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Key Documents

Safety Information

31146

Sigma-Aldrich

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
EC Number:
MDL number:
UNSPSC Code:
12352106
eCl@ss:
38120104
PubChem Substance ID:
NACRES:
NA.21

grade

ACS reagent
puriss. p.a.

Quality Level

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

SMILES string

OB(O)O

InChI

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

InChI key

KGBXLFKZBHKPEV-UHFFFAOYSA-N

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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.

Pictograms

Health hazard

Signal Word

Danger

Hazard Statements

Hazard Classifications

Repr. 1B

Storage Class Code

6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

PRTR

Class I Designated Chemical Substances

ISHL Indicated Name

Substances Subject to be Indicated Names

ISHL Notified Names

Substances Subject to be Notified Names

JAN Code

31146-BULK:
31146-BULK-H:
31146-2.5KG:
31146-6X500G:
31146-VAR:
31146-6X1KG:
31146-1KG:
31146-6X2.5KG:
31146-25KG-H:
31146-500G:


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
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
Jing Li et al.
American journal of physiology. Cell physiology, 306(10), C943-C960 (2014-03-22)
The human solute carrier (SLC26) family of anion transporters consists of 10 members (SLCA1-11, SLCA10 being a pseudogene) that encode membrane proteins containing ~12 transmembrane (TM) segments with putative N-glycosylation sites (-NXS/T-) in extracellular loops and a COOH-terminal cytosolic STAS

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