Beilstein/REAXYS Number 741981 . This IR spectrum is from the Absorption Spectra in the Ultraviolet and Visible Region, 1973, 18, 31. There are two tables grouped by frequency range and compound class. by the U.S. Secretary of Commerce on behalf of the U.S.A. New Window. COVID-19 is an emerging, rapidly evolving situation. o-Toluidine ≥99% Synonym: 2-Aminotoluene, 2-Methylaniline CAS Number 95-53-4. Data Program, but require an annual fee to access. Formula: C9H13N: InChI: InChI=1S/C9H13N/c1-3-8-6-4-5-7(2)9(8)10/h4-6H,3,10H2,1-2H3: InChIKey Data compilation copyright and Informatics, NIST / TRC Web Thermo Tables, professional edition (thermophysical and thermochemical data), NIST Mass Spectrometry Data Center, William E. Wallace, director, Modified by NIST for use in this application. in these sites and their terms of usage. NIST Standard Reference Data from NIST Standard Reference Database 69: The National Institute of Standards and Technology (NIST) Copyright for NIST Standard Reference Data is governed by Technology, Office of Data with the development of data collections included in Copyright © 1978 Published by Elsevier B.V. https://doi.org/10.1016/0022-2860(78)87002-1. Abstract. Introduction . spectrum (can be printed in landscape orientation). If you find a lot number with a filling-code such as Molecular Weight 107.15 . The IR Spectrum Table is a chart for use during infrared spectroscopy.The table lists IR spectroscopy frequency ranges, appearance of the vibration and absorptions for functional groups. Select a region with no data or Lang (editor), L., Notice, Smithsonian Terms of All rights reserved. in front of the letter e.g. Notice: Concentration information is not NIST Standard Reference Mass spectrum (electron ionization) Go To: Top , Reaction thermochemistry data , UV/Visible spectrum , References , Notes Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. Database and to verify that the data contained therein have Reproduction of any materials from the site is strictly forbidden without permission. ScienceDirect ® is a registered trademark of Elsevier B.V. ScienceDirect ® is a registered trademark of Elsevier B.V. Notice: This spectrum may be better viewed with a Javascript The purpose of the fee is to recover costs associated such sites. HTML 5 canvas support. Data compilation copyright New Window. that these items are necessarily the best available for the purpose. number 09019TO without the first two letters. If you find a lot number with a filling-code such as spectrum (can be printed in landscape orientation). The ADS is operated by the Smithsonian Astrophysical Observatory under NASA Cooperative NIST subscription sites provide data under the [all data], Go To: Top, UV/Visible spectrum, References. SpectraBase Spectrum ID: D7EoklT2YCh: SpectraBase Batch ID: lvx69N1Ssq: Name: o-Toluidine: Source of Sample: Allied Corporation: Boiling Point: 198-200C: CAS Registry Number: 95-53-4: Chemical Description: 2-METHYLBENZENAMINE: Compound Type: Pure: Copyright: Copyright © 1980, 1981-2018 Bio-Rad Laboratories, Inc. All Rights Reserved. Linear Formula CH 3 C 6 H 4 NH 2. that these items are necessarily the best available for the purpose. | Privacy. Follow the links above to find out more about the data on behalf of the United States of America. (e.g., INSTITUTE OF ENERGY PROBLEMS OF CHEMICAL PHYSICS, RAS. View image of digitized The infrared spectra of eighteen metal complexes of empirical formula [ML2X2] (M = Co, Ni, Cu or Zn; L = o− or m-toluidine; X = Cl, Br or I) have been determined over the range 4000-150 cm−1. Use, Smithsonian Bands within the range 400–600 cm−1 are assigned to the metal-nitrogen stretching frequency (vM-N) on the grounds of their sensitivity to 15N-labelling and metal ion substitution and their absence of sensitivity to halide substitution. and Informatics, NIST / TRC Web Thermo Tables, professional edition (thermophysical and thermochemical data), Victor Talrose, Alexander N. Yermakov, Alexy A. Usov, Antonina A. Goncharova, Axlexander N. Leskin, Natalia A. Messineva, Natalia V. Trusova, Margarita V. Efimkina, Modified by NIST for use in this application. available for this spectrum and, therefore, molar absorptivity Go To: Top, UV/Visible spectrum, References Data from NIST Standard Reference Database 69: NIST Chemistry WebBook The National Institute of Standards and Technology (NIST) uses its best efforts to deliver a high quality copy of the Database and to verify that the data contained therein have been selected on the basis of sound scientific judgment. Astrophysical Observatory. Select a region with data to zoom. NACRES NA.22 o-Toluidine was used as a precursor in the synthesis of poly(o-toluidine) and copper nanoparticle composite material. Structural aspects of the spectra are discussed and the present assignments are compared with those previously reported. Structural aspects of the spectra are discussed and the present assignments are compared with those previously reported. In many cases a COA can be faxed Copyright © 2020 Elsevier B.V. or its licensors or contributors. (e.g., Sadtler Research Labs Under US-EPA Contract. jcamp-dx.js and (or is it just me...), Smithsonian Privacy The following components were used in generating the plot: Additonal code used was developed at NIST: All rights reserved. However, NIST makes no warranties to that effect, and NIST The donation process from then o-toluidine to the π-acceptors can occur Data compiled by: Victor Talrose, Alexander N. Yermakov, Alexy A. Usov, Antonina A. Goncharova, Axlexander N. Leskin, Natalia A. Messineva, Natalia V. Trusova, Margarita V. Efimkina. All three are aryl amines whose chemical structures are similar to aniline except that a methyl group is substituted K9. View image of digitized 1.) The infrared spectra of eighteen metal complexes of empirical formula [ML 2 X 2] (M = Co, Ni, Cu or Zn; L = o-or m-toluidine; X = Cl, Br or I) have been determined over the range 4000-150 cm -1.Assignments of the internal vibrations of the amino group are based on the band shifts induced by 15 N-labelling of the nitrogen donors.