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2-Tridecanone

  • Product Name 2-Tridecanone
  • cas 593-08-8
  • purity 99%
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Buy cost-effective 99% pure 2-Tridecanone 593-08-8 now

  • Molecular Formula: C13H26O
  • Molecular Weight: 198.349
  • Appearance/Colour: white to slightly yellow crystalline solid 
  • Melting Point: 24-27 °C(lit.) 
  • Refractive Index: n20/D 1.435(lit.)  
  • Boiling Point: 263.839 °C at 760 mmHg 
  • Flash Point: 83.293 °C 
  • PSA: 17.07000 
  • Density: 0.826 g/cm3 
  • LogP: 4.49630 

2-Tridecanone(Cas 593-08-8) Usage

Preparation

By heating a mixture of lauric acid and acetic acid over thorium oxide at 450°C.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

Ketones, such as 2-Tridecanone, are reactive with many acids and bases liberating heat and flammable gases (e.g., H2). The amount of heat may be sufficient to start a fire in the unreacted portion of the ketone. Ketones react with reducing agents such as hydrides, alkali metals, and nitrides to produce flammable gas (H2) and heat. Ketones are incompatible with isocyanates, aldehydes, cyanides, peroxides, and anhydrides. They react violently with aldehydes, HNO3, HNO3 + H2O2, and HClO4.

Fire Hazard

2-Tridecanone is combustible.

Definition

ChEBI: A methyl ketone that is tridecane in which the methylene hydrogens at position 2 are replaced by an oxo group.

Taste threshold values

Taste characteristics at 10 ppm: fatty and earthy with a fatty mouthfeel and with a dairy, ketonic, waxy, creamy, cheesy, dairy and coconut.

General Description

White crystalline solid.

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

593-08-8 Relevant articles

REVERSIBLE PROTONATION OF A VINYL SELENIDE DURING ITS ACID CATALYZED HYDROLYSIS

Piquard, J. L.,Hevesi, L.

, p. 1901 - 1902 (1980)

Partially reversible protonation is show...

-

Seebach,D. et al.

, p. 3509 - 3512 (1973)

-

Oxidative Cleavage of Alkenes by O2with a Non-Heme Manganese Catalyst

Bennett, Elliot L.,Brookfield, Adam,Guan, Renpeng,Huang, Zhiliang,Mcinnes, Eric J. L.,Robertson, Craig M.,Shanmugam, Muralidharan,Xiao, Jianliang

supporting information, p. 10005 - 10013 (2021/07/19)

The oxidative cleavage of C═C double bon...

Highly productive α-alkylation of ketones with alcohols mediated by an Ir-oxalamidato/solid base catalyst system

Maeda, Hironori,Nara, Hideki,Shimizu, Hideo

supporting information, p. 2772 - 2779 (2020/12/29)

An Ir-oxalamidato complex in combination...

Mild Deprotection of Dithioacetals by TMSCl/NaI Association in CH3CN

Yao, Yunxin,Zhao, Guangkuan,Hamze, Abdallah,Alami, Mouad,Provot, Olivier

, p. 5775 - 5779 (2020/08/17)

A mild process using a combination of TM...

Nickel/Photoredox-Catalyzed Methylation of (Hetero)aryl Chlorides Using Trimethyl Orthoformate as a Methyl Radical Source

Kariofillis, Stavros K.,Shields, Benjamin J.,Tekle-Smith, Makeda A.,Zacuto, Michael J.,Doyle, Abigail G.

supporting information, p. 7683 - 7689 (2020/04/22)

Methylation of organohalides represents ...

593-08-8 Process route

1-Decanol
112-30-1

1-Decanol

acetone
67-64-1

acetone

tridecan-2-one
593-08-8

tridecan-2-one

laurone
540-09-0

laurone

Conditions
Conditions Yield
With [Cp*2Ir2(μ-N,N′-bis(5-tert-butyl-4-hydroxy-2-methylphenyl)oxalamidato)Cl2]; calcium hydroxide; at 120 ℃; for 15h; under 2250.23 Torr; Autoclave; Inert atmosphere;
84%
tridecan-2-ol
59812-98-5,101186-18-9,112711-14-5,1653-31-2

tridecan-2-ol

tridecan-2-one
593-08-8

tridecan-2-one

Conditions
Conditions Yield
With Iron(III) nitrate nonahydrate; 2,2,6,6-tetramethyl-piperidine-N-oxyl; oxygen; sodium chloride; In 1,2-dichloro-ethane; at 25 ℃; for 21h; under 760.051 Torr;
99%
With Iodine monochloride; caesium carbonate; In dichloromethane; at 0 - 20 ℃; for 3h; Green chemistry;
91%
With chromium(VI) oxide; In acetone;

593-08-8 Upstream products

  • 143-07-7
    143-07-7

    lauric acid

  • 917-54-4
    917-54-4

    methyllithium

  • 112-16-3
    112-16-3

    n-dodecanoyl chloride

  • 1007476-32-5
    1007476-32-5

    sodium ethyl acetylacetate enolate

593-08-8 Downstream products

  • 2801-87-8
    2801-87-8

    4-methylpentadecane

  • 59812-98-5
    59812-98-5

    tridecan-2-ol

  • 629-50-5
    629-50-5

    Tridecane

  • 13205-57-7
    13205-57-7

    1-methyl-dodecylamine

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