ProName:Benzene-1,3,5-tricarbaldehyde CasNo:3163-76-6 Molecular Formula:C9H6O3 Appearance:Powder Application:as ligands of porous materials DeliveryTime:2~3days PackAge:1gm, 2gm, 5gm, 10gm and customized pac... Port:S
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inquiryDayangchem'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
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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 manufacturin
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inquiry1.In No Less 10 years exporting experience. you 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 Specializ
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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
Hunan chemfish Pharmaceutical co.,Ltd.located in Lugu High-tech industral park ,Hunan province . with its own R&D center and more than 10000㎡manufacture plant . Chemfish owns 40 reactors from 1000L to 8000L. With complete auxiliary equipment as
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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
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
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inquiryWhy Choose Us: 1. Factory direct sales, so we can provide the competitive price and high quality product base on 8 years of production and R&D experience. 2. It is available in stock for quick shipment.Products could be packaged according to cu
We 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
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inquiry1,3,5-Benzenetricarboxaldehyde Basic information Product Name: 1,3,5-Benzenetricarboxaldehyde Synonyms: 1,3,5-Benzenetricarboxaldehyde;1,3,5-TRIFORMYLBENZENE;1,3,5-Benzenetricarbaldehyde;Benzene-1,3,5-tricarbaldehyde;triforMylbenzene;benzene-1,
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inquiryfactory?direct?saleAppearance:White Powder Storage:Store In Dry, Cool And Ventilated Place Package:25kg/drum, also according to the clients requirement Application:It is widely used as a thickener, emulsifier and stabilizer Transportation:By Sea Or B
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inquiryShandong Mopai Biotechnology 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 chemicals. W
Cas:3163-76-6
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inquiry1.Applied in food field.it can improve the immune system and prolong life. 2.Appliedin cosmetic field.it can improve the skin care. 3.Applied in pharmaceutical field.it can treat various dieases. 4.Our product quality assurance will make our customer
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inquiryHigh quality,stable supply chain.Appearance:white/off-white or light yellow Storage:Store in cool and dry place, keep away from strong light and heat. Package:aluminum bottle,glass bottle,PTFE bottle,cardboard drum Application:This product can be use
We are a Union of chemistry in China, consists of chemists,engineers, laboratories,factories in China. We organize surplus capacity of R&D and production as well as custom synthesis for chemical products and chemical business project. We are supp
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inquiry1, High quality with competitive price:2, Fast and safe delivery3.Excellent pre-sales and after-sales service4. Well-trained and professional technologist and sales with rich experience in the field for 5-10 yearsAppearance:see detailed specification
Stock products, own laboratory Package:Grams, Kilograms Application:For R&D Transportation:According to customer request Port:Shanghai
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inquiryLower price, sample is available,SDS test documents are available,large stock in warehouseAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:Fine chemical intermediates, used as the main raw material for the synthe
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inquiryR & D enterprises have their own stock in stock Package:1kg Application:pharmaceutical intermediates
Acmec is a leading manufacturer and supplier of biochemical reagents and life science products. We have over 40,000 items in stock (real-time inventory) and offer discounted prices to registered members of the online store ( www.acmec.com.cn ) Appea
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inquiryShanghai Finebiotech Co.,Ltd.was established in 2020, which providing professional chemical services. As a customer-oriented company, we have distinguished ourself from others in providing worldwide customers with cost-effective and efficient service
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 and international standards.2. Now we have established long-term stable re
1.Our services:A.Supply sampleB.The packing also can be according the customers` requirmentC.Any inquiries will be replied within 24 hoursD.we provide Commerical Invoice, Packing List, Bill of loading, COA , Health certificate and Origin certificate.
Cas:3163-76-6
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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? We can also provide MT1 peptide powder2.
Ansciep 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
Cas:3163-76-6
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inquiryWe are a trading company aiming at providing high-quality services to customers. Established for many years, with good reputation in the industry Storage:Sealed and preserved Application:Fine chemical intermediates, used as the main raw material for
We product this chemical more than 10 years . We are very experience to export it to many countries, Our superior & stable quality , competitive price gain warm reception from our customers. Application:Chemical intermediate
Conditions | Yield |
---|---|
With 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione In tert-butyl alcohol for 5h; Reflux; | 100% |
With pyridinium chlorochromate | 99% |
With Dess-Martin periodane In dichloromethane for 15h; | 98% |
triformylmethane
benzene-1,3,5-trialdehyde
Conditions | Yield |
---|---|
In water at 20℃; for 168h; | 96% |
Conditions | Yield |
---|---|
With 1,4-dichloro-1,4-diazoniabicyclo[2,2,2]octane bis-chloride; water at 40℃; for 0.333333h; pH=7; | 90% |
(i) (irradiation), Br2, (ii) aq. H2SO4; Multistep reaction; | |
Multi-step reaction with 4 steps 1: bromine / 160 °C / Irradiation.UV-Licht 2: tetrachloromethane; dibenzoyl peroxide; <α,α'>azoisobutyronitrile; N-bromo-succinimide 3: methanol / Behandeln der Reaktionsloesung mit warmer wss. Natriumperchlorat-Loesung 4: N,N-dimethyl-4-nitroso-aniline / Hydrolysieren des Reaktionsprodukts View Scheme | |
Multi-step reaction with 3 steps 1: bromine / 160 °C / Irradiation.UV-Licht 2: tetrachloromethane; dibenzoyl peroxide; <α,α'>azoisobutyronitrile; N-bromo-succinimide 3: hexamethylenetetramine View Scheme | |
Multi-step reaction with 2 steps 1: N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile) / tetrachloromethane / 15 h / 85 °C 2: sodium methylate; 2-nitropropane / methanol; ethyl acetate / 6 h / 30 °C View Scheme |
1,3,5-Tris(bromomethyl)benzene
benzene-1,3,5-trialdehyde
Conditions | Yield |
---|---|
Stage #1: 1,3,5-Tris(bromomethyl)benzene With 2-nitropropane; sodium methylate In methanol; ethyl acetate at 30℃; for 6h; Stage #2: With water In methanol; ethyl acetate | 80.8% |
With 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione In dimethyl sulfoxide at 20℃; | 57% |
With 2-nitropropane; sodium ethanolate In ethanol; dimethyl sulfoxide for 3h; Ambient temperature; | 52% |
Conditions | Yield |
---|---|
With sulfuric acid In water for 1h; | 80% |
With morpholine for 4h; Reflux; | 60% |
With sulfuric acid | |
(i) Mor, (ii) aq. HCl; Multistep reaction; |
(E)-3-(dimethylamino)acrolein
benzene-1,3,5-trialdehyde
Conditions | Yield |
---|---|
With acetic acid for 10h; Heating; | 60% |
1,3,5-benzene tris(carbonyl chloride)
A
Isophthalaldehyde
B
benzene-1,3,5-trialdehyde
Conditions | Yield |
---|---|
With hydrogen; thiourea; Pd-BaSO4 In xylene for 10h; Heating; | A 19% B 59% |
benzene-1,3,5-trialdehyde
Conditions | Yield |
---|---|
With sodium bis(2-methoxyethoxy)aluminium hydride In toluene at 0 - 20℃; for 6h; | 55% |
sorbic Acid
N,N-dimethyl-formamide
A
benzene-1,3,5-trialdehyde
B
2-chlorobenzene-1,3,5-tricarboxaldehyde
Conditions | Yield |
---|---|
With trichlorophosphate at 80 - 90℃; | A 37% B 5% |
3-penten-2-ol
N,N-dimethyl-formamide
A
Isophthalaldehyde
B
benzene-1,3,5-trialdehyde
Conditions | Yield |
---|---|
With trichlorophosphate for 6h; Heating; | A 26% B 6% |
With trichlorophosphate for 6h; Heating; other 3-buten-2-ols; | A 26% B 6% |
Conditions | Yield |
---|---|
With hydrogen; thiourea; Pd-BaSO4 In xylene for 10h; | 12% |
With lithium aluminium tetrahydride; tert-butyl alcohol In diethyl ether; diethylene glycol dimethyl ether | |
With lithium tri-t-butoxyaluminum hydride | |
Multi-step reaction with 2 steps 1: benzene; pyridine 2: LiAlH4 View Scheme |
1,3,5-tris(3,5-dimethylpyrazolyl-1-carbonyl)benzene
benzene-1,3,5-trialdehyde
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride |
benzene-1,3,5-trialdehyde
Conditions | Yield |
---|---|
With p-dimethylaminonitrosobenzene Hydrolysieren des Reaktionsprodukts; |
Conditions | Yield |
---|---|
With tetracarbonyl nickel |
3,3-diethoxypropanal
A
benzene-1,3,5-trialdehyde
B
(E)-3-[2-((Z)-2-Hydroxy-vinyl)-furan-3-yloxy]-propenal
E
(E)-3-[2-((Z)-2-{(E)-1-Hydroxy-3-[2-((Z)-2-hydroxy-vinyl)-furan-3-yloxy]-allyloxy}-vinyl)-furan-3-yloxy]-propenal
F
(E)-3-[2-((Z)-2-{(E)-1-Hydroxy-3-[2-((Z)-2-{(E)-1-hydroxy-3-[2-((Z)-2-hydroxy-vinyl)-furan-3-yloxy]-allyloxy}-vinyl)-furan-3-yloxy]-allyloxy}-vinyl)-furan-3-yloxy]-propenal
Conditions | Yield |
---|---|
In water for 240h; |
1,4-dihydrobenzoic acid
N,N-dimethyl-formamide
benzene-1,3,5-trialdehyde
Conditions | Yield |
---|---|
With trichlorophosphate 1.) room temp., 1 h; Yield given. Multistep reaction; |
cyclohexadieneacetyl chloride
N,N-dimethyl-formamide
benzene-1,3,5-trialdehyde
Conditions | Yield |
---|---|
With trichlorophosphate 1.) room temp., 1 h; Yield given. Multistep reaction; |
penta-1,3-diene
N,N-dimethyl-formamide
benzene-1,3,5-trialdehyde
Conditions | Yield |
---|---|
(i) PCl5, (ii) H2O; Multistep reaction; |
N,N-dimethyl-formamide
benzene-1,3,5-trialdehyde
Conditions | Yield |
---|---|
(i) chloromethylene-dimethyl-ammonium chloride, CHCl3, (ii) H2O; Multistep reaction; |
tetrahydrofuran
1,3,5-tris(3,5-dimethylpyrazolyl-1-carbonyl)benzene
benzene-1,3,5-trialdehyde
benzene-1,3,5-trialdehyde
Conditions | Yield |
---|---|
With Pd-BaSO4 Hydrogenation; |
benzene-1,3,5-tricarboxylic acid
A
Isophthalaldehyde
B
benzene-1,3,5-trialdehyde
Conditions | Yield |
---|---|
With hydrogen; 2,2-dimethylpropanoic anhydride; tetrakis(triphenylphosphine) palladium(0) In tetrahydrofuran at 80℃; under 22501.8 Torr; for 24h; | A 6 % Chromat. B 86 % Spectr. |
Conditions | Yield |
---|---|
In 1,4-dioxane; water at 70℃; for 3h; |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 79 percent / LiAlH4 2: 98 percent / Dess-Martin reagent / CH2Cl2 / 15 h View Scheme | |
Multi-step reaction with 2 steps 1: lithium aluminium tetrahydride / tetrahydrofuran / 14 h / 0 - 20 °C / Inert atmosphere 2: 2-iodoxybenzoic acid / tert-butyl alcohol / 2 h / 95 °C / Reflux; Inert atmosphere View Scheme | |
Multi-step reaction with 2 steps 1: lithium aluminium tetrahydride / tetrahydrofuran / 16 h / 0 - 70 °C / Inert atmosphere 2: 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione / acetonitrile / 1 h / 80 °C / Inert atmosphere View Scheme | |
Multi-step reaction with 2 steps 1: lithium aluminium tetrahydride / tetrahydrofuran / Reflux 2: pyridinium chlorochromate View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 90 percent / SOCl2, DMF / 2.5 h / Heating 2: 12 percent / H2, thiourea / Pd/BaSO4 / xylene / 10 h View Scheme | |
Multi-step reaction with 3 steps 1: SOCl2 2: benzene; pyridine 3: LiAlH4 View Scheme | |
Stage #1: benzene-1,3,5-tricarboxylic acid With sulfuric acid In methanol for 12h; Reflux; Stage #2: With lithium aluminium tetrahydride In tetrahydrofuran at 0℃; for 12h; Inert atmosphere; Stage #3: With pyridinium chlorochromate In diethyl ether; dichloromethane | |
Stage #1: benzene-1,3,5-tricarboxylic acid With sulfuric acid In methanol for 12h; Reflux; Stage #2: With lithium aluminium tetrahydride In tetrahydrofuran at 0℃; for 12h; Inert atmosphere; | |
Multi-step reaction with 3 steps 1.1: sulfuric acid / 24 h / Reflux 2.1: lithium aluminium tetrahydride / tetrahydrofuran / 0 °C / Inert atmosphere 2.2: 24 h / Reflux 3.1: pyridinium chlorochromate / dichloromethane / 6 h / 20 °C View Scheme |
3,5-bis(bromomethyl)toluene
benzene-1,3,5-trialdehyde
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: tetrachloromethane; dibenzoyl peroxide; <α,α'>azoisobutyronitrile; N-bromo-succinimide 2: methanol / Behandeln der Reaktionsloesung mit warmer wss. Natriumperchlorat-Loesung 3: N,N-dimethyl-4-nitroso-aniline / Hydrolysieren des Reaktionsprodukts View Scheme | |
Multi-step reaction with 2 steps 1: tetrachloromethane; dibenzoyl peroxide; <α,α'>azoisobutyronitrile; N-bromo-succinimide 2: hexamethylenetetramine View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: Br2 / Irradiation 2: H2SO4 View Scheme | |
Multi-step reaction with 2 steps 1: Br2 / 155 - 180 °C / Irradiation 2: (i) Mor, (ii) aq. HCl View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: lithium borohydride / tetrahydrofuran 2: pyridinium chlorochromate View Scheme |
benzene-1,3,5-trialdehyde
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: lithium aluminium tetrahydride / tetrahydrofuran / 0 °C / Inert atmosphere 1.2: 24 h / Reflux 2.1: pyridinium chlorochromate / dichloromethane / 6 h / 20 °C View Scheme |
Conditions | Yield |
---|---|
In dichloromethane at 20℃; for 12h; | 100% |
With trifluoroacetic acid In dichloromethane at 20℃; for 120h; | 83% |
With trifluoroacetic acid In dichloromethane at 20℃; | 83% |
With trifluoroacetic acid In dichloromethane at 20℃; | 83% |
In dichloromethane at 20℃; | 70% |
Conditions | Yield |
---|---|
In methanol; chloroform at 20℃; for 1h; Inert atmosphere; | 98% |
benzene-1,3,5-trialdehyde
malononitrile
1,3,5-tris(2',2'-ethenyldicarbonnitrile)benzene
Conditions | Yield |
---|---|
With 1,2,4,5-tetramethylbenzene; C193H176N12O6Zn2(4+) In chloroform-d1; [D3]acetonitrile at 20℃; for 48h; Reagent/catalyst; Knoevenagel Condensation; | 97% |
With piperidine In 1,2-dimethoxyethane at 20℃; for 0.5h; | 95% |
With piperidine In butan-1-ol at 50℃; for 8h; | 87% |
With boron trioxide In ethanol for 2h; Heating; | 15% |
Conditions | Yield |
---|---|
Stage #1: 3,6-dioxa-1,8-diaminooctane; benzene-1,3,5-trialdehyde In chloroform-d1 at 20℃; for 1h; Stage #2: C96H118N2O2(2+)*2F6P(1-) In chloroform-d1 at 20℃; for 2h; | 97% |
Conditions | Yield |
---|---|
In dichloromethane at 20℃; Cooling with ice; | 96% |
In ethyl acetate at 22℃; for 72.5h; | 74% |
In methanol Inert atmosphere; Cooling with ice; |
benzene-1,3,5-trialdehyde
3-amino-2,4,6-trinitrotoluene
Conditions | Yield |
---|---|
With piperidine In benzene for 16h; Knoevenagel Condensation; Dean-Stark; Reflux; | 96% |
Conditions | Yield |
---|---|
With trifluoroacetic acid In chloroform for 4h; Reflux; | 95% |
Conditions | Yield |
---|---|
In methanol at 20℃; for 49h; Solvent; | 95% |
Conditions | Yield |
---|---|
With trifluoroacetic acid In dichloromethane at 20℃; for 48h; | 94% |
Conditions | Yield |
---|---|
With acetic acid In acetonitrile at 20℃; for 168h; | 92% |
Conditions | Yield |
---|---|
With piperidine In benzene for 14h; Knoevenagel Condensation; Dean-Stark; Reflux; | 90.3% |
benzene-1,3,5-trialdehyde
1,2-Dihydro-N-phenylcyclohepta[b]pyrrol-2-one
Conditions | Yield |
---|---|
With trifluoroacetic acid In dichloromethane at 20℃; for 48h; | 90% |
benzene-1,3,5-trialdehyde
thiosemicarbazide
2,2′,2″-(benzene-1,3,5-triyltris(methanylylidene))tris(hydrazinecarbothioamide)
Conditions | Yield |
---|---|
With acetic acid In methanol for 4h; Reflux; | 90% |
Conditions | Yield |
---|---|
In methanol for 24h; Reflux; | 90% |
Conditions | Yield |
---|---|
With acetic acid In acetonitrile at 20℃; for 36h; Concentration; | 90% |
Conditions | Yield |
---|---|
With sodium ethanolate In ethanol for 3h; Knoevenagel Condensation; Reflux; | 90% |
(S,S)-N-methyl-1,2-diphenylethylenediamine
benzene-1,3,5-trialdehyde
C54H48N6
Conditions | Yield |
---|---|
Stage #1: (S,S)-N-methyl-1,2-diphenylethylenediamine; benzene-1,3,5-trialdehyde In dichloromethane at 20℃; for 3h; Inert atmosphere; Stage #2: With N-Bromosuccinimide In dichloromethane at 0 - 20℃; Inert atmosphere; | 88% |
benzene-1,3,5-trialdehyde
3,5-bis(trifluoromethyl)phenylacetonitrile
Conditions | Yield |
---|---|
With sodium ethanolate In ethanol for 3h; Knoevenagel Condensation; Reflux; | 88% |
Conditions | Yield |
---|---|
With triethylamine In methanol; dichloromethane at 20℃; for 240h; | 87% |
benzene-1,3,5-trialdehyde
2,2-Dimethyl-1,3-propanediol
5-(5,5-Dimethyl-[1,3]dioxan-2-yl)-benzene-1,3-dicarbaldehyde
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid | 86% |
Conditions | Yield |
---|---|
In dichloromethane at 20℃; for 120h; | 85% |
benzene-1,3,5-trialdehyde
N-benzylhydroxylamine hydrochloride
Conditions | Yield |
---|---|
With sodium hydrogencarbonate; sodium sulfate In tetrahydrofuran at 90℃; under 11251.1 Torr; for 6h; Microwave irradiation; | 85% |
Conditions | Yield |
---|---|
With trifluoroacetic acid In dichloromethane at 20℃; for 120h; | 83% |
benzene-1,3,5-trialdehyde
Conditions | Yield |
---|---|
With ammonium acetate; acetic acid at 140℃; for 15h; | 83% |
Conditions | Yield |
---|---|
With trifluoroacetic acid In chloroform for 4h; Reflux; | 82% |
benzene-1,3,5-trialdehyde
[(p-methylphenyl)sulfonylmethyl]isonitrile
C15H9N3O3
Conditions | Yield |
---|---|
With potassium carbonate In methanol at 70℃; van Leusen oxazole synthesis; | 81% |
Conditions | Yield |
---|---|
In dichloromethane at 20℃; for 96h; Cooling with ice; | 81% |
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