Welcome to LookChem.com Sign In|Join Free
  • or
2-Naphthalenol, 1-[(2-hydroxy-5-methylphenyl)azo]-, also known as 1-(2-hydroxy-5-methylphenylazo)-2-naphthol, is an organic compound with the chemical formula C17H14N2O2. It is a derivative of naphthalene, featuring an azo group (-N=N-) connecting a 2-naphthol moiety to a 2-hydroxy-5-methylphenyl group. This yellow crystalline solid is primarily used as a dye, specifically in the coloration of plastics, textiles, and leather. It is known for its good solubility in organic solvents and its ability to form stable colorations. The compound is also characterized by its melting point, which is around 180°C, and it is sensitive to light, which can lead to color changes over time. Due to its chemical structure, it is classified as a potentially hazardous substance and requires proper handling and disposal to minimize environmental and health risks.

4866-96-0

Post Buying Request

4866-96-0 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

4866-96-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4866-96-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,6 and 6 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4866-96:
(6*4)+(5*8)+(4*6)+(3*6)+(2*9)+(1*6)=130
130 % 10 = 0
So 4866-96-0 is a valid CAS Registry Number.

4866-96-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[(2-hydroxy-5-methylphenyl)hydrazinylidene]naphthalen-2-one

1.2 Other means of identification

Product number -
Other names 1-<2-Hydroxy-5-methyl-phenylazo>-2-hydroxy-naphthalin

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:4866-96-0 SDS

4866-96-0Downstream Products

4866-96-0Relevant academic research and scientific papers

An Azo Coupling Strategy for Protein 3-Nitrotyrosine Derivatization

Liu, Yuxin,Zhou, Pengcheng,Da, Honghong,Jia, Huiyi,Bai, Feifei,Hu, Guodong,Zhang, Baoxin,Fang, Jianguo

, p. 11228 - 11232 (2019)

Herein, a strategy for the selective derivatization of 3-nitrotyrosine-containing proteins using the classic azo coupling reaction as the key step is described. This novel approach featured multiple advantages and was successfully applied to detect picomole levels of protein tyrosine nitration in biological samples.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 4866-96-0