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Phosphonic Acid, Phosphorous Acid, Phosphorus Trihydroxide, Orthophosphorus Acid, Dihydroxyphosphine Oxide, Trihydroxyphosphine, 13598-36-2

Phosphonic Acid, Phosphorous Acid, Phosphorus Trihydroxide, Orthophosphorus Acid, Dihydroxyphosphine Oxide, Trihydroxyphosphine, 13598-36-2

PHOSPHONIC ACID (PHOSPHOROUS ACID, H₃PO₃)

1. Chemical Identity and Material Classification

  • Chemical Name: Phosphonic Acid, Phosphorous Acid, Orthophosphorous Acid

  • Synonyms: Phosphorus Trihydroxide, Dihydroxyphosphine Oxide, Trihydroxyphosphine, Hydrogen Phosphonate

  • CAS Number: 13598-36-2

  • Molecular Formula: H₃PO₃

  • Molecular Weight: 82.00 g/mol

  • EC Number: 237-066-7

  • MDL Number: MFCD00137263

  • RTECS Number: SZ6400000

  • UN Number: 2834 (Phosphorous acid, solid)

2. Physical Properties

2.1 General Physical Properties

Property Value
Appearance White to colorless crystalline solid
Crystal form Rhombohedral or plate-like crystals
Odor Odorless (slight pungent odor when heated)
Density (25°C) 1.651 g/cm³
Melting point 73°C (163°F)
Boiling point 200°C (decomposes)
Decomposition temperature >180°C (forms H₃PO₄ + PH₃ – highly toxic)
Vapor pressure (20°C) 0.001 Pa (very low)
Refractive index (nD) 1.491 (at 25°C)
Bulk density (tapped) 0.9–1.1 g/cm³ (powdered form)

2.2 Thermal Properties

Parameter Value
Enthalpy of fusion ~12–15 kJ/mol
Heat of decomposition Endothermic (produces H₃PO₄ and PH₃)
Specific heat capacity (C_p, 25°C) ~1.2 J/(g·K)
Thermal conductivity (solid) ~0.3 W/(m·K)

3. Chemical Structure and Acid-Base Properties

3.1 Molecular Structure

  • Structure type: Phosphorus oxoacid with P–H bond (unlike phosphoric acid)

  • Molecular geometry: Tetrahedral (P center with OH, OH, H, and O)

  • Actual formula: HP(O)(OH)₂ (contains one P–H bond and two P–OH groups)

  • Tautomerism: Exists predominantly as HP(O)(OH)₂ (not P(OH)₃)

  • P–H bond: Characteristic band at ~2300–2400 cm⁻¹ in IR spectrum

3.2 Acid Dissociation Constants (pKa, 25°C)

Dissociation pKa Value Description
First dissociation pKa₁ 1.29 HP(O)(OH)₂ → HP(O)(OH)O⁻ + H⁺
Second dissociation pKa₂ 6.74 HP(O)(OH)O⁻ → HP(O)O₂²⁻ + H⁺
Third dissociation pKa₃ ~12–14 (very weak) Not typically considered
  • Acidity comparison: Stronger than phosphoric acid (H₃PO₄ pKa₁ = 2.14)

  • Dibasic nature: Despite formula H₃PO₃, only two acidic hydrogens (third hydrogen is directly bonded to P, non-acidic)

4. Solubility Behavior

Solvent Solubility (g/100 mL) Temperature
Water Highly soluble (≈ 300 g/100 mL) 20°C
Water Completely miscible 80°C
Ethanol 100 g/100 mL (soluble) 20°C
Methanol Soluble 20°C
Acetone 50 g/100 mL 20°C
Diethyl ether Slightly soluble 20°C
Benzene Insoluble 20°C
Toluene Insoluble 20°C
Chloroform Insoluble 20°C

5. Chemical Properties and Reactivity

5.1 Oxidation (Air)

Property Description
Oxidation in air Slowly oxidized by atmospheric oxygen to phosphoric acid (H₃PO₄)
Rate Slow at room temperature; accelerated by heat and moisture
Reaction 2H₃PO₃ + O₂ → 2H₃PO₄

5.2 Thermal Decomposition

Parameter Description
Decomposition onset >180°C
Decomposition reaction 4H₃PO₃ → 3H₃PO₄ + PH₃ (phosphine – highly toxic, flammable)
PH₃ hazards Extremely toxic (LC₅₀ ~ 11 ppm), pyrophoric, explosive with air
Warning Do not heat phosphorous acid above 180°C without proper ventilation!

5.3 Reducing Agent Properties (Strong Reducer)

Reducing property Value / Description
Standard redox potential E° (HPO₃²⁻/H₃PO₃) ~ -0.5 V
Ag⁺ reduction 2Ag⁺ + H₃PO₃ + H₂O → 2Ag (s) + H₃PO₄ + 2H⁺
Hg²⁺ reduction Reduces Hg²⁺ to Hg⁰ or Hg₂²⁺
Cu²⁺ reduction Reduces Cu²⁺ to Cu⁺ or Cu⁰
Fe³⁺ reduction Fe³⁺ + H₃PO₃ + H₂O → Fe²⁺ + H₃PO₄ + 2H⁺
Iodate reduction IO₃⁻ + H₃PO₃ → I⁻ + H₃PO₄ (used in analytical chemistry)
Sulfuric acid reduction H₂SO₄ + H₃PO₃ → SO₂ (g) + H₃PO₄ + H₂O (when heated)

5.4 Reactions with Bases and Amines

Reaction Description
With NaOH H₃PO₃ + NaOH → NaH₂PO₃ + H₂O (sodium dihydrogen phosphite)
With 2NaOH H₃PO₃ + 2NaOH → Na₂HPO₃ + 2H₂O (disodium hydrogen phosphite)
With amines Forms phosphite salts (exothermic) – used in stabilizer production

5.5 Reactions with Metal Salts

Metal Reaction Product Note
Lead (Pb) PbHPO₃ (lead phosphite) Plastic stabilizer (e.g., dibasic lead phosphite)
Calcium (Ca) CaHPO₃ Intermediate for various applications
Zinc (Zn) ZnHPO₃ Used in corrosion inhibition

6. Production Methods

6.1 Phosphorus Trichloride Hydrolysis (Primary Industrial Method)

  • Reaction: PCl₃ + 3H₂O → H₃PO₃ + 3HCl (exothermic, vigorous)

  • Process: PCl₃ added slowly to water with stirring and cooling → hydrolysis reaction → hydrogen chloride (HCl) released as by-product → HCl recovered as hydrochloric acid → solution refined → cooled → crystallized → decolorized → dried

  • Yield: 90–95%

  • Purity achieved: 98–99.5%

  • By-product: HCl (valuable – sold as hydrochloric acid)

6.2 Phosphite Method (Alternative)

  • Process: From phosphite salts using mineral acid → yields phosphorous acid

  • Less common: Used for specialty grades

6.3 Purification

  • Recrystallization from water or ethanol

  • Activated carbon treatment: For color removal (decolorization)

7. Quality Specifications

7.1 Technical Grade

Parameter Specification
Purity (H₃PO₃, w/w) ≥ 98.0–99.0%
Phosphoric acid (H₃PO₄) ≤ 0.5–1.0%
Chloride (Cl) ≤ 0.02%
Sulfate (SO₄) ≤ 0.02%
Iron (Fe) ≤ 0.002%
Heavy metals (as Pb) ≤ 0.001%
Water insolubles ≤ 0.1%
Color White (APHA ≤ 20)

7.2 Reagent Grade

Parameter Specification
Purity (H₃PO₃, w/w) ≥ 99.0–99.5%
Phosphoric acid (H₃PO₄) ≤ 0.2%
Chloride (Cl) ≤ 0.005%
Sulfate (SO₄) ≤ 0.005%
Iron (Fe) ≤ 0.0005%
Heavy metals (as Pb) ≤ 0.0005%
Reducing power Passes test (e.g., reduces Ag⁺)

8. Industrial Applications

8.1 Plastic Stabilizers (Largest Use)

Application Product Typical Loading
PVC heat stabilizers Dibasic lead phosphite (2PbO·PbHPO₃·0.5H₂O) 1–5 phr
Polycarbonate stabilizer Phosphite esters 0.1–1%
Nylon antioxidant For nylon 1010 0.1–0.5%
Polyester stabilizer Prevents degradation during processing 0.1–0.3%

8.2 Water Treatment and Corrosion Control

Parameter Value
Application Scale inhibitor, corrosion inhibitor for cooling water systems
Mechanism Phosphite ions (HPO₃²⁻) chelate metal ions, form protective films
Typical dosage 5–50 mg/L
Synergists Zinc salts, phosphonates, polyacrylates
Boiler water treatment Oxygen scavenger (reduces dissolved O₂)

8.3 Agriculture (Pesticide Intermediate)

Application Product Importance
Organophosphorus pesticides Glyphosate (herbicide) precursor via oxidation Very large volume
Fungicides Fosetyl-Al (aluminum tris-O-ethylphosphonate) Systemic fungicide
Plant nutrition Phosphite fertilizers (not a direct P source – phosphite is not metabolized as phosphate) Foliar application for disease control

8.4 Chemical Industry (Reducing Agent)

Application Description
Organic synthesis Reduction of nitro compounds to amines
Dye industry Reducing agent in dye manufacturing
Pharmaceutical intermediates Synthesis of various phosphonate drugs
Antioxidant Prevents oxidation in various formulations

8.5 Analytical Chemistry

Application Description
Iodate determination Reduces IO₃⁻ to I⁻ – used in iodometric titrations
Mercury determination Reduces Hg²⁺ to Hg⁰ (cold vapor AAS)
Copper determination Reduces Cu²⁺ to Cu⁺ (colorimetric methods)
Gold/silver determination Reduces Au³⁺/Ag⁺ to metallic Au/Ag
Cadmium determination Interference suppression in some methods
Reducing agent General purpose reducing agent in analytical procedures

9. Chemical Reactions of Industrial Importance

9.1 Synthesis of Phosphites (Esters)

Reaction Product Application
H₃PO₃ + 3ROH (with catalyst) (RO)₃P (trialkyl phosphite) Antioxidants, flame retardants
H₃PO₃ + 2ROH (RO)₂PHO (dialkyl phosphite) Pesticide intermediates
H₃PO₃ + 4ROH + olefin Phosphonate esters PVC stabilizers

9.2 Synthesis of Glyphosate (Herbicide)

  • Route: H₃PO₃ + formaldehyde + glycine → oxidation → glyphosate (N-(phosphonomethyl)glycine)

  • Reaction steps:

    1. H₃PO₃ + CH₂O → HOCH₂P(O)(OH)₂ (hydroxymethylphosphonic acid)

    2. Reaction with glycine → iminodiacetic acid derivative

    3. Oxidation → glyphosate

  • Global importance: One of the largest volume herbicides worldwide

9.3 Synthesis of Stabilizers

  • Dibasic lead phosphite: 2PbO + PbHPO₃ → (2PbO·PbHPO₃) – PVC heat stabilizer

  • Calcium/zinc phosphites: Emerging non-toxic stabilizer alternatives

10. Safety and Toxicology

Parameter Value
Oral LD₅₀ (rat) 1,895 mg/kg (moderately toxic)
Oral LD₅₀ (mouse) 2,172 mg/kg
Skin corrosion Corrosive (R35 – Causes severe burns)
Eye damage Severe damage (corrosive)
Inhalation hazard Irritating to respiratory tract; decompose to PH₃ at high temperature
Mutagenicity Negative (Ames test)
Carcinogenicity Not classified (IARC Group 3)
OSHA PEL (as P) Not specifically established
ACGIH TLV Not specifically established
PH₃ by-product hazard Extremely toxic – avoid heating above 180°C in open vessels

11. Safety Precautions and Personal Protective Equipment (PPE)

  • Hazards:

    • Corrosive – causes severe skin burns and eye damage (R35)

    • Harmful if swallowed (R22)

    • Decomposes above 180°C to release toxic, flammable phosphine (PH₃)

    • Hygroscopic – absorbs moisture from air

  • Reactivity:

    • Incompatible with strong bases (neutralization – exothermic)

    • Incompatible with oxidizing agents (reaction can be violent)

    • Reacts with metals (may release hydrogen gas)

    • Slow oxidation in air to H₃PO₄

  • PPE (mandatory):

    • Chemical-resistant gloves (nitrile, neoprene, or butyl rubber, EN 374)

    • Chemical splash goggles (EN 166) or full face shield

    • Protective clothing (acid-resistant apron or suit)

    • Respiratory protection (P2/P3 filter for dust; SCBA if heating)

  • Engineering controls:

    • Local exhaust ventilation (LEV) for powder handling

    • Eyewash stations and safety showers within immediate vicinity

  • First aid:

    • Inhalation: Remove to fresh air; if breathing difficulty, administer oxygen; seek medical attention

    • Skin contact: Remove contaminated clothing; wash with copious water for at least 15 minutes; seek medical attention

    • Eye contact: Rinse with water for 15–20 minutes, lifting eyelids; seek immediate medical attention

    • Ingestion: Rinse mouth; do NOT induce vomiting; drink milk or water; seek immediate medical attention

12. Environmental Fate and Disposal

Parameter Value
Biodegradation Not readily biodegradable (inorganic/organic hybrid)
Ecotoxicity (fish, LC₅₀, 96 hours) 100–500 mg/L (moderate toxicity)
Daphnia magna (EC₅₀, 48 hours) 50–200 mg/L
Environmental persistence Oxidizes to phosphate (H₃PO₄) over time
Eutrophication potential Lower than phosphate (phosphite is not bioavailable to algae)
Disposal method Neutralization with lime (Ca(OH)₂) → calcium phosphite sludge → landfill
Waste code (EU) 16 06 03* (hazardous – if contaminated)

13. Storage and Shelf Life

  • Storage conditions:

    • Cool, dry, well-ventilated area (15–30°C)

    • Keep tightly closed in original packaging (hygroscopic)

    • Store away from strong bases, oxidizing agents, and metals

    • Avoid high temperatures (>150°C) – decomposition to PH₃

    • Protect from moisture (prevents caking and oxidation)

    • Use corrosion-resistant storage (plastic, glass-lined, or stainless steel)

  • Shelf life:

    • Sealed container (dry): 24–36 months

    • Opened container: 6–12 months (if properly resealed, stored under inert gas)

  • Degradation indicator:

    • Caking/hardening (moisture absorption)

    • Yellow discoloration (oxidation to H₃PO₄)

    • Loss of reducing power (analytical test)

14. Transport Information

Regulation Classification
UN Number 2834 (Phosphorous acid, solid)
ADR/RID Class 8 (Corrosive), Packing group III
IMDG Class 8, PG III
IATA Class 8, PG III
Proper shipping name Phosphorous acid (solid)
Hazard label Corrosive (8)
Marine pollutant No
Special provision Not applicable

15. Analytical Methods

15.1 Assay Determination (Alkaline Titration)

Parameter Value
Principle Titration of phosphorous acid with NaOH using phenolphthalein indicator
Reaction H₃PO₃ + 2NaOH → Na₂HPO₃ + 2H₂O
Equivalent weight 41.00 g/eq (H₃PO₃/2)
Interferences H₃PO₄ (phosphoric acid) titrates as monobasic in same pH range

15.2 Phosphite vs. Phosphate Determination

Method Principle
Iodometric titration H₃PO₃ reduces I₂ to I⁻ (H₃PO₄ does not)
Redox titration with KMnO₄ H₃PO₃ reduces MnO₄⁻ (H₃PO₄ does not)
Spectrophotometric (phosphomolybdate) Phosphate gives blue color; phosphite does not react under standard conditions

15.3 Reducing Power Test (Silver Nitrate)

Parameter Value
Principle H₃PO₃ reduces Ag⁺ to metallic Ag (dark precipitate)
Reaction 2Ag⁺ + H₃PO₃ + H₂O → 2Ag (s) + H₃PO₄ + 2H⁺
Indication Formation of dark (brown/black) silver deposit

16. Synonyms and Common Names

  • English: Phosphonic acid, Phosphorous acid, Orthophosphorous acid, Phosphorus trihydroxide, Dihydroxyphosphine oxide, Trihydroxyphosphine

  • French: Acide phosphoreux

  • German: Phosphonsäure, Phosphorige Säure

  • Spanish: Ácido fosforoso

  • Italian: Acido fosforoso

  • Turkish: Fosfonik asit, Fosforlu asit, Ortofosforlu asit

17. Standards Compliance

Standard Compliance
REACH (EC 1907/2006) Registered (EC 237-066-7)
TSCA (US) Listed
RoHS Compliant (not restricted)
FDA (21 CFR) Limited indirect food contact (as antioxidant in polymers)

18. Why Choose Phosphonic Acid? (Technical Summary)

Advantage Description
Strong reducing agent Reduces Ag⁺, Hg²⁺, Cu²⁺, Fe³⁺, IO₃⁻ – useful in analytical chemistry and metal recovery
Dibasic acid (pKa₁ = 1.29) Stronger acidity than H₃PO₄ – effective for pH control
Key precursor for phosphite stabilizers Essential for PVC heat stabilizers (dibasic lead phosphite)
Glyphosate intermediate Critical raw material for world's most widely used herbicide
Corrosion inhibition Effective in water treatment formulations (scale/corrosion control)
Versatile synthesis Produces phosphite esters (antioxidants, flame retardants, pesticide intermediates)
Hygroscopic but stable (if kept dry) Easy to handle under proper conditions
Cost-effective Lower cost than many specialty phosphorus compounds
Limitation note: Corrosive – requires careful handling. Decomposes to toxic, pyrophoric PH₃ above 180°C – never heat without ventilation. Slowly oxidizes in air to H₃PO₄. Not a direct plant nutrient (phosphite must be oxidized to phosphate for plant uptake).

19. Limitations and Precautions

Limitation Description / Solution
Corrosive nature Requires acid-resistant equipment and PPE
PH₃ formation above 180°C Do not heat above 180°C without inert atmosphere and proper ventilation/scavenging
Air oxidation Slowly converts to H₃PO₄ – store in sealed containers, use under inert gas for long-term storage
Hygroscopic Absorbs moisture from air – causes caking, reduced purity
Not a direct fertilizer Phosphite is not metabolized by plants (must oxidize to phosphate) – do not use as sole P source
Metal corrosion Corrosive to many metals (use plastic, glass-lined, or 316 stainless steel equipment)
Toxic by-products Thermal decomposition yields PH₃ (extremely toxic, pyrophoric) – ensure adequate ventilation

20. Sectoral Suitability Summary Table

Sector Application Typical Concentration/Usage Alternatives
Plastics PVC heat stabilizer (dibasic lead phosphite) 1–5 phr Calcium/zinc stabilizers, organotins
Plastics Polycarbonate/nylon antioxidant 0.1–1% Hindered phenols, phosphites
Water Treatment Corrosion/scale inhibitor 5–50 mg/L Phosphonates (ATMP, HEDP), polyacrylates
Agriculture Glyphosate production (herbicide) Large volume feedstock None (key intermediate)
Agriculture Fosetyl-Al fungicide production Intermediate None
Chemical Industry Phosphite esters (antioxidants, flame retardants) Varies Phosphorus trichloride (alternative route)
Analytical Chemistry Reducing agent (Hg, Au, Ag, I determination) 0.1–1% solution Stannous chloride, hydroxylamine
Dye Industry Reducing agent in dye synthesis Process dependent Sodium dithionite, zinc dust
Metal Treatment Metal surface passivation 1–5% solution Phosphoric acid
Laboratory General reducing reagent 0.1–1 M Sodium sulfite, ascorbic acid

This TDS is prepared in compliance with ISO 11014-1 format and is intended for chemical engineers, water treatment specialists, plastics compounders, agrochemical manufacturers, analytical chemists, and procurement professionals. Certificates of Analysis (CoA), Safety Data Sheets (SDS), reducing power test reports, and sample validation reports are available upon request.

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