What is the FEMA 2763?

FEMA 2763 is colorless to pale yellow solid, while it's Molecular Formula is C14H28O. colorless to pale yellow solid A major component of the essential oil found in the leaves of Azadirachta indica.

What is the CAS number for FEMA 2763?

The CAS number of FEMA 2763 is 124-25-4.

What is FEMA 2763 (124-25-4) used for?

Myristaldehyde has a strong, fatty, orris-like odor with a sweet, fatty, “citrus-peel” flavor (diluted). Industrially prepared from the corresponding myristic acid.InChI:InChI=1/C11H20O2/c1-2-3-4-5-6-7-10-8-9-11(12)13-10/h10H,2-9H2,1H3/t10-/m0/s1

What is the FEMA 2763?

FEMA 2763 is colorless to pale yellow solid, while it's Molecular Formula is C14H28O. colorless to pale yellow solid A major component of the essential oil found in the leaves of Azadirachta indica.

What is the CAS number for FEMA 2763?

The CAS number of FEMA 2763 is 124-25-4.

What is FEMA 2763 (124-25-4) used for?

Myristaldehyde has a strong, fatty, orris-like odor with a sweet, fatty, “citrus-peel” flavor (diluted). Industrially prepared from the corresponding myristic acid.InChI:InChI=1/C11H20O2/c1-2-3-4-5-6-7-10-8-9-11(12)13-10/h10H,2-9H2,1H3/t10-/m0/s1

Pharmaceutical

Your Location:Home > Pharmaceutical > FEMA 2763

Product classification

FEMA 2763

CAS：124-25-4
purity：99%

Inquiry

Details

Buy Good Quality FEMA 2763 124-25-4 with a minimum purity of 99%

Molecular Formula: C14H28O
Molecular Weight: 212.376
Appearance/Colour: colorless to pale yellow solid
Vapor Pressure: 0.00271mmHg at 25°C
Melting Point: 23°C(lit.)
Refractive Index: 1.449
Boiling Point: 271.59 °C at 760 mmHg
Flash Point: 121.502 °C
PSA： 17.07000
Density: 0.827g/cm³
LogP: 4.88640

FEMA 2763(Cas 124-25-4) Usage

Preparation	Industrially prepared from the corresponding myristic acid
Synthesis Reference(s)	Canadian Journal of Chemistry, 46, p. 75, 1968 DOI: 10.1139/v68-013
Metabolism	See monograph on aldehyde C-8*
Chemical Structure	Tetradecane with two hydrogens attached to a terminal carbon replaced by an oxo group.
Definition	ChEBI: A long-chain fatty aldehyde that is tetradecane in which two hydrogens attached to a terminal carbon are replaced by an oxo group. It is found in coriander.
Taste threshold values	Taste characteristics at 10 ppm: fatty, lactonic, coconut, woody and fishy with a fruity nuance

InChI:InChI=1/C11H20O2/c1-2-3-4-5-6-7-10-8-9-11(12)13-10/h10H,2-9H2,1H3/t10-/m0/s1

124-25-4 Relevant articles

Long tailed cage amines: Synthesis, metal complexation, and structure

Dittrich, Birger,Harrowfield, Jack M.,Koutsantonis, George A.,Nealon, Gareth L.,Skelton, Brian W.

, p. 3433 - 3448 (2010)

The generation of amphiphiles derived fr...

Synthesis and preferred conformations of all regio- and diastereoisomeric methyl 2,3-fluorohydroxyalkanoates

Husstedt, Wibke S.,Wiehle, Susanne,Stillig, Christian,Bergander, Klaus,Grimme, Stefan,Haufe, Guenter

, p. 355 - 363 (2011)

Selective syntheses of enantiopure regio...

Flexible, polymer-supported synthesis of sphingosine derivatives provides ceramides with enhanced biological activity

El-Dahshan, Adeeb,Al-Gharabli, Samer I.,Radetzki, Silke,Al-Tel, Taleb H.,Kumar, Pradeep,Rademann, J?rg

, p. 5506 - 5512 (2014)

A polymer-supported route for the synthe...

Copper-Catalyzed Asymmetric Conjugate Additions of Bis(pinacolato)diboron and Dimethylzinc to Acyl- N-methylimidazole Michael Acceptors: A Highly Stereoselective Unified Strategy for 1,3,5,... n (OH, Me) Motif Synthesis

Lauberteaux, Jimmy,Crévisy, Christophe,Baslé, Olivier,De Figueiredo, Renata Marcia,Mauduit, Marc,Campagne, Jean-Marc

, p. 1872 - 1876 (2019)

A unified strategy for the construction ...

Protolichesterinic acid derivatives: α-Methylene-γ-lactones as potent dual activators of PPARγ and Nrf2 transcriptional factors

Le Lamer, Anne-Cécile,Authier, Hélène,Rouaud, Isabelle,Coste, Agnès,Boustie, Jo?l,Pipy, Bernard,Gouault, Nicolas

, p. 3819 - 3822 (2014)

PPARγ and Nrf2 are important transcripti...

Synthesis and characterization of a Ni nanoparticle stabilized on Ionic liquid-functionalized magnetic Silica nanoparticles for tandem oxidative reaction of primary alcohols

Hosseinzadeh-Khanmiri, Rahim,Kamel, Yaser,Keshvari, Zahra,Mobaraki, Ahmad,Shahverdizadeh, Gholam Hossein,Vessally, Esmail,Babazadeh, Mirzaagha

, (2018)

In this research, preparation of the mag...

Oxidation of long-chain alcohols to aldehydes by the dipyridine chromic anhydride complex

Valicenti,Holman

, p. 389 - 392 (1976)

The oxidation of alcohols by the dipyrid...

-

Beard,C.D. et al.

, p. 7944 - 7949 (1974)

Selectivity control in oxidation of 1-tetradecanol on supported nano Au catalysts

Martínez-González,Ivanova, Svetlana,Domínguez, María I.,Cortés Corberán

, p. 113 - 119 (2016)

Selective oxidation of tetradecanol, a m...

Chiral geminal disilyl alkane compound, synthesis method and applications thereof

-

Paragraph 0204; 0205; 0206; 0207; 0209, (2019/01/14)

The present invention discloses a chiral...

Racemic gem disilyl alkane compound containing four silicon-hydrogen bonds, and sybthesis method and application of compound

-

Paragraph 0263-0268; 0269, (2019/05/15)

The invention discloses a racemic gem di...

Total Synthesis of the Proposed Structure of Mycobactin J

Ghosh, Chiranjit,Pal, Sujit,Patel, Akanksha,Kapur, Manmohan

supporting information, p. 6511 - 6515 (2018/10/20)

The total synthesis of the proposed stru...

124-25-4 Process route

: 112-72-1
1-Tetradecanol

: 124-25-4,511542-15-7
myristylaldehyde

: 3234-85-3
myristic acid tetradecyl ester

Conditions

Conditions	Yield
With oxygen; In n-heptane; at 80 ℃; for 6h; under 750.075 Torr; Temperature; Solvent; Green chemistry;

: 112-72-1
1-Tetradecanol

: 124-25-4,511542-15-7
myristylaldehyde

: 3234-85-3
myristic acid tetradecyl ester

: 544-63-8
n-tetradecanoic acid