Product Detail Minimum Order Qty. 10 Gram
Cas:95-63-6
Min.Order:10 Gram
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Type:Trading Company
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
Cas:95-63-6
Min.Order:25 Kilogram
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Type:Lab/Research institutions
inquirybest service, quality anAppearance:Colorless transparent liquid Storage:Store in dry, dark and ventilated place. Package:according to the clients requirement Application:It is an important raw material and intermediate used in Organic Synthesis, Ph
Cas:95-63-6
Min.Order:1 Kilogram
FOB Price: $3.0
Type:Lab/Research institutions
inquiry1.Hefei TNJ Chemical Industry Co.Limited(ISO9001:2008),are strong in the field of Pharmaceuticals,food additives,plant extract and fine chemical for more than 10 years. 2.Full experience of large numbers container loading in main Chinese seap
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
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
Our 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
CHENGDU YANXI is a comprehensive manufacturer and an international distribution of products throughout the world. Specialized in Scrap metal, Chemical raw materials, Paper products and color industry. We aim to become leading position in global dis
Cas:95-63-6
Min.Order:1 Kilogram
FOB Price: $3.0
Type:Trading Company
inquiry1,2,4-Trimethylbenzene Basic information Product Name: 1,2,4-Trimethylbenzene Synonyms: 1,3,4-TRIMETHYLBENZENE;1,2,4-TRIMETHYLBENZENE;PSI-CUMENE;PSEUDOCUMENE;PSEUDOCUMOL;PSC;TRIMETHYLBEN
Cas:95-63-6
Min.Order:1 Kilogram
Negotiable
Type:Lab/Research institutions
inquiryPseudocumene (PSC) Chemical name: 1,2,4-Trimethylbenzene (TMB) Molecular formula: C9H12 Molecular weight: 546.78 Structural formula: UN No.: 3295 CAS NO.: 95-63-6 Appearance: Colorless Clear Liquid Storage:Store in cool and dry p
Cas:95-63-6
Min.Order:5 Metric Ton
FOB Price: $1.0 / 2.0
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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
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
Cas:95-63-6
Min.Order:0 Metric Ton
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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
Cas:95-63-6
Min.Order:4 Kilogram
Negotiable
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
Cas:95-63-6
Min.Order:10 Gram
FOB Price: $100.0
Type:Lab/Research institutions
inquiry1,2,4-Trimethyl Benzene from Wuxi TAA Chemical Industry Co.,Ltd. 1.A strong technical force and advanced processing equipments. The quality of the products has been strictly inspected and all kinds of index have reached or exceeded domestic an
Cas:95-63-6
Min.Order:1 Metric Ton
FOB Price: $1.0
Type:Other
inquiryProduct 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,
Cas:95-63-6
Min.Order:1 Metric Ton
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Type:Lab/Research institutions
inquiryLocated in Hangzhou National Hi-Tech Industrial Development Zone, zhongqichem is a technical company mainly focus on the Custom synthesis, manufacturing, sales of chemicals to various industries. Benefiting from the outstanding customer service an
Hebei Lead Bio-Chemicals Co., Ltd. established in 2006, devolved in resurching, manufacturing and supplying of pharmaceuticals,food ingredients, cosmetics,health care products, Chinese herb, plant extracts and some fine chemicals,is one of leading gr
Cas:95-63-6
Min.Order:0
Negotiable
Type:Manufacturers
inquirySuperior quality, moderate price & quick delivery. Appearance:colorless transparent liquid Storage:stored in a cool, dry and ventilated place to provent sun and rain Package:25kg/drum, or as per your request. Application:Used as Pharmaceuti
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
R & D enterprises have their own stock in stock Package:1kg Application:pharmaceutical intermediates
Best service,high quality and cheap price. Storage:Keep away from heat,sparks and flames. Package:25kg/50kg/200kg drum or Customer demand Application:Used as pharmaceutical intermediates Transportation:BY sea/air or by courier
Our clients, like BASF,CHEMO,Brenntag,ASR,Evonik,Merck and etc.Appearance:COA Storage:in stock Application:MSDS/TDS
Cangzhou Enke Pharma Tech Co.,ltd. is located in Cangzhou City, Hebei province ,where is a famous petroleum chemical industry city?in China. Enke Pharma a high-tech enterprise ,and we are dedicated to developing and manufacturing new api,?intermediat
Product Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard
Cas:95-63-6
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 1,2,4-Trimethylbenzene Application:sell high purity of 1,2,4-Trimethylbenzene
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
Cas:95-63-6
Min.Order:0
Negotiable
Type:Lab/Research institutions
inquiryConditions | Yield |
---|---|
With palladium/alumina; hydrogen In hexane at 325℃; Flow reactor; Green chemistry; | A 96.2% B 3.8% |
With hydrogen In hexane at 325℃; Flow reactor; Green chemistry; | A 15.9% B 84.2% |
Conditions | Yield |
---|---|
Stage #1: 2,3-dimethyl-buta-1,3-diene; crotonaldehyde at 150℃; for 3h; Diels-Alder Cycloaddition; Stage #2: With 5%-palladium/activated carbon In ethyl acetate at 260℃; | 95% |
2,3,5-Trimethyl-(4-methylphenylsulfonyloxy)benzene
1,2,4-Trimethylbenzene
Conditions | Yield |
---|---|
With sodium tetrahydroborate; bis(triphenylphosphine)nickel(II) chloride; tricyclohexylphosphine In tetrahydrofuran at 60℃; for 14h; | 93% |
Conditions | Yield |
---|---|
With (η4-1,5-hexadiene)(1,3-bis(2,6-diisopropylphenyl)-1,3-dihydro-2H-imidazol-2-ylidene)nickel In BENZENE-d6 at 20℃; | 91% |
Conditions | Yield |
---|---|
With palladium/alumina; hydrogen In hexane at 325℃; Flow reactor; Green chemistry; | A 84.8% B 6.5% |
With hydrogen In hexane at 325℃; Flow reactor; Green chemistry; | A 19.5% B 73.2% |
3,4-dimethylcyclohex-3-ene-1-carboxaldehyde
A
o-xylene
B
1,2,4-Trimethylbenzene
Conditions | Yield |
---|---|
With hydrogen In hexane at 325℃; Flow reactor; Green chemistry; | A 17.5% B 80.9% |
With palladium/alumina; hydrogen In hexane at 325℃; Flow reactor; Green chemistry; | A 73% B 27% |
Conditions | Yield |
---|---|
With sodium tetrahydroborate; (-) In ethanol at 20℃; for 2h; | 63% |
With phosphorus; hydrogen iodide | |
With diethyl ether; magnesium Zersetzen der Reaktionsprodukte mit Wasser; |
Conditions | Yield |
---|---|
In benzene-d6 1 turnover/day, catalytic react., 25°C; products detd. by NMR and GC; | A 45% B 55% |
o-xylene
A
2-Ethyltoluene
B
1,2,4-Trimethylbenzene
C
1,2,3-trimethylbenzene
D
2-methyl-benzyl alcohol
E
1,2-bis(2-methylphenyl)ethane
Conditions | Yield |
---|---|
With peracetic acid at 20 - 22℃; Product distribution; Irradiation; λ>2900 Angstroem; | A 9.3% B n/a C n/a D 36.9% E n/a |
para-xylene
A
4-Methylbenzyl alcohol
B
1,2,4-Trimethylbenzene
C
4-methylethylbenzene
D
1,2-di-p-tolylethane
Conditions | Yield |
---|---|
With peracetic acid at 20 - 22℃; Product distribution; Irradiation; λ>2900 Angstroem; | A 32.3% B 5.9% C 10.2% D n/a |
m-xylene
A
1-Methyl-3-ethylbenzene
B
1,2,4-Trimethylbenzene
C
1,2,3-trimethylbenzene
D
1,2-di-m-tolylethane
E
3-methylbenzyl alcohol
F
1,3,5-trimethyl-benzene
Conditions | Yield |
---|---|
With peracetic acid at 20 - 22℃; Product distribution; Irradiation; λ>2900 Angstroem; | A 7.4% B n/a C n/a D n/a E 30% F n/a |
o-xylene
A
3,4-Dimethylphenol
B
2-Ethyltoluene
C
1,2,4-Trimethylbenzene
D
2,3-Dimethylphenol
E
2-methyl-benzyl alcohol
F
1,2-bis(2-methylphenyl)ethane
Conditions | Yield |
---|---|
With peracetic acid at 20 - 22℃; Product distribution; Irradiation; λ=2537 Angstroem; | A n/a B 24.3% C n/a D n/a E 15.1% F n/a |
para-xylene
A
2,5-Dimethylphenol
B
4-Methylbenzyl alcohol
C
1,2,4-Trimethylbenzene
D
4-methylethylbenzene
E
1,2-di-p-tolylethane
Conditions | Yield |
---|---|
With peracetic acid at 20 - 22℃; Product distribution; Irradiation; λ=2537 Angstroem; | A 6.1% B 13.5% C 8.4% D 23.5% E n/a |
acetone
A
ethane
B
propane
C
o-xylene
D
1,2,4-Trimethylbenzene
E
toluene
F
benzene
Conditions | Yield |
---|---|
Zeolite HZSM-5(1) at 350℃; under 760 Torr; for 1h; Product distribution; Mechanism; 1)other times 2)other zeolites 3) impregnation of zeolites with basic oxides; | A 3.4% B 8.1% C 11% D 7.8% E 15.4% F 3.7% G n/a |
para-xylene
A
o-xylene
B
1,2,4-Trimethylbenzene
C
m-xylene
D
toluene
Conditions | Yield |
---|---|
Product distribution; Irradiation; other xylene, also with DCA; | A 0.4% B 13.2% C 1.2% D 5% |
Conditions | Yield |
---|---|
With hydrogenchloride at 50 - 60℃; Einleiten von HCl, Kochen des Reaktionsprodukts mit aethanol. NaOH und Hydrogenolyse des gebildeten Aethylaether-Gemisches an Kupferchromit bei 300grad unter Druck; |
Conditions | Yield |
---|---|
With aluminium trichloride at 95℃; |
Conditions | Yield |
---|---|
With aluminium trichloride at 130 - 140℃; |
Conditions | Yield |
---|---|
With hydrogenchloride Erwaermen der Reaktionsprodukte mit Zinkstaub und wss. NaOH auf 100grad; | |
With hydrogenchloride Erwaermen der Reaktionsprodukte mit Zinkstaub und wss. NaOH auf 100grad; |
Conditions | Yield |
---|---|
With hydrogenchloride Erwaermen der Reaktionsprodukte mit Zinkstaub und wss. NaOH auf 100grad; | |
With hydrogenchloride Erwaermen der Reaktionsprodukte mit Zinkstaub und wss. NaOH auf 100grad; |
Conditions | Yield |
---|---|
With phosphorus pentoxide |
Conditions | Yield |
---|---|
With aluminium trichloride at 80℃; |
Conditions | Yield |
---|---|
With phosphorus pentaoxide | |
With zinc(II) chloride | |
With phosphorus pentoxide |
Conditions | Yield |
---|---|
With phosphorus pentoxide | |
With zinc(II) chloride |
Conditions | Yield |
---|---|
unter geringem Ueberdruck; |
1,1,3-trimethylcyclohexane
1,2,4-Trimethylbenzene
Conditions | Yield |
---|---|
With Pt/Al2O3; hydrogen at 300℃; | |
With Pt/Al2O3; s-butyl chloride at 300℃; |
bis-(2,4-dimethyl-phenyl)methane
1,2,4-Trimethylbenzene
Conditions | Yield |
---|---|
With hydrogen; nickel; tungsten at 450℃; under 13974.6 Torr; | |
With molybdenum oxide-aluminium oxide; hydrogen at 300℃; |
Conditions | Yield |
---|---|
With tetrahydrofuran; lithium aluminium tetrahydride; lithium hydride | |
With diethyl ether; magnesium Zersetzen der Reaktionsprodukte mit Wasser; |
Conditions | Yield |
---|---|
Diazotization.Reduktion mit Zinn in alkal. Loesung; |
Conditions | Yield |
---|---|
With phosphorus pentoxide |
1,2,4-Trimethylbenzene
1,2,4-tribromo-3,5,6-trimethyl-benzene
Conditions | Yield |
---|---|
With benzyltrimethylazanium tribroman-2-uide; zinc(II) chloride In acetic acid at 70℃; for 24h; | 99% |
Conditions | Yield |
---|---|
With sulfuric acid; dihydrogen peroxide; iodine; iron(II) sulfate; sodium bromide In dichloromethane; water at 0℃; | 97.3% |
With hydrogenchloride; sodium hypochlorite; sodium bromide In water at 29.85℃; for 8h; Product distribution; Further Variations:; Temperatures; | 96.2% |
With bromine; iron; acetic acid |
Conditions | Yield |
---|---|
With N,N,N-trimethylbenzenemethanaminium dichloroiodate; zinc(II) chloride In acetic acid for 48h; Ambient temperature; | 97% |
With iodine; Selectfluor In acetonitrile at 55 - 65℃; for 1.5h; | 88% |
With aluminum oxide; iodine; copper dichloride at 60℃; for 3h; also other polymethylbenzenes; | 97 % Chromat. |
Conditions | Yield |
---|---|
With air; acetic acid; 1N,3N,5N-trihydroxy-1,3,5-triazin-2,4,6[1H,3H,5H]-trione; cobalt(II) acetate; zirconyl acetate at 150℃; under 15200 Torr; for 6h; | 97% |
With 7H2O*3H3N*3H(1+)*[FeMo6O18(OH)6](3-); sodium carbonate; acetic acid at 100℃; under 750.075 Torr; for 12h; Reagent/catalyst; Temperature; Inert atmosphere; | 97% |
With cobalt(II) acetate; manganese(II) acetate; acetic acid at 110 - 220℃; under 14251.4 - 16501.7 Torr; Pressure; Temperature; | 96.32% |
2-mesitylenesulphonyl chloride
1,2,4-Trimethylbenzene
1,3,5-trimethyl-2-(2,4,5-trimethyl-benzenesulfonyl)-benzene
Conditions | Yield |
---|---|
With aluminum (III) chloride In dichloromethane at 25℃; for 2h; Inert atmosphere; | 96% |
With aluminum (III) chloride In dichloromethane at 20℃; for 2h; | 96% |
1,2,4-Trimethylbenzene
ethyl-methyl-malonyl dichloride
2-ethyl-2,4,5,7-tetramethylindan-1,3-dione
Conditions | Yield |
---|---|
AlCl3 In dichloromethane | 93% |
Conditions | Yield |
---|---|
With phthalic anhydride; dihydrogen peroxide In neat (no solvent) at 118 - 120℃; for 2.5h; Reagent/catalyst; Temperature; Time; Solvent; | 92% |
With dihydrogen peroxide; acetic anhydride; methyltrioxorhenium(VII) In water at 60℃; | 37% |
With 3-chloro-benzenecarboperoxoic acid In chloroform at 60 - 70℃; for 0.5h; | 16.5% |
[(η6-benzene)IrH2(P(iPr)3)]BF4
1,2,4-Trimethylbenzene
[(η6-1,2,4-trimethylbenzene)IrH2(P(iPr)3)]BF4
Conditions | Yield |
---|---|
In acetone under Ar; a soln. of Ir complex in acetone was treated with a 10-fold excess of the arene and stirred for 1 h; the soln. was concd., treated with a mixt. of (C2H5)2O/THF, the ppt. wasfiltered, washed with (C2H5)2O, dried in vac.; elem. anal.; | 92% |
1,2,4-Trimethylbenzene
5-chloro-1,2,4-trimethylbenzene
Conditions | Yield |
---|---|
With hydrogenchloride; sodium chloride; sodium hydroxide In water; acetonitrile Solvent; Reagent/catalyst; | 91.2% |
With benzyltrimethylazanium tetrachloro-λ3-iodanuide In acetic acid for 20h; Ambient temperature; | 52% |
With chlorine im Dunkeln; | |
With aluminium trichloride; sulfuryl dichloride |
Conditions | Yield |
---|---|
With antimony pentafluoride; fluorosulphonic acid at 0℃; for 1h; | A 90% B 1% |
With antimony pentafluoride; fluorosulphonic acid at 0℃; for 1h; Yields of byproduct given. Title compound not separated from byproducts; | A 90 % Chromat. B n/a |
3,3-Dimethylacryloyl chloride
1,2,4-Trimethylbenzene
2',3,4',5'-tetramethylcrotonophenone
Conditions | Yield |
---|---|
With aluminium trichloride | 89% |
With aluminium trichloride In nitromethane |
Conditions | Yield |
---|---|
With In(OSO2CF3)3 for 0.133333h; Friedel-Crafts acylation reaction; microwave irradiation; | 89% |
1,2,4-Trimethylbenzene
A
isophthalic acid
B
terephthalic acid
C
1,2,4-benzene tricarboxylic acid
Conditions | Yield |
---|---|
With oxygen; titanium(IV) isopropylate; tetrabutoxytitanium; manganese(II) acetate; cobalt(II) acetate; ammonium bromide; cerous nitrate In water; acetic acid at 150 - 225℃; under 5250.53 - 18751.9 Torr; for 1.2 - 1.25h; Product distribution / selectivity; | A n/a B n/a C 88.3% |
Conditions | Yield |
---|---|
In further solvent(s) N2-atmosphere; equimolar amts. of TlCl and AlCl3, stirring in 1,2,4-trimethylbenzene at room temp.; filtration, slow cooling to 0°C (crystn.); elem. anal.; | 86% |
1,2,4-Trimethylbenzene
Conditions | Yield |
---|---|
With trifluorormethanesulfonic acid In dichloromethane at -40℃; for 0.0166667h; | 86% |
Conditions | Yield |
---|---|
Stage #1: 1,2,4-Trimethylbenzene With formic acid; dihydrogen peroxide; calcium chloride at 50 - 90℃; for 5h; Stage #2: With sodium dithionite In water at 45℃; for 2h; Temperature; Reagent/catalyst; | 85.6% |
With peracetic acid; sodium disulfite 1) acetic acid, 70 deg C, 1 h; 2) water, 20 deg C, 0.5 h.; Yield given. Multistep reaction; | |
Multi-step reaction with 3 steps 1: sodium bromide; sulfuric acid; iron(II) sulfate; iodine; dihydrogen peroxide / dichloromethane; water / 0 °C 2: potassium dichromate; sulfuric acid; copper(II) sulfate / water; acetonitrile / 45 °C 3: sodium carbonate; hydrogen / 80 °C View Scheme |
4,4,5,5-pentamethyl-2-(1'-n-butyl-pyrazole-4'-yl)-4,5-dihydro-1H-imidazolyl-3-oxide-1-oxyl
1,2,4-Trimethylbenzene
Conditions | Yield |
---|---|
In further solvent(s) dissolving mixt. of copper compd. and nitronyl nitroxide deriv. in 1,2,4-trimethylbenzene with heating to 70°C for 2-3 min; cooling to room temp., keeping with slow evapn. at 5°C for 1-2 d,filtration, washing with cold heptane, air drying, elem. anal.; | 85% |
1,2,4-Trimethylbenzene
Conditions | Yield |
---|---|
Stage #1: 1,2,4-Trimethylbenzene; (E)-5-(4-chlorophenyl)-1-phenylpent-4-en-2-yn-1-one With trifluorormethanesulfonic acid In dichloromethane at 20℃; Stage #2: With water In dichloromethane | 85% |
1,2,4-Trimethylbenzene
acetic acid
A
2,3,5-Trimethyl-1,4-benzoquinone
B
Duroquinone
C
2,3,5-trimethylanisole
D
2,3,6-trimethylphenyl acetate
E
1-methoxy-2,4,5-trimethylbenzene
F
3-acetoxy-2,5-dihydroxy-5-carboxy-2,3,5-trimethylpentan-4-olide
Conditions | Yield |
---|---|
With peracetic acid at 70℃; for 0.5h; Product distribution; Kinetics; Thermodynamic data; other reaction time: 4 h.; | A 16% B 0.03% C 0.02% D 0.03% E 0.04% F 82.6% |
Conditions | Yield |
---|---|
With water at 100℃; for 10h; Sealed tube; Green chemistry; regioselective reaction; | 82% |
Conditions | Yield |
---|---|
at 160℃; for 72h; complexation; | 81% |
[IrCl(C8H3(CH3)3C4F4)]2
1,2,4-Trimethylbenzene
[Ir(C8H3(CH3)3C4F4)(C6H3(CH3)3)](1+)*ClO4(1-)=[Ir(C8H3(CH3)3C4F4)(C6H3(CH3)3)]ClO4
Conditions | Yield |
---|---|
In dichloromethane byproducts: AgCl; stirring, 1h; filtering off pptd. AgCl (kieselgur); concentrating; addn. of ether; pptn.; recrystn. (dichloromethane/ether); elem. anal.; | 81% |
1,2,4-Trimethylbenzene
4-chlorobenzoyl chloride
4'-bromo-2,4,5-trimethylbenzophenone
Conditions | Yield |
---|---|
Stage #1: 4-chlorobenzoyl chloride With aluminum (III) chloride In dichloromethane at -20℃; Friedel Crafts acylation; Inert atmosphere; Stage #2: 1,2,4-Trimethylbenzene In dichloromethane Friedel Crafts acylation; Stage #3: With hydrogenchloride; water In dichloromethane | 81% |
1,2,4-Trimethylbenzene
(E)-5-phenyl-1-(4-methylphenyl)pent-4-en-2-yn-1-one
Conditions | Yield |
---|---|
Stage #1: 1,2,4-Trimethylbenzene; (E)-5-phenyl-1-(4-methylphenyl)pent-4-en-2-yn-1-one With trifluorormethanesulfonic acid In dichloromethane at 20℃; Stage #2: With water In dichloromethane | 80% |
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