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255653

trans-2-Nonenal

Name: <I>trans</I>-2-Nonenal
Brand: ALDRICH

95%

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

Assay:

95%

Form:

liquid

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Properties

vapor density

>1 (vs air)

Quality Level

100

assay

95%

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

SMILES string

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

InChI

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

InChI key

BSAIUMLZVGUGKX-BQYQJAHWSA-N

Description

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pictograms

GHS07

signalword

Warning

hcodes

H315,H319,H335

pcodes

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

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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Antimalarials based on the dioxane scaffold of plakortin. A concise synthesis and SAR studies.

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

The formation of cis-3-nonenal, trans-2-nonenal and hexanal from linoleic acid hydroperoxide isomers by a hydroperoxide cleavage enzyme system in cucumber (Cucumis sativus) fruits.

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

Evaluation of the toxicity of stress-related aldehydes to photosynthesis in chloroplasts.

Jun'ichi Mano et al.

Planta, 230(4), 639-648 (2009-07-07)

Aldehydes produced under various environmental stresses can cause cellular injury in plants, but their toxicology in photosynthesis has been scarcely investigated. We here evaluated their effects on photosynthetic reactions in chloroplasts isolated from Spinacia oleracea L. leaves. Aldehydes that are

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