- Product Name 2-Tridecanone
- cas 593-08-8
- purity 99%
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
-
-
112-30-1
1-Decanol
-
-
67-64-1
acetone
-
-
593-08-8
tridecan-2-one
-
-
540-09-0
laurone
| 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%
|
-
-
59812-98-5,101186-18-9,112711-14-5,1653-31-2
tridecan-2-ol
-
-
593-08-8
tridecan-2-one
| 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
lauric acid
-
917-54-4
methyllithium
-
112-16-3
n-dodecanoyl chloride
-
1007476-32-5
sodium ethyl acetylacetate enolate
593-08-8 Downstream products
-
2801-87-8
4-methylpentadecane
-
59812-98-5
tridecan-2-ol
-
629-50-5
Tridecane
-
13205-57-7
1-methyl-dodecylamine