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544000

Sigma-Aldrich

5-Hexynoic acid

97%

Synonym(s):

4-Ethynylbutyric acid, 5-Hexyn-1-oic acid

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About This Item

Linear Formula:
CH≡C(CH2)3CO2H
CAS Number:
Molecular Weight:
112.13
Beilstein:
1743192
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

97%

refractive index

n20/D 1.449 (lit.)

bp

224-225 °C (lit.)

density

1.016 g/mL at 25 °C (lit.)

SMILES string

OC(=O)CCCC#C

InChI

1S/C6H8O2/c1-2-3-4-5-6(7)8/h1H,3-5H2,(H,7,8)

InChI key

VPFMEXRVUOPYRG-UHFFFAOYSA-N

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General description

5-Hexynoic acid is an alkynoic acid. It undergoes gold-catalyzed cyclization to form the corresponding methylene lactones.

Application

5-Hexynoic acid may be used in the preparation of:
  • 5-hexynoic acid methyl ester
  • 5,6-dicarba-closo-dodecaboranyl hexynoic acid
  • 5,8,11-dodecatriynoic acid
  • 5-isocyanato-1-pentyne

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

230.0 °F - closed cup

Flash Point(C)

110 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 3 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

544000-VAR:
544000-5G:
544000-BULK:
544000-25G:


Certificates of Analysis (COA)

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Juan M Castro et al.
Scientific reports, 9(1), 165-165 (2019-01-19)
The self-reproduction of supramolecular assemblies based on the synthesis and self-assembly of building blocks is a critical step towards the construction of chemical systems with autonomous, adaptive, and propagation properties. In this report, we demonstrate that giant vesicles can grow
A mild access to ?-or ?-alkylidene lactones through gold catalysis.
Harkat H, et al.
Tetrahedron Letters, 47(35), 6273-6276 (2006)
Synthesis of a Tyr3-octreotate conjugated closo-carborane [HC2B10H10]: a potential compound for boron neutron capture therapy.
Schirrmacher E, et al.
Tetrahedron Letters, 44(51), 9143-9145 (2003)
Cobalt-catalyzed cocyclizations of isocyanato alkynes: a regiocontrolled entry into 5-indolizinones. Application to the total synthesis of camptothecin.
Earl RA and Vollhardt KPC.
Journal of the American Chemical Society, 105(23), 6991-6993 (1983)
Synthesis of 5, 8, 11-dodecatriynoic acid and its use in the synthesis of arachidonic acid and related acids.
Fryer RI, et al.
The Journal of Organic Chemistry, 40(3), 348-350 (1975)

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