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Phosphorous acid tris(2-nonylphenyl) ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

16784-72-8

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16784-72-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16784-72-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,7,8 and 4 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 16784-72:
(7*1)+(6*6)+(5*7)+(4*8)+(3*4)+(2*7)+(1*2)=138
138 % 10 = 8
So 16784-72-8 is a valid CAS Registry Number.

16784-72-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name tris(2-nonylphenyl) phosphite

1.2 Other means of identification

Product number -
Other names Tri(nonylated phenyl)phosphite

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:16784-72-8 SDS

16784-72-8Upstream product

16784-72-8Downstream Products

16784-72-8Relevant academic research and scientific papers

COUMESTAN-LIKE ANTIOXIDANTS AND UV ABSORBANTS

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, (2011/01/05)

The present invention relates to derivatives of the 1H-pyrano[4,3-b]benzofuran-1-one structure and their nitrogen analogues which possess powerful antioxidant properties combined with a highly effective UV absorbing functionality in one molecule. These compounds are especially useful in cosmetical and dermatological formulations.

Hydroxy-substituted N-alkoxy hindered amines and compositions stabilized therewith

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, (2008/06/13)

Hindered amines substituted on the N-atom with an hydroxy-substituted alkoxy moiety are particularly effective in stabilizing organic polymer compositions against the deleterious effects of oxidative, thermal and actinic radiation where the presence of the OH group on the compounds adds important properties not otherwise attainable.

Substituted 5-heteroaryl-2-(2-hydroxyphenyl)-2h-benzotriazole UV absorbers, a process for preparation thereof and compositions stabilized therewith

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, (2008/06/13)

Compounds of formula I or II where R is a heteroaryl moiety, such as 3-pyridyl, or T is a heteroaryl moiety, such as thien-2,5-diyl, and E1and E2are independently hydrogen, alkyl, aralkyl and the like, are prepared by reaction of a benzotriazole substituted on the 5-position of the benzo ring by a halogen atom with a heteroarylboronic acid or ester in the presence of a transition-metal catalyst, such as palladium (II) diacetate. The benzotriazole compounds of formula I are particularly efficacious as stabilizers for automotive coatings and candle wax.

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