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Merck

31146

Ácido bórico

puriss. p.a., ACS reagent, reag. ISO, reag. Ph. Eur., buffer substance, ≥99.8%

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Fórmula lineal:
H3BO3
Número CAS:
Peso molecular:
61.83
PubChem Substance ID:
eCl@ss:
38120104
UNSPSC Code:
12352106
NACRES:
NA.21
EC Number:
233-139-2
MDL number:
Assay:
≥99.8%
Form:
powder or crystals
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Quality Level

agency

USP/NF, reag. ISO, reag. Ph. Eur.

vapor pressure

2.6 mmHg ( 20 °C)

grade

ACS reagent, puriss. p.a.

assay

≥99.8%

form

powder or crystals

impurities

≤0.005% insoluble in methanol, ≤0.05% with methanol-HCl non-volat. matter

pH

3.6-4.0 (20 °C, 4%)

mp

160 °C (dec.) (lit.)

solubility

water: soluble

density

1.440 g/cm3

anion traces

chloride (Cl-): ≤3 mg/kg, phosphate (PO43-): ≤5 mg/kg, sulfate (SO42-): ≤5 mg/kg

cation traces

As: ≤5 mg/kg, Ca: ≤10 mg/kg, Cd: ≤5 mg/kg, Cu: ≤5 mg/kg, Fe: ≤1 mg/kg, Mg: ≤5 mg/kg, Pb: ≤5 mg/kg, Zn: ≤5 mg/kg

SMILES string

OB(O)O

InChI

1S/BH3O3/c2-1(3)4/h2-4H

InChI key

KGBXLFKZBHKPEV-UHFFFAOYSA-N

General description

Boric acid can be used as a Lewis acid catalyst in organic synthesis to facilitate various organic reactions, including dehydration, hydrolysis, decarboxylation, and condensation reactions. It produces different borate anions and salts and can react with alcohols to produce borate esters. It is also used as a buffering agent and pH adjuster.
Boric acid is a very weak acid, having pH in the range of 3.6-4.0. Coulometric method for the determination of boric acid has been reported.

Application

Boric acid can be used as a precursor to synthesize boron carbon oxynitride thin films by the atmospheric pressure chemical vapor deposition (APCVD) method using carbon-rich methane and nitrogen-rich ammonia.


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pictograms

Health hazard

signalword

Danger

hcodes

Hazard Classifications

Repr. 1B

Clase de almacenamiento

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable



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Catanzaro EJ, et al.
Boric Acid: Isotopic and Assay Standard Reference Materials, 1-1 (1970)
One-pot synthesis of 3, 4-dihydropyrimidin-2(1H)-ones using boric acid as catalyst.
Tu S, et al.
Tetrahedron Letters, 44(32), 6153-6155 (2003)
L Romano et al.
The Journal of antimicrobial chemotherapy, 55(1), 110-114 (2004-12-03)
There is very little information, to date, on the antifungal activity of bergamot oil. In this study, we investigated the in vitro activity of three bergamot oils (natural essence, furocoumarin-free extract and distilled extract) against clinically relevant Candida species. We