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Chemical Structure| 600-15-7 Chemical Structure| 600-15-7
Chemical Structure| 600-15-7

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Synonyms: α-Hydroxybutyric acid

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Product Details of 2-Hydroxybutyric acid

CAS No. :600-15-7
Formula : C4H8O3
M.W : 104.10
SMILES Code : CCC(O)C(O)=O
Synonyms :
α-Hydroxybutyric acid
MDL No. :MFCD00070502
InChI Key :AFENDNXGAFYKQO-UHFFFAOYSA-N
Pubchem ID :11266

Safety of 2-Hydroxybutyric acid

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H303-H315-H318-H335
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340+P312-P305+P351+P338+P310-P312-P332+P313-P403+P233-P405-P501

Application In Synthesis of 2-Hydroxybutyric acid

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 600-15-7 ]

[ 600-15-7 ] Synthesis Path-Downstream   1~6

  • 3
  • [ 584-03-2 ]
  • [ 5077-67-8 ]
  • [ 600-15-7 ]
YieldReaction ConditionsOperation in experiment
With 1% platinum on charcoal; oxygen; In water; at 100℃; under 2250.23 Torr; for 24h; Reactions were carried out using a Radley?s low pressure glass reactor (50 ml). A butanediol in water (20 ml, 0.6 M) and the catalyst(butanediol/metal ratio2000) were added into the reactor,which was then pressurized with oxygen (3 bar). The reaction mixture was heated to 100 C for 24 h under constant stirring(1000 rpm), then cooled to room temperature and analyzed. 1H-NMR spectroscopy was used for product identification; spectrawere acquired over a 16 scan period using a Bruker 400 MHz DPXsystem with a 5 mm auto tune broadband probe. All samples were prepared as dilute solutions in D2O. Carbon mass balances were calculated and were between 96 and 104percent. Blank reactions have also been carried out with no oxidation activity detected in the absence of catalyst or with the KB-B carbon support.
45%Spectr.; 55%Spectr. With oxygen; In water; at 100℃; under 2250.23 Torr; for 24h; General procedure: (0017) Reactions were carried out using a Radley's low pressure glass reactor (50ml). A butanediol in water (20ml, 0.6M) and the catalyst (butanediol/metal ratio=2000) were added into the reactor, which was then pressurized with oxygen (3bar). The reaction mixture was heated to 100°C for 24h under constant stirring (1000rpm), then cooled to room temperature and analyzed. 1H NMR spectroscopy was used for product identification; spectra were acquired over a 16 scan period using a Bruker 400MHz DPX system with a 5mm auto tune broadband probe. All samples were prepared as dilute solutions in D2O. Carbon mass balances were calculated and were between 96 and 104percent. Blank reactions have also been carried out with no oxidation activity detected in the absence of catalyst or with the KB-B carbon support.
  • 4
  • [ 584-03-2 ]
  • [ 802294-64-0 ]
  • [ 5077-67-8 ]
  • [ 600-15-7 ]
YieldReaction ConditionsOperation in experiment
With Au-Pd/carbon catalyst; oxygen; In water; at 100℃; under 2250.23 Torr; for 24h; Reactions were carried out using a Radley?s low pressure glass reactor (50 ml). A butanediol in water (20 ml, 0.6 M) and the catalyst(butanediol/metal ratio2000) were added into the reactor,which was then pressurized with oxygen (3 bar). The reaction mixture was heated to 100 C for 24 h under constant stirring(1000 rpm), then cooled to room temperature and analyzed. 1H-NMR spectroscopy was used for product identification; spectrawere acquired over a 16 scan period using a Bruker 400 MHz DPXsystem with a 5 mm auto tune broadband probe. All samples were prepared as dilute solutions in D2O. Carbon mass balances were calculated and were between 96 and 104percent. Blank reactions have also been carried out with no oxidation activity detected in the absence of catalyst or with the KB-B carbon support.
6%Spectr.; 46%Spectr.; 45%Spectr. With oxygen; In water; at 100℃; under 2250.23 Torr; for 24h; General procedure: (0017) Reactions were carried out using a Radley's low pressure glass reactor (50ml). A butanediol in water (20ml, 0.6M) and the catalyst (butanediol/metal ratio=2000) were added into the reactor, which was then pressurized with oxygen (3bar). The reaction mixture was heated to 100°C for 24h under constant stirring (1000rpm), then cooled to room temperature and analyzed. 1H NMR spectroscopy was used for product identification; spectra were acquired over a 16 scan period using a Bruker 400MHz DPX system with a 5mm auto tune broadband probe. All samples were prepared as dilute solutions in D2O. Carbon mass balances were calculated and were between 96 and 104percent. Blank reactions have also been carried out with no oxidation activity detected in the absence of catalyst or with the KB-B carbon support.
  • 5
  • [ 584-03-2 ]
  • [ 64-19-7 ]
  • [ 802294-64-0 ]
  • [ 5077-67-8 ]
  • [ 600-15-7 ]
YieldReaction ConditionsOperation in experiment
With oxygen; In water; at 100℃; under 2250.23 Torr; for 24h; Reactions were carried out using a Radley?s low pressure glass reactor (50 ml). A butanediol in water (20 ml, 0.6 M) and the catalyst(butanediol/metal ratio2000) were added into the reactor,which was then pressurized with oxygen (3 bar). The reaction mixture was heated to 100 C for 24 h under constant stirring(1000 rpm), then cooled to room temperature and analyzed. 1H-NMR spectroscopy was used for product identification; spectrawere acquired over a 16 scan period using a Bruker 400 MHz DPXsystem with a 5 mm auto tune broadband probe. All samples were prepared as dilute solutions in D2O. Carbon mass balances were calculated and were between 96 and 104percent. Blank reactions have also been carried out with no oxidation activity detected in the absence of catalyst or with the KB-B carbon support.
7%Spectr.; 11%Spectr.; 28%Spectr.; 54%Spectr. With oxygen; In water; at 100℃; under 2250.23 Torr; for 24h; General procedure: (0017) Reactions were carried out using a Radley's low pressure glass reactor (50ml). A butanediol in water (20ml, 0.6M) and the catalyst (butanediol/metal ratio=2000) were added into the reactor, which was then pressurized with oxygen (3bar). The reaction mixture was heated to 100°C for 24h under constant stirring (1000rpm), then cooled to room temperature and analyzed. 1H NMR spectroscopy was used for product identification; spectra were acquired over a 16 scan period using a Bruker 400MHz DPX system with a 5mm auto tune broadband probe. All samples were prepared as dilute solutions in D2O. Carbon mass balances were calculated and were between 96 and 104percent. Blank reactions have also been carried out with no oxidation activity detected in the absence of catalyst or with the KB-B carbon support.
7%Spectr.; 11%Spectr.; 28%Spectr.; 54%Spectr. With oxygen; In water; at 100℃; under 2250.23 Torr; for 24h; General procedure: (0017) Reactions were carried out using a Radley's low pressure glass reactor (50ml). A butanediol in water (20ml, 0.6M) and the catalyst (butanediol/metal ratio=2000) were added into the reactor, which was then pressurized with oxygen (3bar). The reaction mixture was heated to 100°C for 24h under constant stirring (1000rpm), then cooled to room temperature and analyzed. 1H NMR spectroscopy was used for product identification; spectra were acquired over a 16 scan period using a Bruker 400MHz DPX system with a 5mm auto tune broadband probe. All samples were prepared as dilute solutions in D2O. Carbon mass balances were calculated and were between 96 and 104percent. Blank reactions have also been carried out with no oxidation activity detected in the absence of catalyst or with the KB-B carbon support.
  • 6
  • [ 584-03-2 ]
  • [ 64-19-7 ]
  • [ 5077-67-8 ]
  • [ 600-15-7 ]
YieldReaction ConditionsOperation in experiment
With oxygen; In water; at 100℃; under 2250.23 Torr; for 24h; Reactions were carried out using a Radley?s low pressure glass reactor (50 ml). A butanediol in water (20 ml, 0.6 M) and the catalyst(butanediol/metal ratio2000) were added into the reactor,which was then pressurized with oxygen (3 bar). The reaction mixture was heated to 100 C for 24 h under constant stirring(1000 rpm), then cooled to room temperature and analyzed. 1H-NMR spectroscopy was used for product identification; spectrawere acquired over a 16 scan period using a Bruker 400 MHz DPXsystem with a 5 mm auto tune broadband probe. All samples were prepared as dilute solutions in D2O. Carbon mass balances were calculated and were between 96 and 104percent. Blank reactions have also been carried out with no oxidation activity detected in the absence of catalyst or with the KB-B carbon support.
 

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