Skip to Content
Merck
CN
All Photos(1)

Documents

W361305

Sigma-Aldrich

ε-Decalactone

≥99%

Synonym(s):

7-Butyl-2-oxepanone

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C10H18O2
CAS Number:
5579-78-2
Molecular Weight:
170.25
FEMA Number:
3613
EC Number:
226-963-9
MDL number:
MFCD00209538
UNSPSC Code:
12164502
PubChem Substance ID:
24901809
Flavis number:
10.029
NACRES:
NA.21

biological source

synthetic

Quality Level

400

Agency

meets purity specifications of JECFA

Assay

≥99%

refractive index

n20/D 1.461 (lit.)

bp

117 °C/3 mmHg (lit.)

density

0.976 g/mL at 25 °C (lit.)

application(s)

flavors and fragrances

Organoleptic

coconut; creamy; sweet

SMILES string

CCCCC1CCCCC(=O)O1

InChI

1S/C10H18O2/c1-2-3-6-9-7-4-5-8-10(11)12-9/h9H,2-8H2,1H3

InChI key

YKVIWISPFDZYOW-UHFFFAOYSA-N

Related Categories

Disclaimer

For R&D or non-EU Food use. Not for retail sale.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

WGK

WGK 2

Flash Point(F)

closed cup

Flash Point(C)

closed cup

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

M Furukawa et al.
Biochemical and biophysical research communications, 199(1), 41-45 (1994-02-28)
Lipase from Pseudomonas cepacia was modified with 2,4-bis[O-methoxypoly(ethylene glycol)]-6-chloro-s-triazine, activated PEG2, to form PEG-lipase. The PEG-lipase is soluble and active in organic solvents. It catalyzes alcoholysis of racemic epsilon-decalactone with ethanol in 1,1,1-trichloroethane to form (R)-hydroxydecanoic acid ethyl ester. No
K Juni et al.
Critical reviews in therapeutic drug carrier systems, 3(3), 209-232 (1987-01-01)
Poly(hydroxy acids) so far have been examined for use in drug delivery in limited number, while the advantageous use of the polymers has been recognized due to their biodegradability and biocompatibility. Homo- and copolymers of lactic acid and glycolic acid

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service