hexamethylenediamine mass spectrum

05427ES–021 - enter the lot number 05427ES without the filling-code If your The molecule is a diamine, consisting of a hexamethylene hydrocarbon chain terminated with amine functional groups. Mass spectral interpretation is the method employed to identify the chemical formula, characteristic fragment patterns and possible fragment ions from the mass spectra. Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others. The diamine also serves as a cross-linking agent in epoxy resins. NIST Standard Reference CopyCopied, NAQMVNRVTILPCV-UHFFFAOYSA-N [4][7] Nonetheless, like other basic amines, it can cause serious burns and severe irritation. on behalf of the United States of America. Hexamethylenediamine was first reported by Theodor Curtius. -021. The great majority of the diamine is consumed by the production of nylon 66 via condensation with adipic acid. A C6 alkane-alpha,omega-diamine. Korksäure", "SRIC Report - Report 31C - Advances in Adiponitrile (ADN) and Hexamethylenediamine (HMDA) Processes | IHS Markit", https://en.wikipedia.org/w/index.php?title=Hexamethylenediamine&oldid=988879466, Articles with changed ChemSpider identifier, Articles with changed DrugBank identifier, Pages using collapsible list with both background and text-align in titlestyle, Articles containing unverified chemical infoboxes, Creative Commons Attribution-ShareAlike License, 39 to 42 °C (102 to 108 °F; 312 to 315 K), This page was last edited on 15 November 2020, at 20:14. Please login to see your pricing and orders. Hexamethylenediamine is moderately toxic, with LD50 of 792–1127 mg/kg. PubChem Substance ID 24895434. But this isn't produced by the same ion as the same m/z value peak in pentane. IR Spectrum; Mass spectrum (electron ionization) Options: Switch to calorie-based units; Data at NIST subscription sites: NIST / TRC Web Thermo Tables, professional edition (thermophysical and thermochemical data) NIST subscription sites provide data under the NIST Standard Reference Data Program, but require an annual fee to access. Technology, Office of Data 39-42 °C, 312-315 °K, 102-108 °F. This MassBank Record with Accession JP003998 contains the MS mass spectrum of 'HEXAMETHYLENEDIAMINE' with the InChIKey 'NAQMVNRVTILPCV-UHFFFAOYSA-N'. shall not be liable for any damage that may result from The mass spectrum of dodecane on the right illustrates the behavior of an unbranched alkane. This MassBank Record with Accession JP003998 contains the MS mass spectrum of 'HEXAMETHYLENEDIAMINE'. STBB0728K9 - enter the lot number STBB0728 without the filling-code The great majority of the diamine is consumed by the production of nylon 66 via condensation with adipic acid. Using the chemical formula of a single isotope you can get the exact mass and the relative abundance percentage of that isotope. Solubility in Water. Combustible. Contact | Privacy. Data from NIST Standard Reference Database 69: The National Institute of Standards and Technology (NIST) Consequently, the radical cation character of the molecular ion (m/z = 170) is delocalized over all the covalent bonds. Hexamethylenediamine is the organic compound with the formula H2N(CH2)6NH2. These other products include 1,2-Cyclohexanediamine, hexamethyleneimine, and the triamine bis(hexamethylenetriamine). Density. CopyCopied, InChI=1S/C6H16N2/c7-5-3-1-2-4-6-8/h1-8H2 If you find a lot number with a filling-code such as If you find a lot number such as TO09019TO - enter the lot It is commonly used for the identification of organic compounds from electron ionization mass spectrometry. Data compiled by: Coblentz Society, Inc. K9. If you remember, the m/z = 57 peak in pentane was produced by [CH 3 CH 2 CH 2 CH 2] +. Pricing & availability is not currently available. Since there are no heteroatoms in this molecule, there are no non-bonding valence shell electrons. The mass spectrum of pentan-3-one. presented with a COA Request form. Exact Mass: 116.13100: Molecular Weight: 116.20500: PSA: 52.04000: LogP: 1.86480 In some cases, a COA may not be available on-line. Site Use Terms CopyCopied, CSID:13835579, http://www.chemspider.com/Chemical-Structure.13835579.html (accessed 06:59, Nov 25, 2020) 0.84 g/mL −1. Melting Point. © 2020  Merck KGaA, Darmstadt, Germany and/or its affiliates. NIST subscription sites provide data under the More important for COO: enter a "0" if only two numbers are such sites. Spectrum solutions u ...(More). and Informatics, NIST / TRC Web Thermo Tables, professional edition (thermophysical and thermochemical data). uses its best efforts to deliver a high quality copy of the All rights reserved. Hexamethylenediamine 98% Synonym: 1,6-Diaminohexane, 1,6-Hexanediamine, HMDA CAS Number 124-09-4. Mass Spectrometry; Metal Catalysts for Organic Synthesis; Monofunctional & alpha,omega-Bifunctional Alkanes; Nucleosides, Nucleotides & Related Reagents; Oxidation; Peptide Synthesis Reagents; Phase-Transfer Catalysts; Phenylpropanoids & Aromatic Polyketides; Polyamines; Polymerization Initiators; Reagents for Electrophoresis Korksäure", "SRIC Report - Report 31C - Advances in Adiponitrile (ADN) and Hexamethylenediamine (HMDA) Processes | IHS Markit", https://en.wikipedia.org/w/index.php?title=Hexamethylenediamine&oldid=988879466, Creative Commons Attribution-ShareAlike License, 39 to 42 °C (102 to 108 °F; 312 to 315 K), This page was last edited on 15 November 2020, at 20:14. This process operates without ammonia and at lower pressure and temperature.[4]. However, NIST makes no warranties to that effect, and NIST 205 °C, 477.7 °K, 400 °F. Follow the links above to find out more about the data Boiling Point. The yield is good, but commercially significant side products are generated by virtue of reactivity of partially hydrogenated intermediates. About 1 billion kilograms are produced annually.[4]. Type in Product Names, Product Numbers, or CAS Numbers to see suggestions. 1,6-Hexanediamine, 70 Percent Solution in Water, also known as hexamethylenediamine, is used for the production of polymers which takes advantage of its bifunctional structure. 1,6-Diaminohexane, Go To: Top, References, Notes Data compilation copyrightby the U.S. Secretary of Commerce on behalf of the U.S.A.All rights reserved. 1,6-Hexanediamine, Reagent, also known as hexamethylenediamine, is used for the production of polymers which takes advantage of its bifunctional structure and its cross-linking properties. Customer Service, Synonym: Where appropriate, many finished products are traceable to NIST Standard Reference Materials. Corrosive/Harmful/Irritant/Hygroscopic/Store under Argon, DANGER: CORROSIVE, burns skin, eyes, and lungs. All Rights Reserved. Standard Reference Data Act. Hexamethylenediamine is used almost exclusively for the production of polymers, an application that takes advantage of its structure. National Institute of Standards and Manufacturing, quality control testing, and packaging are all performed in Spectrum's own facilities. Hexamethylenediamine is stable in air but combustible. Nitrogen Compounds - Organic Building Blocks, P260 - P280 - P301 + P312 + P330 - P303 + P361 + P353 - P305 + P351 + P338. to you upon submission of this form. Structure, properties, spectra, suppliers and links for: 1,6-HEXANEDIAMINE, Hexamethylenediamine, 124-09-4. Except where otherwise noted, data are given for materials in their. MDL number MFCD00008243. It can be used as a:• Reactant for the synthesis of dialkyl hexamethylene-1,6-dicarbamate with alkyl carbamate in the presence of various metal catalysts via the transesterification reaction.• Surface modifier for chlorinated and fluorinated nanodiamond synthesized by detonation.• Reactant with adipic acid for the synthesis of nylon 6-6 by polycondensation. The Reag ...(More), 1,6-Hexanediamine, 70 Percent Solution in Water, also known as hexamethylenediamine, is used for the production of polymers which takes advantage of its bifunctional structure. This time the base peak (the tallest peak - and so the commonest fragment ion) is at m/z = 57. The diamine also serves as a cross-linking agent in epoxy resins. Plot a mass spectrum given a list of peak masses and intensities with this online tool. Hexamethylenediamine is used almost exclusively for the production of polymers, an application that takes advantage of its structure. Hexamethylenediamine is stable in air but combustible. the Reaction mass of 7-azatridecane-1,13-diamine and hexamethylenediamine EC Number: 907-605-7 CAS Number: 68815-47-4 Molecular formula: C6H16N2 (HMD) C12H29N3 (BHT) IUPAC Name: Reaction mass of 7-azatridecane-1,13-diamine and hexamethylenediamine . The colorless solid (yellowish for some commercial samples) has a strong amine odor.

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