1999-4-7 C8H8O2 m-Toluic acid

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10 Gram	Negotiable

10 Gram

Negotiable

Min.Order :10 Gram
Purity: 99%
Payment Terms : L/C,D/A,D/P,T/T,Other

Keywords

1999-4-7 C8H8O2 m-Toluic acid 1999-4-7 C8H8O2

Quick Details

Appearance:white powder
Application:Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts;Organic acids;intermediates
PackAge:Woven bag
ProductionCapacity:1|Kilogram|Day
Storage:Normal temperature
Transportation:Ocean shipping Express delivery

Superiority:

m-Toluic acid Basic information

Product Name:	m-Toluic acid
Synonyms:	RARECHEM AL BO 0048;M-TOLUIC ACID;M-TOLUYLIC ACID;M-METHYLBENZOIC ACID;METHYLBENZOIC(M-) ACID;beta-methylbenzoic acid;3-TOLUIC ACID;3-METHYLBENZOIC ACID
CAS:	99-04-7
MF:	C8H8O2
MW:	136.15
EINECS:	202-723-9
Product Categories:	Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts;Organic acids;intermediates
Mol File:	99-04-7.mol

m-Toluic acid Chemical Properties

mp	108 °C
bp	263 °C(lit.)
density	1.054 g/mL at 25 °C(lit.)
refractive index	1.509
Fp	150 °C
Water Solubility	<0.1 g/100 mL at 19 ºC
Merck	14,9535
BRN	970526
Stability:	Stable. Combustible. Incompatible with strong oxidizing agents.
CAS DataBase Reference	99-04-7(CAS DataBase Reference)
NIST Chemistry Reference	Benzoic acid, 3-methyl-(99-04-7)
EPA Substance Registry System	Benzoic acid, 3-methyl-(99-04-7)

Safety Information

Hazard Codes	Xn
Risk Statements	22
Safety Statements	22-24/25-36
WGK Germany	3
RTECS	XU1200000
HS Code	29163900

MSDS Information

Provider	Language
3-Methylbenzoic acid	English
SigmaAldrich	English
ACROS	English
ALFA	English

m-Toluic acid Usage And Synthesis

Chemical Properties	off-white crystalline solid
General Description	White to yellowish crystals or mostly yellow flaky solid (with some white flakes). Has a floral-honey odor.
Air & Water Reactions	Fine dust dispensed in air in sufficient concentrations, and in the presence of an ignition source is a potential dust explosion hazard. . Insoluble in water.
Reactivity Profile	m-Toluic acid is a carboxylic acid. Carboxylic acids donate hydrogen ions if a base is present to accept them. They react in this way with all bases, both organic (for example, the amines) and inorganic. Their reactions with bases, called "neutralizations", are accompanied by the evolution of substantial amounts of heat. Neutralization between an acid and a base produces water plus a salt. Carboxylic acids with six or fewer carbon atoms are freely or moderately soluble in water; those with more than six carbons are slightly soluble in water. Soluble carboxylic acid dissociate to an extent in water to yield hydrogen ions. The pH of solutions of carboxylic acids is therefore less than 7.0. Many insoluble carboxylic acids react rapidly with aqueous solutions containing a chemical base and dissolve as the neutralization generates a soluble salt. Carboxylic acids in aqueous solution and liquid or molten carboxylic acids can react with active metals to form gaseous hydrogen and a metal salt. Such reactions occur in principle for solid carboxylic acids as well, but are slow if the solid acid remains dry. Even "insoluble" carboxylic acids may absorb enough water from the air and dissolve sufficiently in m-Toluic acid to corrode or dissolve iron, steel, and aluminum parts and containers. Carboxylic acids, like other acids, react with cyanide salts to generate gaseous hydrogen cyanide. The reaction is slower for dry, solid carboxylic acids. Insoluble carboxylic acids react with solutions of cyanides to cause the release of gaseous hydrogen cyanide. Flammable and/or toxic gases and heat are generated by the reaction of carboxylic acids with diazo compounds, dithiocarbamates, isocyanates, mercaptans, nitrides, and sulfides. Carboxylic acids, especially in aqueous solution, also react with sulfites, nitrites, thiosulfates (to give H2S and SO3), dithionites (SO2), to generate flammable and/or toxic gases and heat. Their reaction with carbonates and bicarbonates generates a harmless gas (carbon dioxide) but still heat. Like other organic compounds, carboxylic acids can be oxidized by strong oxidizing agents and reduced by strong reducing agents. These reactions generate heat. A wide variety of products is possible. Like other acids, carboxylic acids may initiate polymerization reactions; like other acids, they often catalyze (increase the rate of) chemical reactions. m-Toluic acid is incompatible with strong oxidizers.
Fire Hazard	Flash point data for m-Toluic acid are not available; however, m-Toluic acid is probably combustible.

m-Toluic acid Preparation Products And Raw materials

Preparation Products	3-Carboxybenzaldehyde-->3-(4-Methylpiperazin-1-ylmethyl)benzoic acid-->Methyl 3-(morpholinomethyl)benzoate ,98%-->METHYL 3-((PYRROLIDIN-1-YL)METHYL)BENZOATE-->3-(BROMOMETHYL)BENZOIC ACID-->3-BENZOYLPHENYLACETIC ACID-->3-Methylbenzophenone-->N,N-Diethyl-3-methylbenzamide
Raw materials	m-Xylene-->1,3-Bisbenzyl-2-oxoimidazolidine-4,5-dicarboxylic acid

Details:

m-Toluic acid Basic information

Product Name:	m-Toluic acid
Synonyms:	RARECHEM AL BO 0048;M-TOLUIC ACID;M-TOLUYLIC ACID;M-METHYLBENZOIC ACID;METHYLBENZOIC(M-) ACID;beta-methylbenzoic acid;3-TOLUIC ACID;3-METHYLBENZOIC ACID
CAS:	99-04-7
MF:	C8H8O2
MW:	136.15
EINECS:	202-723-9
Product Categories:	Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts;Organic acids;intermediates
Mol File:	99-04-7.mol

m-Toluic acid Chemical Properties

mp	108 °C
bp	263 °C(lit.)
density	1.054 g/mL at 25 °C(lit.)
refractive index	1.509
Fp	150 °C
Water Solubility	<0.1 g/100 mL at 19 ºC
Merck	14,9535
BRN	970526
Stability:	Stable. Combustible. Incompatible with strong oxidizing agents.
CAS DataBase Reference	99-04-7(CAS DataBase Reference)
NIST Chemistry Reference	Benzoic acid, 3-methyl-(99-04-7)
EPA Substance Registry System	Benzoic acid, 3-methyl-(99-04-7)

Safety Information

Hazard Codes	Xn
Risk Statements	22
Safety Statements	22-24/25-36
WGK Germany	3
RTECS	XU1200000
HS Code	29163900

MSDS Information

Provider	Language
3-Methylbenzoic acid	English
SigmaAldrich	English
ACROS	English
ALFA	English

m-Toluic acid Usage And Synthesis

Chemical Properties	off-white crystalline solid
General Description	White to yellowish crystals or mostly yellow flaky solid (with some white flakes). Has a floral-honey odor.
Air & Water Reactions	Fine dust dispensed in air in sufficient concentrations, and in the presence of an ignition source is a potential dust explosion hazard. . Insoluble in water.
Reactivity Profile	m-Toluic acid is a carboxylic acid. Carboxylic acids donate hydrogen ions if a base is present to accept them. They react in this way with all bases, both organic (for example, the amines) and inorganic. Their reactions with bases, called "neutralizations", are accompanied by the evolution of substantial amounts of heat. Neutralization between an acid and a base produces water plus a salt. Carboxylic acids with six or fewer carbon atoms are freely or moderately soluble in water; those with more than six carbons are slightly soluble in water. Soluble carboxylic acid dissociate to an extent in water to yield hydrogen ions. The pH of solutions of carboxylic acids is therefore less than 7.0. Many insoluble carboxylic acids react rapidly with aqueous solutions containing a chemical base and dissolve as the neutralization generates a soluble salt. Carboxylic acids in aqueous solution and liquid or molten carboxylic acids can react with active metals to form gaseous hydrogen and a metal salt. Such reactions occur in principle for solid carboxylic acids as well, but are slow if the solid acid remains dry. Even "insoluble" carboxylic acids may absorb enough water from the air and dissolve sufficiently in m-Toluic acid to corrode or dissolve iron, steel, and aluminum parts and containers. Carboxylic acids, like other acids, react with cyanide salts to generate gaseous hydrogen cyanide. The reaction is slower for dry, solid carboxylic acids. Insoluble carboxylic acids react with solutions of cyanides to cause the release of gaseous hydrogen cyanide. Flammable and/or toxic gases and heat are generated by the reaction of carboxylic acids with diazo compounds, dithiocarbamates, isocyanates, mercaptans, nitrides, and sulfides. Carboxylic acids, especially in aqueous solution, also react with sulfites, nitrites, thiosulfates (to give H2S and SO3), dithionites (SO2), to generate flammable and/or toxic gases and heat. Their reaction with carbonates and bicarbonates generates a harmless gas (carbon dioxide) but still heat. Like other organic compounds, carboxylic acids can be oxidized by strong oxidizing agents and reduced by strong reducing agents. These reactions generate heat. A wide variety of products is possible. Like other acids, carboxylic acids may initiate polymerization reactions; like other acids, they often catalyze (increase the rate of) chemical reactions. m-Toluic acid is incompatible with strong oxidizers.
Fire Hazard	Flash point data for m-Toluic acid are not available; however, m-Toluic acid is probably combustible.

m-Toluic acid Preparation Products And Raw materials

Preparation Products	3-Carboxybenzaldehyde-->3-(4-Methylpiperazin-1-ylmethyl)benzoic acid-->Methyl 3-(morpholinomethyl)benzoate ,98%-->METHYL 3-((PYRROLIDIN-1-YL)METHYL)BENZOATE-->3-(BROMOMETHYL)BENZOIC ACID-->3-BENZOYLPHENYLACETIC ACID-->3-Methylbenzophenone-->N,N-Diethyl-3-methylbenzamide
Raw materials	m-Xylene-->1,3-Bisbenzyl-2-oxoimidazolidine-4,5-dicarboxylic acid

HenNan sunlake enterprise corporation is located in Henan Province , The central plain of China , Which enjoys favorable geogeaphical position and convenient transportion, The com[any was established in june. 1998 , until now having more than 18 years experience in manufacturing & exporting chemical raw material .

Sunlake is a professional manufacturer engaged in producing and selling chemicals,including Organic & inorganic chemicals , pigments & Dyestuffs , Water treatment chemicals , Food & FEED additives and others . these products have been being well exported to europe , southeast Asia , the Middle East , Africa , South America and some other countries and areas.

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