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262536

Sigma-Aldrich

trans-3-Nonen-2-one

95%

Synonym(s):

(3E)-3-Nonen-2-one, (3E)-Non-3-en-2-one, (E)-3-Nonen-2-one

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About This Item

Linear Formula:
CH3(CH2)4CH=CHCOCH3
CAS Number:
18402-83-0
Molecular Weight:
140.22
MDL number:
MFCD00010241
UNSPSC Code:
12352100
PubChem Substance ID:
24855748
NACRES:
NA.22

Assay

95%

refractive index

n20/D 1.449 (lit.)

bp

85 °C/12 mmHg (lit.)

density

0.848 g/mL at 25 °C (lit.)

SMILES string

[H]\C(CCCCC)=C(\[H])C(C)=O

InChI

1S/C9H16O/c1-3-4-5-6-7-8-9(2)10/h7-8H,3-6H2,1-2H3/b8-7+

InChI key

HDKLIZDXVUCLHQ-BQYQJAHWSA-N

Application

trans-3-Nonen-2-one has been used:
  • as substrate to investigate steady-state kinetics of NADPH oxidation
  • in the preparation of azido quinolone

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

179.6 °F - closed cup

Flash Point(C)

82 °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’.

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Ryan A Dick et al.
The Journal of biological chemistry, 279(17), 17269-17277 (2004-02-18)
NADPH-dependent alkenal/one oxidoreductase (AOR) from the rat is a phase 2/antioxidative enzyme that is known to catalyze the reduction of the carbon-carbon double bond of alpha,beta-unsaturated aldehydes and ketones. It is also known for its leukotriene B(4) 12-hydroxydehydrogenase activity. In
Hajoong Lee et al.
The Journal of organic chemistry, 75(5), 1756-1759 (2010-02-10)
We describe the assembly of a 960-member library of tricyclic 2,3-dihydro-4-quinolones using a combination of solution-phase high-throughput organic synthesis and parallel chromatographic purification. The library was produced with high efficiency and complete chemo- and diastereoselectivity by diversification of an azide-bearing
Emiliano Ventura et al.
Food additives & contaminants. Part A, Chemistry, analysis, control, exposure & risk assessment, 37(8), 1253-1263 (2020-05-14)
Selective androgen receptor modulators (SARMs) are a class of new emerging "designer" steroid compounds gaining popularity over more well established anabolic-androgenic steroids (AAS) amongst both non-professional and elite athletes. Moreover, due to their anabolic activity, SARM compounds may also potentially
Emiliano Ventura et al.
Journal of chromatography. A, 1600, 183-196 (2019-05-06)
A semi-quantitative method was developed to monitor the misuse of 15 SARM compounds belonging to nine different families, in urine matrices from a range of species (equine, canine, human, bovine and murine). SARM residues were extracted from urine (200 μL) with

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