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inquiryItems Standard Result Appearance White powder Conforms Assay 98%-100% 99%
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inquiryHigh quality Tetrapropyl ammonium chloride CAS 5810-42-4 with attractive price Company profile Wuhan Fortuna Chemical Co.,Ltd established in 2006, is a big integrative chemical enterprise being engaged in Pharmaceutical & its intermediates,
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inquiryName: (5Z)-5-[(2-methoxynaphthalen-1-yl)methylidene]-1-phenyl-2-thioxodihydropyrimidine-4,6(1H,5H)-dione CAS:5810-42-4 MF: C22H16N2O3S Appearance:White Powder Storage:Store in cool and dry place, away from sun light. Package:25KG Application:Synthe
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inquiryOur company was built in 2009 with an ISO certificate.In the past 5 years, we have grown up as a famous fine chemicals supplier in China and we had established stable business relationships with Samsung,LG,Merck,Thermo Fisher Scientific and so on.O
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inquiryBest quality & Attractive price & Professional service; Trial & Pilot & Commercial Hisunny Chemical is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality intermediates, specia
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inquiryOur 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 present
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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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inquiryCompany Introduction 1. Established in 2005, with two independent business divisions: Fine chemicals division; Pharmaceutical division. 2. Main product: Optical brightener Textile auxiliary Dye stuff Pigments
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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
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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
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inquiryHunan 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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inquiryWe are leading fine chemicals supplier in China with ISO certificate, Our main business covers the fields below: 1.Noble Metal Catalysts (Pt.Pd...) 2.Organic Phosphine Ligands (Tert-butyl-phosphine.Cyclohexyl-phosphine...) 3.OLED
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inquiryProduct Name: Tetrapropyl ammonium chloride Synonyms: TETRAPROPYLAMMONIUMCHLORIDE,94%;Tetra-n-propylammoniumchloride,98%;1-PROPANAMINIUM,N,N,N-TRIPROPYL-,CHLORIDE;Tetra-n-propylammonium chloride, 99+%;Tetrapropylazanium chloride;Tetrapropylamin
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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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inquiryProduct name: Tetrapropyl Ammonium Chloride CAS No.:5810-42-4 Molecule Formula:C22H16N2O3S Molecule Weight:388.44 Purity: 99.0% Package: 25kg/drum Description:White crystals or powder Manufacture Standards:Enterprise Standard
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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
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inquirystock,low price,high quality,high purity,good sevice Appearance:5810-42-4 Storage:Preserve In Well-Closed, Light-Resistant and Tight Containers. Store In Cool & Dry Place Package:1g,5g,50g,100g,1kg...more Application:R&D Transportation:byland,by ai
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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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inquiryWuhu Nuovo Chemical Technology Co., Ltd. was established in August 2014, mainly engaged in the development, production and sales of ionic liquids, ribose, nucleosides, nucleotides and related chemicals; Products are mainly used in new energy, new ma
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inquiry3,5-bis(bis[(N'-tert-butylureayl)-N-ethyl]aminomethyl)-1H-pyraze
Tetrapropylammonium chloride
water
cobalt(II) chloride
Conditions | Yield |
---|---|
With KH In N,N-dimethyl acetamide byproducts: KCl; (Ar); a soln. of ligand treated with KH, CoCl2 added, stirred for 30 min, H2O added, stirred for 30 min, N(C3H7)4Cl added, stirred for 1 h; evapd. (vac., at room temp.), washed (Et2O), dried (vac.), dissolved in CH2Cl2, filtered, evapd. (vac.); elem. anal.; | 99% |
acetamide
3,5-bis(bis[(N'-isopropylureayl)-N-ethyl]aminomethyl)-1H-pyraze
Tetrapropylammonium chloride
cobalt(II) chloride
Conditions | Yield |
---|---|
With KH In N,N-dimethyl acetamide byproducts: KCl; (Ar); a soln. of C3H2N2(CH2N(C2H4NHC(O)NHCH(CH3)2)2)2 treated with KH, CoCl2 added, stirred, acetamide added, stirred, N(C3H7)4Cl added, stirred; evapd. (vac., at room temp.), washed (Et2O), dried (vac.), dissolved in CH2Cl2, filtered, evapd. (vac.); elem. anal.; | 99% |
acetamide
3,5-bis(bis[(N'-tert-butylureayl)-N-ethyl]aminomethyl)-1H-pyraze
Tetrapropylammonium chloride
cobalt(II) chloride
Conditions | Yield |
---|---|
With KH In N,N-dimethyl acetamide byproducts: KCl; (Ar); a soln. of C3H2N2(CH2N(C2H4NHC(O)NHC(CH3)3)2)2 treated with KH, CoCl2 added, stirred for 30 min, acetamide added, stirred for 30 min, N(C3H7)4Cl added, stirred for 1 h; evapd. (vac., at room temp.), washed (Et2O), dried (vac.), dissolved in CH2Cl2, filtered, evapd. (vac.); | 99% |
N,N-dimethyl acetamide
3,5-bis(bis[(N'-isopropylureayl)-N-ethyl]aminomethyl)-1H-pyraze
Tetrapropylammonium chloride
cobalt(II) acetate
Conditions | Yield |
---|---|
With KH In N,N-dimethyl acetamide byproducts: KCl, KCH3COO; (Ar); a soln. of C3H2N2(CH2N(C2H4NHC(O)NHC(CH3)3)2)2 treated with KH, Cosalt added, stirred, N(C3H7)4Cl added, stirred; evapd. (vac., at room temp.), washed (Et2O), dried (vac.), dissolved in CH2Cl2, filtered, evapd. (vac.); elem. anal.; | 99% |
N,N-dimethyl acetamide
3,5-bis(bis[(N'-tert-butylureayl)-N-ethyl]aminomethyl)-1H-pyraze
Tetrapropylammonium chloride
cobalt(II) acetate
Conditions | Yield |
---|---|
With KH In N,N-dimethyl acetamide byproducts: KCl, KCH3COO; (Ar); a soln. of C3H2N2(CH2N(C2H4NHC(O)NHC(CH3)3)2)2 treated with KH, Cosalt added, stirred for 30 min, N(C3H7)4Cl added, stirred for 1 h; evapd. (vac., at room temp.), washed (Et2O), dried (vac.), dissolved in CH2Cl2, filtered, evapd. (vac.); elem. anal.; | 99% |
dichloromethane
3-(bis[(N'-tert-butylureaylato)-N-ethyl]aminatomethyl)-5-tert-butyl-1H-pyrazole
Tetrapropylammonium chloride
water
cobalt(II) acetate
Conditions | Yield |
---|---|
With KH In N,N-dimethyl acetamide byproducts: KCl; (Ar); a soln. of ligand treated with KH, Co salt added, stirred, filtered, H2O added, stirred for 30 min, N(C3H7)4Cl added, stirred for 1 h; dissolved in CH2Cl2, filtered, evapd. (vac.), washed (Et2O/pentane), dried (vac.); elem. anal.; | 95% |
Tetrapropylammonium chloride
Conditions | Yield |
---|---|
Stage #1: 1,10-bis(phenyliodonium)-closo-decaborate With n-butyllithium In tetrahydrofuran; hexane at -10 - -5℃; for 1h; Inert atmosphere; Stage #2: Tetrapropylammonium chloride Inert atmosphere; | 95% |
dichloromethane
3,5-bis(bis[(N'-isopropylureayl)-N-ethyl]aminomethyl)-1H-pyraze
Tetrapropylammonium chloride
water
cobalt(II) chloride
Conditions | Yield |
---|---|
With KH In N,N-dimethyl acetamide byproducts: KCl; (Ar); a soln. of ligand treated with KH, CoCl2 added, stirred, H2O added, stirred, N(C3H7)4Cl added, stirred; evapd. (vac., at room temp.), washed (Et2O), dried (vac.), dissolved in CH2Cl2, filtered, evapd. (vac.); elem. anal.; | 94% |
Conditions | Yield |
---|---|
In water K3Co(CN)6 in H2O was added under stirring to soln. of ligand and Sn-complex in H2O, 15 min; filtered, washed with H2O, dried at room temp. for ca. 10 h; elem. anal.; | 90% |
Tetrapropylammonium chloride
Conditions | Yield |
---|---|
In water SnFe-complex was reacted with ligand in H2O, stirred for 12 h; filtered, washed with H2O, dried; elem. anal.; | 90% |
Tetrapropylammonium chloride
tetra(n-propyl)ammonium dicarbonyldichlororhodate(I)
Conditions | Yield |
---|---|
With CO; HCl In hydrogenchloride stirring Rh-complex (in concd. HCl) under CO for 2 d, addn. of Pr4NCl (in CH2Cl2), shaking; sepn. of org. layer, drying (MgSO4), crystn. on Et2O addn.; elem. anal.; | 90% |
Conditions | Yield |
---|---|
for 6h; Reflux; | 90% |
Tetrapropylammonium chloride
dihydrogen peroxide
ClH2O6W(1-)*C12H28N(1+)
Conditions | Yield |
---|---|
Stage #1: dihydrogen peroxide; ortho-tungstic acid In water at 31.84℃; for 0.5h; Stage #2: Tetrapropylammonium chloride With hydrogenchloride In water at -0.16℃; for 0.666667h; | 88% |
Tetrapropylammonium chloride
antimony(III) chloride
Conditions | Yield |
---|---|
In further solvent(s) solvent: 1.2-C2H4Cl2; dropwise addn. of SbCl3 soln. at room temp. with stirring; 1 h; filtration; crystn. from 1.2-C2H4Cl2 or EtOH; elem. anal.; | 85% |
Tetrapropylammonium chloride
Conditions | Yield |
---|---|
In acetonitrile at 20℃; for 1h; Inert atmosphere; Schlenk technique; Reflux; | 82% |
Conditions | Yield |
---|---|
In dichloromethane; water | 81% |
Tetrapropylammonium chloride
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide (N2); mixture in DMF is heated at 60°C for 18 h; filtration, addn. of ether to the filtrate, after 3 d solid is washed (acetonitrile, ether), recrystn. (hot acetonitrile), elem. anal.; | 80% |
Conditions | Yield |
---|---|
With methanol In methanol addn. of a soln. of ammonium salt in methanol to a soln. of W6Cl18 in methanol; sepn. of ppt.; | 80% |
Tetrapropylammonium chloride
Conditions | Yield |
---|---|
In acetonitrile (N2); mixture in acetonitrile is refluxed for 24 h; addn. of ether, solid is collected, recrystd. by ether diffusion into a soln. of DMF, after 5 d solid is collected, washed (ether), dried, elem. anal.; | 78% |
Tetrapropylammonium chloride
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide filtering, addn. of ether, elem. anal.; | 75% |
Tetrapropylammonium chloride
A
(CH3)3Sn(H2O)(1+)
Conditions | Yield |
---|---|
In water; acetonitrile (Me2Sn(CH2)3SnMe)1.5Co(CN)6 suspended in soln. of (n-Pr)4NCl in H2O (plus a few drops of MeCN; stirred for 24 h; filtered; washed (cold H2O); dried; elem. anal.; | A n/a B 75% |
phenyl trimethylsilyl selenide
Tetrapropylammonium chloride
cadmium(II) chloride
Conditions | Yield |
---|---|
In dichloromethane CdCl2, N(nPr)4Cl were dissolved in CH2Cl2, ligand was added, stirred overnight, Et2O was added; elem. anal.; | 70% |
Tetrapropylammonium chloride
zinc
[(C3H7)4N](1+)*[C6H5ZnCl2](1-)=[(C3H7)4N][C6H5ZnCl2]
Conditions | Yield |
---|---|
With C6H5Cl In acetonitrile; benzene Electrolysis; (N2); electrolysis of soln. of arylhalogenide and Pr4NBr in MeCN/benzene with Zn anode during 6 h; filtered soln. was pptd. by addn. of Et2O, ppt. washed with PE and dried; elem. anal.; | 69% |
Tetrapropylammonium chloride
Conditions | Yield |
---|---|
With H2O In N,N-dimethyl-formamide (N2); mixture in DMF containing water is heated at 60°C for 18 h; filtration, addn. of ether, obtained oil is washed (acetonitrile, ether), obtained powder is dissolved in DMF, ether is diffused for 7 d, crystals are washed (ether); | 66% |
Conditions | Yield |
---|---|
In acetonitrile reflux (1 h); filtration, concn. (in air, room temperature), dissolution (CH3CN), recrystn. (CH3CN/toluene), filtration, washing (MeOH and ether), drying; elem. anal.; | 66% |
Trifluoromethanesulfonyl fluoride
Tetrapropylammonium chloride
methylmagnesium chloride
tetrapropylammonium tris(trifluoromethanesulfonyl)methide
Conditions | Yield |
---|---|
Stage #1: Trifluoromethanesulfonyl fluoride; methylmagnesium chloride In tetrahydrofuran at 0 - 50℃; Inert atmosphere; Stage #2: Tetrapropylammonium chloride In tetrahydrofuran; water | 62% |
piperidine
Tetrapropylammonium chloride
piperidinium (2,7-dimethoxy-9H-fluoren-9-ylidine)methanedithioate
Conditions | Yield |
---|---|
In dichloromethane byproducts: colloidal Pt, piperidinium chloride; room temp.; to a suspn. of PtCl2 in CH2Cl2 were added piperidine and ammonium-compound, the soln. was filtered through Celite, dithioate was added, the mixt. was stirred for 1 h; partially evapd., the solid was filtered off, washed with CH2Cl2 and methanol, vac.-dried; elem. anal.; | 60% |
3,5-bis(bis[(N'-isopropylureayl)-N-ethyl]aminomethyl)-1H-pyraze
Tetrapropylammonium chloride
cobalt(II) chloride
Conditions | Yield |
---|---|
With potassium hydride In N,N-dimethyl acetamide byproducts: KCl; (under Ar); KH in N,N-dimethylacetamide added to ligand at room temp., CoCl2 added at room temp., (CH3CH2CH2)4NCl added; | 60% |
3,5-bis(bis[(N'-tert-butylureayl)-N-ethyl]aminomethyl)-1H-pyraze
Tetrapropylammonium chloride
cobalt(II) chloride
Conditions | Yield |
---|---|
With potassium hydride In N,N-dimethyl acetamide byproducts: KCl; (under Ar); KH in N,N-dimethylacetamide added to ligand at room temp., CoCl2 added at room temp., (CH3CH2CH2)4NCl added; | 60% |
lithium selenide
Tetrapropylammonium chloride
Conditions | Yield |
---|---|
In tetrahydrofuran (N2); mixture is stirred for 30 min; ppt. is collected, dissolved in DMF, slow diffusion of ether for 3 d, crystals are collected; | 57% |
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