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150-83-4

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150-83-4 Usage

Chemical Properties

white crystalline powder

Uses

Different sources of media describe the Uses of 150-83-4 differently. You can refer to the following data:
1. Optically active 3-hydroxybutyric acids are key intermediates of the biosynthesis and metabolism of fatty acids and exist widely in biological systems.
2. (±)-Sodium 3-hydroxybutyrate has been used in a study to understand the effect of butyrate on fibroblast growth factor 21 (FGF21), which is involved in fatty acid ?-oxidation in liver. It may be used in the preparation of poly(3-hydroxybutyrate).

Application

DL-β-Hydroxybutyric acid sodium salt has been used:as a standard for quantifying blood plasma and milk β-hydroxybutyric acid in Danish Jersey cows.to investigate its anticonvulsant effects in epilepsy induced rats.to induce hyperketonemia in Holstein dairy cows.

Definition

ChEBI: An organic sodium salt resulting from the replacement of the proton from the carboxy group of 3-hydroxybutyric acid by a sodium ion.

Biological Functions

Neuroprotective compound in experimental models of neurodegenerative diseases. Shown to be oxidized as an energetic substrate in the brain during starvation. May inhibit brain glucose oxidation, which may account for the suppression of hepatic glucose production observed after administration of ketone bodies in humans.

Biological Activity

β-Hydroxybutyric acid is a ketone body present in the rumen epithelium of liver cells. Its interconversion to acetoacetate influences the acid-base balance and is coupled NADH generation from (nicotinamide adenine dinucleotide) NAD+, measured fluorimetrically. A high plasma level of β-hydroxybutyric acid is implicated in diabetic ketoacidosis. It traverses the blood-brain barrier as a monocarboxylic acid. β-Hydroxybutyric acid may play a protective role in dopaminergic neurodegeneration in Parkinson′s disease model. β-Hydroxybutyric acid is a ligand for G protein-coupled receptor(GPR109A) and favors inhibition of secretion, transcription and translation of growth hormone (GH) and prolactin (PRL) gene in cow anterior pituitary cells (DCAPCs).

Biochem/physiol Actions

β-Hydroxybutyric acid is a ketone body present in the rumen epithelium of liver cells. Its interconversion to acetoacetate influences the acid-base balance and is coupled NADH generation from (nicotinamide adenine dinucleotide) NAD+, measured fluorimetrically. A high plasma level of β-hydroxybutyric acid is implicated in diabetic ketoacidosis. It traverses the blood-brain barrier as a monocarboxylic acid. β-Hydroxybutyric acid may play a protective role in dopaminergic neurodegeneration in Parkinson′s disease model. β-Hydroxybutyric acid is a ligand for G protein-coupled receptor(GPR109A) and favors inhibition of secretion, transcription and translation of growth hormone (GH) and prolactin (PRL) gene in cow anterior pituitary cells (DCAPCs).

Check Digit Verification of cas no

The CAS Registry Mumber 150-83-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,5 and 0 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 150-83:
(5*1)+(4*5)+(3*0)+(2*8)+(1*3)=44
44 % 10 = 4
So 150-83-4 is a valid CAS Registry Number.
InChI:InChI=1/C4H8O3.Na/c1-3(5)2-4(6)7;/h3,5H,2H2,1H3,(H,6,7);

150-83-4 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
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  • Alfa Aesar

  • (A11613)  Sodium 3-hydroxybutyrate, 98%   

  • 150-83-4

  • 5g

  • 279.0CNY

  • Detail
  • Alfa Aesar

  • (A11613)  Sodium 3-hydroxybutyrate, 98%   

  • 150-83-4

  • 25g

  • 1095.0CNY

  • Detail
  • Aldrich

  • (54965)  (±)-Sodium3-hydroxybutyrate  ≥99.0% (NT)

  • 150-83-4

  • 54965-10G-F

  • 625.95CNY

  • Detail
  • Aldrich

  • (54965)  (±)-Sodium3-hydroxybutyrate  ≥99.0% (NT)

  • 150-83-4

  • 54965-50G-F

  • 2,254.59CNY

  • Detail

150-83-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name DL-3-Hydroxybutyric acid, sodium salt

1.2 Other means of identification

Product number -
Other names Sodium 3-hydroxybutyrate

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:150-83-4 SDS

150-83-4Upstream product

150-83-4Relevant articles and documents

Catalyzed dehydrogenative coupling of primary alcohols with water, methanol, or amines

Zweifel, Theo,Naubron, Jean-Valere,Gruetzmacher, Hansjoerg

supporting information; experimental part, p. 559 - 563 (2009/04/14)

A working partnership: Metal-ligand cooperativity is responsible for the high activity of the rhodium amido complex 1 in the dehydrogenative coupling of primary alcohols with water, methanol, or amines, including ammonia (see scheme), to give carboxylic acids, methyl carboxylates, or amides, respectively. The catalysis proceeds under mild reaction conditions in the presence of a recyclable hydrogen acceptor A. The multistep mechanism was elucidated by computational methods. (Chemical Equation Presented)

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