dichloromethane
water
Dimethyl(phenyl)phosphine
zinc
B
cobalt
C
zinc(II) chloride
Conditions | Yield |
---|---|
In dichloromethane | A n/a B 99% C n/a D n/a |
dichloromethane
tributylphosphine
water
cobalt(II) chloride
zinc
B
cobalt
C
zinc(II) chloride
Conditions | Yield |
---|---|
In dichloromethane | A n/a B 99% C n/a D n/a |
dichloromethane
water
diphenyl(methyl)phosphine
cobalt(II) chloride
zinc
B
cobalt
C
zinc(II) chloride
Conditions | Yield |
---|---|
In dichloromethane | A n/a B 99% C n/a D n/a |
dichloromethane
water
triphenylphosphine
cobalt(II) chloride
zinc
B
cobalt
C
zinc(II) chloride
Conditions | Yield |
---|---|
In dichloromethane | A n/a B 99% C n/a D n/a |
Conditions | Yield |
---|---|
In neat (no solvent) byproducts: HCl, hexamethyldisiloxane; Room temperature.; | 96% |
(1,3-di-tert-butyl-2,4-diethyl-1,3,2,4-diazadiboretidine)-zinc-dichloride
2,2-dimethyl-3-butyne
A
1,3-di-tert-butyl-2,4-diethyl-4-(3,3-dimethylbutynyl)-1,3-diazonia-2,4-diborata-1,3-butadiene
B
zinc(II) chloride
Conditions | Yield |
---|---|
In dichloromethane room temp.; ZnCl2 filtered off; distn.; | A 64% B 95% |
(1,3-di-tert-butyl-2,4-diethyl-1,3,2,4-diazadiboretidine)-zinc-dichloride
phenylacetylene
A
1,3-di-tert-butyl-2,4-diethyl-4-(phenylethynyl)-1,3-diazonia-2,4-diborata-1,3-butadiene
B
zinc(II) chloride
Conditions | Yield |
---|---|
In dichloromethane room temp.; ZnCl2 filtered off; distn. at 121°C, 0.002 Torr; | A 80% B 92% |
(1,3-di-tert-butyl-2,4-diethyl-1,3,2,4-diazadiboretidine)-zinc-dichloride
propynoic acid methyl ester
A
1,3-di-tert-butyl-2,4-diethyl-4-{(methoxycarbonyl)ethynyl}-1,3-diazonia-2,4-diborata-1,3-butadiene
B
zinc(II) chloride
Conditions | Yield |
---|---|
In dichloromethane ZnCl2 filtered off; | A 78% B 88% |
tetrahydrofuran
vanadium(III) chloride
zinc
A
bis(triisopropylcyclopentadienyl)vanadium(II)
C
zinc(II) chloride
Conditions | Yield |
---|---|
In tetrahydrofuran refluxing (stirring, overnight), evapn.; extg. (hexanes), evapn.; | A 85% B n/a C n/a |
(1,3-di-tert-butyl-2,4-diethyl-1,3,2,4-diazadiboretidine)-zinc-dichloride
acetylene
A
1,3,8,10-tetra-tert-butyl-2,4,7,9-tetraethyl-1,3,8,10-tetraazonia-2,4,7,9-tetraborata-1,3,7,9-decatetraene-5-yne
B
zinc(II) chloride
Conditions | Yield |
---|---|
In dichloromethane 2 h at room temp.; ZnCl2 filtered off; distn. at 140°C, 0.002 Torr; 1(H), (11)B, (13)C NMR, MS; elem. anal.; | A 71% B 82% |
chlorine dioxide
water
zinc
D
zinc(II) chloride
Conditions | Yield |
---|---|
In water on react. of excess aq. ClO2 with fine Zn filings, formation of oxide; yield with most favorable conditions;; | A 4% B 57% C 33% D 6% |
In water on react. of excess aq. ClO2 with fine Zn filings, formation of oxide; yield with most favorable conditions;; | A 4% B 57% C 33% D 6% |
bis(2,4,6-trimethylphenyl)-zinc
vanadium(V) oxychloride
A
mesityl vanadium(V)oxiddichloride
C
zinc(II) chloride
Conditions | Yield |
---|---|
In hexane under Ar; 41 mmol ZnMes2 added to 82 mmol VOCl3 in hexane at -20°C; mixt. stirred at room temp. for 2-3 h; dark-blue ppt. (VOCl2*ZnCl2) filtered off; filtrate concd. and cooled; elem. anal.; | A 46% B n/a C n/a |
In pentane under Ar; 41 mmol ZnMes2 added to 82 mmol VOCl3 in pentane at -20°C; mixt. stirred at room temp. for 2-3 h; dark-blue ppt. (VOCl2*ZnCl2) filtered off; filtrate concd. and cooled; elem. anal.; | A 46% B n/a C n/a |
Conditions | Yield |
---|---|
With BF3 or BCl3 or BBr3 In neat (no solvent) byproducts: B(C2H5)3; on heating ofmixture of methylchloride and boron halid (BF3, BCl3, BBr3) with powdered Zn at 325 up to 350 °C, forming of B(CH3)3 and ZnCl2 on cooling down at -80°C;; | |
With BF3 or BCl3 or BBr3 In neat (no solvent) byproducts: B(C2H5)3; on heating ofmixture of methylchloride and boron halid (BF3, BCl3, BBr3) with powdered Zn at 325 up to 350 °C, forming of B(CH3)3 and ZnCl2 on cooling down at -80°C;; |
Conditions | Yield |
---|---|
In neat (no solvent) calcination of ZnO and NH4Cl;; |
Conditions | Yield |
---|---|
In neat (no solvent) heating up to red heat;; | |
In water slow react. with concd. aq. NH4Cl;; | |
In water slow react. with concd. aq. NH4Cl;; |
Conditions | Yield |
---|---|
byproducts: NH3, H2; corrosion of zinc in the battery, depending on activity of manganese (in battery);; | |
byproducts: NH3, H2; corrosion of zinc in the battery;; | |
byproducts: NH3, H2; corrosion of zinc in the battery;; |
zinc(II) carbonate
zinc(II) chloride
Conditions | Yield |
---|---|
In hydrogenchloride dissolving ZnCO3 in aq. HCl;; not isolated;; |
Conditions | Yield |
---|---|
In hydrogenchloride; water soln. conc. by heating; solidified material vac. dried at 200°C; then purifn. by sublimation at 450°C under vac.; detd. by XRD andX-ray fluorescence spect.; |
Conditions | Yield |
---|---|
With 1percent Co or Ni In neat (no solvent) on react. of Zn carbonate in presence of 1% CO or Ni with Cl2; dry method;; | |
With 1percent Co or Ni In neat (no solvent) on react. of Zn carbonate in presence of 1% CO or Ni with Cl2; dry method;; |
Conditions | Yield |
---|---|
With air In water treatment of ZnCO3 with industrial FeCl2-soln. under injection of air;; |
Conditions | Yield |
---|---|
In neat (no solvent) calcination of NaCl with Zn2P4O7;; evaporation of ZnCl2;; |
zinc(II) chloride
Conditions | Yield |
---|---|
In neat (no solvent) byproducts: H2O; under He or Ar, heated to 400°C; salt melted and boiled; after water vapor ceased escaping dry Cl2 fed into reactor and temp. raised to 650°C; |
Conditions | Yield |
---|---|
With iron(II) sulfate In not given byproducts: Fe(OH)3; Zn production from industrial wastes; detailed description given;; ZnCl2 not isolated;; | |
With FeSO4 In not given byproducts: Fe(OH)3; Zn production from industrial wastes; detailed description given;; ZnCl2 not isolated;; | |
With iron(II) sulfate In not given byproducts: Fe(OH)3; Zn production from industrial wastes; detailed description given;; ZnCl2 not isolated;; |
Conditions | Yield |
---|---|
In neat (no solvent) giving ZnBr2 into contact with Cl2;; | |
In neat (no solvent) giving ZnBr2 into contact with Cl2;; |
Conditions | Yield |
---|---|
With ammonium molibdate; 1,8-diazabicyclo[5.4.0]undec-7-ene at 240℃; for 3h; | 100% |
Conditions | Yield |
---|---|
With sodium hydroxide In water at 5 - 20℃; for 18h; Heating / reflux; | 100% |
Conditions | Yield |
---|---|
Stage #1: L-Aspartic acid; zinc(II) oxide In water at 60 - 90℃; Stage #2: zinc(II) chloride In water | 100% |
zinc(II) chloride
Conditions | Yield |
---|---|
With NaOH In water byproducts: KCl, NaCl; addn. of soln. of Co complex to soln. of ZnCl2, stirring, addn. of aq. NaOH, heating to 66°C, 10 min; filtration, washing with warm H2O (four times), air-drying; elem. anal.; | 100% |
diclofenac sodium
zinc(II) chloride
{Zn(C6H3Cl2NHC6H4CH2COO)2(H2O)}
Conditions | Yield |
---|---|
With H2O; KOH In water byproducts: NaCl; mixing aq. soln. of the components, adjusting to pH 5.5-7.5 with KOH and stirring at room temp. for 4-6 h; filtn., washing with water, drying over silica gel (vac.) and over P4O10 at 90°C (vac.); | 100% |
Conditions | Yield |
---|---|
In further solvent(s) byproducts: MeCl; slow heating in neat Ph(Me)P(O)OMe until complete pptn.; particle size and polymerization degree depending on heating rate; | 100% |
Zinc and its compounds are on the Community Right-To-Know List. Reported in EPA TSCA Inventory. EPA Genetic Toxicology Program.
OSHA PEL: Fume: TWA 1 mg/m3; STEL 2 mg/m3
ACGIH TLV: TWA 1 mg/m3; STEL 2 mg/m3 (fume)
DOT Classification: 8; Label: Corrosive
For occupational chemical analysis use OSHA: #ID-125 g.
Zinc chloride, with the CAS register number 7646-85-7, is a chemical compound with the formula ZnCl2. The substance is white crystalline solid. Its EINECS register number is 231-592-0. When dissolved in water, Zinc chloride is a strong acid. In addition, it is hygroscopic and even deliquescent, therefore, the samples of Zinc chloride should be protected from sources of moisture, including the water vapor present in ambient air. Zinc chloride is soluble in ethanol, glycerol and acetone.
Properties: Zinc chloride has a specific gravity of 2.75, a pH of 4 and a burning taste. The anhydrous Zinc chloride which is white in color is known for its solubility in water. Zinc chloride is an ionic salt, though some covalent character is indicated by its low melting point (275 °C) and its high solubility in solvents such as diethyl ether. It behaves as a mild Lewis acid, and aqueous solutions have a pH around 4. It is hydrolyzed to an oxychloride when hydrated forms are heated.
In alkali solution in the presence of OH- ion various zinc hydroxychloride anions are present in solution, e.g. ZnOH3Cl2-, ZnOH2Cl22-, ZnOHCl32-, and Zn5OH2Cl3·H2O (simonkolleite) precipitates. The use of Zinc chloride as a flux, sometimes in a mixture with ammonium chloride, involves the production of HCl and its subsequent reaction with surface oxides. In aqueous solution, Zinc chloride is a useful source of Zn2+ for the preparation of other zinc salts, for example zinc carbonate:
ZnCl2(aq) + Na2CO3(aq) → ZnCO3(s) + 2 NaCl(aq)
Preparation: Zinc chloride is an important compound and it is exists in its nine crystalline forms which are either colorless or white. It is actually a granular powder which we obtain by heating calcium chloride and zinc sulfate together.
Zinc chloride can also be prepared from zinc and hydrogen chloride.
Zn + 2 HCl → ZnCl2 + H2
Hydrated forms and aqueous solutions of Zinc chloride may be readily prepared similarly by treating Zn metal with hydrochloric acid. Zinc oxide and zinc sulfide react with HCl:
ZnS(s) + 2 HCl(aq) → ZnCl2(aq) + H2S(g)
Uses: Historically a dilute aqueous solution of Zinc chloride was used as a disinfectant under the name "Burnett's Disinfecting Fluid". It is also used in some commercial brands of antiseptic mouthwash. Zinc chloride finds wide application in textile processing, metallurgical fluxes, and organic synthesis. Concentrated aqueous solutions of Zinc chloride have the interesting property of dissolving starch, silk, and cellulose.
In the laboratory, Zinc chloride finds wide use, principally as a moderate-strength Lewis acid. It can catalyse (A) the Fischer indole synthesis, and also (B) Friedel-Crafts acylation reactions involving activated aromatic rings. Ninhydrin reacts with amino acids and amines to form a coloured compound "Ruhemann's purple"(RP). Spraying with a Zinc chloride solution forms a 1:1 complex (RP)ZnCl(H2O)2 which is more readily detected as it fluoresces better than Ruhemann's purple.
When you are using Zinc chloride, please be cautious about it. The substance is Corrosive, harmful if swallowed and dangerous for the environment. It can cause burns and is toxic to aquatic organisms which may cause long-term adverse effects in the aquatic environment. In case of contact with eyes, you should rinse immediately with plenty of water and seek medical advice. Whenever you will use or contact it, you need wear suitable protective clothing, gloves and eye/face protection. In case of accident or if you feel unwell seek medical advice immediately (show the label where possible). This material and its container must be disposed of as hazardous waste.
Descriptors computed from structure of Zinc chloride:
(1)Canonical SMILES: Cl[Zn]Cl
(2)InChI: InChI=1S/2ClH.Zn/h2*1H;/q;;+2/p-2
(3)InChIKey: JIAARYAFYJHUJI-UHFFFAOYSA-L
The toxicity data about Zinc chloride is as follows:
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
child | TDLo | oral | 169mg/kg (169mg/kg) | LUNGS, THORAX, OR RESPIRATION: DYSPNEA BLOOD: "CHANGES IN SERUM COMPOSITION (E.G., TP, BILIRUBIN, CHOLESTEROL)" SKIN AND APPENDAGES (SKIN): "DERMATITIS, OTHER: AFTER SYSTEMIC EXPOSURE" | Annals of Emergency Medicine. Vol. 23, Pg. 1383, 1994. |
guinea pig | LD50 | oral | 200mg/kg (200mg/kg) | Food Research. Vol. 7, Pg. 313, 1942. | |
guinea pig | LDLo | intraperitoneal | 173mg/kg (173mg/kg) | Archives of Environmental Health. Vol. 11, Pg. 201, 1965. | |
man | TCLo | inhalation | 4800mg/m3/30M (4800mg/m3) | LUNGS, THORAX, OR RESPIRATION: OTHER CHANGES | Personal Communication from J.J. Ferry, Area Manager, Industrial & Environmental Hygiene, General Electric Co., 1 River Rd., Schenectady, NY 12345, Jan. 10, 1974Vol. 10JAN1974, |
mouse | LD50 | intraperitoneal | 24mg/kg (24mg/kg) | Toxicology and Applied Pharmacology. Vol. 63, Pg. 461, 1982. | |
mouse | LD50 | intravenous | 9090ug/kg (9.09mg/kg) | Indian Journal of Pharmacology. Vol. 23, Pg. 153, 1991. | |
mouse | LD50 | oral | 329mg/kg (329mg/kg) | Indian Journal of Pharmacology. Vol. 23, Pg. 153, 1991. | |
mouse | LD50 | subcutaneous | 330mg/kg (330mg/kg) | Oyo Yakuri. Pharmacometrics. Vol. 8, Pg. 1067, 1974. | |
rabbit | LDLo | intravenous | 11mg/kg (11mg/kg) | Toxicology and Applied Pharmacology. Vol. 9, Pg. 269, 1966. | |
rat | LCLo | inhalation | 1960mg/m3/10M (1960mg/m3) | SENSE ORGANS AND SPECIAL SENSES: OTHER: EYE BEHAVIORAL: EXCITEMENT | Archives of Toxicology. Vol. 59, Pg. 160, 1986. |
rat | LD | intratracheal | > 1500uL/kg (1.5mL/kg) | LUNGS, THORAX, OR RESPIRATION: ACUTE PULMONARY EDEMA LUNGS, THORAX, OR RESPIRATION: OTHER CHANGES | American Review of Respiratory Disease. Vol. 141(Suppl), Pg. A3-A937, 1990. |
rat | LD50 | intraperitoneal | 58mg/kg (58mg/kg) | SENSE ORGANS AND SPECIAL SENSES: MIOSIS (PUPILLARY CONSTRICTION): EYE VASCULAR: BP ELEVATION NOT CHARACTERIZED IN AUTONOMIC SECTION | Veterinary and Human Toxicology. Vol. 30, Pg. 224, 1988. |
rat | LD50 | intravenous | 3690ug/kg (3.69mg/kg) | Indian Journal of Pharmacology. Vol. 23, Pg. 153, 1991. | |
rat | LD50 | oral | 350mg/kg (350mg/kg) | Food Research. Vol. 7, Pg. 313, 1942. |
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