Chemical Formula:
The chemical formula for boric acid is
and generally referred to as, because it contains boron (B) bonded by three hydroxyl (-OH) groups.
Appearance:
It is normally a white, crystalline solid or colorless powder.
Solubility:
Boric acid is soluble in water (approximately 5.7 g/100 mL at 20°C) and also soluble in alcohol and glycerol.
Melting Point:
Boric acid melting point is about 170°C or 338°F.
Boiling Point:
It decomposes before boiling, so a boiling point is not typically defined.
Density:
The density of boric acid is approximately 1.44 g/cm³.
pH:
Aqueous solutions of boric acid are slightly acidic with a pH in the range of 5.0 to 5.5.
Hygroscopic Nature:
Boric acid is slightly hygroscopic or capable of absorbing moisture from the air, which may influence its storage and handling.
Stability:
Boric acid is stable under normal conditions. It does not react violently with most substances but can undergo hydrolysis in strong bases.
Toxicity:
Even though believed to be safe in small quantities, boric acid is found to be toxic at higher concentrations. Hence, it has to be treated with care, especially when it comes in a concentrated form.
Acidic Character
Weak Acid: Boric acid is a Lewis acid and a weak acid. The weak acid gives a proton (H⁺) but to a lesser extent compared with the strong acids.
Equilibrium in Solution: Boric acid partially ionizes in aqueous solution
Reaction with Bases
Neutralization: Boric acid reacts with strong bases to produce borate ions. It reacts with sodium hydroxide (NaOH)
Dehydration and Decomposition
Thermal Stability: When boric acid is heated, it loses its water of crystallization and is thermally decomposed to metaboric acid. Upon further heating, it continues its decomposition into yet more compounds.
Complex Formation
Coordination Chemistry: Boric acid can be used to synthesize some complexes with various kinds of ligands. Boric acid will react with alcohols to form borate esters, which are applied in organic syntheses.
Reaction with Alcohols
Borate Ester Formation: Boric acid reacts with alcohols to produce borate esters, which can be applied in organic syntheses:
Interaction with Metals
Metal Borates: Boric acid can react with metal oxides or hydroxides, yielding their corresponding metal borates. For example, it reacts with magnesium oxide
MgO to give magnesium borate.
Antimicrobial Properties
Interference with cellular process: Boric acid has some antimicrobial properties due to interference with cellular processes in some microorganisms. Hence, it is used in antifungal and antiseptic purposes.
Buffering Action
pH Stabilization: The Boric acid acts as a buffer, holding constant the stable pH of biological and chemical systems, in spite of some small additions of acids or bases.
Medical: Is used as an antiseptic and antifungal agent, commonly in eye wash solutions.
Pest Control: Acts as an insecticide for pests like cockroaches and ants.
Industrial: In the production of glass and ceramics, and also as a part of fiber optics.
pH Buffering: Maintains constant pH levels in pools, cosmetics, and pharmaceuticals
Agriculture: Provides boron required for plant growth when added to the fertilizers.
Household : Used as a cleaner and as a deodorizer.
Textiles : Imparts flame retardancy to fabrics
Boric acid is a versatile compound employed in various fields, including medicine, agriculture, and industry. The versatility of the compound will be determined from all these diverse uses of boric acid, ranging from being an antiseptic, insecticide, and pH stabilizer, among others, in both its manufacturing and environmental management. It is only when one gains knowledge on all these diverse applications of boric acid that its benefit may be made use of to maximum effectiveness while keeping use safe. As research continues to explore its potential, boric acid will probably remain an essential component in various sectors.
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Chemical Formula:
The chemical formula for boric acid is
and generally referred to as, because it contains boron (B) bonded by three hydroxyl (-OH) groups.
Appearance:
It is normally a white, crystalline solid or colorless powder.
Solubility:
Boric acid is soluble in water (approximately 5.7 g/100 mL at 20°C) and also soluble in alcohol and glycerol.
Melting Point:
Boric acid melting point is about 170°C or 338°F.
Boiling Point:
It decomposes before boiling, so a boiling point is not typically defined.
Density:
The density of boric acid is approximately 1.44 g/cm³.
pH:
Aqueous solutions of boric acid are slightly acidic with a pH in the range of 5.0 to 5.5.
Hygroscopic Nature:
Boric acid is slightly hygroscopic or capable of absorbing moisture from the air, which may influence its storage and handling.
Stability:
Boric acid is stable under normal conditions. It does not react violently with most substances but can undergo hydrolysis in strong bases.
Toxicity:
Even though believed to be safe in small quantities, boric acid is found to be toxic at higher concentrations. Hence, it has to be treated with care, especially when it comes in a concentrated form.
Acidic Character
Weak Acid: Boric acid is a Lewis acid and a weak acid. The weak acid gives a proton (H⁺) but to a lesser extent compared with the strong acids.
Equilibrium in Solution: Boric acid partially ionizes in aqueous solution
Reaction with Bases
Neutralization: Boric acid reacts with strong bases to produce borate ions. It reacts with sodium hydroxide (NaOH)
Dehydration and Decomposition
Thermal Stability: When boric acid is heated, it loses its water of crystallization and is thermally decomposed to metaboric acid. Upon further heating, it continues its decomposition into yet more compounds.
Complex Formation
Coordination Chemistry: Boric acid can be used to synthesize some complexes with various kinds of ligands. Boric acid will react with alcohols to form borate esters, which are applied in organic syntheses.
Reaction with Alcohols
Borate Ester Formation: Boric acid reacts with alcohols to produce borate esters, which can be applied in organic syntheses:
Interaction with Metals
Metal Borates: Boric acid can react with metal oxides or hydroxides, yielding their corresponding metal borates. For example, it reacts with magnesium oxide
MgO to give magnesium borate.
Antimicrobial Properties
Interference with cellular process: Boric acid has some antimicrobial properties due to interference with cellular processes in some microorganisms. Hence, it is used in antifungal and antiseptic purposes.
Buffering Action
pH Stabilization: The Boric acid acts as a buffer, holding constant the stable pH of biological and chemical systems, in spite of some small additions of acids or bases.
Medical: Is used as an antiseptic and antifungal agent, commonly in eye wash solutions.
Pest Control: Acts as an insecticide for pests like cockroaches and ants.
Industrial: In the production of glass and ceramics, and also as a part of fiber optics.
pH Buffering: Maintains constant pH levels in pools, cosmetics, and pharmaceuticals
Agriculture: Provides boron required for plant growth when added to the fertilizers.
Household : Used as a cleaner and as a deodorizer.
Textiles : Imparts flame retardancy to fabrics
Boric acid is a versatile compound employed in various fields, including medicine, agriculture, and industry. The versatility of the compound will be determined from all these diverse uses of boric acid, ranging from being an antiseptic, insecticide, and pH stabilizer, among others, in both its manufacturing and environmental management. It is only when one gains knowledge on all these diverse applications of boric acid that its benefit may be made use of to maximum effectiveness while keeping use safe. As research continues to explore its potential, boric acid will probably remain an essential component in various sectors.
Other Related Sections
NCERT Solutions | Sample Papers | CBSE SYLLABUS| Calculators | Converters | Stories For Kids | Poems for Kids| Learning Concepts | Practice Worksheets | Formulas | Blogs | Parent Resource
Admissions Open for
The chemical formula for Aluminum Bromide is AlBr₃.
Aluminum Bromide is used primarily as a catalyst in organic synthesis, particularly in the bromination of aromatic compounds. It also has applications in the production of other chemicals and in certain types of chemical research.
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