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Potassium tert-butoxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 865-47-4 Structure
  • Basic information

    1. Product Name: Potassium tert-butoxide
    2. Synonyms: BuOk(PotassiuM tert-butoxide);PotassiuM tert-butoxide reagent grade, >=98%;PotassiuM tert-butoxide solution 1.0 M in THF;PotassiuM tert-butoxide subliMed grade, 99.99% trace Metals basis;PotassiuM tert-butoxide, 1.0 M solution in tert-Butanol , SpcSeal;PotassiuM tert-butoxide, 1.0 M solution in THF, SpcSeal;PotassiuM tert-butoxide, 1.8 M solution in THF, SpcSeal;PotassiuM tert-butyl alcohol
    3. CAS NO:865-47-4
    4. Molecular Formula: C4H9KO
    5. Molecular Weight: 112.21
    6. EINECS: 212-740-3
    7. Product Categories: Pharmaceutical intermediates;straight chain compounds;Classes of Metal Compounds;K (Potassium) Compounds (excluding simple potassium salts);Typical Metal Compounds;Micro/Nanoelectronics;Chemical Synthesis;Organic Bases;Synthetic Reagents;Organic BasesMicro/Nanoelectronics;Potassium;Solution Deposition Precursors;metal alkoxide;25mL Sure/Seal Reagents;Chemical Synthesis;Materials Science;Organic Bases;Organometallic Reagents;Solution Deposition Precursors;Synthetic Reagents
    8. Mol File: 865-47-4.mol
  • Chemical Properties

    1. Melting Point: 256-258 °C (dec.)(lit.)
    2. Boiling Point: 275°C
    3. Flash Point: 54 °F
    4. Appearance: White to off-white/Solution
    5. Density: 0.910 g/mL at 20 °C
    6. Vapor Pressure: 1 mm Hg ( 220 °C)
    7. Refractive Index: N/A
    8. Storage Temp.: Flammables area
    9. Solubility: Soluble in hexane, toluene, diethyl ether and terahydrofuran.
    10. PKA: pK1:18(25°C)
    11. Water Solubility: REACTS
    12. Sensitive: Moisture Sensitive
    13. Stability: Stable, but reacts violently with water and acids, possibly leading to fire. Incompatible with water, acids, halogenated hydroca
    14. BRN: 3556712
    15. CAS DataBase Reference: Potassium tert-butoxide(CAS DataBase Reference)
    16. NIST Chemistry Reference: Potassium tert-butoxide(865-47-4)
    17. EPA Substance Registry System: Potassium tert-butoxide(865-47-4)
  • Safety Data

    1. Hazard Codes: F,C,Xi
    2. Statements: 11-19-22-34-35-14-20-36/37-37
    3. Safety Statements: 16-26-36/37/39-43-45-7/9-8-43A-33-27-29
    4. RIDADR: UN 3274 3/PG 2
    5. WGK Germany: 1
    6. RTECS:
    7. F: 10-21
    8. TSCA: Yes
    9. HazardClass: 8
    10. PackingGroup: I
    11. Hazardous Substances Data: 865-47-4(Hazardous Substances Data)

865-47-4 Usage

Chemical Description

Potassium tert-butoxide is a strong base used in organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 865-47-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,6 and 5 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 865-47:
(5*8)+(4*6)+(3*5)+(2*4)+(1*7)=94
94 % 10 = 4
So 865-47-4 is a valid CAS Registry Number.
InChI:InChI=1/C4H10O.K/c1-4(2,3)5;/h5H,1-3H3;/q;+1

865-47-4 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
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  • Detail
  • Alfa Aesar

  • (A13947)  Potassium tert-butoxide, 97%   

  • 865-47-4

  • 25g

  • 251.0CNY

  • Detail
  • Alfa Aesar

  • (A13947)  Potassium tert-butoxide, 97%   

  • 865-47-4

  • 100g

  • 356.0CNY

  • Detail
  • Alfa Aesar

  • (A13947)  Potassium tert-butoxide, 97%   

  • 865-47-4

  • 250g

  • 492.0CNY

  • Detail
  • Alfa Aesar

  • (A13947)  Potassium tert-butoxide, 97%   

  • 865-47-4

  • 500g

  • 883.0CNY

  • Detail
  • Alfa Aesar

  • (A13947)  Potassium tert-butoxide, 97%   

  • 865-47-4

  • 1000g

  • 1590.0CNY

  • Detail
  • Aldrich

  • (156671)  Potassiumtert-butoxide  reagent grade, ≥98%

  • 865-47-4

  • 156671-5G

  • 503.10CNY

  • Detail
  • Aldrich

  • (156671)  Potassiumtert-butoxide  reagent grade, ≥98%

  • 865-47-4

  • 156671-25G

  • 510.12CNY

  • Detail
  • Aldrich

  • (156671)  Potassiumtert-butoxide  reagent grade, ≥98%

  • 865-47-4

  • 156671-100G

  • 696.15CNY

  • Detail
  • Aldrich

  • (156671)  Potassiumtert-butoxide  reagent grade, ≥98%

  • 865-47-4

  • 156671-500G

  • 1,647.36CNY

  • Detail
  • Aldrich

  • (156671)  Potassiumtert-butoxide  reagent grade, ≥98%

  • 865-47-4

  • 156671-2.5KG

  • 5,692.05CNY

  • Detail
  • Aldrich

  • (659878)  Potassiumtert-butoxide  sublimed grade, 99.99% trace metals basis

  • 865-47-4

  • 659878-5G

  • 607.23CNY

  • Detail
  • Aldrich

  • (659878)  Potassiumtert-butoxide  sublimed grade, 99.99% trace metals basis

  • 865-47-4

  • 659878-25G

  • 1,993.68CNY

  • Detail

865-47-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Potassium tert-butanolate

1.2 Other means of identification

Product number -
Other names potassium,2-methylpropan-2-olate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Intermediates,Laboratory chemicals
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:865-47-4 SDS

865-47-4Synthetic route

tert-butyl alcohol
75-65-0

tert-butyl alcohol

potassium tert-butylate
865-47-4

potassium tert-butylate

Conditions
ConditionsYield
With potassium amalgam; catalyst comprising porous iron for 2.2h; Conversion of starting material;
With potassium amalgam; catalyst comprising porous iron for 1.7h; Conversion of starting material;
With potassium amalgam; nonporous iron for 15h; Conversion of starting material;
2-phenethyl iodide
17376-04-4

2-phenethyl iodide

potassium tert-butylate
865-47-4

potassium tert-butylate

styrene
292638-84-7

styrene

Conditions
ConditionsYield
In tert-butyl alcohol at 40℃; Rate constant; Mechanism; secondary α-deuterium isotope effects investigated;100%
1-fluoro-2-phenylethane
458-87-7

1-fluoro-2-phenylethane

potassium tert-butylate
865-47-4

potassium tert-butylate

styrene
292638-84-7

styrene

Conditions
ConditionsYield
18-crown-6 ether In tert-butyl alcohol at 40℃; Rate constant; Mechanism; secondary α-deuterium isotope effects investigated; also in absence of catalyst;100%
potassium tert-butylate
865-47-4

potassium tert-butylate

2-phenylethyl chloride
622-24-2

2-phenylethyl chloride

styrene
292638-84-7

styrene

Conditions
ConditionsYield
18-crown-6 ether In tert-butyl alcohol at 40℃; Rate constant; Mechanism; secondary α-deuterium isotope effects investigated; also in absence of catalyst;100%
potassium tert-butylate
865-47-4

potassium tert-butylate

1-phenyl-2-bromoethane
103-63-9

1-phenyl-2-bromoethane

styrene
292638-84-7

styrene

Conditions
ConditionsYield
In tert-butyl alcohol at 40℃; Rate constant; Mechanism; secondary α-deuterium isotope effects investigated;100%
potassium tert-butylate
865-47-4

potassium tert-butylate

4-chlorobenzoyl chloride
586-75-4

4-chlorobenzoyl chloride

tert-butyl-4-bromobenzoate
59247-47-1

tert-butyl-4-bromobenzoate

Conditions
ConditionsYield
In tetrahydrofuran at 0 - 20℃; for 2h; Inert atmosphere;100%
In diethyl ether for 1h; Substitution;95%
In tetrahydrofuran at -78 - 20℃; for 2h;95%
potassium tert-butylate
865-47-4

potassium tert-butylate

benzylmercury(II) chloride
2117-39-7

benzylmercury(II) chloride

phosphonic acid diethyl ester
762-04-9

phosphonic acid diethyl ester

dibenzylmercury(II)
780-24-5

dibenzylmercury(II)

Conditions
ConditionsYield
In dimethyl sulfoxide Hg deriv. adding to a stirred soln. of potassium tert-butoxide and diethyl phosphite in N2-purged DMSO, stirring for 5 min;100%
In dimethyl sulfoxide Hg deriv. adding to a stirred soln. of potassium tert-butoxide and diethyl phosphite in N2-purged DMSO, stirring for 39.5 h;51%
C14H25B9N2

C14H25B9N2

potassium tert-butylate
865-47-4

potassium tert-butylate

C14H24B9N2(1-)*K(1+)

C14H24B9N2(1-)*K(1+)

Conditions
ConditionsYield
In tetrahydrofuran for 0.5h;100%
tert-butyl 4-(2,6-dichloro-4-pyridyl)pyrrolo[2,3-b]pyridine-1-carboxylate

tert-butyl 4-(2,6-dichloro-4-pyridyl)pyrrolo[2,3-b]pyridine-1-carboxylate

potassium tert-butylate
865-47-4

potassium tert-butylate

4-(2-tert-butoxy-6-chloro-4-pyridyl)-1H-pyrrolo[2,3-b]pyridine

4-(2-tert-butoxy-6-chloro-4-pyridyl)-1H-pyrrolo[2,3-b]pyridine

Conditions
ConditionsYield
Stage #1: tert-butyl 4-(2,6-dichloro-4-pyridyl)pyrrolo[2,3-b]pyridine-1-carboxylate; potassium tert-butylate In toluene at 100℃; for 5h;
Stage #2: With hydrogenchloride In water; toluene for 0.166667h;
100%
2,3-dichloropyrazine
4858-85-9

2,3-dichloropyrazine

potassium tert-butylate
865-47-4

potassium tert-butylate

2-(tert-butoxy)-3-chloropyrazine

2-(tert-butoxy)-3-chloropyrazine

Conditions
ConditionsYield
In tetrahydrofuran for 1h; Inert atmosphere; Cooling with ice;100%
C12H7ClINO

C12H7ClINO

potassium tert-butylate
865-47-4

potassium tert-butylate

tert-butyl (4-chloro-2-iodophenyl)(propa-1,2-dien-1-yl)carbamate

tert-butyl (4-chloro-2-iodophenyl)(propa-1,2-dien-1-yl)carbamate

Conditions
ConditionsYield
In tetrahydrofuran at -78℃; for 2h; Inert atmosphere;100%
potassium tert-butylate
865-47-4

potassium tert-butylate

1,1,4,4-tertakis(trimethylsilyl)octamethylcyclohexasilane
99548-02-4

1,1,4,4-tertakis(trimethylsilyl)octamethylcyclohexasilane

C17H51Si9(1-)*K(1+)

C17H51Si9(1-)*K(1+)

Conditions
ConditionsYield
In 1,2-dimethoxyethane at 20℃; for 2h; Inert atmosphere;100%
potassium tert-butylate
865-47-4

potassium tert-butylate

C35H45FeN4O2(1+)*I(1-)

C35H45FeN4O2(1+)*I(1-)

C39H54FeN4O3

C39H54FeN4O3

Conditions
ConditionsYield
In benzene-d6 for 0.333333h; Inert atmosphere;100%

865-47-4Upstream product

865-47-4Relevant articles and documents

Unusual Reactivity of Silicon Grease Towards Metal Alkoxides: Serendipity for Structural Chemistry

Nahrstedt, Vanessa,Raauf, Aida,Hegemann, Corinna,Brune, Veronika,Schl?fer, Johannes,Mathur, Sanjay

, p. 1102 - 1109 (2021)

Controlled synthesis of moisture sensitive metal alkoxides demands the use of silicon grease for the inert synthetic manipulation of starting materials using glass apparatus to avoid adventitious hydrolysis. Spontaneous reaction of the siloxane units (?OSi(Me3)2)n) with the synthesized alkoxides often leads to molecular metal alkoxides based siloxane frameworks. These spontaneous incorporation of siloxane units into homo- and heterometallic alkoxide building blocks lead to the new multinuclear homo- and heterometallic alkoxide-siloxide compounds [Ce2(OtBu)4{Me2Si(OtBu)O}2(NO3)2] (1), [Zr{(OiPr)2{Me2SiO2}Sr{Zr2(OiPr)8}}2] (2) and [Sn2In2O2{Me2Si(OiPr)O}(OiPr)5]2 (3). Multifunctional coordination properties of these siloxane units enable the molecular approach to synthetically demanding polymetallic complexes for potential MOx-SiOx nanocomposites fabrication.

Synthesis and photochromic properties of new naphthopyrans

Zhao, Qian,Yang, Yanhua,Duan, Yingxiang,Tao, Xian,Shen, YingZhong

, p. 840 - 847 (2018/11/10)

[Figure not available: see fulltext.] Two novel isomeric naphthopyrans substituted with phenyl (13-butyl-6,7-dimethoxy-3,3-bis(6-methoxybiphenyl-3-yl)-3,13-dihydrobenzo[h]indeno[2,1-f]chromen-13-ol) and 4-(naphthalen-1-yl)phenyl (13-butyl-6,7-dimethoxy-3,3-bis[6-methoxy-4'-(naphthalenyl)-biphenyl-3-yl]-3,13-dihydrobenzo[h]indeno[2,1-f]chromen-13-ol) moieties were synthesized. Their photochromism, electrochemical and fluorescent properties were investigated. They displayed faster color fading rate and larger fluorescence quantum yield than 13-butyl-6,7-dimethoxy-3,3-bis(4-methoxyphenyl)-3,13-dihydrobenzo[h]indeno[2,1-f]chromen-13-ol. Moreover, they showed excellent photochromic and fluorescent properties both in solution and in polymethylmethacrylate film. In addition, cyclic voltammetry tests showed that the aromatic substituents had a significant effect on the electrochemical behavior of the naphthopyran derivatives.

Efficient Synthesis of N-Substituted 2,4-Azepandione Ring System as an Active Intermediate for Heterocyclic Syntheses

Waly, Mohamed A.,Yossif, Shiam A.,Ibrahim, Ismail T.,Sofan, Mamdouh A.

, p. 1318 - 1326 (2017/03/27)

An improved efficient synthesis for 2,4-azepandiones (3, 8, and 14) could be achieved by a careful control of the reaction conditions to cyclize ethyl 4-(N-acetylarylamino) butanoate (1, 7, and 13), respectively. The ethyl 4-arylamino butanoate (9 or 12) was prepared by stirring the ethyl 4-bromobutanoate and substituted anilines at room temperature. Then, they were acetylated with acetyl chloride and triethylamine under the conditions that avoid the formation of 2-pyrrolidinone derivatives 10. Due to the rapid decomposition of the acetylated product (7 or 13) to its starting material (9 or 12), the reaction mixture is directly transferred without workup to the next cyclization step. The azepandione synthesis is favored by using a weak base at low temperature, where it is in a competition with the other modes of ring closure. The structures of the new compounds were supported by correct analytical and spectral data.

Apparatus for producing of potassium tert -butoxide

-

Paragraph 0028; 0029, (2017/07/01)

The utility model relates to an apparatus for producing of potassium tert -butoxide, including: reation kettle (1), reation kettle (1) loop through delivery pump (2), heater (3) are connected with pervaporation membrane separation unit (4), the export of holding back the side of pervaporation membrane separation unit (4) is connected with reation kettle (1), the infiltration side of pervaporation membrane separation unit (4) is provided with vacuum pump (5) and penetrant condenser (6), and (6) exit of penetrant condenser still is connected with infiltration fluid reservoir (7) and infiltration liquid pump (8). The utility model discloses process is simple, and conversion is rateed highly, and factor of safety is high, does not introduce the third component, and operating power consumption is low, and energy utilization is high.

Preparation method for low residual granular sodium alkoxide or potassium alcoholate

-

Paragraph 0039-0040, (2017/01/17)

The invention provides a preparation method for low residual granular sodium alkoxide or potassium alcoholate. The method includes using sodium or potassium and alcohol as raw materials, mixing the mixture with a solvent, reacting in inert gas atmosphere by using a microwave heating method, and removing the residual alcohol and solvent in the presence of microwave after the reaction to get the granular sodium alkoxide or potassium alcoholate. The microwave frequency is 2450 +/- 50 MHz. The method can prepare sodium alkoxide or potassium alcoholate with low residual solvent, and the prepared sodium alkoxide or potassium alcoholate is large granular solid, so that the development from powdered product to granular product can be realized, and the problems of residual solvent and potential risk troubled human for a long time can be overcome.

Method and device for producing potassium tert-butoxide

-

Paragraph 0026, (2017/06/02)

The invention relates to a device and technology for producing potassium tert-butoxide. The technology includes the following specific steps that 1, tertiary butanol and potassium hydroxide are reacted in a reaction kettle, and the liquid-phase reactant is fed into a pervaporation membrane for dehydration; 2, the material obtained through dehydration is returned into the reaction kettle to continue to participate in reacting. According to the device and technology, the process is simple, the reaction conversion ratio is high, the safety coefficient is high, third components are avoided, running energy consumption is low, and the energy utilization ratio is high.

Structurally Simple Benzyl-Type Photolabile Protecting Groups for Direct Release of Alcohols and Carboxylic Acids

Wang, Pengfei,Lu, Wenya,Devalankar, Dattatray A.,Ding, Zhenying

, p. 2114 - 2117 (2015/05/13)

Structurally simple benzyl-type photolabile protecting groups (PPGs) have been developed to release alcohols and carboxylic acids. Release of two substrates from one PPG chromophore has also been accomplished. (Chemical Equation Presented).

Phosphorescent OLED and hole transporting materials for phosphorescent OLEDs

-

Page/Page column, (2014/05/07)

The present invention relates to phosphorescent organic light-emitting diodes (OLEDs) comprising a hole-transporting or a hole-transporting and an electron-blocking layer comprising an N,N,N',N'-tetraaryl-phenylene-3,5-diamine or an N,N,N',N'-tetraaryl-1,1'-biphenyl-3,3'-diamine matrix compound and to new N,N,N',N'-tetraarylsubstituted m-arylene diamine compounds useful as hole-transporting and electron-blocking layer matrices in phosphorescent OLEDs.

Novel antimalarial 3-azabicyclo[3.2.2]nonane derivatives

-

, (2011/04/24)

The present invention relates to novel 3-azabicyclo[3.2.2]nonane derivatives of the general formula (I) or a pharmaceutically acceptable salt thereof wherein R1, R2, R3, R4, R5, R6, R7, R8, R9 and R10 are as defined in the specification. The novel 3-azabicyclo[3.2.2]nonane derivatives are particularly useful for treatment and prevention of malaria and trypanosomiasis.

SPIRO COMPOUNDS USEFUL AS ANTAGONISTS OF THE H1 RECEPTOR

-

Page/Page column 32, (2009/03/07)

The invention provides a compound of formula (I) or a pharmaceutically acceptable salt thereof, for treating diseases and conditions of the central nervous system (CNS), in particular sleep disorders.

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