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Cyclohexadecanol, also known as cyclohexadecan-1-ol or 1-cyclohexadecanol, is a cyclic alcohol with the molecular formula C16H32O. It is a colorless to pale yellow liquid with a characteristic odor. This organic compound consists of a cyclohexane ring fused to a decyl chain, making it a member of the cycloalkanol family. Cyclohexadecanol is used in various applications, including as a fragrance ingredient in perfumes and as a chemical intermediate in the synthesis of other compounds. It is also known for its potential use as a biofuel additive and as a component in the production of lubricants and surfactants. Due to its complex structure, cyclohexadecanol exhibits unique chemical properties and reactivity, making it an interesting subject for research and development in the field of organic chemistry.

2565-90-4

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2565-90-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2565-90-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,6 and 5 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2565-90:
(6*2)+(5*5)+(4*6)+(3*5)+(2*9)+(1*0)=94
94 % 10 = 4
So 2565-90-4 is a valid CAS Registry Number.

2565-90-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name epoxy-cyclohexadecane

1.2 Other means of identification

Product number -
Other names Cyclohexadecanol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2565-90-4 SDS

2565-90-4Downstream Products

2565-90-4Relevant academic research and scientific papers

Macrocyclic Side-Chain Monomers for Photoinduced ATRP: Synthesis and Properties versus Long-Chain Linear Isomers

Barbon, Stephanie M.,Rolland, Manon,Anastasaki, Athina,Truong, Nghia P.,Schulze, Morgan W.,Bates, Christopher M.,Hawker, Craig J.

, p. 6901 - 6910 (2018)

The photoinduced atom transfer radical polymerization of traditionally challenging hydrophobic monomers (lauryl C12, stearyl C18, and docosyl C22-acrylate) and novel cyclic isomers (C12, C16, and C17) is reported. By the judicious selection of commercially available solvents and catalytic systems, polymers with a high degree of control over dispersity (D ≈ 1.1) and end-group fidelity were obtained over a wide range of molecular weights. This level of control provides access to unique hydrophobic materials (random, block, and homopolymers) with significant differences in properties observed due to the isomeric form of the hydrocarbon side chain (macrocyclic versus linear).

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