Product Name

  • Name

    n-Butanoic acid

  • EINECS 203-532-3
  • CAS No. 107-92-6
  • Article Data1027
  • CAS DataBase
  • Density 0.987 g/cm3
  • Solubility miscible with water
  • Melting Point -6 - -3 °C
  • Formula C4H8O2
  • Boiling Point 164.3 °C at 760 mmHg
  • Molecular Weight 88.1063
  • Flash Point 69 °C
  • Transport Information UN 2820 8/PG 3
  • Appearance colourless liquid
  • Safety 26-36-45
  • Risk Codes 34
  • Molecular Structure Molecular Structure of 107-92-6 (n-Butanoic acid)
  • Hazard Symbols IrritantXi,CorrosiveC
  • Synonyms n-Butanoic acid;n-Butyric acid;(3R,4S)-1-Benzoyl-3-(1-methoxy-1-methylethoxy)-4-phenyl-2-azetidinone;Butyricacid (6CI,7CI,8CI);1-Propanecarboxylic acid;Ethylacetic acid;Honey robber;NSC 8415;Propylformic acid;
  • PSA 37.30000
  • LogP 0.87110

Synthetic route

2-butenoic acid
3724-65-0

2-butenoic acid

butyric acid
107-92-6

butyric acid

Conditions
ConditionsYield
With potassium hydroxide; hydrogen; [RhCl(Ph3P)2]; Ph2PO2CCH=CMe2 In acetone at 22℃; under 2280 Torr; for 17h;100%
With sodium tetrahydroborate; sodium hydroxide In water at 20 - 60℃;90%
With sodium hydroxide; hydrogen; nickel In water hydrogen generated in situ electrochemically on Raney nickel electrode;60%
butyraldehyde
123-72-8

butyraldehyde

butyric acid
107-92-6

butyric acid

Conditions
ConditionsYield
With 2,2,2-trichloroethylperoxycarbonic acid; dihydrogen peroxide In dichloromethane Ambient temperature;100%
With C4H11FeMo6NO24(3-)*3C16H36N(1+); water; oxygen; sodium carbonate at 50℃; under 760.051 Torr; for 8h; Green chemistry;99%
With 4H3N*4H(1+)*CuMo6O18(OH)6(4-); water; oxygen; sodium carbonate at 50℃; under 760.051 Torr; for 12h;98%
butan-1-ol
71-36-3

butan-1-ol

butyric acid
107-92-6

butyric acid

Conditions
ConditionsYield
With ammonium cerium (IV) nitrate; sodium trimethylsilylpropionate-d4; C18H22N4O2Ru(2+)*2F6P(1-); water at 20℃; for 0.5h;100%
With oxygen In water at 80℃; under 760.051 Torr; for 24h;99.7%
With potassium hydroxide at 50℃; electrolysis;98.8%
2-oxopentanoic acid sodium salt
13022-83-8

2-oxopentanoic acid sodium salt

butyric acid
107-92-6

butyric acid

Conditions
ConditionsYield
With calcium hypochlorite; acetic acid In dichloromethane; water; acetonitrile for 3h; Ambient temperature;96%
5-methyl-1-propyl-2,7,8-trioxabicyclo[3.2.1]octane
199921-04-5

5-methyl-1-propyl-2,7,8-trioxabicyclo[3.2.1]octane

butyric acid
107-92-6

butyric acid

Conditions
ConditionsYield
Stage #1: 5-methyl-1-propyl-2,7,8-trioxabicyclo[3.2.1]octane With pyridinium p-toluenesulfonate In methanol; water at 22℃; for 1.5h; Ring cleavage;
Stage #2: With lithium hydroxide In tetrahydrofuran at 22℃; for 6h; Hydrolysis;
96%
Conditions
ConditionsYield
With palladium 10% on activated carbon; W(OTf)6; hydrogen at 135℃; under 760.051 Torr; for 12h;96%
With palladium on activated carbon; W(OTf)6; hydrogen In neat (no solvent) at 135℃; under 760.051 Torr; for 12h;96%
With hydrogen at 200 - 247℃; under 15514.9 Torr; for 5.66667h; Inert atmosphere;94.2 %Chromat.
2-ethyl-1,3-hexane diol
94-96-2

2-ethyl-1,3-hexane diol

A

2-ethyl-1-hydroxy-3-hexanone
27970-80-5

2-ethyl-1-hydroxy-3-hexanone

B

butyric acid
107-92-6

butyric acid

Conditions
ConditionsYield
With dihydrogen peroxide; Na12[WZn3(H2O)2(ZnW9O34)2] at 75℃; for 7h;A 95%
B 4%
With Na12[WZn3(H2O)2(ZnW9O34)2]; dihydrogen peroxide at 85℃; for 7h;
With SiW11Zn; dihydrogen peroxide In water at 89.85℃; for 9h;
butanoic acid anhydride
106-31-0

butanoic acid anhydride

4-chloro-N-(2-fluoro-5-chlorophenyl)-N-(1R)-(2-hydroxy-1-methylpentyl)benzenesulfonamide
691909-53-2

4-chloro-N-(2-fluoro-5-chlorophenyl)-N-(1R)-(2-hydroxy-1-methylpentyl)benzenesulfonamide

butyric acid
107-92-6

butyric acid

Conditions
ConditionsYield
With dmap; triethylamine In dichloromethane94%
tributyl-amine
102-82-9

tributyl-amine

A

N,N-(di-n-butyl)butyramide
14287-95-7

N,N-(di-n-butyl)butyramide

B

butyric acid
107-92-6

butyric acid

Conditions
ConditionsYield
With benzyl(triethyl)ammoniumpermanganate In dichloromethaneA 93%
B 5%
diethyl sulphide
352-93-2

diethyl sulphide

2-oxopentanoic acid
1821-02-9

2-oxopentanoic acid

A

diethyl sulphide
70-29-1

diethyl sulphide

B

carbon dioxide
124-38-9

carbon dioxide

C

butyric acid
107-92-6

butyric acid

Conditions
ConditionsYield
With oxygen; methylene blue In pyridine; acetonitrile for 2h; Irradiation;A 92%
B n/a
C 19%
butanoic acid ethyl ester
105-54-4

butanoic acid ethyl ester

butyric acid
107-92-6

butyric acid

Conditions
ConditionsYield
With octadecyltriethoxysilane-treated high-silica Hβ-20 zeolite In water at 130℃; for 24h; Reagent/catalyst;92%
With PIPES buffer; Candida rugosa lipase In water; toluene Rate constant; other enzymes, other solvent;
With Candida antarctica lipase B; 4-nitro-phenol; MOPS buffer In water at 25℃; pH=7.2; Enzyme kinetics; Further Variations:; Reagents; Enzymatic reaction;
butan-1-ol
71-36-3

butan-1-ol

A

butyraldehyde
123-72-8

butyraldehyde

B

butyric acid
107-92-6

butyric acid

Conditions
ConditionsYield
With sodium bromate; Ru2(dmnapy)Cl4 for 0.25h; Ambient temperature;A 91.5%
B 2.5%
With C30H24N2O7W; dihydrogen peroxide In water; acetonitrile for 14h; Reflux;A 67%
B 23%
With tert.-butylhydroperoxide; chromium tetra(tert-butoxide) In benzene at 20℃; for 24h;A 16%
B 53%
butyraldehyde
123-72-8

butyraldehyde

A

peroxybutyric acid
13122-71-9

peroxybutyric acid

B

butyric acid
107-92-6

butyric acid

Conditions
ConditionsYield
With oxygen In neat (no solvent) at 30 - 40℃; with solvent (benzene);A 0.8%
B 90.5%
With oxygen; palladium diacetate; tetrabutyl-ammonium chloride In chlorobenzene at 10℃; Rate constant; Product distribution; other catalysts;
With tetrachloromethane; oxygen; ozone at -20 - -10℃;
propyl cyanide
109-74-0

propyl cyanide

butyric acid
107-92-6

butyric acid

Conditions
ConditionsYield
enzyme from Synechocystis sp. PCC 6803 In phosphate buffer at 30℃; for 12h; pH=7.2;90%
With benzene-1,2-dicarboxylic acid for 0.666667h; microwave irradiation;83%
With chaetomium globosum (Q2GR86); water Reagent/catalyst; Enzymatic reaction;
With nitrilase from Gordonia terrae In aq. phosphate buffer at 35℃; for 1h; pH=8; Enzymatic reaction;
5-methyl-6-methylthio-3-pyridinecarboxamide

5-methyl-6-methylthio-3-pyridinecarboxamide

ethyl 2-diazo-3-oxobutanoate
2009-97-4

ethyl 2-diazo-3-oxobutanoate

butyric acid
107-92-6

butyric acid

Conditions
ConditionsYield
rhodium(II) acetate In chloroform90%
trans-4-Octene
14850-23-8

trans-4-Octene

A

1-nitrobutane
627-05-4

1-nitrobutane

B

butyric acid
107-92-6

butyric acid

Conditions
ConditionsYield
A 90%
B n/a
succinic acid
110-15-6

succinic acid

A

tetrahydrofuran
109-99-9

tetrahydrofuran

B

4-butanolide
96-48-0

4-butanolide

C

Butane-1,4-diol
110-63-4

Butane-1,4-diol

D

butyric acid
107-92-6

butyric acid

E

n-butane
106-97-8

n-butane

F

butan-1-ol
71-36-3

butan-1-ol

Conditions
ConditionsYield
With hydrogen In 1,4-dioxane at 139.84℃; under 60006 Torr; for 24h; Catalytic behavior; Reagent/catalyst; Time; Autoclave; Overall yield = > 99 %;A 0.2%
B 3.1%
C 89%
D n/a
E n/a
F 7.6%
phenyl butyl ketone
1009-14-9

phenyl butyl ketone

A

propionaldehyde
123-38-6

propionaldehyde

B

butyraldehyde
123-72-8

butyraldehyde

C

propionic acid
802294-64-0

propionic acid

D

benzoic acid
65-85-0

benzoic acid

E

butyric acid
107-92-6

butyric acid

Conditions
ConditionsYield
With 5% active carbon-supported ruthenium; water; oxygen; calcium oxide at 100℃; for 12h; Reagent/catalyst; Time;A n/a
B n/a
C n/a
D 89%
E n/a
butyroin
496-77-5

butyroin

butyric acid
107-92-6

butyric acid

Conditions
ConditionsYield
With sodium hypochlorite In acetonitrile at 20℃; for 1h;88%
With dihydrogen peroxide; tris(cetylpyridinium) 12-tungstophosphate In chloroform for 24h; Heating;9%
octane-4,5-diol
22607-10-9

octane-4,5-diol

butyric acid
107-92-6

butyric acid

Conditions
ConditionsYield
With sodium hypochlorite In acetonitrile at 20℃; for 1.5h;88%
ethylmalonic acid
601-75-2

ethylmalonic acid

butyric acid
107-92-6

butyric acid

Conditions
ConditionsYield
In water for 0.25h; Decarboxylation; microwave irradiation;87%
In neat (no solvent) at 141℃; Kinetics; Thermodynamic data; ΔH(excit.), ΔS(excit.), ΔF(excit.);
butyric acid hydrazide
3538-65-6

butyric acid hydrazide

butyric acid
107-92-6

butyric acid

Conditions
ConditionsYield
With water; 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione In chloroform at 20℃; for 1h;87%
With sulfuric acid at 70 - 80℃; Equilibrium constant; Kinetics;
With sulfuric acid In water at 55℃; Mechanism; Rate constant;
With perchloric acid; water; potassium hexacyanoferrate(III) at 30℃; Rate constant; Thermodynamic data; Mechanism; Ea, ΔH(excit.), ΔG(excit.), ΔS(excit.), also in the presence of NaClO4, NaNO3, NaCl, KCl or LiCl, also in methanol, effect of substrate, K4Fe(CN)6 and HClO4 concentrations;
β-Propiolactone
57-57-8

β-Propiolactone

methylmagnesium bromide
75-16-1

methylmagnesium bromide

butyric acid
107-92-6

butyric acid

Conditions
ConditionsYield
copper(l) chloride at 0℃; for 0.25h;87%
β-Propiolactone
57-57-8

β-Propiolactone

methylmagnesium halogenide

methylmagnesium halogenide

butyric acid
107-92-6

butyric acid

Conditions
ConditionsYield
With copper(l) chloride In tetrahydrofuran at 0℃; for 0.25h;87%
butyraldehyde
123-72-8

butyraldehyde

A

butyl butyrate
109-21-7

butyl butyrate

B

butyric acid
107-92-6

butyric acid

C

butan-1-ol
71-36-3

butan-1-ol

Conditions
ConditionsYield
With dihydridotetrakis(triphenylphosphine)ruthenium; water; 1-Phenylbut-1-en-3-one In 1,2-dimethoxyethane at 180℃; for 24h; Product distribution; Mechanism; in the absence of hydrogen acceptor (benzalacetone); other aldehydes;A n/a
B 85%
C n/a
Conditions
ConditionsYield
With potassium permanganate; iron(III) chloride In acetone at -78 - 20℃; for 29h;85%
allyl butyrate
2051-78-7

allyl butyrate

butyric acid
107-92-6

butyric acid

Conditions
ConditionsYield
Stage #1: allyl butyrate With sodium tetrahydroborate In dimethyl sulfoxide at 20℃;
Stage #2: With hydrogenchloride; water In dimethyl sulfoxide for 0.5h; chemoselective reaction;
85%
(5R)-5-phenylmorpholin-3-one
192815-71-7

(5R)-5-phenylmorpholin-3-one

A

(3R)-3-phenylmorpholine
138713-44-7, 74572-03-5

(3R)-3-phenylmorpholine

B

butyric acid
107-92-6

butyric acid

Conditions
ConditionsYield
With [RuCl2(N-heterocyclic carbene)(bis[2-(diphenylphosphino)ethyl]amine)]; caesium carbonate In toluene; butan-1-ol at 150℃; under 37503.8 Torr; for 6h; Schlenk technique; Autoclave;A 85%
B 10%
ethanol
64-17-5

ethanol

butyric acid
107-92-6

butyric acid

butanoic acid ethyl ester
105-54-4

butanoic acid ethyl ester

Conditions
ConditionsYield
zirconium(IV) oxide at 200℃; in vapor-phase;100%
With HZSM-5 at 170℃; for 12h; Temperature;99%
With Thermomyces lanuginosus lipase immobilized in an ionic-exchange resin at 30℃; for 6h; Concentration; Temperature; Sonication; Molecular sieve; Enzymatic reaction;90%
butyric acid
107-92-6

butyric acid

butan-1-ol
71-36-3

butan-1-ol

butyl butyrate
109-21-7

butyl butyrate

Conditions
ConditionsYield
With [Al(H2O)6][MS]3 In cyclohexane for 1h; Reagent/catalyst; Dean-Stark; Reflux;100%
With Candida antarctica B lipase In 2,2,4-trimethylpentane at 40℃; for 3h; Enzymatic reaction;98%
With DOOl-AlCl3 superacid resin for 1.5h; Heating;97%
butyric acid
107-92-6

butyric acid

butanamide
541-35-5

butanamide

Conditions
ConditionsYield
With Candida antarctica lipase B; ammonium carbamate In various solvent(s) at 25℃; for 408h; Substitution;100%
Stage #1: butyric acid With niobium pentachloride In dichloromethane
Stage #2: With ammonia In dichloromethane at 45 - 50℃; for 1h;
98%
With Candida antarctica lipase B; ammonium carbamate In various solvent(s) at 35℃; for 72h; Substitution;91%
cyclohexanecarbaldehyde
2043-61-0

cyclohexanecarbaldehyde

butyric acid
107-92-6

butyric acid

2-(Cyclohexyl-hydroxy-methyl)-butyric acid
114049-45-5

2-(Cyclohexyl-hydroxy-methyl)-butyric acid

Conditions
ConditionsYield
With lithium diisopropyl amide In tetrahydrofuran100%
3-(2-vinyloxyethoxy)-1,2-propylene carbonate
54107-24-3

3-(2-vinyloxyethoxy)-1,2-propylene carbonate

butyric acid
107-92-6

butyric acid

Butyric acid 1-[2-(2-oxo-[1,3]dioxolan-4-ylmethoxy)-ethoxy]-ethyl ester
127827-84-3

Butyric acid 1-[2-(2-oxo-[1,3]dioxolan-4-ylmethoxy)-ethoxy]-ethyl ester

Conditions
ConditionsYield
With heptafluorobutyric Acid at 75℃; for 3h;100%
2-(3,4-dimethoxyphenyl)-ethylamine
120-20-7

2-(3,4-dimethoxyphenyl)-ethylamine

butyric acid
107-92-6

butyric acid

4-formyl-3,5-dimethoxyphenoxy-Merrifield resin

4-formyl-3,5-dimethoxyphenoxy-Merrifield resin

N-(3,4-Dimethoxyphenethyl)butyramide
81165-56-2

N-(3,4-Dimethoxyphenethyl)butyramide

Conditions
ConditionsYield
Stage #1: 2-(3,4-dimethoxyphenyl)-ethylamine; 4-formyl-3,5-dimethoxyphenoxy-Merrifield resin With sodium tris(acetoxy)borohydride In acetic acid; N,N-dimethyl-formamide at 20℃; for 69h; Solid phase reaction; reductive amination;
Stage #2: butyric acid With benzotriazol-1-ol; dicyclohexyl-carbodiimide In N,N-dimethyl-formamide at 20℃; for 15h; Solid phase reaction; acylation;
Stage #3: With dimethylsulfide; water; trifluoroacetic acid In dichloromethane at 20℃; for 15h; Solid phase reaction; cleavage of amide;
100%
2-(3-methoxyphenyl)-1-ethanamine
2039-67-0

2-(3-methoxyphenyl)-1-ethanamine

butyric acid
107-92-6

butyric acid

4-formyl-3,5-dimethoxyphenoxy-Merrifield resin

4-formyl-3,5-dimethoxyphenoxy-Merrifield resin

N-[2-(3-Methoxyphenyl)ethyl]butanamide
138505-09-6

N-[2-(3-Methoxyphenyl)ethyl]butanamide

Conditions
ConditionsYield
Stage #1: 2-(3-methoxyphenyl)-1-ethanamine; 4-formyl-3,5-dimethoxyphenoxy-Merrifield resin With sodium tris(acetoxy)borohydride In acetic acid; N,N-dimethyl-formamide at 20℃; for 69h; Solid phase reaction; reductive amination;
Stage #2: butyric acid With benzotriazol-1-ol; dicyclohexyl-carbodiimide In N,N-dimethyl-formamide at 20℃; for 15h; Solid phase reaction; acylation;
Stage #3: With dimethylsulfide; water; trifluoroacetic acid In dichloromethane at 20℃; for 15h; Solid phase reaction; cleavage of amide;
100%
o-methoxy-2-phenylethylamine
2045-79-6

o-methoxy-2-phenylethylamine

butyric acid
107-92-6

butyric acid

4-formyl-3,5-dimethoxyphenoxy-Merrifield resin

4-formyl-3,5-dimethoxyphenoxy-Merrifield resin

N-butanoyl-2-(2-methoxyphenyl)ethanamine

N-butanoyl-2-(2-methoxyphenyl)ethanamine

Conditions
ConditionsYield
Stage #1: o-methoxy-2-phenylethylamine; 4-formyl-3,5-dimethoxyphenoxy-Merrifield resin With sodium tris(acetoxy)borohydride In acetic acid; N,N-dimethyl-formamide at 20℃; for 69h; Solid phase reaction; reductive amination;
Stage #2: butyric acid With benzotriazol-1-ol; dicyclohexyl-carbodiimide In N,N-dimethyl-formamide at 20℃; for 15h; Solid phase reaction; acylation;
Stage #3: With dimethylsulfide; water; trifluoroacetic acid In dichloromethane at 20℃; for 15h; Solid phase reaction; cleavage of amide;
100%
4-Methoxyphenethylamine
55-81-2

4-Methoxyphenethylamine

butyric acid
107-92-6

butyric acid

4-formyl-3,5-dimethoxyphenoxy-Merrifield resin

4-formyl-3,5-dimethoxyphenoxy-Merrifield resin

N-butanoyl-2-(4-methoxyphenyl)ethanamine

N-butanoyl-2-(4-methoxyphenyl)ethanamine

Conditions
ConditionsYield
Stage #1: 4-Methoxyphenethylamine; 4-formyl-3,5-dimethoxyphenoxy-Merrifield resin With sodium tris(acetoxy)borohydride In acetic acid; N,N-dimethyl-formamide at 20℃; for 69h; Solid phase reaction; reductive amination;
Stage #2: butyric acid With benzotriazol-1-ol; dicyclohexyl-carbodiimide In N,N-dimethyl-formamide at 20℃; for 15h; Solid phase reaction; acylation;
Stage #3: With dimethylsulfide; water; trifluoroacetic acid In dichloromethane at 20℃; for 15h; Solid phase reaction; cleavage of amide;
100%
2-(3-chlorophenyl)ethylamine
13078-79-0

2-(3-chlorophenyl)ethylamine

butyric acid
107-92-6

butyric acid

4-formyl-3,5-dimethoxyphenoxy-Merrifield resin

4-formyl-3,5-dimethoxyphenoxy-Merrifield resin

N-[2-(3-chloro-phenyl)-ethyl]-butyramide

N-[2-(3-chloro-phenyl)-ethyl]-butyramide

Conditions
ConditionsYield
Stage #1: 2-(3-chlorophenyl)ethylamine; 4-formyl-3,5-dimethoxyphenoxy-Merrifield resin With sodium tris(acetoxy)borohydride In acetic acid; N,N-dimethyl-formamide at 20℃; for 69h; Solid phase reaction; reductive amination;
Stage #2: butyric acid With benzotriazol-1-ol; dicyclohexyl-carbodiimide In N,N-dimethyl-formamide at 20℃; for 15h; Solid phase reaction; acylation;
Stage #3: With dimethylsulfide; water; trifluoroacetic acid In dichloromethane at 20℃; for 15h; Solid phase reaction; cleavage of amide;
100%
n-butyl isonitrile
2769-64-4

n-butyl isonitrile

2,3-di-O-tert-butyldimethylsilyl-1,4-dideoxy-1,4-imino-1,N-dehydrothreitol

2,3-di-O-tert-butyldimethylsilyl-1,4-dideoxy-1,4-imino-1,N-dehydrothreitol

butyric acid
107-92-6

butyric acid

(3S,4S)-3,4-Bis-(tert-butyl-dimethyl-silanyloxy)-1-butyryl-pyrrolidine-2-carboxylic acid butylamide

(3S,4S)-3,4-Bis-(tert-butyl-dimethyl-silanyloxy)-1-butyryl-pyrrolidine-2-carboxylic acid butylamide

Conditions
ConditionsYield
In methanol for 18h; Joullie-Ugi coupling;100%
(S)-5-phenylpent-1-en-3-amine
380848-17-9

(S)-5-phenylpent-1-en-3-amine

butyric acid
107-92-6

butyric acid

N-(1-phenethyl-allyl)-butyramide
380848-27-1

N-(1-phenethyl-allyl)-butyramide

Conditions
ConditionsYield
Stage #1: butyric acid With 4-methyl-morpholine; isobutyl chloroformate In tetrahydrofuran at -20℃; for 0.75h;
Stage #2: With pyridine; 4-hydroxy-3-nitrobenzophenone resin In tetrahydrofuran; N,N-dimethyl-formamide for 12h;
Stage #3: (S)-5-phenylpent-1-en-3-amine In dichloromethane for 24h; Further stages.;
100%
C16H35NO2Si2

C16H35NO2Si2

n-butyl isonitrile
2769-64-4

n-butyl isonitrile

butyric acid
107-92-6

butyric acid

C25H52N2O4Si2

C25H52N2O4Si2

Conditions
ConditionsYield
In methanol for 18h; Ugi-type reaction;100%
chlorosulfuric acid chloromethyl ester
49715-04-0

chlorosulfuric acid chloromethyl ester

butyric acid
107-92-6

butyric acid

chloromethyl n-butyrate
33657-49-7

chloromethyl n-butyrate

Conditions
ConditionsYield
With tetrabutylammomium bromide; sodium hydrogencarbonate In dichloromethane; water at 20℃; for 16h;100%
With tetra(n-butyl)ammonium hydrogensulfate; potassium carbonate In dichloromethane; water at 20℃; for 4h; Inert atmosphere;58%
With sodium hydrogencarbonate; tetra(n-butyl)ammonium hydrogen sulfate In dichloromethane; water41%
With tetra(n-butyl)ammonium hydrogensulfate; sodium hydrogencarbonate In dichloromethane; water at 0℃; for 1h;31%
(S)-valinol
2026-48-4

(S)-valinol

butyric acid
107-92-6

butyric acid

(S)-2-butyl-4-isopropyloxazoline
906672-84-2

(S)-2-butyl-4-isopropyloxazoline

Conditions
ConditionsYield
Zn4(OAc)6O In chlorobenzene for 12h; Product distribution / selectivity; Heating / reflux;100%
Zn4(OCOCF3)6O In chlorobenzene for 12h; Product distribution / selectivity; Heating / reflux;100%
cycl-isopropylidene malonate
2033-24-1

cycl-isopropylidene malonate

butyric acid
107-92-6

butyric acid

5-butanoyl-2,2-dimethyl-1,3-dioxane-4,6-dione
72546-06-6

5-butanoyl-2,2-dimethyl-1,3-dioxane-4,6-dione

Conditions
ConditionsYield
With dmap; dicyclohexyl-carbodiimide In dichloromethane at 20℃;100%
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; for 16h; Inert atmosphere;100%
With dmap In dichloromethane; N,N-dimethyl-formamide
cholinium hydrogen carbonate
78-73-9

cholinium hydrogen carbonate

butyric acid
107-92-6

butyric acid

2-hydroxy-N,N,N-trimethylethan-1-aminium butyrate
93458-02-7

2-hydroxy-N,N,N-trimethylethan-1-aminium butyrate

Conditions
ConditionsYield
In water at 20℃;100%
In water at 20℃;
at 75℃; for 12h;
C15H21NO3
1381872-39-4

C15H21NO3

Boc-L-phenylalaninal
72155-45-4

Boc-L-phenylalaninal

butyric acid
107-92-6

butyric acid

C33H48N2O8
1381872-97-4

C33H48N2O8

Conditions
ConditionsYield
In dichloromethane Passerini reaction;100%
p-hydroxyphenethyl alcohol
501-94-0

p-hydroxyphenethyl alcohol

butyric acid
107-92-6

butyric acid

2-(4-hydroxylphenyl)ethyl butyrate
386263-87-2

2-(4-hydroxylphenyl)ethyl butyrate

Conditions
ConditionsYield
With Candida antarctica at 45℃; for 24h;100%
With di-isopropyl azodicarboxylate; triphenylphosphine In tetrahydrofuran at 0 - 20℃; for 24h;
N-(2-aminoethyl)-4-methyl-N-(prop-2-yn-1-yl)benzenesulfonamide
1438397-77-3

N-(2-aminoethyl)-4-methyl-N-(prop-2-yn-1-yl)benzenesulfonamide

butyric acid
107-92-6

butyric acid

N-[2-(N-propargyl-N-tosylamino)ethyl]butyramide

N-[2-(N-propargyl-N-tosylamino)ethyl]butyramide

Conditions
ConditionsYield
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; for 0.5h;100%
i-Amyl alcohol
123-51-3

i-Amyl alcohol

butyric acid
107-92-6

butyric acid

isopentyl butanoate
106-27-4

isopentyl butanoate

Conditions
ConditionsYield
With Candida antarctica lipase B at 50℃; for 4h; Molecular sieve; Ionic liquid; Green chemistry; Enzymatic reaction;99.9%
copper methanesulfonate In cyclohexane at 130 - 135℃; for 2.5h;96%
With salicylic acid resin supported FeCl3 In benzene at 125℃; for 1.96667h;95.8%
Citronellol
106-22-9

Citronellol

butyric acid
107-92-6

butyric acid

3,7-dimethyl-6-octenyl butyrate
141-16-2

3,7-dimethyl-6-octenyl butyrate

Conditions
ConditionsYield
With Candida antarctica lipase B at 50℃; for 4h; Molecular sieve; Ionic liquid; Green chemistry; Enzymatic reaction;99.9%
In n-heptane at 40℃; for 24h; lipozyme IM 20 (immobilized Mucor miehi lipase);94.66%
In water at 30℃; for 18h; lipase from Aspergillus niger; Yield given;
Geraniol
106-24-1

Geraniol

butyric acid
107-92-6

butyric acid

Geranyl butyrate
106-29-6

Geranyl butyrate

Conditions
ConditionsYield
With Candida antarctica lipase B at 50℃; for 4h; Molecular sieve; Ionic liquid; Green chemistry; Enzymatic reaction;99.9%
With sodium hydroxide at 80℃; for 8h;66.94%
In hexane at 30℃; for 72h; Corynebacterium sp. S-401;23%
Nerol
106-25-2

Nerol

butyric acid
107-92-6

butyric acid

butyric acid β-neryl ester
999-40-6

butyric acid β-neryl ester

Conditions
ConditionsYield
With Candida antarctica lipase B at 50℃; for 4h; Molecular sieve; Ionic liquid; Green chemistry; Enzymatic reaction;99.9%
With dmap; dicyclohexyl-carbodiimide In dichloromethane Steglich Esterification;
methanol
67-56-1

methanol

butyric acid
107-92-6

butyric acid

butanoic acid methyl ester
623-42-7

butanoic acid methyl ester

Conditions
ConditionsYield
With aluminum(III) sulphate octadecahydrate at 110℃; for 0.166667h; Sealed tube; Microwave irradiation;99.7%
With NiO/SiO2 at 360℃; Reagent/catalyst;97.98%
With 1-methyl-3-(4-sulfobutyl)-1H-imidazol-3-ium hydrogensulfate at 80℃; for 2h;96%
butyric acid
107-92-6

butyric acid

peroxybutyric acid
13122-71-9

peroxybutyric acid

Conditions
ConditionsYield
With dihydrogen peroxide; KU-2 x 8 cation-exchange resin In 1,4-dioxane at 19.9℃; Mechanism; Product distribution; Kinetics; other temperatures;99.2%
With tetraacetyl diborate; xylene unter vermindertem Druck unter Entfernen von Essigsaeure und Behandeln des Reaktionsprodukts mit Wasserstoffperoxid in Aether;
With dihydrogen peroxide
With sulfuric acid; dihydrogen peroxide at -10 - -5℃; Oxidation;
butyric acid
107-92-6

butyric acid

recorcinol
108-46-3

recorcinol

1-(2,4-dihydroxyphenyl)butan-1-one
4390-92-5

1-(2,4-dihydroxyphenyl)butan-1-one

Conditions
ConditionsYield
With boron trifluoride diethyl etherate In chlorobenzene at 80℃; Friedel-Crafts Acylation;99%
With zinc(II) chloride In toluene Reflux;89.3%
With PPA

Butyric acid Specification

The IUPAC name of this chemical is Butyric acid. With the CAS registry number 107-92-6 and EINECS registry number 203-532-3, it is also named as ethylacetic acid. In addition, the molecular formula is C4H8O2. It is an oily colorless liquid that is easily soluble in water, ethanol, and ether, and can be separated from an aqueous phase by saturation with salts such as calcium chloride. And it has an unpleasant smell and acrid taste. Besides, it is found in butter, parmesan cheese, vomit, and as a product of anaerobic fermentation (including in the colon and as body odor). 

Physical properties about this chemical are: (1)ACD/LogP: 0.70; (2)# of Rule of 5 Violations: 0; (3)ACD/BCF (pH 5.5): 1; (4)ACD/BCF (pH 7.4): 1; (5)ACD/KOC (pH 5.5): 8.756; (6)ACD/KOC (pH 7.4): 1; (7)#H bond acceptors: 2; (8)#H bond donors: 1; (9)#Freely Rotating Bonds: 2; (10)Polar Surface Area: 37.3 Å2; (11)Index of Refraction: 1.411; (12)Molar Refractivity: 22.145 cm3; (13)Molar Volume: 89.188 cm3; (14)Polarizability: 8.779 ×10-24cm3; (15)Surface Tension: 32.584 dyne/cm; (16)Density: 0.988 g/cm3; (17)Flash Point: 69.712 °C; (18)Enthalpy of Vaporization: 42.395 kJ/mol; (19)Boiling Point: 164.348 °C at 760 mmHg; (20)Vapour Pressure: 1.351 mmHg at 25°C.

Preparation of Butyric acid: It is industrially prepared by the fermentation of sugar or starch, brought about by the addition of putrefying cheese, with calcium carbonate added to neutralize the acids formed in the process. In addition, it can be prepared by butan-1-ol. The other product is butyraldehyde. This reaction will need reagent NaBrO3 and catalyst Ru2(dmnapy)Cl4. The reaction time is 15 hours with ambient temperature. The yield is about 91.5%.

Butyric acid can be prepared by butan-1-ol. The other product is butyraldehyde

Uses of Butyric acid: it can be used as food, perfume and fishing bait additives, an animal feed supplement, an approved food flavouring. In addition, it is used in the preparation of various butyrate esters. Besides, it can react with 4-methyl-quinoline to get 4-methyl-2-propyl-quinoline. This reaction will need reagents sulfuric acid and iron(III) sulfate, and solvent H2O. The reaction time is 20 hours with irradiation. The yield is about 76%.

Butyric acid can react with 4-methyl-quinoline to get 4-methyl-2-propyl-quinoline

When you are using this chemical, please be cautious about it as the following:
This chemical can cause burns. During using it, wear suitable protective clothing. In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. And in case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.).

You can still convert the following datas into molecular structure:
(1)SMILES: CCCC(=O)O
(2)InChI: InChI=1/C4H8O2/c1-2-3-4(5)6/h2-3H2,1H3,(H,5,6)
(3)InChIKey: FERIUCNNQQJTOY-UHFFFAOYAP

The toxicity data is as follows:

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
mouse LC inhalation > 500mg/m3 (500mg/m3) LUNGS, THORAX, OR RESPIRATION: STRUCTURAL OR FUNCTIONAL CHANGE IN TRACHEA OR BRONCHI Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 23(5), Pg. 31, 1958.
mouse LD50 intraperitoneal 3180mg/kg (3180mg/kg)   Journal of Pharmacy and Pharmacology. Vol. 21, Pg. 85, 1969.
mouse LD50 intravenous 800mg/kg (800mg/kg) BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD Acta Pharmacologica et Toxicologica. Vol. 18, Pg. 141, 1961.
mouse LD50 subcutaneous 3180mg/kg (3180mg/kg)   Journal of Pharmacy and Pharmacology. Vol. 21, Pg. 85, 1969.
mouse LDLo oral 500mg/kg (500mg/kg) GASTROINTESTINAL: NECROTIC GHANGES

KIDNEY, URETER, AND BLADDER: OTHER CHANGES

BLOOD: CHANGES IN SPLEEN
Toksikologiya Novykh Promyshlennykh Khimicheskikh Veshchestv. Toxicology of New Industrial Chemical Substances. For English translation, see TNICS*. Vol. 4, Pg. 19, 1962.
rabbit LD50 skin 530uL/kg (0.53mL/kg)   Union Carbide Data Sheet. Vol. 4/10/1968,
rat LC inhalation > 500mg/m3 (500mg/m3) LUNGS, THORAX, OR RESPIRATION: STRUCTURAL OR FUNCTIONAL CHANGE IN TRACHEA OR BRONCHI Toksikologiya Novykh Promyshlennykh Khimicheskikh Veshchestv. Toxicology of New Industrial Chemical Substances. For English translation, see TNICS*. Vol. 4, Pg. 19, 1962.
rat LD50 oral 2gm/kg (2000mg/kg)   "Toxicometric Parameters of Industrial Toxic Chemicals Under Single Exposure," Izmerov, N.F., et al., Moscow, Centre of International Projects, GKNT, 1982Vol. -, Pg. 30, 1982.

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