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Singlet, doublet, etc. This ester is the main constituent of the essential banana oil. %��������� eBiochemicals provides information on the Isoamyl acetate(3-Methylbutyl acetate;Acetic acid isoamyl ester; Isopentyl acetate; isopentyl acetate): structure, NMR,MS,IR,spectral data, msds, molecular formula, cas, physical and chemical properties, and suppliers. 4 0 obj stream 142 °C Alfa Aesar: 288 F (142.2222 °C) NIOSH NS9800000 145 °C Food and Agriculture Organization of the United Nations 3-Methylbutyl acetate: 143 °C OU Chemical Safety Data (No longer updated) More details: 142 °C Alfa Aesar B21618: 142 °C (Literature) LabNetwork LN00163295 142 °C FooDB FDB008132: 287-289 F / 760 mmHg (141.6667-142.7778 °C / 760 mmHg) Wikidata Q221307 x�\I�G���h—��z_,�����q@B�&42�2�����ZY�M?AR�{�/3+++�����o�˿�uC��i*�a*߿.W�+�>��._�PV��W��.M'm�26�����)_=��������|z_�uy���y~[�������[��/s�N}V�E7_ݖO��-�P��r���/]uE낵措�:����� ꦹ�m��r�&5��54 fU2�G���3C����`�X����ج�?�-g6+�>�K�����l˛?����������_�GU�r`r�����r�����.w$��T�P�ϗvP����W>:��36N�_�:�l�s��P��Z�7���M-F�#��-����ʛ��L�|���M��/���ȯ"�A�Eđ�|zHǯ���|]��\�7��h�!D�n��}'7���� zF�~�ReP/n�\���K;Mf^u�QA�ml(Y }{i���|UUu9�����8������P�P��in�U��iFZ��i�Àa�?ۼ�� Welcome to eBiochemicals. +86-400-6021-666 service@molbase.com ISOAMYL ALCOHOL 30899-19-5 NMR spectrum, ISOAMYL ALCOHOL H-NMR spectral analysis, ISOAMYL ALCOHOL C-NMR spectral analysis ect. Compound Isoamyl acetate with free spectra: 3 NMR and 9 FTIR. The synthesis of esters directly from alcohols and carboxylic acids plays an important 2Lp�������y0v�)fI��e���S@W��n�K7t����. A 4.0 B 2.0 C 1.6 D 1.4 E 0.9 * assign signals A-E to protons on the structure of the product* O OHHO + << /Length 5 0 R /Filter /FlateDecode >> %PDF-1.3 1H NMR Analysis of Isoamyl Acetate (Banana Oil) Signal Integration (# of H’s) Expected Chemical Shift (ppm) Observed Chemical Shift (ppm) # of 3-bond Neighbors (n) Multiplicity/ Splitting (m = n+1) ex. ChemicalBook ProvideIsoamyl acetate(123-92-2) 13C NMR,IR2,MS,IR3,IR1,1H NMR,Raman,ESR,13C NMR,Spectrum The aim of this project is the synthesis of a specific ester, the isoamyl acetate, which is obtained by the condensation of isoamyl acohol with acetic acid through a Fischer-Speier esterification. 13C Nuclear Magnetic Resonance (NMR) Chemical Shifts of Isoamyl acetate with properties.

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