23708-56-7

Basic information

• Product Name: 6-UNDECANOL
• Synonyms: UNDECANOL-6;6-UNDECANOL;DIAMYL CARBINOL;Di-n-amyl carbinol~Di-n-pentyl carbinol;undecan-6-ol;6-UNDECANOL 97%;6-Undecanol,97%;6-Hendecanol
• CAS NO: 23708-56-7
• Molecular Formula: C₁₁H₂₄O
• Molecular Weight: 172.31
• EINECS: 245-837-4
• Mol File: 23708-56-7.mol
• Article Data: 18

Chemical Properties

• Melting Point: 25-26°C
• Boiling Point: 117-118°C 16mm
• Flash Point: 60 °C
• Appearance: /
• Density: 0,83 g/cm3
• Vapor Pressure: 0.0132mmHg at 25°C
• Refractive Index: 1.4374
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: 15.58±0.20(Predicted)
• CAS DataBase Reference: 6-UNDECANOL(CAS DataBase Reference)
• NIST Chemistry Reference: 6-UNDECANOL(23708-56-7)
• EPA Substance Registry System: 6-UNDECANOL(23708-56-7)

Safety Data

• Safety Statements: 24/25
• RIDADR: 1993
• HazardClass: 3.2
• PackingGroup: III
• Hazardous Substances Data: 23708-56-7(Hazardous Substances Data)

Usage

General Description

6-Undecanol, also known as undecyl alcohol, is an organic compound with the chemical formula CH3(CH2)9CH2OH. It is classified as a long-chain primary alcohol and is derived from the hydrogenation of undecylenic acid. 6-Undecanol is a colorless liquid with a mild, fatty odor and is insoluble in water but soluble in most organic solvents. It is commonly used in the production of pharmaceuticals, perfumes, and cosmetics, as well as in the manufacture of plasticizers, lubricants, and surfactants. Additionally, it has applications in the synthesis of flavoring compounds and as a chemical intermediate in the production of other chemicals. Due to its low toxicity and favorable physical properties, 6-Undecanol is widely used in various industrial and commercial applications.

InChI:InChI=1/C11H24O/c1-3-5-7-9-11(12)10-8-6-4-2/h11-12H,3-10H2,1-2H3

Upstream product

• 927-49-1 dipentyl ketone 
• 73587-64-1 undec-4t-en-6-one 
• 64-17-5 ethanol 
• 110-53-2 1-Bromopentane 
• 109-94-4 formic acid ethyl ester 
• 142-61-0 Hexanoyl chloride 
• 64214-56-8 N-methoxy-N-methylhexanoamide 
• 142-62-1 hexanoic acid 
• 621-84-1 O-benzyl carbamate 
• 67-64-1 acetone 
• 71-36-3 butan-1-ol 
• 60045-12-7 tert-Butyl-dimethyl-(1-pentyl-hexyloxy)-silane 
• 543-59-9 1-Chloropentane 
• 66-25-1 hexanal 

Downstream Products

• 927-49-1 dipentyl ketone 
• 4941-53-1 5-undecene 
• 1051938-75-0 undec-6-yl benzoate 
• 5422-52-6 α-n-pentylheptanoic acid 
• 27610-92-0 2-butyloctanoic acid 
• 1315330-96-1 N,N'-bis(2,6-diisopropylphenyl)-1,7-bis(6-undecanoxy)perylene-3,4,9,10-tetracarboxylic diimide 
• 1315330-98-3 N-(2,6-diisopropylphenyl)-N'-{4-[2-methyl-5-(cyanoacrylic acid)-3-thienyl]-phenyl}-1,7-bis(6-undecanoxy)perylene-3,4,9,10-tetracarboxylic diimide 
• 1315330-97-2 N-(2,6-diisopropylphenyl)-1,7-bis(6-undecanoxy)perylene-3,4,9,10-tetracarboxylic 3,4-anhydride 9,10-imide 
• 1315331-00-0 N-(2,6-diisopropylphenyl)-N'-(3-carboxy-2-pyrazyl)-1,7-bis(6-undecanoxy)perylene-3,4,9,10-tetracarboxylic diimide 
• 1315330-99-4 N-(2,6-diisopropylphenyl)-N'-(3-carboxy-2-pyridil)-1,7-bis(6-undecanoxy)perylene-3,4,9,10-tetracarboxylic diimide 
• 1120-21-4 n-Undecane 
• 61405-58-1 sulfuric acid mono-(1-pentyl-hexylester); sodium-salt 
• 20351-26-2 6-chloro-undecane 
• 65633-70-7 2-[4-(4-Chloro-phenoxy)-phenoxy]-propionic acid 1-pentyl-hexyl ester 

Relevant articles and documents

METHOD FOR PRODUCING HIGHER LINEAR FATTY ACIDS OR ESTERS

The present invention relates to a method of producing linear fatty acids comprising 7 to 28 carbon atoms or esters thereof using a combined biotechnological and chemical method. In particular, the present invention relates to a method of producing dodecanoic acid (i.e. lauric acid), via higher alkanones, preferably 6-undecanone.

IONIZABLE CATIONIC LIPID FOR RNA DELIVERY

What is described is a compound of formula I consisting of a compound in which R1 is a branched chain alkyl consisting of 10 to 31 carbons; R2 is a linear alkyl, alkenyl, or alkynyl consisting of 2 to 20 carbons; L1 and L2 are the same or different, each a linear alkylene of 1 to 20 carbons or a linear alkenylene of 2 to 20 carbons; X1 is S or O; R3 is a linear or branched alkylene consisting of 1 to 6 carbons; and R4 and R5 are the same or different, each a hydrogen or a linear or branched alkyl consisting of 1 to 6 carbons; or a pharmaceutically acceptable salt thereof.

Stereoselective direct reductive amination of ketones with electron-deficient amines using Re2O7/NaPF6 catalyst

The first example of direct reductive amination (DRA) of ketones with electron-deficient amines (EDA) such as Cbz-, Boc-, EtOCO-, Fmoc-, Bz-, ArSO2-, etc. protected amines have been achieved using catalytic Re2O7/NaPF6. Excellent chemoselectivities as well as diastereoselectivity (for 2-alkyl cyclohexanones) were obtained. The Royal Society of Chemistry 2013.