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14422-78-7

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14422-78-7 Usage

Type

Chemical compound

Uses

Fluorescent labeling reagent for proteins and amino acids; detection and quantification of peptides and proteins in complex mixtures; studying protein-protein interactions, enzyme activity, and protein folding; development of sensors for detecting small molecules; analysis of environmental samples

Properties

Strong UV absorption; emits strong fluorescence

Precautions

Toxic and can be harmful if ingested or inhaled

Check Digit Verification of cas no

The CAS Registry Mumber 14422-78-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,4,2 and 2 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 14422-78:
(7*1)+(6*4)+(5*4)+(4*2)+(3*2)+(2*7)+(1*8)=87
87 % 10 = 7
So 14422-78-7 is a valid CAS Registry Number.

14422-78-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(diethylamino)naphthalene-1,4-dione

1.2 Other means of identification

Product number -
Other names 2-Diethylamino-1,4-naphthoquinone

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:14422-78-7 SDS

14422-78-7Relevant articles and documents

Naphthoquinone Colouring Matters. Part 6. Colour and Constitution of Electron Donor-substituted 2-Aryl- and 2-Vinyl-1,4-naphthoquinones.

Blackburn, Christopher,Griffiths, John

, p. 1556 - 1574 (2007/10/02)

The visible absorption spectroscopic properties of 2-aryl-1,4-naphthoquinones containing amino-groups in the 4'-position of the aryl ring or in the 3-position of the quinonoid ring, and also of the related 2-aminovinyl-1,4-naphthoquinones, are described.P

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