5458-99-1

Basic information

• Product Name: 3-[(2-HYDROXYETHYL)AMINO]PROPANOIC ACID
• Synonyms: 3-[(2-HYDROXYETHYL)AMINO]PROPANOIC ACID;3-(2-HYDROXY-ETHYLAMINO)-PROPIONIC ACID;AKOS BBV-004511;UKRORGSYN-BB BBV-004511;PPDDDJFBMYJHBK-UHFFFAOYSA-N
• CAS NO: 5458-99-1
• Molecular Formula: C₅H₁₁NO₃
• Molecular Weight: 133.15
• Mol File: 5458-99-1.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 344.9°C at 760 mmHg
• Flash Point: 162.4°C
• Appearance: /
• Density: 1.188g/cm³
• Vapor Pressure: 4.03E-06mmHg at 25°C
• Refractive Index: 1.481
• Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
• Solubility: DMSO (Slightly, Heated, Sonicated), Methanol (Slightly, Sonicated), Water (Sligh
• CAS DataBase Reference: 3-[(2-HYDROXYETHYL)AMINO]PROPANOIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 3-[(2-HYDROXYETHYL)AMINO]PROPANOIC ACID(5458-99-1)
• EPA Substance Registry System: 3-[(2-HYDROXYETHYL)AMINO]PROPANOIC ACID(5458-99-1)

Safety Data

• Hazardous Substances Data: 5458-99-1(Hazardous Substances Data)

Usage

General Description

3-[(2-HYDROXYETHYL)AMINO]PROPANOIC ACID, also known as serine, is an amino acid that is essential for the synthesis of proteins and the proper functioning of the nervous system. It is classified as a non-essential amino acid, meaning it can be synthesized by the human body and is also found in many common foods. Serine plays a crucial role in the biosynthesis of purines and pyrimidines, which are essential components of DNA and RNA. It also acts as a precursor for the synthesis of other important molecules such as phospholipids, which are essential for the structure and function of cell membranes. In addition, serine is involved in the formation of creatine, a molecule that provides energy for muscle contractions. Overall, 3-[(2-HYDROXYETHYL)AMINO]PROPANOIC ACID is a vital compound for various biological processes within the human body.

InChI:InChI=1/C5H11NO3/c7-4-3-6-2-1-5(8)9/h6-7H,1-4H2,(H,8,9)

Upstream product

• 141-43-5 ethanolamine 
• 79-10-7 acrylic acid 
• 57-57-8 β-Propiolactone 

Downstream Products

• 330788-60-8 N-{4-[4-Amino-1-(1-{3-[(2-hydroxyethyl)amino]propanoyl}-4-piperidyl)-1H-pyrazolo[3,4-d]pyrimidin-3-yl]-2-fluorophenyl}-N'-(3-methylphenyl)urea Monoacetate Salt 

Relevant articles and documents

Bis[N-(2-hydroxyethyl)-β-alaninato]-copper(II)

The CuII ion in the title complex, [Cu(C5H 10NO3)2] or [Cu(He-ala)2] [He-ala = W-(2-hydroxyethyl)-β-alaninate], resides at the inversion centre of a square bipyramid comprised of two facially arranged tridentate He-ala ligands. Each He-ala ligand binds to a CuII ion by forming one six-membered β-alaninate chelate ring in a twist conformation and one five-membered ethanolamine ring in an envelope conformation, with Cu-N = 2.017 (2) A, Cu-OCoo = 1.968 (1) A and Cu-OOH = 2.473 (2) A. The [Cu(He-ala)2] molecules are involved in a network of O-H...O and N-H...O hydrogen bonds, forming layers parallel to the (101) plane. The layers are connected into a three-dimensional structure by van der Waals interactions, so that the molecular centres form pseudo-face-centered close packing.

Cross-linked hyaluronate compounds

There is disclosed a cross-linked hyaluronate compound obtained by reacting a sodium hyaluronate compound with a polfunctional aziridine compound as a cross-linking agent. The polyfunctional aziridine compound was added to hyaluronan of various molecular weights in an equivalent ratio of HA/AZ of 1:1 to 1:10, preferably, 1:3 to 1:10, more preferably, 1:3 to 1:5; most preferably 1:4 to 1:5. The polymeric hydrogel compounds obtained are useful to prevent the formation of post-operative adhesions, designing tissue engineering applications, and the like.