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Butyraldehyde

analytical standard, contains ~0.1% 2,6-di-tert-butyl-4-methylphenol and ~1% water as stabilizer

Synonyme(s) :

Butanal

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About This Item

Formule linéaire :
CH3CH2CH2CHO
Numéro CAS:
Poids moléculaire :
72.11
Numéro Beilstein :
506061
Numéro CE :
Numéro MDL:
Code UNSPSC :
85151701
ID de substance PubChem :
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

Densité de vapeur

2.5 (vs air)

Pression de vapeur

90 mmHg ( 20 °C)

Pureté

≥97.0% (GC)

Température d'inflammation spontanée

390 °F

Durée de conservation

limited shelf life, expiry date on the label

Contient

~0.1% 2,6-di-tert-butyl-4-methylphenol and ~1% water as stabilizer

Limite d'explosivité

12.5 %

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Indice de réfraction

n20/D 1.377-1.387
n20/D 1.380 (lit.)

Point d'ébullition

75 °C (lit.)

Pf

−96 °C (lit.)

Densité

0.8 g/mL at 25 °C (lit.)

Application(s)

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

Format

neat

Chaîne SMILES 

[H]C(=O)CCC

InChI

1S/C4H8O/c1-2-3-4-5/h4H,2-3H2,1H3

Clé InChI

ZTQSAGDEMFDKMZ-UHFFFAOYSA-N

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Description générale

Butyraldehyde (BA) belongs to the class of volatile organic compounds (VOCs).
This substance is listed on the positive list of the EU regulation 10/2011 for plastics intended to come into contact with food. Find all available reference materials for compounds listed in 10/2011 here

Application

BA has been used as an analytical reference standard for the analysis of BA in:
  • Air samples by pentafluorophenyl hydrazine derivatization followed by analysis using gas chromatography (GC) equipped with flame ionization detector (FID).
  • Ambient air by GC coupled to mass spectrometry (MS).

It may be used as an analytical reference standard for the analysis of BA in:
  • Environmental samples by 2,4-dinitrophenylhydrazine derivatization followed by analysis using rapid resolution liquid chromatography-ultraviolet diode array detector (RRLC-UV-DAD) and RRLC coupled to ion-trap mass spectrometer (IT-MS) operating under the atmospheric pressure chemical ionization (APCI) mode.
  • Saliva samples by magnetic-stirring-assisted micro-solid-phase extraction (μ-SPE) and headspace GC combined with ion-mobility spectrometry (IMS).

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Pictogrammes

FlameExclamation mark

Mention d'avertissement

Danger

Mentions de danger

Classification des risques

Eye Irrit. 2 - Flam. Liq. 2

Code de la classe de stockage

3 - Flammable liquids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

<50.0 °F - Pensky-Martens closed cup

Point d'éclair (°C)

< 10 °C - Pensky-Martens closed cup


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Certificats d'analyse (COA)

Lot/Batch Number

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Critical role of a pre-purge setup in the thermal desorption analysis of volatile organic compounds by gas chromatography with mass spectrometry.
Kim YH and Kim KH
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Analysis of 31 hydrazones of carbonyl compounds by RRLC-UV and RRLC-MS (/MS): a comparison of methods.
Ochs SDM, et al.
Journal of Spectroscopy (New York, NY, United States), 2015(14), 2455-2462 (2015)
Extraction of toxic compounds from saliva by magnetic-stirring-assisted micro-solid-phase extraction step followed by headspace-gas chromatography-ion mobility spectrometry.
Criado-Garcia L and Arce L
Analytical and Bioanalytical Chemistry, 408(24), 6813-6822 (2016)
Experimental validation of an effective carbon number-based approach for the gas chromatography-mass spectrometry quantification of `compounds lacking authentic standards or surrogates?.
Kim YH, et al.
Analytica Chimica Acta, 830(, author=, 32-41 (2014)
The effect of solvent selection in the gas chromatographic analysis of carbonyls in air samples after derivatization with pentafluorophenyl hydrazine.
Ullah MA, et al.
Atmospheric Research, 166(, author=, 101-109 (2015)

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