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:111-27-3
Min.Order:100 Gram
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inquiryOur clients, like BASF,CHEMO,Brenntag,ASR,Evonik,Merck and etc.Appearance:COA Storage:in stock Application:MSDS/TDS
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Cas:111-27-3
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inquiryItems Standard Result Appearance colorless liquid colorless liquid Odor It has a fruity aro
Cas:111-27-3
Min.Order:1 Gram
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inquiryProduct description: Product name Hexyl alcohol CAS number 111-27-3 Assay ≥99% Appearance Colorless liquid Capacity 2000mt/year Application Flavor, surfactants, plasticizers,
Cas:111-27-3
Min.Order:1 Kilogram
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Type:Lab/Research institutions
inquiryProduct Name n-Hexanol CAS No. 111-27-3 Chemical formula C6H14O Purity 99%min
Cas:111-27-3
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inquiryThe above product is Ality Chemical's strong item with best price, good quality and fast supply. Ality Chemical has been focusing on the research and production of this field for over 14 years. At the same time, we are always committed to providi
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Cas:111-27-3
Min.Order:1 Gram
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inquiryColorcom is a global leader in industrial chemical manufacturing and is continuously innovating and transforming to exceed client expectations and industry standards. Colorcom prides itself on superior customer and technical focus, while focusing on
1-Hexanol CAS 111-27-3 Hexyl alcohol CAS no 111-27-3 n-Hexanol 1-Hexanol Manufacturer High quality Best price In stock factory CAS 111-27-3 1-Hexanol COA TDS price MSDS highly quality and immedaite delivery Name Hexyl alcohol Syno
Cas:111-27-3
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inquiryName:1-Hexanol CAS NO:111-27-3 Grade:Medical scientific research and export Molecular formula:C6H14O Molecular weight:102.17 Product Quality 12 years of chemical raw materials Mature operation of the industry System stability Data storage
Cas:111-27-3
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inquiryOur company was built in 2009 with an ISO certificate.In the past 5 years, we have grown up as a famous fine chemicals supplier in China and we had established stable business relationships with Samsung,LG,Merck,Thermo Fisher Scientific and so on.O
Cas:111-27-3
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inquiryWith our good experience, we offer detailed technical support and advice to assist customers. We communicate closely with customers to establish their quality requirements. Consistent Quality Our plant has strict quality control in each manufacturing
Cas:111-27-3
Min.Order:1 Kilogram
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inquiryWITH US,YOUR MONEY IN SAFE,YOUR BUSINESS IN SAFE 1)Quick Response Within 12 hours; 2)Quality Guarantee: All products are strictly tested by our QC, confirmed by QA and approved by third party lab in China, USA, Canada, Germany, UK, Italy, France et
Cas:111-27-3
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inquiryOur Advantage: high quality with competitive price High quality standard: BP/USP/EP Enterprise standard All purity customized Fast and safe delivery We have reliable forwarder who can help us deliver our goods more fast and safe. We
Cas:111-27-3
Min.Order:10 Kilogram
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inquiryAbout Product Details 1-Hexanol Basic infor
Cas:111-27-3
Min.Order:1 Kilogram
FOB Price: $3.0 / 5.0
Type:Lab/Research institutions
inquiryProduct Name:1-Hexanol CAS No.:111-27-3 EINECS: 203-852-3 Molecular Formula: C6H14O Molecular Weight: 102.17 Appearance:Colorless transparent liquid Appearance: Colorless Liquid Storage:RT. Package:drum Application:Agrochemical Intermediates
1. Guaranteed purity; 2. Large quantity in stock; 3. Largest manufacturer; 4. Best service after shipment with email; 5. High quality & competitive price; Appearance:liquid Storage:Store in sealed containers at cool & dry pla
Cas:111-27-3
Min.Order:100 Gram
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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
Cas:111-27-3
Min.Order:1 Kilogram
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Type:Lab/Research institutions
inquiryProduct Name: 1-Hexanol CAS: 111-27-3 MF: C6H14O MW: 102.17 EINECS: 203-852-3 by Plant (Food/Spice/Herb) Mol File: 111-27-3.mol 1-Hexanol Structure 1-Hexanol Chemical Properties Melting point -52 °C (lit.) Boiling point
Beluga chemical professional supply High quality1-Hexanol CAS 111-27-3 1. Beluga Chemical has a professional RESEARCH and development team and strong technical force to ensure technical support and research capabilities. 2. Made in China and expo
Cas:111-27-3
Min.Order:1 Gram
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Type:Lab/Research institutions
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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Cas:111-27-3
Min.Order:10 Gram
Negotiable
Type:Trading Company
inquiry1-Hexanol CAS:111-27-3 Specification Item Specifications Results Appearance Colorless liquid Conforms Odor With fruit fragrance Confo
1. Timely and efficient service to ensure communication with customers 2. Produce products of different specifications and sizes according to your requirements. 3. Quality procedures and standards recognized by SGS. Advanced plant equipment ensures
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
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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
Cas:111-27-3
Min.Order:1 Gram
Negotiable
Type:Lab/Research institutions
inquiryConditions | Yield |
---|---|
With sodium aluminum tetrahydride In tetrahydrofuran at 0℃; for 0.5h; | 100% |
With C30H34Cl2N2P2Ru; potassium methanolate; hydrogen In tetrahydrofuran at 100℃; under 38002.6 - 76005.1 Torr; for 15h; Glovebox; Autoclave; | 93% |
With ethanol; ruthenium(bis[2‐(ethylsulfanyl)ethyl]amine)(dichloro)(triphenylphosphine); potassium tert-butylate In toluene at 80℃; for 16h; Catalytic behavior; Reagent/catalyst; | 89% |
Conditions | Yield |
---|---|
With Na-phosphate buffer; horse liver NADH; NAD; sodium formate; <(C5Me5)Rh(bpy-5-OAc)(H2O)>Cl2 at 25℃; for 30h; Product distribution; Mechanism; other ketones, other times, other temperatures, other enzymes; | 100% |
With sodium aluminum tetrahydride In tetrahydrofuran at 0℃; for 0.0833333h; Product distribution; other aldehydes, ketones, carboxylic acids (also sodium salts), acid chlorides, esters, lactones, epoxides, amides, nitriles, nitrogen and sulfur compounds; var. temp., time and ratio of reagents; | 100% |
With sodium aluminum tetrahydride In tetrahydrofuran at 0℃; for 0.0833333h; | 100% |
Conditions | Yield |
---|---|
With C39H39N6ORu(1+)*Br(1-); potassium methanolate; hydrogen In tetrahydrofuran at 70℃; under 37503.8 Torr; for 4h; Reagent/catalyst; | 100% |
With C56H70Cl3N10Ru2(1+)*F6P(1-); potassium tert-butylate; hydrogen In tetrahydrofuran; dodecane at 70℃; under 37503.8 Torr; for 16h; Inert atmosphere; Glovebox; Autoclave; | 100% |
With C30H26Cl2N3PRu; hydrogen; sodium ethanolate In toluene at 80℃; under 38002.6 Torr; for 16h; Catalytic behavior; Autoclave; Inert atmosphere; Schlenk technique; | 95% |
2,4,6-triisopropyl-benzenesulfonic acid n-hexylester
A
1,3,5-triisopropyl benzene
B
hexan-1-ol
Conditions | Yield |
---|---|
With lithium amalgam In N,N-dimethyl-formamide; toluene Product distribution; Mechanism; further solvents; | A 100% B 100% |
Conditions | Yield |
---|---|
With C56H70Cl3N10Ru2(1+)*F6P(1-); potassium tert-butylate; hydrogen In tetrahydrofuran; dodecane at 70℃; under 37503.8 Torr; for 16h; Inert atmosphere; Glovebox; Autoclave; | 100% |
With C66H102N4OP2Ru; hydrogen In toluene at 105℃; under 22502.3 Torr; for 20h; Inert atmosphere; Glovebox; | 99% |
With C31H26ClN2OPRu; hydrogen; sodium methylate In tetrahydrofuran at 80℃; for 2h; | 98% |
Conditions | Yield |
---|---|
With C56H70Cl3N10Ru2(1+)*F6P(1-); potassium tert-butylate; hydrogen In tetrahydrofuran; dodecane at 70℃; under 37503.8 Torr; for 16h; Inert atmosphere; Glovebox; Autoclave; | 100% |
Conditions | Yield |
---|---|
silica-supported prop-1-ylsulfonic acid In methanol | 99.6% |
With silica gel; iron(III) chloride for 45h; Ambient temperature; | 98.5% |
ammonium cerium(IV) nitrate In alkaline aq. solution; acetonitrile at 70℃; for 2h; pH=8; Decomposition; | 94% |
Conditions | Yield |
---|---|
Stage #1: 1-hexene With 9-bora-bicyclo[3.3.1]nonane Stage #2: With sodium peroxoborate tetrahydrate | 99% |
Stage #1: 1-hexene With borane-THF In tetrahydrofuran at 25℃; for 0.0138889h; Flow reactor; Stage #2: With dihydrogen peroxide; sodium hydroxide In tetrahydrofuran; ethanol; water at 20℃; for 0.00555556h; Flow reactor; | 88% |
With di-n-pentylbromoborane; alkaline H2O2; sodium hydride 1.) diglyme, room temperature, 7 h; further dialkylbromoboranes; Yield given. Multistep reaction; |
hexyl 2,4,6-trimethylbenzenesulfonate
A
1,3,5-trimethyl-benzene
B
hexan-1-ol
Conditions | Yield |
---|---|
With lithium amalgam In N,N-dimethyl-formamide; toluene Product distribution; Mechanism; further solvents; | A 85% B 99% |
Conditions | Yield |
---|---|
With hydrogen; copper-palladium; silica gel In ethanol at 25℃; under 760 Torr; Kinetics; | A 99% B n/a |
With hydrogen In methanol at 30℃; under 760.051 Torr; for 3h; | A 99% B 1% |
With hydrogen In methanol at 20℃; under 150.015 - 900.09 Torr; for 0.0116667h; Inert atmosphere; Schlenk technique; Green chemistry; | A n/a B n/a |
Conditions | Yield |
---|---|
With water In aq. phosphate buffer at 20℃; pH=7.4; Electrolysis; Inert atmosphere; Enzymatic reaction; | 98.3% |
With hydrogen; Rh/Al2O3; molybdenum hexacarbonyl In 1,2-dimethoxyethane at 150℃; under 76000 Torr; for 16h; | 95% |
With 1,1,3,3-Tetramethyldisiloxane; copper(II) bis(trifluoromethanesulfonate) In toluene at 80℃; for 16h; sealed tube; | 94% |
Conditions | Yield |
---|---|
With C24H20ClN2OPRu; potassium tert-butylate; hydrogen In tetrahydrofuran at 110℃; under 10640.7 Torr; for 36h; Inert atmosphere; Schlenk technique; | 98% |
With ethanol; sodium | |
With sodium aluminum tetrahydride In tetrahydrofuran for 12h; Ambient temperature; |
Conditions | Yield |
---|---|
With lithium amalgam In 1,4-dioxane; isopropyl alcohol at 23℃; for 2h; | A 98% B 98% |
Conditions | Yield |
---|---|
With sodium tetrahydroborate; palladium diacetate In methanol at 20℃; for 0.5h; | 98% |
Conditions | Yield |
---|---|
With hydrogen In tetrahydrofuran at 30℃; under 760.051 Torr; for 6h; | A 98% B 2% |
Conditions | Yield |
---|---|
In sodium hydroxide; water | 97% |
1-(2-Thioxo-thiazolidin-3-yl)-hexan-1-one
hexan-1-ol
Conditions | Yield |
---|---|
With sodium tetrahydroborate; water In tetrahydrofuran Ambient temperature; | 96% |
benzenesulfonic acid n-hexylester
A
lithium benzenesulfinate
B
hexan-1-ol
Conditions | Yield |
---|---|
With lithium amalgam In N,N-dimethyl-formamide; toluene at 23℃; for 2h; Product distribution; Mechanism; further solvents (effect of pKa); | A 95% B 95% |
4-methylbenzenesulfonic acid n-hexylester
A
p-toluene sulfinic acid
B
hexan-1-ol
Conditions | Yield |
---|---|
With lithium amalgam In 1,4-dioxane; isopropyl alcohol at 23℃; for 2h; | A 95% B 95% |
4-chlorobenzenesulfonic acid n-hexylester
A
4-chlorobenzenesulfinic acid
B
hexan-1-ol
Conditions | Yield |
---|---|
With lithium amalgam In 1,4-dioxane; isopropyl alcohol at 23℃; for 2h; | A 91% B 95% |
Conditions | Yield |
---|---|
With aniline; (ϖ-allyl)palladium triflate based catalyst at 50℃; for 2h; | 94% |
With lithium aluminium tetrahydride; bis(cyclopentadienyl)titanium dichloride In tetrahydrofuran for 8h; Ambient temperature; | 84% |
tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride; polydimethylsiloxane In methanol; water at 50℃; for 24h; | 77% |
Conditions | Yield |
---|---|
Stage #1: 2-hexen-1-ol With lithium triethylborohydride; cobalt(II) bromide In tetrahydrofuran Inert atmosphere; Glovebox; Stage #2: With hydrogen In tetrahydrofuran at 60℃; under 7500.75 Torr; for 3h; | 94% |
Conditions | Yield |
---|---|
Stage #1: 1-hexene With Thexylboran Stage #2: With sodium peroxoborate tetrahydrate | A n/a B 93% |
With borane-THF; dihydrogen peroxide; sodium carbonate 1.) THF, 0 deg C; 2.) H2O/THF, 50 deg C, 1 h; Yield given. Multistep reaction. Yields of byproduct given; | |
With dimesitylboron hydride In tetrahydrofuran at 25℃; for 8h; Yields of byproduct given. Title compound not separated from byproducts; | A n/a B 96 % Chromat. |
4-methoxybenzenesulfonic acid n-hexylester
A
4-methoxybenzenesulfinic acid
B
hexan-1-ol
Conditions | Yield |
---|---|
With lithium amalgam In N,N-dimethyl-formamide at 23℃; for 2h; | A 93% B 90% |
1-(tert-butyldimethylsilyl)oxyhexane
hexan-1-ol
Conditions | Yield |
---|---|
With diisobutylaluminium hydride In dichloromethane; toluene at 23℃; for 2h; | 93% |
Conditions | Yield |
---|---|
With carbonylchloro[4,5-bis(diisopropylphosphinomethyl)acridine]hydridoruthenium(II); water; hydrogen In 1,4-dioxane at 135℃; under 3750.38 Torr; for 48h; Pressure; Schlenk technique; Inert atmosphere; | 93% |
2,4-hexadiene-1-ol
A
(Z)-3-Hexen-1-ol
B
(E)-3-hexen-1-ol
C
hex-4-en-1-ol
D
hexan-1-ol
Conditions | Yield |
---|---|
With hydrogen; (methyl benzoate)Cr(CO)6 In methanol at 190 - 200℃; under 36775.4 Torr; for 2h; | A 92.5% B 4.6% C 2.3% D 0.6% |
With hydrogen; (1,2,4,5-tetramethylbenzene)tricarbonylchromium(0) In methanol at 190 - 200℃; under 36775.4 Torr; for 4h; Product distribution; other arene ligands, other solvents; also in absence of arene ligands; |
Conditions | Yield |
---|---|
With hydrogen In 1,2-dimethoxyethane at 80℃; under 60006 Torr; for 2h; Reagent/catalyst; Pressure; Solvent; Temperature; | A 92.3% B 8% |
With hydrogen; (acetylacetonato)dicarbonylrhodium (l); molybdenum hexacarbonyl In 1,4-dioxane at 150℃; under 75007.5 Torr; for 3h; | A 79% B 7% |
Conditions | Yield |
---|---|
With Na12(Ga4(1,5-bis(2,3-dihydroxybenzamido)naphthalene))6; [(DMPE)Rh(COD)][BF4]; hydrogen In water-d2 at 20℃; for 12h; Reagent/catalyst; | 92% |
Conditions | Yield |
---|---|
at 20 - 50℃; for 1h; Temperature; | 100% |
at 100 - 110℃; | |
at 20 - 135℃; |
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at -15℃; for 1h; Green chemistry; | 100% |
With triethylamine | 99% |
With triethylamine In dichloromethane at 0 - 20℃; | 99% |
Conditions | Yield |
---|---|
With C19H35Cl2CoN2P; sodium triethylborohydride In toluene at 150℃; for 24h; | 100% |
With chloro(η5-pentamethylcyclopentadienyl)(L-prolinato)iridium(III) In toluene at 95℃; for 24h; Inert atmosphere; Sealed tube; | 98% |
With chloro(η5-pentamethylcyclopentadienyl)(L-prolinato)iridium(III) In toluene at 95℃; for 24h; | 98% |
Conditions | Yield |
---|---|
With dilithium tetra(tert-butyl)zincate In toluene at 0℃; for 1h; Inert atmosphere; | 100% |
With pseudomonas fuorescens lipase immobilized on multiwall carbon nano-tubes at 50℃; for 5h; Green chemistry; | 99% |
With sulfuric acid beim Erhitzen; | |
With aluminium trichloride at 105℃; | |
In diethyl ether at 35℃; Candida cylindracea lipase; |
Conditions | Yield |
---|---|
With C23H42N2OP2Ru for 12h; Reflux; Inert atmosphere; Darkness; | 100% |
Ru complex at 157℃; for 24h; Inert atmosphere; | 99% |
With calcium hypochlorite In water; acetic acid; acetonitrile at 0℃; for 1h; | 98% |
Conditions | Yield |
---|---|
With 4 A molecular sieve; tetrabutylammonium periodite; sodium ruthenate(VI) In dichloromethane at 20℃; for 24h; Oxidation; | 100% |
With 4 A molecular sieve; tetrabutylammonium perchlorate; Ru-Cu-Al-hydrotalcite In toluene at 60℃; for 24h; | 100% |
With iodosylbenzene; Cl-CH2-PS supported 5-amino-1,10-phenanthroline-Ru In acetonitrile at 60℃; for 2h; | 100% |
Conditions | Yield |
---|---|
With air; potassium carbonate In water at 66.84℃; for 24h; | 100% |
With oxygen In water at 80℃; under 760.051 Torr; for 24h; | 99.3% |
Stage #1: hexan-1-ol 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; | 99% |
3-tert-butoxycarbonyl-2-chloro-1,3,2-oxazaphospholidine
hexan-1-ol
3-tert-butoxycarbonyl-2-hexyloxy-1,3,2-oxazaphospholidine
Conditions | Yield |
---|---|
With triethylamine In dichloromethane -60 deg C to r.t., 1 h; | 100% |
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In benzene | 100% |
toluene-4-sulfonic acid In toluene for 18h; Heating / reflux; | 96% |
With toluene-4-sulfonic acid | 84% |
With toluene-4-sulfonic acid In benzene for 16h; Heating; | 84% |
hexan-1-ol
Conditions | Yield |
---|---|
With polyvinylpyridine polymer-supported dimethylaminopyridine; polystyrene-bound N-cyclohexylcarbodiimide In dichloromethane at 20℃; | 100% |
Conditions | Yield |
---|---|
With triphenylphosphine; diethylazodicarboxylate In tetrahydrofuran; toluene at 0 - 20℃; for 0.5h; Inert atmosphere; | 100% |
With triphenylphosphine; diethylazodicarboxylate In tetrahydrofuran at 20℃; for 1h; | 95% |
Conditions | Yield |
---|---|
With triethylsilane; t-Bu-P4 In hexane; dimethyl sulfoxide at 100℃; for 2h; | 100% |
Conditions | Yield |
---|---|
at 85℃; for 24h; | 100% |
4-[(6,7-dimethoxy-4-quinolyl)oxy]-2,5-dimethylaniline
bis(trichloromethyl) carbonate
sodium hydrogencarbonate
hexan-1-ol
Conditions | Yield |
---|---|
With triethylamine In methanol; dichloromethane; chloroform; toluene | 100% |
Conditions | Yield |
---|---|
With copper(II) bis(trifluoromethanesulfonate) at 100℃; for 0.0833333h; Microwave irradiation; | 100% |
Conditions | Yield |
---|---|
With oxidase In water at 40℃; for 1.5h; Reformatsky Reaction; | 100% |
With oxygen In neat (no solvent) at 45℃; for 7h; Solvent; Temperature; | 50 %Chromat. |
Conditions | Yield |
---|---|
With bismuth(lll) trifluoromethanesulfonate In 1,2-dichloro-ethane at 80℃; for 24h; Reagent/catalyst; Inert atmosphere; Schlenk technique; chemoselective reaction; | 100% |
With toluene-4-sulfonic acid In neat (no solvent) at 120℃; for 24h; Inert atmosphere; Sealed tube; | 98% |
With p-toluene sulfonic acid - choline chloride covalently immobilized on polymeric microspheres coated iron oxide magnetic nanoparticles In neat (no solvent) at 120℃; for 12h; Reagent/catalyst; Solvent; chemoselective reaction; | 90% |
Conditions | Yield |
---|---|
With bismuth(lll) trifluoromethanesulfonate In 1,2-dichloro-ethane at 80℃; for 24h; Inert atmosphere; Schlenk technique; chemoselective reaction; | 100% |
hexan-1-ol
Conditions | Yield |
---|---|
With C28H27F6N3O3S In tetrahydrofuran at 25℃; for 72h; Inert atmosphere; | 100% |
Conditions | Yield |
---|---|
With nickel(II) sulfate hexahydrate; 4,4'-Dimethoxy-2,2'-bipyridin; C41H40O16; N-ethyl-N,N-diisopropylamine In acetonitrile at 20℃; for 24h; Schlenk technique; Irradiation; Inert atmosphere; | 100% |
Conditions | Yield |
---|---|
silica-supported prop-1-ylsulfonic acid In acetonitrile for 0.166667h; | 99.8% |
With sulfated zirconia In dichloromethane for 1h; Ambient temperature; | 96% |
With aminosulfonic acid at 15℃; for 4.5h; | 96% |
Conditions | Yield |
---|---|
With sodium hydroxide for 0.0194444h; microwave irradiation; | 99% |
With H3[P(Mo3O10)4]*nH2O at 20℃; for 0.1h; | 97% |
With zirconium phosphate In neat (no solvent) at 60℃; for 0.5h; Green chemistry; | 96% |
Conditions | Yield |
---|---|
With C19H35Cl2CoN2P; sodium triethylborohydride In toluene at 150℃; for 24h; Catalytic behavior; Reagent/catalyst; Solvent; Temperature; Molecular sieve; Schlenk technique; | 99% |
With C15H15ClN7Ru(1+)*Cl(1-); sodium tetraphenyl borate; 1,2-bis-(diphenylphosphino)ethane at 165℃; for 12h; Reagent/catalyst; Schlenk technique; Inert atmosphere; | 98% |
With [Py(NP(iPr)2)(NHP(iPr)2)Ir(cod)]; potassium tert-butylate In diethylene glycol dimethyl ether at 110℃; for 24h; Inert atmosphere; | 95% |
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