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Merck

31146

Boric acid

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

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About This Item

Linear Formula:
H3BO3
CAS Number:
Molecular Weight:
61.83
PubChem Substance ID:
eCl@ss:
38120104
UNSPSC Code:
12352106
NACRES:
NA.21
EC Number:
233-139-2
MDL number:

Product Name

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

InChI key

KGBXLFKZBHKPEV-UHFFFAOYSA-N

InChI

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

SMILES string

OB(O)O

grade

ACS reagent
puriss. p.a.

agency

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

vapor pressure

2.6 mmHg ( 20 °C)

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

Quality Level

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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.

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.

pictograms

Health hazard

signalword

Danger

hcodes

Hazard Classifications

Repr. 1B

Storage Class

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
L Charlet Bhami et al.
Journal of vector borne diseases, 52(2), 147-152 (2015-06-30)
The use of low concentrations of boric acid as a potential and effective control agent for the eggs and immature stages of Aedes aegypti L. and Aedes albopictus Skuse (Diptera: Culicidae) is found to be safe and effective as compared
Albert Serrà et al.
ACS nano, 8(5), 4630-4639 (2014-05-03)
Electrodeposition from microemulsions using ionic liquids is revealed as a green method for synthesizing magnetic alloyed nanoparticles, avoiding the use of aggressive reducing agents. Microemulsions containing droplets of aqueous solution (electrolytic solution containing Pt(IV) and Co(II) ions) in an ionic

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