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1-ISOPROPYL-3-P-TOLYLTRIAZENE, also known as IPT, is a chemical compound characterized by its molecular formula C10H14N4. It presents as a clear to light yellow liquid with a slightly aromatic scent. IPT is recognized for its role as a radical inhibitor and stabilizer in industrial applications, particularly in the production of rubber, plastics, paint, and coatings. Its functionality is attributed to its ability to scavenge free radicals and prevent chain reactions that could result in the degradation and instability of products. Moreover, IPT has garnered interest for its potential as a novel cancer therapy, given its capacity to inhibit tumor cell growth and induce apoptosis, although further research is required to explore its full medicinal potential.

50707-41-0

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50707-41-0 Usage

Uses

Used in Chemical Industry:
1-ISOPROPYL-3-P-TOLYLTRIAZENE is used as a radical inhibitor and stabilizer for its ability to scavenge free radicals and prevent chain reactions that can lead to the degradation and instability of rubber, plastics, paint, and coatings.
Used in Pharmaceutical Research:
1-ISOPROPYL-3-P-TOLYLTRIAZENE is studied as a potential novel therapy for cancer due to its capacity to inhibit tumor cell growth and induce apoptosis in cancer cells, although further research is necessary to fully understand its potential medicinal applications.

Check Digit Verification of cas no

The CAS Registry Mumber 50707-41-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,7,0 and 7 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 50707-41:
(7*5)+(6*0)+(5*7)+(4*0)+(3*7)+(2*4)+(1*1)=100
100 % 10 = 0
So 50707-41-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H15N3/c1-8(2)11-13-12-10-6-4-9(3)5-7-10/h4-8H,1-3H3,(H,11,12)

50707-41-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Isopropyl-3-<i>p</i>-tolyltriazene

1.2 Other means of identification

Product number -
Other names 1-Isopropyl-3-p-tolyltriazene

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:50707-41-0 SDS

50707-41-0Relevant academic research and scientific papers

Process for preparing mitomycin analogs

-

, (2008/06/13)

The present invention provides novel mitomycin analogs containing a disulfide group and processes for the preparation thereof. These compounds are mitomycin A analogs in which the 7-alkoxy group bears an organic substituent incorporating a disulfide group

STRUCTURAL EFFECT ON THE MECHANISTIC PATHWAY OF THE DECOMPOSITION OF 3-ALKYL-1-ARYLTRIAZENES: A KINETIC STUDY

Laila, Abdulhameed A. R.

, p. 453 - 456 (2007/10/02)

A kinetic study of the reaction between 3-alkyl-1-aryltriazenes and substituted acetic acids has been made in solvent acetone over the temperature range 21-37 deg C.Ea is 17.3 +/- 0.3 kcal mol-1 and log A is 10.3 +/- 0.1.Influence of the substituents on the reaction rate has been analyzed.The Hammett correlation with ? gave a ρ value of -0.96 for para-aryl substituted triazenes and +0.35 for meta- and para-substituted phenylacetic acid.The rate of decomposition of triazenes is also affected by changing the alkyl group.From these results a duality in mechanism is proposed; first, a simultaneous protonation and alkyl group expulsion to be the rate-determining step when R is tertiary, benzylic and possibly secondary.Secondly, a concerted mechanism for the protonation of nitrogen and cleavage of the N-R bond for primary alkyl groups.

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