Aspartic acid, homopolymer, sodium salt

Product Information

Molecular Formula
(C4H7NO4)x.xNa
Description
One of the non-essential amino acids commonly occurring in the L-form. It is found in animals and plants, especially in sugar cane and sugar beets. It may be a neurotransmitter.
Synonyms
DL-Aspartic acid, homopolymer, sodium salt
Flash Point
Not applicable
Density
1.21 g/cm3
Storage
−20°C
Grade
Industrial grade

Computed Properties

Hydrogen Bond Donor Count
1
Hydrogen Bond Acceptor Count
5
Rotatable Bond Count
1
Exact Mass
177.00139620 g/mol
Monoisotopic Mass
177.00139620 g/mol
Topological Polar Surface Area
106Ų
Heavy Atom Count
11
Formal Charge
0
Complexity
122
Isotope Atom Count
0
Defined Atom Stereocenter Count
1
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
3
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
CN-114106788-A Industrial circulating cooling liquid 2021-12-15
CN-114057804-A Preparation method and application of polycarboxylic acid anti-wrinkle antibacterial finishing agent 2021-12-07
CN-114107270-A L-aspartic acid beta-decarboxylase mutant 2021-12-07
CN-113974171-A Slightly water-soluble composition, slightly water-soluble food or medicine and preparation method thereof 2021-11-08
CN-113908290-A Multifunctional nano composite and preparation method and application thereof 2021-10-22
CN-113816876-A Cardanol cyclic carbonate ether carboxylate anionic surfactant and preparation method thereof 2021-09-18
CN-113735724-A Aspartic acid sodium diacetate and preparation method thereof 2021-09-08
CN-113604415-A Application of recombinant bacillus subtilis and method for producing tetrahydropyrimidine by using wastewater generated in enzymatic synthesis of N-acetylneuraminic acid 2021-09-01
CN-113621549-A Application of recombinant bacillus subtilis and method for producing tetrahydropyrimidine by using waste water generated in enzymatic synthesis of nicotinamide mononucleotide 2021-09-01
CN-113637624-A Recombinant bacillus subtilis, application thereof and method for producing tetrahydropyrimidine by using waste water generated in glutathione synthesis by enzyme method 2021-09-01

Literatures

PMID Publication Date Title Journal
36251573 2022-10-27 Sebetralstat (KVD900): A Potent and Selective Small Molecule Plasma Kallikrein Inhibitor Featuring a Novel P1 Group as a Potential Oral On-Demand Treatment for Hereditary Angioedema Journal of medicinal chemistry
35483150 2022-06-01 Cineole alleviates the BPA-inhibited NETs formation by regulating the p38 pathway-mediated programmed cell death Ecotoxicology and environmental safety
32363662 2020-08-01 Bisphenol A exposure disrupts aspartate transport in HepG2 cells Journal of biochemical and molecular toxicology
30844808 2019-01-01 A Phase 2 Study of PCI-27483, a Factor VIIa Inhibitor in Combination with Gemcitabine for Advanced Pancreatic Cancer Oncology
28470569 2018-01-01 Transport of BMAA into Neurons and Astrocytes by System xc Neurotoxicity research
28548828 2017-09-15 Screening of Pro-Asp Sequences Exposed on Bacteriophage M13 as an Ideal Anchor for Gold Nanocubes ACS synthetic biology
28682067 2017-07-27 Expanding the Antiviral Spectrum of 3-Fluoro-2-(phosphonomethoxy)propyl Acyclic Nucleoside Phosphonates: Diamyl Aspartate Amidate Prodrugs Journal of medicinal chemistry
28257918 2017-05-01 Ceftriaxone-mediated upregulation of the glutamate transporter GLT-1 contrasts neurotoxicity evoked by kainate in rat organotypic spinal cord cultures Neurotoxicology
26707656 2016-04-01 Persistent elevation of D-Aspartate enhances NMDA receptor-mediated responses in mouse substantia nigra pars compacta dopamine neurons Neuropharmacology
25849139 2015-05-14 Aspartic acid based nucleoside phosphoramidate prodrugs as potent inhibitors of hepatitis C virus replication Organic & biomolecular chemistry
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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