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Merck
CN

255653

trans-2-Nonenal

97%

Synonym(s):

(2E)-2-Nonenal, (2E)-Non-2-enal, (2E)-Nonen-1-al, (E)-2-Nonen-1-al, (E)-2-Nonenal, (E)-Non-2-enal, (E)-Nonen-1-al, 2-trans-Nonenal, trans-2-Nonen-1-al

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About This Item

Linear Formula:
CH3(CH2)5CH=CHCHO
CAS Number:
18829-56-6
Molecular Weight:
140.22
NACRES:
NA.22
PubChem Substance ID:
24855471
UNSPSC Code:
12352100
EC Number:
242-609-6
MDL number:
MFCD00007012

Key Documents

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Product Name

trans-2-Nonenal, 97%

InChI key

BSAIUMLZVGUGKX-BQYQJAHWSA-N

InChI

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

SMILES string

[H]C(=O)C(\[H])=C(/[H])CCCCCC

vapor density

>1 (vs air)

assay

97%

form

liquid

refractive index

n20/D 1.453 (lit.)

bp

88-90 °C/12 mmHg (lit.)

density

0.846 g/mL at 25 °C (lit.)

functional group

aldehyde

Quality Level

100

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pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk

WGK 2

flash_point_f

183.2 °F - closed cup

flash_point_c

84 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
MKCX0486
MKCS0175
MKCP7728
MKCL0482
MKCF4235

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T Galliard et al.
Biochimica et biophysica acta, 441(2), 181-192 (1976-08-23)
1. A particulate enzyme fraction and an acetone powder preparation from cucumber fruits cleaved 9- and 13-hydroperoxyoctadecadienoic acids to form volatile aldehydes and oxoacid fragments. 2. From the 9-hydroperoxide, the major volatile fragments were cis-3-nonenal and trans-2-nonenal using particulate enzyme
Jan Hubert et al.
Experimental & applied acarology, 44(4), 315-321 (2008-04-19)
The toxicities of three plant volatiles, (2E)-hexenal, (2E, 6Z)-nonadienal and (2E)-nonenal, intermediate products of the oxylipin biosynthesis pathway, were tested on three mites of importance for medical purposes and as pests. The aldehydes were diluted in hexane separately and incorporated
Caterina Fattorusso et al.
Bioorganic & medicinal chemistry, 19(1), 312-320 (2010-12-03)
In our search for new antimalarial agents inspired by natural products, we describe herein the synthesis, the evaluation of in vitro antiplasmodial activity, and the SAR studies for a series of endoperoxide antimalarials based on the plakortin scaffold. These simplified
Xiaochun Zhu et al.
Chemical research in toxicology, 22(8), 1386-1397 (2009-06-23)
Autoxidation of linoleic acid (LA) enhanced by Fe(II)/ascorbate generates unsaturated hydroperoxides which undergo further oxidative evolution resulting in a mixture of electrophiles, including epoxyketooctadecenoic acid and dienones with intact C-18 chains as well as oxidative cleavage products such as 4-hydroxy-2(E)-nonenal
A M Barron et al.
Endocrinology, 150(7), 3228-3236 (2009-03-14)
The benefits of estrogen replacement as a preventative treatment for Alzheimer's disease (AD) are subject to debate. Because the effects of estrogen depletion and replacement on accumulation of the neurotoxic beta-amyloid (A beta) peptide in transgenic animal models of AD
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