4609-87-4

Basic information

• Product Name: 1-NITRODECANE
• Synonyms: 1-NITRODECANE;1-NITRODECANE 97%
• CAS NO: 4609-87-4
• Molecular Formula: C₁₀H₂₁NO₂
• Molecular Weight: 187.28
• Mol File: 4609-87-4.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 272.04°C (estimate)
• Flash Point: 95.2°C
• Appearance: /
• Density: 0.9085 (estimate)
• Vapor Pressure: 0.0239mmHg at 25°C
• Refractive Index: 1.4337
• CAS DataBase Reference: 1-NITRODECANE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-NITRODECANE(4609-87-4)
• EPA Substance Registry System: 1-NITRODECANE(4609-87-4)

Safety Data

• Hazardous Substances Data: 4609-87-4(Hazardous Substances Data)

Usage

Properties of 1-Nitrodecane

A chemical compound consisting of 10 carbon atoms, 21 hydrogen atoms, 1 nitrogen atom, and 2 oxygen atoms.

Organic Compound

Composed of elements such as carbon, hydrogen, and others, typically derived from living organisms or their products.

Nitro Group Attachment

A functional group consisting of an oxygen atom and a nitrogen atom (-NO2) attached to a hydrocarbon chain, which significantly influences the compound's properties.

Decane Chain

A 10-carbon alkane chain (C10H22) to which the nitro group is attached.

Synthetic Intermediate

Commonly used as a precursor in the synthesis of various chemicals and pharmaceuticals.

Colorless Liquid

A transparent liquid without any color.

Sweet Odor

A slightly pleasant and sweet smell, though not necessarily indicative of its safety.

Insolubility in Water

1-Nitrodecane does not dissolve or mix well with water.

Solubility in Organic Solvents

The compound dissolves easily in organic solvents, such as alcohols, ethers, and hydrocarbons.

Irritant

1-Nitrodecane can cause irritation to the eyes and skin upon contact.

Health Hazards

Exposure to high concentrations of 1-Nitrodecane can lead to harmful health effects.

Handling Precautions

It is important to handle 1-Nitrodecane with care, using proper personal protective equipment and in well-ventilated areas to minimize exposure and risks.

InChI:InChI=1/C10H21NO2/c1-2-3-4-5-6-7-8-9-10-11(12)13/h2-10H2,1H3

Upstream product

• 124-18-5 decane 
• 2050-77-3 Iododecane 
• 112-29-8 1-bromo dodecane 
• 2016-57-1 1-aminodecane 
• 68-12-2 N,N-dimethyl-formamide 
• 62103-13-3 1-azidodecane 
• 5509-08-0 decyl p-toluenesulfonate 

Downstream Products

• 1975-78-6 n-decanenitrile 
• 112-31-2 caprinaldehyde 
• 26228-72-8 N-decylhydroxyl-amine 
• 95421-85-5 (cis-4-nonyl-2-oxa-3-azabicyclo<3.2.0>hept-3-en-1-yl)diphenylphosphine oxide 
• 1144110-50-8 C₂₄H₃₃NO₆S₂ 
• 1402832-97-6 1-(p-chlorophenylthio)-1-nitrodecane 
• 2016-57-1 1-aminodecane 

Relevant articles and documents

Modular Regiospecific Synthesis of Nitrated Fatty Acids

Endogenous nitrated fatty acids are an important class of signaling molecules. Herein a modular route for the efficient and regiospecific preparation of nitrooleic acids as well as various analogues is described. The approach is based on a simple set of alkyl halides as common building blocks and a Henry reaction/Burgess dehydration sequence for the formation of the key nitroalkene moiety.

Sequential continuous flow processes for the oxidation of amines and azides by using HOF·MeCN

The generation and use of the highly potent oxidising agent HOF·MeCN in a controlled single continuous flow process is described. Oxidations of amines and azides to corresponding nitrated systems by using fluorine gas, water and acetonitrile by sequential gas-liquid/liquid-liquid continuous flow procedures are reported. Oxidation in flow: The oxidation of amines and azides to the corresponding nitrated systems by using fluorine gas, water and acetonitrile by sequential gas-liquid/liquid-liquid continuous flow procedures are reported. Copyright

Oxidation of azides by the HOF·CH3CN: A novel synthesis of nitro compounds

The HOF·CH3CN complex, readily prepared by passing F 2 through aqueous acetonitrile, is an exceptionally efficient oxygen transfer agent. It is unique in its capacity to oxidize various azides into the corresponding nitro derivatives. This method requires short reactions times and room temperature or below, and the desired nitro compounds were usually isolated in very good yields. The respective nitroso derivatives are believed to be the intermediates in this reaction. Functional groups such as aromatic rings, ketones, nitriles, halides, alcohols, and esters are tolerated. Sulfides react with HOF·CH3CN usually at the same rate as azides. Amines and olefins, however, react faster, so they have to be protected first. Nitro derivatives with various oxygen isotopes can be made using the labeled H 18OF·CH3CN. In the case of chiral azides the stereochemistry around the nitrogen-bonded carbons is retained.