BHB (Mg/Ca/Na salts have no single CAS)

Basic information

  • Product Name:BHB (Mg/Ca/Na salts have no single CAS)
  • CasNo.:300-85-6
  • MF:C4H8O3
  • MW:104.106

Physical and Chemical Properties

  • Purity:99%
  • Boiling Point:174-175℃
  • Packing:
  • Throughput:
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Product Details

CasNo: 300-85-6

MF: C4H8O3

Cost-effective and customizable BHB (Mg/Ca/Na salts have no single CAS) 300-85-6 factory

  • Molecular Formula:C4H8O3
  • Molecular Weight:104.106
  • Vapor Pressure:0.000979mmHg at 25°C 
  • Melting Point:174-175℃ 
  • Refractive Index:n20/D 1.443(lit.)  
  • Boiling Point:269.216 °C at 760 mmHg 
  • PKA:4.36±0.10(Predicted) 
  • Flash Point:121.011 °C 
  • PSA:57.53000 
  • Density:1.196 g/cm3 
  • LogP:-0.15810 

3-HYDROXYBUTYRIC ACID(Cas 300-85-6) Usage

Definition

ChEBI: A straight-chain 3-hydroxy monocarboxylic acid comprising a butyric acid core with a single hydroxy substituent in the 3- position; a ketone body whose levels are raised during ketosis, used as an energy source by the brain during fasting in humans. Also u ed to synthesise biodegradable plastics.

InChI:InChI=1/C4H8O3/c1-3(5)2-4(6)7/h3,5H,2H2,1H3,(H,6,7)/p-1/t3-/m1/s1

300-85-6 Relevant articles

Nitrogen-doped cobalt nanocatalysts for carbonylation of propylene oxide

Chen, Lin,He, Lin,Xia, Chungu,Yang, Bingxiao,Zeng, Bo,Zhu, Gangli

, (2020/07/16)

Nitrogen-doped cobalt nanoparticles load...

Synthesis of α,β- and β-Unsaturated Acids and Hydroxy Acids by Tandem Oxidation, Epoxidation, and Hydrolysis/Hydrogenation of Bioethanol Derivatives

Faria, Jimmy,Komarneni, Mallik R.,Li, Gengnan,Pham, Tu,Resasco, Daniel E.,Ruiz, Maria P.,Santhanaraj, Daniel

supporting information, p. 7456 - 7460 (2020/03/23)

We report a reaction platform for the sy...

PtII-Catalyzed Hydroxylation of Terminal Aliphatic C(sp3)?H Bonds with Molecular Oxygen

Janssen, Michiel,De Vos, Dirk E.

supporting information, p. 10724 - 10734 (2019/07/15)

The practical application of Shilov-type...

Method for preparing 3- hydroxybutyrate

-

Paragraph 0056-0058; 0060-0062; 0064-0066, (2019/03/08)

The invention discloses a method for pre...

300-85-6 Process route

(E)-but-2-enoic acid
107-93-7

(E)-but-2-enoic acid

propene
187737-37-7,13987-01-4,15220-87-8,9003-07-0,676-63-1,25085-53-4

propene

crotonic acid isopropyl ester
6284-46-4,17377-84-3,18060-77-0

crotonic acid isopropyl ester

isopropyl alcohol
67-63-0,8013-70-5

isopropyl alcohol

3-Hydroxybutyric acid
300-85-6,625-71-8,26063-00-3,29435-48-1

3-Hydroxybutyric acid

Conditions
Conditions Yield
With water; at 230 ℃; for 1h; Product distribution; 1M Solution of acid.;
4 % Chromat.
2 % Chromat.
3.3 % Chromat.
butyric acid
107-92-6

butyric acid

4-hydroxybutanoic acid
591-81-1

4-hydroxybutanoic acid

3-Hydroxybutyric acid
300-85-6,625-71-8,26063-00-3,29435-48-1

3-Hydroxybutyric acid

Conditions
Conditions Yield
With carbon monoxide; oxygen; trifluoroacetic acid; palladium on activated charcoal; copper dichloride; at 75 ℃; for 18h; under 56887.8 Torr; Title compound not separated from byproducts.;
24 % Spectr.
22%

300-85-6 Upstream products

  • 110-86-1
    110-86-1

    pyridine

  • 60-29-7
    60-29-7

    diethyl ether

  • 141-82-2
    141-82-2

    malonic acid

  • 75-07-0
    75-07-0

    acetaldehyde

300-85-6 Downstream products

  • 541-50-4
    541-50-4

    2-acetoacetic acid

  • 110-15-6
    110-15-6

    succinic acid

  • 1487-49-6
    1487-49-6

    3-hydroxybutyric acid methyl ester

  • 77-92-9
    77-92-9

    citric acid