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579661

Sigma-Aldrich

Decanoic acid-10-13C

99 atom % 13C

Synonym(s):

Capric acid-10-13C

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About This Item

Linear Formula:
13CH3(CH2)8CO2H
CAS Number:
287111-32-4
Molecular Weight:
173.26
MDL number:
MFCD01075564
UNSPSC Code:
51113400
PubChem Substance ID:
329758381
Note: This product can be packaged on demand. For information on pricing, availability and packaging of custom sizes, please contact Stable Isotopes Customer Service

isotopic purity

99 atom % 13C

form

solid

bp

268-270 °C (lit.)

mp

30-32 °C (lit.)

density

0.898 g/mL at 25 °C

mass shift

M+1

SMILES string

[13CH3]CCCCCCCCC(O)=O

InChI

1S/C10H20O2/c1-2-3-4-5-6-7-8-9-10(11)12/h2-9H2,1H3,(H,11,12)/i1+1

InChI key

GHVNFZFCNZKVNT-OUBTZVSYSA-N

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1 of 4

This Item
488658587818616125
Decanoic acid-10-13C 99 atom % 13C

579661

Decanoic acid-10-13C

Decanoic acid-1-13C 99 atom % 13C

488658

Decanoic acid-1-13C

Decanoic acid-1,2-13C2 99 atom % 13C

587818

Decanoic acid-1,2-13C2

Decanoic-10,10,10-d3 acid 99 atom % D, 99% (CP)

616125

Decanoic-10,10,10-d3 acid

isotopic purity

99 atom % 13C

isotopic purity

99 atom % 13C

isotopic purity

99 atom % 13C

isotopic purity

99 atom % D

mass shift

M+1

mass shift

M+1

mass shift

M+2

mass shift

M+3

form

solid

form

solid

form

solid

form

solid

bp

268-270 °C (lit.)

bp

268-270 °C (lit.)

bp

268-270 °C (lit.)

bp

268-270 °C (lit.)

mp

30-32 °C (lit.)

mp

30-32 °C (lit.)

mp

30-32 °C (lit.)

mp

30-32 °C (lit.)

density

0.898 g/mL at 25 °C

density

0.898 g/mL at 25 °C

density

0.903 g/mL at 25 °C

density

0.908 g/mL at 25 °C

Packaging

This product may be available from bulk stock and can be packaged on demand. For information on pricing, availability and packaging, please contact Stable Isotopes Customer Service.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Aquatic Chronic 3 - Eye Irrit. 2 - Skin Irrit. 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

230.0 °F - closed cup

flash_point_c

110 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

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    EW0855

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    Suren Husinec et al.
    Organic letters, 13(9), 2286-2289 (2011-03-31)
    A base promoted cyclization of the protected N-propargylaminopyridines was shown to be an efficient method for the preparation of imidazo[1,2-a]pyridine derivatives. The reactions were carried out with a small excess of base, at room temperature or slightly above producing the
    Richard Ducray et al.
    Bioorganic & medicinal chemistry letters, 21(16), 4698-4701 (2011-07-22)
    We disclose a novel series of insulin-like growth factor-1 receptor kinase inhibitors based on the 3-(pyrimidin-4-yl)-imidazo[1,2-a]pyridine scaffold. The influence on the inhibitory activity of substitution on the imidazopyridine and at the C5 position of the pyrimidine is discussed. In the
    Ebrahim Kianmehr et al.
    Journal of combinatorial chemistry, 12(1), 41-44 (2009-11-13)
    A one-pot, three-component reaction between pyridine, phenacyl bromide, and thiocyanate is described. The reaction afforded the corresponding special type of fully substituted imidazo[1,2-a]pyridine derivatives in good yields without using any catalyst or activation.
    Richard Ducray et al.
    Bioorganic & medicinal chemistry letters, 21(16), 4702-4704 (2011-07-19)
    Following the discovery of imidazopyridine 1 as a potent IGF-1R tyrosine kinase inhibitor, the aniline part has been modified with the aim to optimize the properties of this series. The structure-activity relationships against IGF-1R kinase activity as well as inhibition
    Hongpeng Sun et al.
    The Journal of organic chemistry, 77(23), 10745-10751 (2012-11-22)
    An efficient tandem route to the synthesis of 3H-1,2a(1),3-triazaacenaphthylene derivatives of the cyclazine family has been developed. Target compounds were obtained in moderate to good yields by a Yb(OTf)(3)/Ag(2)CO(3)-catalyzed, three-component domino reaction. This in turn will set the stage for
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