Quick Details Classification: Other CAS No.: 1310-65-2 MF: LiOH.H2O Place of Origin: China (Mainland) Grade Standard: high purity Purity: 56.5%min
Cas:1310-66-3
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inquiryItems standard Results Appearance White crystalline grain White crystalline grain LIOH.H2O 99
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Cas:1310-66-3
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inquiryProduct Name Lithium Hydroxide CAS No. 1310-66-3 Molecular Formula LiOH·H2O Molecular Weight 41.96 g·mol−1 LiOH
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Cas:1310-66-3
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inquiryProduct Name: Lithium hydroxide monohydrate CAS: 1310-66-3 MF: Li.HO.H2O MW: 41.96 EINECS: 603-454-3 Mol File: 1310-66-3.mol Lithium hydroxide monohydrate Structure Lithium hydroxide monohydrate Chemical Properties Melting point
Cas:1310-66-3
Min.Order:1 Gram
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inquiryPacking: According to customer requirements Delivery time: In stock or depands Port of shipment: Ningbo/Shanghai/Qingdao OEM/ODM:Welcome Sample:We can offer our existing samples at once Appearance:white powder/ Refer to COA Storage:Refer to COA
Cas:1310-66-3
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Cas:1310-66-3
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Cas:1310-66-3
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Cas:1310-66-3
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Cas:1310-66-3
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Cas:1310-66-3
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inquiryLithium hydroxide monohydrate CAS: 1310-66-3 Specification Lithium hydroxide mono (Industrial grade) CAS No: 1310-66-3 Appearance: White crystal LiOH: 56.5% min. CO32-: 0.5% max K: 0.005% max Na: 0.005% max Mg: 0.005% max Mn: 0.005% max Si : 0.005%
Cas:1310-66-3
Min.Order:1 Kilogram
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inquiryAppearance:white powder Storage:Store in a cool,dry place and keep away from direct strong light Package:As customer request Application:Used for research and industrial manufacture. Transportation:Common products:Sea/Air/Courie
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Min.Order:100 Metric Ton
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Cas:1310-66-3
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Cas:1310-66-3
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inquiryPyrroloquinoline quinone cas 72909-34-3 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
Cas:1310-66-3
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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
Conditions | Yield |
---|---|
In ethanol; water boiling soln. of LiOH in 62.8 vol.-% alcohol, pptn. of hydrate on vaporization or cooling ;; | |
With sulfuric acid In water vaporization of cold. concd. LiOH soln. over H2SO4;; | |
In water aq. LiOH soln.; various conditions;; |
Conditions | Yield |
---|---|
With sulfuric acid In sulfuric acid Electrolysis; electrochemical conversion of LiCO3 into LiOH in aq. H2SO4 at temp. 30-40°C in membrane electrolyzer is suggested; soln. of LiOH cooled, evapd. and LiOH*H2O crystd.; product washed with LiOH soln. and dried; elem. anal.; |
lithium hydroxide monohydrate
Conditions | Yield |
---|---|
In water Electrolysis; formation by electrolysis of aq. LiCl with a Hg-circulation cathode;; the formed LiOH*H2O is free of Cl(1-), SO4(2-), PO4(3-) and Fe(3+);; | |
In water |
Conditions | Yield |
---|---|
In water formation as precipitate on evaporation a aq. soln. of LiOH;; | |
In water formation as precipitate on evaporation a aq. soln. of LiOH;; |
Conditions | Yield |
---|---|
With caustic lime In water reaction of Li2CO3 with caustic lime in aq. soln.;; | |
With caustic lime In water |
n-butyllithium
A
lithium hydroxide monohydrate
Conditions | Yield |
---|---|
In hexane 1.6 M n-BuLi in hexane, 48 h; ppt. was washed thoroughly with hexane and EtOH, dried in vac., elem. anal., detected by X-ray powder diffractometry; | A n/a B 0% C n/a |
n-butyllithium
A
lithium hydroxide monohydrate
Conditions | Yield |
---|---|
In hexane 1.6 M n-BuLi in hexane, 48 h; ppt. was washed thoroughly with hexane and EtOH, dried in vac., elem. anal., detected by powder X-ray diffractometry; | A n/a B 0% C n/a |
Conditions | Yield |
---|---|
In neat (no solvent) stored in open air for 8 wk; detd. by X-ray diffraction; |
Conditions | Yield |
---|---|
In neat (no solvent) stored in open air for 8 wk; detd. by X-ray diffraction; |
Conditions | Yield |
---|---|
In neat (no solvent) stored in open air for 8 wk; detd. by X-ray diffraction; |
lithium hydroxide monohydrate
Conditions | Yield |
---|---|
In neat (no solvent) stored in open air for 1 wk; detd. by X-ray diffraction; |
Conditions | Yield |
---|---|
With air for 1h; |
Conditions | Yield |
---|---|
With air at 20℃; for 0.5h; |
Conditions | Yield |
---|---|
With air at 20℃; for 0.5h; |
lithium hydroxide monohydrate
phosphoric acid
Conditions | Yield |
---|---|
In water evpn. of stoich. soln. of Fe(NO3)3*9H2O and LiH2PO4 at 20°C; two-steps termal treatment at 350 and 700°C under N2/H2 during 10 h; WO 2002/099913 A1; sintered for 12 h at 800°C (under Ar) for electrical measurements; detd. by XRD; | 100% |
lithium hydroxide monohydrate
phosphoric acid
Conditions | Yield |
---|---|
In water pptd. in soln. of Mn(NO3)2*4H2O (0.1M), H3PO4 (0.1M), LiNO3 (1M) and LiOH*H2O (0.3M) after 5 d under refluxing and stirring (pH=10); Chem. Mater., 16, 93 (2004); sintered for 12 h at 900°C (under air) for electrical conductivity measurements; detd. by XRD; | 100% |
lithium hydroxide monohydrate
5-bromosalicylaldehyde thiosemicarbazone
water
Conditions | Yield |
---|---|
In water LiOH and ligand were mixed at 100°C, soln. of Fe salt was added to refluxing mixt., stirring for 30 min; soln. was cooled to room temp. overnight, ppt. was filtered off, washed with water, dried in vac. first at room temp., then at 50°C overnight; elem. anal.; | 100% |
lithium hydroxide monohydrate
Conditions | Yield |
---|---|
In tetrahydrofuran at 0 - 20℃; | 100% |
lithium hydroxide monohydrate
Conditions | Yield |
---|---|
In water; acetonitrile at 22℃; for 24h; Inert atmosphere; | 100% |
Conditions | Yield |
---|---|
In water all manipulations under inert atm.; excess of complex suspended in waterand treated with hydroxide, stirred for 15 min; filtered, washed with water, filtrate evapd. to dryness; | 99% |
lithium hydroxide monohydrate
[Ni(2-(2-hydroxymethyl)amino-3-oximobutane(1-))3(μ3-O)]ClO4
Conditions | Yield |
---|---|
In methanol (under aerobic conditions); Ni-complex refluxed with LiOH*H2O in MeOH; | 99% |
lithium hydroxide monohydrate
benzo[ghi]perylene 1,2,4,5,10,11-hexacarboxylic trianhydride
Conditions | Yield |
---|---|
In methanol at 80℃; for 24h; | 99% |
Conditions | Yield |
---|---|
In neat (no solvent) mixed in stoich. ratio, heated at 60 °C for 2 h, pressed; dried at 120 °C for 7 h, at 150 °C for 16 h; | 97% |
Conditions | Yield |
---|---|
for 15h; Heating; | 96% |
Conditions | Yield |
---|---|
In melt mixing of LiOH*H2O, LiNO3 and MnO2 by grinding in a mortar, heating at 280°C for 12 h in air, cooling to room temp.; washing with distd. water, centrifuging, drying at 80°C under vac.; | 95% |
lithium hydroxide monohydrate
bis(fluorosulfonyl)imide ammonium salt
Conditions | Yield |
---|---|
at -5℃; for 0.5h; Temperature; | 95% |
In isopropyl alcohol at 20℃; for 7h; Solvent; | 91% |
In water at 20℃; for 1.5h; Inert atmosphere; | 89% |
In Isopropyl acetate at 31 - 35℃; under 65.0315 Torr; for 4h; Temperature; Solvent; Pressure; Reflux; | 114.8 g |
lithium hydroxide monohydrate
ethyl 2,2-bis(3,5-bis(2-methoxyphenyl)-1H-pyrazol-1-yl)acetate
Conditions | Yield |
---|---|
In tetrahydrofuran; water at 20℃; | 94% |
lithium hydroxide monohydrate
Conditions | Yield |
---|---|
In tetrahydrofuran; methanol; water at 20℃; for 3h; | 94% |
Conditions | Yield |
---|---|
In water lithium hydroxide slurried in a small amt. of water, gallia added; mixt. stirred at ca. 40°C (40 min); addn. of silica; boiling, evapn. to dryness; residue dried at 120°C (2 h); addn. of water, heating at 180°C (4-5 d); filtration, washing, drying; elem. anal.; | 92% |
Conditions | Yield |
---|---|
In water lithium hydroxide slurried in a small amt. of water, gallia added; mixt. stirred at ca. 40°C (40 min); addn. of silica; boiling, evapn. to dryness; residue dried at 120°C (2 h); addn. of water, heating at 180°C (6 d); filtration, washing, drying; elem. anal.; | 92% |
lithium hydroxide monohydrate
Conditions | Yield |
---|---|
With CH3COOH In tetrahydrofuran; water under N2; soln. of Mn compd. in THF treated with aq. soln. of LiOH (1:10molar ratio), mixt. stirred for 25 h, Et2O and water added, phases sepd ., glacial acetic acid added dropwise to aq. soln.; ppt. sepd., washed with water; elem. anal.; | 92% |
Conditions | Yield |
---|---|
In water at 200℃; for 72h; | 92% |
Conditions | Yield |
---|---|
In water heating (80°C), pptn.; filtn., washing (H2O, EtOH), drying (air atm.); | 91.2% |
lithium hydroxide monohydrate
ethanol
1-(5-acetyl-2,4-dihydroxyphenyl)-1-ethanone
water
acetylacetone
Conditions | Yield |
---|---|
for 7h; Reflux; | 90% |
Conditions | Yield |
---|---|
With strontium(II) hydroxide octahydrate; potassium hydroxide In water at 180℃; for 24h; High pressure; Autoclave; | 90% |
lithium hydroxide monohydrate
ethanol
1-(5-acetyl-2,4-dihydroxyphenyl)-1-ethanone
water
copper(II) sulfate
Conditions | Yield |
---|---|
for 7h; Reflux; | 89% |
Conditions | Yield |
---|---|
In ethanol; water the components were dissolved in boiling water, after cooling EtOH was added and the solution was reheated to boiling, allowed to stand for one day at room temp. with occasional shaking; filtrated, washed with 96% EtOH, dried in air, recrystd. from H2O/ethanol; elem. anal., crude (+)-Ir(en)3Cl3 was sepd. by evapn., dissoln. in 12 M HCl, pptn. by ethanol, 1 h, heating at 160°C; | A 87% B n/a |
lithium hydroxide monohydrate
(((CH3)3C)2C6H3)3C27H11N4ONi
Conditions | Yield |
---|---|
With (COCl)2; SnCl4 In benzene Ni compd. added to toluene soln. of porphyrin; 24 h at 100°C; evapd.; chromd. (slica gel, CH2Cl2); LiOH*H2O and water added to dioxane soln.; refluxed (24 h); evapd.; toluene added; evapd.; chromd. (silica gel, CH2Cl2-hexane, CH2Cl2-AcOH); evapd.; benzene and (COCl)2 added; stirred (room temp., 2 h); solvent distd.; SnCl4 added; 1 h at room temp.; CH2Cl2 added; aq. NaOH added; org. phase washed (water); dried (Na2SO4); evapd.; chromd.(silica gel, hexane-CH2Cl2); crystd. (CH2Cl2-MeOH); elem. anal.; | 87% |
lithium hydroxide monohydrate
N,N'-ethylenebis(L-aspartic acid) tetramethyl ester
Conditions | Yield |
---|---|
In water aq. LiOH added to a soln. of the ligand in MeOH; stirred overnight untilcomplete hydrolysis (checked by TLC) and evapd.; residue dissolved in a small amt. of water, and aq. soln. of Eu salt added; left to stand for 8 h; ppt. removed by filtration; filtrate evapd.; residue purified by repptn.in H2O-EtOH and gel filtration; elem. anal.; | 87% |
Conditions | Yield |
---|---|
In water H2MoO4*H2O (1 mmol) added to aq. soln. of LiOH*H2O (2 mmol), stirred for20 min; filtered, allowed to stant (air) at room temp. for 1 week; | 87% |
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