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Key words & phrases: 1-propanol n-propyl alcohol image diagram on how to interpret and explain the mass spectrum of propan-1-ol m/z m/e base peaks, image and diagram of the mass spectrum of propan-1-ol, details of the mass spectroscopy of propan-1-ol, low and high resolution mass spectrum of propan-1-ol, prominent m/z peaks in the mass spectrum ...

Mass MS2014-05103CW 1-propanol C3H8O (Mass of molecular ion: 60) Source Temperature: 250 °C Sample Temperature: 250 °C Reservoir, 70 eV

IR Spectrum. Go To: Top, Condensed phase thermochemistry data, References, Notes. Data compiled by: Coblentz Society, Inc. GAS (SATURATED); DOW KBr FOREPRISM-GRATING; DIGITIZED BY NIST FROM HARD COPY (FROM TWO SEGMENTS) 2, 4 cm-1 resolution

This page contains chemical ionization mass spectrometry data obtained at Widener University for Chem 465, Advanced Spectroscopy.

The 1 H NMR spectrum of propanol shows the -CH 2 - attached to the alcohol as a triplet at 3.58 ppm. This shows that the signal is being split by the adjacent -CH 2 - group and not the alcohol -OH. The signal for the proton attached to the oxygen appears as a singlet at 2.26 ppm.

Propan-1-ol is the parent member of the class of propan-1-ols that is propane in which a hydrogen of one of the methyl groups is replaced by a hydroxy group. It has a role as a protic solvent and a metabolite. It is a short-chain primary fatty alcohol and a member of propan-1-ols.

Chung, H.-Y.; Yung, I.K.S.; Ma, W.C.J.; Kim, J.-S., Analysis of volatile components in frozen and dried scallops (Patinopecten yessoensis) by gas chromatography/mass spectrometry, Food Res. Int., 2002, 35, 1, 43-53, https://doi.org/10.1016/S0963-9969(01)00107-7.

This MassBank Record with Accession MSBNK-Fac_Eng_Univ_Tokyo-JP007679 contains the MS mass spectrum of '1-PROPANOL' with the InChIKey 'BDERNNFJNOPAEC-UHFFFAOYSA-N'.

Mass Spectrometry. As noted in Section 12.3, alcohols undergo fragmentation in the mass spectrometer by two characteristic pathways, alpha cleavage and dehydration. In the alpha-cleavage pathway, a C–C bond nearest the hydroxyl group is broken, yielding a neutral radical plus a resonance-stabilized, oxygen-containing cation.