Ethylboronic acid Chemical Properties

Melting point:

161-162°C

Boiling point:

154.0±23.0 °C(Predicted)

Density 

0.941±0.06 g/cm3(Predicted)

storage temp. 

Inert atmosphere,Store in freezer, under -20°C

solubility 

DMSO (Slightly), Water (Slightly)

form 

Crystalline Powder, Needles or Flakes

pka

10.18±0.43(Predicted)

color 

White to slightly yellow

Sensitive 

Hygroscopic

BRN 

1731546

InChI

InChI=1S/C2H7BO2/c1-2-3(4)5/h4-5H,2H2,1H3

InChIKey

PAVZHTXVORCEHP-UHFFFAOYSA-N

SMILES

C(B(O)O)C

CAS DataBase Reference

4433-63-0(CAS DataBase Reference)

NIST Chemistry Reference

Ethyldihydroxyborane(4433-63-0)

Safety Information

Hazard Codes 

Xi,Xn

Risk Statements 

36/37/38-22

Safety Statements 

37/39-26-36

WGK Germany 

WGK 3

TSCA 

No

HazardClass 

IRRITANT, KEEP COLD

HS Code 

29319090

Storage Class

11 - Combustible Solids

Hazard Classifications

Eye Irrit. 2
Skin Irrit. 2
STOT SE 3

MSDS

• Language:English Provider:ACROS
• Language:English Provider:ALFA

Ethylboronic acid Usage And Synthesis

Chemical Properties

white to slightly yellow crystalline powder,

Uses

Ethylboronic Acid is the sole precursor in the successful preparation of boron-doped graphene (B-doped graphene) films with large area.

Synthesis

Alkylboronic acid pinacol ester (2 mmol) and methanol (10 mL) were charged into a 10 mL glass vial with a magnetic stirring bar, potassium hydrofluoride (2 mL, 4.5 M saturated aqueous solution) was added slowly and dropwise to the mixture, and the mixture was stirred for 1 hour at room temperature. All volatile compounds were then removed under vacuum, and the organic residue was redissolved in methanol (6 mL), followed by the addition of water (6-10 mL) and evaporation of all volatile compounds (this process was performed 3 times). The solid residue was stirred with dry acetone (8 mL), then the liquid phase was carefully decanted and the residual inorganic salts were washed with more acetone (3 ?? 2 mL), the filtrate was collected, and the filtrate was concentrated in vacuo to give the potassium ethyltrifluoroborate salt intermediate.

Potassium alkyltrifluoroborate (0.4 mmol) and water (1 mL) were injected into a 10 mL glass vial fitted with a magnetic stirring bar, then silica (100 mg) was added to the vial, and the mixture was stirred for 1-2 hr at room temperature, and the progress of the reaction was monitored by 11B-NMR, and when the reaction had proceeded to its full extent, a mixture of ethyl acetate and ether (10 mL) was used to The mixture was diluted and the organic phase was separated by filtering the mixture through diatomaceous earth. The aqueous phase was extracted with a mixed solution of ethyl acetate and ether, and the combined organic layers were dried with anhydrous sodium sulfate, and finally the target product was obtained by removing the solvent in vacuum.

Ethylboronic acid(4433-63-0)Related Product Information

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