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inquiryItems Standard Result Appearance White crystalline powder Complies Assay 98.0%min
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inquiryHebei 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
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inquiryHigh purity CAS 557-34-6 Zinc acetate in stock Our main business covers the fields below: 1.Noble Metal Catalysts (Pt.Pd...) 2.Organic Phosphine Ligands (Tert-butyl-phosphine.Cyclohexyl-phosphine...) 3.OLED intermediates (Fluorene,Carba
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inquiryProduct name Zinc acetate Synonyms Acetic acid, zinc(II) salt;aceticacid,zinc(ii)salt;ai3-04465;Dicarbomethoxyzinc;Zinc acetate, pure, 99%;zinc acetate solution;Zinkdi(acetat);zinc(+2) cation diaceta
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inquiryZinc acetate CAS: 557-34-6 Specification Items Specification Result Assay 99%-102% Conforms
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inquiryPRODUCT DETAILS
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inquiryZinc acetate,anhydrous Grade U.S.P Technical pure Assay% 99.0-101.0 99.0-102.0 pH of a 5% solution at 25℃ 6.0-7.0 6.0-7.0
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Zinc acetate CAS 557-34-6 Description Purity: 99% Min Application: Intermediates Appearance: Powder Package: Bag Delivery: 3-5days Our Advantage & Service 1.Top quality: Using high quality material and establishing a strict quality
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inquiryAllyl acetate
phenylzinc chloride
A
allylbenzene
B
biphenyl
C
zinc diacetate
Conditions | Yield |
---|---|
tetrakis(triphenylphosphine) palladium(0) In tetrahydrofuran Ar atmosphere; stirring (20°C, 5 mole-% catalyst, 5 h); | A 100% B 0% C n/a |
Conditions | Yield |
---|---|
With acetic acid In diethyl ether N2 atmosphere; dropwise addn. of CH3COOH in Et2O to soln. of ZnEt2 (molar ratio Zn/acid 1:2), pptn.; filtration off, washing (Et2O), drying (vac.); | 99% |
Conditions | Yield |
---|---|
at 20℃; for 0.166667h; Inert atmosphere; | A 95% B 82 mg |
Conditions | Yield |
---|---|
In acetic acid Electrolysis; on electrolysis of Na acetate in acetic acid at 280V, 7mA/cmxcm, formation of acetate at Zn anode;; | 85% |
In acetic acid Electrolysis; on electrolysis of Na acetate in acetic acid at 280V, 7mA/cmxcm, formation of acetate at Zn anode;; | 85% |
poly(methacrylic acid)
acetic acid
zinc(II) carbonate
A
zinc diacetate
B
zinc methacryliate acetate
Conditions | Yield |
---|---|
In water at 20℃; for 2h; | A n/a B 43% |
Conditions | Yield |
---|---|
With zinc hydroxide | |
With zinc(II) nitrate |
Conditions | Yield |
---|---|
at 250 - 280℃; Ueberleiten ueber Zinkstaub; |
Conditions | Yield |
---|---|
at 150℃; |
zinc diacetate
Conditions | Yield |
---|---|
With acetic acid In water |
Conditions | Yield |
---|---|
In not given prepn. from ZnCO3 and carboxylic acid in molar ratio 1:2; | |
In not given neutralizing acetic acid with the carbonate; slow evapn.; | |
In water at 100℃; for 3h; |
Conditions | Yield |
---|---|
With chloroform byproducts: H2O; on dehydration of dihydrate with chloroform;; | |
In neat (no solvent) byproducts: H2O; loss of 2 mole H2O at 100 °C;; | |
In neat (no solvent) byproducts: H2O; vac. dehydration at 363 K, according to: G. Maslowska, A. Baranowska, Prod. Eighth Conf. Coord. Chem., Smolenice, Bratislava, 1980, pp. 269-273; |
Conditions | Yield |
---|---|
In neat (no solvent) on react. of acetic anhydride with Zn acetate dihydrate at 10°C for a period of 27 hours;; | |
In neat (no solvent) on react. of acetic anhydride with Zn acetate dihydrate at 10°C for a period of 27 hours;; |
Conditions | Yield |
---|---|
In carbon disulfide byproducts: N2; decompn. of nitrosoacetanilide with Zn dust and forming of Zn acetate and N2;; |
zinc diacetate
Conditions | Yield |
---|---|
With acetic acid In hydrogenchloride; water; acetic acid ZnO dissoln. in solvents mixt.; evapn. to dryness (hot plate, 90°C), further drying (vac. desiccator, 4 h); X-ray diffraction; | |
With acetic acid In water; acetic acid ZnO dissoln. in solvents mixt.; concn. (hot plate, 90°C), air-cooling to room temp. (28+/-2°C), crystn. for 24 h, filtn., washing (ethyl alcohol), drying (vac. desiccator, 2 h); X-ray diffraction; |
Conditions | Yield |
---|---|
In water shaken for 24 h at 25.0°C; evapn. of filtrate to dryness; |
Conditions | Yield |
---|---|
In acetic acid on slow heating of Zn with glacial acetic acid;; |
Conditions | Yield |
---|---|
In acetic acid byproducts: C6H5CH2OCOCH3; addn. of mixt. of benzaldehyde and excess acetic acid to zinc dust, stirring ( room temp., 12 h); filtration; |
zinc diacetate
Conditions | Yield |
---|---|
With H2O In neat (no solvent, solid phase) byproducts: Zn(OH)2; decompn. in solid state (moisture); IR-spectroscopy; |
zinc diacetate
Conditions | Yield |
---|---|
With acetic acid on treating with acetic acid;; | |
With acetic acid | |
With acetic acid | |
With acetic acid on treating with acetic acid;; |
Conditions | Yield |
---|---|
In neat (no solvent) on react. of acetic anhydride with Zn(OH)2 at 138°C for a period of 4 hours;; | |
at 138°C, some acetate is formed;; | |
at 138°C, some acetate is formed;; | |
In neat (no solvent) on react. of acetic anhydride with Zn(OH)2 at 138°C for a period of 4 hours;; |
Conditions | Yield |
---|---|
In water in 0.1n soln.;; | A n/a B >99 |
Conditions | Yield |
---|---|
In water Kinetics; dissolving both components in distilled water; stoichiometric concentrations: Zn 0.1 - 0.8 M, acetate 0.1 - 0.4 M; pH of solution from 4 to 6;; ultrasonic absorptions spectra;; |
Conditions | Yield |
---|---|
2,6-bis[(di-t-butylphosphino)methyl]phenyl palladium trifluoroacetate In benzene CO2 was reacted with ZnMe2 in C6H6 in presence of Pd catalyst at room temp.; | |
Pd(methyl)((1,3-bis[(di-tert-butylphosphino)methyl]benzene)(-1H)) In benzene CO2 was reacted with ZnMe2 in C6H6 in presence of Pd catalyst at 100°C; | |
Pd(acetyl)((1,3-bis[(di-tert-butylphosphino)methyl]benzene)(-1H)) In benzene CO2 was reacted with ZnMe2 in C6H6 in presence of Pd catalyst at 100°C; |
zinc diacetate
(22S)-22-Hydroxy-6β-methoxy-3α,5α-cyclocholest-24-ene
A
(22S)-3β-Acetoxy-22-hydroxycholesta-5,24-diene
B
Acetic acid (S)-1-[(S)-1-((3S,10R,13S)-3-acetoxy-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)-ethyl]-4-methyl-pent-3-enyl ester
Conditions | Yield |
---|---|
In acetic acid for 1h; Heating; | A 100% B n/a |
zinc diacetate
Conditions | Yield |
---|---|
In methanol; chloroform at 20℃; for 0.333333h; | 100% |
zinc diacetate
Conditions | Yield |
---|---|
In methanol; chloroform for 0.25h; Heating; | 100% |
Conditions | Yield |
---|---|
In methanol; chloroform for 1h; Heating; | 100% |
zinc diacetate
Conditions | Yield |
---|---|
In methanol; chloroform; water at 20℃; for 0.5h; | 100% |
zinc diacetate
Conditions | Yield |
---|---|
In methanol; chloroform at 20℃; for 0.166667h; | 100% |
Conditions | Yield |
---|---|
In ethanol at 20℃; for 0.166667h; Product distribution / selectivity; | 100% |
Conditions | Yield |
---|---|
100% |
C20H6N4(CH3)4(C2H5)2(C2H4COOC3H6C6H4N(CH3)2)(C2H4COOC2H4SC10H4O2(CH3))
zinc diacetate
Zn(C20H4N4(CH3)4(C2H5)2(C2H4COOC3H6C6H4N(CH3)2)(C2H4COOC2H4SC10H4O2(CH3)))
Conditions | Yield |
---|---|
In methanol treatment of the ligand with a methanol soln. of zinc acetate; | 100% |
zinc diacetate
Conditions | Yield |
---|---|
In methanol; dichloromethane refluxing of porphyrine with Zn(OAc)2 in CH2Cl2-MeOH for 1.5 h under argon; column chromy. (alumina); | 100% |
phosphoric acid
zinc diacetate
water
1,2-diaminocyclohexane
Conditions | Yield |
---|---|
In water hydrothermal conditions, 180°C; | 100% |
Conditions | Yield |
---|---|
In water hydrothermal conditions, molar ratio BPO4:Zn(OAc)2:diaminocyclohexane:water 2:1:2.5:117, , pH=8, 210°C; elem. anal.; | 100% |
Conditions | Yield |
---|---|
In methanol; chloroform dry N2-atmosphere; stirring, refluxing (10 h, dark); evapn. (vac.), washing (MeOH), drying; | 100% |
Conditions | Yield |
---|---|
In methanol | 100% |
sarcosine
zinc diacetate
fullerene-C60
[Zn(C20H8N4((C4H9)2C6H3)3(C6H4)(C10H2N2O4)(C6H4)(CH3NC2H3)C60)]
Conditions | Yield |
---|---|
In toluene C60, C20H10N4((C4H9)2C6H3)3(C6H4)2(C10H2N2O4)(CHO), N-methylglycine (toluene) heated under N2 in dark for 6 h; cooled to 25°C, evapd. to dryness (reduced pressure); chromy. sepd., dissolved (CH3Cl), added Zn(OAc)2 in CH3OH, heated for 30 min; washed twice (H2O), dried (anhydrous Na2SO4), solvent evapd., chromy., reprecipitated from benzene-methanol; | 100% |
Pyromellitic dianhydride
4-hexadecylaniline
zinc diacetate
[Zn(C20H8N4((C4H9)2C6H3)3(C6H4)(C10H2N2O4)(C6H4)(C16H33))]
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide (C20H10N4((C4H9)2C6H3)3(C6H4))NH2, C10H2O6, (C16H33)NH(C6H5) (dry DMF) heated under N2 in dark for 22 h, cooled to 25°C, evapd. to dryness (reduced pressure); chromy., dissolved (CHCl3), added Zn(OAc)2 in CH3OH, heated for 30 min; washed twice (H2O), dried (anhydrous Na2SO4), solvent evapd., chromy., reprecipitated from chloroform-methanol; | 100% |
zinc diacetate
zinc(II) 5-[1'-(hexylaminomethyl)ferrocenyl]-10,15,20-tri(p-tolyl)porphyrin
Conditions | Yield |
---|---|
In methanol; dichloromethane; water Fe(C5H4CH2NH(CH2)5CH3)(C5H4)-substituted porphyrin reacted with ZnOAc2 in CH2Cl2/MeOH/H2O for 10 h; chromy. (SiO2, CH2Cl2/MeOH); elem. anal.; | 100% |
zinc diacetate
zinc(II) 5,10,15-triphenyl-20-(2,6-dimethyl-4-[2-(trimethylsilyl)ethynyl]phenyl)porphyrin
Conditions | Yield |
---|---|
In chloroform reaction for 2.5 h; | 100% |
zinc diacetate
Conditions | Yield |
---|---|
In chloroform reaction for 1 h; | 100% |
zinc diacetate
ZnC20H8N4(C6H5)3C6H2(CH3)2CCC6H4ZnC20H8N4(C6H2(CH3)3)3
Conditions | Yield |
---|---|
In chloroform stirring (room temp., 1 h); filtration, concn.; | 100% |
zinc diacetate
[2-hydroxy-5,10,15,20-tetrakis(3',5'-di-tert-butylphenyl)porphinato]zinc(II)
Conditions | Yield |
---|---|
With sodium hydride; Benzaldoxime In methanol; dichloromethane; mineral oil mixt. refluxing in dark for 45 min, solvent complete removal; residue chromy. (silica, DCM), recrystn. (DCM/MeOH); | 100% |
zinc diacetate
Conditions | Yield |
---|---|
In methanol; dichloromethane reaction of zinc compd. with porphyrin deriv. in MeOH/CH2Cl2 at room temp. for 12 h; | 100% |
zinc diacetate
diphenyl[10,20-diphenylporphyrinatozinc(II)-5-yl]phosphine oxide
Conditions | Yield |
---|---|
In methanol; dichloromethane a soln. of zinc acetate in methanol was added to a soln. of porphyrin inCH2Cl2, the mixt. was refluxed for 2 h; ppt. was filtered, washed three times with methanol; | 100% |
zinc diacetate
Zn(C20H8N4(C6H4CH3)3)C6H4CH2NC6H4C(CH3)2COC6H3NO2CHCH
Conditions | Yield |
---|---|
In chloroform (Ar); stirring a soln. of ligand with excess of zinc salt in CHCl3 overnight; column chromy (SiO2); | 100% |
zinc diacetate
meso-pentyldipyrromethane
5-formyl-1,1,3,3-tetramethylisoindolin-2-yloxyl
5,10,15-tri-n-pentyl-20-(1',1',3',3'-tetramethylisoindolin-2'-yloxyl-5'-yl)porphyrinato zinc(II)
Conditions | Yield |
---|---|
With trifluoroacetic acid; 2,3-dicyano-5,6-dichloro-p-benzoquinone In methanol; dichloromethane; chloroform to soln. of 5-formyl-1,1,3,3-tetramethylisoindolin-2-yloxyl, 5-pentyldipyrromethane in CH2Cl2 under Ar, trifluoroacetic acid added, stirred for 20 min, 2,3-dichloro-5,6-dicyano-1,4-benzoquinone added stirred, evapd. to dryness, chromy., refluxed,....; elem. anal.; | 100% |
Conditions | Yield |
---|---|
In chloroform excess of Zn(II) acetate, reflux; | 100% |
zinc diacetate
Conditions | Yield |
---|---|
In chloroform excess of Zn(II) acetate, reflux; | 100% |
zinc diacetate
Conditions | Yield |
---|---|
In chloroform excess of Zn(II) acetate, reflux; | 100% |
Conditions | Yield |
---|---|
In dimethyl sulfoxide stirring; filtn., washing (DMSO, hot H2O, acetone), drying (60°C, 24 h); elem. anal.; | 100% |
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