1,2-EPOXYTETRADECANE

  • Name:1,2-EPOXYTETRADECANE
  • CAS:3234-28-4
  • Purity:99%
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Details

Top Quality 1,2-EPOXYTETRADECANE 3234-28-4 Hot Sell In Stock

  • Molecular Formula:C14H28 O
  • Molecular Weight:212.376
  • Vapor Pressure:0.00163mmHg at 25°C 
  • Melting Point:185-186 °C (decomp) 
  • Refractive Index:1.4408 
  • Boiling Point:303.9°Cat760mmHg 
  • Flash Point:99.3°C 
  • PSA:12.53000 
  • Density:0.86g/cm3 
  • LogP:4.69620 

1,2-EPOXYTETRADECANE(Cas 3234-28-4) Usage

Air & Water Reactions

1,2-EPOXYTETRADECANE is sensitive to exposure to moisture. Insoluble in water.

Reactivity Profile

1,2-EPOXYTETRADECANE, an epoxide, is incompatible with strong acids, caustics, and peroxides. . Epoxides are highly reactive. They polymerize in the presence of catalysts or when heated. These polymerization reactions can be violent. Compounds in this group react with acids, bases, and oxidizing and reducing agents. They react, possibly violently with water in the presence of acid and other catalysts.

Health Hazard

ACUTE/CHRONIC HAZARDS: 1,2-EPOXYTETRADECANE is a local irritant.

Fire Hazard

1,2-EPOXYTETRADECANE is probably combustible.

Flammability and Explosibility

Nonflammable

General Description

Clear colorless mobile liquid with an ether-like odor.

InChI:InChI=1/C14H28O/c1-2-3-4-5-6-7-8-9-10-11-12-14-13-15-14/h14H,2-13H2,1H3

3234-28-4 Relevant articles

Proton Switch in the Secondary Coordination Sphere to Control Catalytic Events at the Metal Center: Biomimetic Oxo Transfer Chemistry of Nickel Amidate Complex

Kim, Soohyung,Jeong, Ha Young,Kim, Seonghan,Kim, Hongsik,Lee, Sojeong,Cho, Jaeheung,Kim, Cheal,Lee, Dongwhan

supporting information, p. 4700 - 4708 (2021/02/12)

High-valent metal-oxo species are key in...

Enantioselective organocatalysis-based synthesis of 3-hydroxy fatty acids and fatty γ-lactones

Bourboula, Asimina,Limnios, Dimitris,Kokotou, Maroula G.,Mountanea, Olga G.,Kokotos, George

, (2019/06/10)

3-Hydroxy fatty acids have attracted the...

Dinuclear Iron(III) and Nickel(II) Complexes Containing N-(2-Pyridylmethyl)-N′-(2-hydroxyethyl)ethylenediamine: Catalytic Oxidation and Magnetic Properties

Jeong, Ah Rim,Shin, Jong Won,Jeong, Jong Hwa,Bok, Kwon Hee,Kim, Cheal,Jeong, Donghyun,Cho, Jaeheung,Hayami, Shinya,Min, Kil Sik

, p. 3023 - 3033 (2017/03/13)

Dinuclear FeIII and NiII complexes, [(ph...

Trinuclear nickel and cobalt complexes containing unsymmetrical tripodal tetradentate ligands: Syntheses, structural, magnetic, and catalytic properties

Shin, Jong Won,Jeong, Ah Rim,Lee, Sun Young,Kim, Cheal,Hayami, Shinya,Min, Kil Sik

, p. 14089 - 14100 (2016/11/06)

The coordination chemistries of the tetr...

3234-28-4 Process route

1-tetradecene
1120-36-1

1-tetradecene

1,2-epoxytetradecane
3234-28-4

1,2-epoxytetradecane

Conditions
Conditions Yield
With 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at 4 ℃; for 18h;
96%
With Ni(dmp)2; oxygen; isovaleraldehyde; In 1,2-dichloro-ethane; for 47h; under 760 Torr; Ambient temperature;
89%
With 3-chloro-benzenecarboperoxoic acid;
87%
With Ni(N-(2-pyridylmethyl)-N’-(2-hydroxyethyl)ethylenediamine)(N3)2; 3-chloro-benzenecarboperoxoic acid; In dichloromethane; acetonitrile; at 20 ℃; for 0.166667h;
43.1%
With [(N-(2-pyridylmethyl)iminodiethanol)2Co3(CH3COO)4]; 3-chloro-benzenecarboperoxoic acid; In dichloromethane; acetonitrile; at 20 ℃; for 0.166667h; Catalytic behavior;
34.3%
With [NiII(2-(di(pyridin-2-ylmethyl)amino)-N-(2-(5-methylpyridin-2-yl)phenyl)acetamidate)](ClO4); 3-chloro-benzenecarboperoxoic acid; In acetonitrile; at 25 ℃; for 0.166667h; Reagent/catalyst;
20.3%
With oxygen; bis(acetylacetonato)dioxidomolybdenum(VI); In 1,2-dichloro-benzene; at 110 ℃; for 8.2h; Further byproducts given. Yields of byproduct given;
46.3 % Chromat.
With 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at 25 ℃; for 48h;
87.9 g
With dihydrogen peroxide; n-tetradecanoic acid; at 25 ℃; for 24h; immobilised Candida antarctica lipase (comp. A and B);
85 % Chromat.
With Sal-Phe-Mn; oxygen; at 120 ℃; for 10h;
With dihydrogen peroxide;
With Novozym 435; dihydrogen peroxide; carbonic acid dimethyl ester; at 40 ℃; for 16h;
69 % Chromat.
Multi-step reaction with 2 steps
1.1: potassium ferricyanide; aq. K2CO3; potassium osmate / quinuclidine / 2-methyl-propan-2-ol / 72 h
1.2: 88 percent / aq. sodium sulfite / 2-methyl-propan-2-ol / 2 h
2.1: HBr / acetic acid / 0.5 h
2.2: 93 percent / K2CO3 / methanol / 2 h
With potassium osmate(VI); hydrogen bromide; potassium carbonate; potassium hexacyanoferrate(III); Quinuclidine; In acetic acid; tert-butyl alcohol;
With 3-chloro-benzenecarboperoxoic acid; In dichloromethane;
With peracetic acid; manganese(II) perchlorate; ammonium bicarbonate; In water; acetic acid; acetonitrile; at 20 ℃; for 0.666667h;
85 %Chromat.
With peracetic acid; C26H30F6MnN8O8S2; In dichloromethane; acetonitrile; at 0 ℃; for 0.55h;
With cobalt(II) perchlorate hexahydrate; 3-chloro-benzenecarboperoxoic acid; In acetonitrile; at 20 ℃; for 0.166667h;
With C60H46Co4F10N4O14S2; 3-chloro-benzenecarboperoxoic acid; In dichloromethane; acetonitrile; at 20 ℃; Catalytic behavior;
76.4 %Chromat.
tetradecane-1,2-diol
21129-09-9

tetradecane-1,2-diol

1,2-epoxytetradecane
3234-28-4

1,2-epoxytetradecane

Conditions
Conditions Yield
tetradecane-1,2-diol; With hydrogen bromide; In acetic acid; for 0.5h;
With potassium carbonate; In methanol; for 2h;
93%

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