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MilliporeSigma

W256102

Sigma-Aldrich

cis-3-hexenal solution

50% in triacetin, stabilized

Sinónimos:

Disolución de (Z)-3-hexenal

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About This Item

Fórmula lineal:
CH3CH2CH2CH=CHCHO
Número de CAS:
Peso molecular:
98.14
FEMA Number:
2561
Council of Europe no.:
2008
MDL number:
UNSPSC Code:
12164502
PubChem Substance ID:
Flavis number:
5.075
NACRES:
NA.21

biological source

synthetic

Quality Level

grade

Fragrance grade
Halal
Kosher

agency

follows IFRA guidelines

reg. compliance

EU Regulation 1223/2009
FDA 21 CFR 117

contains

α-tocopherol as stabilizer (synthetic)

concentration

50% in triacetin

refractive index

n20/D 1.44

bp

20 °C/0.2 mmHg

density

0.982 g/mL at 25 °C

application(s)

flavors and fragrances

documentation

see Safety & Documentation for available documents

food allergen

no known allergens

fragrance allergen

no known allergens

organoleptic

apple; fatty; green; fruity

storage temp.

2-8°C

SMILES string

CC\C=C/CC=O

InChI

1S/C6H10O/c1-2-3-4-5-6-7/h3-4,6H,2,5H2,1H3/b4-3-

InChI key

GXANMBISFKBPEX-ARJAWSKDSA-N

Application

La disolución de cis-3-hexenal puede utilizarse como patrón para identificar y cuantificar los compuestos orgánicos volátiles emitidos por las plantas heridas utilizando espectrometría de masas por ionización química.

Disclaimer

Para I+D y uso alimentario fuera de la UE. No para venta al por menor.

pictograms

FlameExclamation mark

signalword

Warning

hcodes

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 3

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

96.0 °F

flash_point_c

35.55 °C

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Gunda Thöming et al.
Journal of agricultural and food chemistry, 63(8), 2127-2136 (2015-02-13)
In herbivorous insects specialized on few plant species, attraction to host odor may be mediated by volatiles common to all host species, by specific compounds, or combinations of both. The pea moth Cydia nigricana is an important pest of the
Identification and Characterization of (3
Eleni A Spyropoulou et al.
Frontiers in plant science, 8, 1342-1342 (2017-08-22)
Marie Engelberth et al.
Plants (Basel, Switzerland), 8(6) (2019-06-20)
Green leaf volatiles (GLVs), which have mostly been described as providers of protection against insect herbivory and necrotrophic pathogen infections, were recently shown to provide significant fortification against cold stress damage. It was further demonstrated that cold-damaged maize seedlings released
Jurgen Engelberth et al.
Plants (Basel, Switzerland), 9(2) (2020-02-12)
Green leaf volatiles (GLVs) are commonly released by plants upon damage, thereby providing volatile signals for other plants to prepare against the major causes of damage, herbivory, pathogen infection, and cold stress. However, while the biosynthesis of these compounds is
Tatyana Savchenko et al.
Planta, 245(6), 1179-1192 (2017-03-18)
This study describes a new role for hydroperoxide lyase branch of oxylipin biosynthesis pathway in protecting photosynthetic apparatus under high light conditions. Lipid-derived signaling molecules, oxylipins, produced by a multi-branch pathway are central in regulation of a wide range of

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