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205605

Sigma-Aldrich

1-Methylcyclopropanecarboxylic acid

98%

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About This Item

Linear Formula:
CH3C3H4CO2H
CAS Number:
6914-76-7
Molecular Weight:
100.12
Beilstein:
2039384
EC Number:
230-020-7
MDL number:
MFCD00001290
UNSPSC Code:
12352100
PubChem Substance ID:
24852211
NACRES:
NA.22

Assay

98%

form

solid

bp

183-185 °C (lit.)

mp

30-32 °C (lit.)

functional group

carboxylic acid

SMILES string

CC1(CC1)C(O)=O

InChI

1S/C5H8O2/c1-5(2-3-5)4(6)7/h2-3H2,1H3,(H,6,7)

InChI key

DIZKLZKLNKQFGB-UHFFFAOYSA-N

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Application

1-Methylcyclopropanecarboxylic acid was used in the structure-activity studies of small carboxylic acids (SCAs). It was also used in the identification of selective orthosteric ligands for both free fatty acid receptor 2 (FFA2) and free fatty acid receptor 3 (FFA3).

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

183.2 °F - closed cup

Flash Point(C)

84 °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.

JAN Code

205605-1G:
205605-BULK:
205605-50G:
205605-5G:
205605-VAR:

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Certificates of Analysis (COA)

Lot/Batch Number
BGBB7749
BGBC0020
BGBB2938V
BGBB2938
1434042

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Johannes Schmidt et al.
The Journal of biological chemistry, 286(12), 10628-10640 (2011-01-12)
Free fatty acid receptor 2 (FFA2; GPR43) is a G protein-coupled seven-transmembrane receptor for short-chain fatty acids (SCFAs) that is implicated in inflammatory and metabolic disorders. The SCFA propionate has close to optimal ligand efficiency for FFA2 and can hence
Brian D Hudson et al.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 26(12), 4951-4965 (2012-08-25)
When it is difficult to develop selective ligands within a family of related G-protein-coupled receptors (GPCRs), chemically engineered receptors activated solely by synthetic ligands (RASSLs) are useful alternatives for probing receptor function. In the present work, we explored whether a

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