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Cas:546-89-4
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inquiryThe above product is Ality Chemical's strong item with best price, good quality and fast supply. Ality Chemical has been focusing on the research and production of this field for over 14 years. At the same time, we are always committed to providi
Shanghai Seasonsgreen Chemical is a high-tech research and development, production, sale and custom synthesis set in one high-tech chemical products enterprises. Our sales and marketing division is located in Shanghai, serving international pharmaceu
Cas:546-89-4
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Cas:546-89-4
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inquiryStock products, own laboratory Appearance:White to yellow Powder or Crystals Storage:Room Temperature Package:Grams, Kilograms Application:For R&D Transportation:According to customer request Port:shanghai
Cas:546-89-4
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inquiryProduct Name: Lithium acetate Synonyms: LITHIUM ACETATE;LITHIUM ACETATE PHIX(R) BUFFER;ACETIC ACID LITHIUM SALT;Lithiumacetat;lithiumethanate;Lithiumethanoat;lithiumethanoate;quilone CAS: 546-89-4 MF: C2H3LiO2
Cas:546-89-4
Min.Order:1 Gram
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inquiryOur 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
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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:546-89-4
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inquiryProduct Name: Lithium acetate Synonyms: LITHIUM ACETATE;LITHIUM ACETATE PHIX(R) BUFFER;ACETIC ACID LITHIUM SALT;LithiumAcetateDihydrateA.R.;Lithiumacetatehydrate,Puratronic,99.998%(metalsbasis);Lithium acet
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Cas:546-89-4
Min.Order:1 Kilogram
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Type:Lab/Research institutions
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Cas:546-89-4
Min.Order:1 Kilogram
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Type:Lab/Research institutions
inquiry1,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 qualifie
Cas:546-89-4
Min.Order:1 Kilogram
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Type:Lab/Research institutions
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
Cas:546-89-4
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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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Cas:546-89-4
Min.Order:1 Gram
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inquiryLithium acetate Chemical Properties Melting point 283-285 °C (lit.) solubility H2O: 5 M at 20 °C, clear, colorless form Powder or Crystals color White to yellow Water Solubility 40.8 g/100 mL (20 ºC) Merck 14,5521
Cas:546-89-4
Min.Order:1 Gram
FOB Price: $66.0
Type:Lab/Research institutions
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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Cas:546-89-4
Min.Order:1 Kilogram
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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
1.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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Cas:546-89-4
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inquiryhigh purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:drum and bag Application:for pharma use Transportation:by sea or air Port:Beijing or Guangzhou
high purity,in stock Package:25kg/drum,or as per customers'demand Application:API,or Intermediates,fine chemicals Transportation:air,sea,courier
R & D enterprises have their own stock in stock Package:1kg Application:pharmaceutical intermediates
Q1: Are you a manufacturer Answer: Yes, we are factory founded on 2012.Q2: How to contact with us Click "contact supplier" And then send us message the product you interest in, you will get reply within 12 hours.Q3:Which kind of payment terms do you
Acmec is a leading manufacturer and supplier of biochemical reagents and life science products. We have over 40,000 items in stock (real-time inventory) and offer discounted prices to registered members of the online store ( www.acmec.com.cn ) Appea
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inquiryhigh quality Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea
TAIHO Unique Advantages:1.We're factory2.Free samples available3.Commodity inspection can be done4.ISO9001,Kosher certifications5.10 years experiences Storage:Store in cool &dry place Package:aluminium foil bag/fiber can/plastic drum Application:comp
lithium pentafluorobenzenesulfinate
mercury(II) diacetate
A
C6F5HgO(O)CCH3
B
lithium acetate
Conditions | Yield |
---|---|
In water in aq. suspension at 25°C, molar ratio of LiOS(O)C6F5 and Hg comp. = 1.0:2.1, immediately react.; | A 55% B n/a |
In water in aq. suspension at 25°C, molar ratio of LiOS(O)C6F5 and Hg comp. = 1.0:2.1, immediately react.; | A 55% B n/a |
lithium tert-butyl hydroperoxide
acetone
A
formaldehyd
B
lithium formate
C
lithium acetate
D
tert-butyl alcohol
Conditions | Yield |
---|---|
lithium tert-butoxide In n-heptane at 40℃; Rate constant; Kinetics; other solvents and inhibitors investigated; Energy of activation, A-factor;; |
lithium tert-butyl hydroperoxide
A
lithium formate
B
lithium acetate
C
lithium tert-butoxide
D
tert-butyl alcohol
Conditions | Yield |
---|---|
In various solvent(s) at 80℃; for 8h; Yield given. Yields of byproduct given; | |
In toluene; cyclohexene at 85℃; for 5h; Kinetics; Product distribution; other solvent, other temperature, other time; | |
In toluene; cyclohexene at 85℃; for 5h; Yield given. Yields of byproduct given; |
n-butyllithium
[bis(acetoxy)iodo]benzene
A
1-iodo-butane
B
iodobenzene
C
octane
D
n-hexan-2-one
E
lithium acetate
F
benzene
Conditions | Yield |
---|---|
In tetrahydrofuran at -5℃; for 0.0833333h; Product distribution; Mechanism; various amounts of nBuLi, other iodine compounds, various organolithium reagents; |
A
lithium formate
B
lithium acetate
C
lithium tert-butoxide
D
tert-butyl alcohol
Conditions | Yield |
---|---|
1-amino-naphthalene In n-heptane at 80℃; Thermodynamic data; Rate constant; other temperature, other solvent, reaction energy, activation entropy, activation enthalpy, gibbs function; |
Conditions | Yield |
---|---|
In acetic acid equilibrium in glacial acetic acid;; |
lithium acetate dihydrate
lithium acetate
Conditions | Yield |
---|---|
In solid heating at 50-195°C; | |
In neat (no solvent, solid phase) 110-180°C; XRD; |
Conditions | Yield |
---|---|
In neat (no solvent) Ar; |
Conditions | Yield |
---|---|
In neat (no solvent) thermolysis in the absence of O2; |
Conditions | Yield |
---|---|
With perchloric acid; water; lithium perchlorate; 2-amino-2-hydroxymethyl-1,3-propanediol pH=7.3 - 8.9; Activation energy; Kinetics; Mechanism; Temperature; |
Conditions | Yield |
---|---|
With lithium hexafluorophosphate; oxygen Electrochemical reaction; |
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 125℃; for 120h; Inert atmosphere; | 5.2 g |
Conditions | Yield |
---|---|
With tetra-(n-butyl)ammonium iodide In water at 55℃; for 6h; Temperature; | 94.15% |
hudrochloranilic acid
tetraethylammonium bromide
lithium acetate
acetone
Conditions | Yield |
---|---|
In water | 94% |
Conditions | Yield |
---|---|
With bis[2-(2-methoxyethoxy)ethyl] 4-oxo-4H-pyran-2,6-dicarboxylate In acetonitrile at 80℃; for 24h; Reagent/catalyst; | 94% |
9,10-Dihydrobenzopyrene
lithium acetate
(+/-)-trans-9-acetoxy-10-bromo-9,10,11,12-tetrahydrobenzopyrene
Conditions | Yield |
---|---|
With N-bromoacetamide In acetic acid for 1.5h; Ambient temperature; | 92% |
lithium acetate
tetra-μ-acetato-diruthenium(II,II)-bis(tetrahydrofuran)
Conditions | Yield |
---|---|
In methanol Ru-salt was heated under reflux for 20 min in MeOH contg. Li(O2CMe) under Ar; the soln. was cooled to ambient temp., filtered off, recrystd. from THF at -20°C; | 92% |
lithium acetate
cyclohexa-1,3-diene
cis-1-acetoxy-4-chlorocyclohex-2-ene
Conditions | Yield |
---|---|
With p-benzoquinone; lithium chloride; palladium diacetate In water; acetic acid Ambient temperature; | 89% |
With palladium diacetate; p-benzoquinone; lithium chloride In acetic acid at 20℃; for 5h; diastereoselective reaction; | 18.7 g |
lithium acetate
1,4-but-2-ynoic acid benzyl ester
Conditions | Yield |
---|---|
With acetic acid-d; palladium diacetate for 14h; Ambient temperature; | 87% |
dibenzo-18-crown-6
lithium acetate
1,1'-(6,7,9,10,17,18,20,21-octahydrodibenzo[b,k]-[1,4,7,10,13,16]hexaoxacyclooctadecine-2,13-diyl)diethanone
Conditions | Yield |
---|---|
With PPA at 68 - 72℃; for 2h; | 86% |
1,2-Dihydroacridine
lithium acetate
Conditions | Yield |
---|---|
With N-bromoacetamide In acetic acid for 4h; Ambient temperature; | 85% |
lithium acetate
5,6-dihydro-naphthalene-2-carboxylic acid
8-Acetyl-7-bromo-5,6,7,8-tetrahydronaphthalene-2-carboxylic acid
Conditions | Yield |
---|---|
With N-bromoacetamide In acetic acid for 3h; Ambient temperature; | 85% |
lithium acetate
O6-<2-(4-nitrophenyl)ethyl>-9-<3',5'-O-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)-2'-O-<(trifluoromethyl)sulfonyl>-β-D-ribofuranosyl>guanine
Conditions | Yield |
---|---|
With N,N,N,N,N,N-hexamethylphosphoric triamide In N,N-dimethyl-formamide Ambient temperature; | 85% |
lithium acetate
cyclohexa-1,3-diene
trans-(±)-4-(acetoxy)cyclohex-2-en-1-yl acetate
Conditions | Yield |
---|---|
With oxygen; palladium diacetate; iron(II) phthalocyanine; 2-(phenylsulfinyl)-1,4-benzoquinone In acetic acid under 760 Torr; for 5.5h; Mechanism; Ambient temperature; or 1,4-hydroquinone/DMSO , other benzoquinones, time course of the reaction, stereoselectivity, other diene; | 85% |
With oxygen; palladium diacetate; iron(II) phthalocyanine; 2-(phenylsulfinyl)-1,4-benzoquinone In acetic acid under 760 Torr; for 5.5h; Ambient temperature; | 85% |
With manganese(IV) oxide; palladium diacetate; acetic acid; p-benzoquinone In pentane at 25℃; for 72h; | 79% |
Conditions | Yield |
---|---|
With bis[2-(2-methoxyethoxy)ethyl] 4-oxo-4H-pyran-2,6-dicarboxylate In acetonitrile at 80℃; for 24h; Reagent/catalyst; | 85% |
cyclohepta-3,5-dien-1-ol
lithium acetate
meso-(1R,4R,6R)-3,6-Diacetoxy-4-cyclohepten-1-ol
Conditions | Yield |
---|---|
With manganese(IV) oxide; palladium diacetate; p-benzoquinone In acetic acid at 25℃; for 64h; | 84% |
With manganese(IV) oxide; p-benzoquinone; palladium diacetate In acetic acid for 41h; Ambient temperature; | 75% |
Conditions | Yield |
---|---|
palladium diacetate In acetic acid for 20h; Ambient temperature; | 83% |
palladium diacetate In acetic acid Product distribution; or sodium, various times; other 2-alkynoic acid derivatives; |
lithium acetate
7,8-Dihydronaphthalene-2-carboxylic acid
5-Acetyl-6-bromo-5,6,7,8-tetrahydronaphthalene-2-carboxylic acid
Conditions | Yield |
---|---|
With N-bromoacetamide In acetic acid for 3h; Ambient temperature; | 83% |
lithium acetate
phenylpropynoic acid methyl ester
(Z)-3-Acetoxy-3-phenyl-acrylic acid methyl ester
Conditions | Yield |
---|---|
palladium diacetate In acetic acid for 22h; Ambient temperature; | 83% |
lithium acetate
Methyl 2-butynoate
β-acetoxy-crotonic acid methyl ester
Conditions | Yield |
---|---|
palladium diacetate In acetic acid for 15h; Ambient temperature; | 83% |
lithium acetate
1-Benzyl-3-(2-cyclohexa-2,4-dienyl-ethyl)-urea
Acetic acid (3aS,7aS)-1-(toluene-4-sulfonyl)-2,3,3a,4,5,7a-hexahydro-1H-indol-5-yl ester
Conditions | Yield |
---|---|
With palladium diacetate; p-benzoquinone In acetic acid; acetone for 16h; Ambient temperature; | 82% |
lithium acetate
3,4-Dihydroacridine
Conditions | Yield |
---|---|
With N-bromoacetamide In acetic acid for 4h; Ambient temperature; | 81% |
lithium acetate
triphenylantimony
triphenylantimony(V) diacetate
Conditions | Yield |
---|---|
In acetonitrile Electrolysis; N2 atmosphere, ambient temp.; constant current electrolysis (Pt plate and wire electrodes); extraction (ether), washing of extracts (water, brine), drying (MgSO4),solvent removal, recrystn. (ethanol); | 81% |
Conditions | Yield |
---|---|
With N2H4 In water to Pu-compd. in H2O added with stirring CH3COOLi, N2H4 and Sr(NO3)2 in H2O, coagulated for ca. 30 min; filtered in vac., washed with cold H2O, dried in an air flow for 3 h, elem. anal.; | 80% |
lithium acetate
cyclohexa-1,3-diene
cis-2-cyclohexenyl-1,4-diacetate
Conditions | Yield |
---|---|
With manganese(IV) oxide; palladium diacetate; acetic acid; p-benzoquinone; lithium chloride In pentane at 25℃; for 72h; | 79% |
With palladium diacetate; acetic acid In pentane |
lithium acetate
1,4-but-2-ynoic acid benzyl ester
(Z)-3-Acetoxy-but-2-enoic acid benzyl ester
Conditions | Yield |
---|---|
palladium diacetate In acetic acid for 8.5h; Ambient temperature; | 78% |
lithium acetate
Conditions | Yield |
---|---|
In dimethyl sulfoxide at 40℃; for 18h; Inert atmosphere; Sealed tube; | 78% |
lithium acetate
6-(benzyloxy)-1,3-cycloheptadiene
1β-acetoxy-4β-chloro-6α-(benzyloxy)-2-cycloheptene
Conditions | Yield |
---|---|
With p-benzoquinone; lithium chloride; palladium diacetate In acetic acid | 77% |
Conditions | Yield |
---|---|
With (1,4,7,10-tetraoxacyclododecane) In dimethyl sulfoxide for 10h; Reagent/catalyst; Reflux; | 77% |
Conditions | Yield |
---|---|
palladium diacetate In trifluoroacetic acid for 5h; Ambient temperature; | 76% |
Conditions | Yield |
---|---|
Stage #1: lithium acetate With bromobenzene; lithium; 1,1,1,3,3,3-hexamethyl-disilazane In tetrahydrofuran at 20℃; Stage #2: 2-Adamantanone In tetrahydrofuran at 20℃; for 2h; Reflux; Stage #3: With sulfuric acid In tetrahydrofuran; water Cooling; | 76% |
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