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inquiryHebei yanxi chemical co., LTD is a professional research, development and production of lead acetate benzene acetamide enterprise backbone members by local well-known entrepreneurs and professional senior engineers in the party's "low carb
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inquiryUnique advantages for alpha-Terpineol Cas 10482-56-1 Guaranteed the purity High quality & competitive price Quality control Fast feedback Prompt shipment Appearance:Liquid Storage:2-8°C Package:180kg/drum Application:Food and Pharm Transp
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inquiryhigh quality Appearance:white 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 Port:shanghai
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Shanghai Seasonsgreen Chemical is a high-tech research and development, production, sale and custom synthesis set in one high-tech chemical products enterprises. Our sales and marketing division is located in Shanghai, serving international pharmaceu
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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
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inquiry1. Direct manufacturer 2. Stock available 3. Stable and fine quality 4. Premium service Appearance:transparent thick liquid Storage:2-8°C Package:bag/bottle/drum Application:for production of perfume compound Transport
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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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inquiryProduct Name Terpineol Synonyms TERPINEOL;TERPINEOL 101 (ALPHA);TERPINEOL 200 (ALPHA);TERPINEOL 318 TYPE;TERPINEOL 350;TERPINEOL, A-;TERPINEOL-ALPHA;Terpineol - Mixed Isomers CAS 800
Appearance:Colourless to Off-White Oil solid Storage:Store below +30°C. Package:25kg/Drum Application:(S)-α-Terpineol comes from the essential oil extracted from the leaves of Zanthoxylum ailanthoides Sieb. Et Zucc. collected from Guizhou which po
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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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inquiry(-)-alpha-Terpineol CAS:10482-56-1 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 organic inte
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inquiryProduct Detail Minimum Order Qty. 10 Gram
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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
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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
Our Services 1. New Molecules R&D 2. Own test center HPLC NMR GC LC-MS 3. API and Intermediates from China reputed manufacturers 4. Documents support COA MOA MSDS DMF open part Our advantages 1. Government awarded company. Top 100 enter
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inquiry1. 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
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inquiryHangzhou KeyingChem Co., Ltd. exported this product to many countries and regions at best price. If you are looking for the material’s manufacturer or supplier in China, KeyingChem is your best choice. Pls contact with us freely for getting det
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inquiryA 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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inquiryProName:High Content Natural Extract α-terpine... CasNo:10482-56-1 Appearance:Powder Application:API, Pharmaceutical excipients, Nutrit... DeliveryTime:Shiping within 3 working days after co... PackAge:25kgs/Drum or According client'
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inquiryJ&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
Our Advantages Production: Advanced chemical equipment with years of experience Staffs for producing various extract products. Quality Control:A complete set of Testing Professional and Analysis Equipment ensures the Quality Requirements and Specif
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inquiryGMP standard, high purity, competitive price, in stock 1. Quick Response: within 6 hours after receiving your email. 2. Quality Guarantee: All products are strictly tested by our QC, confirmed by QA, and approved by a third-party lab in China, USA,
1-methyl-1-(4-methyl-3-cyclohexenyl)ethyl hydroperoxide
(-)-(S)-α-terpineol
Conditions | Yield |
---|---|
With triphenylphosphine In dichloromethane at 0℃; for 0.0833333h; | 94% |
methylmagnesium bromide
benzyl (1S)-4-methylcyclohex-3-ene-1-carboxylate
(-)-(S)-α-terpineol
Conditions | Yield |
---|---|
In tetrahydrofuran at 0 - 20℃; for 13h; | 86% |
N-<(R)-1-phenylethyl>-O-<(3S,4S)-8-hydroxy-1-p-menthen-3-yl>urethane
(-)-(S)-α-terpineol
Conditions | Yield |
---|---|
With sodium; lithium In various solvent(s) at 0℃; | 35% |
(-)-α-pinene
(-)-(S)-α-terpineol
Conditions | Yield |
---|---|
With formic acid Erwaermen des Reaktionsprodukts mit wss.-aethanol. Kalilauge; |
beta-pinene
(-)-(S)-α-terpineol
Conditions | Yield |
---|---|
With nitric acid; potassium nitrate Behandeln des Reaktionsprodukts mit wss. Ammoniak und Zink; |
beta-pinene
A
δ-terpineol
B
(-)-(S)-α-terpineol
C
(+)-8-bromo-α-fenchol
Conditions | Yield |
---|---|
With N-Bromosuccinimide; acetic acid; zinc 1.) acetone, water, 30 min, 2.) ether, 30 min; Multistep reaction; |
(-)-(S)-α-terpineol
Conditions | Yield |
---|---|
With water; sodium nitrite unter Kuehlung; |
Conditions | Yield |
---|---|
anschl. Erhitzen mit 10prozentig. wss. KOH auf 160grad; |
diethyl ether
N-(R)-(+)-bornylamine
water
A
camphene
B
(-)-(S)-α-terpineol
C
(+)-camphene hydrate
Conditions | Yield |
---|---|
das Hydrogensulfat reagiert; |
(4S)-α-terpineol 8-O-β-D-glucopyranoside
(-)-(S)-α-terpineol
Conditions | Yield |
---|---|
With water; β-glucosidase at 37℃; for 24h; Hydrolysis; Enzymatic reaction; | 1.4 mg |
(-)-(S)-limonene
(-)-(S)-α-terpineol
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: dioxygen; bis(1-morpholinocarbamoyl-4,4-dimethyl-1,3-pentanedionato)Co; triethylsilane / 1,2-dichloro-ethane / 24 h / 20 °C 1.2: 8 percent / HCl / methanol; H2O / 0.08 h 2.1: 94 percent / triphenylphosphine / CH2Cl2 / 0.08 h / 0 °C View Scheme | |
Multi-step reaction with 2 steps 1.1: dioxygen; bis(1-morpholinocarbamoyl-4,4-dimethyl-1,3-pentanedionato)Co; triethylsilane / 1,2-dichloro-ethane / 1 h / 20 °C 1.2: 36 percent / HCl / methanol; H2O / 0.08 h 2.1: 94 percent / triphenylphosphine / CH2Cl2 / 0.08 h / 0 °C View Scheme | |
Stage #1: (-)-(S)-limonene With mercury(II) diacetate In tetrahydrofuran; water Stage #2: With sodium tetrahydroborate; sodium hydroxide |
(-)-(S)-α-terpineol
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 5.5 mg / tannase, Aspergillus oryzae; H2O / 3 h / 30 °C / Enzymatic reaction 2: 1.4 mg / β-glucosidase; H2O / 24 h / 37 °C / Enzymatic reaction View Scheme |
6-(1-hydroxy-1-methylethyl)-3-methyl-2-cyclohexen-1-one
(-)-(S)-α-terpineol
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 1.) LiAlH4 / 1.) Et2O, room temperature, 24 h, 2.) benzene, room temperature, 24 h 2: 1.) n-BuLi / 1.) THF, hexane, 0 deg C, 1 h, 2.) THF, hexane, -78 deg C, 30 min 3: 35 percent / Li, Na / various solvent(s) / 0 °C View Scheme |
(-)-(S)-α-terpineol
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 1.) n-BuLi / 1.) THF, hexane, 0 deg C, 1 h, 2.) THF, hexane, -78 deg C, 30 min 2: 35 percent / Li, Na / various solvent(s) / 0 °C View Scheme |
nerol β-D-glucopyranoside
A
(-)-(S)-α-terpineol
B
Cyclohepta-1,3,5-triene
Conditions | Yield |
---|---|
With water pH=2.5; |
2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide
(-)-(S)-α-terpineol
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: silver(l) oxide / diethyl ether / 220 h / 20 °C / Darkness 2: water / pH 2.5 View Scheme |
α-D-glucopyranose peracetylate
(-)-(S)-α-terpineol
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: acetic anhydride; hydrogen bromide / water / 3 h / Cooling with ice 2: silver(l) oxide / diethyl ether / 220 h / 20 °C / Darkness 3: water / pH 2.5 View Scheme |
4-(allyloxy)-4-oxobutanoic acid
(-)-(S)-α-terpineol
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide In dichloromethane at 20℃; under 11250900 Torr; for 24h; | 95% |
methyl hydrogen succinate
(-)-(S)-α-terpineol
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide In dichloromethane at 20℃; under 11250900 Torr; for 24h; | 92% |
(-)-(S)-α-terpineol
Conditions | Yield |
---|---|
With N-Bromosuccinimide; water In acetone | 87% |
(-)-(S)-α-terpineol
Conditions | Yield |
---|---|
With thallium(III) acetate In water; acetic acid for 1h; Ambient temperature; | 86% |
(-)-(S)-α-terpineol
Conditions | Yield |
---|---|
With Oxone; acetyl methyl β-cyclodextrin; sodium hydrogencarbonate; edetate disodium In acetonitrile at 20℃; for 0.666667h; | 85% |
(-)-(S)-α-terpineol
Conditions | Yield |
---|---|
With thionyl chloride; N,N-dimethyl-formamide In dichloromethane at 0 - 5℃; Inert atmosphere; | 81.64% |
(3R-cis)-1-benzoyl-3-(1-methoxy-1-methylethoxy)-4-phenyl-2-azetidinone
(-)-(S)-α-terpineol
Conditions | Yield |
---|---|
Stage #1: (-)-(S)-α-terpineol With lithium hexamethyldisilazane In tetrahydrofuran at -45℃; for 1h; Stage #2: (3R-cis)-1-benzoyl-3-(1-methoxy-1-methylethoxy)-4-phenyl-2-azetidinone In tetrahydrofuran at 0℃; for 2h; Stage #3: With water; acetic acid In tetrahydrofuran at 0℃; for 3h; | 80% |
(-)-(S)-α-terpineol
(S)-(+)-2-methoxy-2-trifluoromethyl-2-phenylacetyl chloride
Conditions | Yield |
---|---|
With dmap In 1,2-dichloro-ethane at 70℃; for 18h; | 76% |
(-)-(S)-α-terpineol
Conditions | Yield |
---|---|
With sodium periodate; ruthenium(III) chloride trihydrate In tetrachloromethane; water; acetonitrile at 0 - 20℃; | 68% |
(-)-(S)-α-terpineol
Conditions | Yield |
---|---|
With bismuth(lll) trifluoromethanesulfonate In 1,2-dichloro-ethane at 80℃; Inert atmosphere; | 67% |
1,1,1,2,2,2-hexamethyldisilane
(-)-(S)-α-terpineol
(S)-trimethyl(2-(4-methylcyclohex-3-enyl)propan-2-yloxy)silane
Conditions | Yield |
---|---|
With 1% Au/TiO2 In ethyl acetate at 55℃; for 3h; | 62% |
(-)-(S)-α-terpineol
Conditions | Yield |
---|---|
With tris(pentafluorophenyl)borane monohydrate; trimethylsilylazide In nitromethane at 23℃; for 1h; Sealed tube; | 58% |
Conditions | Yield |
---|---|
With pyridinium p-toluenesulfonate In dichloromethane for 0.5h; Heating; | 52% |
(-)-(S)-α-terpineol
benzyl chloroformate
Conditions | Yield |
---|---|
Stage #1: (-)-(S)-α-terpineol With 3,6‐di‐tert‐butyl‐9‐mesityl‐10‐phenylacridin‐10‐ium tetrafluoroborate; ammonium carbonate; 2-amino-benzenethiol In dichloromethane; acetonitrile at 20℃; for 12h; Schlenk technique; Inert atmosphere; Sealed tube; Irradiation; Stage #2: benzyl chloroformate | 51% |
(-)-(S)-α-terpineol
t-butyl 3-(trichloromethyl)-1,2-oxaziridine-2-carboxylate
Conditions | Yield |
---|---|
Stage #1: (-)-(S)-α-terpineol With lithium hexamethyldisilazane In tetrahydrofuran at -78℃; Metallation; Stage #2: t-butyl 3-(trichloromethyl)-1,2-oxaziridine-2-carboxylate In tetrahydrofuran at -78 - 20℃; Substitution; Further stages.; | 50% |
4-fluorobenzonitrile
(-)-(S)-α-terpineol
Conditions | Yield |
---|---|
With 15-crown-5; sodium hydride In tetrahydrofuran; mineral oil at 60℃; for 20h; Inert atmosphere; | 17% |
(-)-(S)-α-terpineol
A
5-(1-Hydroxy-1-methyl-ethyl)-2-methyl-cyclohex-2-enone
B
(S)-4-(1-hydroxy-1-methylethyl)-1-cyclohexene-1-carboxaldehyde
Conditions | Yield |
---|---|
With air; GifIV = pyridine; acetic acid; iron(II) chloride; zinc | A 6.3% B 1.4% |
(-)-(S)-α-terpineol
limonene.
Conditions | Yield |
---|---|
With pyrographite at 200℃; |
(-)-(S)-α-terpineol
homoterpenylmethylketone
Conditions | Yield |
---|---|
With jones reagent |
(-)-(S)-α-terpineol
(-)-(1R,2R,4S)-1,3,3-trimethyl-2-oxabicyclo[2.2.2]octane-6-ol
Conditions | Yield |
---|---|
With dioxyphthalic acid |
(-)-(S)-α-terpineol
A
(-)-trans-sobrerol
B
(S)-4-(1-hydroxy-1-methylethyl)-1-cyclohexene-1-methanol
C
(4R,6R)-6-hydroxy-4-(1-hydroxyisopropyl)-1-methylcyclohexene
Conditions | Yield |
---|---|
With Nicotiana tabacum Product distribution; effect of incubation time; | |
With sodium phosphate buffer; Nicotiana tabacum; oxygen; NADPH at 30℃; for 2h; Product distribution; hydroxylation, various substrartes, hydroxylase activity under different reaction conditions; |
(-)-(S)-α-terpineol
Conditions | Yield |
---|---|
With bromine In diethyl ether for 6h; Ambient temperature; |
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