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 quantities
Simagchem, your partner in China as a premier supply of bulk specialty chemicals for industry and life science. We introduce experienced quality product and exceptional JIT service with instant market intelligence in China to benefit our customers
high quality Appearance:White or off-white Solid 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
Aniline 1. Physical and chemical properties Appearance: Colorless to yellow liquid Molecular Weight: 93.13g/moL Molecular Formula: C6H7N Density: 1.
The 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
Hebei 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
Name Anili
Product Description Product name Aniline CAS 62-53-3 Assay 99% Appearance Colorless oily liquid
Product Name Aniline Synonyms ai3-03053;amino-benzen;Aminophen;Anilin;anilin(czech);Anilina;anilina(italian,polish);Aniline reagent CAS 62-53-3 MF C6H7N
Our company has been in existence for 10 years since its establishment. We have our own unique team. The company integrates independent research and development, production and sales. We have established famous brands at home and abroad. At prese
Cas:62-53-3
Min.Order:1 Metric Ton
FOB Price: $1200.0 / 1700.0
Type:Trading Company
inquirySuperiority We can customize and synthesize products that other suppliers may not be able to provide. Advantage cof, mof ligand manufacturer Product Detail bes
Cas:62-53-3
Min.Order:100 Kilogram
Negotiable
Type:Trading Company
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
Hangzhou 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
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
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:62-53-3
Min.Order:10 Gram
FOB Price: $100.0
Type:Lab/Research institutions
inquirySuperior quality Appearance:colourless liquid Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:100g/bottle,1kg/bottle,25kg/drum or as per your request Application:Used as Pharmaceutical Intermediates Transportation
Product name: Aniline CAS No.: 62-53-3 Molecule Formula:C6H7N Molecule Weight:93.13 Purity: 99.0% Package: 200kg/drum Description:Colorless to yellow liquid Manufacture Standards:Enterprise Standard TESTING ITEMS
Hangzhou Huarong Pharm Co., Ltd.established since 2006 , has been actively developing specialty products for Finished Dosages, APIs, Intermediates, and Fine chemicals markets in North America, Europe, Korea, Japan, Mid-East and all over the World. Hu
Appearance:95%+ Package:R&D,Pilot run Transportation:per client require Port:Express ,Air, Sea
high 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 purity,in stock Package:25kg/drum,or as per customers'demand Application:API,or Intermediates,fine chemicals Transportation:air,sea,courier
Jinhua huayi chemical co., ltd. is dedicated to the development, production and marketing of chemicals. On the basis of equality and mutual benefit, and under the principle of customer first, credit first, quality first, we are ready to join hands
R & D enterprises have their own stock in stock Package:1kg Application:pharmaceutical intermediates
high purity Storage:normal temperature Package:DRUM Application:mainly for medical use for R&Dpurpose use only Transportation:AIR,SEA Port:BEIJING,SHANGHAI,TIANJIN,SHENZHEN
Product Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard
Cas:62-53-3
Min.Order:1 Kilogram
FOB Price: $112.0
Type:Trading Company
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
Amoychem is committed to providing the top-quality chemical products and services Internationally. We offer our customers with friendly, professional service and reliable, high performance products that have been manufactured according to the accredi
sell high purity of Aniline Application:sell high purity of Aniline
1,we produce and sell good chemicals around the world. 2,our success rate is about 95%. this means, if customer order is accepted, the probability that the customer will obtain the ordered substances, is 95%. 3,our staff consists of highl
Hangzhou ZeErRui Chemical Co., Ltd. located in Lingang industrial areas, our plant covers an area of 6000 square meters.ZeErRui dedicated to the development, production and marketing of chemicals. We have earned ourselves a good reputation at home an
Conditions | Yield |
---|---|
With copper(I) oxide; ammonium hydroxide In 1-methyl-pyrrolidin-2-one at 80℃; for 15h; | 100% |
With ammonia; copper In water at 100℃; for 24h; Ullmann reaction; | 99.1% |
With copper(l) iodide; 2-carboxyquinoline N-oxide; potassium carbonate; ammonium hydroxide In dimethyl sulfoxide at 80℃; for 23h; Inert atmosphere; | 98% |
Conditions | Yield |
---|---|
With hydrogen; platinum In water at 20℃; Product distribution; other temp.; | 100% |
With ethanol; water; tetrabutylammonium hypophosphite; benzene; palladium on activated charcoal for 5h; Product distribution; Heating; hydrogenation in a biphasic solvent system; | 100% |
With hydrogen; Pd in AV-17-8-Pd In ethanol at 40℃; under 760 Torr; Rate constant; | 100% |
Conditions | Yield |
---|---|
With ammonia borane; gold on titanium oxide In ethanol at 20℃; for 0.5h; Inert atmosphere; | A 92% B 100% |
With samarium; iodine; ammonium chloride In tetrahydrofuran; water at 20℃; for 4h; Reduction; | A 56% B 20% |
Electrolysis; |
Conditions | Yield |
---|---|
With hydrazine hydrate In ethanol; water at 80℃; chemoselective reaction; | 100% |
With ammonium hydroxide; nickel boride at 40℃; for 0.5h; Product distribution; further medium: 3N HCl; | 94.4% |
With copper(I) chloride; potassium borohydride In methanol for 0.416667h; Product distribution; Ambient temperature; reduction of aromatic nitro compounds, nitrozobenzene, azobenzene and azoxybenzene with potassium borohydride-copper(I) chloride to primary amines; | 94% |
Conditions | Yield |
---|---|
With sodium hydrogen telluride In diethyl ether; ethanol for 0.25h; Ambient temperature; | 100% |
With iron(III)-acetylacetonate; hydrazine hydrate In methanol at 150℃; for 0.05h; Microwave irradiation; chemoselective reaction; | 99% |
With dibutyltin In benzene at 15℃; for 5h; other reagents; | 98% |
Conditions | Yield |
---|---|
With tris-(2-chloro-ethyl)-amine; trifluorormethanesulfonic acid; trifluoroacetic acid In chloroform at 40℃; for 12h; Product distribution; Mechanism; various acids, various substrates; | 100% |
With trifluorormethanesulfonic acid; trimethylsilylazide at 55℃; for 0.833333h; Product distribution; Mechanism; other arenes or substituted arenes; var. temperatures and time; | 95% |
With trifluorormethanesulfonic acid; trimethylsilylazide In chloroform at 90℃; under 5250.53 Torr; for 0.0466667h; Flow reactor; | 86% |
Conditions | Yield |
---|---|
With sodium hydroxide In ethanol; water at 100℃; for 0.666667h; Product distribution; | 100% |
3-(4-nitro-phenoxy)-benz[d]isothiazole-1,1-dioxide
A
aniline
B
saccharin
Conditions | Yield |
---|---|
With sodium hypophosphite; palladium on activated charcoal In water; benzene for 0.25h; Heating; | A 100% B n/a |
Conditions | Yield |
---|---|
With sodium hypochlorite; sodium hydroxide In 1,4-dioxane; water at 80℃; for 0.25h; Hofmann degradation; | 100% |
With sodium hydroxide; benzyltrimethylazanium tribroman-2-uide In water for 2h; Ambient temperature; | 72% |
With water; bromine; sodium hydroxide Hofmann Rearrangement; Cooling with ice; |
Conditions | Yield |
---|---|
With hydrazine hydrate In ethanol; water at 80℃; chemoselective reaction; | 100% |
With sodium tetrahydroborate; meso-tetraphenylporphyrin iron(III) chloride In methanol; diethylene glycol dimethyl ether at 25℃; for 3h; Product distribution; Further Variations:; Reagents; | 98% |
With hydrogen In ethanol at 30℃; under 1875.19 Torr; for 1h; Irradiation; Autoclave; | 95% |
Conditions | Yield |
---|---|
With hydrogen; palladium In ethanol; acetic acid under 2585.7 Torr; | A 100% B n/a |
A
bis(p-bromophenyl)arsinic acid
B
aniline
Conditions | Yield |
---|---|
With water In diethyl ether | A 100% B n/a |
t-butyl N-phenyl sulfinamoyl acetate
benzylamine
A
Benzylamino-thioxo-acetic acid tert-butyl ester
B
aniline
Conditions | Yield |
---|---|
In diethyl ether for 72h; Ambient temperature; | A 63% B 100% |
In diethyl ether for 72h; Mechanism; Ambient temperature; reaction of other substituted t-butyl sulfinamoyl acetates; | A 63% B 100% |
Conditions | Yield |
---|---|
With copper(I) chloride; potassium borohydride In methanol for 0.25h; Product distribution; Ambient temperature; reduction of aromatic nitro compounds , nitrosobenzene, azobenzene and azoxybenzene with potassium borohydride-copper(I) chloride to primary amines; | 100% |
With N-doped TiO2 In methanol at 20℃; for 3h; UV-irradiation; Inert atmosphere; | 92% |
With 4,4'-di-tert-butylbiphenyl; lithium; nickel dichloride In tetrahydrofuran at 20℃; for 10h; Reduction; deoxygenation; | 66% |
Conditions | Yield |
---|---|
With H2 In not given Ru compound heated at 80°C under CO-H2 (1:1); | 100% |
carbon monoxide
aniline
Conditions | Yield |
---|---|
With H2 In not given Ru compound heated at 80°C under CO-H2 (1:1); | 100% |
Conditions | Yield |
---|---|
With iron(III) oxide; sodium hydroxide; copper(l) iodide; ammonia In ethanol; water at 90℃; for 16h; | 100% |
With copper(I) oxide; ammonium hydroxide In 1-methyl-pyrrolidin-2-one at 80℃; for 15h; | 99% |
With ammonia; triethylamine In water at 20℃; for 2.5h; Reagent/catalyst; Solvent; Time; | 98% |
anilino(tert-butyldimethyl)silane
aniline
Conditions | Yield |
---|---|
With silica gel In ethanol; water at 20℃; for 2h; | 100% |
2-methyl-1,2,3,4-tetrahydroquinolin-4-yl-(phenyl)amine
A
2-methylquinoline
B
aniline
Conditions | Yield |
---|---|
With palladium dichloride In acetonitrile | A 100% B 100% |
Conditions | Yield |
---|---|
With ammonium formate In water; isopropyl alcohol at 20℃; for 3h; | 99% |
With hydrogen; triethylamine In water at 120 - 140℃; under 22502.3 - 37503.8 Torr; | 99% |
With hydrogen; NiCl2-Li-[poly(2-vinyl-naphthalene)-co-(divinylbenzene)] In tetrahydrofuran at 20℃; under 760.051 Torr; for 2h; | 98% |
Conditions | Yield |
---|---|
With hydrogen; triethylamine In water at 120 - 140℃; under 22502.3 - 37503.8 Torr; | 99% |
With lithium at 230℃; Zersetzen der Reaktionsprodukte mit Wasser; | |
With potassium fluoride; polymethylhydrosiloxane; palladium diacetate In tetrahydrofuran at 20℃; for 0.75h; | 94 % Spectr. |
Conditions | Yield |
---|---|
With ammonium formate In water at 20℃; for 3h; | 99% |
With ammonium formate; PdMCM-41 In methanol at 69.84℃; for 0.666667h; | 95% |
With palladium on activated charcoal; formic acid; N,N-dimethyl-formamide for 3h; Heating; | 90% |
Conditions | Yield |
---|---|
With hydrogen; triethylamine In water at 120 - 140℃; under 22502.3 - 37503.8 Torr; Temperature; | 99% |
With methanol; gold; hydrogen; caesium carbonate at 100℃; under 3800.26 Torr; for 155h; | 80% |
Stage #1: 4-bromo-aniline With palladium dichloride In water at 20℃; for 0.0333333h; Stage #2: With 1,1,3,3-Tetramethyldisiloxane for 0.383333h; | 79% |
Conditions | Yield |
---|---|
With water at 100℃; for 10h; Inert atmosphere; | 99% |
HY-Zeolite In dichloromethane for 1.5h; Heating; | 92% |
With 3-butyl-l-methyl-1H-imidazol-3-iumtrifloroacetate In 1,4-dioxane; water at 70 - 72℃; for 1h; | 92% |
Conditions | Yield |
---|---|
With hydrogen; 5% rhodium-on-charcoal; tris(acetylacetonato)cobalt In tetrahydrofuran at 20℃; for 16h; | A 99% B 89% |
With hydrogen; 5% rhodium-on-charcoal; iron(II) acetate In tetrahydrofuran at 20℃; for 16h; | A 98% B 80% |
With hydrogen; 5% rhodium-on-charcoal In tetrahydrofuran at 20℃; for 16h; Product distribution / selectivity; | A 93% B 31% |
With hydrogen at 110℃; under 4560.31 Torr; for 24h; Autoclave; chemoselective reaction; |
Conditions | Yield |
---|---|
With 40% potassium fluoride/alumina for 0.0666667h; Microwave irradiation; Neat (no solvent); | A 90% B 99% |
Conditions | Yield |
---|---|
With ammonium formate In water; isopropyl alcohol at 20℃; for 3h; | 99% |
With Raney aluminium-nickel alloy; water; sodium hydroxide In dimethoxymethane at 25℃; for 17h; |
Conditions | Yield |
---|---|
With ammonium formate In water; isopropyl alcohol at 20℃; for 3h; | 99% |
With methylene blue; sodium hydroxide Kinetics; Concentration; pH-value; Temperature; Irradiation; |
Conditions | Yield |
---|---|
With hydrogen In ethanol at 109.84℃; under 18751.9 Torr; for 7.5h; Autoclave; Green chemistry; chemoselective reaction; | 99% |
Cyclopentene oxide
aniline
trans-2-(phenylamino)cyclopentanol
Conditions | Yield |
---|---|
With zirconium(IV) chloride at 20℃; for 0.25h; | 100% |
With lithium bromide at 20℃; for 5h; | 100% |
With sulfated zirconia In neat (no solvent) at 20℃; for 0.5h; regioselective reaction; | 98% |
Conditions | Yield |
---|---|
With copper(II) bis(trifluoromethanesulfonate) In water at 20℃; for 0.0166667h; | 100% |
With aluminum oxide for 5h; Milling; | 100% |
sodium hydrogen sulfate; silica gel at 56 - 58℃; for 0.0244444h; microwave irradiation; | 98% |
Conditions | Yield |
---|---|
In diethyl ether Ring cleavage; Substitution; | 100% |
In dichloromethane at 20℃; for 1h; | 100% |
at 20℃; for 2h; | 99% |
Conditions | Yield |
---|---|
Stage #1: phthalic anhydride; aniline In N,N-dimethyl acetamide at 20℃; for 24h; Stage #2: In N,N-dimethyl acetamide; xylene at 140℃; for 48h; | 100% |
In 1,2-dichloro-benzene at 180 - 190℃; for 5h; Dean-Stark; | 100% |
In 1,2-dichloro-benzene at 180 - 190℃; for 5h; Dean-Stark; | 100% |
Phenyl glycidyl ether
aniline
N-(2-hydroxy-3-phenoxypropyl)aniline
Conditions | Yield |
---|---|
With zirconium(IV) chloride at 20℃; for 0.25h; | 100% |
With lithium bromide at 20℃; for 5h; | 100% |
silica gel at 20℃; for 3h; | 100% |
cyclohexane-1,2-epoxide
aniline
2-(phenylamino)cyclohexan-1-ol
Conditions | Yield |
---|---|
In water at 60℃; for 18h; | 100% |
With acetic acid at 20 - 25℃; for 1h; Temperature; Reagent/catalyst; | 100% |
With PhCNAl(OC(CF3)2PhCH3)3 at 25℃; for 4h; Inert atmosphere; Neat (no solvent); | 99% |
cyclohexane-1,2-epoxide
aniline
trans-(2-(phenylamino)cyclohexanol)
Conditions | Yield |
---|---|
With bis(trifluoromethane)sulfonimide lithium at 20℃; for 20h; without solvent; | 100% |
With zirconium(IV) chloride at 20℃; for 0.25h; | 100% |
Montmorillonite K 10 at 20℃; for 3h; Product distribution; Further Variations:; Catalysts; reaction times; | 100% |
Conditions | Yield |
---|---|
With pyridine; aluminum oxide at 93 - 95℃; for 1h; microwave irradiation; | 100% |
In dichloromethane at 20℃; Inert atmosphere; | 100% |
In dichloromethane at 21℃; Inert atmosphere; | 100% |
Conditions | Yield |
---|---|
With acetic acid In 1,2-dichloro-ethane at 20℃; for 24h; Inert atmosphere; | 100% |
With formic acid In ethanol; water at 20℃; for 0.0166667h; Green chemistry; | 99% |
at 20℃; for 14h; Molecular sieve; | 98% |
Conditions | Yield |
---|---|
With pyridine In toluene for 12h; | 100% |
With triethylamine In dichloromethane at 20℃; Inert atmosphere; | 100% |
With triethylamine In ethyl acetate at 0 - 20℃; | 94% |
Conditions | Yield |
---|---|
In chloroform Ambient temperature; | 100% |
In benzene Heating; | 74% |
In water at 20℃; for 2h; | 69% |
2-ethoxycarbonyl-1-cyclopentanone
aniline
2-(N-phenylcarbamoyl)cyclopentanone
Conditions | Yield |
---|---|
In neat (no solvent) at 180℃; for 0.75h; Microwave irradiation; Green chemistry; | 100% |
In 5,5-dimethyl-1,3-cyclohexadiene at 160℃; Inert atmosphere; | 90% |
With dmap In toluene for 9.5h; Reflux; Inert atmosphere; | 39% |
3,4,5-trimethoxy-benzaldehyde
aniline
N-(3,4,5-trimethoxybenzylidene)aniline
Conditions | Yield |
---|---|
In chloroform Ambient temperature; | 100% |
sodium hydrogen sulfate; silica gel at 60 - 62℃; for 0.025h; microwave irradiation; | 94% |
In ethanol at 20℃; | 87% |
Conditions | Yield |
---|---|
Stage #1: trityl chloride; aniline at 190℃; for 0.5h; Stage #2: With hydrogenchloride In methanol for 0.5h; Reflux; | 100% |
at 50℃; for 1.5h; | 63% |
With pyridine at 20℃; for 24h; Substitution; | 44% |
Conditions | Yield |
---|---|
With tri-n-butyl-tin hydride; silica gel at 20℃; for 1h; | 100% |
With sodium tetrahydroborate; triethylamine In methanol | 100% |
With sodium tris(acetoxy)borohydride In 1,2-dichloro-ethane at 18℃; for 1h; Solvent; Reagent/catalyst; Green chemistry; | 100% |
Conditions | Yield |
---|---|
In chloroform Ambient temperature; | 100% |
In toluene at 120℃; for 24h; | 100% |
With alumina-entrapped Ag at 120℃; under 750.075 Torr; for 1h; Inert atmosphere; Autoclave; | 100% |
benzaldehyde
aniline
(E)-N-benzylidenebenzenamine
Conditions | Yield |
---|---|
In ethanol for 6h; Reflux; | 100% |
In toluene Inert atmosphere; Schlenk technique; Molecular sieve; | 100% |
With silica gel In ethanol at 20℃; Ultrasound irradiation; | 99% |
Conditions | Yield |
---|---|
In chloroform Ambient temperature; | 100% |
In toluene for 1h; Ambient temperature; | 100% |
In benzene for 4h; Reflux; Dean-Stark; | 100% |
Conditions | Yield |
---|---|
at 50℃; for 4h; | 100% |
With sodium sulfate In dichloromethane for 4h; Reflux; | 100% |
In methanol at 20℃; for 1h; | 98% |
Conditions | Yield |
---|---|
With pyridine; aluminum oxide at 92 - 94℃; for 0.0166667h; microwave irradiation; | 100% |
With triethylamine In dichloromethane at 0 - 20℃; for 16h; Inert atmosphere; | 100% |
With triethylamine In tetrahydrofuran at 0 - 20℃; for 2.5h; Inert atmosphere; Schlenk technique; Glovebox; | 99.5% |
Conditions | Yield |
---|---|
With triethylamine In dichloromethane | 100% |
In acetic acid for 0.0833333h; | 98% |
In hexane | 95% |
Conditions | Yield |
---|---|
With aluminum oxide for 5h; Milling; | 100% |
sodium hydrogen sulfate; silica gel at 58 - 60℃; for 0.0208333h; microwave irradiation; | 96% |
With aqueous extract of pericarp of Sapindus trifoliatus fruits at 20℃; for 0.333333h; | 93% |
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 20℃; for 2.5h; | 100% |
With pyridine Reflux; | 95% |
With pyridine at 20℃; Inert atmosphere; Reflux; | 91% |
Conditions | Yield |
---|---|
In toluene Heating; | 100% |
sodium hydrogen sulfate; silica gel at 56 - 58℃; for 0.0222222h; microwave irradiation; | 95% |
magnesium(II) perchlorate In 1,2-dichloro-ethane at 20℃; for 4h; | 94% |
Conditions | Yield |
---|---|
With iron(III) chloride hexahydrate In toluene for 6.5h; Solvent; Reagent/catalyst; Reflux; | 100% |
at 20 - 120℃; for 15h; | 99% |
at 120℃; for 15h; | 99% |
Conditions | Yield |
---|---|
With dmap; 2-chloro-1-(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,12,12,12-henicosafluorododecyl)pyridinium trifluoromethanesulfonate; triethylamine In N,N-dimethyl-formamide at 20℃; for 1h; | 100% |
With dmap; 2-chloro-1-(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,12,12,12-henicosafluorododecyl)pyridinium trifluoromethanesulfonate; triethylamine In N,N-dimethyl-formamide at 20℃; for 1h; | 100% |
With zinc(II) oxide for 2.33h; Reflux; chemoselective reaction; | 99% |
Conditions | Yield |
---|---|
In water at 20℃; for 24h; Michael condensation; | 100% |
With Nafion(R) SAC-13 In acetonitrile at 20℃; for 12h; | 98% |
With bis(trifluoromethanesulfonyl)amide In acetonitrile for 4h; Michael addition; | 98% |
Conditions | Yield |
---|---|
With potassium carbonate; sodium iodide In acetonitrile for 3h; Reflux; | 100% |
With potassium carbonate; sodium iodide In acetonitrile for 3h; Reflux; | 100% |
With triethylamine In ethanol for 4h; Heating; | 22% |
Conditions | Yield |
---|---|
With ammonium formate; palladium on activated charcoal In water; isopropyl alcohol at 20℃; for 0.5h; | 100% |
With 1.1 wt% Pd/NiO; hydrogen In ethanol at 25℃; under 760.051 Torr; for 10h; | 98% |
With sodium tetrahydroborate In tetrahydrofuran at 20℃; | 96% |
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