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ChemicalBook--->CAS DataBase List--->7664-38-2

7664-38-2

7664-38-2 Structure

7664-38-2 Structure
IdentificationMore
[Name]

Phosphorous acid
[CAS]

7664-38-2
[Synonyms]

EXTRAN AP 21
EXTRAN(R) AP 21
EXTRAN(R) AP21, ACID RINSE DETERGENT WITH PHOSPHORIC ACID
EXTRAN(R) AP21 DETERGENT
FEMA 2900
H3PO4
O-PHOSPHORIC ACID
ORTHOPHOSPHORIC ACID
PHOSPHATE ATOMIC SPECTROSCOPY STANDARD
PHOSPHORIC ACID, ORTHO
PHOSPHORIC ACID, POLY
PHOSPHORIC(V) ACID
PHOSPHOROUS ACID
PHOSPHOROUS ICP STANDARD
PHOSPHORUS ICP STANDARD
U.N. 1805
Acide phosphorique
acidephosphorique
acidephosphorique(french)
acidephosphoriquesolutions
[EINECS(EC#)]

231-633-2
[Molecular Formula]

H3O4P
[MDL Number]

MFCD00011340
[Molecular Weight]

98
[MOL File]

7664-38-2.mol
Chemical PropertiesBack Directory
[Appearance]

Phosphoric acid is a colorless, odorless, crystalline solid or a thick syrupy liquid. Physical state is strength and temperature dependent.
[Melting point ]

~40 °C(lit.)
[Boiling point ]

158 °C(lit.)
[density ]

1.685 g/mL at 25 °C(lit.)
[vapor density ]

3.4 (vs air)
[vapor pressure ]

2.2 mm Hg ( 20 °C)
[FEMA ]

2900
[refractive index ]

n20/D 1.433
[storage temp. ]

no restrictions.
[solubility ]

H2O: soluble
[form ]

Solid or Viscous Liquid
[pka]

2.1-7.2-12.3(at 25℃)
[color ]

≤10(APHA)
[Specific Gravity]

1.7
[Odor]

Odorless
[PH]

<0.5 (100g/l, H2O, 20℃)
[PH Range]

1.5
[Water Solubility ]

MISCIBLE
[Usage]

Phosphorous acid is used for reaction with inorganic and organic products, for water treatment, industrial and agricultural uses. It is also used to bleach industrial and cleaning supplies. Contact
[λmax]

λ: 260 nm Amax: ≤0.05
λ: 280 nm Amax: ≤0.04
[Merck ]

14,7344
[BRN ]

1921286
[Dielectric constant]

61.0
[Exposure limits]

TLV-TWA 1 mg/m3 (ACGIH, MSHA, and OSHA); TLV-STEL 3 mg/m3 (ACGIH).
[InChIKey]

NBIIXXVUZAFLBC-UHFFFAOYSA-N
[LogP]

-2.15
[Uses]

Phosphoric Acid is an acidulant that is an inorganic acid produced by burning phosphorus in an excess of air, producing phosphorus pentoxide which is dissolved in water to form orthophosphoric acid of varying concentrations. it is a strong acid which is soluble in water. the acid salts are termed phosphates. it is used as a flavoring acid in cola and root beer beverages to provide desirable acidity and sourness. it is used as a synergistic antioxidant in vegetable shorten- ings. in yeast manufacture, it is used to maintain the acidic ph and provide a source for phosphorus. it also functions as an acidulant in cheese. it is also termed orthophosphoric acid.
[CAS DataBase Reference]

7664-38-2(CAS DataBase Reference)
[NIST Chemistry Reference]

Phosphoric acid(7664-38-2)
[EPA Substance Registry System]

7664-38-2(EPA Substance)
Safety DataBack Directory
[Hazard Codes ]

C,Xn,T,F
[Risk Statements ]

R34:Causes burns.
R35:Causes severe burns.
R22:Harmful if swallowed.
R39/23/24/25:Toxic: danger of very serious irreversible effects through inhalation, in contact with skin and if swallowed .
R36/38:Irritating to eyes and skin .
R23/24/25:Toxic by inhalation, in contact with skin and if swallowed .
R11:Highly Flammable.
[Safety Statements ]

S7:Keep container tightly closed .
S16:Keep away from sources of ignition-No smoking .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37:Wear suitable protective clothing and gloves .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
S1/2:Keep locked up and out of the reach of children .
S24/25:Avoid contact with skin and eyes .
[RIDADR ]

UN 3453 8/PG 3
[WGK Germany ]

3
[RTECS ]

TB6300000
[F ]

3-10
[TSCA ]

Yes
[HazardClass ]

8
[PackingGroup ]

III
[HS Code ]

28092000
[Safety Profile]

Human poison by ingestion. Moderately toxic by skin contact. A corrosive irritant to eyes, skin, and mucous membranes, and a systemic irritant by inhalation. A common air contaminant. A strong acid. Mixtures with nitromethane are explosive. Reacts with chlorides + stainless steel to form explosive hydrogen gas. Potentially violent reaction with solum tetrahydroborate. Dangerous; when heated to decomposition it emits toxic fumes of POx
[Hazardous Substances Data]

7664-38-2(Hazardous Substances Data)
[IDLA]

1,000 mg/m3
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Hydrogen peroxide-->Celite-->Phosphorus-->Barium hydroxide-->White phosphorus-->ROCK PHOSPHATE-->Phosphate rock powder-->phosphoric acid by wet process-->Ammonium bisulfate-->Sodium molybdate dihydrate-->CALCIUM SULFATE HEMIHYDRATE-->Microvoid filter film
[Preparation Products]

Pyrophosphoric acid-->amphoteric polyacrylamide-->3-METHYLTHIOPHENE-2-CARBONYL CHLORIDE-->Ferric pyrophosphate-->IODOCYCLOHEXANE-->2-ACETYL-5-CYANOTHIOPHENE-->alcohol polyoxyethylene ether phosphoric monoester ethanolamine-->ZINC PHOSPHATE, MONOBASIC-->Aluminium phosphate-->Phosphatizing liquid-->Sodium dihydrogen phosphate-->Cefcapene pivoxil-->Acid modified starch-->Aluminum dihydrogen phosphate-->4-Chromanone-->2-Acetyl-3-methylthiophene-->2-(2-Bromoethyl)-1,3-dioxolane-->4,4'-Bis(bromomethyl)biphenyl-->Phosphoric acid, calcium salt (1:)-->Maddrell's salt for food-->TSP-->Sewerage inhibitor-->Phosphatizing agent-->Starch, phosphate-->4′-Ethoxyacetophenone-->Conditioner for metal surface-->SODIUM PHOSPHOTUNGSTATE-->Monosodium phosphate-->MAGNESIUM HYDROGEN PHOSPHATE TRIHYDRATE-->AMMONIUM PHOSPHOMOLYBDATE-->2-ACETYL-5-IODOTHIOPHENE-->MAGNESIUM PHOSPHATE-->Alendronic acid-->Disodium hydrogen phosphate dihydrate-->ZINC DIHYDROGEN PHOSPHATE-->Phosphomolybdic Acid-->hydration catalyst for propylene-->Tetrabutylammonium phosphate-->non-dip adhesive nodule-holeless honeycomb structural adhesive J-23-2-->Aluminum triphosphate
Hazard InformationBack Directory
[General Description]

A clear colorless liquid or transparent crystalline solid. The pure solid melts at 42.35°C and has a density of 1.834 g/cm3. Liquid is usually an 85% aqueous solution. Shipped as both a solid and liquid. Corrosive to metals and tissue. Used in making fertilizers and detergents and in food processing.
[Reactivity Profile]

PHOSPHORIC ACID(7664-38-2) reacts exothermically with bases. May react with active metals, including such structural metals as aluminum and iron, to release hydrogen, a flammable gas. Can initiate the polymerization of certain classes of organic compounds. Reacts with cyanide compounds to release gaseous hydrogen cyanide. May generate flammable and/or toxic gases in contact with dithiocarbamates, isocyanates, mercaptans, nitrides, nitriles, sulfides, and strong reducing agents. Forms explosive mixture with nitromethane. Reacts violently with sodium tetrahydroborate. In the presence of chlorides can corrode stainless steel to form explosive hydrogen gas. Emits toxic and irritating fumes of oxides of phosphorus when heated to decomposition [Lewis, 3rd ed., 1993, p. 1029].
[Air & Water Reactions]

Soluble in water with small release of heat.
[Health Hazard]

Burns on mouth and lips, sour acrid taste, severe gastrointestinal irritation, nausea, vomiting, bloody diarrhea, difficult swallowing, severe abdominal pains, thirst, acidemia, difficult breathing, convulsions, collapse, shock, death.
[Potential Exposure]

Phosphoric acid is used in the manufacture of fertilizers, phosphate salts; polyphosphates, detergents, activated carbon; animal feed; ceramics, dental cement; pharmaceuticals, soft drinks; gelatin, rust inhibitors; wax, and rubber latex. Exposure may also occur during electropolishing, engraving, photoengraving, lithographing, metal cleaning; sugar refining; and water-treating.
[Fire Hazard]

Non-combustible, substance itself does not burn but may decompose upon heating to produce corrosive and/or toxic fumes. Some are oxidizers and may ignite combustibles (wood, paper, oil, clothing, etc.). Contact with metals may evolve flammable hydrogen gas. Containers may explode when heated.
[First aid]

Move victim to fresh air. Call 911 or emergency medical service. Give artificial respiration if victim is not breathing. Do not use mouth-to-mouth method if victim ingested or inhaled the substance; give artificial respiration with the aid of a pocket mask equipped with a one-way valve or other proper respiratory medical device. Administer oxygen if breathing is difficult. Remove and isolate contaminated clothing and shoes. In case of contact with substance, immediately flush skin or eyes with running water for at least 20 minutes. For minor skin contact, avoid spreading material on unaffected skin. Keep victim warm and quiet. Effects of exposure (inhalation, ingestion or skin contact) to substance may be delayed. Ensure that medical personnel are aware of the material(s) involved and take precautions to protect themselves. Medical observation is recommended for 2448 hours after breathing overexposure, as pulmonary edema may be delayed. As first aid for pulmonary edema, a doctor or authorized paramedic may consider administering a drug or other inhalation therapy.
[Shipping]

UN1805 Phosphoric acid solution, Hazard class: 8; Labels: 8-Corrosive material. UN3543 Phosphoric acid solid, Hazard class: 8; Labels: 8-Corrosive material.
[Incompatibilities]

The substance is a medium strong acid. Incompatible with strong caustics; most metals. Readily attacks and reacts with metals forming flammable hydrogen gas. Do not mix with solutions containing bleach or ammonia. Violently polymerizes on contact with azo compounds; epoxides, and other polymerizable compounds. Decomposes on contact with metals, alcohols, aldehydes, cyanides, ketones, phenols, esters, sulfides, halogenated organics; producing toxic fumes. Corrosive to common metals and possibly to some rubbers and plastics.
[Chemical Properties]

Phosphoric acid is a colorless, odorless, crystalline solid or a thick syrupy liquid. Physical state is strength and temperature dependent.
Concentrated phosphoric acid occurs as a colorless, odorless, syrupy liquid. It has a pleasing acid taste when suitably diluted.
Pure phosphoric acid, also called orthophosphoric acid, is a clear, colorless, mineral acid with moderate strength. It is normally marketed as an aqueous solution of 75–85% in which it exists as a clear, viscous liquid.
Phosphoric acid
Food-grade phosphoric acid is used to acidify foods and beverages. It provides a tangy or sour taste and, being a mass-produced chemical, is available cheaply and in large quantities. Phosphoric acid, used in many soft drinks, has been linked to lower bone density in epidemiological studies. In brief, phosphoric acid is a strong acid and common industrial chemical used in the manufacture of a wide number of products, notably porcelain and metal cleaners, detergents, and fertilisers. It is also used as a food additive and is a major constituent of many soft drinks. Low phosphate concentrations are found in drinking water to which it is added in some areas in order to reduce lead solubility.
[Waste Disposal]

Add slowly to solution of soda ash and slaked lime with stirring, then flush to sewer with large volumes of water.
[Physical properties]

Chemists refer to orthophosphoric acid as phosphoric acid, which is the IUPAC name for this compound. The prefix “ortho” is used to distinguish the acid from other phosphoric acids, which are generally called polyphosphoric acids. Orthophosphoric acid is a nontoxic, rather weak triprotic acid. When pure, it is a solid at STP. Orthophosphoric acid is a very polar molecule which makes it highly soluble in water. The valence state of phosphorous in orthophosphoric acid and other phosphoric acids is +5. Triprotic means that the orthophosphoric acid molecule can dissociate up to three times, producing a hydrogen cation, H+, each time.
[Occurrence]

Phosphoric acid is a natural constituent of many fruits and their juices.
[History]

Phosphoric acid was produced but not identified by alchemists in ancient times. It derives its name from the element phosphorus, which was discovered in 1669 by Henning Brand (1630 1710).Scheele subsequently isolated phosphorus from bone ash and produced phosphoric acid by reacting phosphorus and nitric acid. Scheele's method replaced bone as the main source of phosphorus rather than urine.
John Bennett Lawes (1814 1900) patented a process in 1841 of making superphosphate from bones and later extended his process to phosphates obtained from rock. Superphosphates are made by treating Ca3(PO4)2 with sulfuric acid to make more soluble calcium hydrogen phosphates: Ca3(PO4)2 + 2H2SO4 Ca(H2PO4)2 + 2CaSO4. In this reaction Ca(H2PO4)2 is monobasic calcium phosphate, which is also called superphosphate. Calcium hydrogen phosphates (superphosphates) are more water soluble and therefore more readily available to plants.
[Definition]

ChEBI: A phosphorus oxoacid that consits of one oxo and three hydroxy groups joined covalently to a central phosphorus atom.
[Production Methods]

The major sources of H3PO4 traditionally have been mineral deposits of phosphate rock. Mining operations are extensive in a number of locations, including the United States (Florida), the Mediterranean area, and Russia, among others. The major constituent of most phosphate rocks is fluorapatite, 3Ca3(PO4)2·CaF2. The supply of high-grade phosphates, the raw material of choice for producing high-purity phosphoric acid by the wet process, is rapidly decreasing in some areas.
Two major methods are utilized for the production of phosphoric acid from phosphate rock. The wet process involves the reaction of phosphate rock with sulfuric acid to produce phosphoric acid and insoluble calcium sulfates. Many of the impurities present in the phosphate rock are also solubilized and retained in the acid so produced. While they are of no serious disadvantage when the acid is to be used for fertilizer manufacture, their presence makes the product unsuitable for the preparation of phosphatic chemicals.
In the other method, the furnace process, phosphate rock is combined with coke and silica and reduced at high temperature in an electric furnace, followed by condensation of elemental phosphorus. Phosphoric acid is produced by burning the elemental phosphorus with air and absorbing the P2O5 in water. The acid produced by this method is of high purity and suitable for nearly all uses with little or no further treatment.
[Production Methods]

The majority of phosphoric acid is made by digesting phosphate rock (essentially tricalcium phosphate) with sulfuric acid; the phosphoric acid is then separated by slurry filtration. Purification is achieved via chemical precipitation, solvent extraction, crystallization, or ion exchange.
[Brand name]

Pharmaceutic aid (solvent).
[Hazard]

Phosphoric acid is water soluble and absorbs oxygen readily, and the specific gravity is 1.89, which is heavier than water. It is toxic by ingestion and inhalation and an irritant to the skin and eyes, with a TLV of 1 mg/m3 of air. The four-digit UN identification number is 1805. The NFPA 704 designation is health 3, flammability 0, and reactivity 0. The primary use of phosphoric acid is in chemical analysis and as a reducing agent.
[Flammability and Explosibility]

Nonflammable
[Agricultural Uses]

Phosphoric acid (H3PO4), also known as orthophosphoric acid, is the most significant source of phosphate fertilizers. Phosphoric acid based fertilizers mainly include ammonium phosphate, diammonium phosphate and monoammonium phosphate.
Phosphoric acid is deliquescent and commercially the most important derivative of phosphorus, accounting for over 90% of the phosphate rock mined. The white rhombic solid is highly soluble in water and ethanol, and the concentrated aqueous solution is generally available for use.
Phosphoric acid is used in several industries other than the fertilizer industry. Most elemental phosphorus is converted into phosphoric acid for non-fertilizer use. There are two basic processes for the production of phosphoric acid.
Metaphosphoric acid is obtained by heating phosphoric acid until dense white fumes begin to appear. The product is highly deliquescent and glassy in appearance. Its salts are known as metaphosphates. Orthophosphoric acid is the most common and is used as an important phosphate ingredient in commercial fertilizers.
[Pharmaceutical Applications]

Phosphoric acid is widely used as an acidifying agent in a variety of pharmaceutical formulations. It is used in pharmaceutical products as part of a buffer system when combined with a phosphate salt such as sodium phosphate, monobasic or dibasic. It is also widely used in food preparations as an acidulant, flavor, and synergistic antioxidant (0.001–0.005%) and sequestrant.
Therapeutically, dilute phosphoric acid has been used welldiluted in preparations used in the treatment of nausea and vomiting. Phosphoric acid 35% gel has also been used to etch tooth enamel and to enhance delivery of drugs through the nail.
) Nanosized hydroxyapatite powder was made by combining phosphoric acid with egg shells.
[Industrial uses]

As a cleanser for metals, phosphoric acid produces a light etch on steel, aluminum, or zinc, which aids paint adhesion. Deoxidine is a phosphoric acid cleanser for metals. Nielite D is phosphoric acid with a rust inhibitor, used as a nonfuming pickling acid for steel. Albrite is available in 75, 80, and 85% concentrations in food and electronic grades, both high-purity specifications. DAB and Phosbrite are called Bright Dip grades, for cleaning applications. Phosphoric anhydride, or phosphorus pentoxide, P2O5, is a white, water-soluble powder used as a dehydrating agent and also as an opalizer for glass. It is also used as a catalyst in asphalt coatings to prevent softening at elevated temperatures and brittleness at low temperatures.
[Biochem/physiol Actions]

Phosphoric acid is commonly used in fertilizer industry. It is also used in the manufacture of insecticide and pesticide.
[Safety]

In the concentrated form, phosphoric acid is an extremely corrosive and harmful acid. However, when used in pharmaceutical formulations it is usually very diluted and is generally regarded as an essentially nontoxic and nonirritant material.
The lowest lethal oral dose of concentrated phosphoric acid in humans is reported to be 1286 mL/kg.
(rabbit, skin): 2.74 g/kg
(rat, oral): 1.53 g/kg
[Synthesis]

The elemental phosphorus is burned to produce phosphorous pentoxide (P2O5), which is then hydrated. The heat is then removed and the phosphoric acid (H3PO4) is collected as a fine mist. Another important source of phosphoric acid is from phosphate rocks by treatment with sulfuric acid; this is the so-called wet-acid process. The synthesis of pure phosphoric acid involves several steps including a time-consuming, expensive step, the sublimation of white phosphorus.
[Carcinogenicity]

Phosphoric acid was not mutagenic in bacterial assays.
[storage]

When stored at a low temperature, phosphoric acid may solidify, forming a mass of colorless crystals, comprising the hemihydrate, which melts at 28°C. Phosphoric acid should be stored in an airtight container in a cool, dry place. Stainless steel containers may be used.
[Regulatory Status]

GRAS listed. Accepted as a food additive in Europe. Included in the FDA Inactive Ingredients Database (infusions, injections, oral solutions, topical creams, lotions, ointments and solutions, and vaginal preparations). Included in nonparenteral and parenteral medicines licensed in the UK. Included in the Canadian List of Acceptable Non-medicinal Ingredients.
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

Phosphorous acid(10294-56-1).msds
Questions and Answers (Q&A)Back Directory
[Overview]

Phosphoric acid has a molecular formula of H3PO4. The pure product appears as colorless transparent viscous liquid or oblique crystals, is odorless and tastes very sour. 85% phosphoric acid is colorless and transparent or slightly light, thick liquid. It has a melting point of 42.35 ℃, the proportion of 1.70, high boiling point acid, being miscible with water at any ratio with a boiling point of 213 ℃ (lost 1/2 water), generating pyrophosphoric acid. Being heated to 300 °C into metaphosphoric acid. The relative density is 181.834. It is easily soluble in water, soluble in ethanol. Phosphoric acid is a common inorganic acid, being a moderately strong acid. Its acidity is weaker than sulfuric acid, hydrochloric acid and nitric acid, but stronger than acetic acid, boric acid, carbonic acid and other weak acid.
Phosphoric acid was prepared first by Robert Boyle in 1694 by dissolving phosphorus pentoxide in water. Phosphoric acid is probably the most important compound of phosphorus. It is the second largest inorganic chemical by volume, after sulfuric acid, marketed in the United States. The single most important application of this acid is manufacturing phosphate salts for fertilizers. Such fertilizer phosphates include sodium, calcium, ammonium, and potassium phosphates. Other applications are in metal pickling and surface treatment for removal of metal oxides from metal surfaces; electropolishing of aluminum; as a bonding agent in various refractory products such as alumina and magnesia; as a catalyst in making nylon and gasoline; as a dehydrating agent; in fireproofing wood and fabrics; in lithographic engraving; in textile dyeing; in dental cement; in coagulating rubber latex; in purifying hydrogen peroxide; and as a laboratory reagent. Dilute solutions of phosphoric acid are used as additives to carbonated beverages for a pleasing sour taste. Also, dilute acid is used in refining sugar; as a nutrient; and as a buffering agent in preparing jam, jelly, and antibiotics. The commercial phosphoric acid is 85% (w/w) in strength.
Phosphoric acid also has been used in the manufacture of sodium phosphate, ferric phosphate, and penicillin for the regulation of pH; for the manufacture of zinc phosphate as dental adhesive; its plastic can be used for the catalyst of the phenolic resin condensation; the desiccant during the production of dyes and intermediates; in the printing industry, it can be used for the preparation of the cleaning agent for wiping off the printing plate stains; in match, it can be used for the impregnation of match stick; it can make the burned match stick exist in the carbon-like type instead of ash type; it is more secure upon using; in metallurgical industry, it is used for the production of refractory mud to improve the duration of life of steel surface; it can be used as the coagulation agent of the rubber slurry and the raw material for the production of inorganic binder agent; it can be applied to metal anti-rust paint; used as acid flavoring agent in food industry.
[description]

Phosphoric acid was prepared first by Robert Boyle in 1694 by dissolving phosphorus pentoxide in water. Phosphoric acid is probably the most important compound of phosphorus. It is the second largest inorganic chemical by volume, after sulfuric acid, marketed in the United States.
The single most important application of Phosphoric acid is manufacturing phosphate salts for fertilizers. Such fertilizer phosphates include sodium, calcium, ammonium, and potassium phosphates. Other applications are in metal pickling and surface treatment for removal of metal oxides from metal surfaces; electropolishing of aluminum; as a bonding agent in various refractory products such as alumina and magnesia; as a catalyst in making nylon and gasoline; as a dehydrating agent; in fireproofing wood and fabrics; in lithographic engraving; in textile dyeing; in dental cement; in coagulating rubber latex; in purifying hydrogen peroxide; and as a laboratory reagent. Dilute solutions of phosphoric acid are used as additives to carbonated beverages for a pleasing sour taste. Also, dilute acid is used in refining sugar; as a nutrient; and as a buffering agent in preparing jam, jelly, and antibiotics. The commercial phosphoric acid is 85% (w/w) in strength.
[Preparation]

Low-purity technical grade phosphoric acid for use in fertilizers is produced from phosphate rocks by digestion with concentrated sulfuric acid. The apatite types, primarily consisting of calcium phosphate phosphate rocks, are used: Ca3(PO4)2 + 3H2SO4 + 6H2O → 2H3PO4 + 3(CaSO4•2H2O)
The insoluble calcium sulfate slurry is filtered out. Acid from this wet process is impure but can be purified by various methods. Purification steps involve precipitation, solvent extraction, crystallization, and ion exchange techniques.
Phosphoric acid also can be made by many different methods. Dissolution of phosphorus pentoxide in water and boiling yields phosphoric acid. Pure phosphoric acid can be obtained by burning phosphorus in a mixture of air and steam:
P4 (l) + 5O2 (g) →P4O10 (s)
P4O10 (s) + H2O (g) → 4H3PO4 (l)
The acid also may be prepared by heating violet phosphorus with 33% nitric acid:
4P + 10HNO3 + H2O → 4H3PO4 + 5NO ↑ + 5NO2 ↑
or by heating red phosphorus with nitric acid (1:1). The overall equation is:
P + 3HNO3 → H3PO4 + NO + 2NO2
[Toxicity]

ADI 0 to 70 mg / kg (total phosphate content in terms of phosphorus, FAO / WHO, 2001).
GRAS (FDA, § 182.1073, 2000).
LD501530mg / kg (rat, oral).
In case of daily intake of 2 ~ 4 g, it can cause mild diarrhea. The amount of sour agent used as a cola drink is 0.02% to 0.06%.
Spectrum DetailBack Directory
[Spectrum Detail]

Phosphoric acid(7664-38-2)IR
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

Phosphoricacid,85wt%solutioninwater,foranalysis(7664-38-2)
[Alfa Aesar]

Orthophosphoric acid, 85% w/w aq. soln., ACS(7664-38-2)
[Sigma Aldrich]

7664-38-2(sigmaaldrich)
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