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Potassium acetylide is a chemical compound consisting of potassium and the acetylide ion (C2^-2), characterized by its high reactivity and flammability. It is synthesized by reacting acetylene gas with a potassium solution in liquid ammonia, and is known for its strong basic and nucleophilic properties in various chemical reactions.

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  • 1111-63-3 Structure
  • Basic information

    1. Product Name: potassium acetylide
    2. Synonyms: potassium acetylide;Ethynylpotassium;Monopotassium acetylide;Potassioethyne
    3. CAS NO:1111-63-3
    4. Molecular Formula: C2HK
    5. Molecular Weight: 102.218
    6. EINECS: 214-181-0
    7. Product Categories: N/A
    8. Mol File: 1111-63-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Vapor Pressure: 69700mmHg at 25°C
    7. Refractive Index: N/A
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: potassium acetylide(CAS DataBase Reference)
    11. NIST Chemistry Reference: potassium acetylide(1111-63-3)
    12. EPA Substance Registry System: potassium acetylide(1111-63-3)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1111-63-3(Hazardous Substances Data)

1111-63-3 Usage

Uses

Used in Organic Synthesis:
Potassium acetylide is utilized as a strong base and nucleophile in organic synthesis for facilitating a range of chemical reactions. Its reactivity allows it to participate in the formation of new chemical bonds, making it a valuable component in the synthesis of complex organic molecules.
Used in the Production of Alkenes and Alkynes:
In the chemical industry, potassium acetylide is employed in the production of specific types of alkenes and alkynes, which are essential building blocks for a variety of organic compounds and materials.
Used in Research and Development:
Due to its unique reactivity, potassium acetylide is also used in research and development settings to explore new chemical reactions and investigate the properties of novel compounds.
Safety Considerations:
Given its potential to react violently with water and its explosive nature when in contact with certain organic compounds, potassium acetylide must be handled and stored with extreme caution under controlled conditions to ensure safety.

Check Digit Verification of cas no

The CAS Registry Mumber 1111-63-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,1 and 1 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1111-63:
(6*1)+(5*1)+(4*1)+(3*1)+(2*6)+(1*3)=33
33 % 10 = 3
So 1111-63-3 is a valid CAS Registry Number.
InChI:InChI=1/C2.K/c1-2;/q-2;+1

1111-63-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Potassium acetylide

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
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:1111-63-3 SDS

1111-63-3Relevant articles and documents

Evidence of solubility of the acetylide ion C22-: Syntheses and crystal structures of K2C2·2NH 3, Rb2C2·2NH3, and Cs 2C2·7NH3

Hamberger, Markus,Liebig, Stefan,Friedrich, Ute,Korber, Nikolaus,Ruschewitz, Uwe

supporting information, p. 13006 - 13010 (2013/03/13)

Most alkali- and alkaline-earth-metal acetylides of composition A 2IC2 (AI=Li-Cs) and (AE)IIC 2 ((AE)II=Mg-Ba) have been known since the 19th century.[1,2] Very early crystal structure investigations had already revealed that they contA In C2 2- dumbbells,[3, 4] but the complex phase behavior of these compounds was elucidated only very recently.[5] In the first half of the last century, CaC2 in particular, which is accessible from CaO and coal, attracted a lot of interest as an industrial feedstock of acetylene by hydrolysis.[6] Owing to the limited petroleum resources, this reaction has found a revival within the last years.[7] Apart from hydrolysis however, reports on further reactions of alkali- and alkaline-earthmetal acetylides are quite rare, which is surely due in part to the fact that these compounds are insoluble in common solvents.[8] However, during the synthesis of ternary copper acetylides AICuC2 with AI=K-Cs, we observed that a suspension of AI 2C2 in liquid ammonia reacts with CuI at temperatures as low as -78°C within minutes.[9] To clarify whether this reaction can be interpreted as a (low) solubility of A I 2C2 in liquid ammonia, we decided to investigate the system AI 2C2/ NH3(l) in more detAIl. The versatility of liquid ammonia to stabilize unusual mAIn-group-element clusters has been shown by several impressive examples.[10] Herein we report the crystal structures of the ammoniates K2C2·2NH3 (1), Rb2C2·2NH3 (2), and Cs2C2·7NH3 (3),[11a-c] which are the first examples of binary acetylide solvates. Additionally, the crystal structure of [Li(NH3)4]C2H (4),[11d] which contA Ins the hydrogen acetylide anion C2H-, is briefly presented.

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