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inquiry1. Product advantages ♦ High purity, all above 98.5%, no impurities after dissolution ♦ We will test each batch to ensure quality ♦ OEM and private brand services designed for free ♦ Various cap colors available ♦ W
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inquiry1.No Less 8 years exporting experience. Clients can 100% received goods 2.Lower Price with higher quality 3,Free sample 4,We are sincerely responsible for the "product quality" and "After Service" Upbio is Specialized
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inquiryAbout Product Details Items Specifications Test Results Appearance White to white crystalline powde
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inquiry(R)-3-Hydroxy Myristic Acid CAS:28715-21-1 Qingdao Belugas Import and Export Co., Ltd. is a scientific and technological company integrating research and development, production and trade of chemical intermediates, specializing in high quality organ
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inquiryHello, dear friend! I'm Hansen and Allen from China. Welcome to my lookchem mall! The following is a brief introduction of our company's products and services. If you are interested in our products, please contact us by emai
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inquiryHenan Wentao Chemical Product Co.,Ltd is Located in Zhengzhou High-tech Development Zone with import and export license, We passed ISO 9001:2008 as well, Henan Wentao has developed more than 1000 compounds, which are widely used in the fields of prod
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inquiryZibo Hangyu Biotechnology Development Co., Ltd is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality pharmaceuticals, intermediates, special chemicals and OLED intermediates and other fine chemi
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inquiry3-HYDROXYTETRADECANOIC ACID Basic information Product Name: 3-HYDROXYTETRADECANOIC ACID Synonyms: DL-BETA-HYDROXYMYRISTIC ACID;HYDROXYMYRISTIC ACID, 3-;(+/-)-3-HYDROXYTETRADECANOIC ACID;3-HYDROXYTETRADECANOIC ACID;3-HYDROXY C14:0 ACID;3-HYDROXYMYRIS
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inquiryhigh purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:drum and bag Application:for pharma use Transportation:by sea or air Port:Beijing or Guangzhou
high qualityAppearance:white crystalline powder Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea
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inquiryJ&H CHEM is one of China's leading providers of integrated fine chemical services including offering, research and development, Custom manufacturing business, as well as other Value-added customer services, for diversified range products of chemicals
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inquiryAnsciep Chemical is a professional enterprise manufacturing and distributing fine chemicals and speciality chemicals. We have been dedicated to heterocycle compounds and phenyl rings for tens of years. This is our mature product for export. Our quali
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inquiry3-HYDROXYTETRADECANOIC ACIDAppearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:pharmaceutical intermediate Transportation:by air, by sea, by express
factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
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inquiry28715-21-1 Application:intermediate
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inquiryStock products, own laboratory Package:Grams, Kilograms Application:For R&D Transportation:According to customer request Port:Shanghai
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factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
3-HYDROXYTETRADECANOIC ACID Basic information Product Name: 3-HYDROXYTETRADECANOIC ACID Synonyms: DL-BETA-HYDROXYMYRISTIC ACID;HYDROXYMYRISTIC ACID, 3
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inquiryKnown for its best quality and competitve price, this chemicals we offered is widely appreciated by our customers. Our advantages:1, High quality with competitive price:1) Standard:BP/USP/EP/Enterprise standard2) All Purity≥99%4) We are manufactureAp
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inquiryHuBei ipure is a diversified product production and operation enterprise, with API, pharma intermediates, and other fine chemicals as well as R&D and pigments development and sales as one of the large enterprises, with more than 130 acres of pl
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inquiryYinghao Pharm products include: leader molecule, heterocyclic compounds,chiral compounds, photoelectric materials, biochemical reagents etc. For example:benzene, pyrimidine, boricacid,pyridine, pyrazole, imidazole, pyrrole, fluorine and other derivat
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inquirymethyl 3-oxotetradecanoate
(R)-3-hydroxytetradecanoic acid
Conditions | Yield |
---|---|
Stage #1: methyl 3-oxotetradecanoate With hydrogen; (R)-2,2'-bis(diphenylphosphanyl)-1,1'-binaphthyl; ruthenium trichloride In methanol at 40 - 50℃; under 3361.46 Torr; for 20h; Stage #2: With lithium hydroxide In tetrahydrofuran; water | 100% |
With sodium hydroxide; hydrogen; acetic acid; L-Tartaric acid; (R,R)-tartaric acid-NaBr-Raney nickel ((R,R)-TA-NaBr-MRNi); sodium bromide 1.) C2H5COOCH3, 100 deg C, 100 kg/cm2; Yield given. Multistep reaction; | |
Multi-step reaction with 2 steps 1: 95.6 percent / H2 / (R)-ruthenium 2,2'-bis(diphenylphosphino)-1,1'-binaphthyl / methanol / 5 h / 100 °C / 3750.3 Torr 2: 97.6 percent / lithium hydroxide monohydrate / methanol; H2O / 12 h View Scheme |
methyl (R)-3-hydroxytetradecanoate
(R)-3-hydroxytetradecanoic acid
Conditions | Yield |
---|---|
With lithium hydroxide monohydrate In tetrahydrofuran; water at 20℃; for 2h; | 98% |
With lithium hydroxide In methanol; water for 12h; | 97.6% |
With sodium hydroxide In tetrahydrofuran; water Reflux; | 96% |
(R)-1-cyanotridecan-2-ol
(R)-3-hydroxytetradecanoic acid
Conditions | Yield |
---|---|
With hydrogenchloride In dichloromethane at 100℃; for 12h; Hydrolysis; | 95% |
(R)-tert-butyl 3-hydroxytetradecanoate
(R)-3-hydroxytetradecanoic acid
Conditions | Yield |
---|---|
With triethylsilane; trifluoroacetic acid In dichloromethane at 20℃; for 0.75h; | 87% |
(R)-3-hydroxytetradecanoic acid ethyl ester
(R)-3-hydroxytetradecanoic acid
Conditions | Yield |
---|---|
With potassium hydroxide In ethanol | 76% |
With ethanol; potassium hydroxide |
3-hydroxytetradecanoic acid
(R)-3-hydroxytetradecanoic acid
Conditions | Yield |
---|---|
With dexamfetamine |
Ethyl 3-hydroxytetradecanoate
(R)-3-hydroxytetradecanoic acid
Conditions | Yield |
---|---|
In diethyl ether (saponification); |
vinyl acetate
3-hydroxytetradecanoic acid
A
(R)-3-hydroxytetradecanoic acid
B
(S)-3-acetoxytetradecanoic acid
Conditions | Yield |
---|---|
With di-tert-butyl-4-methylphenol In tetrahydrofuran at 65℃; for 3h; Pseudomonas lipase; |
3-oxomyristic acid
A
(R)-3-hydroxytetradecanoic acid
B
tridecan-2-one
Conditions | Yield |
---|---|
With potassium dihydrogenphosphate; baker's yeast; D-glucose In water at 28℃; for 48h; Yield given. Yields of byproduct given; |
(3R)-1-trimethylsilyl-tetradec-1-yn-3-ol
A
(R)-3-hydroxytetradecanoic acid
B
(3S)-3-hydroxytetradecanoic acid
Conditions | Yield |
---|---|
With sodium hydroxide; bis(cyclohexanyl)borane; dihydrogen peroxide 1) THF, 0 deg C; 2) 40-50 deg C; Yield given. Multistep reaction. Title compound not separated from byproducts; |
n-dodecanoyl chloride
(R)-3-hydroxytetradecanoic acid
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1.1: pyridine / CH2Cl2 / 3 h / 0 - 20 °C 1.2: 77.9 percent / methanol / 3 h / Heating 2.1: 95.6 percent / H2 / (R)-ruthenium 2,2'-bis(diphenylphosphino)-1,1'-binaphthyl / methanol / 5 h / 100 °C / 3750.3 Torr 3.1: 97.6 percent / lithium hydroxide monohydrate / methanol; H2O / 12 h View Scheme |
1-tridecene
(R)-3-hydroxytetradecanoic acid
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: K3Fe(CN)6; K2CO3; water / 4,6-bis(9-O-dihydroquinidinyl)-2,5-diphenylpyrimidine; OsO4 / 2-methyl-propan-2-ol; toluene / 24 h / 20 °C 2: 92 percent / pyridine; thionyl chloride / 5 h / 0 °C 3: 86 percent / dimethylformamide / 12 h / 90 °C 4: 95 percent / aq. HCl / CH2Cl2 / 12 h / 100 °C View Scheme |
(R)-1,2-dihydroxytridecane
(R)-3-hydroxytetradecanoic acid
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 92 percent / pyridine; thionyl chloride / 5 h / 0 °C 2: 86 percent / dimethylformamide / 12 h / 90 °C 3: 95 percent / aq. HCl / CH2Cl2 / 12 h / 100 °C View Scheme |
(4R)-4-undecyl-1,3,2-dioxathiolane-2-oxide
(R)-3-hydroxytetradecanoic acid
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 86 percent / dimethylformamide / 12 h / 90 °C 2: 95 percent / aq. HCl / CH2Cl2 / 12 h / 100 °C View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 1.) CuI / 1.) THF, -30 deg C, 30 min, 2.) THF, a) -30 deg C, 1 h, b) RT, overnight 2: 76 percent / aq. KOH / ethanol View Scheme |
n-dodecanoyl chloride
(R)-3-hydroxytetradecanoic acid
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 2: di-t-butyl-p-cresol / tetrahydrofuran / 3 h / 65 °C / Pseudomonas lipase View Scheme |
2,2-dimethyl-4,6-dioxo-5-dodecanoyl-1,3-dioxane
(R)-3-hydroxytetradecanoic acid
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: methanol / 5 h / Heating 2: 1.) H2, AcOH, 2.) NaOH / 1.) (R,R)-tartaric acid-NaBr-Raney nickel ((R,R)-TA-NaBr-MRNi) / 1.) C2H5COOCH3, 100 deg C, 100 kg/cm2 View Scheme |
(R)-(-)-1-tetradecyn-3-ol
(R)-3-hydroxytetradecanoic acid
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 1) 2.4 eq. n-BuLi; 2) 1.4 M H2SO4 / 1) THF, -78 deg C; 2) from -20 deg C to room temperature 2: 1) 2 eq. dicyclohexylborane; 2) NaOH, H2O2 / 1) THF, 0 deg C; 2) 40-50 deg C View Scheme |
tetradec-1-yn-3-one
(R)-3-hydroxytetradecanoic acid
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 1.4 eq. R-Alpine-Borane / neat (no solvent) / 8 h / 0 - 20 °C 2: 1) 2.4 eq. n-BuLi; 2) 1.4 M H2SO4 / 1) THF, -78 deg C; 2) from -20 deg C to room temperature 3: 1) 2 eq. dicyclohexylborane; 2) NaOH, H2O2 / 1) THF, 0 deg C; 2) 40-50 deg C View Scheme |
1,4-dioxane
methyl (R)-3-hydroxytetradecanoate
(R)-3-hydroxytetradecanoic acid
Conditions | Yield |
---|---|
With hydrogenchloride; sodium hydroxide In methanol; water |
n-tetradecanoic acid
A
2-hydroxytetradecanoic acid
B
(R)-3-hydroxytetradecanoic acid
Conditions | Yield |
---|---|
With recombinant Bacillus subtilis cytochrome P450(BSβ) F79L mutant; dihydrogen peroxide at 37℃; for 0.0166667h; pH=7; Kinetics; Concentration; Reagent/catalyst; aq. phosphate buffer; Enzymatic reaction; regioselective reaction; |
jagaricin
A
D-allo-threonine
B
(2S,3S)-2-amino-3-hydroxybutanoic acid
C
L-threonine
D
D-Glutamin
E
(R)-3-hydroxytetradecanoic acid
F
dehydrobutyrine
G
tyrosine
H
glycine
I
L-histidine
Conditions | Yield |
---|---|
With hydrogenchloride; phenol In water at 105℃; Reagent/catalyst; |
(+/-)-3-hydroxytetradecanoic acid methyl ester
A
(R)-3-hydroxytetradecanoic acid
B
(S)-methyl 3-hydroxymyristate
Conditions | Yield |
---|---|
With Porcine Pancreas Lipase; water In aq. phosphate buffer at 36℃; for 7h; pH=7.6; enantioselective reaction; | A n/a B n/a |
With Porcine Pancreas Lipase; water In aq. phosphate buffer at 36℃; for 7h; pH=7.6; Resolution of racemate; enantioselective reaction; | A n/a B n/a |
(+/-)-3-hydroxytetradecanoic acid methyl ester
A
(R)-3-hydroxytetradecanoic acid
B
(S)-methyl 3-hydroxymyristate
C
(3S)-3-hydroxytetradecanoic acid
Conditions | Yield |
---|---|
With Porcine Pancreas Lipase; water In aq. phosphate buffer at 36℃; for 7h; pH=7.6; Resolution of racemate; enantioselective reaction; | A n/a B n/a C n/a |
lauric acid
(R)-3-hydroxytetradecanoic acid
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1.1: magnesium ethylate / 1,4-dioxane 1.2: 20 °C 2.1: hydrogen; dichloro-R-2,2′-bis(diphenylphosphino)-1,1′-binaphthyl ruthenium / methanol / 20 h / 50 °C / 3102.97 Torr / Inert atmosphere 3.1: lithium hydroxide monohydrate / water; tetrahydrofuran / 2 h / 20 °C View Scheme |
Conditions | Yield |
---|---|
With hydrogenchloride In water at 123℃; for 23h; |
1-hydroxy-pyrrolidine-2,5-dione
(R)-3-hydroxytetradecanoic acid
Conditions | Yield |
---|---|
With 2`,3`-dideoxycytidine In tetrahydrofuran for 12h; Ambient temperature; | 100% |
methanol
(R)-3-hydroxytetradecanoic acid
methyl (R)-3-hydroxytetradecanoate
Conditions | Yield |
---|---|
With boron trifluoride at 100℃; for 0.0333333h; | 100% |
With boron trifluoride at 105℃; for 0.75h; |
(R)-3-hydroxytetradecanoic acid
α-bromoacetophenone
(3R)-3-hydroxytetradecanoic acid phenacyl ester
Conditions | Yield |
---|---|
With triethylamine In ethyl acetate | 98% |
With triethylamine In ethyl acetate 1.) 0 deg C, 10 min, 2.) room temp.; | 94% |
With triethylamine In ethyl acetate | 93% |
(R)-3-hydroxytetradecanoic acid
benzyl chloride
3-hydroxy-D-tetradecanoic acid benzyl ester
Conditions | Yield |
---|---|
In tetrahydrofuran; dimethyl sulfoxide at 50℃; | 97% |
(R)-3-hydroxytetradecanoic acid
benzyl 2-amino-2-deoxy-4,6-O-isopropylidene-β-D-glucopyranoside
benzyl 2-deoxy-2-<(3R)-3-hydroxytetradecanamido>-4,6-O-isopropylidene-β-D-glucopyranoside
Conditions | Yield |
---|---|
With 3-{[(ethylimino)methylene]-amino}-N,N,N-trimethyl-1-propanaminium iodide In dichloromethane | 95% |
With dicyclohexyl-carbodiimide In dichloromethane for 3h; Ambient temperature; Yield given; |
(R)-3-hydroxytetradecanoic acid
{(2R,3R,4S,5S,6S)-6-[(2R,3S,4R,5R,6S)-5-Amino-6-((2R,3S,4R,5R,6R)-5-amino-3,4-bis-benzyloxy-6-methoxy-tetrahydro-pyran-2-ylmethoxy)-4-benzyloxy-2-hydroxymethyl-tetrahydro-pyran-3-yloxy]-3,4,5-tris-benzyloxy-tetrahydro-pyran-2-yl}-methanol
C89H124N2O18
Conditions | Yield |
---|---|
With N-ethylmorpholine;; benzotriazol-1-ol; dicyclohexyl-carbodiimide In 1,4-dioxane at 20℃; for 2h; | 88% |
(R)-3-hydroxytetradecanoic acid
triethylsilyl chloride
(R)-3-O-triethylsilyl myristic acid
Conditions | Yield |
---|---|
In pyridine at 60℃; for 2h; | 85.6% |
(R)-3-hydroxytetradecanoic acid
2-(trimethylsilyl)ethyl 2-amino-2-deoxy-4,6-O-isopropylidene-β-D-glucopyranoside
2-(trimethylsilyl)ethyl 2-deoxy-2-<(3R)-3-hydroxytetradecanamido>-4,6-O-isopropylidene-β-D-glucopyranoside
Conditions | Yield |
---|---|
With N-(3-dimethylaminopropyl)-N-ethylcarbodiimide In dichloromethane Ambient temperature; | 84% |
1-hydroxy-pyrrolidine-2,5-dione
(R)-3-hydroxytetradecanoic acid
N-(R)-3-hydroxytetradecanoyloxysuccinimide
Conditions | Yield |
---|---|
With dicyclohexyl-carbodiimide In ethyl acetate at 0℃; for 16h; | 80% |
1H-imidazole
(R)-3-hydroxytetradecanoic acid
tert-butyldimethylsilyl chloride
Conditions | Yield |
---|---|
In methanol; dichloromethane; chloroform | 79% |
(R)-3-hydroxytetradecanoic acid
(R)-1,3-dihydroxytetradecane
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride In tetrahydrofuran for 2.5h; Ambient temperature; | 76% |
(R)-3-hydroxytetradecanoic acid
1,3,4,6-tetra-O-acetyl-D-glucosamine hydrochloride
1,3,4,6-tetra-O-acetyl-2-deoxy-<(3R)-3-hydroxytetradecanamido>-β-D-glucopyranose
Conditions | Yield |
---|---|
With triethylamine; dicyclohexyl-carbodiimide In pyridine for 48h; Ambient temperature; | 68% |
(R)-3-hydroxytetradecanoic acid
(S)-methyl 3-(tert-butoxy)-2-((R)-2-((tert-butoxycarbonyl)amino)-3-((2-hydroxyethyl)thio)propanamido)propanoate
methyl (L-(thio-((R)-ethyl 3-hydroxytetradecanoate))-N-(tert-butoxycarbonyl))cysteyl-L-(3-O-(tert-butyl))serate
Conditions | Yield |
---|---|
With 4-methyl-morpholine; dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; | 63% |
(R)-3-hydroxytetradecanoic acid
benzyl bromide
3-hydroxy-D-tetradecanoic acid benzyl ester
Conditions | Yield |
---|---|
With triethylamine In ethyl acetate for 72h; Ambient temperature; | 61% |
With tetra-(n-butyl)ammonium iodide; triethylamine In ethyl acetate at 20℃; for 18h; |
(R)-3-hydroxytetradecanoic acid
Fmoc-Leu-OH
L-Asn(Trt)
Fmoc-L-Gln(Trt)-OH
Conditions | Yield |
---|---|
Stage #1: Fmoc-Leu-OH With N-ethyl-N,N-diisopropylamine; HATU In N,N-dimethyl-formamide at 20℃; for 6h; Weinreb amide resin; Stage #2: With piperidine In N,N-dimethyl-formamide for 0.05h; Weinreb amide resin; Stage #3: (R)-3-hydroxytetradecanoic acid; L-Asn(Trt); Fmoc-L-Gln(Trt)-OH Further stages; | 60% |
(R)-3-hydroxytetradecanoic acid
Fmoc-Val-OH
L-Asn(Trt)
Fmoc-L-Gln(Trt)-OH
Conditions | Yield |
---|---|
Stage #1: Fmoc-Val-OH With N-ethyl-N,N-diisopropylamine; HATU In N,N-dimethyl-formamide at 20℃; for 6h; Weinreb amide resin; Stage #2: With piperidine In N,N-dimethyl-formamide for 0.05h; Weinreb amide resin; Stage #3: (R)-3-hydroxytetradecanoic acid; L-Asn(Trt); Fmoc-L-Gln(Trt)-OH Further stages; | 53% |
diazomethane
(R)-3-hydroxytetradecanoic acid
methyl (R)-3-hydroxytetradecanoate
Conditions | Yield |
---|---|
In diethyl ether Yield given; |
methanol
(R)-3-hydroxytetradecanoic acid
A
methyl (R)-3-hydroxytetradecanoate
B
(S)-methyl 3-hydroxymyristate
Conditions | Yield |
---|---|
With hydrogenchloride for 2h; Ambient temperature; Yield given. Title compound not separated from byproducts; |
(R)-3-hydroxytetradecanoic acid
Benzyl-6-O-<6-O-acetyl-2-amino-3-O-<α,α-D2>benzyl-2-desoxy-4-O-(diphenoxyphosphoryl)-β-D-glucopyranosyl>-2-amino-3,4-di-O-<α,α-D2>benzyl-2-desoxy-β-D-glucopyranosid-dihydrochlorid
Benzyl-6-O-<6-O-acetyl-3-O-<α,α-D2>benzyl-2-desoxy-4-O-(diphenoxyphosphoryl)-2-<(R)-3-hydroxytetradecanoylamino>-β-D-glucopyranosyl>-3,4-di-O-<α,α-D2>benzyl-2-desoxy-2-<(R)-3-hydroxytetradecanoylamino>-β-D-glucopyranosid
Conditions | Yield |
---|---|
With cyclohexyl(2-morpholinoethyl)carbodiimide metho-p-toluenesulfonate; benzotriazol-1-ol; triethylamine 1.) DMF, 60 min, 2.) DMF, 1 h; Yield given. Multistep reaction; |
Conditions | Yield |
---|---|
With cyclohexyl-(2-morpholinoethyl)carbodiimide metho-p-toluenesulfonate; benzotriazol-1-ol; triethylamine 1.) DMF, 60 min, RT, 2.) DMF, 8 h, RT; Yield given. Multistep reaction; |
(R)-3-hydroxytetradecanoic acid
C34H34(2)H2NO9P*ClH
Benzyl-6-O-acetyl-3-O-<α,α-D2>benzyl-2-desoxy-4-O-(diphenoxyphosphoryl)-2-<(R)-3-hydroxytetradecanoylamino>-β-D-glucopyranosid
Conditions | Yield |
---|---|
With cyclohexyl(2-morpholinoethyl)carbodiimide metho-p-toluenesulfonate; benzotriazol-1-ol; triethylamine 1.) DMF, 60 min, 2.) DMF, 40 min, RT; Yield given. Multistep reaction; |
(R)-3-hydroxytetradecanoic acid
1,3-di-O-acetyl-2-amino-4,6-O-benzylidene-2-deoxy-β-D-glucopyranose hydrochloride
Conditions | Yield |
---|---|
With triethylamine; dicyclohexyl-carbodiimide In pyridine | |
With triethylamine; dicyclohexyl-carbodiimide In pyridine |
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