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W281107

Sigma-Aldrich

Octyl octanoate

≥98%, FG

Synonym(s):

Octyl caprylate

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About This Item

Empirical Formula (Hill Notation):
C16H32O2
CAS Number:
2306-88-9
Molecular Weight:
256.42
FEMA Number:
2811
EC Number:
218-980-5
Council of Europe no.:
395
MDL number:
MFCD00129710
UNSPSC Code:
12164502
PubChem Substance ID:
24901190
Flavis number:
9.114
NACRES:
NA.21

biological source

synthetic

Quality Level

400

grade

FG
Kosher

Agency

meets purity specifications of JECFA

reg. compliance

EU Regulation 1334/2008 & 872/2012

Assay

≥98%

refractive index

n20/D 1.435 (lit.)

bp

307 °C (lit.)

mp

−18 °C (lit.)

density

0.859 g/mL at 25 °C (lit.)

application(s)

flavors and fragrances

Documentation

see Safety & Documentation for available documents

food allergen

no known allergens

Organoleptic

coconut; oily; fruity; sweet

SMILES string

CCCCCCCCOC(=O)CCCCCCC

InChI

1S/C16H32O2/c1-3-5-7-9-11-13-15-18-16(17)14-12-10-8-6-4-2/h3-15H2,1-2H3

InChI key

DJNTZVRUYMHBTD-UHFFFAOYSA-N

Related Categories

Storage Class Code

10 - Combustible liquids

WGK

nwg

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Seyed Mehdi Razavi et al.
Natural product research, 24(18), 1704-1709 (2009-07-17)
The hydrodistillated essential oils from leaves and fruits of Ecballium elaterium were analysed by GC-MS. Octyl octanoate (30.0%), 3-(6,6- dimethyl-5-oxohept-2-enyl)-cyclohexanone (20.4%) and hexahydro farnesyl acetone (19.1%) were the main components among 21 constituents characterised in the leaf oil. Twenty-one compounds
R A Stenning et al.
Bio/technology (Nature Publishing Company), 11(11), 1299-1301 (1993-11-01)
The distribution of water and the formation of microphases during the synthesis of octyl octanoate and the hydrolysis of triolein catalyzed by immobilized lipase have been directly monitored in real time using confocal laser microscopy.
Elinor M Lichtenberg et al.
Behavioral ecology and sociobiology, 65(4), 763-774 (2011-04-09)
Foragers can improve search efficiency, and ultimately fitness, by using social information: cues and signals produced by other animals that indicate food location or quality. Social information use has been well studied in predator-prey systems, but its functioning within a
Dirk Louis P Schorkopf et al.
Proceedings. Biological sciences, 274(1611), 895-898 (2007-01-26)
Stingless bees of the species Trigona spinipes (Fabricius 1793) use their saliva to lay scent trails communicating the location of profitable food sources. Extracts of the cephalic labial glands of the salivary system (not the mandibular glands, however) contain a
Mehdi Sabzichi et al.
Colloids and surfaces. B, Biointerfaces, 159, 620-628 (2017-09-03)
Drug delivery-based nanoparticles have been emerged to be an alternative and efficient approach to cancer therapy compared to conventional systems. Here, we investigated the role of all-trans retinoic acid (ATRA) formulated with precirol in increasing doxorubicin (Dox) induced apoptosis and
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