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HENAN SUNLAKE ENTERPRISE CORPORATION99-66-1 C8H16O2 2-Propylpentanoic acid//file1.lookchem.com/cas/reactions/2021/06/01/1750447.png
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99-66-1 C8H16O2 2-Propylpentanoic acid CAS NO.99-66-1

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

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Product Details

Keywords

  • 99-66-1 C8H16O2 2-Propylpentanoic acid
  • 99-66-1
  • C8H16O2

Quick Details

  • ProName: 99-66-1 C8H16O2 2-Pr...
  • CasNo: 99-66-1
  • Molecular Formula: C8H16O2
  • Appearance: white powder
  • Application: For treatment and management of seizur...
  • DeliveryTime: 5-7 days after payment
  • PackAge: Woven bag
  • Port: Tianjin Shanghai
  • ProductionCapacity: 1 Kilogram/Day
  • Purity: 99%
  • Storage: Normal temperature
  • Transportation: Ocean shipping Express delivery
  • LimitNum: 10 Gram

Superiority

2-propylpentanoic acid basic information
product name: 2-propylpentanoic acid
synonyms: (n-c3h7)2chcooh;2 pp (base);2-n-propylpentanoicacid;2-n-propylvalericacid;2-propylpentansαure;2-propylvaleriansαure;2-propyl-valericaci;44089
cas: 99-66-1
mf: c8h16o2
mw: 144.21
einecs: 202-777-3
product categories: pharmaceutical raw materials;organic acids;antiepileptic;all aliphatics;valproic acid series;aliphatics;intermediates & fine chemicals;pharmaceuticals
mol file: 99-66-1.mol
2-propylpentanoic acid structure
2-propylpentanoic acid chemical properties
bp 220 °c(lit.)
density 0.92
refractive index n20/d 1.425(lit.)
fp 232 °f
storage temp. 2-8°c
solubility h2o: slightly soluble
water solubility slightly soluble
merck 14,9913
brn 1750447
cas database reference 99-66-1(cas database reference)
nist chemistry reference valproic acid(99-66-1)
epa substance registry system pentanoic acid, 2-propyl-(99-66-1)
safety information
hazard codes xn,t,f
risk statements 22-36/37/38-39/23/24/25-23/24/25-11
safety statements 26-45-36/37-16-7
ridadr un 1230 3/pg 2
wgk germany 3
rtecs yv7875000
hazardclass 8
packinggroup iii
hs code 29159080
hazardous substances data 99-66-1(hazardous substances data)
msds information
provider language
valproic acid english
sigmaaldrich english
acros english
alfa english
2-propylpentanoic acid usage and synthesis
chemical properties colorless liquid
usage antiepileptic; increases levels of -aminobutyric acid(gaba) in the brain. anticonvulsant that also has efficacy as a mood stabilizer in bipolar disorder
usage antiepileptic; anticonvulsant that also acts as a mood stabilizer for those with bipolar disorder.
usage for treatment and management of seizure disorders, mania, and prophylactic treatment of migraine headache. in epileptics, valproic acid is used to control absence seizures, tonic-clonic seizures (grand mal), complex partial seizures, and the seizures asso
general description clear colorless liquid.
air & water reactions insoluble in water.
reactivity profile 2-propylpentanoic 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 2-propylpentanoic 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. 2-propylpentanoic acid is incompatible with bases, oxidizing agents and reducing agents. 2-propylpentanoic acid is corrosive. .
fire hazard 2-propylpentanoic acid is combustible.
2-propylpentanoic acid preparation products and raw materials
raw materials 2,2-dipropylmalonic acid

Details

2-propylpentanoic acid basic information
product name: 2-propylpentanoic acid
synonyms: (n-c3h7)2chcooh;2 pp (base);2-n-propylpentanoicacid;2-n-propylvalericacid;2-propylpentansαure;2-propylvaleriansαure;2-propyl-valericaci;44089
cas: 99-66-1
mf: c8h16o2
mw: 144.21
einecs: 202-777-3
product categories: pharmaceutical raw materials;organic acids;antiepileptic;all aliphatics;valproic acid series;aliphatics;intermediates & fine chemicals;pharmaceuticals
mol file: 99-66-1.mol
2-propylpentanoic acid structure
2-propylpentanoic acid chemical properties
bp 220 °c(lit.)
density 0.92
refractive index n20/d 1.425(lit.)
fp 232 °f
storage temp. 2-8°c
solubility h2o: slightly soluble
water solubility slightly soluble
merck 14,9913
brn 1750447
cas database reference 99-66-1(cas database reference)
nist chemistry reference valproic acid(99-66-1)
epa substance registry system pentanoic acid, 2-propyl-(99-66-1)
safety information
hazard codes xn,t,f
risk statements 22-36/37/38-39/23/24/25-23/24/25-11
safety statements 26-45-36/37-16-7
ridadr un 1230 3/pg 2
wgk germany 3
rtecs yv7875000
hazardclass 8
packinggroup iii
hs code 29159080
hazardous substances data 99-66-1(hazardous substances data)
msds information
provider language
valproic acid english
sigmaaldrich english
acros english
alfa english
2-propylpentanoic acid usage and synthesis
chemical properties colorless liquid
usage antiepileptic; increases levels of -aminobutyric acid(gaba) in the brain. anticonvulsant that also has efficacy as a mood stabilizer in bipolar disorder
usage antiepileptic; anticonvulsant that also acts as a mood stabilizer for those with bipolar disorder.
usage for treatment and management of seizure disorders, mania, and prophylactic treatment of migraine headache. in epileptics, valproic acid is used to control absence seizures, tonic-clonic seizures (grand mal), complex partial seizures, and the seizures asso
general description clear colorless liquid.
air & water reactions insoluble in water.
reactivity profile 2-propylpentanoic 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 2-propylpentanoic 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. 2-propylpentanoic acid is incompatible with bases, oxidizing agents and reducing agents. 2-propylpentanoic acid is corrosive. .
fire hazard 2-propylpentanoic acid is combustible.
2-propylpentanoic acid preparation products and raw materials
raw materials 2,2-dipropylmalonic 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.
we sincerely welcome foreign friends to visit our plant for cooperation. with the idea of "quality first,credit priority, excellent service", we are highly acknowledged by customers for good quality and competitive price. more importantly , the company has a strong r & d team, who are professional engineers and scholars with ph. d. .so we are confident to serve you better with our high - quality products and professional team.
we are taking great efforts to provide our customers with demanded goods and professional services, and continuously improve our core ability of competition and get the momentum for sustainable development, and finally make us being a reliable and professional wupplier in international market. we welcome any serious inquiries from all customers of the world, and sincerely hope to cooperate with you for a brilliant future!
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