20633-13-0

Basic information

• Product Name: Nonylnitrate
• Synonyms: Nitric acid nonyl ester;Nonylnitrate
• CAS NO: 20633-13-0
• Molecular Formula: C₉H₁₉NO₃
• Molecular Weight: 189.25
• Mol File: 20633-13-0.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 233.6°C at 760 mmHg
• Flash Point: 76.9°C
• Appearance: /
• Density: 0.964g/cm³
• Vapor Pressure: 0.0843mmHg at 25°C
• Refractive Index: 1.437
• CAS DataBase Reference: Nonylnitrate(CAS DataBase Reference)
• NIST Chemistry Reference: Nonylnitrate(20633-13-0)
• EPA Substance Registry System: Nonylnitrate(20633-13-0)

Safety Data

• Hazardous Substances Data: 20633-13-0(Hazardous Substances Data)

Usage

Synthesis Reference(s)

Tetrahedron, 30, p. 2467, 1974 DOI: 10.1016/S0040-4020(01)97118-2

InChI:InChI=1/C9H19NO3/c1-2-3-4-5-6-7-8-9-13-10(11)12/h2-9H2,1H3

Upstream product

• 124-11-8 non-1-ene 
• 4282-42-2 1-iodononane 
• 693-58-3 1-Bromononane 
• 143-08-8 nonyl alcohol 

Downstream Products

• 143-08-8 nonyl alcohol 
• 4282-42-2 1-iodononane 

Relevant articles and documents

Practical catalytic nitration directly with commercial nitric acid for the preparation of aliphatic nitroesters

To pursue a sustainable and efficient approach for aliphatic nitroester preparation from alcohol, europium-triflate-catalyzed nitration, which directly uses commercial nitric acid, has been successfully developed. Gram scalability with operational ease showed its practicability.

Preparation of alkyl nitrates, nitrites, and thiocyanates from alcohols utilizing trichloroisocyanuric acid with triphenylphosphine

Alcohols in acetonitrile are converted into alkyl nitrates, nitrites, or thiocyanates by the action of triphenylphosphine and trichloroisocyanuric acid along with silver nitrate, silver nitrite, or sodium thiocyanate, respectively.

Electroorganic chemistry; 145: Coupling reaction of an olefin with a radical NO.3 generated by anodic oxidation of NO-3

When NO-3 is electrochemically oxidized in the presence of a variety of terminal and 1,2-disubstituted olefins 1 in a mixed solvent system (MeCN:H2O:Et2O = 10:2:1), a radical NO.3 is generated from NO-3 and nitrate esters 3 are formed by a new coupling reaction of the olefin with the radical. The products 3 can be further transformed into the corresponding alcohols 4 and alkyl iodides 5. Under the same reaction conditions, 1,1-di- and 1,1,2-trisubstituted olefins 6 do not give nitrate esters but afford oxazoline derivatives 7. (1S,5S)-(-)-β-Pinene (13) is diastereoselectively transformed into (1S,2R,5S)-(-)-myrtanol (14) by this technique.