75-98-9 C5H10O2 Pivalic 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

75-98-9 C5H10O2 Pivalic acid 75-98-9 C5H10O2

Quick Details

Appearance:white powder
Application:Intermediates;Building Blocks;C1 to C5;Carbonyl Compounds;Carboxylic Acids;Chemical Synthesis;Organic Building Blocks;Synthesizing medicine intermediate
PackAge:Woven bag
ProductionCapacity:1|Kilogram|Day
Storage:Normal temperature
Transportation:Ocean shipping Express delivery

Superiority:

Pivalic acid Basic information

Product Name:	Pivalic acid
Synonyms:	RARECHEM AL BO 0076;NEOPENTANOIC ACID;PIVALIC ACID;TRIMETHYLACETIC ACID;CARBOXYLIC ACID C5;ALPHA,ALPHA-DIMETHYLPROPIONIC ACID;2,2-DIMETHYLPROPIONIC ACID;2,2-DIMETHYLPROPANOIC ACID
CAS:	75-98-9
MF:	C5H10O2
MW:	102.13
EINECS:	200-922-5
Product Categories:	Intermediates;Building Blocks;C1 to C5;Carbonyl Compounds;Carboxylic Acids;Chemical Synthesis;Organic Building Blocks;Synthesizing medicine intermediate
Mol File:	75-98-9.mol

Pivalic acid Chemical Properties

mp	32-35 °C(lit.)
bp	163-164 °C(lit.)
density	0.889 g/mL at 25 °C(lit.)
vapor density	3.6 (vs air)
vapor pressure	9.75 mm Hg ( 60 °C)
refractive index	1.393
Fp	147 °F
storage temp.	2-8°C
Water Solubility	25 g/L (20 ºC)
Merck	14,7511
BRN	969480
CAS DataBase Reference	75-98-9(CAS DataBase Reference)
NIST Chemistry Reference	Pivalic acid(75-98-9)
EPA Substance Registry System	Propanoic acid, 2,2-dimethyl-(75-98-9)

Safety Information

Hazard Codes	C
Risk Statements	21/22-34
Safety Statements	26-36/37/39-45
RIDADR	UN 3261 8/PG 2
WGK Germany	1
RTECS	TO7700000
HazardClass	8
PackingGroup	II
Hazardous Substances Data	75-98-9(Hazardous Substances Data)

MSDS Information

Provider	Language
SigmaAldrich	English
ACROS	English
ALFA	English

Pivalic acid Usage And Synthesis

Chemical Properties	white crystalline low melting mass
Usage	Pivalic Acid is a metabolite of oral cephem (β-lactam) antibiotics such as S-1108, containing pivaloyl moieties.
General Description	Pivalic acid is a colored crystalline solid of low toxicity that is soluble in water, ethyl alcohol and diethyl ether.
Air & Water Reactions	With mixing, water soluble.
Reactivity Profile	Pivalic 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 Pivalic 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.
Health Hazard	CALL FOR MEDICAL AID. SOLID: Irritating to eyes and skin. Harmful if swallowed. IF IN EYES OR ON SKIN, flush with running water for at least 15 minutes; hold eyelids open if necessary. Wash skin with soap and water. Remove and isolate contaminated clothing and shoes at the site. If SWALLOWED and victim is UNCONSCIOUS OR HAVING CONVULSIONS, do nothing except keep victim warm. Because of low volatility, it is relatively harmless when inhaled at normal ambient temperature (around 20°C). It is slightly toxic by ingestion or skin absorption. The vapor is irritating at elevated temperatures. Can cause considerable discomfort by oral routes; may cause reversible or irreversible changes to exposed tissue, not permanent injury or death.
Fire Hazard	COMBUSTIBLE. Produces vapors irritating to eyes and skin. Decomposes to produce acrid smoke and fumes.

Pivalic acid Preparation Products And Raw materials

Raw materials	Chloroform-->Formic acid-->CARBON MONOXIDE-->ISOBUTYLENE-->2-Methyl-1-propanol-->2-Chloro-2-methylpropane-->TRIMETHYLACETONITRILE
Preparation Products	Pivaloyl chloride-->Clomazone-->2-tert-Butylpyridine-4-carboxylic acid ,97%-->3-(3-METHOXYPHENYL)PROPIONIC ACID-->2-TERT-BUTYLPYRIDINE-4-CARBONITRILE-->3-(2,2-DIMETHYL-PROPIONYLAMINO)-ISONICOTINIC ACID-->tert-Butyl peroxypivalate -->3-CHLORO-2,2-DIMETHYLPROPIONIC ACID

Details:

Pivalic acid Basic information

Product Name:	Pivalic acid
Synonyms:	RARECHEM AL BO 0076;NEOPENTANOIC ACID;PIVALIC ACID;TRIMETHYLACETIC ACID;CARBOXYLIC ACID C5;ALPHA,ALPHA-DIMETHYLPROPIONIC ACID;2,2-DIMETHYLPROPIONIC ACID;2,2-DIMETHYLPROPANOIC ACID
CAS:	75-98-9
MF:	C5H10O2
MW:	102.13
EINECS:	200-922-5
Product Categories:	Intermediates;Building Blocks;C1 to C5;Carbonyl Compounds;Carboxylic Acids;Chemical Synthesis;Organic Building Blocks;Synthesizing medicine intermediate
Mol File:	75-98-9.mol

Pivalic acid Chemical Properties

mp	32-35 °C(lit.)
bp	163-164 °C(lit.)
density	0.889 g/mL at 25 °C(lit.)
vapor density	3.6 (vs air)
vapor pressure	9.75 mm Hg ( 60 °C)
refractive index	1.393
Fp	147 °F
storage temp.	2-8°C
Water Solubility	25 g/L (20 ºC)
Merck	14,7511
BRN	969480
CAS DataBase Reference	75-98-9(CAS DataBase Reference)
NIST Chemistry Reference	Pivalic acid(75-98-9)
EPA Substance Registry System	Propanoic acid, 2,2-dimethyl-(75-98-9)

Safety Information

Hazard Codes	C
Risk Statements	21/22-34
Safety Statements	26-36/37/39-45
RIDADR	UN 3261 8/PG 2
WGK Germany	1
RTECS	TO7700000
HazardClass	8
PackingGroup	II
Hazardous Substances Data	75-98-9(Hazardous Substances Data)

MSDS Information

Provider	Language
SigmaAldrich	English
ACROS	English
ALFA	English

Pivalic acid Usage And Synthesis

Chemical Properties	white crystalline low melting mass
Usage	Pivalic Acid is a metabolite of oral cephem (β-lactam) antibiotics such as S-1108, containing pivaloyl moieties.
General Description	Pivalic acid is a colored crystalline solid of low toxicity that is soluble in water, ethyl alcohol and diethyl ether.
Air & Water Reactions	With mixing, water soluble.
Reactivity Profile	Pivalic 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 Pivalic 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.
Health Hazard	CALL FOR MEDICAL AID. SOLID: Irritating to eyes and skin. Harmful if swallowed. IF IN EYES OR ON SKIN, flush with running water for at least 15 minutes; hold eyelids open if necessary. Wash skin with soap and water. Remove and isolate contaminated clothing and shoes at the site. If SWALLOWED and victim is UNCONSCIOUS OR HAVING CONVULSIONS, do nothing except keep victim warm. Because of low volatility, it is relatively harmless when inhaled at normal ambient temperature (around 20°C). It is slightly toxic by ingestion or skin absorption. The vapor is irritating at elevated temperatures. Can cause considerable discomfort by oral routes; may cause reversible or irreversible changes to exposed tissue, not permanent injury or death.
Fire Hazard	COMBUSTIBLE. Produces vapors irritating to eyes and skin. Decomposes to produce acrid smoke and fumes.

Pivalic acid Preparation Products And Raw materials

Raw materials	Chloroform-->Formic acid-->CARBON MONOXIDE-->ISOBUTYLENE-->2-Methyl-1-propanol-->2-Chloro-2-methylpropane-->TRIMETHYLACETONITRILE
Preparation Products	Pivaloyl chloride-->Clomazone-->2-tert-Butylpyridine-4-carboxylic acid ,97%-->3-(3-METHOXYPHENYL)PROPIONIC ACID-->2-TERT-BUTYLPYRIDINE-4-CARBONITRILE-->3-(2,2-DIMETHYL-PROPIONYLAMINO)-ISONICOTINIC ACID-->tert-Butyl peroxypivalate -->3-CHLORO-2,2-DIMETHYLPROPIONIC 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 .

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