibbs, Timothy J. K.,Boomhoff, Michael,Tomkinson, Nicholas C. O.
, p. 1573 - 1576 (2008/02/04)
A mild and efficient method for the monocarboxymethylation of primary amines that takes place under aqueous conditions at room temperature is described. Treatment of an aqueous solution of a variety of primary amines with two equivalents of glyoxylic acid
Synthesis of Strombine. A New Method for Monocarboxymethylation of Primary Amines
Kihlberg, Jan,Bergman, Rolf,Wickberg, Boerje
, p. 911 - 916 (2007/10/02)
Many common methods for monocarboxymethylation of primary amines give various amounts of dialkylated by-products.In this work the reaction of two equivalents of glyoxilic acid with representative primary aliphatic and aromatic amines, as well as with amino acids and a dipeptide, is shown to give only the N-(carboxymethyl)-N-formyl derivative of the amine under mild conditions in carboxylic acid solvents.Hydrolysis then produces the monocarboxymethylated primary amine in good to exellent overall yield.Proof that the intermediate product is not obtained via the Leuckart reaction is given.
