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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Glycine, N-(2-hydroxyethyl)-

OCCNCC(=O)O Request for Quotation
Chemical Name: Glycine, N-(2-hydroxyethyl)-
CAS Number: 5835-28-9
Product Number: AG00EF2H(AGN-PC-0JO5TA)
Synonyms:
MDL No:
Molecular Formula: C4H9NO3
Molecular Weight: 119.1192

Identification/Properties

Properties
MP:
>140°C (dec.)
BP:
339.3°C at 760 mmHg
Storage:
Keep in dry area;-10 ℃;
Form:
Solid
Computed Properties
Molecular Weight:
119.12g/mol
XLogP3:
-3.6
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
119.058g/mol
Monoisotopic Mass:
119.058g/mol
Topological Polar Surface Area:
69.6A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
73.7
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-((2-Hydroxyethyl)amino)acetic acid, commonly known in the field of chemistry as glycine betaine or N-trimethylglycine, holds a pivotal role in chemical synthesis due to its versatile applications. As a zwitterionic amino acid derivative, this compound demonstrates remarkable properties that make it a valuable asset in various synthetic processes.One significant application of 2-((2-Hydroxyethyl)amino)acetic acid lies in its utility as a stabilizing agent for proteins and enzymes. Its ability to interact with biomolecules through both ionic and hydrogen bonding allows for the preservation of protein structure and function under harsh conditions, such as high temperatures or extreme pH levels. This feature makes it an essential component in the formulation of enzyme-based biocatalysts for industrial processes.Furthermore, this compound is utilized in the synthesis of betaine-based surfactants and detergents. By incorporating 2-((2-Hydroxyethyl)amino)acetic acid into the molecular structure of surfactants, manufacturers can enhance the solubility and stability of these compounds in aqueous solutions. This, in turn, improves the efficiency of cleaning products and enhances their performance in various applications, ranging from household cleaning to industrial processes.Moreover, 2-((2-Hydroxyethyl)amino)acetic acid serves as a precursor in the synthesis of quaternary ammonium compounds, which find applications as antimicrobial agents, phase transfer catalysts, and conditioning agents in personal care products. Its unique chemical structure allows for the modification of properties to tailor the functionality of these compounds according to specific requirements, making it a versatile building block in organic synthesis.In conclusion, the diverse applications of 2-((2-Hydroxyethyl)amino)acetic acid in chemical synthesis underscore its importance as a multifunctional compound with significant contributions to various industries, including biotechnology, pharmaceuticals, and materials science.