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Items Standard Result Appearance White to pale yellow crystal Complies Odor Characteristi
Cas:334-48-5
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inquiryProduct name: Decanoic acid CAS: 334-48-5 MF: C10H20O2 MW: 172.26 EINECS: 206-376-4 Purity:
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Capric acid CAS: 334-48-5 Specification Item Standard Structural data confirmation 1. H-NMR: The data of structure are identical with reference standard 2. HPLC-MS: Ensure the mol
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Cas:334-48-5
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Cas:334-48-5
Min.Order:10 Gram
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inquiryProduct Name: Decanoic acid Synonyms: acidedecanoique;Caprinsαure;Caprynic acid;caprynicacid;Decansαure;Decatoicacid;Decoic acid;decoicacid CAS: 334-48-5 MF: C10H20O2 MW: 172.26 EINECS: 206-376-4 Product Categories: Pharmace
Cas:334-48-5
Min.Order:1 Kilogram
Negotiable
Type:Lab/Research institutions
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Company Introduction 1. Established in 2005, with two independent business divisions: Fine chemicals division; Pharmaceutical division. 2. Main product: Optical brightener Textile auxiliary Dye stuff Pigments
Packing: According to customer requirements Delivery time: In stock or depands Port of shipment: Ningbo/Shanghai/Qingdao OEM/ODM:Welcome Sample:We can offer our existing samples at once Transportation:Express/Sea/Air Port:Ningbo/Shanghai/Qingd
Conditions | Yield |
---|---|
With selenium(IV) oxide; dihydrogen peroxide In tetrahydrofuran for 4h; Heating; | 100% |
With palladium 10% on activated carbon; water; sodium hydroxide at 80℃; under 600.06 Torr; for 6h; | 99% |
With dihydrogen peroxide In acetic acid at 90℃; for 7h; | 97% |
1-decanoic acid
Conditions | Yield |
---|---|
With trifluoroacetic acid for 15h; Product distribution; | 100% |
1-decanoic acid
Conditions | Yield |
---|---|
With lithium hydroxide In tetrahydrofuran; water at 20℃; Inert atmosphere; | 100% |
Conditions | Yield |
---|---|
With 1-methyl-pyrrolidin-2-one; buta-1,3-diene; nickel dichloride In tetrahydrofuran at -78 - 0℃; for 1h; Inert atmosphere; | 99% |
1-decanoic acid
Conditions | Yield |
---|---|
With palladium 10% on activated carbon; W(OTf)6; hydrogen; acetic acid at 180℃; under 15001.5 Torr; for 10h; Reagent/catalyst; Temperature; Pressure; Autoclave; | 99% |
With palladium 10% on activated carbon; W(OTf)6; hydrogen; acetic acid at 180℃; under 22801.5 Torr; Pressure; Temperature; Reagent/catalyst; | 95% |
n-decanal oxime
1-decanoic acid
Conditions | Yield |
---|---|
With [hydroxy(tosyloxy)iodo]benzene; water In dimethyl sulfoxide at 20℃; for 24h; | 99% |
Conditions | Yield |
---|---|
Stage #1: 1-decyne With 1-methyl-pyrrolidin-2-one; C17H11ClF6N2Ru(1+) In water at 25℃; for 24h; Inert atmosphere; Stage #2: With [bis(acetoxy)iodo]benzene at 25℃; for 1h; | 98% |
1-decanoic acid
Conditions | Yield |
---|---|
With aluminium(III) triflate; 5%-palladium/activated carbon; hydrogen; acetic acid at 180℃; under 15201 Torr; | 98% |
With palladium 10% on activated carbon; W(OTf)6; hydrogen; acetic acid at 180℃; under 22502.3 Torr; for 10h; Reagent/catalyst; Pressure; Temperature; Autoclave; | 94% |
With palladium on activated charcoal; W(OTf)6; hydrogen; acetic acid at 180℃; under 22502.3 Torr; for 10h; Autoclave; | 94% |
1-decanoic acid
Conditions | Yield |
---|---|
Stage #1: Decanoic acid, tert-butyldimethylsilyl ester; carbon tetrabromide In ethanol at 20℃; for 0.5h; Irradiation; Stage #2: In ethanol at 20℃; for 1h; | 97% |
Conditions | Yield |
---|---|
With 4-acetylamino-2,2,6,6-tetramethylpiperidine-1-oxoammonium tetrafluoroborate In water; acetonitrile at 20℃; | 95% |
With [bis(acetoxy)iodo]benzene; iodine In acetonitrile at 20℃; for 2h; | 94% |
With Cu(II)-complex of salen-H4; dihydrogen peroxide In acetonitrile at 80℃; for 8h; | 93% |
Conditions | Yield |
---|---|
With sodium hypochlorite; lithium hypochlorite In ethanol at 77℃; for 4h; | 94% |
With sodium hypobromide |
Caprinsaeure-4-methoxybenzylester
A
1-decanoic acid
B
tri(p-bromophenyl)amine
C
4-methoxy-benzaldehyde
Conditions | Yield |
---|---|
With 2,6-dimethylpyridine; 2a(1+)(.) In water; acetonitrile oxidative electrolysis; Yield given; | A 93% B n/a C n/a |
Conditions | Yield |
---|---|
With formic acid; triethylamine at 100℃; Knoevenagel condensation; | 93% |
1-decanoic acid
Conditions | Yield |
---|---|
With ammonium chloride; zinc In ethanol for 0.25h; Heating; | 92% |
Conditions | Yield |
---|---|
With potassium hydroxide; polystyrene-CH2=O(CH2CH2O)6.4H copolymer at 25℃; for 17h; | 91% |
With potassium hydroxide; polystyrene-CH2=O(CH2CH2O)6.4H at 25℃; for 17h; Product distribution; various esters, saponification, different poly(ethylene glycol)s grafted copolymers; | 91% |
With Rhodococcus sp. LKE-028 esterase at 70℃; pH=11; aq. buffer; Enzymatic reaction; |
Conditions | Yield |
---|---|
Stage #1: 1-undecene With ozone In water; acetonitrile at 0℃; Inert atmosphere; Stage #2: With sodium chlorite In water; acetonitrile at 15 - 20℃; under 760.051 Torr; Inert atmosphere; Stage #3: With sodium hydrogen sulfate In water; acetonitrile at 35℃; for 0.166667h; Inert atmosphere; | 91% |
Decanoic acid benzhydryl ester
A
benzophenone
B
1-decanoic acid
C
4-bromo-N,N-bis(4-nitrophenyl)benzeneamine
Conditions | Yield |
---|---|
With 2c (1+)(.); sodium hydrogencarbonate In water; acetonitrile oxidative electrolysis; Yield given; | A n/a B 90% C n/a |
Conditions | Yield |
---|---|
With dipyridinium dichromate In N,N-dimethyl-formamide for 20h; Ambient temperature; | A n/a B 87% |
Conditions | Yield |
---|---|
With [2,2]bipyridinyl; bis(1,5-cyclooctadiene)nickel (0); zinc In N,N-dimethyl acetamide at 80℃; for 12h; | 87% |
Decanoic acid 2,4-dimethoxy-benzyl ester
A
1-decanoic acid
B
tri(p-bromophenyl)amine
C
2,4-Dimethoxybenzaldehyde
Conditions | Yield |
---|---|
With 2,6-dimethylpyridine; 2a-radical-kation In water; acetonitrile oxidative electrolysis; Yield given; | A 86% B n/a C n/a |
Conditions | Yield |
---|---|
With water; difluoro[4-(trifluoromethyl)phenyl]-λ3-bromane In dichloromethane at 0℃; for 1h; Baeyer-Villiger type oxidation; Inert atmosphere; | A 6 %Chromat. B 80% |
With water; difluoro[4-(trifluoromethyl)phenyl]-λ3-bromane In acetonitrile at 0℃; for 1h; Baeyer-Villiger type oxidation; Inert atmosphere; | A 69 %Chromat. B 27 %Chromat. |
Conditions | Yield |
---|---|
With sodium periodate; cetyltributylphosphonium bromide In chloroform; water for 8h; Heating; | A 78% B 20 % Chromat. |
Conditions | Yield |
---|---|
With 2,2,6,6-tetramethyl-piperidine-N-oxyl; oxone; potassium bromide; methyltrioxorhenium(VII) In acetonitrile at 0℃; for 4h; | A 78% B 6% |
With palladium 10% on activated carbon; water; sodium hydroxide at 80℃; under 600.06 Torr; for 6h; | A 6% B 60% |
With 10% Ru/C; water; oxygen In toluene at 90℃; under 760.051 Torr; for 24h; | A 14% B 59% |
tridecane-2,4-dione
1-decanoic acid
Conditions | Yield |
---|---|
With ammonium cerium(IV) nitrate In acetonitrile at 20℃; for 4h; | 75% |
With iodine; oxygen In ethyl acetate for 10h; Mercury lamp irradiation; | 61% |
Conditions | Yield |
---|---|
With oxygen; cobalt(II) acetate; manganese(II) acetate In acetic acid at 130℃; for 5h; | 74% |
C19H40O2Si
1-decanoic acid
Conditions | Yield |
---|---|
Stage #1: C19H40O2Si; carbon tetrabromide In ethanol at 20℃; for 0.5h; Irradiation; Stage #2: In ethanol at 20℃; for 4h; | 73% |
Conditions | Yield |
---|---|
With 10% Pt/activated carbon; oxygen In water at 80℃; for 6h; Green chemistry; chemoselective reaction; | A 14% B 72% |
non-1-ene
carbon monoxide
A
2-methylnonanoic acid
B
1-decanoic acid
Conditions | Yield |
---|---|
With water; triphenylphosphine; tin(ll) chloride; palladium dichloride In acetone at 90℃; under 18240 Torr; for 6h; | A 15% B 71% |
With water; triphenylphosphine; palladium dichloride In acetone at 90℃; under 9880 Torr; for 6h; Product distribution; further reagent, further pressure, further amounts of reagents, selectivity; | A 16% B 66% |
bis-triphenylphosphine-palladium(II) chloride; triphenylphosphine In 1,4-dioxane at 95℃; under 15200 Torr; for 4h; Product distribution; Rate constant; other catalyst; |
dichloromethane
1-Decanol
A
1-decanoic acid
B
Methylendidecanoat
C
decanoyloxymethyl chloride
Conditions | Yield |
---|---|
With benzyl(triethyl)ammoniumpermanganate | A 15% B 71% C 13% |
oct-1-ene
bromoacetic acid
A
5-hexyldihydro-2(3H)-furanone
B
1-decanoic acid
Conditions | Yield |
---|---|
With dibenzoyl peroxide In benzene for 5h; Heating; | A 68% B 6.5% |
With dibenzoyl peroxide In benzene for 5h; Heating; other olefins; | A 68% B 6.5% |
With dibenzoyl peroxide In benzene for 5h; Mechanism; Heating; other α-bromocarboxylic acids; | A 68% B 6.5% |
Conditions | Yield |
---|---|
With oxalyl dichloride; N,N-dimethyl-formamide In dichloromethane at 0 - 20℃; for 4h; | 100% |
With Amberlite IRA 93 (PCl5 form) In 1,2-dichloro-ethane for 2h; Heating; | 86% |
With phosphorus trichloride at 60 - 100℃; |
1-decanoic acid
(R,S)-2,2-dimethyl-1,3-dioxolane-4-methanol
(2,2-dimethyl-1,3-dioxolane-4-yl)methyl caprate
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide Esterification; | 100% |
With dmap; dicyclohexyl-carbodiimide In diethyl ether at 20 - 25℃; for 4.5h; Esterification; | |
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 0 - 20℃; for 16h; |
1,3-dioxan-5-yl 4-methylbenzene-1-sulfonate
1-decanoic acid
decanoic acid 3-hydroxy-2-(toluene-4-sulfonyloxy)-propyl ester
Conditions | Yield |
---|---|
With boron trifluoride diethyl etherate; trifluoroacetic anhydride In tetrahydrofuran at 20℃; for 2h; acylolysis; | 100% |
1-decanoic acid
Conditions | Yield |
---|---|
With camphor sulphuric acid for 18h; Heating; | 100% |
Conditions | Yield |
---|---|
With zirconium(IV) oxychloride In 1,3,5-trimethyl-benzene at 162℃; for 24h; | 100% |
With choline chloride; zinc(II) chloride at 110℃; for 6h; | 99% |
ZrOCl2 hydrate In 1,3,5-trimethyl-benzene at 165℃; for 24h; Product distribution / selectivity; | 100 %Chromat. |
HfOCl2 hydrate In 1,3,5-trimethyl-benzene at 165℃; for 24h; Product distribution / selectivity; | 99.2 %Chromat. |
ZrOCl2/ZrO2 catalyst In 1,3,5-trimethyl-benzene at 165℃; for 24h; Product distribution / selectivity; | 56 %Chromat. |
Conditions | Yield |
---|---|
With Bu4NHSO4; sodium hydrogencarbonate In CH2Cl2:H2O | 100% |
1-decanoic acid
cholinium hydrogen carbonate
(2-hydroxyethyl)trimethylammonium decanoate
Conditions | Yield |
---|---|
In water at 20℃; | 100% |
In water at 20℃; |
1-decanoic acid
pregabilin
(S)-3-(aminomethyl)-5-methylhexanoic acid caprate
Conditions | Yield |
---|---|
In tert-butyl methyl ether for 0.75h; | 100% |
cycl-isopropylidene malonate
1-decanoic acid
5-decanoyl-6-hydroxy-2,2-dimethyl-4H-1,3-dioxin-4-one
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide In dichloromethane at 20℃; for 7h; | 100% |
With dmap; triethylamine; dicyclohexyl-carbodiimide In dichloromethane at 0 - 20℃; Inert atmosphere; | 65% |
Conditions | Yield |
---|---|
Stage #1: Nα-Fmoc-Nδ-(acetyl)-Nδ-(benzoyloxy)-L-ornithine With N-ethyl-N,N-diisopropylamine In dichloromethane for 1h; Stage #2: 1-decanoic acid; Fmoc-Ser(tBu)-OH; Fmoc-Orn(Boc)-OH With piperidine In N,N-dimethyl-formamide Further stages; | 100% |
1-decanoic acid
Conditions | Yield |
---|---|
With ammonium hydroxide pH=8; | 100% |
1-decanoic acid
(+)-O-Demethyltramadol
(+)-(1R,2R)-3-[2-(dimethylamino)-methyl-1-hydroxycyclohexyl]phenol decanoate
Conditions | Yield |
---|---|
In pentane at 20 - 30℃; for 24.5h; Product distribution / selectivity; | 99.2% |
Conditions | Yield |
---|---|
With tetrachloromethane at 20℃; for 12h; UV-irradiation; | 99% |
With Mesoscopically Assembled SulfatedZirconia Nanoparticles at 49.84℃; for 8h; Catalytic behavior; Reagent/catalyst; Temperature; | 97% |
With sulfuric acid; acetonitrile at 80 - 85℃; for 16 - 18h; | 97% |
Conditions | Yield |
---|---|
With Bromotrichloromethane; 4-(diphenylphosphino)-benzyltrimethylammonium bromide; triethylamine In tetrahydrofuran at 60℃; for 6h; Inert atmosphere; | 99% |
With 4-methyl-morpholine; C14H12Cl2N4O3 In dichloromethane for 2h; | 93% |
at 150℃; for 0.5h; microwave irradiation; | 85% |
With 2,6-lutidinium perchlorate; triphenylphosphine In dichloromethane at 40℃; for 6.5h; constant-current electrolysis; | 61% |
Stage #1: benzylamine With Sphingomonas sp. HXN-200 lipase expressed in Escherichia coli cells In hexane; water at 30℃; for 0.0833333h; Enzymatic reaction; Stage #2: 1-decanoic acid In hexane; water at 30℃; for 8h; Enzymatic reaction; | 55% |
Conditions | Yield |
---|---|
With piperidine; silica gel In methanol; acetonitrile Kolbe electrolytic synthesis; Electrolysis; cooling; | 99% |
With potassium hydroxide In methanol at 20℃; for 0.166667h; pH=6; Kolbe Electrolysis; |
Conditions | Yield |
---|---|
With iron(III) chloride hexahydrate In 1,3,5-trimethyl-benzene for 12h; Reflux; | 99% |
Conditions | Yield |
---|---|
With iron(III) chloride hexahydrate In 1,3,5-trimethyl-benzene for 12h; Reflux; | 99% |
2,3,4,6-Tetra-O-benzyl-D-glucopyranose
1-decanoic acid
Conditions | Yield |
---|---|
With (R)-(+)-2-phenyl-2,3-dihydrobenzo[d]imidazo[2,1-b]thiazole; 2,2-dimethylpropanoic anhydride; N-ethyl-N,N-diisopropylamine In chloroform at 20℃; for 24h; Inert atmosphere; diastereoselective reaction; | A 99% B n/a |
Conditions | Yield |
---|---|
With nano sulfated-TiO2 In neat (no solvent) at 80℃; under 760.051 Torr; for 1.5h; | 98% |
In n-heptane at 25℃; for 4h; Chromobacterium viscosum (CV) lipase immobilised in MBGs (microemulsion-based gels); | 93% |
With toluene-4-sulfonic acid | |
With hydrogenchloride |
Conditions | Yield |
---|---|
With hydrogen; Rh/Al2O3; molybdenum hexacarbonyl In 1,2-dimethoxyethane at 150℃; under 76000 Torr; for 16h; | 98% |
With samarium diiodide; water; triethylamine In tetrahydrofuran at 20℃; for 3h; Inert atmosphere; | 98% |
With hydrogen In hexane at 250℃; under 30003 Torr; for 3h; | 96.3% |
Conditions | Yield |
---|---|
With niobium(V) oxide In o-xylene for 30h; Reflux; Inert atmosphere; | 98% |
With Titania nano-particle at 110℃; for 0.5h; | 95% |
Heating; | 84% |
Conditions | Yield |
---|---|
With nano sulfated-TiO2 In neat (no solvent) at 80℃; under 760.051 Torr; for 1.5h; | 98% |
With acid activated Indian bentonite In toluene for 8h; Heating; | 85% |
With sulfuric acid Reflux; | 66.3% |
1-hydroxy-pyrrolidine-2,5-dione
1-decanoic acid
N-decanoyloxysuccinimide
Conditions | Yield |
---|---|
With dicyclohexyl-carbodiimide In ethyl acetate for 6h; | 98% |
Stage #1: 1-decanoic acid With bis(trichloromethyl) carbonate; triethylamine In dichloromethane at 0℃; Stage #2: 1-hydroxy-pyrrolidine-2,5-dione In dichloromethane at 20℃; for 0.5h; | 93% |
With dicyclohexyl-carbodiimide In tetrahydrofuran for 3h; | 87% |
1-decanoic acid
6-(bromoacetyl)amino-2,3-dimorpholinoquinoxaline
Conditions | Yield |
---|---|
With 18-crown-6 ether; potassium hydrogencarbonate In acetonitrile for 0.833333h; Ambient temperature; | 98% |
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