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Benzenamine, 4-(1,1-dimethylethyl)-N-hydroxy-, also known as tert-butyl-N-hydroxybenzeneamine or hydroxylamine-O-tert-butylbenzene, is an organic compound with the chemical formula C10H15NO. It is a derivative of aniline, where a tert-butyl group (1,1-dimethylethyl) is attached to the para position of the benzene ring, and a hydroxylamine group (N-hydroxy) is present. Benzenamine, 4-(1,1-dimethylethyl)-N-hydroxy- is a colorless to pale yellow liquid with a molecular weight of 165.23 g/mol. It is used as a stabilizer and antioxidant in various industrial applications, particularly in the production of polymers and plastics, due to its ability to scavenge free radicals and prevent oxidative degradation. The compound is also known for its reactivity in chemical synthesis, often used as an intermediate in the preparation of other organic compounds.

13252-73-8

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13252-73-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13252-73-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,5 and 2 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 13252-73:
(7*1)+(6*3)+(5*2)+(4*5)+(3*2)+(2*7)+(1*3)=78
78 % 10 = 8
So 13252-73-8 is a valid CAS Registry Number.

13252-73-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-tert-butylphenyl)hydroxylamine

1.2 Other means of identification

Product number -
Other names 4-tert-Butylphenylhydroxylamin

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:13252-73-8 SDS

13252-73-8Upstream product

13252-73-8Relevant academic research and scientific papers

Integrating replication processes with mechanically interlocked molecular architectures

Vidonne, Annick,Philp, Douglas

, p. 8464 - 8475 (2008/12/22)

A kinetic model for the integration of self-replication with the formation of a mechanically interlocked molecular architecture, namely a rotaxane, is presented. The logical steps required to convert this model into molecular structures through consideration of the design criteria highlighted by the model are discussed and executed. Ultimately, despite careful design, the rotaxane synthesised did not replicate as expected. The reasons for this failure are traced by experiment and computation to the sub-optimal association constant for the pseudorotaxane complex required to form the replicating rotaxane. Additionally, a deleterious supramolecular steric effect, operating through the proximity of the macrocyclic component of the pseudorotaxane to the transition state for the stoppering reaction is identified computationally.

13C NMR studies of p-substituted nitrosobenzenes

Al-Tahou, Baheeja M.,Gowenlock, Brian G.

, p. 353 - 355 (2007/10/02)

The 13C NMR spectra of a wide range of monomeric para-substituted nitrosobenzenes have been determined end the results related to a wide range of published data for other para-disubstituted benzenes.It is shown that the nitroso substituent exercises a different pattern of effect for the 13C chemical shifts at the ipso C atom from at least twenty eight other substituents.It is noted that when the para substituent is a ?-donor, the nitroso group functions in a different manner from that operative when the para substituent is a ?-acceptor, a general possibility that has already been suggested in the recent literature.

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