Our Advantage Rich Experience Our products are sold all over Europe,North&South America, Sino-East, Asia and pacific area as well as Africa,we establish long term. Quality service Company cooperates with research institutes. We strictly con
Cas:10544-50-0
Min.Order:1 Kilogram
FOB Price: $1.0 / 10.0
Type:Trading Company
inquiryWITH US,YOUR MONEY IN SAFE,YOUR BUSINESS IN SAFE 1)Quick Response Within 12 hours; 2)Quality Guarantee: All products are strictly tested by our QC, confirmed by QA and approved by third party lab in China, USA, Canada, Germany, UK, Italy, France et
Cas:10544-50-0
Min.Order:1 Kilogram
FOB Price: $139.0 / 210.0
Type:Trading Company
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
Cas:10544-50-0
Min.Order:1 Kilogram
Negotiable
Type:Lab/Research institutions
inquiryCyclic octaatomic sulfur CAS:10544-50-0 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
Cas:10544-50-0
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
Cas:10544-50-0
Min.Order:1 Kilogram
Negotiable
Type:Lab/Research institutions
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
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:10544-50-0
Min.Order:10 Gram
FOB Price: $100.0
Type:Lab/Research institutions
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,
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
Cas:10544-50-0
Min.Order:0
Negotiable
Type:Trading Company
inquiryZhenyu biotech exported this product to many countries and regions at best price. if you are looking for the material's manufacturer or supplier in china, zhenyu biotech is your best choice. pls contact with us freely for getting detailed
Cas:10544-50-0
Min.Order:1 Kilogram
FOB Price: $2.0
Type:Lab/Research institutions
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:10544-50-0
Min.Order:1 Gram
Negotiable
Type:Lab/Research institutions
inquiryTriumph has the complete production of G- KG - MT service chain,we can make the new technology into productivity quickly in the research and development of new products. Main Business Custom Synthesis:
GOLDEN PHARMA CO.,LIMITED.is a professional pharmaceutical company,our team have more than 20years expereince in pharmaceutical production and sales. we are a professional technical enterprise specializing in the R & D, production,QA regulation
We produce carbomer by our own factory,carbomer 940 is our best seller.It is used for cosmetic and medical.And we also become agent for lubrizol.Our carbomer 940 get high viscosity and good transparency.The price will depond on the market,surely supp
Lower 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
Hangzhou Dingyan Chem is a leading manufacturer and supplier of chemicals in China.We develop,produce and distribute high quality pharmaceuticals, intermediates, special chemicals and other fine chemicals.Appearance:A white or almost white crystallin
Cas:10544-50-0
Min.Order:0
Negotiable
Type:Trading Company
inquiryJ&H CHEM is one of China's leading providers of integrated fine chemical services including offering, research and development, Custom manufacturing business, as well as other Value-added customer services, for diversified range products of chemicals
Cas:10544-50-0
Min.Order:0
Negotiable
Type:Lab/Research institutions
inquiryhigh purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:Foil bag; Drum; Plastic bottle Application:Pharma;Industry;Agricultural Transportation:by sea or air Port:Beijing or Guangzhou
Cas:10544-50-0
Min.Order:0
Negotiable
Type:Lab/Research institutions
inquiry1.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.
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 highly qualified in
Cas:10544-50-0
Min.Order:0
Negotiable
Type:Lab/Research institutions
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
Cyclic octaatomic sulfurAppearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:pharmaceutical intermediate Transportation:by air, by sea, by express
factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
Cas:10544-50-0
Min.Order:0
Negotiable
Type:Lab/Research institutions
inquiry1. Timely and efficient service to ensure communication with customers2. Produce products of different specifications and sizes according to your requirements.3. Quality procedures and standards recognized by SGS. Advanced plant equipment ensures sta
Cas:10544-50-0
Min.Order:0
Negotiable
Type:Lab/Research institutions
inquiryChangzhou Helios Biochemical Co., Ltd is a leading manufacturer and supplier for medical intermediates and pesticide intermediates . We specialize in custom synthesis of benzene ring, pyridine and pyrimidine derivatives to help customers to accelerat
Cas:10544-50-0
Min.Order:0
Negotiable
Type:Lab/Research institutions
inquiryThe factory supplies Application:manufacturing supplies
factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
Conditions | Yield |
---|---|
decompn. under argon at about 800 K; | A 100% B 100% C 100% |
A
sulfur
Conditions | Yield |
---|---|
In chlorobenzene at 132℃; for 1h; Solvent; Reagent/catalyst; Inert atmosphere; | A 100% B 96% |
hydrogen sulfide
oxygen
A
sulfur
B
Sulfate
C
sulfite(2-)
Conditions | Yield |
---|---|
With air; iron(III) chloride In water H2S and air were bubbled into soln. FeCl3 in N-methylpyrrolidinone-H2O (95:5) at room temp. for 300 h; | A 98.72% B 0.09% C 0.02% |
With air; Iron(III) nitrate nonahydrate In water H2S and air were bubbled into soln. Fe(NO3)3*9H2O in N-methylpyrrolidinone-H2O (95:5) at room temp. for 24 h; | A 63.03% B n/a C n/a |
With air; iron(III) chloride In further solvent(s) H2S and air were bubbled into soln. FeCl3 in N-methylpyrrolidinone at room temp. for 100-313 h; sulfur was filtered off; | |
With air; iron(III) chloride hexahydrate In water H2S and air were bubbled into soln. FeCl3*6H2O in N-methylpyrrolidinone-H2O (95:5) at room temp. for 198 h; | |
With air; iron(III) chloride In water H2S and air were bubbled into soln. FeCl3 in N-methylpyrrolidinone-H2O (95:5) at room temp. for 300 h; |
dibenzylamine
A
sulfur
Conditions | Yield |
---|---|
In dichloromethane for 7h; Reflux; | A 98% B 82% |
A
sulfur
Conditions | Yield |
---|---|
at 230℃; for 0.166667h; Reagent/catalyst; Solvent; Inert atmosphere; | A 97% B 65% |
A
sulfur
B
1,4-bis(trimethylsilyl)-2,3,6,7-tetrathiacyclooctane
D
ethenyltrimethylsilane
Conditions | Yield |
---|---|
In benzene byproducts: Cu2Cl2, CO; 80°C, 8 h; filtn., washing ppt. (hot benzene), chromy. of filtrate after removing solvent; | A 90% B 10% C n/a D 96% |
Conditions | Yield |
---|---|
With (NH4)2S(x) In tetrahydrofuran; methanol addn. of a soln. of (NH4)2S(x) in methanol to a soln. of (C5Me5)ReOCl2 in THF and stirring for 4 h; removal of the solvent and chromatography of the residue on silica gel, elution of S8 with toluene/hexane and elution of (C5Me5)ReS3S4 with CH2Cl2, recrystn. from CHCl3/hexane at -25°C; | A n/a B 95.8% |
pyrrolidine
A
sulfur
D
2-amino-6-ethoxy-4-phenylpyridine-3,5-dicarbonitrile
Conditions | Yield |
---|---|
In dichloromethane for 0.166667h; Solvent; Temperature; Time; Reflux; | A 95% B 78% C 14% D 6% |
piperidine
A
sulfur
D
2-amino-6-ethoxy-4-phenylpyridine-3,5-dicarbonitrile
Conditions | Yield |
---|---|
In dichloromethane for 3.5h; Time; Reflux; | A 94% B 74% C 11% D 10% |
N-butylamine
A
sulfur
Conditions | Yield |
---|---|
In dichloromethane for 4h; Reflux; | A 94% B 32% |
carbon disulfide
2-Aminophenyl disulfide
A
sulfur
B
2-Mercaptobenzothiazole
Conditions | Yield |
---|---|
With sodium hydrogensulfide In water at 80℃; for 10h; Catalytic behavior; Reagent/catalyst; Solvent; Temperature; Autoclave; Green chemistry; | A 73% B 94% |
Conditions | Yield |
---|---|
With SO2 In sulfur dioxide under inert atmosphere, SO2 condensed into the flask, allowed to stand overnight at 25°C; removal of SO2, extn. (CS2), filtered, removal of CS2, washed with CHCl3: S8, Mo-compd. isolated from the extn. residue; | A n/a B 92% |
Conditions | Yield |
---|---|
With NaF In acetonitrile byproducts: NaCl; exclusion of moisture; addn. of org.compd. suspn. of Mo-compd. and NaF in MeCN, refluxing (4 h); filtn., partial evapn., cooling (5°C), filtn., washing (MeCN), drying (N2 stream); elem. anal.; | A n/a B 90% C n/a |
carbon disulfide
bis(2-amino-5-methoxyphenyl)disulfide
A
sulfur
B
6-methoxy-1,3-benzothiazole-2-thiol
Conditions | Yield |
---|---|
With sodium hydrogensulfide In water at 80℃; for 4h; Inert atmosphere; Green chemistry; | A n/a B 90% |
morpholine
A
sulfur
D
2-amino-6-ethoxy-4-phenylpyridine-3,5-dicarbonitrile
Conditions | Yield |
---|---|
In dichloromethane for 13h; Time; Reflux; | A 89% B 77% C 2% D 12% |
carbon disulfide
2-[(2-amino-5-methylphenyl)dithio]-4-methylphenylamine
A
sulfur
B
2-mercapto-6-methylbenzothiazole
Conditions | Yield |
---|---|
With sodium hydrogensulfide In water at 80℃; for 10h; Inert atmosphere; Green chemistry; | A n/a B 89% |
Conditions | Yield |
---|---|
With air; iron(III) sulfate pentahydrate In water H2S and air were bubbled into soln. Fe2(SO4)3*5H2O in N-methylpyrrolidinone-H2O (95:5) at room temp. for 80.5 h; | A 88.5% B n/a |
A
sulfur
Conditions | Yield |
---|---|
With sodium hydride In tetrahydrofuran at 66℃; for 2h; Reagent/catalyst; Solvent; | A 88% B 88% |
diethylamine
A
sulfur
E
2-amino-6-ethoxy-4-phenylpyridine-3,5-dicarbonitrile
Conditions | Yield |
---|---|
In dichloromethane for 3.5h; Reflux; | A 86% B 84% C 5% D 2% E 6% |
carbon disulfide
6,6′-disulfanediylbis(2-methylaniline)
A
sulfur
B
2-Mercapto-4-methyl-benzothiazole
Conditions | Yield |
---|---|
With sodium hydrogensulfide In water at 80℃; for 10h; Inert atmosphere; Green chemistry; | A n/a B 86% |
A
sulfur
B
benzo[d]oxazole-2-carbonitrile
Conditions | Yield |
---|---|
at 200℃; for 0.0166667h; Reagent/catalyst; Solvent; Inert atmosphere; | A 60% B 85% |
A
sulfur
B
benzo[d]oxazole-2-carbonitrile
Conditions | Yield |
---|---|
With triethylamine In chlorobenzene at 132℃; for 24h; Solvent; Reagent/catalyst; | A 85% B 45% |
2,2′-disulfanediylbis(4-bromoaniline)
carbon disulfide
A
sulfur
B
6-bromo-2-mercaptobenzothiazole
Conditions | Yield |
---|---|
With sodium hydrogensulfide In water at 80℃; for 4h; Inert atmosphere; Green chemistry; | A n/a B 85% |
Conditions | Yield |
---|---|
With NaF In acetonitrile byproducts: NaCl; exclusion of moisture; addn. of NaF to suspn. of Mo-compd. in MeCN, addn. of org. compd. with stirring (room temp.), stirring (2 h); filtn., parial evapn., cooling (5°C), filtn., washing (MeCN), drying (vac.); elem. anal.; | A n/a B 78% C n/a |
carbon disulfide
2-[(2-amino-5-chlorophenyl)dithio]-4-chlorophenylamine
A
sulfur
B
6-chloro-2-mercaptobenzothiazole
Conditions | Yield |
---|---|
With sodium hydrogensulfide In water at 80℃; for 4h; Inert atmosphere; Green chemistry; | A n/a B 76% |
sulfuryl dichloride
bissulphane
sulfur dichloride
A
sulfur
Conditions | Yield |
---|---|
In carbon disulfide Ar; S-compds. soln. addn. dropwise to Se-compd. soln. at -78°C; elem. anal., (77)Se-NMR; | A n/a B 73% |
Conditions | Yield |
---|---|
With N,N-dimethyl-formamide In N,N-dimethyl-formamide; toluene dissolving in DMF/toluene mixt. 4:3 (shaking, 8 h); sepn. of S8 (filtration off), addn. of toluene and hexane to filtrate, washing (toluene), drying (vac., heating on water bath); elem. anal.; | A n/a B 72% |
carbon disulfide
2-[2-amino-5-(methylsulfonyl)phenyl]dithio-4-(methylsulfonyl)phenylamine
A
sulfur
Conditions | Yield |
---|---|
With sodium hydrogensulfide In water at 80℃; for 8h; Inert atmosphere; Green chemistry; | A n/a B 71% |
Conditions | Yield |
---|---|
In carbon disulfide Ar; S-compd. soln. addn. dropwise to Se-compd. soln. at -78°C, mixt. allowing to warm slowly to room temp. (stirring, 12 h); elem. anal., (77)Se-NMR; | A n/a B 70% |
carbon disulfide
6,6′-disulfanediylbis(2-fluoroaniline)
A
2-mercapto-4-fluorobenzothiazole
B
sulfur
Conditions | Yield |
---|---|
With sodium hydrogensulfide In water at 80℃; for 10h; Inert atmosphere; Green chemistry; | A 65% B n/a |
sulfur
sodium tetrahydroborate
ammonia
ammonia borane complex
Conditions | Yield |
---|---|
In ammonia to NaBH4 in a flask at -40°C NH3 is condensed, then slowly S8 isadded (5 h), to the mixt. (after 3 h) CH2Cl2 is added, then the mixt. is warmed to room temp.; residue is extd. with CH2Cl2, the soln. is evapd., elem. anal.; | 100% |
sulfur
Conditions | Yield |
---|---|
In chloroform complex was reacted with excess S8, CHCl3, 48 h, heating; | A 33% B 100% |
sulfur
Conditions | Yield |
---|---|
In chloroform complex was reacted with excess S8, CHCl3, 48 h, heating; | 100% |
In chloroform N2 bubbled through soln. of S in CHCl3 for several hours, Co-compd. added and mixt. boiled for 2d, alumina added and solvent removed; chromy. (alumina, hexane, hexane-ether); | 97% |
sulfur
Conditions | Yield |
---|---|
In chloroform complex was reacted with excess S8, CHCl3, 48 h, heating; | A 33% B 100% |
sulfur
A
(η-cyclopentadienyl)(1,2-diphenyl-1,2-ethylenedithiolato)cobalt(III)
Conditions | Yield |
---|---|
In chloroform complex was reacted with excess S8, CHCl3, 48 h, heating; | A 100% B 33% |
Conditions | Yield |
---|---|
In toluene inert atmosphere; molar ratio Cr:S=2:1, ambient temp.; | 100% |
In tetrahydrofuran inert atmosphere; molar ratio Cr:S=2:1, ambient temp.; | 100% |
In tetrahydrofuran Soln. of reagents (1 equiv of S) in THF was stirred at ambient temp. for 1 h (inert atm.); chromy. on silica column; eluent - benzene-ether; evapd., dissolved in hexane-ether, cooling overnight at -17°C; elem. anal.;; | 99% |
Conditions | Yield |
---|---|
With hydrogen fluoride at -83.37 - 20℃; for 72h; Schlenk technique; | 100% |
sulfur
bromine
arsenic pentafluoride
B
arsenic(III) fluoride
Conditions | Yield |
---|---|
In sulfur dioxide 1 d; slow removal of solvent, cooling to 0°C; | A 99.7% B n/a |
Conditions | Yield |
---|---|
In liquid sulphur dioxide byproducts: AsF3; 77 K, then room temp; 13 d;; elem. anal.;; | A 99.1% B n/a |
sulfur
caesium carbonate
Conditions | Yield |
---|---|
In ammonia NH3 (liquid); Ar-atmosphere; stoich. amts., sealed silica tube, 160°C, 4 d; solvent removal; elem. anal.; | 99% |
sulfur
Conditions | Yield |
---|---|
In chloroform N2 bubbled through soln. of S in CHCl3 for several hours, Co-compd. added and mixt. boiled for 2d, alumina added and solvent removed; chromy. (alumina, hexane, hexane-ether); | 99% |
Conditions | Yield |
---|---|
In chloroform N2 bubbled through soln. of S in CHCl3 for several hours, Co-compd. added and mixt. boiled for 2d, alumina added; chromy. (alumina, hexane, hexane-ether); | 99% |
sulfur
A
(η-cyclopentadienyl)(1,2-diphenyl-1,2-ethylenedithiolato)cobalt(III)
Conditions | Yield |
---|---|
In chloroform N2 bubbled through soln. of S in CHCl3 for several hours, Co-compd. added and mixt. boiled for 2d, alumina added and solvent removed; chromy. (alumina, hexane, hexane-ether), elem. anal.; | A 99% B 10% |
pyridine
sulfur
Conditions | Yield |
---|---|
In toluene N2-atmosphere; S8 (1/8 eqiuv.); stirring overnight; | 99% |
In toluene crystn. on pentane addn. and cooling (-40°C); | 76% |
In toluene inert atmosphere; stirring (-40°C, 40 h); solvent redn. (vac.), crystn. (pentane layering, -40°C); elem. anal.; | 76% |
sulfur
cis-sulfhydrylphenyl[bis(dicyclohexylphosphino)ethane]platinum(II)
Conditions | Yield |
---|---|
In benzene-d6 N2-atmosphere, NMR tube; stirring (room temp., 2 h); not isolated, detd. by NMR spectroscopy; | 99% |
sulfur
cis-sulfhydrylneopentenyl[bis(dicyclohexylphosphino)ethane]platinum(II)
Conditions | Yield |
---|---|
In tetrahydrofuran-d8 N2-atmosphere, NMR tube; stirring (room temp., 1 h); not isolated, detd. by NMR spectroscopy; | 99% |
sulfur
cis-methylhydrido{bis(dicyclohexylphosphino)ethane}platinum(II)
cis-sulfhydrylmethyl[bis(dicyclohexylphosphino)ethane]platinum(II)
Conditions | Yield |
---|---|
In tetrahydrofuran-d8 N2-atmosphere, NMR tube; stirring (room temp., 0.5 h); not isolated, detd. by NMR spectroscopy; | 99% |
Conditions | Yield |
---|---|
In tetrahydrofuran Sonication; sonication of a mixt. of iron complex with sulfur in THF for 30 minr 15 min; evapn.; elem. anal.; | 99% |
sulfur
n-butyllithium
N,N-dimethylferrocenesulfonamide
water
2,2''-bis(N,N-dimethylsulfanoylferrocenyl)-1,1''-disulfide
Conditions | Yield |
---|---|
With O2 In tetrahydrofuran; hexane (N2); addn. of BuLi in hexane to soln. of iron compd. with stirring at 0°C, stirring for 1 h, addn. of sulphur, stirring at room temp. for 2 h, stirring at room temp. under O2; pouring into cold aqueous HCl, extn. (CHCl3), drying under MgSO4, evapn., chromy. (silica gel, chloroform), elem. anal.; | 99% |
sulfur
bismuth
Conditions | Yield |
---|---|
In neat (no solvent) mixt. K2S, Bi, P, and S in sealed evacuated ampule was heated in furnaceto 600°C over 12 h, held there for 12 h, and cooled to room temp . for 6 h; | 99% |
Conditions | Yield |
---|---|
With sodium tetrahydroborate In ethanol treatment of (O(CC3H7)4C)W(CO)5 with sulfur in the presence of NaBH4 in EtOH; | 99% |
sulfur
(S)-(-)-2-di-ortho-tolyl-phosphino-1-dimethylaminoferrocene
(S)-(+)-2-di-ortho-tolyl-phosphinothioyl-1-dimethylaminoferrocene
Conditions | Yield |
---|---|
In toluene (Ar); Schlenk technique; mixt. of Fe complex and S8 in toluene was heated at 40°C for 2 h; cooled to room temp.; filtered; chromd. (silica gel, hexane/Et2O, 90/10); elem. anal.; | 99% |
Conditions | Yield |
---|---|
In sulfur dioxide stirring (room temp., overnight); slow removal of solvent over 4 h, filtration; | 98.5% |
Conditions | Yield |
---|---|
With methylamine In neat (no solvent) to NaBH4 in a flask at -10°C is condensed MeNH2, then is slowly added sulfur (2 h), the mixt. is stirred overnight and MeNH2 evapd., to the mixt. is added benzene and warmed to room temp.; residue is extd. with benzene, the soln. is evapd., elem. anal.; | 98% |
sulfur
bis(cyclopentadienyl)titanium dichloride
Conditions | Yield |
---|---|
With lithium triethylborohydride In tetrahydrofuran byproducts: LiCl; A soln. of S and LiEt3BH was treated dropwise with a THF soln. of complex, stirred at room temp. overnight (N2 atm.);; evapd., extd. with CH2Cl2, filtered, evapd., elem. anal.;; | 98% |
With hydrogen sulfide; ammonia In water S8 and concd. aq. NH3 placed in bottle, H2S bubbled with stirring for 1h, degassed for 10 min (vac.), H2O and CHCl3 added with stirring, complex added with stirring, reacted for 20 h; H2O added, extd. (CHCl3), extracts filtered, solvent removed (vac.), dried (vac. at 75°C); | 88% |
In dimethyl sulfoxide stirring (90°C, 20-30 min);; solvent removal (reduced pressure), extn. (CH2Cl2), filtration, chromy. (SiO2, CH2Cl2);; | 20% |
sulfur
GeN(C(CH3)3)Si(CH3)N(C(CH3)3)Si(NC(CH3)3)(CH3)N(C(CH3)3)
Conditions | Yield |
---|---|
In toluene soln. added S8; evapd.; | 98% |
sulfur
Conditions | Yield |
---|---|
In chloroform N2 bubbled through soln. of S in CHCl3 for several hours, Co-compd. added and mixt. boiled for 2d, alumina added and solvent removed; chromy. (alumina, hexane, hexane-ether), elem. anal.; | 98% |
About|Contact|Cas|Product Name|Molecular|Country|Encyclopedia
Message|New Cas|MSDS|Service|Advertisement|CAS DataBase|Article Data|Manufacturers | Chemical Catalog
©2008 LookChem.com,License: ICP
NO.:Zhejiang16009103
complaints:service@lookchem.com Desktop View