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293393

Hexanoamide

98%

Synonym(s):

Caproamide

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About This Item

Linear Formula:
CH3(CH2)4CONH2
CAS Number:
628-02-4
Molecular Weight:
115.17
NACRES:
NA.22
PubChem Substance ID:
24857654
UNSPSC Code:
12352100
EC Number:
211-024-8
MDL number:
MFCD00008046
Assay:
98%
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assay

98%

mp

100-102 °C (lit.)

functional group

amide

SMILES string

CCCCCC(N)=O

InChI

1S/C6H13NO/c1-2-3-4-5-6(7)8/h2-5H2,1H3,(H2,7,8)

InChI key

ALBYIUDWACNRRB-UHFFFAOYSA-N

General description

Hexanoamide is the most rapidly hydrolysed substrate for amidase from Aspergillus nidulans. Zirconium mediated conversion of hexanoamide to hexanenitrile has been reported.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
MKCJ7230
11128AD
23523JS
13416HB
09421DI

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Jianfei Zheng et al.
Bioconjugate chemistry, 19(6), 1227-1234 (2008-05-30)
Molecular conjugates of hormone receptor-ligands with molecular probes or functional domains are finding diverse applications in chemical biology. Whereas many examples of hormone conjugates that target steroid hormone receptors have been reported, practical ligand conjugates that target the nuclear thyroid
Alexandra Thomas et al.
Cancers, 12(8) (2020-08-23)
Pancreatic cancer remains a recalcitrant neoplasm associated with chemoresistance and high fatality. Because it is frequently resistant to apoptosis, exploiting autophagic cell death could offer a new treatment approach. We repurpose echinomycin, an antibiotic encapsulated within a syndecan-1 actively targeted
Aliphatic and enantioselective amidases: from hydrolysis to acyl transfer activity.
D Fournand et al.
Journal of applied microbiology, 91(3), 381-393 (2001-09-15)
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Global Trade Item Number

SKUGTIN
293393-1G04061826072042