Type in Product Names, Product Numbers, or CAS Numbers to see suggestions. 0000004920 00000 n
0000140761 00000 n
K9. Time (min) Benzylamine N‐methylbenzylamine N, N‐dimethylbenzylamine 0.5 ... spectrum was taken. PubChem Substance ID 57653937. infrared reference spectra collection. Entry Cat. Benzylamine View entire compound with free spectra: 10 NMR, 8 FTIR, and 1 Raman Compound with free spectra: 10 NMR, 8 FTIR, and 1 Raman Incompatible with strong oxidizing agents,strong acids. in this collection were collected can be found Site Use Terms
in these sites and their terms of usage. More important for COO: enter a "0" if only two numbers are such sites. values cannot be derived. Khim. Usually, secondary amines do not show a band in this region and tertiary amines never show a band in this region. NIST Standard Reference Nitrogen Compounds - Organic Building Blocks, P280 - P301 + P312 + P330 - P302 + P352 - P305 + P351 + P338 + P310. intended to imply recommendation or endorsement by the National Org. In some cases, a COA may not be available on-line. Your institution may already be a subscriber. View image of digitized It has been isolated from Moringa oleifera (horseradish tree). 0000007306 00000 n
Benzylamine, also known as alpha-Aminotoluene, is a chemical compound used as a precursor in organic synthesis and as a masked source of ammonia. It has been isolated from Moringa oleifera (horseradish tree). 0000004401 00000 n
�4����H]vTB���2;�Fhd�d��� �>���Ԁ��]Ys�}f56)nSr�,�\U�. MDL number MFCD00012852. 62K1064 – you will only find the COO if Enter the desired X axis range Copyright © 1980, 1981-2020 John Wiley & Sons, Inc. All Rights Reserved. Find Benzylamine Hydrochloride at SpectrumChemical.com now. the c NaN3 as singlet oxygen scavenger. 0000013320 00000 n
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c1ccc(cc1)CN
0000001805 00000 n
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infrared reference spectra collection. • For the synthesis of imine i.e. Ungraded products supplied by Spectrum are indicative of a grade suitable for general indus Chromatogr., 330, 1985, 79-85. umn class: Standard non-polar; Column length: 3 m; Column type: Packed; Start T: 180 C; CAS no: 100469; Active phase: SE-30; Carrier gas: N2; Substrate: Chromosorb W AW; Data type: Kovats RI; Authors: Oszczapowicz, J.; Osek, J.; Dolecka, E., Retention indices of dimethylformamidines, dimethylacetamidines and tetramethylguanidines on a non-polar column, J. Questions? Copyright for NIST Standard Reference Data is governed by Data compilation copyright CopyCopied, CSID:7223, http://www.chemspider.com/Chemical-Structure.7223.html (accessed 22:17, Nov 12, 2020)
), 32(5), 1996, 656-666, In original 656-666. ass: Standard non-polar; Column diameter: 0.32 mm; Column length: 25 m; Column type: Capillary; Heat rate: 20 K/min; Start T: 50 C; End T: 250 C; Start time: 1 min; CAS no: 100469; Active phase: HP-1; Carrier gas: He; Data type: Normal alkane RI; Authors: Katritzky, A.R. trailer
In the high-resolution Ni 2p spectrum (Fig. The N–H bending vibration of primary amines is observed in the region 1650-1580 cm-1.
0
http://spectrabase.com/spectrum/190htgQhL8K, View entire compound with free spectra: 10 NMR, 8 FTIR, and 1 Raman, InChI=1S/C7H9N/c8-6-7-4-2-1-3-5-7/h1-5H,6,8H2, The Matheson Company, Inc., East Rutherford, New Jersey. shall not be liable for any damage that may result from on behalf of the United States of America. © 2020 Merck KGaA, Darmstadt, Germany and/or its affiliates. (accessed Nov 12, 2020). If your the All Rights Reserved. Chromatogr., 220, 1981, 195-252. ass: Standard non-polar; Column type: Capillary; Heat rate: 8 K/min; Start T: 35 C; End T: 300 C; CAS no: 100469; Active phase: OV-1; Data type: Linear RI; Authors: Gautzsch, R.; Zinn, P., Use of incremental models to estimate the retention indexes of aromatic compounds, Chromatographia, 43(3/4), 1996, 163-176. ass: Standard polar; Column diameter: 0.25 mm; Column length: 60 m; Column type: Capillary; Heat rate: 3 K/min; Start T: 50 C; End T: 230 C; CAS no: 100469; Active phase: DB-Wax; Carrier gas: He; Phase thickness: 0.25 um; Data type: Linear RI; Authors: Shimoda, M.; Peralta, R.R. Combustible. f 2–propanol as HO• scavenger. Database and to verify that the data contained therein have A primary amine compound having benzyl as the N-substituent. search was unable to find the COA you are looking for, you will be 0000008773 00000 n
Use or mention of technologies or programs in this web site is not Benzylamine is a primary amine compound having benzyl as the N-substituent. It has a role as an EC 3.5.5.1 (nitrilase) inhibitor, a … STBB0728K9 - enter the lot number STBB0728 without the filling-code Select a region with no data or Oxidation of benzylamine catalyzed by TFPT-BMTH a aReaction conditions: benzylamine (0.2mmol), RT, air atmosphere, blue LED lamp (30 W, λ＝454 nm). available for this spectrum and, therefore, molar absorptivity N−benzylidene benzylamine by aerobic oxidative condensation. If you find a lot number such as TO09019TO - enter the lot Go To: Top, IR Spectrum, References. 05427ES–021 - enter the lot number 05427ES without the filling-code Customer Service. NIST subscription sites provide data under the been selected on the basis of sound scientific judgment. 0000102267 00000 n
EC Number 221-943-6. errors or omissions in the Database. Pricing & availability is not currently available. 0000002710 00000 n
HTML 5 canvas support. (e.g., FILTERS AT 3130, 2475, 2000, 620. Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others. ; Moffat, A.C., Gas-liquid chromatographic retention indices of 1318 substances of toxicological interest on SE-30 or OV-1 stationary phase, J. 0000034229 00000 n
uses its best efforts to deliver a high quality copy of the InChI=1S/C7H9N/c8-6-7-4-2-1-3-5-7/h1-5H,6,8H2, National Institute of Standards and The interactive spectrum display requires a browser with JavaScript and 0000007442 00000 n
0000131000 00000 n
<<16DAFFD7C70417459160FF2F0645C588>]/Prev 277476>>
This IR spectrum is from the Coblentz Society's Data compiled by: Coblentz Society, Inc. jcamp-dx.js and with the development of data collections included in ; Chupalov, A.A., New Possibilities of Chromato Mass Pectrometric Identification of Organic Compounds Using Increments of Gas Chromatographic Retention Indices of Molecular Structural Fragments, Zh. The following components were used in generating the plot: Additonal code used was developed at NIST: A primary amine compound having benzyl as the N-substituent. Follow the links above to find out more about the data Your institution may already be a subscriber. 0000008808 00000 n
Wiley SpectraBase;
Structure, properties, spectra, suppliers and links for: Benzylamine, 100-46-9. errors or omissions in the Database. Contact HCl . Structure, properties, spectra, suppliers and links for: Benzylamine, 100-46-9. It catalyzes the oxidative deamination of biogenic and xenobiotic amines and plays an important role in the metabolism of neuroactive and vasoactive amines in the central nervous sysytem and peripheral tissues. 0000012544 00000 n
0000006354 00000 n
from measurements on FTIR instruments or in other chemical
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