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1115-63-5

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  • Potassium L-Aspartate Factory CAS 1115-63-5 L-Aspartic acid potassium salt CAS no 1115-63-5 L-Aspartic acid,potassium salt (1:1)

    Cas No: 1115-63-5

  • USD $ 3.5-5.0 / Kiloliter

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1115-63-5 Usage

Description

L-Aspartic Acid Potassium Salt, also known as potassium aspartate, is a non-essential amino acid derivative that exists in a white crystalline powder form. It is a naturally occurring compound and plays a significant role in various biological processes.

Uses

Used in Pharmaceutical and Biomedical Applications:
L-Aspartic Acid Potassium Salt is used as a key component in the preparation of perforated patch-clamp intracellular solutions. This application is crucial for studying ion channels and membrane transport mechanisms in cells.
Used in Clinical Diagnostics:
In the field of clinical diagnostics, L-Aspartic Acid Potassium Salt is utilized as a component in the Serum Glutamate-Oxaloacetate Transaminase (SGOT) assay. This assay is essential for measuring the levels of SGOT enzyme in blood samples, which can be indicative of various health conditions, including liver damage.
Used in Cellular and Molecular Research:
L-Aspartic Acid Potassium Salt is also employed as a component in an internal solution (IS) for the MitoFlash assay. This assay is designed to detect mitochondrial flashes in permeabilized cells, providing valuable insights into cellular metabolism and mitochondrial function.

Biochem/physiol Actions

L-Aspartic acid is an endogenous N-methyl-D-aspartate (NMDA) receptor agonist.

Check Digit Verification of cas no

The CAS Registry Mumber 1115-63-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,1 and 5 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1115-63:
(6*1)+(5*1)+(4*1)+(3*5)+(2*6)+(1*3)=45
45 % 10 = 5
So 1115-63-5 is a valid CAS Registry Number.
InChI:InChI=1/C4H7NO4.K.H2O/c5-2(4(8)9)1-3(6)7;;/h2H,1,5H2,(H,6,7)(H,8,9);;1H2/q;+1;/p-1/t2-;;/m0../s1

1115-63-5 Well-known Company Product Price

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  • Sigma-Aldrich

  • (11230)  L-Asparticacidpotassiumsalt  puriss. p.a., ≥99.0% (anhydrous basis)

  • 1115-63-5

  • 11230-100G-F

  • 634.14CNY

  • Detail
  • Sigma

  • (A6558)  L-Asparticacidpotassiumsalt  ≥98% (HPLC)

  • 1115-63-5

  • A6558-25G

  • 362.70CNY

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  • Sigma

  • (A6558)  L-Asparticacidpotassiumsalt  ≥98% (HPLC)

  • 1115-63-5

  • A6558-100G

  • 1,035.45CNY

  • Detail
  • Sigma

  • (A6558)  L-Asparticacidpotassiumsalt  ≥98% (HPLC)

  • 1115-63-5

  • A6558-1KG

  • 6,119.10CNY

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1115-63-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name L-ASPARTIC ACID POTASSIUM SALT

1.2 Other means of identification

Product number -
Other names L-Aspartate Potassium

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1115-63-5 SDS

1115-63-5Synthetic route

L-Aspartic acid
56-84-8

L-Aspartic acid

potassium hydrogen L-aspartate
1115-63-5

potassium hydrogen L-aspartate

Conditions
ConditionsYield
With potassium hydroxide In water Ambient temperature;100%
potassium hydrogen L-aspartate
1115-63-5

potassium hydrogen L-aspartate

Potassium; 3-carboxy-3-oxo-propionate
53413-14-2

Potassium; 3-carboxy-3-oxo-propionate

Conditions
ConditionsYield
With potassium hydroxide; 3-{[tris(hydroxymethyl)methyl]amino}propanesulfonic acid; potassium chloride; R292D mutant aspartate aminotransferase In water at 25℃; Equilibrium constant;

1115-63-5Upstream product

1115-63-5Relevant articles and documents

Metal Ion Binding by Amino Acids. - Preparation and Crystal Structures of Lithium Hydrogen L-Aspartate Hydrate and Potassium Hydrogen L-Aspartate Dihydrate

Schmidbaur, Hubert,Bach, Ina,Wilkinson, Dallas L.,Mueller, Gerhard

, p. 1427 - 1432 (2007/10/02)

Lithium hydrogen L-aspartate, prepared by neutralisation of lithium carbonate with aqueous L-aspartic acid L-AspH2, crystallizes as the monohydrate Li(L-AspH) * H2O.Saturated solutions show pH 7.30.Potassium hydrogen L-aspartate, synthesized similarly from L-AspH2 and KOH, crystallizes from aqueous solutions (pH 7.52) as the dihydrate K(L-AspH) * 2 H2O.The NMR spectra of the two complexes exhibit no major differences. - Crystalline Li(L-AspH) * H2O has a layer structure, in which each lithium atom is in a tetrahedral environment of four oxygen atoms belonging to four different amino acids.The hydrate water molecule and the nitrogen function (protonated to give an ammonium center) have no metal contacts, but are components of a network of hydrogen bonds interconnecting the layers.One of the carboxylate oxygen atoms is in a bridging position between the metal atoms, which are arranged in pairs and participate in edge-sharing six-membered rings.In each of the layers large empty channels are formed. - Crystals of K(L-AspH) * 2 H2O show a chain structure with the potassium atoms exhibiting coordination number 7.The metal atoms are again arranged in double strings with the β-carboxylate oxygen atoms of the L-AspH(1-) counter anions in chelating and bridging positions.The α-carboxylate and protonated amino functions show no metal contacts, but are part of the hydrogen-bonding system interconnecting the chains of the coordination polymer.Both hydrate water molecules are K-coordinated, one in a metal-bridging position. - Keywords: L-Aspartate complexes / Lithium hydrogen L-aspartate hydrate / Potassium hydrogen L-aspartate dihydrate / Amino acid complexes

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