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Nonacosan-1-ol, also known as 1-Nonacosanol, is a long-chain fatty alcohol with the chemical formula C29H60O. It is a white, waxy solid with a melting point of approximately 76-77°C. nonacosan-1-ol is a member of the aliphatic alcohols family and consists of a 29-carbon straight chain with a hydroxyl group at one end. Nonacosan-1-ol is found in various natural sources, such as beeswax and some plant waxes, and is used in the synthesis of various chemicals, including surfactants, lubricants, and emulsifiers. Due to its high molecular weight and unique properties, it has potential applications in the pharmaceutical, cosmetic, and chemical industries.

6624-76-6

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6624-76-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6624-76-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,2 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6624-76:
(6*6)+(5*6)+(4*2)+(3*4)+(2*7)+(1*6)=106
106 % 10 = 6
So 6624-76-6 is a valid CAS Registry Number.

6624-76-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Nonacosanol

1.2 Other means of identification

Product number -
Other names 1-Nonacosanol

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:6624-76-6 SDS

6624-76-6Downstream Products

6624-76-6Relevant academic research and scientific papers

Anti-inflammatory and ulcerogenic activity of newer phytoisolates of Swertia alata C.B. Clarke

Bajaj, Sakshi,Wakode, Sharad,Kaur, Avneet,Fuloria, Shivkanya,Fuloria, Neeraj

, p. 5055 - 5065 (2021)

The present study was intended to evaluate the in?vitro (COX-1/COX-2) and in?vivo anti-inflammatory and ulcerogenic activity of newer phytoconstituents isolated from the aerial parts of Swertia alata C.B. Clarke (Gentianaceae). For isolation of newer phyt

A New Synthesis of Long Chain Acid Esters and Carbinols

Rao, S. Jagadishwar,Bhalerao, U. T.,Tilak, B. D.

, p. 208 - 211 (2007/10/02)

A versatile synthesis of difficulty accessible long chain acid esters and carbinols is described.The synthesis involves acylations at 2- and 5-positions of thiophene.Thioketalation of the resulting ketoesters followed by Raney nickel desulfurization yield acid esters which on LAH reduction give the corresponding carbinols.

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