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172839

Sigma-Aldrich

2-十三烷酮

99%

同義詞:

甲基十一烷酮

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About This Item

線性公式:
CH3(CH2)10COCH3
CAS號碼:
分子量::
198.34
Beilstein:
1757402
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

化驗

99%

形狀

solid

折射率

n20/D 1.435 (lit.)

bp

134 °C/10 mmHg (lit.)
263 °C (lit.)

mp

24-27 °C (lit.)

密度

0.822 g/mL at 25 °C (lit.)

SMILES 字串

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 密鑰

CYIFVRUOHKNECG-UHFFFAOYSA-N

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一般說明

2-十三酮是从 竹叶花椒叶中所提取精油的一种成分。

應用

2-十三酮曾用于研究土壤改良剂对洋葱鳞茎的影响

象形圖

Environment

訊號詞

Warning

危險聲明

防範說明

危險分類

Aquatic Acute 1 - Aquatic Chronic 1

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 2

閃點(°F)

224.6 °F - closed cup

閃點(°C)

107 °C - closed cup

個人防護裝備

Eyeshields, Gloves


分析證明 (COA)

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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)
Yasumasa Shikichi et al.
Bioscience, biotechnology, and biochemistry, 76(2), 407-409 (2012-02-09)
(R)-10-Methyl-2-tridecanone, the female sex pheromone of the southern corn rootworm (Diabrotica undecimpunctata howardi Barber), was synthesized in 9 steps from methyl (S)-3-hydroxy-2-methylpropanoate in a 15.7% overall yield. Olefin cross metathesis between (R)-6-methyl-1-nonene and 5-hexen-2-one employing Grubbs' first-generation catalyst was the
N W Kimps et al.
Medical and veterinary entomology, 25(2), 202-208 (2010-11-16)
2-Tridecanone and 2-undecanone are both found naturally in the trichomes of wild tomato plants and are important in plant resistance to herbivory. 2-Undecanone is the U.S. Environmental Protection Agency (EPA)-registered active ingredient in the commercially available arthropod repellent, BioUD(®) .
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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