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Cas:112-86-7
Min.Order:1 Metric Ton
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Type:Manufacturers
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Cas:112-86-7
Min.Order:1 Kilogram
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Type:Lab/Research institutions
inquiryHigh quality Erucic Acid Cas 112-86-7 with steady supply Company profile Wuhan Fortuna Chemical Co.,Ltd established in 2006, is a big integrative chemical enterprise being engaged in Pharmaceutical & its intermediates, Food/Feed additives, F
Cas:112-86-7
Min.Order:10 Kilogram
FOB Price: $10.0
Type:Trading Company
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Cas:112-86-7
Min.Order:1 Gram
FOB Price: $0.1
Type:Manufacturers
inquiryhebei yanxi chemical co., LTD who registered capital of 10 million yuan, nearly to $2 million, we have a pharmaceutical raw materials factory production of pharmaceutical raw materials, and a reagent r&d center, and we do research and developm
Cas:112-86-7
Min.Order:1 Metric Ton
FOB Price: $1.0 / 3.0
Type:Trading Company
inquiryOur main production base is located in Xuzhou industry park. We are certified both to the ISO 9001 and ISO 14001 Standards, have a safety management system in place.Our R&D team masters core technology for process-design of target building block
Product Name: Erucic Acid Synonyms: 13C DOCOSENOIC ACID;(13Z)-13-Docosenoic acid;(z)-13-docosenoicaci;(Z)-docos-13-enoicacid;13-cis-Docosenoicacid;13-Docosenoic acid, (Z)-;13-Docosenoicacid,(13Z)-;Erucasαure CAS: 112-86-7 MF: C22H42O2 MW:
Cas:112-86-7
Min.Order:1 Kilogram
FOB Price: $500.0
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
Cas:112-86-7
Min.Order:1 Gram
FOB Price: $1.0 / 99.0
Type:Trading Company
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Cas:112-86-7
Min.Order:1 Kilogram
FOB Price: $139.0 / 210.0
Type:Trading Company
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Cas:112-86-7
Min.Order:10 Kilogram
Negotiable
Type:Trading Company
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 We can also provide MT1 peptide powd
Cas:112-86-7
Min.Order:1 Kilogram
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Cas:112-86-7
Min.Order:1 Kilogram
Negotiable
Type:Lab/Research institutions
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Cas:112-86-7
Min.Order:1 Kilogram
FOB Price: $32.0 / 36.0
Type:Trading Company
inquiryErucic Acid CAS: 112-86-7 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 intermediates
Cas:112-86-7
Min.Order:1 Gram
Negotiable
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
About Product Details
Cas:112-86-7
Min.Order:1 Kilogram
FOB Price: $3.0 / 10.0
Type:Lab/Research institutions
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Cas:112-86-7
Min.Order:1 Kilogram
Negotiable
Type:Lab/Research institutions
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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Zibo 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
Cas:112-86-7
Min.Order:10 Gram
FOB Price: $100.0
Type:Lab/Research institutions
inquiryShandong Baimao Chemical Co., Ltd is a private joint-stock fine chemical enterprises, with a sound management system. Long-term commitment to chemical products research and development, production and marketing. Our products include organic chemical
Cas:112-86-7
Min.Order:5 Metric Ton
FOB Price: $120.0 / 150.0
Type:Trading Company
inquiryManufacture High Quality Best Price For Erucic acidAppearance:White crystalline powder Storage:Store in dry,dark,ventilated place Package:according to customers' requirements Application:Pharmaceutical intermediates Transportation:By air(EMS or EUB o
Cas:112-86-7
Min.Order:1 Gram
Negotiable
Type:Other
inquiryWe are one of a few suppliers that can offer custom synthesis service of this product We are specialized in custom synthesis, chemical/pharmaceutical/ pesticides outsourcing and contract research. We are committed to prov
Cas:112-86-7
Min.Order:100 Gram
FOB Price: $100.0 / 2000.0
Type:Lab/Research institutions
inquirySuperior quality, moderate price & quick delivery. Appearance:white powder Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:25kg/drum, or as per your request. Application:Used as Pharmaceutical Intermediates Tr
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,
Our Advantages A. International Top level TechnologyOur company owned biomedicine experts are famous at home and abroad with rich experience in research and development in the field of efficient chiral functional molecules research and development an
Conditions | Yield |
---|---|
With lithium hydroxide monohydrate In tetrahydrofuran; water at 20℃; | 86% |
pyridine
ethanol
docos-13-enoic acid-anhydride
A
cis-13-docosenoic acid
B
ethyl (13Z)-13-docosenoate
Conditions | Yield |
---|---|
erucic acid anhydride; |
cis-13-docosenoic acid
Conditions | Yield |
---|---|
at 175℃; |
ethanol
docos-13-enoic acid-anhydride
A
cis-13-docosenoic acid
B
ethyl (13Z)-13-docosenoate
Conditions | Yield |
---|---|
erucic acid anhydride; |
cis-Octadecenoic acid
adipic acid monomethyl ester
cis-13-docosenoic acid
Conditions | Yield |
---|---|
With methanol; sodium methylate Electrolysis.Hydrolyse des gebildeten Erucasaeure-methylesters durch Erwaermen mit wss.-methanol.Natronlauge; |
Conditions | Yield |
---|---|
With nickel Hydrogenation; | |
With quinoline; ethyl acetate Hydrogenation.Lindlar-Katalysator; |
13-hydroxy-docosanoic acid
cis-13-docosenoic acid
Conditions | Yield |
---|---|
at 220℃; under 7 Torr; |
Conditions | Yield |
---|---|
erucic acid anhydride; |
Conditions | Yield |
---|---|
Kinetics; |
cis-13-docosenoic acid
Conditions | Yield |
---|---|
With ethanol; sodium |
cis-13-docosenoic acid
Conditions | Yield |
---|---|
With ethanol; sodium |
Conditions | Yield |
---|---|
Hydrogenation; |
cis-13-docosenoic acid
Conditions | Yield |
---|---|
With potassium hydroxide | |
With potassium hydroxide ueber mehrere Stufen; | |
With lead(II) oxide bei Extraktion mit Aether bleibt erucasaures Blei ungeloest, das mit Salzsaeure zerlegt wird; | |
With hydrogenchloride Destillieren die untere, die Methylester enthaltende Schicht bei 25 mm, Verseifen die ueber 240grad siedende Hauptfraktion und Umkrystallisieren die abgeschiedene Erucasaeure bei 0-5grad aus einem Gemisch von Alkohol und Aceton; |
Conditions | Yield |
---|---|
erucic acid dichloride; |
13,14-dibromo-docosanoic acid
cis-13-docosenoic acid
Conditions | Yield |
---|---|
erucic acid dibromide; |
Conditions | Yield |
---|---|
ν-chloro-erucic acid; |
Conditions | Yield |
---|---|
μ-bromo-erucic acid; |
Conditions | Yield |
---|---|
With aluminum isopropoxide Einw. von Bromwasserstoff auf das entstandene Saeuregemisch und Behandlung mit Zink; |
docos-13-enoic acid-anhydride
A
cis-13-docosenoic acid
B
ethyl (13Z)-13-docosenoate
Conditions | Yield |
---|---|
erucic acid anhydride; |
Conditions | Yield |
---|---|
erucic acid dichloride; |
13-iodo-docosanoic acid
A
cis-13-docosenoic acid
Conditions | Yield |
---|---|
With potassium hydroxide |
tetradec-5-ynoic acid
cis-13-docosenoic acid
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: methanol; sodium / Electrolysis.Behandlung des Reaktionsprodukts mit wss.-aethanol.Kalilauge 2: methanol; sodium / Electrolysis.anschliessenden Behandlung mit wss.-aethanol.Kalilauge 3: quinoline; ethyl acetate / Hydrogenation.Lindlar-Katalysator View Scheme |
pentadec-6-ynoic acid
cis-13-docosenoic acid
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: methanol; sodium / Electrolysis.Behandlung des Reaktionsprodukts mit wss.-aethanol.Kalilauge 2: methanol; sodium / Electrolysis.anschliessenden Behandlung mit wss.-aethanol.Kalilauge 3: quinoline; ethyl acetate / Hydrogenation.Lindlar-Katalysator View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: methanol; sodium / Electrolysis.anschliessenden Behandlung mit wss.-aethanol.Kalilauge 2: quinoline; ethyl acetate / Hydrogenation.Lindlar-Katalysator View Scheme |
dodec-6-ynedioic acid monomethyl ester
cis-13-docosenoic acid
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: methanol; sodium / Electrolysis.Behandlung des Reaktionsprodukts mit warmer wss.-aethanol.Kalilauge 2: methanol; sodium / Electrolysis.Behandlung des Reaktionsprodukts mit wss.-aethanol.Kalilauge 3: methanol; sodium / Electrolysis.anschliessenden Behandlung mit wss.-aethanol.Kalilauge 4: quinoline; ethyl acetate / Hydrogenation.Lindlar-Katalysator View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: methanol; sodium / Electrolysis.Behandlung des Reaktionsprodukts mit warmer wss.-aethanol.Kalilauge 2: methanol; sodium / Electrolysis.Behandlung des Reaktionsprodukts mit wss.-aethanol.Kalilauge 3: methanol; sodium / Electrolysis.anschliessenden Behandlung mit wss.-aethanol.Kalilauge 4: quinoline; ethyl acetate / Hydrogenation.Lindlar-Katalysator View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: methanol; sodium / Electrolysis.Behandlung des Reaktionsprodukts mit warmer wss.-aethanol.Kalilauge 2: methanol; sodium / Electrolysis.Behandlung des Reaktionsprodukts mit wss.-aethanol.Kalilauge 3: methanol; sodium / Electrolysis.anschliessenden Behandlung mit wss.-aethanol.Kalilauge 4: quinoline; ethyl acetate / Hydrogenation.Lindlar-Katalysator View Scheme |
cis-13-docosenoic acid
Conditions | Yield |
---|---|
With Candida antarctica Lipase A; sodium chloride In aq. phosphate buffer; isopropyl alcohol pH=7.5; Catalytic behavior; Enzymatic reaction; |
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride In tetrahydrofuran for 3.5h; Heating; | 100% |
With lithium aluminium tetrahydride In diethyl ether at 0 - 20℃; for 2.25h; Inert atmosphere; Green chemistry; | 96.2% |
With lithium aluminium tetrahydride | |
With lithium aluminium tetrahydride In diethyl ether | |
Multi-step reaction with 2 steps 1: sulfuric acid / Reflux 2: lithium aluminium tetrahydride / tetrahydrofuran / 20 °C / Inert atmosphere View Scheme |
Conditions | Yield |
---|---|
With [1,3-bis(2,4,5-Me3Ph)-2-imidazolidinylidene]Ru=CHPh(PCy3)Cl2 at 45℃; for 24h; | A 100% B n/a |
Stage #1: cis-13-docosenoic acid; dichloro(tricyclohexylphosphino)(benzylidene)(1,3-dimesityl-4,5-dihydroimidazol-2-ylidene)ruthenium(III) at 45℃; for 72h; Neat (no solvent); Stage #2: With ethyl vinyl ether Product distribution / selectivity; | A 70% B n/a |
cis-13-docosenoic acid
N-{2-[(2,6-dimethylphenyl)-amino]-2-oxoethyl}-N,N-diethyl-benzenemethanaminium eruciate
Conditions | Yield |
---|---|
In methanol at 30 - 60℃; for 1 - 2h; | 100% |
cis-13-docosenoic acid
2-(pyridin-4-yl)-thiazolidine-4-carboxylic acid
Conditions | Yield |
---|---|
In pyridine (6 ml)-methylene chloride | 99% |
Conditions | Yield |
---|---|
With ammonia; zircornium(IV) n-propoxide at 165℃; for 6h; Reagent/catalyst; | 98.8% |
Multi-step reaction with 2 steps 1: oxalyl dichloride / dichloromethane / Inert atmosphere 2: ammonium hydroxide View Scheme |
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide In dichloromethane for 1h; | 96% |
Conditions | Yield |
---|---|
With Zn-MCM-22 catalyst at 80 - 340℃; under 15001.5 Torr; for 6h; Inert atmosphere; Large scale; | 96% |
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; for 24h; |
Conditions | Yield |
---|---|
With choline chloride; zinc(II) chloride at 110℃; for 12h; | 95% |
Conditions | Yield |
---|---|
Stage #1: cis-13-docosenoic acid With dihydrogen peroxide In formic acid; water at 20℃; Stage #2: With potassium hydroxide In water for 4h; Reflux; | 94% |
With formic acid; dihydrogen peroxide | 91% |
With potassium hydroxide; potassium permanganate; water at 0℃; |
cis-13-docosenoic acid
4-bromopiperidine hydrobromide
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; for 18h; Inert atmosphere; | 94% |
Conditions | Yield |
---|---|
With choline chloride; zinc(II) chloride at 110℃; for 12h; | 93% |
Conditions | Yield |
---|---|
With sodium methylate In methanol for 0.533333h; electrolysis, 1A (1F/mol), Pt-plate anode, titanium cathode; | 92% |
cis-13-docosenoic acid
1-amino-3-(dimethylamino)propane
N-erucamidopropyl-N,N-dimethylamine
Conditions | Yield |
---|---|
With sodium fluoride at 155 - 160℃; for 10h; Inert atmosphere; | 92% |
With aluminum oxide; sodium fluoride at 160℃; for 10h; Inert atmosphere; | 82% |
With aluminum oxide; sodium fluoride In neat (no solvent) at 155 - 160℃; for 10h; Inert atmosphere; |
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide In chloroform at 20℃; Cooling with ice; | 91.8% |
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℃; |
Conditions | Yield |
---|---|
With chloroformic acid ethyl ester; triethylamine In acetonitrile for 0.5h; Ambient temperature; | 90% |
cis-13-docosenoic acid
Conditions | Yield |
---|---|
With acridine; dichloro(dimethylglyoxime)(dimethylglyoximato)cobalt(III) In dichloromethane; acetonitrile at 25 - 27℃; for 36h; Irradiation; | 90% |
Stage #1: cis-13-docosenoic acid With bis(1,5-cyclooctadiene)diiridium(I) dichloride; triphenylphosphine; potassium iodide at 20℃; for 0.5h; Inert atmosphere; Schlenk technique; Stage #2: With acetic anhydride at 160℃; for 5h; Inert atmosphere; Schlenk technique; regioselective reaction; | |
With bis(1,5-cyclooctadiene)diiridium(I) dichloride; N,N-diphenylaminobenzene; acetic anhydride; potassium iodide at 160℃; for 12h; Inert atmosphere; Green chemistry; chemoselective reaction; |
(3aR,5S,5aR,8aS,8bR)-2,2,7,7-Tetramethyl-tetrahydro-bis[1,3]dioxolo[4,5-b;4',5'-d]pyran-5-carbaldehyde
cis-13-docosenoic acid
4-methoxycarbonyl-1-isocyanobenzene
Conditions | Yield |
---|---|
In dichloromethane at 20℃; Passerini Condensation; | 90% |
cis-13-docosenoic acid
N1,N8-bis(tert-butoxycarbonyl)spermidine
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; for 48h; Inert atmosphere; | 89.4% |
Conditions | Yield |
---|---|
With oxygen; ozone In water; acetone at 0℃; Flow reactor; | A 74% B 88% |
cis-13-docosenoic acid
(Z)-N-hydroxydocos-13-enamide
Conditions | Yield |
---|---|
With hydroxylamine hydrochloride; potassium hydroxide In methanol for 24h; Reflux; | 85% |
Stage #1: cis-13-docosenoic acid With 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide; triethylamine In ethyl acetate; acetonitrile at 20℃; for 0.5h; Stage #2: With hydroxylamine hydroxide In ethyl acetate; acetonitrile at 20℃; | 72% |
Conditions | Yield |
---|---|
Stage #1: cis-13-docosenoic acid With O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; for 2h; Stage #2: 2,2'-iminobis[ethanol] In dichloromethane at 20℃; for 18h; | 83% |
cis-13-docosenoic acid
tolyldocosanoic acid
Conditions | Yield |
---|---|
With sulfuric acid In toluene | 82% |
Conditions | Yield |
---|---|
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine In dichloromethane at 20℃; for 14h; Inert atmosphere; | 82% |
Conditions | Yield |
---|---|
Stage #1: cis-13-docosenoic acid With 2,6-dimethylpyridine; potassium osmate(VI) dihydrate; sodium periodate In 1,3-dioxane; water at 20℃; for 16h; Inert atmosphere; Stage #2: With sodium tetrahydroborate In tetrahydrofuran at 0 - 20℃; for 3.25h; Inert atmosphere; | 81% |
With sodium hydroxide; sodium tetrahydroborate; ozone 1.) ethanol, cyclohexane, 0 deg C, 2.) water, ethanol, cyclohexane, room temp., 10 h; Yield given. Multistep reaction; | |
Stage #1: cis-13-docosenoic acid With ozone In ethanol; cyclohexane at 0 - 5℃; Ozonolysis; Stage #2: With potassium borohydride Reduction; | |
Stage #1: cis-13-docosenoic acid With ozone In ethanol; cyclohexane at 0 - 5℃; for 4h; Stage #2: With potassium borohydride In methanol at 0℃; for 8h; Further stages.; | |
Multi-step reaction with 2 steps 1: O3 / ethanol; cyclohexane / 0 - 5 °C 2: KBH4 View Scheme |
cis-13-docosenoic acid
1-O-cholesteryl-β-D-galactopyranoside
cholesteryl 6-O-erucoyl-β-D-galactopyranoside
Conditions | Yield |
---|---|
Stage #1: cis-13-docosenoic acid With pyridine; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine at 20℃; for 0.5h; Inert atmosphere; Stage #2: 1-O-cholesteryl-β-D-galactopyranoside at 20℃; for 36h; Inert atmosphere; regioselective reaction; | 81% |
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In pyridine at 0 - 20℃; for 48h; | 52% |
Conditions | Yield |
---|---|
With piperazine; 9-(2-chlorophenyl)acridine; tetrakis(acetonitrile)copper(I)tetrafluoroborate In dichloromethane at 25 - 27℃; for 14h; Irradiation; | 80% |
vinyl acetate
cis-13-docosenoic acid
(Z)-Docos-13-enoic acid vinyl ester
Conditions | Yield |
---|---|
With palladium diacetate; potassium hydroxide for 24h; Ambient temperature; | 79% |
cis-13-docosenoic acid
hexadecanoic acid 2-decanoyloxy-1-hydroxymethyl-ethyl ester
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide In dichloromethane at 20℃; for 1h; Esterification; | 77% |
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