PRODUCTS

PHENYL SALICYLATE

Salol = Phenyl salicylate

CAS Number :118-55-8
EC Number: 204-259-2

Phenyl salicylate or salol is the organic compound with the formula C6H5O2C6H4OH.
Phenyl salicylate is a white solid. It is sometimes used in sunscreens and as an antiseptic.

Production and reactions
The title compound was first synthesized in 1883 by the Polish chemist and doctor Marceli Nencki (who did not publish his findings) and later independently in 1885 by the German chemist Richard Seifert (de) (1861–1919) (who published his findings). ).
It is synthesized by heating salicylic acid with phenol in the presence of phosphoryl chloride.
Phenyl salicylate also results from heating salicylic acid:

2 HOC6H4CO2H → C6H5O2C6H4OH + CO2 + H2O
Transformation requires dehydration and decarboxylation. Heating phenyl salicylate in turn gives xanthone.

2 C6H5O2C6H4OH → 2 C6H5OH + O[C6H4]2CO + CO2
Phenyl salicylate In this conversion, besides carbon dioxide, phenol is also produced.

salo reaction
Phenyl salicylate In the Salol reaction, phenyl salicylate reacts with o-toluidine in 1,2,4-trichlorobenzene to the corresponding amide o-salicylotoluide at elevated temperatures. Salicylates are a type of medicine.

Medical
Phenyl salicylate has been used as an antiseptic based on antibacterial activity upon hydrolysis in the small intestine.

Phenyl salicylate acts as a mild analgesic.

History
Swiss physician Hermann Sahli (sometimes spelled "Saly") (1856–1933) sought a substitute for sodium salicylate, which was used to treat rheumatoid arthritis but was not tolerated by some patients.
That's why Dr. Sahli asked Polish chemist and doctor Marceli Nencki from Bern, Switzerland, if Nencki knew of a salicylate compound that was devoid of the side effects of sodium salicylate.
Nencki proposed phenyl salicylate, which he synthesized circa 1883.
Nencki had not published his findings while investigating how phenyl salicylate behaves in the body.
Meanwhile, the German chemist Richard Seifert (de) (1861–1919), a student of the German chemist Rudolf Wilhelm Schmitt (de) (1830-1898), independently synthesized phenyl salicylate in 1885.
In 1885, Seifert accepted a position at (de) the Heyden chemical company in Radebeul, Germany, which produced salicylic acid.
The United States granted Nencki and Seifert a patent for the production of phenyl salicylate, while Germany granted a patent to the company Nencki and Heyden for its production.
The Heyden company later sold phenyl salicylate as a medicine under the trade name "Salol", an abbreviation for "salicylate of phenol."
Among other applications, Salol was used as an orally administered antiseptic for the small intestine where the compound was hydrolyzed to salicylic acid and phenol.

Names
Preferred IUPAC name
Phenyl 2-hydroxybenzoate
Other Names: Salo

identifiers
CAS Number :118-55-8
chebi: 34918
ChEMBL    : ChEMBL1339216
ChemSpider: 8058 ☒
ECHA Information Card:    100.003.873
EC Number    : 204-259-2
Barrel : C14163    ☒
Cage : C026041
PubChem Client ID    : 8361
UNII    : 28A37T47QO control
CompTox Control Panel (EPA)    : DTXSID6021957

Features
Chemical formula:    C13H10O3
Molar mass:    214.22 g/mol
Appearance:    White solid
Density    : 1.25 g/cm3
Melting point    : 41.5 °C (106.7 °F; 314.6 K)
Boiling point    : 173 °C (343 °F; 446 K) at 12 mmHg
Solubility in water:    1 g/6670 mL
Magnetic susceptibility (χ):    -123.2·10−6 cm3/mol
Refractive index (nD):    1.615[2]

Pharmacology
ATC code: G04BX12 (WHO)

hazards
Flash point: 137.3[2] °C (279.1 °F; 410.4 K)

Phenyl salicylate is a benzoate ester, the phenyl ester of salicylic acid.
Also known as salol, it can be formed by heating salicylic acid with phenol and is used in the manufacture of some polymers, lacquers, adhesives, waxes and lacquers.
Phenyl salicylate acts as an ultraviolet filter. It is a benzoate ester, a member of phenols and a member of salicylates.
Phenyl salicylate is derived from a salicylic acid.

Phenyl salicylate is a phenyl ester of 2-hydroxybenzoic acid.
Phenyl salicylate is used in some manufacturing processes of polymers, lacquers, adhesives, waxes and lacquers.
Phenyl salicylate is an active ingredient in some pharmaceutical products as a mild analgesic to relieve pain by releasing salicylate.
Phenyl salicylate can also be found in some antiseptic agents.
Phenyl salicylate is synthesized by heating salicylic acid with phenol [MSDS]. Phenyl salicylate is used as a food additive in the USA.
This compound belongs to the class of organic compounds known as depsids and depsidones.
These are either a polyphenolic compound consisting of two or more monocyclic aromatic units linked by an ester bond (depsid) or polycyclic compounds, a compound containing the depsidon structure (depsidone).

This compound belongs to the class of organic compounds known as depsids and depsidones.
These are polyphenolic compounds, a polyphenolic compound consisting of two or more monocyclic aromatic units linked by an ester bond (depsid), or a compound containing the depsidon structure (depsidone).

Phenyl salicylate has several medicinal uses.
Phenyl salicylate can be used as an analgesic to relieve pain, an antiseptic with antibacterial action, and also a type of antipyretic for the treatment of fever.
Phenyl salicylate is also used to treat inflammation of the lower urinary tract.
Phenyl salicylate is no longer widely applied in human medical practice, but is still used in veterinary medicine MSDS.

When combined with methenamine, benzoic acid, phenyl salicylate, methylene blue, and hyoscyamine sulfate, it is used to relieve discomfort, pain, frequent urination, and urinary tract cramps/spasms caused by a urinary tract infection or urinary tract infection. a diagnostic procedure

Phenyl Salicylate distribution volume
Steady-state plasma salicylate concentrations increase more proportionally with increasing dosages; The time required to reach steady state increases with increasing daily dose.
Dosing intervals of 8-12 hours are sufficient to maintain plasma salicylate concentrations within the normal range of therapeutic anti-inflammatory concentrations.

Metabolism
It is hydrolyzed to salicylic acid. Salicylic acid elimination kinetics are dependent on drug concentration due to the limited capacity of two major biotransformation pathways: formation of salicylic acid and salicylic phenolic glucuronide.

The metabolism of this drug, like other salicylates, occurs mainly in the liver.

Salicylic acid metabolism occurs via glucuronide formation (to produce salicyluric acid) and salicyl phenolic glucuronide formation by conjugation with glycine (to produce salicyluric acid) and oxidation to form gentisic acid.
The rate of formation of salicylic phenolic glucuronide and salicyluric acid is readily saturated at low salicylic acid concentrations, and their formation can be described by Michaelis-Menten kinetics.

way of elimination
Please refer to Aspirin for elimination route.
Half life
Mean half-life of 1.1 hours
Adverse effects can be divided into several categories
Eyes: irritation
Skin: skin irritation
Cardiovascular: rapid pulse, flushing
Central Nervous System — blurred vision, dizziness
Respiratory—shortness of breath or difficulty breathing, irritation of the respiratory system
Genitourinary — difficult voiding, acute urinary retention
Gastrointestinal - dry mouth, nausea/vomiting

Synonyms: Salo
Linear Formula: 2-(HO)C6H4CO2C6H5
CAS Number:118-55-8
Molecular Weight: 214.22
Beilstein:393969
EC Number: 204-259-2
MDL number:MFCD00002213
Flavis number: 9.689

analysis: ≥99%
bp: 172-173 °C/12 mmHg (lights up)
width: 41-43 °C (lit)
SMILES string: Oc1cccccc1C(=O)Oc2cccccc2
InChI: 1S/C13H10O3/c14-12-9-5-4-8-11(12)13(15)16-10-6-2-1-3-7-10/h1-9.14H
InChI switch: ZQBAKBUEJOMQEX-UHFFFAOYSA-N

Name:    phenyl 2-hydroxybenzoate
CAS Number:    118-55-8
ECHA EINECS - REACH Pre-Registration:    204-259-2
FDA UNII:    28A37T47QO
Nikkaji Web:    J5300G
Beilstein Number:    0393969
MDL:    MFCD00002213
CoE Number:    11814
XlogP3:    3.80 (estimated)
Molecular Weight:    214.22030000
Formula:    C13 H10 O3
BioActivity Summary:    listing

A benzoate ester, which is the phenyl ester of salicylic acid.
Also known as salol, it can be formed by heating salicylic acid with phenol and is used in the manufacture of some polymers, lacquers, adhesives, waxes and lacquers.

Air and Water Reactions
It is insoluble in water.
Fire danger
Flash point data are not available for this chemical, but it is likely flammable. (NTP, 1992)
health hazard
SYMPTOMS: Signs of exposure to this compound include skin, eye and mucous membrane irritation.

ACUTE/CHRONIC HAZARDS: This compound is a mild skin and eye irritant. (NTP, 1992)
Reactivity Profile
Not compatible with brominated water, ferric salts, camphor, phenol, chloral hydrate, monobrominated camphor, thymol or urethane in trituration. (NTP, 1992).
The Reagents Below Belongs to the Group(s)

Fire extinguishing
Fires involving this material can be controlled with a dry chemical, carbon dioxide or Halon extinguisher. (NTP, 1992)
Non-Fire Intervention
MINOR SPILLS AND LEAKAGE: If a spill occurs while working with this chemical, REMOVE ALL SOURCES OF FIRE FIRST, then moisten the solid spill with ethanol and transfer the moistened material to a suitable container.
Use absorbent paper moistened with ethanol to remove any remaining material.
Seal absorbent paper and any clothing that may be contaminated in a vapor-proof plastic bag for final disposal.
Wash all solvent-contaminated surfaces with ethanol, then wash with a soap and water solution.
Do not re-enter the contaminated area until the Security Officer (or other responsible person) has verified that the area has been properly cleaned.

STORAGE PRECAUTIONS: You should store this material in the refrigerator. (NTP, 1992)
protective clothing
RECOMMENDED RESPIRATOR: Where pure test chemical is weighed and diluted, use a NIOSH approved half-face respirator equipped with an organic vapor/acid gas cartridge (specific for organic vapors, HCl, acid gas and SO2) with dust/mist filter. (NTP, 1992)
DuPont Tychem® Suit Fabrics
No information available.
First aid
EYES: First check if the victim has contact lenses and remove them if they are. While simultaneously calling a hospital or poison control center, flush the victim's eyes with water or normal saline for 20 to 30 minutes.
Do not put any ointment, oil, or medication in the victim's eyes without specific instructions from a physician.
Even if no symptoms (such as redness or irritation) develop, IMMEDIATELY transport the victim to hospital after rinsing eyes.

SKIN: IMMEDIATELY flush affected skin with water while removing and isolating all contaminated clothing. Gently wash all affected skin areas with soap and water.
If symptoms such as redness or irritation occur, IMMEDIATELY call a doctor and be prepared to transport the victim to hospital for treatment.

INHALATION: IMMEDIATELY leave contaminated area; Take deep breaths for fresh air.
If symptoms (such as wheezing, coughing, shortness of breath or burning in the mouth, throat or chest) develop, call a doctor and be prepared to transport the victim to hospital.
Provide appropriate respiratory protection to rescuers entering an unknown atmosphere.
A Self-Contained Breathing Apparatus (SCBA) should be used whenever possible; otherwise, use a higher or equal level of protection than recommended under Protective Clothing.

INGESTION: DO NOT induce vomiting. If the victim is conscious and not convulsing, give 1 or 2 glasses of water to dilute the chemical and IMMEDIATELY call a hospital or poison control center.
If advised by a doctor, be prepared to transport the victim to the hospital.
If the victim is having a seizure or is unconscious, do not give anything by mouth, make sure the airway is clear, and lay the victim on their side with the head lower than the body.
DON'T MAKE VOMITING. IMMEDIATELY transport the victim to the hospital. (NTP, 1992)

Phenyl salicylate, also known as salol or musol, belongs to the class of organic compounds known as depsids and depsidones.
Phenyl salicylate is a polyphenolic compound consisting of two or more monocyclic aromatic units connected by an ester bond (depsid) or polycyclic compounds, a compound containing the depsidon structure (depsidone).
Phenyl salicylate is a mild, sweet and balmy-tasting compound.
Phenyl salicylate is a potentially toxic compound. Phenyl salicylate is used as a food additive.
Phenyl salicylate is hydrolyzed to salicylic acid. It is used in the treatment of inflammation in the lower urinary tract.

It belongs to the class of organic compounds known as depsids and depsidones.
These are either a polyphenolic compound consisting of two or more monocyclic aromatic units linked by an ester bond (depsid) or polycyclic compounds, a compound containing the depsidon structure (depsidone).

Phenyl salicylate Properties
Melting point: 41-43 °C (lights up)
Boiling point: 172-173 °C/12 mmHg (lights up)
Density 1,250g/cm3
FEMA: 3960 | phenyl salicylate
refractive index: 1.5090 (estimated)
Flash point: >230 °F
storage temperature: 2-8°C
Solubility : dioxane: 0.1 g/mL, clear, colorless
form : Fine Crystalline Powder
pka: 8.71±0.10(estimated)
White color
Solubility in Water: It is soluble in alcohol, ether, chloroform, turpentine, acetone and benzene.
It is slightly soluble in chloroformbenzene. It is insoluble in water.
Price: 14.7310
JECFA Number: 736
BRN: 393969
Stability: Photosensitive. Incompatible with strong oxidants. flammable.
Food Added Substances (formerly EAFUS): Phenyl Salicylate
CAS Database Reference : 118-55-8(CAS Database Reference)
FDA 21 CFR: 177.11010; 310,545
EWG's Meal Ratings: 1-3
FDA UNII: 28A37T47QO
ATC code: G04BX12
NIST Chemistry Reference: Benzoic acid, 2-hydroxy-, phenyl ester(118-55-8)

Phenyl salicylate, 99%, C13H10O3, CAS Number-118-55-8, salol, salphenyl, phenyl salicylate, 2-phenoxycarbonylphenol, salicylic acid, phenyl ester, benzoic acid, 2-hydroxy-, phenyl ester, phenyl-2-hydroxybenzoate , musol, phenol salicylate, 2-hydroxybenzoic acid phenyl ester, 250g, 98.5% min. (GK)

The phenyl salicylate Thermo Scientific branded product was originally part of the Acros Organics product portfolio.
Some documents and label information may refer to the old brand.

• CosIng database:
- perfumery: used for perfume and aromatic raw materials.
- antimicrobial: helps control the growth of microorganisms on the skin.
- denaturant: makes cosmetics tasteless. Mostly added
to cosmetics containing ethyl alcohol.

• Other:
- UV filtering without demanding protection against UV damage, instead protection against, for example, chapped lips.
- Antibacterial additive in mouthwash to control bacterial growth that can cause minor bleeding in the gums (gingivitis). See also the heading “medical products” in the text below.
- Emollient – smooth dry skin; hand and face cream
- Prophylactic use - It is not allowed to be used as an active ingredient in products similar to medicinal products, but as a claim from the cosmetic industry as it is on the limit of medicinal products.

Applied PS concentrations
perfume

It is based on the assumption that Phenyl Salicylate is 0.02% and the fragrance blend is used at 20% in a consumer product.
Antibacterial 1.5% salol, the amount requested by a Norwegian industrial company for use in an oral hygiene product.
UV filtering Usage levels: 2 – 10%; for example 10% in a lip product (“ointment” for chapped lip (Appendix 1 and references herein).
- Limited applications at present other than for perfumery purposes, but PS is still used in mouthwash, hairspray and conditioners; moisturizers or semi-solid sticks for dry skin, chapped hands and feet, for example. An online search in March 2011 showed at least 10 concrete products containing PS.
Examples of cosmetic products containing PS are listed in Appendix 2. EWG Skin Deep Cosmetic Database
It contained zero products with PS, and the German database (Codecheck.info) contained only one product with PS.

medical products
- PS has antiseptic effects for intestinal release in tablet formulations ("coatings").
- PS is also a mild analgesic, antipyretic, anti-rheumatic agent (similar to other salicylates such as aspirin).
- used against PS cheilitis (red, blistering, itchy rash chapped lips susceptible to Staphylococcus infections); products against sore throat; laryngitis. (Council of Europe, 2006; (Chemicalland [online]).

Other products
Once used in sunscreens, Phenyl Salicylate is today mostly used in the manufacture of some polymers, polishes, adhesives, waxes and polishes.
Phenyl Salicylate stabilizes plastic against degradation by blocking UV light penetrating plastic and cosmetic packaging and also has some plasticizing properties.

Where is phenyl salicylate found?
Phenyl salicylate is used in the manufacture of polishes, adhesives, waxes and polishes.

What are some products that may contain phenyl salicylate?
adhesives
varnishes
varnishes

A clinician's perspective.
Additional resources and links for phenyl salicylate.
To submit resources or links, please complete the application form at the top of this page.

Salicylic acid, also called ortho-hydroxybenzoic acid, is a white, crystalline solid primarily used in the preparation of aspirin and other pharmaceutical products.
Phenyl salicylate free acid occurs naturally in many plants, especially in small amounts in various Spiraea species.
Phenyl salicylate methyl ester is also widely found in nature; It is the main component of wintergreen oil.
Salicylic acid was first prepared from salicylaldehyde in 1838 by Italian chemist Raffaele Piria.
In 1860, German chemists Hermann Kolbe and Eduard Lautemann discovered a synthesis based on phenol and carbon dioxide.
Today the compound is made from dry sodium phenoxide (sodium phenolate) and carbon dioxide, then treated with acid.

Salicylic acid esterified with methanol in the presence of an acid catalyst yields methyl salicylate, a synthetic wintergreen oil used as a flavoring agent.
Treatment of salicylic acid with phenol yields phenyl salicylate, which is used for sunburn creams and enteric-coated pills and is used to make salicylanilide for use as a fungicide and mildew inhibitor.
Salicylic acid is a component of preparations used to combat warts, corns, calluses and various skin diseases.
Sodium salt is used in the manufacture of certain classes of paints.

Pure salicylic acid crystallizes from hot water as white needles that sublimate intact at temperatures up to 155 °C (311 °F) and melt at 159 °C (318 °F). Above 200 °C (392 °F), acid decomposes into phenol and carbon dioxide.

Who should not take phenyl salicylate?
Phenyl salicylate is contraindicated with this medicine for the following conditions. Consult your doctor if you have any of the following:

Conditions:
thyrotoxicosis
diabetes
low vitamin K levels
anemia
hemophilia
decrease in the blood clotting protein prothrombin
increased risk of bleeding due to a clotting disorder
increased risk of bleeding
thrombotic thrombocytopenic purpura, a type of blood disease
nasal polyp
gastroesophageal reflux disease
stomach or intestinal ulcer
a type of stomach irritation called gastritis
liver problems
severe liver disease
bleeding of the stomach or intestines
decreased kidney function
visible water retention
pregnancy
A patient producing milk and breastfeeding

Explanation
Phenyl salicylate is used as a food additive [EAFUS] ("EAFUS: Anything Added to Food in the United States.
Phenyl salicylate belongs to the family of Hydroxybenzoic Acid Derivatives.
These are compounds containing a hydroxybenzoic acid (or a derivative) with a benzene ring carrying a carboxylic acid.

Compound Type
Ester
Ether
food additive
Food Toxin
metabolism
organic compound
synthetic Compound

Phenyl salicylate (also known as Salol) is an organic compound.
These phenyl salicylate crystals are used in school labs to demonstrate how cooling rates affect crystal size in igneous rocks.

Title: Phenyl Salicylate
CAS Registry Number: 118-55-8
CAS Name: 2-Hydroxybenzoic acid phenyl ester
Trademarks: Salol
Molecular Formula: C13H10O3
Molecular Weight: 214.22
Percent Composition: C 72.89%, H 4.71%, O 22.41%
Literature References: Made by the action of phosphorus oxychloride on a mixture of phenol and salicylic acid.
Properties: White, small crystals or crystalline powder; pleasant aromatic smell and taste. d 1.25; width 41-43°; bp12 173°.
One gram dissolves in 6670 ml of water, 6 ml of alcohol, 1.5 ml of benzene, 5 ml of amyl alcohol, 10 ml of paraffin, 4 ml of almond oil.
Sol in acetone, chloroform, ether, oils; Very little sol in glycerol. Solubility in g/100 g at 25°: absolute ethanol 53; ethyl acetate 470; methyl ethyl ketone 620; toluene 460; Stoddard solver 88; water less than 0.1%. Incompatible.
Bromine water, iron salts; camphor in trituration, monobrominated camphor, phenol, chloral hydrate, thymol or urethane.
Melting point: mp 41-43°
Boiling point: bp12 173°
Density: d 1.25
Use: In the manufacture of various polymers for the plastics industry, as well as in varnishes, adhesives, waxes, varnishes.
In sunscreens and creams.
As a light absorber to prevent discoloration of plastics. It has some plasticizing properties.
Therap-Cat: Analgesic, antipyretic, anti-inflammatory.
Therap-Cat-Vet: Used externally as a disinfectant, internally as an intestinal antiseptic and antipyretic.
Keywords: Analgesic (Non-Narcotic); Anti-inflammatory (Nonsteroidal); Salicylic Acid Derivatives; antipyretic

Explanation
synonym: hello
Formula: C13H10O3
Formula Weight: 214.22
CAS No.: 118-55-8
Storage Code: Green—general chemical storage

Laboratory Grade - Medium purity. It is suitable for educational laboratories. Use for qualitative analysis, not quantitative analysis.

This product is specially produced for use in science laboratories; Certificate of analysis is not available.

The mechanism of hydrolysis of phenyl salicylate and catechol monobenzoate in neutral and alkaline solutions was investigated.
It was concluded that phenyl salicylate provides general intramolecular base catalysis of the ionized phenolic group in the non-buffer-catalyzed portion of these reactions.

Eyes: Immediately flush eyes with excess water for 15 minutes, occasionally lifting upper and lower eyelids.
Skin: Immediately flush skin with excess water for 15 minutes while removing contaminated clothing.
Ingestion: Call Poison Control immediately. Rinse mouth with cold water. Give the victim 1-2 glasses of water or milk to drink.
Try to vomit immediately.
Inhalation: Remove to fresh air. If not breathing, give artificial respiration.

Emits pungent fumes when heated to decomposition.
Protective equipment and precautions for firefighters: Use foam or dry chemical to extinguish fire.
Firefighters must wear full firefighting gear and respiratory protection (SCBA). Cool the container with water spray.
The material is not susceptible to mechanical impact or static discharge.

Handling: Use with adequate ventilation and do not breathe dust or vapours.
Avoid contact with skin, eyes or clothing. Wash your hands thoroughly after handling.
Storage: Store [Green Storage] in General Storage with other items that do not have specific storage hazards.
Store in a cool, dry, well-ventilated, locked warehouse away from incompatible materials.

Use ventilation to keep airborne concentrations below exposure limits.
Have approved eyewash facility, safety shower and fire extinguishers available.
Wear chemical-resistant clothing such as chemical splash goggles and gloves and apron. Wash hands thoroughly after handling material and before eating or drinking. Use NIOSH approved respirator with powder cartridge.
Exposure guidelines: Phenyl Salicylate: OSHA PEL: N/A, ACGIH: TLV: N/A, STEL: N/A.

C13H10O3, a white, crystalline, aromatic powder produced by the interaction of salicylic acid and phenol, is used as a preservative, as a light absorber in sunscreen preparations, and primarily as an antipyretic and antiseptic in medicine; hello

What is phenyl salicylate and where is it found?
Phenyl salicylate is used as an analgesic, antipyretic and rheumatic agent.
Phenyl salicylate is also used in the manufacture of polymer plastics, lacquers, waxes, lacquers, adhesives.
It is found in cosmetics, some sun oils and creams. It can be found in some disinfectants and intestinal antiseptic agents for veterinary use.
Further research may identify additional product or industrial uses for this chemical.

What else is phenyl salicylate called?
Phenyl salicylate chemical can be defined by different names including: 2-Hydroxybenzoic acid phenyl ester 2-Phenoxycarbonylphenol, Benzoic acid, 2-hydroxy-, phenyl ester Phenylester kiseline salicilov, Mussol, Phenol salicylate, Phenyl 2 hydroxybenzoate, Salol, Salfenil Manufacturers chemicals It may not be a complete list as it has stripped and deleted product lines.

INCI name: phenyl salicylate
EINECS/ELINCS number: 204-259-2
Functions (INCI)
Antimicrobial: It slows down the growth of microorganisms on the skin and prevents bacterial growth.
Denaturant: Makes cosmetics tasteless. Mainly added to cosmetics containing ethyl alcohol
Perfume: Used for perfume and aromatic raw materials

Uses of Phenyl Salicylate
Phenyl Salicylate is used to prevent:

ache
Phenyl salicylate medication may be prescribed for other uses. Ask your doctor or pharmacist for more information.

Other urological
Phenyl Salicylate Interactions
This is not a complete list of Phenyl Salicylated drug interactions.
Ask your doctor or pharmacist for more information.

Phenyl Salicylate and Pregnancy
Tell your doctor if you are pregnant or planning to become pregnant.

The FDA classifies drugs based on safety for use during pregnancy.
Five categories - A, B, C, D and X - are used to classify possible risks to an unborn baby when a drug is taken during pregnancy.

Phenyl salicylate, also called Salol, has several medicinal properties.
Phenyl salicylate can serve as an analgesic, that is, it relieves pain, as an antiseptic, that is, it has antibacterial properties, and can be used as an antipyretic, that is, to treat fever.
Some of the medical uses of phenyl salicylate include an external disinfectant, an active ingredient in sunscreens, and an oral medication to treat urinary tract pain.
Phenyl salicylate can also be found in the enteric coating of pills and mixed with alcohol or oils to create a topical treatment for inflammation.

Phenyl Salicylate, Crystal, Purified is used in the production of some polymers, polishes, adhesives, waxes and polishes.
Purified Grade describes chemicals of good quality where there are no official standards and are normally limited to inorganic chemicals.

Synonyms :
phenyl salicylate
118-55-8
PHENYL 2-HYDROXYBENZOATE
hello
phenol salicylate
salphenyl
Mosol
Benzoic acid, 2-hydroxy-, phenyl ester
2-phenoxycarbonylphenol
Salicylic acid, phenyl ester
2-Hydroxybenzoic acid phenyl ester
Phenyl-2-hydroxybenzoate
2-Hydroxy-benzoic acid phenyl ester
Fenylester kyseliny salicylove
MGK 33406
Salicylic Acid Phenyl Ester
UNII-28A37T47QO
Seesorb 201
Seesorb K 201
2-Hydroxybenzoic acid, phenyl ester
MFCD00002213
SHEBI:34918
28A37T47QO
NSC33406
NSC-33406
NCGC00090887-02
DSSTox_CID_1957