69300-15-8

Basic information

• Product Name: 2-METHYLDECANONITRILE
• Synonyms: 2-methyl-decanenitril;2-Methyldecanenitrile;2-methyl-Decanenitrile;Decanenitrile,2-methyl-;FRUTONILE;2-METHYLDECANONITRILE;2-Methyldecannitril;2-Cyanodecane
• CAS NO: 69300-15-8
• Molecular Formula: C₁₁H₂₁N
• Molecular Weight: 167.29
• EINECS: 273-960-3
• Product Categories: Aliphatics
• Mol File: 69300-15-8.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 251℃
• Flash Point: 129℃
• Appearance: /
• Density: 0.820
• Vapor Pressure: 0.021mmHg at 25°C
• Refractive Index: 1.432
• Solubility: Dichloromethane, Hexanes
• CAS DataBase Reference: 2-METHYLDECANONITRILE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-METHYLDECANONITRILE(69300-15-8)
• EPA Substance Registry System: 2-METHYLDECANONITRILE(69300-15-8)

Safety Data

• Hazardous Substances Data: 69300-15-8(Hazardous Substances Data)

Usage

Uses

2-METHYLDECANONITRILE is used in the perfume composition.

InChI:InChI=1/C11H21N/c1-3-4-5-6-7-8-9-11(2)10-12/h11H,3-9H2,1-2H3

Upstream product

• 693-54-9 Decan-2-one 
• 143-33-9 sodium cyanide 
• 1720-38-3 1,9-decadiyne 
• 151-50-8 potassium cyanide 
• 598-56-1 N,N-dimethyl-ethanamine 
• 7309-46-8 methyl n-butylcyanoacetate 
• 111-83-1 1-bromo-octane 
• 107-12-0 propiononitrile 

Downstream Products

• 19009-56-4 2-methyldecanal 

Relevant articles and documents

Preparation method of alkyl nitrile compound

The invention discloses a preparation method of an alkyl nitrile compound. Specifically, the preparation method comprises the following step: in an organic solvent, in the presence of a protective gasand under the action of a catalyst, carrying out a reduction reaction as shown in the specification on olefin as shown in a formula I, a cyanation reagent and water, wherein the alkyl nitrile compound 1 is a compound II and/or a compound III. The preparation method provided by the invention is mild in condition, can realize hydrocyanation of olefin more safely and efficiently, and has good substrate universality and functional group compatibility.

Ketone precursors for organoleptic compounds

The invention discloses ketones of formula I: wherein, Y is an optionally substituted alkyl, cycloalkyl, or cycloalkylalkyl, wherein each alkyl group is straight or branched and each alkyl and cycloalkyl group is saturated or unsaturated; R1is hydrogen or a C1-6alkyl group that is substituted, saturated or unsaturated, straight or branched; A is a chromophoric substituted aromatic ring or ring system; n is an integer; and with the proviso that formula I is not 2-ethoxy-1-phenyl-ethanone. These compositions are useful for the delivery of organoleptic compounds, especially of flavors, fragrances, masking agents and antimicrobial compounds.

Hydrocyanation of α,ω-Diynes Catalyzed by Tetracyanonickelate. Regiospecific Synthesis of a New Series of Acyclic Dinitriles

Hydrocyanation of α,ω-diynes without the use of HCN has been described.Cyanonickelate, prepared by reducing 2- with NaBH4 or Zn in the presence of excess KCN in water or ethylene glycol, catalyzes hydrocyanation of α,ω-diynes, HCC(CH2)nCCH to give quantitatively CH3CH(CN)(CH2)nCH(CN)CH3, a new series of acyclic dinitriles.Importance of the preliminary formation of a (?-acetylene)nickel(0) complex for the hydrocyanation has been suggested.