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124-07-2

Basic Information
CAS No.: 124-07-2
Name: Octanoic acid
Molecular Structure:
Molecular Structure of 124-07-2 (Octanoic acid)
Formula: C8H16O2
Molecular Weight: 144.21
Synonyms: 1-Heptanecarboxylic acid;n-Caprylic acid;n-Octanoic acid;n-Octylic acid;
EINECS: 204-677-5
Density: 0.929 g/cm3
Melting Point: 16 °C
Boiling Point: 239.33 °C at 760 mmHg
Flash Point: 107.379 °C
Solubility: 0.68 g/L (20 ºC)
Appearance: colourless oily liquid
Hazard Symbols: CorrosiveC,IrritantXi
Risk Codes: 34
Safety: 26-36/39-45-36/37/39-25-27
Transport Information: UN 3265 8/PG 3
PSA: 37.30000
LogP: 2.43150
Synthetic route
1974-04-5

2-bromoheptane

124-38-9

carbon dioxide

124-07-2

Octanoic acid

Conditions
ConditionsYield
With nickel(II) iodide; manganese; C36H40N2 In N,N-dimethyl-formamide at 25℃; under 760.051 Torr; for 20h; regioselective reaction;92%
With rubidium carbonate; diethyl 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate; (4s,6s)-2,4,5,6-tetra(9H-carbazol-9-yl)isophthalonitrile; (6,6’-dimethyl-2,2'-bipyridine)nickel(II) dibromide; tetra-(n-butyl)ammonium iodide In N,N-dimethyl-formamide at 10℃; under 750.075 Torr; for 20h; Schlenk technique; Sealed tube; Irradiation;48%
Stage #1: 2-bromoheptane; carbon dioxide With nickel(II) bromide dimethoxyethane; C32H32N2; C42H34F10IrN4(1+)*F6P(1-); N-ethyl-N,N-diisopropylamine; lithium tert-butoxide In N,N-dimethyl-formamide at 30℃; for 24h; Microwave irradiation; Schlenk technique;
Stage #2: With hydrogenchloride In water; N,N-dimethyl-formamide Reagent/catalyst;
25%
Stage #1: carbon dioxide With nickel(II) iodide; manganese; C36H40N2 In N,N-dimethyl-formamide at 25℃; under 760.051 Torr; Schlenk technique;
Stage #2: 2-bromoheptane In N,N-dimethyl-formamide at 25℃; under 760.051 Torr; for 20h; Schlenk technique;
Stage #3: With hydrogenchloride In water; N,N-dimethyl-formamide Reagent/catalyst;
76 %Spectr.
111-87-5

octanol

124-07-2

Octanoic acid

Conditions
ConditionsYield
With nitric acid for 0.333333h; Ambient temperature; sonication;100%
With nitric acid for 0.333333h; Ambient temperature; sonication;100%
With ruthenium trichloride; iodobenzene; potassium peroxomonosulfate In water; acetonitrile at 20℃; for 16h;100%
124-13-0

Octanal

124-07-2

Octanoic acid

Conditions
ConditionsYield
With tris[2-(4,6-difluorophenyl)pyridinato-C2,N]-iridium(III); oxygen In acetonitrile at 20℃; Irradiation; Sealed tube; Green chemistry; chemoselective reaction;99%
With diphenyl diselenide; dihydrogen peroxide In water at 20℃; for 3h; Green chemistry;99%
With copper acetylacetonate; oxygen; sodium hydroxide; 1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene In water at 50℃; under 760.051 Torr; for 12h; Sealed tube;99%
124-38-9

carbon dioxide

124-07-2

Octanoic acid

Conditions
ConditionsYield
With nickel(II) iodide; manganese; C36H40N2 In N,N-dimethyl-formamide at 25℃; under 760.051 Torr; for 20h; regioselective reaction;81%
1974-04-5

2-bromoheptane

124-38-9

carbon dioxide

B

124-07-2

Octanoic acid

Conditions
ConditionsYield
Stage #1: 2-bromoheptane; carbon dioxide With nickel(II) iodide; manganese; 2,9-diethyl-4,7-diphenyl-1,10-phenanthroline In N,N-dimethyl-formamide at 30℃; under 760.051 Torr; for 17h; Schlenk technique;
Stage #2: With hydrogenchloride In water; N,N-dimethyl-formamide Reagent/catalyst; Temperature; Solvent;
A n/a
B 72%
With rubidium carbonate; diethyl 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate; (4s,6s)-2,4,5,6-tetra(9H-carbazol-9-yl)isophthalonitrile; (6,6’-dimethyl-2,2'-bipyridine)nickel(II) dibromide In N,N-dimethyl-formamide at 10℃; under 750.075 Torr; for 20h; Reagent/catalyst; Schlenk technique; Sealed tube; Irradiation; Overall yield = 48 %; Overall yield = 17.3 mg;
998-93-6

4-bromoheptane

124-38-9

carbon dioxide

124-07-2

Octanoic acid

Conditions
ConditionsYield
With nickel(II) iodide; manganese; C36H40N2 In N,N-dimethyl-formamide at 25℃; under 760.051 Torr; for 20h; regioselective reaction;72%
698-76-0

6-propyl-tetrahydro-pyran-2-one

124-07-2

Octanoic acid

Conditions
ConditionsYield
With palladium on activated carbon; W(OTf)6; hydrogen In neat (no solvent) at 135℃; under 760.051 Torr; for 12h;98%
With palladium 10% on activated carbon; W(OTf)6; hydrogen at 135℃; under 760.051 Torr; for 12h;92%
124-38-9

carbon dioxide

B

124-07-2

Octanoic acid

Conditions
ConditionsYield
Stage #1: 3-bromoheptane; carbon dioxide With nickel(II) iodide; manganese; C36H40N2 In N,N-dimethyl-formamide at 25℃; under 760.051 Torr; for 17h; Schlenk technique;
Stage #2: With hydrogenchloride In water; N,N-dimethyl-formamide
A n/a
B 81%
124-38-9

carbon dioxide

5011-57-4

2-(p-toluenesulfonyl)heptane

124-07-2

Octanoic acid

Conditions
ConditionsYield
With nickel(II) iodide; manganese; C36H40N2 In N,N-dimethyl-formamide at 25℃; under 760.051 Torr; for 20h; regioselective reaction;56%

dimethyl 2-((5-(hydroxymethyl)furan-2-yl)methylene)malonate

124-07-2

Octanoic acid

Conditions
ConditionsYield
With palladium 10% on activated carbon; W(OTf)6; hydrogen; acetic acid at 180℃; under 22502.3 Torr; for 10h; Autoclave;80%
With palladium on activated charcoal; W(OTf)6; hydrogen; acetic acid at 180℃; under 22502.3 Torr; for 10h; Autoclave;80%
998-93-6

4-bromoheptane

124-38-9

carbon dioxide

B

124-07-2

Octanoic acid

Conditions
ConditionsYield
Stage #1: 4-bromoheptane; carbon dioxide With nickel(II) iodide; manganese; C36H40N2 In N,N-dimethyl-formamide at 25℃; under 760.051 Torr; for 17h; Schlenk technique;
Stage #2: With hydrogenchloride In water; N,N-dimethyl-formamide
A n/a
B 72%
oxone

oxone

Os(VIII)

Os(VIII)

124-11-8

non-1-ene

124-07-2

Octanoic acid

Conditions
ConditionsYield
With hydrogenchloride; sodium sulfate; OsO4 In ethyl acetate; N,N-dimethyl-formamide; tert-butyl alcohol90%
1871-67-6

(E)-oct-2-enoic acid

124-07-2

Octanoic acid

Conditions
ConditionsYield
With carbon monoxide; hydrogen; triethylamine; acetylacetonatodicarbonylrhodium(l); triphenylphosphine In dichloromethane at 25℃; under 7500.75 Torr; for 24h;42%
124-38-9

carbon dioxide

4883-86-7

4-heptyltoluene-p-sulphonate

124-07-2

Octanoic acid

Conditions
ConditionsYield
With nickel(II) iodide; manganese; C36H40N2 In N,N-dimethyl-formamide at 25℃; under 760.051 Torr; for 20h; regioselective reaction;50%
14779-25-0

3-(5-methylfuran-2-yl) acrylic acid

124-07-2

Octanoic acid

Conditions
ConditionsYield
With palladium on activated charcoal; W(OTf)6; hydrogen; acetic acid at 180℃; under 22502.3 Torr; for 10h; Autoclave;86%
111-87-5

octanol

A

111-66-0

oct-1-ene

B

124-07-2

Octanoic acid

Conditions
ConditionsYield
With 1,10-Phenanthroline; oxygen; cobalt(II) nitrate In dimethyl sulfoxide at 100℃; under 9000.9 Torr; for 12h;A 36%
B 53%
124-11-8

non-1-ene

124-07-2

Octanoic acid

Conditions
ConditionsYield
Stage #1: non-1-ene With oxygen; ozone In tetrahydrofuran at 0℃;
Stage #2: With semicarbazide hydrochloride In tetrahydrofuran at 0 - 20℃; Inert atmosphere;
95%
Stage #1: non-1-ene With ozone In dichloromethane; acetic acid at 0℃;
Stage #2: With semicarbazide hydrochloride In dichloromethane; acetic acid at 0 - 20℃;
95%
With Oxone; osmium(VIII) oxide In N,N-dimethyl-formamide; tert-butyl alcohol at 20℃; for 3h;90%
592-76-7

1-Heptene

124-38-9

carbon dioxide

B

124-07-2

Octanoic acid

Conditions
ConditionsYield
With nickel(II) iodide; manganese; Bathocuproine; water In N,N-dimethyl-formamide at 50℃; under 760.051 Torr; for 40h;A n/a
B 49%
5663-96-7

oct-2-ynoic acid

124-07-2

Octanoic acid

Conditions
ConditionsYield
With ethanol; lithium; nickel dichloride; 4,4'-di-tert-butylbiphenyl In tetrahydrofuran at 20℃; for 12h;93%
With sodium hydroxide; Triethoxysilane; water; palladium diacetate for 4h; Ambient temperature;92%
With sodium tetrahydroborate; sodium hydroxide In water at 20 - 60℃;92%
With ethanol; sodium
111-11-5

methyl octanate

A

7377-03-9

caprylohydroxamic acid

B

124-07-2

Octanoic acid

Conditions
ConditionsYield
With hydroxylamine nitrate; sodium hydroxide In methanol at 0 - 50℃; for 3h;A 84%
B 3 g
124-11-8

non-1-ene

20478-70-0

decanoic acid hydrazide

A

124-07-2

Octanoic acid

B

N'-[(1E)-octylidene]decanohydrazide

Conditions
ConditionsYield
Stage #1: non-1-ene With oxygen; ozone In tetrahydrofuran at 0℃;
Stage #2: decanoic acid hydrazide In tetrahydrofuran at 0 - 20℃; for 72h;
A 12%
B 78%
111-87-5

octanol

A

124-13-0

Octanal

B

124-07-2

Octanoic acid

Conditions
ConditionsYield
With hydrogenchloride; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; sodium nitrite In dichloromethane; water at 20℃; under 760.051 Torr; for 12h; in air;A 92%
B 5.2%
With Succinimide; sodium hypochlorite solution; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; potassium carbonate In ethyl acetate at 0 - 10℃; for 2h;A 86%
B 7%
With potassium chromate; copolyesteramide (from N,N'-bis(4-methoxycarbonylbenzoyl)hexamethylenediamine, 1,6-hexanediol, poly(ethylene glycol)); sulfuric acid In dichloromethane at -5℃; for 0.25h;A 83%
B 2.1%
1871-67-6

(E)-oct-2-enoic acid

201230-82-2

carbon monoxide

A

124-13-0

Octanal

B

124-07-2

Octanoic acid

C

1039763-53-5

C9H16O3

Conditions
ConditionsYield
With tris(2,4-di-tert-butylphenyl)phosphite; hydrogen; acetylacetonatodicarbonylrhodium(l) In dichloromethane at 25℃; under 7500.75 Torr; for 24h;A 23%
B 33%
C 12%
592-77-8

hept-2-ene

124-38-9

carbon dioxide

B

124-07-2

Octanoic acid

Conditions
ConditionsYield
With nickel(II) iodide; manganese; Bathocuproine; water In N,N-dimethyl-formamide at 50℃; under 760.051 Torr; for 40h;A n/a
B 15%
1456-12-8

methyl ester of 5-methyl-3-(2-furyl)propanoic acid

124-07-2

Octanoic acid

Conditions
ConditionsYield
With hydrogen; trifluoroacetic acid In n-heptane at 190℃; under 22502.3 Torr; for 10h; Reagent/catalyst; Temperature; Pressure; Autoclave; High pressure;91 %Chromat.
1871-67-6

(E)-oct-2-enoic acid

201230-82-2

carbon monoxide

A

124-13-0

Octanal

B

124-07-2

Octanoic acid

Conditions
ConditionsYield
With hydrogen; acetylacetonatodicarbonylrhodium(l) In dichloromethane at 25℃; under 7500.75 Torr; for 24h;
With hydrogen; acetylacetonatodicarbonylrhodium(l) In dichloromethane at 25℃; under 7500.75 Torr; for 20.5h;A 91 % Chromat.
B 4.5 % Spectr.
111-87-5

octanol

A

124-07-2

Octanoic acid

B

2306-88-9

octyl octylate

Conditions
ConditionsYield
With sodium bromate; sodium hydrogensulfite for 2h; Ambient temperature;A 3%
B 94%
Stage #1: octanol With gold on titanium oxide In water at 90℃; for 0.166667h; Inert atmosphere;
Stage #2: With dihydrogen peroxide In water at 90℃; for 1.08333h; Inert atmosphere; chemoselective reaction;
A 90%
B n/a
With sodium tungstate; dihydrogen peroxide In water at 90℃; for 4h;A 87%
B 2%
124-11-8

non-1-ene

1576-35-8

toluene-4-sulfonic acid hydrazide

A

124-07-2

Octanoic acid

B

4-methyl-N'-octylidenebenzene-1-sulfonohydrazide

4-methyl-N'-octylidenebenzene-1-sulfonohydrazide

Conditions
ConditionsYield
Stage #1: non-1-ene With oxygen; ozone In dichloromethane; acetic acid at 0℃;
Stage #2: toluene-4-sulfonic acid hydrazide In dichloromethane; acetic acid at 20℃; Inert atmosphere;
A 19%
B 42%
64-17-5

ethanol

124-13-0

Octanal

124-07-2

Octanoic acid

Conditions
ConditionsYield
With oxygen at 100℃; under 3750.38 Torr; for 5h; Autoclave;11 %Chromat.
64-17-5

ethanol

124-13-0

Octanal

A

54889-48-4

1,1-diethoxy-octane

B

124-07-2

Octanoic acid

C

106-32-1

octanoic acid ethyl ester

Conditions
ConditionsYield
With oxygen at 100℃; under 3750.38 Torr; for 5h; Autoclave;A 27 %Chromat.
B 8 %Chromat.
C 7 %Chromat.
With oxygen at 100℃; under 3750.38 Torr; for 5h; Reagent/catalyst; Autoclave;A 8 %Chromat.
B 13 %Chromat.
C 58 %Chromat.
With oxygen at 100℃; under 3750.38 Torr; for 5h; Reagent/catalyst; Autoclave;A 63 %Chromat.
B 6 %Chromat.
C 12 %Chromat.
124-07-2

Octanoic acid

54107-24-3

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

127827-87-6

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

Conditions
ConditionsYield
With heptafluorobutyric Acid at 75℃; for 3h;100%
124-07-2

Octanoic acid

59565-09-2

2-(vinyloxy)ethyl isothiocyanate

Octanoic acid (2-vinyloxy-ethyl)-amide

Conditions
ConditionsYield
With triethylamine at 45 - 50℃; for 1h;100%
124-07-2

Octanoic acid

125034-39-1

2-(Trimethylsilyl)ethyl 6-O-tert-butyldimethylsilyl-2-deoxy-4-O-diphenoxyphosphinyl-3-O-<(3R)-3-hydroxytetradecanoyl>-2-<(3R)-3-<(2-trimethylsilylethoxy)methoxy>tetradecanamido>-β-D-glucopyranoside

125056-34-0

2-(Trimethylsilyl)ethyl 6-O-tert-butyldimethylsilyl-2-deoxy-4-O-diphenoxyphosphinyl-3-O-<(3R)-3-octanoyloxytetradecanoyl>-2-<(3R)-3-<(2-trimethylsilylethoxy)methoxy>tetradecanamido>-β-D-glucopyranoside

Conditions
ConditionsYield
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane Ambient temperature;100%
124-07-2

Octanoic acid

142-82-5

n-heptane

Conditions
ConditionsYield
With palladium on silica gel; hydrogen at 300℃; under 760.051 Torr; for 4h; Temperature; Flow reactor;100%
With hydrogen; silica gel; palladium at 330℃; Ni/Al2O3, 180 deg C;97%
With Au0012O19676(00)Pd042(98)Si038; hydrogen at 260℃; under 760.051 Torr; Catalytic behavior; Reagent/catalyst;
124-07-2

Octanoic acid

3945-69-5

4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride

octanoic acid 4,6-dimethoxy-[1,3,5]triazin-2-yl ester

Conditions
ConditionsYield
In 1,2-dimethoxyethane at 0℃; for 3h; Condensation;100%
124-07-2

Octanoic acid

C8H16O2*C19H21NO

Conditions
ConditionsYield
In tetrahydrofuran at 40 - 50℃; for 5h;100%
124-07-2

Octanoic acid

642-72-8

benzydamine

C19H23N3O*C8H16O2

Conditions
ConditionsYield
In tetrahydrofuran at 40 - 50℃; for 5h;100%
124-07-2

Octanoic acid

3375-31-3

palladium diacetate

palladium dioctanoate

Conditions
ConditionsYield
In cyclohexane at 40℃; Solvent;100%
143-07-7

lauric acid

75-94-5

trichlorovinylsilane

124-07-2

Octanoic acid

544-63-8

n-tetradecanoic acid

1330066-17-5

C36H68O6Si

Conditions
ConditionsYield
In toluene at 60 - 150℃; for 4h;99.82%
124-07-2

Octanoic acid

36653-82-4

1-Hexadecanol

29710-31-4

Octanoic acid, hexadecyl ester

Conditions
ConditionsYield
With choline chloride; zinc(II) chloride at 110℃; for 6h;99%
With immobilized lipase Novozym 435 from Candida antarctica B supported on a macroporous acrylic resin In carbon dioxide at 63.7℃; under 76657.7 Torr; for 0.333333h; Supercritical conditions; Enzymatic reaction; liquid CO2;99.5%

rhodium(III) hydroxide

124-07-2

Octanoic acid

dirhodium(II) tetraoctanoate

Conditions
ConditionsYield
at 105℃; for 6h; Temperature; Concentration;99.24%
124-07-2

Octanoic acid

56-81-5

glycerol

538-23-8

tricaprilin

Conditions
ConditionsYield
With acetic acid at 275℃; for 0.5h;99.2%
With tungsten(VI) oxide at 175℃; under 1 Torr; for 22h; Reagent/catalyst;93%
at 100℃; Beim Erhitzen in Gegenwart von aus Naphthalin,Oelsaeure und konz.Schwefelsaeure in Petrolaether dargestelltem Twitchells Reagens;
67-56-1

methanol

124-07-2

Octanoic acid

111-11-5

methyl octanate

Conditions
ConditionsYield
polyaniline sulfate at 70℃; for 24h;99%
With N-Bromosuccinimide at 70℃; for 2h; Time;97%
With 1,3-dibromo-5,5-dimethylimidazolidine-2,4-dione at 70℃; for 2h;97%
124-07-2

Octanoic acid

111-87-5

octanol

Conditions
ConditionsYield
With samarium diiodide; heptanal; samarium(III) trifluoromethanesulfonate In tetrahydrofuran; methanol; potassium hydroxide at 20℃; for 0.075h; Reduction;99%
With 1,1,3,3-Tetramethyldisiloxane; copper(II) bis(trifluoromethanesulfonate) In toluene at 80℃; for 16h; sealed tube;91%
With hydrogen In neat (no solvent) at 180℃; under 37503.8 Torr; for 12h;91%
124-07-2

Octanoic acid

7377-03-9

caprylohydroxamic acid

Conditions
ConditionsYield
With Novozym 435 (Candida antarctica lipase B on Lewatit E); hydroxylamine In water at 40℃; for 20h; Condensation; Enzymatic reaction;99%
Stage #1: Octanoic acid With acetic anhydride for 0.166667h;
Stage #2: With hydroxylamine hydrochloride for 0.666667h;
95.81%
With liverextract; hydroxylamine
With hydroxylamine; 1,1'-carbonyldiimidazole
With hydroxylamine; adenosine monophosphate ligase SfaB from Streptomyces thioluteus; ATP; magnesium chloride; Cleland's reagent In aq. buffer at 30℃; for 6h; pH=8; Enzymatic reaction;
124-07-2

Octanoic acid

100-51-6

benzyl alcohol

10276-85-4

benzyl caprylate

Conditions
ConditionsYield
With [Cl(C6F13C2H4)2SnOSn(C2H4C6F13)2Cl]2 In various solvent(s) at 150℃; for 10h;99%
With pyrographite; toluene-4-sulfonic acid for 0.00777778h; Esterification; Microwave irradiation (675 W);90%
With tris(2-methoxyphenyl)bismuthine In benzene for 12h; Heating;86%
124-07-2

Octanoic acid

98-52-2

4-(1,1-dimethylethyl)-cyclohexanol

octanoic acid 4-tert-butyl-cyclohexyl ester

Conditions
ConditionsYield
With pyridine; <(chlorosulfinyloxy)methylene>dimethylammonium chloride In dichloromethane at 20℃; for 6h;99%
124-07-2

Octanoic acid

108-93-0

cyclohexanol

1551-42-4

octanoic acid cyclohexyl ester

Conditions
ConditionsYield
With pyridine; <(chlorosulfinyloxy)methylene>dimethylammonium chloride In dichloromethane at 20℃; for 6h;99%
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    Octanoic acid

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    Min.Order: 1 Kilogram

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    Specifications CAS No.: 124-07-2 Other Names: caprylic acid MF: C16H30O4Sn EINECS No.: 204-677-5 Place of Origin: Henan, China (Main

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    124-07-2

    MSDS/COA Download

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    Min.Order: 1 Metric Ton

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  • Octanoic Acid

  • Casno:

    124-07-2

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    Octanoic Acid

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    124-07-2

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  • Octanoic acid

  • Casno:

    124-07-2

    Octanoic acid

    Min.Order: 1 Kilogram

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    Octanoic acid CAS RN: 124-07-2 Molecular formula: C8H16O2 Molecular weight: 144.21 Properties: Colorless and transparent liquid, no mechanical impurity.

    Founded in 2008, East Chemsources Limited is a professional manufacturer of supplier in food and beverage, pharmaceuticals, cosmetics and other industries. pharmaceutical field in

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  • Casno:

    124-07-2

    124-07-2 Octanoicacid

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  • n-Octanoic Acid

  • Casno:

    124-07-2

    n-Octanoic Acid

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  • N-Octanoic acid

  • Casno:

    124-07-2

    N-Octanoic acid

    Min.Order: 1 Kilogram

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    Product Name 1-Heptanecarboxylic acid;1-heptanecarboxylicacid;1-octanoic acid;acidecaprylique;acideoctanoique;Caprylsαure;Emery 657;Emery657 Synonyms 124-07-2 CAS C8H16O2

    Welcome to Henan Sinotech! Sinotech Corporation has exceptional sourcing ability for chemicals used in Organic Fine Chemicals and APIs; Inorganic chemicals; Flame Retardants;OLED

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    124-07-2

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    124-07-2

    Octanoic acid 124-07-2

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  • Octanoic acid

  • Casno:

    124-07-2

    Octanoic acid

    Min.Order: 1 Kilogram

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  • Casno:

    124-07-2

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    Min.Order: 1 Kilogram

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    Business Type:Trading Company

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  • Casno:

    124-07-2

    MSDS/COA Download

    BLOOM TECH Advanced API/Technology support Octanoic acid CAS 124-07-2

    Min.Order: 1 Gram

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  • Casno:

    124-07-2

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    Min.Order: 10 Gram

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    Business Type:Trading Company

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  • Octanoic acid 124-07-2

  • Casno:

    124-07-2

    Octanoic acid 124-07-2

    Min.Order: 1 Kilogram

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  • Casno:

    124-07-2

    Octanoic acid CAS NO.124-07-2

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  • Octanoic acid

  • Casno:

    124-07-2

    Octanoic acid

    Min.Order: 1 Kilogram

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  • Casno:

    124-07-2

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    Prouduct name: Octanoic acid CAS: 124-07-2 Appearance: colourless oily liquid Purity: 99% Min Certification of Octanoic acid CAS 124-07-2 Item Specifications Result

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    124-07-2

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    124-07-2

    MSDS/COA Download

    Monad Medicine 99% Purity CAS#124-07-2 Octanoic acid

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    Name: Octanoic acid Appearance: Liquid CAS Number: 124-07-2 Package: According to the customer's request Export Port: Wuhan, Shanghai, Shenzhen, Guangzhou, etc, Purity: 99% min Storage condition: Refrigerator store (w

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    124-07-2

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    Business Type:Trading Company

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  • Casno:

    124-07-2

    Octanoic acid

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  • Casno:

    124-07-2

    Octanoic acid

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    124-07-2

    Octanoic acid 124-07-2

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  • Octanoic acid

  • Casno:

    124-07-2

    Octanoic acid

    Min.Order: 100 Metric Ton

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    124-07-2

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  • OCTANOIC ACID

  • Casno:

    124-07-2

    OCTANOIC ACID

    Min.Order: 1 Gram

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    124-07-2

    Octanoic acid

    Min.Order: 0

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    Address:No.200 Zhenhua Rd.Xihu Industrial Park, Hangzhou 310030, China

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  • Casno:

    124-07-2

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    124-07-2

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    124-07-2

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  • Casno:

    124-07-2

    Octanoic acid

    Min.Order: 0

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Reported in EPA TSCA Inventory.

Specification

The IUPAC name of this chemical is Octanoic acid. With the CAS registry number 124-07-2 and EINECS registry number 204-677-5, it is also named as 1-Heptanecarboxylicacid. In addition, the molecular formula is C8H16O2 and the molecular weight is 144.21. It is a kind of colourless oily liquid and belongs to the classes of Miscellaneous Natural Products; Alkylcarboxylic Acids; Monofunctional & alpha,omega-Bifunctional Alkanes; Monofunctional Alkanes. And it is minimally soluble in water with a slightly unpleasant rancid-like smell and taste.

Physical properties about this chemical are: (1)ACD/LogP: 2.74; (2)ACD/LogD (pH 5.5): 1.94; (3)ACD/LogD (pH 7.4): 0.146; (4)ACD/BCF (pH 5.5): 11.324; (5)ACD/BCF (pH 7.4): 1; (6)ACD/KOC (pH 5.5): 117.554; (7)ACD/KOC (pH 7.4): 1.887; (8)#H bond acceptors: 2; (9)#H bond donors: 1; (10)#Freely Rotating Bonds: 6; (11)Polar Surface Area: 37.3 Å2; (12)Index of Refraction: 1.437; (13)Molar Refractivity: 40.676 cm3; (14)Molar Volume: 155.215 cm3; (15)Polarizability: 16.125 ×10-24cm3; (16)Surface Tension: 33.075 dyne/cm; (17)Density: 0.929 g/cm3; (18)Flash Point: 107.379 °C; (19)Enthalpy of Vaporization: 50.325 kJ/mol; (20)Boiling Point: 239.33 °C at 760 mmHg; (21)Vapour Pressure: 0.022 mmHg at 25°C.

Preparation of Octanoic acid: it can be prepared by octanoyl chloride. The other product is octanoic acid octyl ester. This reaction will need reagent LiInH4 and solvent diethyl ether. The reaction should react in temperature of 0 °C for 1 hour and in the room temperature for 12 hours. The yield is about 22%.

Octanoic acid can be prepared by octanoyl chloride

Uses of Octanoic acid: it is used commercially in the production of esters used in perfumery and also in the manufacture of dyes. And it is also used in the treatment of some bacterial infections and used as an algaecide, bactericide, and fungicide in nurseries, greenhouses, garden centers, and interiorscapes on ornamentals. Moreover, it is also used as disinfectant in health care facilities, schools/colleges, animal care/veterinary facilities, industrial facilities, office buildings, recreational facilities. In addition, it can be used to get octan-1-ol. This reaction will need reagents Sm and 10percent HCl and solvent methanol. The reaction time is 30 minutes with ambient temperature. The yield is about 39%.

Octanoic acid can be used to get octan-1-ol.

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, gloves and eye/face protection and avoid contact with eyes. 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: CCCCCCCC(=O)O
(2)InChI: InChI=1/C8H16O2/c1-2-3-4-5-6-7-8(9)10/h2-7H2,1H3,(H,9,10)
(3)InChIKey: WWZKQHOCKIZLMA-UHFFFAOYAH

The toxicity data is as follows:

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
mouse LD50 intravenous 600mg/kg (600mg/kg) BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD Acta Pharmacologica et Toxicologica. Vol. 18, Pg. 141, 1961.
rabbit LD50 skin > 5gm/kg (5000mg/kg)   Food and Cosmetics Toxicology. Vol. 19, Pg. 237, 1981.
rat LD50 oral 10080mg/kg (10080mg/kg) BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)

GASTROINTESTINAL: "HYPERMOTILITY, DIARRHEA"
Food and Cosmetics Toxicology. Vol. 2, Pg. 327, 1964.