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172839

2-Tridecanone

Name: 2-Tridecanone
Brand: ALDRICH

99%

Synonym(s):

Methyl undecyl ketone

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About This Item

Linear Formula:

CH₃(CH₂)₁₀COCH₃

CAS Number:

593-08-8

Molecular Weight:

198.34

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24850421

EC Number:

209-784-0

Beilstein/REAXYS Number:

1757402

MDL number:

MFCD00008968

Assay:

99%

Form:

solid

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Properties

Quality Level

100

assay

99%

form

solid

refractive index

n20/D 1.435 (lit.)

bp

134 °C/10 mmHg (lit.), 263 °C (lit.)

mp

24-27 °C (lit.)

density

0.822 g/mL at 25 °C (lit.)

functional group

ketone

SMILES string

CCCCCCCCCCCC(C)=O

InChI

1S/C13H26O/c1-3-4-5-6-7-8-9-10-11-12-13(2)14/h3-12H2,1-2H3

InChI key

CYIFVRUOHKNECG-UHFFFAOYSA-N

Description

General description

2-Tridecanone is a component of the essential oil obtained from the leaves of Zanthoxylum alatum.

Application

2-Tridecanone was used to study the impact of soil amendments in onion bulbs.

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pictograms

GHS09

signalword

Warning

hcodes

H410

pcodes

P273 - P391 - P501

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1

Storage Class

11 - Combustible Solids

wgk

WGK 2

flash_point_f

224.6 °F - closed cup

flash_point_c

107 °C - closed cup

ppe

Eyeshields, Gloves

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Antioxidant and antimicrobial properties of the essential oil and extracts of Zanthoxylum alatum grown in north-western Himalaya.

Sanjay Guleria et al.

TheScientificWorldJournal, 2013, 790580-790580 (2013-06-20)

The essential oil obtained from the fresh leaves of Zanthoxylum alatum was analysed by gas chromatography/mass spectrometry (GC/MS). Fourteen components were identified, and linalool (30.58%), 2-decanone (20.85%), β -fenchol (9.43%), 2-tridecanone (8.86%), β -phellandrene (5.99%), Sabinene (4.82%), and α -pinene

Persistence of 2-tridecanone on the leaves of seven vegetables.

G F Antonious

Bulletin of environmental contamination and toxicology, 73(6), 1086-1093 (2005-01-28)

Fatty acid elongation in the biosynthesis of (Z)-10-heptadecen-2-one and 2-tridecanone in ejaculatory bulb microsomes of Drosophila buzzatii.

P J Skiba et al.

Insect biochemistry and molecular biology, 24(8), 847-853 (1994-09-01)

A fatty acid chain elongation process is involved in incorporation of saturated and unsaturated fatty acyl-CoA esters into 2-tridecanone and (Z)-10-heptadecen-2-one by Drosophila buzzatii. The microsomal fraction from mature male ejaculatory bulbs is chain-length specific and requires malonyl-CoA (or acetyl-CoA

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Global Trade Item Number

SKU	GTIN
172839-25G	04061838346490