Home Other Building Blocks 1633-83-6
1633-83-6,MFCD00006584
Catalog No.:AA001TXI

1633-83-6 | 1,4-Butane sultone

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Purity
Availability
Price(USD)
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5g
98%
in stock  
$6.00   $4.00
- +
10g
98%
in stock  
$7.00   $5.00
- +
25g
98%
in stock  
$9.00   $7.00
- +
100g
98%
in stock  
$23.00   $16.00
- +
500g
98%
in stock  
$105.00   $74.00
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  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Application
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA001TXI
Chemical Name:
1,4-Butane sultone
CAS Number:
1633-83-6
Molecular Formula:
C4H8O3S
Molecular Weight:
136.1695
MDL Number:
MFCD00006584
SMILES:
O=S1(=O)CCCCO1
NSC Number:
71999
Properties
Properties
 
BP:
299.9°C at 760 mmHg  
Form:
Liquid  
MP:
12-15 °C(lit.)  
Refractive Index:
n20/D 1.464(lit.)  
Solubility:
54g/l (decomposition)  
Stability:
Moisture Sensitive  
Storage:
Inert atmosphere;Room Temperature;  

Computed Properties
 
Complexity:
153  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
8  
Hydrogen Bond Acceptor Count:
3  
XLogP3:
0.1  

Upstream Synthesis Route

[1]Patent:CN108558821,2018,A,.Locationinpatent:Paragraph0020;0021;0022

[2]Patent:CN106397392,2017,A,.Locationinpatent:Paragraph0050;0056;0062;0067;0073;0078;0084;0095

[3]BulletindesSocietesChimiquesBelges,1955,vol.64,p.747,752,768

[4]BulletindesSocietesChimiquesBelges,1955,vol.64,p.747,752,768

[5]BulletindesSocietesChimiquesBelges,1955,vol.64,p.747,752,768

[6]JustusLiebigsAnnalenderChemie,1954,vol.586,p.158,163

[7]JournaloftheAmericanChemicalSociety,1954,vol.76,p.5357,5360

[8]JustusLiebigsAnnalenderChemie,1954,vol.586,p.158,163

[1]PhosphorusandSulfurandtheRelatedElements,1987,vol.31,p.161-176

[2]PhosphorusandSulfurandtheRelatedElements,1987,vol.31,p.161-176

[1]PhosphorusandSulfurandtheRelatedElements,1987,vol.31,p.161-176

[1]PhosphorusandSulfurandtheRelatedElements,1987,vol.31,p.161-176

[1]PhosphorusandSulfurandtheRelatedElements,1987,vol.33,p.165-172

Downstream Synthesis Route

[1]Patent:CN108558821,2018,A.Locationinpatent:Paragraph0020;0021;0022

[2]Patent:CN106397392,2017,A.Locationinpatent:Paragraph0050;0056;0062;0067;0073;0078;0084;0095

[3]BulletindesSocietesChimiquesBelges,1955,vol.64,p.747,752,768

[4]BulletindesSocietesChimiquesBelges,1955,vol.64,p.747,752,768

[5]BulletindesSocietesChimiquesBelges,1955,vol.64,p.747,752,768

[6]JustusLiebigsAnnalenderChemie,1954,vol.586,p.158,163

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Literature

Title: Silica-supported sulfonic acid-functionalized ionic liquid coated with [bmim][PF6] as a scavenger for the synthesis of amides.

Journal: Molecular diversity 20110201

Title: A novel supramolecular organogel nanotubular template approach for conducting nanomaterials.

Journal: The journal of physical chemistry. B 20100121

Title: Self-assembled cylindrical and vesicular molecular templates for polyaniline nanofibers and nanotapes.

Journal: The journal of physical chemistry. B 20090827

Title: Masked imidazolyl-dipyrromethanes in the synthesis of imidazole-substituted porphyrins.

Journal: The Journal of organic chemistry 20061110

Title: Quantitative structure-activity relationship modeling of acute toxicity of quaternary alkylammonium sulfobetaines to Daphnia magna.

Journal: Environmental toxicology and chemistry 20040901

Application
1,4-Butane sultone serves as a valuable building block in various chemical reactions and synthesis routes. It finds application as a key reactant in the preparation of conjugated polymers, including polybetaine and poly[2-ethynyl-N-(4-sulfobutyl)pyridinium betaine] (PESPB). Additionally, it is utilized in the synthesis of Bronsted acid catalysts such as 4-(succinimido)-1-butane sulfonic acid and poly(4-vinylpyridinium butane sulfonic acid) hydrogen sulfate. These catalysts play a crucial role in facilitating the synthesis of diverse organic compounds, including 1-amidoalkyl-2-naphthols, substituted quinolines, and pyrano[4,3-b]pyran derivatives. 1,4-Butane sultone's versatility makes it a valuable component in organic synthesis, enabling the development of various functional materials and catalysts for applications across different fields of chemistry.
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