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Cycloheptadecanol is a cyclic alcohol with the molecular formula C17H36O. It is a colorless to pale yellow liquid with a floral, green, and woody odor. This organic compound is composed of a 17-carbon cyclic structure with a hydroxyl group attached to one of the carbon atoms. Cycloheptadecanol is used in the fragrance industry as a fixative and scent enhancer, and it can be found in various perfumes, cosmetics, and personal care products. It is also used as a flavoring agent in food and beverages, imparting a creamy, floral, and woody taste. The compound is synthesized through various chemical processes, and its stability and low volatility make it a valuable component in the creation of long-lasting fragrances and flavors.

4429-77-0

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4429-77-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4429-77-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,2 and 9 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4429-77:
(6*4)+(5*4)+(4*2)+(3*9)+(2*7)+(1*7)=100
100 % 10 = 0
So 4429-77-0 is a valid CAS Registry Number.
InChI:InChI=1/C17H34O/c18-17-15-13-11-9-7-5-3-1-2-4-6-8-10-12-14-16-17/h17-18H,1-16H2

4429-77-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name cycloheptadecanol

1.2 Other means of identification

Product number -
Other names Civetol,dihydro

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:4429-77-0 SDS

4429-77-0Relevant 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 (2018/09/12)

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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