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Merck

W309311

Sigma-Aldrich

2-Undecanone

greener alternative

natural, FCC, FG

Sinónimos:

Methyl nonyl ketone

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About This Item

Fórmula lineal:
CH3(CH2)8COCH3
Número de CAS:
Peso molecular:
170.29
FEMA Number:
3093
Beilstein/REAXYS Number:
1749573
EC Number:
Council of Europe no.:
150c
MDL number:
UNSPSC Code:
12164502
PubChem Substance ID:
Flavis number:
7.016
NACRES:
NA.21

grade

FG
Halal
Kosher
natural

Quality Level

agency

meets purity specifications of JECFA

reg. compliance

EU Regulation 1334/2008 & 178/2002
FCC
FDA 21 CFR 172.515

vapor density

5.9 (vs air)

vapor pressure

<1 mmHg ( 20 °C)

greener alternative product characteristics

Less Hazardous Chemical Syntheses
Use of Renewable Feedstocks
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

refractive index

n20/D 1.43 (lit.)

bp

231-232 °C (lit.)

mp

11-13 °C (lit.)

density

0.825 g/mL at 25 °C (lit.)

application(s)

flavors and fragrances

documentation

see Safety & Documentation for available documents

food allergen

no known allergens

greener alternative category

organoleptic

fatty; waxy; fruity

SMILES string

CCCCCCCCCC(C)=O

InChI

1S/C11H22O/c1-3-4-5-6-7-8-9-10-11(2)12/h3-10H2,1-2H3

InChI key

KYWIYKKSMDLRDC-UHFFFAOYSA-N

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General description

2-Undecanone occurs naturally in wild tomato. It is also found in Ruta chalepensis essential oil and hop oil. Due to its insect repellant activity, 2-undecanone is being considered as a natural non-toxic alternative to N,N-diethyl-3-methylbenzamide or DEET.
We are committed to bringing you greener alternative products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product is Biobased and thus aligns with "Less Hazardous Chemical Syntheses" and "Use of Renewable Feedstocks".

Application

  • Larvicididal Activity of Natural Repellents Against the Dengue Vector, Aedes aegypti: This paper details the use of natural compounds like 2-Undecanone as effective larvicidal agents against vectors of significant human diseases, showcasing their role in developing non-toxic, eco-friendly insect control solutions (Zhang et al., 2020).

  • Control of Filth Flies, Cochliomyia macellaria (Diptera: Calliphoridae), Musca domestica (Diptera: Muscidae), and Sarcophaga bullata (Diptera: Sarcophagidae), Using Novel Plant-Derived Methyl Ketones: Investigates the efficacy of 2-Undecanone in managing common pest flies, underlining its potential as a biopesticide and organic solvent in public health and safety applications (Deguenon et al., 2019).

Biochem/physiol Actions

Taste: @ 10 ppm.

pictograms

Environment

signalword

Warning

hcodes

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1

Storage Class

10 - Combustible liquids

wgk_germany

WGK 2

flash_point_f

192.2 °F - closed cup

flash_point_c

89 °C - closed cup

ppe

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)


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Visite la Librería de documentos

2?Undecanone, a constituent of the glandular trichomes of Lycopersicon hirsutum f. glabratum: Effects on Heliothis zea and Manduca sexta growth and survival.
Farrar RR & Kennedy GG.
Entomologia Experimentalis et Applicata, 43(1), 17-23 (1987)
Constituents of the essential oil of Ruta chalepensis L. from Turkey.
Baser KHC, et al.
J. Essent. Oil Res., 8(4), 413-414 (1996)
Novel arthropod repellent, BioUD, is an efficacious alternative to deet.
Witting-Bissinger BE, et al.
Journal of Medical Entomology, 45(5), 891-898 (2008)
Release characteristics of the non-toxic insect repellant 2-undecanone from its crystalline inclusion compound with ?-cyclodextrin.
Whang HS & Tonelli A.
Journal of Inclusion Phenomena and Macrocyclic Chemistry, 62(1-2), 127-134 (2008)
George F Antonious et al.
Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes, 50(9), 667-673 (2015-06-17)
Glandular trichomes on the leaves of wild tomato, Lycopersicon hirsutum f. hirsutum Mull, also known as Solanum habrochaites (Solanaceae) synthesize and accumulate high levels of methyl ketones (MKs). The potential of using MKs as alternatives to synthetic acaricides for controlling

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