Dayangchem’s R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. DayangChem can provide different quantiti
Cas:112-85-6
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Cas:112-85-6
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inquiryItems Standard Result Assay (Ursolic acid) 98%min 98.22% -----------------------------------------------------------------------------------------------------------
Cas:112-85-6
Min.Order:1 Gram
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Cas:112-85-6
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Product Name: Docosanoic acid Synonyms: Docosanoic acid(C22:0);1-Docosanoic acid;1-docosanoicacid;B95;B95(acid);behenic;Behensαure;docosanoic CAS: 112-85-6 MF: C22H44O2 MW: 340.58 EINECS: 204-010-8 Product Categories: Sensitizer;Saturat
Cas:112-85-6
Min.Order:1 Kilogram
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Type:Lab/Research institutions
inquiryOur advantages: 1. All inquiries will be replied within 12 hours. 2. Dedication to quality, supply & service. 3. Strictly on selecting raw materials. 4. Reasonable & competitive price, fast lead time. 5. Sample is available for your eva
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Min.Order:1 Kilogram
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inquiryName: Behenic Acid Synonyms: Docosanoic acid CAS: 112-85-6 MF: C22H44O2 Appearance: white powder Storage:Store in cool and dry place, away from sun light. Package: 25kgs/drum Application:Organic synthesis Transportation:By sea or by air Port:Qi
Appearance:White to slightly yellow Crystalline Powder Storage:R T Package:25kg/Barrel Application:Used in the manufacture of behenyl alcohol, behenate and behenic acid amide, widely used in textile, petroleum, detergent, cosmetics and other industr
Cas:112-85-6
Min.Order:1 Kilogram
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Min.Order:1 Kilogram
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inquiryDocosanoic acid is a long-chain fatty acid,it has the following purposes: Waxes, textiles, pharmaceuticals, emulsifiers, and personal care products, lubricants, esters, chemical synthesis, and specialties. It can be used in product formu
Cas:112-85-6
Min.Order:1 Gram
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Type:Trading Company
inquiryDocosanoic acid CAS:112-85-6 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 organic intermediat
Cas:112-85-6
Min.Order:1 Gram
Negotiable
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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
Henan 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
Best quality & Attractive price & Professional service; Trial & Pilot & Commercial Hisunny Chemical is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality intermediates, specia
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J&H CHEM R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. J&H CHEM has some Manufacturing base in Jia
A substitute for perfluorooctanoic acid, mainly used as a surfactant, dispersant, additive, etc Appearance:White solid or Colorless liquid Purity:99.3 % We will ship the goods in a timely manner as required We can provide relevant documents acc
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Min.Order:4 Kilogram
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Type:Lab/Research institutions
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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Min.Order:10 Gram
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inquiryotassium behenate in cosmetics, skin care products in the main role is cleaning agents, foaming agents, surfactants, the risk factor is 1, more safe, can be assured to use, for pregnant women generally no effect, potassium behenate does not cause acn
Superior quality, moderate price & quick delivery. Appearance:white to cream crystals or powder Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:25kg/drum;200kg/drum as per your request Application:Used in the
Product Details Grade: pharmaceutical grade Purity:99%+ ProductionCapacity: 1000 Kilogram/Month Scope of use: For scientific research only(The product must be used legally) Our Advantage 1. Best quality with competitive price. 2. Quick shipping,
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Docosanoic acid Basic information Product Name: Docosanoic acid Synonyms: 1-Docosanoic acid;1-docosanoicacid;B95;B95(acid);behenic;Behensαure;docosanoic;Docosansαure CAS: 112-85-6 MF: C22H44O2 MW: 340.58 EINECS: 204-010-8 Product Catego
Conditions | Yield |
---|---|
With hydrogen In methanol at 20℃; for 4h; | 97.5% |
Conditions | Yield |
---|---|
With palladium 10% on activated carbon; hydrogen In tetrahydrofuran at 20 - 30℃; under 4500.45 - 6000.6 Torr; | 90.3% |
bei der Reduktion an platinierten Platinkathoden.Electrolysis; | |
With selenium at 300℃; |
6-docosenoic acid
n-docosanoic acid
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal In methanol for 6h; | 86% |
Conditions | Yield |
---|---|
With ethanol; platinum Hydrogenation; |
Conditions | Yield |
---|---|
With hydrogen; nickel Hydrogenation; |
Conditions | Yield |
---|---|
With air at 95℃; |
5-oxo-docosanoic acid
n-docosanoic acid
Conditions | Yield |
---|---|
With methanol; sodium; hydrazine; diethylene glycol at 195℃; |
n-docosanoic acid
Conditions | Yield |
---|---|
With potassium hydroxide; hydrazine hydrate; diethylene glycol |
4-oxodocosanoic acid
n-docosanoic acid
Conditions | Yield |
---|---|
With sodium hydroxide; hydrazine hydrate; diethylene glycol at 220℃; |
Conditions | Yield |
---|---|
Hydrogenation; |
Conditions | Yield |
---|---|
With methanol; sodium Electrolysis.und Behandlung des Reaktionsprodukts mit methanol.Natronlauge; |
Conditions | Yield |
---|---|
With potassium hydroxide |
Conditions | Yield |
---|---|
With potassium hydroxide In methanol for 3h; Heating; | A 5 mg B 10 mg |
Conditions | Yield |
---|---|
With pH 1.2 In water at 37℃; Product distribution; var. pH and temperatures; |
A
n-docosanoic acid
Conditions | Yield |
---|---|
With potassium hydroxide In 1,4-dioxane; methanol at 70℃; for 3h; Yield given; |
n-docosanoic acid
Conditions | Yield |
---|---|
With water; zinc at 130℃; |
n-docosanoic acid
Conditions | Yield |
---|---|
With water; zinc at 130℃; |
n-docosanoic acid
Conditions | Yield |
---|---|
With sodium hydroxide; hydrazine hydrate; 2,2'-[1,2-ethanediylbis(oxy)]bisethanol zuletzt bei 200grad nach teilweisem Abdestillieren des Loesungsmittels; |
n-docosanoic acid
Conditions | Yield |
---|---|
With hydrogenchloride; amalgamated zinc |
n-docosanoic acid
Conditions | Yield |
---|---|
With sodium hydroxide |
Conditions | Yield |
---|---|
Hydrogenation; |
n-docosanoic acid
Conditions | Yield |
---|---|
With hydrogenchloride; ethanol; zinc Verseifung etwa entstandenen Esters mit Kalilauge; |
n-docosanoic acid
Conditions | Yield |
---|---|
With oxygen at 150℃; | |
With Nitrogen dioxide at 120 - 130℃; |
docosanoic acid anhydride
n-docosanoic acid
Conditions | Yield |
---|---|
at 200 - 210℃; |
Conditions | Yield |
---|---|
at 210℃; |
Conditions | Yield |
---|---|
Hydrogenation; |
Conditions | Yield |
---|---|
Ce3+ exchanged Y-fanjasite at 150℃; for 48h; | 100% |
Conditions | Yield |
---|---|
at 250℃; for 15h; Inert atmosphere; | 99.6% |
With C28H60O3PS(1+)*CF3O3S(1-) at 80℃; for 6h; Sealed tube; |
Conditions | Yield |
---|---|
Stage #1: n-docosanoic acid With oxalyl dichloride In toluene for 2h; Inert atmosphere; Reflux; Stage #2: With ammonium hydroxide In water | 99% |
With ammonia; zircornium(IV) n-propoxide at 165℃; for 7h; Reagent/catalyst; | 98.7% |
With phosphorus pentachloride at 160℃; man versetzt nach Entfernung des POCl3 mit konz.Ammoniak; | |
Multi-step reaction with 2 steps 1: SOCl2 / Heating 2: ammonia gas / CHCl3 View Scheme | |
Multi-step reaction with 2 steps 1: oxalyl dichloride / dichloromethane / Inert atmosphere 2: ammonium hydroxide View Scheme |
Conditions | Yield |
---|---|
In ammonium hydroxide; ethanol hot (50°C) soln. docosanoic acid in EtOH was added slowly to hot soln. AgNO3 in aq. NH4OH at 50°C in the dark; ppt. was washed with water, extracted with EtOH and dried in vacuo for 12 h; | 99% |
In water dipping Langmuir-Blodgett film of behenic acid on CaF2 substrate into soln. of AgNO3, 15 min; washing with H2O, drying in air; |
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide In dichloromethane for 1h; | 99% |
n-docosanoic acid
n-docosanal
Conditions | Yield |
---|---|
With methylphenylsilane; 2,2-dimethylpropanoic anhydride; Tri(p-tolyl)phosphine; bis(dibenzylideneacetone)-palladium(0) In toluene at 60℃; for 20h; Schlenk technique; Inert atmosphere; | 98% |
Multi-step reaction with 2 steps 1: thionyl chloride / diethyl ether / 20 °C 2: bis(dibenzylideneacetone)-palladium(0); tris(2,4,6-trimethylphenyl)phosphine; triethylsilane / toluene / 1.5 h / 40 °C / Schlenk technique; Inert atmosphere View Scheme |
Conditions | Yield |
---|---|
With triphenylphosphine-sulfur trioxide adduct In neat (no solvent) at 110℃; for 2h; Green chemistry; | 97% |
at 250℃; for 15h; Inert atmosphere; | 92.8% |
Conditions | Yield |
---|---|
Stage #1: n-docosanoic acid With O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine In dichloromethane at 0℃; for 0.166667h; Stage #2: H2N-Arg(Pbf)-Gly-Asp(OtBu)-OtBu In dichloromethane at 0 - 20℃; for 96h; | 96% |
n-docosanoic acid
Conditions | Yield |
---|---|
Stage #1: n-docosanoic acid With oxalyl dichloride; N,N-dimethyl-formamide In dichloromethane at 20℃; for 2h; Stage #2: (2S)-2-amino-N-dodecyl-5-[(N-nitrocarbamimidoyl)amino]pentanamide hydrochloride With triethylamine In tetrahydrofuran at 20℃; | 96% |
Conditions | Yield |
---|---|
With triphenylphosphine-sulfur trioxide adduct In neat (no solvent) at 110℃; for 2h; Green chemistry; | 96% |
n-docosanoic acid
docosanoic acid anhydride
Conditions | Yield |
---|---|
With 4-methyl-morpholine; 2-chloro-4,6-dimethoxy-1 ,3,5-triazine In dichloromethane at 0 - 20℃; for 24h; | 95% |
With acetic anhydride | |
With dicyclohexyl-carbodiimide In dichloromethane at 20℃; for 4h; Acylation; | |
Multi-step reaction with 2 steps 1: 51 percent / N-methylmorpholine / tetrahydrofuran / 1.) 0 to 5 deg C, 24 h 2.) r.t., 14 h 2: CHCl3 View Scheme |
1,3-dioxan-5-yl 4-methylbenzene-1-sulfonate
n-docosanoic acid
Conditions | Yield |
---|---|
With boron trifluoride diethyl etherate; trifluoroacetic anhydride In tetrahydrofuran at 20℃; for 2h; acylolysis; | 95% |
Conditions | Yield |
---|---|
With choline chloride; zinc(II) chloride at 110℃; for 12h; | 95% |
n-docosanoic acid
methyl 2,3-di-O-benzyl-β-D-arabinofuranosyl-(1->2)-3-O-benzyl-α-D-arabinofuranoside
methyl 5-O-behenoyl-2,3-di-O-benzyl-β-D-arabinofuranosyl-(1->2)-5-O-behenoyl-3-O-benzyl-α-D-arabinofuranoside
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide In dichloromethane at 0℃; for 4h; Inert atmosphere; | 95% |
Conditions | Yield |
---|---|
With triethylamine at 160℃; for 5h; Autoclave; Green chemistry; | 95% |
With diiron nonacarbonyl at 180℃; for 1h; Sealed tube; |
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide In dichloromethane at 20℃; for 3h; Esterification; | 94% |
n-docosanoic acid
decanoic acid 3-hydroxy-2-(toluene-4-sulfonyloxy)-propyl ester
docosanoic acid 3-decanoyloxy-2-(toluene-4-sulfonyloxy)-propyl ester
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide In dichloromethane at 20℃; for 1h; Esterification; | 94% |
n-docosanoic acid
hexadecanoic acid 3-hydroxy-2-(toluene-4-sulfonyloxy)-propyl ester
docosanoic acid 3-hexadecanoyloxy-2-(toluene-4-sulfonyloxy)-propyl ester
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide In dichloromethane at 20℃; for 1h; Esterification; | 94% |
n-docosanoic acid
docosanoyl azide
Conditions | Yield |
---|---|
With sodium azide; N-ethyl-N,N-diisopropylamine; (bis-(2-methoxyethyl)amino)sulfur trufluoride In dichloromethane; dimethyl sulfoxide at 0 - 20℃; for 0.5h; | 94% |
Stage #1: n-docosanoic acid With 4-methyl-morpholine; chloroformic acid ethyl ester In tetrahydrofuran at -20℃; for 0.5h; Stage #2: With sodium azide In tetrahydrofuran; water at -5℃; for 0.25h; Inert atmosphere; |
n-docosanoic acid
docosanoyl chloride
Conditions | Yield |
---|---|
With phosgene at 95℃; for 48h; | 93.2% |
With thionyl chloride | |
With thionyl chloride at 85℃; |
n-docosanoic acid
1-amino-3-(dimethylamino)propane
N-(3-(dimethylamino)propyl)docosanamide
Conditions | Yield |
---|---|
With aluminum oxide; sodium fluoride at 165℃; for 11h; Inert atmosphere; | 92.41% |
at 150 - 180℃; for 10.5h; | |
Amidation; |
n-docosanoic acid
(2S,3R,4R)-2-amino-1,4-di-O-benzyl-3-O-(2',3',4',6'-tetra-O-benzyl-β-D-glucopyranosyl)octadecane
(2S,3R,4R)-1,4-di-O-benzyl-3-O-(2',3',4',6'-tetra-O-benzyl-β-D-glucopyranosyl)-2-N-docosanoyl-octadecane
Conditions | Yield |
---|---|
Stage #1: (2S,3R,4R)-2-amino-1,4-di-O-benzyl-3-O-(2',3',4',6'-tetra-O-benzyl-β-D-glucopyranosyl)octadecane With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane; N,N-dimethyl-formamide at 0℃; for 0.5h; activation; Stage #2: n-docosanoic acid With N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; for 3h; Acylation; | 92% |
n-docosanoic acid
Conditions | Yield |
---|---|
Stage #1: (L)-2-hydroxy-1-hexadecyloxycarbonylethylammonium chloride With dmap In chloroform Stage #2: n-docosanoic acid With dicyclohexyl-carbodiimide In chloroform at 20℃; for 20h; | 92% |
chlorosulfuric acid chloromethyl ester
n-docosanoic acid
Conditions | Yield |
---|---|
Stage #1: n-docosanoic acid With tetra(n-butyl)ammonium hydrogensulfate; sodium hydrogencarbonate In dichloromethane; water at 20℃; Stage #2: chlorosulfuric acid chloromethyl ester In dichloromethane; water at 0℃; for 18h; | 92% |
Conditions | Yield |
---|---|
With chloroformic acid ethyl ester; triethylamine In dichloromethane for 0.5h; Ambient temperature; | 90% |
n-docosanoic acid
(2S,3R,4R)-2-amino-1,4-di-O-benzyl-3-O-(2',3',4',6'-tetra-O-benzyl-β-D-galactopyranosyl)octadecane
(2S,3R,4R)-1,4-di-O-benzyl-3-O-(2',3',4',6'-tetra-O-benzyl-β-D-galactopyranosyl)-2-N-docosanoyl-octadecane
Conditions | Yield |
---|---|
Stage #1: (2S,3R,4R)-2-amino-1,4-di-O-benzyl-3-O-(2',3',4',6'-tetra-O-benzyl-β-D-galactopyranosyl)octadecane With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane; N,N-dimethyl-formamide at 0℃; for 0.5h; activation; Stage #2: n-docosanoic acid With N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; for 3h; Acylation; | 90% |
n-docosanoic acid
(2S,3R,4R)-2-amino-3,4-di-O-benzyl-1-O-(2',3',4',6'-tetra-O-benzyl-α-D-galactopyranosyl)octadecane
(2S,3R,4R)-3,4-di-O-benzyl-1-O-(2',3',4',6'-tetra-O-benzyl-α-D-galactopyranosyl)-2-N-docosanoyl-octadecane
Conditions | Yield |
---|---|
Stage #1: (2S,3R,4R)-2-amino-3,4-di-O-benzyl-1-O-(2',3',4',6'-tetra-O-benzyl-α-D-galactopyranosyl)octadecane With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane; N,N-dimethyl-formamide at 0℃; for 0.5h; activation; Stage #2: n-docosanoic acid With N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; for 3h; Acylation; | 90% |
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran at 0 - 20℃; for 22h; | 90% |
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