PRODUCTS

2-METHYLBENZOIC ACID

2-Methylbenzoic acid is an aromatic carboxylic acid with a methyl group in the ortho position, widely used as a versatile intermediate in the synthesis of dyes, pigments, esters, agrochemicals, and pharmaceuticals.
2-Methylbenzoic acid is commonly synthesized by the oxidation of o-xylene, converting one of the methyl groups on the aromatic ring into a carboxylic acid group.
2-Methylbenzoic acid's chemical stability, reactivity, and ability to enhance the performance of functional materials make it valuable across chemical, pharmaceutical, and industrial manufacturing sectors.

CAS Number: 122-79-2
EC Number: 204-575-0
Molecular Formula: C8H8O2
Molecular Weight: 136.15 g/mol

Synonyms: Suberic acid, Octanedioic acid, Octane-1,8-dicarboxylic acid, Octane-1,8-dioic acid, 1,8-Octanedicarboxylic acid, n-Octanedicarboxylic acid, n-Octanedioic acid, 1,8-Dicarboxyoctane, 1,8-Dioctanedioic acid, 1,8-Dioic octane acid, Octane α,ω-dicarboxylic acid, 1,8-Di-carboxylic octane, 1,8-Octanedioic acid, 1,8-Octanoic diacid, α,ω-Octanedioic acid, α,ω-Dicarboxyoctane, α,ω-Dioic octane acid, n-Octane α,ω-dicarboxylic acid, 1,8-Dicarboxylic octane, 1,8-Octane diacid, 1,8-Octanedioate (ion form), Octane-1,8-bis(carboxylic acid), Octane-1,8-biscarboxylate, Octane dicarboxylate, 1,8-Di-carboxyoctane, 1,8-Octanedicarboxylate, Octane-1,8-biscarboxylic acid, Octane-1,8-biscarboxylic, Octane-1,8-COOH, Octanedioic acid (C8 diacid), Octane-dioic acid, Octane-dicarboxylic acid, n-Octane-1,8-dicarboxylic acid, C8 Dicarboxylic acid, Suberic acid (common name), Dioctane diacid, Dioctane dicarboxylic acid, Octane α,ω-diCOOH, Octane-1,8-(COOH)₂, 1,8-Octane-bis(carboxylic acid), Octane-biscarboxylic acid, Octane α,ω-biscarboxylic acid, C8HOOC acid, Octanedioate, n-Octanedicarboxylate, n-Octane-dioic acid, Octane-1,8-biscarboxyl, Octane-1,8-(diacid), Octane-1,8-bis(acid), Suberate (salt form of suberic acid)Synonyms:, (Acetyloxy)benzene, 100843-EP2301983A1, 100843-EP2371831A1, 122-79-2, 355G9R500Y, 4-06-00-00613 (Beilstein Handbook Reference), A0043, ACETATE, PHENYL, Acetates, acetic acid phenyl, Acetic acid phenyl ester, Acetic acid, phenyl ester, ACETIC ACID, PHENYLESTER, Acetic acid,phenyl ester, Acetic acid-phenyl ester, Acetoxybenzene, Acetyl phenol, Acetylphenol, Actate de phnyle, AI3-01972, AKOS002710242, bmse000481, bmse010117, BRN 0636458, C00548, CHEBI:8082, CHEMBL289559, CS-0102517, CS-O-10949, D88203, DTXCID4030178, DTXSID3051626, EC 204-575-0, EINECS 204-575-0, FEMA 3958, FEMA NO. 3958, Fenylester kyseliny octove, Fenylester kyseliny octove [Czech], FT-0659102, FT-0673718, HSDB 2667, HY-128733, MFCD00008699, NCI60_002262, NSC 27795, NSC-27795, NSC27795, Phen-d5-ol, acetate, Phenol acetate, phenoxy ethan-1-one, PHENYL ACETATE, PHENYL ACETATE [FHFI], PHENYL ACETATE [HSDB], PHENYL ACETATE [MI], Phenyl acetate, 99%, Phenyl acetate, analytical standard, Phenyl ester of acetic acid, PhOAc, PIPERAZINECITRATEHYDRATE, PS-5400, Q419645, QY9, SCHEMBL35500, STK022563, UNII-355G9R500Y, W-109455, WLN: 1VOR, 2-Phenylacetate, Benzeneacetate, Benzeneacetic acid, ion(1-) [ACD/Index Name], BENZYLFORMATE, Phenylacetat [German] [ACD/IUPAC Name], Phenylacetate [ACD/IUPAC Name] [Wiki], Phénylacétate [French] [ACD/IUPAC Name], Phenylethanoate, w-Phenylacetate, ω-Phenylacetate, 103-82-2 [RN], 2-phenylethanoate, 3539899 [Beilstein], acetate, phenyl-, A-PHENYL-ACETATE, phenylacetate anion, phenylacetate(1-), phenylacetic acid anion, 122-79-2 [RN], 204-575-0 [EINECS], 355G9R500Y, 636458 [Beilstein], Acétate de phényle [French] [ACD/IUPAC Name], Acetic acid phenyl ester, Acetic acid, phenyl ester [ACD/Index Name], AJ2800000, MFCD00008699 [MDL number], Phenyl acetate [ACD/IUPAC Name] [Wiki], Phenyl-acetat [German] [ACD/IUPAC Name], (2,3,4,5,6-Pentadeuteriophenyl) acetate, [122-79-2] [RN], 1072946-32-7 [RN], 1072946-33-8 [RN], 122-84-9 [RN], 204-578-7 [EINECS], 22705-26-6 [RN], 2-Phenylacetate, 4-06-00-00613 [Beilstein], 4-06-00-00613 (Beilstein Handbook Reference) [Beilstein], 4-08-00-00460 [Beilstein], 4-13-00-00137 [Beilstein], 4'-Methoxyphenyl-2-propanone, Acetic acid phenyl ester; Phenyl ethanoate, Acetic acid, phenylester, Acetic acid-phenyl ester, Acetic acid-phenyl ester, Acetoxybenzene, Acetyl phenol, EINECS 204-575-0, FEMA 3958, Fenylester kyseliny octove, Fenylester kyseliny octove [Czech], MFCD03792523 [MDL number], o-Acetylphenol, PHENOL ACETATE, phenyl acetate on polystyrene, ca 4 mmol/g, PHENYL ACETATE|PHENYL ACETATE, Phenyl Acetate-d5, phenyl acetic acid, Phenyl ester of acetic acid, phenyl ethanoate, Phenylacetate [ACD/IUPAC Name] [Wiki], PS-5400, QY9, UNII:355G9R500Y, UNII-355G9R500Y, WLN: 1VOR

2-Methylbenzoic acid is the ester of phenol and acetic acid.
2-Methylbenzoic acid can be produced by reacting phenol (Which can be produced by decarboxylation of aspirin)with acetic anhydride or acetyl chloride.

2-Methylbenzoic acid can be separated into phenol and an acetate salt, via saponification: heating the 2-Methylbenzoic acid with a strong base, such as sodium hydroxide, will produce phenol and an acetate salt (sodium acetate, if sodium hydroxide were used).

2-Methylbenzoic acid is an aromatic fatty acid metabolite of phenylalanine with potential antineoplastic activity.
Naturally occurring in mammals, 2-Methylbenzoic acid induces differentiation, growth inhibition, and apoptosis in tumor cells.

2-Methylbenzoic acid mechanisms of action include decreased protein prenylation, activation of the peroxisome proliferation-activated receptors, inhibition of DNA methylation, and depletion of glutamine.
2-Methylbenzoic acid belongs to the class of organic compounds known as phenol esters.

These are aromatic compounds containing a benzene ring substituted by a hydroxyl group and an ester group.
2-Methylbenzoic acid has a phenolic-like taste.

2-Methylbenzoic acid is an acetate ester obtained by the formal condensation of phenol with acetic acid.
2-Methylbenzoic acid is a member of 2-Methylbenzoic acids and a member of benzenes.
2-Methylbenzoic acid is functionally related to a phenol.

2-Methylbenzoic acid is a natural product found in Euglena gracilis and Arabidopsis thaliana with data available.
2-Methylbenzoic acid is a metabolite found in or produced by Saccharomyces cerevisiae.

2-Methylbenzoic acid is the ester of acetic acid and phenol and used most often as a solvent.
Ungraded products supplied by Spectrum are indicative of a grade suitable for general industrial use or research purposes and typically are not suitable for human consumption or therapeutic use.

2-Methylbenzoic acid is registered under the REACH Regulation but is not currently being manufactured in and / or imported to the European Economic Area.
2-Methylbenzoic acid is used at industrial sites and in manufacturing.

2-Methylbenzoic acid, belongs to benzene and substituted derivatives class of compounds.
Those are aromatic compounds containing one monocyclic ring system consisting of benzene.

2-Methylbenzoic acid is slightly soluble (in water) and a weakly acidic compound (based on its pKa).
2-Methylbenzoic acid can be synthesized from acetic acid.

2-Methylbenzoic acid is also a parent compound for other transformation products, including but not limited to, hydratropic acid, 2,4,5-trihydroxyphenylacetic acid, and mandelamide.
2-Methylbenzoic acid is a sweet, civet, and floral tasting compound and can be found in a number of food items such as hyssop, cowpea, endive, and shea tree, which makes 2-Methylbenzoic acid a potential biomarker for the consumption of these food products.

2-Methylbenzoic acid can be found primarily in most biofluids, including cerebrospinal fluid (CSF), saliva, feces, and blood.
2-Methylbenzoic acid exists in all living species, ranging from bacteria to humans.

In humans, 2-Methylbenzoic acid is involved in the 2-Methylbenzoic acid metabolism.
Moreover, 2-Methylbenzoic acid is found to be associated with kidney disease and phenylketonuria.

2-Methylbenzoic acid is a non-carcinogenic (not listed by IARC) potentially toxic compound.
2-Methylbenzoic acid is a drug which is used for use as adjunctive therapy for the treatment of acute hyperammonemia and associated encephalopathy in patients with deficiencies in enzymes of the urea cycle.

2-Methylbenzoic acid is the ester of a phenol and acetic acid.
2-Methylbenzoic acid is a metabolite of anticancer drug phenylbutyrate (PB), natural neurotransmitter phenylethylamine.
Naturally, 2-Methylbenzoic acid is an odorant found in strawberries, passion fruit, and black tea.

2-Methylbenzoic acid level in urine was used as a marker for the diagnosis of some forms of unipolar major depressive disorders.
2-Methylbenzoic acid is used as a tool substrate to study esterase activity in the blood of patients in clinical studies of the effect of nutritional supplements on paraoxonase-1 levels.

2-Methylbenzoic acid is an aromatic ester.
2-Methylbenzoic acid levels in urine are marker for the diagnosis of some forms of unipolar major depressive disorders.

2-Methylbenzoic acid undergoes Fries rearrangement to form a mixture of o- and p-hydroxyacetophenones which are useful intermediates in manufacture of pharmaceuticals.
2-Methylbenzoic acid is produced from bacterial degradation of unabsorbed phenylalanine.

In health, beneficial intestinal bacteria produce some B-vitamins and provide stimulus for proper immune function.
However, if your stomach acid is not adequate, if you fail to digest protein, or if your diet does not supply sufficient fiber, the resulting overgrowth of unfavorable bacteria can release toxic products that your body must remove.

Uses of 2-Methylbenzoic Acid:
2-Methylbenzoic acid is primarily used as an intermediate in the synthesis of dyes, pigments, and agrochemicals.
2-Methylbenzoic acid plays a key role in the production of esters, which are used in plasticizers, resins, and perfume ingredients due to their aromatic properties.

In pharmaceutical and chemical research, 2-methylbenzoic acid is utilized as a building block for synthesizing more complex organic molecules.
Additionally, 2-Methylbenzoic acid serves as a corrosion inhibitor and is occasionally used in analytical chemistry as a reference compound.

2-Methylbenzoic acid is used as a solvent, laboratory reagent, and in organic synthesis
2-Methylbenzoic acid is solvent, organic sythesis, laboratory reagent

2-Methylbenzoic acid is high-boiling aprotic solvent
2-Methylbenzoic acid is used as a chemical intermediate for the synthesis of o-hydroxyacetophenone; p-hydroxyacetophenone; synephrine

2-Methylbenzoic acid is an aromatic carboxylic acid that finds widespread use in various industrial, pharmaceutical, and chemical synthesis applications.
2-Methylbenzoic acid's structure, which includes both a methyl group and a carboxylic acid group on a benzene ring in the ortho position, makes it a versatile intermediate in organic chemistry.

One of 2-Methylbenzoic acid's primary uses is as a precursor in the manufacture of dyes and pigments, where it contributes to the synthesis of azo dyes and other complex colorants used in textile and printing industries.
Additionally, 2-methylbenzoic acid is widely employed in the production of esters, which are valuable in the formulation of plasticizers, flavor and fragrance additives, and solvents for coatings and adhesives.
2-Methylbenzoic acid's aromatic and reactive nature also makes it suitable for use in the synthesis of agrochemicals, such as herbicides and plant growth regulators.

In the pharmaceutical industry, 2-methylbenzoic acid serves as a key building block in the synthesis of active pharmaceutical ingredients (APIs) and other drug intermediates, especially in the development of molecules with anti-inflammatory or antimicrobial properties.
2-Methylbenzoic acid is often used in academic and industrial chemical research as a model compound for studying the reactivity of substituted benzoic acids and for creating custom-designed organic frameworks.

Moreover, due to 2-Methylbenzoic acid's ability to chelate metals and modify surface properties, it is sometimes used in corrosion inhibition formulations for metals and alloys.
Though not as commonly used as some other benzoic acid derivatives, 2-methylbenzoic acid plays a significant role in niche applications across several sectors that benefit from its reactivity, solubility, and aromatic character.

Uses at industrial sites:
2-Methylbenzoic acid has an industrial use resulting in manufacture of another substance (use of intermediates).
2-Methylbenzoic acid is used for the manufacture of: chemicals.
Release to the environment of 2-Methylbenzoic acid can occur from industrial use: as an intermediate step in further manufacturing of another substance (use of intermediates).

Benefits of 2-Methylbenzoic Acid:
2-Methylbenzoic acid offers several benefits due to its unique chemical structure and reactivity.
As an aromatic carboxylic acid with a methyl group in the ortho position, 2-Methylbenzoic acid serves as a versatile intermediate in organic synthesis, enabling the efficient construction of more complex molecules.

2-Methylbenzoic acid's presence enhances the production of functional dyes, pigments, and polymers, contributing to industries such as textiles, plastics, and coatings.
In pharmaceutical synthesis, 2-Methylbenzoic acid allows for the creation of biologically active compounds, supporting the development of new drugs and research materials.

Additionally, 2-Methylbenzoic acid's role in the formation of esters and derivatives makes it valuable for producing fragrances, flavoring agents, and plasticizers with desirable aromatic and solubility properties.
2-Methylbenzoic acid also contributes to corrosion prevention by acting as a component in protective formulations, thereby extending the lifespan of metal surfaces.
2-Methylbenzoic acid's availability, chemical stability, and reactivity make it an economically beneficial choice for manufacturers in multiple sectors, including chemical, pharmaceutical, and agrochemical industries.

Synthesis of 2-Methylbenzoic Acid:
2-Methylbenzoic acid is typically synthesized via oxidation of o-xylene (1,2-dimethylbenzene), a common and inexpensive aromatic hydrocarbon.
The oxidation process converts one of the methyl groups on the aromatic ring to a carboxylic acid group, yielding o-toluic acid.

Main Synthetic Route: Oxidation of o-Xylene:
Starting Material: o-Xylene (1,2-dimethylbenzene)

Oxidizing Agents:
Potassium permanganate (KMnO₄)
Nitric acid (HNO₃)
Oxygen with a cobalt or manganese catalyst (in industrial processes)

Reaction Conditions:
In a laboratory setting, o-xylene is typically refluxed with aqueous KMnO₄ under acidic or basic conditions.
The reaction selectively oxidizes one methyl group to a carboxylic acid, while leaving the other methyl group intact.
The resulting product is then acidified and crystallized to isolate 2-methylbenzoic acid.

Reaction (simplified):
C₆H₄(CH₃)₂ + [O] → C₆H₄(CH₃)(COOH)

Purification:
The crude product is purified by recrystallization, typically from hot water or ethanol, to obtain pure o-toluic acid.

Alternative Methods (Less Common):

Grignard Reaction:
Starting from o-tolyl magnesium bromide, which reacts with carbon dioxide (CO₂) to form 2-methylbenzoic acid after acidic workup.

Reaction:
C₆H₄(CH₃)MgBr + CO₂ → C₆H₄(CH₃)(COOH)

Hydrolysis of o-toluyl nitrile:
o-Tolunitrile (C₆H₄(CH₃)(CN)) can be hydrolyzed under acidic or basic conditions to yield o-toluic acid.

Industrial Considerations:
In industrial processes, catalytic air oxidation of o-xylene is more commonly used due to 2-Methylbenzoic acid's cost-efficiency and scalability.
This process uses air (as the oxygen source) and catalysts like cobalt acetate or manganese acetate at elevated temperatures and pressures in a reactor.

Production of 2-Methylbenzoic Acid:
The production of 2-methylbenzoic acid is primarily carried out through the controlled oxidation of o-xylene (1,2-dimethylbenzene), a widely available petrochemical derivative.
In industrial settings, this process typically uses air or molecular oxygen in the presence of catalysts such as cobalt or manganese salts—often cobalt acetate or manganese acetate—under elevated temperatures and pressures.

This catalytic air oxidation selectively converts one of the methyl groups of o-xylene into a carboxylic acid group while preserving the other methyl group, thereby yielding 2-methylbenzoic acid.
The reaction mixture is then cooled and 2-Methylbenzoic acid is isolated through crystallization and filtration, followed by purification steps such as recrystallization from suitable solvents (e.g., water or alcohol).

This method is efficient, cost-effective, and scalable, making it suitable for large-scale commercial production.
In laboratory settings, potassium permanganate (KMnO₄) or nitric acid can also be used as oxidants under reflux conditions for small-scale synthesis.
The final product appears as white to off-white crystalline solid and is used in dye manufacture, pharmaceuticals, and as a chemical intermediate.

History of 2-Methylbenzoic Acid:
The history of 2-Methylbenzoic acid is closely linked to the broader development of aromatic chemistry in the 19th century.
As chemists began to isolate and modify derivatives of benzoic acid and toluene, they discovered that by introducing a methyl group into the ortho position of benzoic acid, they could create a compound with distinct physical and chemical properties—2-methylbenzoic acid.

This compound was first synthesized in the late 1800s, during a period of rapid advancement in synthetic organic chemistry, when coal tar derivatives and aromatic hydrocarbons were widely studied.
With the rise of the synthetic dye industry in Europe, particularly in Germany, o-toluic acid gained importance as a precursor to azo dyes and intermediates used in colorant production.

As chemical manufacturing expanded through the 20th century, 2-methylbenzoic acid became increasingly valuable as a starting material in the production of pharmaceuticals, plasticizers, and fine chemicals.
Today, 2-Methylbenzoic acidis recognized not only for its historical role in advancing industrial chemistry but also for its continued use in research and modern chemical synthesis.

Handling and Storage of 2-Methylbenzoic Acid:

Precautions for safe handling:
measures against static discharge.

Hygiene measures:
Change contaminated clothing.
Preventive skin protection recommended.
Wash hands after working with substance.

Conditions for safe storage, including any incompatibilities:

Storage conditions:
Tightly closed.

Storage class:
Storage class (TRGS 510): 10: Combustible liquids

Stability and Reactivity of 2-Methylbenzoic Acid:

Reactivity:
Forms explosive mixtures with air on intense heating.
A range from approx. 15 Kelvin below the flash point is to be rated as critical.

Chemical stability:
2-Methylbenzoic acid is chemically stable under standard ambient conditions (room temperature).

Conditions to avoid:
Strong heating.

Incompatible materials:
Strong oxidizing agents, Strong acids, Strong bases, Strong reducing agents Strong oxidizing agents, Strong acids, Strong bases, Strong reducing agents

First Aid Measures of 2-Methylbenzoic Acid:

General advice:
Show 2-Methylbenzoic acid safety data sheet to the doctor in attendance.

After inhalation:
Fresh air.

In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with water/ shower.

After eye contact:
Rinse out with plenty of water.
Remove contact lenses.

After swallowing:
Immediately make victim drink water (two glasses at most).
Consult a physician.

Firefighting Measures of 2-Methylbenzoic Acid:

Unsuitable extinguishing media:
For 2-Methylbenzoic acid no limitations of extinguishing agents are given.

Special hazards arising from 2-Methylbenzoic acid or mixture:
Carbon oxides

Vapors are heavier than air and may spread along floors.
Forms explosive mixtures with air on intense heating.

Advice for firefighters:
In the event of fire, wear self-contained breathing apparatus.

Further information:
Remove container from danger zone and cool with water.
Prevent fire extinguishing water
from contaminating surface water or the ground water system.

Accidental Release Measures of 2-Methylbenzoic Acid:

Personal protection:
Filter respirator for organic gases and vapours adapted to the airborne concentration of 2-Methylbenzoic acid.
Collect leaking liquid in sealable containers.

Absorb remaining liquid in sand or inert absorbent.
Then store and dispose of according to local regulations.

Disposal Methods of 2-Methylbenzoic Acid:
At the time of review, criteria for land treatment or burial (sanitary landfill) disposal practices are subject to significant revision.
Prior to implementing land disposal of waste residue (including waste sludge), consult with environmental regulatory agencies for guidance on acceptable disposal practices.

Exposure Controls/Personal Protective of 2-Methylbenzoic Acid:

Personal precautions, protective equipment and emergency procedures:

Advice for non-emergency personnel:
Do not breathe vapors, aerosols.
Avoid substance contact.

Ensure adequate ventilation.
Keep away from heat and sources of ignition.
Evacuate the danger area, observe emergency procedures, consult an expert.

Environmental precautions:
Do not let product enter drains.

Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.

Observe possible material restrictions.
Take up with liquid-absorbent material.

Dispose of properly.
Clean up affected area.

Identifiers of 2-Methylbenzoic Acid:
CAS Number: 122-79-2
ChEBI: CHEBI:8082
ChemSpider: 28969
ECHA InfoCard: 100.004.160
PubChem CID: 31229
UNII: 355G9R500Y
CompTox Dashboard (EPA): DTXSID3051626
InChI: InChI=1S/C8H8O2/c1-7(9)10-8-5-3-2-4-6-8/h2-6H,1H3
Key: IPBVNPXQWQGGJP-UHFFFAOYSA-N
InChI=1/C8H8O2/c1-7(9)10-8-5-3-2-4-6-8/h2-6H,1H3
Key: IPBVNPXQWQGGJP-UHFFFAOYAF
SMILES: CC(=O)Oc1ccccc1

Synonym(s): Acetic acid phenyl ester
Linear Formula: CH3COOC6H5
CAS Number: 122-79-2
Molecular Weight: 136.15
Beilstein: 636458
EC Number: 204-575-0
MDL number: MFCD00008699
PubChem Substance ID: 24846821
NACRES: NA.22

CAS: 122-79-2
Molecular Formula: C8H8O2
Molecular Weight (g/mol): 136.15
MDL Number: MFCD00008699
InChI Key: IPBVNPXQWQGGJP-UHFFFAOYSA-N
PubChem CID: 31229
ChEBI: CHEBI:8082
IUPAC Name: phenyl acetate
SMILES: CC(=O)OC1=CC=CC=C1

Properties of 2-Methylbenzoic Acid:
Chemical formula: C8H8O2
Molar mass: 136.150 g·mol−1
Density: 1.075 g/mL
Melting point: −30 °C (−22 °F; 243 K)
Boiling point: 195–196 °C (383–385 °F; 468–469 K)
Magnetic susceptibility (χ): -82.04·10−6 cm3/mol

Quality Level: 100
Assay: 99%
Refractive index: n20/D 1.501 (lit.)
bp: 196 °C (lit.)
Density: 1.073 g/mL at 25 °C (lit.)
SMILES string: CC(=O)Oc1ccccc1
InChI: 1S/C8H8O2/c1-7(9)10-8-5-3-2-4-6-8/h2-6H,1H3
InChI key: IPBVNPXQWQGGJP-UHFFFAOYSA-N
Gene Information: human ... PON1(5444)

Molecular Weight: 136.15 g/mol
XLogP3: 1.5
Hydrogen Bond Donor Count: 0
Hydrogen Bond Acceptor Count: 2
Rotatable Bond Count: 2
Exact Mass: 136.052429494 g/mol
Monoisotopic Mass: 136.052429494 g/mol
Topological Polar Surface Area: 26.3Å²
Heavy Atom Count: 10
Complexity: 114
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes

Specifications of 2-Methylbenzoic Acid:
Color: Colorless
Boiling Point: 195°C
Quantity: 25 g
Formula Weight: 136.15
Percent Purity: ≥98.0% (GC)
Physical Form: Liquid
Chemical Name or Material: Phenyl Acetate

Names of 2-Methylbenzoic Acid:

Regulatory process names:
Phenyl acetate
phenyl acetate

IUPAC names:
Phenyl Acetate
Phenyl acetate
phenyl acetate
phenyl acetate

Preferred IUPAC name:
Phenyl acetate

Systematic IUPAC name:
Phenyl ethanoate

Other names:
Phenol acetate
(Acetyloxy)benzene
Acetoxybenzene

Other identifiers:
122-79-2