4434-66-6

Basic information

• Product Name: 1-BROMONONADECANE
• Synonyms: 1-bromo-nonadecan;nonadecane,1-bromo-;NONADECYL BROMIDE;1-BROMONONADECANE
• CAS NO: 4434-66-6
• Molecular Formula: C₁₉H₃₉Br
• Molecular Weight: 347.42
• EINECS: 224-641-2
• Mol File: 4434-66-6.mol
• Article Data: 5

Chemical Properties

• Melting Point: 38-41 °C
• Boiling Point: 378.73°C (estimate)
• Flash Point: 155.7°C
• Appearance: /
• Density: 1.0129 (estimate)
• Vapor Pressure: 2.1E-05mmHg at 25°C
• Refractive Index: 1.4751 (estimate)
• BRN: 1703823
• CAS DataBase Reference: 1-BROMONONADECANE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-BROMONONADECANE(4434-66-6)
• EPA Substance Registry System: 1-BROMONONADECANE(4434-66-6)

Safety Data

• Safety Statements: 22-24/25
• WGK Germany: 3
• Hazardous Substances Data: 4434-66-6(Hazardous Substances Data)

Usage

General Description

1-Bromononadecane is a chemical compound with the molecular formula C10H21Br. It is a long-chain alkyl bromide, specifically a bromoalkane, which is commonly used in organic synthesis and as a chemical intermediate. It is a clear, colorless liquid with a slight odor, and it is insoluble in water but soluble in organic solvents such as ethanol and diethyl ether. 1-Bromononadecane has various industrial applications, including as a surfactant, lubricant, and dispersant. It is also used in the production of pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactivity and potential health hazards, 1-Bromononadecane should be handled with care and in accordance with safety guidelines and regulations.

InChI:InChI=1/C19H39Br/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20/h2-19H2,1H3

Upstream product

• 1454-84-8 nonadecan-1-ol 
• 629-04-9 1-Bromoheptane 
• 3344-77-2 12-bromododecanol 
• 646-30-0 nonadecanoic acid 
• 112-47-0 1,10-Decanediol 
• 53463-68-6 1-bromo-10-decanol 
• 51795-88-1 1-bromo-10-(tetrahydropyranyloxy)decane 

Downstream Products

• 55791-68-9 4-Nonadecylamino-benzoic acid ethyl ester 
• 55791-69-0 4-(n-nonadecylamino)benzoic acid 
• 593-50-0 melissyl alcohol 
• 1254966-90-9 5-(nonadecane-1-sulfonyl)-1-phenyl-1H-tetrazole 

Relevant articles and documents

The synthesis of single enantiomers of a meromycolic acid

3-Oxa-2,4-dioxobicyclo[3.1.0]hexane provides a flexible starting material for the preparation of single enantiomers of a meromycolic acid, a long chain fatty acid containing two remote cis-cyclopropanes. (C) 2000 Elsevier Science Ltd.

The synthesis of a single enantiomer of a major α-mycolic acid of M. tuberculosis

We report a synthesis of a single enantiomer of a mycolic acid from Mycobacterium tuberculosis containing a di-cis-cyclopropane. The method can be simply varied to modify the chain lengths or the absolute stereochemistry of either cyclopropane.

UNSATURATED ANALOGUES OF 1-TRIACONTANOL

A simple regio- and stereoselective synthesis of unsaturated analogues of the plant growth stimulator 1-triacontanol from ω-alkyn-1-ols is reported.Starting from the easily accessible 10-undecyn-1-ol, eight n-C30 alcohols containing , (E) -C=C- or (Z) -C=C- group in the position 21 and/or 10 have been prepared.Spectral and gas-chromatographic properties (Kovats retention indices) of the novel compounds are described.