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Citronellal

$52

  • Brand : BIOFRON

  • Catalogue Number : BD-P0657

  • Specification : 96.0%(GC)

  • CAS number : 106-23-0

  • Formula : C10H18O

  • Molecular Weight : 154.253

  • Volume : 0.2ml

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Catalogue Number

BD-P0657

Analysis Method

HPLC,NMR,MS

Specification

96.0%(GC)

Storage

2-8°C

Molecular Weight

154.253

Appearance

liquid

Botanical Source

Structure Type

Monoterpenoids

Category

SMILES

Synonyms

IUPAC Name

Applications

Density

0.8±0.1 g/cm3

Solubility

Flash Point

75.6±0.0 °C

Boiling Point

208.4±9.0 °C at 760 mmHg

Melting Point

InChl

InChl Key

WGK Germany

RID/ADR

HS Code Reference

2912190000

Personal Projective Equipment

Correct Usage

For Reference Standard and R&D, Not for Human Use Directly.

Meta Tag

provides coniferyl ferulate(CAS#:106-23-0) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc. Articles of coniferyl ferulate are included as well.>> amp version: coniferyl ferulate

No Technical Documents Available For This Product.

PMID

31547401

Abstract

Methods

KEYWORDS

Rhododendron flowers; comprehensive two-dimensional gas chromatography-mass spectrometry; odor description; quadrupole time-of-flight mass spectrometry; volatile compounds.

Title

Characterization of Volatile Compounds in Four Different Rhododendron Flowers by GC×GC-QTOFMS

Author

Chen-Yu Qian 1 2, Wen-Xuan Quan 3, Zhang-Min Xiang 4, Chao-Chan Li 5

Publish date

2019 Sep 12;

PMID

31426453

Abstract

Since the 50’s, the massive and “environmental naïve” use of synthetic chemistry has revolutionized the farming community facing the dramatic growth of demography. However, nowadays, the controversy grows regarding the long-term harmful effects of these products on human health and the environment. In this context, the use of essential oils (EOs) could be an alternative to chemical products and a better understanding of their mode of biological action for new and optimal applications is of importance. Indeed, if the biocidal effects of some EOs or their components have been at least partly elucidated at the molecular level, very little is currently known regarding their mechanism of action as herbicides at the molecular level. Here, we showed that cinnamon and Java citronella essential oils and some of their main components, i.e.,, cinnamaldehyde (CIN), citronellal (CitA), and citronellol (CitO) could act as efficient herbicides when spread on A. thaliana leaves. The individual EO molecules are small amphiphiles, allowing for them to cross the mesh of cell wall and directly interact with the plant plasma membrane (PPM), which is one of the potential cellular targets of EOs. Hence, we investigated and characterized their interaction with biomimetic PPM while using an integrative biophysical approach. If CitO and CitA, maintaining a similar chemical structure, are able to interact with the model membranes without permeabilizing effect, CIN belonging to the phenylpropanoid family, is not. We suggested that different mechanisms of action for the two types of molecules can occur: while the monoterpenes could disturb the lipid organization and/or domain formation, the phenylpropanoid CIN could interact with membrane receptors.

KEYWORDS

Essential oils; plant plasma membrane; structure/activity relationships

Title

Insights into the Relationships Between Herbicide Activities, Molecular Structure and Membrane Interaction of Cinnamon and Citronella Essential Oils Components

Author

Laurence Lins 1, Simon Dal Maso 2, Berenice Foncoux 3, Anouar Kamili 3, Yoann Laurin 3, Manon Genva 4, M Haissam Jijakli 2, Caroline De Clerck 2, Marie Laure Fauconnier 4, Magali Deleu 3

Publish date

2019 Aug 16

PMID

31382590

Abstract

A chiral derivatizing agent (CDA) with the aldehyde function has been widely used in discriminating chiral amines because of the easy formation of imines under mild conditions. There is a preference for the use of cyclic aldehydes as a CDA since their lower conformational flexibility favors the differentiation of the diastereoisomeric derivatives. In this study, the imines obtained from the reaction between (S)-citronellal and the chiral amines (sec-butylamine, methylbenzylamine, and amphetamine) were analyzed by the nuclear Overhauser effect (NOE). Through NOE, it was possible to observe that the ends of the molecules were close, suggesting a quasi-folded conformation. This conformation was confirmed by theoretical calculations that indicated the London forces and the molecular orbitals as main justifications for this conformation. This conformational locking explains the good separation of 13C NMR signals between the diastereomeric imines obtained and, consequently, a good determination of the enantiomeric excess using the open chain (S)-citronellal as a CDA.

KEYWORDS

NMR; NOE; conformation; long-chain imine.

Title

An Explanation about the Use of ( S)-Citronellal as a Chiral Derivatizing Agent (CDA) in 1 H and 13 C NMR for Sec-Butylamine, Methylbenzylamine, and Amphetamine: A Theoretical-Experimental Study

Author

Viviani Nardini 1, Vinicius Palaretti 2, Luis Gustavo Dias 2, Gil Valdo Jose da Silva 2

Publish date

2019 Aug 3