3-Butenoic acid

Base Information

Chemical Name:3-Butenoic acid
CAS No.:625-38-7
Molecular Formula:C4H6O2
Molecular Weight:86.0904
Hs Code.:29161900
European Community (EC) Number:210-892-5
NSC Number:44546,43973
DSSTox Substance ID:DTXSID60211539
Nikkaji Number:J102.015C
Wikidata:Q223058
Metabolomics Workbench ID:439
Mol file:625-38-7.mol

Synonyms:3-butenoic acid;vinylacetic acid

Suppliers and Price of 3-Butenoic acid

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

AK Scientific
3-Butenoic acid
5g
$ 25.00

Alfa Aesar
Vinylacetic acid, 96%
25g
$ 98.10

Alfa Aesar
Vinylacetic acid, 96%
100g
$ 315.00

American Custom Chemicals Corporation
3-BUTENOIC ACID 95.00%
1G
$ 628.51

Biosynth Carbosynth
3-Butenoic acid
5 g
$ 95.00

Biosynth Carbosynth
3-Butenoic acid
50 g
$ 350.00

Biosynth Carbosynth
3-Butenoic acid
10 g
$ 150.00

Biosynth Carbosynth
3-Butenoic acid
25 g
$ 250.00

Biosynth Carbosynth
3-Butenoic acid
2 g
$ 60.00

Crysdot
But-3-enoicacid 95+%
100g
$ 408.00

Total 53 raw suppliers

Chemical Property of 3-Butenoic acid

Chemical Property:

Appearance/Colour:clear colourless to yellow liquid
Vapor Pressure:0.714mmHg at 25°C
Melting Point:-39 °C(lit.)
Refractive Index:n20/D 1.423(lit.)
Boiling Point:170.6 °C at 760 mmHg
PKA:4.34(at 25℃)
Flash Point:68.2 °C
PSA：37.30000
Density:1.021 g/cm³
LogP:0.64710
Storage Temp.:2-8°C
Solubility.:Fully miscible.
XLogP3:0.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:86.036779430
Heavy Atom Count:6
Complexity:65.9

Purity/Quality:

97% ^*data from raw suppliers

3-Butenoic acid ^*data from reagent suppliers

Safty Information:

Pictogram(s): C
Hazard Codes:C
Statements: 22-34-68-43-40
Safety Statements: 26-36/37/39-45

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

Chemical Classes:Other Classes -> Organic Acids
Canonical SMILES:C=CCC(=O)O
Uses Vinylacetic acid used in the preparation of strained nitroso Diels-Aldrer adducts which undergo a domino ROC metathesis in the presence of Ru-carbene catalysts and olefins. It is used in the synthesis of polyethylene glycolated boltorn coatings. It was used to study the inhibition of the enzyme-catalyzed conversion of D-tyrosyl- phenylalanyl-glycine to D-tyrosyl-phenylaline amide by non-peptide carboxylic acids. 3-Butenoic acid was used in the synthesis of polyethylene glycolated boltorn coatings. It was used to study the inhibition of the enzyme-catalysed conversion of D-tyrosyl- phenylalanyl-glycine to D-tyrosyl-phenylaline amide by non-peptide carboxylic acids. It was used in preparation of strained nitroso Diels-Aldrer adducts which undergo a domino ROC metathesis in the presence of Ru-carbene catalysts and olefins.

Technology Process of 3-Butenoic acid

There total 74 articles about 3-Butenoic acid which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 95.0%

: 109-75-1
but-3-enenitrile

: 625-38-7
but-3-enoic acid

Guidance literature:: enzyme from Synechocystis sp. PCC 6803; In phosphate buffer; at 30 ℃; for 12h; pH=7.2;
DOI:10.1002/ejoc.200600699

Reference yield: 92.0%

: 2345-51-9
3-butynoic acid

: 625-38-7
but-3-enoic acid

Guidance literature:: With hydrogen; In ethanol; at 20 ℃; for 3h; under 760.051 Torr;
DOI:10.1021/acscatal.5b02518

Reference yield: 87.0%

: 5296-64-0
allyl phenyl thioether

: 124-38-9,18923-20-1
carbon dioxide

: 625-38-7
but-3-enoic acid

Guidance literature:: allyl phenyl thioether; With lithium; In diethyl ether; at 3 - 6 ℃; for 2h;

carbon dioxide;
DOI:10.1016/j.tetlet.2005.04.080