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Merck
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Key Documents

M2265

Sigma-Aldrich

1-Octanoyl-rac-glycerol

≥99%

Synonyme(s) :

Glyceryl 1-monooctanoate, 1-Capryloyl-rac-glycerol, Monocaprylin

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About This Item

Formule empirique (notation de Hill):
C11H22O4
Numéro CAS:
Poids moléculaire :
218.29
Numéro MDL:
Code UNSPSC :
12352211
ID de substance PubChem :
Nomenclature NACRES :
NA.25

Niveau de qualité

Pureté

≥99%

Forme

powder

Groupe fonctionnel

ester

Type de lipide

neutral glycerides

Conditions d'expédition

ambient

Température de stockage

−20°C

Chaîne SMILES 

CCCCCCCC(=O)OCC(O)CO

InChI

1S/C11H22O4/c1-2-3-4-5-6-7-11(14)15-9-10(13)8-12/h10,12-13H,2-9H2,1H3

Clé InChI

GHBFNMLVSPCDGN-UHFFFAOYSA-N

Application


  • Molecular Simulations and Markov State Modeling of Quorum Sensing Regulators: Research revealed the inactive form of the quorum sensing regulator SdiA in Escherichia coli, offering insights into bacterial communication mechanisms that could be influenced by lipid-based signaling molecules such as 1-Octanoyl-rac-glycerol (Grabski et al., 2021).

Actions biochimiques/physiologiques

Monocaprylin (1-octanoyl-rac-glycerol) is used as an antimicrobial monoglycerin with potential to treat bacteria D congolensis and campylobacter infections and to inactivate E. coli, Listeria and Salmonella on biosurfaces.

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, type N95 (US)


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