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Key Documents

75034

Supelco

2,3-Hexanedione

analytical standard

Sinonimo/i:

Acetyl butyryl

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About This Item

Formula condensata:
CH3CH2CH2COCOCH3
Numero CAS:
Peso molecolare:
114.14
Beilstein:
1699896
Numero CE:
Numero MDL:
Codice UNSPSC:
85151701
ID PubChem:
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

Densità del vapore

3.9 (vs air)

Tensione di vapore

10 mmHg ( 20 °C)

Saggio

≥96.0% (GC)

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

Indice di rifrazione

n20/D 1.409
n20/D 1.412 (lit.)

P. eboll.

128 °C (lit.)

Densità

0.934 g/mL at 25 °C (lit.)

applicazioni

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

Formato

neat

Temperatura di conservazione

2-8°C

Stringa SMILE

CCCC(=O)C(C)=O

InChI

1S/C6H10O2/c1-3-4-6(8)5(2)7/h3-4H2,1-2H3
MWVFCEVNXHTDNF-UHFFFAOYSA-N

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Applicazioni

2,3-Hexanedione may be used as an internal standard for the determination of intermediates of advanced glycation end products in the human nail using ultra-performance liquid chromatography coupled with electrospray ionization time-of-flight mass spectrometry (UPLC-ESI-TOFMS).
2,3-Hexanedione may be used as an internal standard for the quantitative determination of methylglyoxal present in the tissues of Sprague–Dawley rats using electrospray ionization liquid chromatography coupled with mass spectrometry(ESI/LC/MS).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Confezionamento

Bottomless glass bottle. Contents are inside inserted fused cone.

Pittogrammi

FlameHealth hazard

Avvertenze

Warning

Indicazioni di pericolo

Classi di pericolo

Flam. Liq. 3 - STOT RE 2 Inhalation

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

3 - Flammable liquids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

82.4 °F - closed cup

Punto d’infiammabilità (°C)

28 °C - closed cup


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Certificati d'analisi (COA)

Lot/Batch Number

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Diacetyl for synthesis

Sigma-Aldrich

8.03528

Diacetyl

Acetoin analytical standard

Supelco

40127-U

Acetoin

2,3-Butanediol analytical standard, mixture of racemic and meso forms

Supelco

42038

2,3-Butanediol

Measurement of methylglyoxal in rat tissues by electrospray ionization mass spectrometry and liquid chromatography
Randell.WE, et al.
Journal of Pharmacological and Toxicological Methods, 51(2), 153-157 (2005)
Jun Zhe Min et al.
Analytical biochemistry, 424(2), 187-194 (2012-03-03)
The resolution of the intermediate advanced glycation end products (AGEs) in the human nail was carried out by the combination of 4,5-dimethyl-1,2-phenylenediamine (DMPD) derivatives and ultra-performance liquid chromatography with electrospray ionization time-of-flight mass spectrometry (UPLC-ESI-TOF-MS). The reaction of the reagent
Molecular mechanism of hexane neuropathy: significant differences in pharmacokinetics between 2.3-, 2.4-, and 2.5-hexanedione.
K Iwasaki et al.
Industrial health, 22(3), 177-187 (1984-01-01)
Thomas R Zilz et al.
Toxicology, 231(2-3), 210-214 (2007-01-19)
The potential cytotoxicity of two hexanedione food additives (2,3 and 3,4 isomers) was evaluated in comparison with the neurotoxic hexane metabolite 2,5-hexanedione in the human SK-N-SH neuroblastoma line using the MTT assay to indicate mitochondrial dehydrogenase activity and flow cytometry
Michael D Coleman et al.
Basic & clinical pharmacology & toxicology, 102(1), 25-29 (2007-11-02)
The effects of the alpha-diketone derivatives 2,3- and 3,4-hexanediones were investigated in three non-neuronal cell lines (MCF7, HepG(2) and CaCo-2) as well as in the neuroblastoma line, SH-SY5Y. The MTT reduction assay was employed to determine the necrotic effects of

Protocolli

-Cymene; 2,5-Dimethylpyrrole; Acetoin, ≥96%, FCC, FG; 2,5-Dimethylpyrazine; 2,6-Dimethylpyrazine; 2-Ethylpyrazine, ≥98%, FG; 2,3-Dimethylpyrazine; 4-Heptanone; 3-Ethylpyridine; 2,3,5-Trimethylpyrazine; Furfural; Pyrrole; Furfuryl acetate; Linalool; Linalyl acetate; 5-Methylfurfural; γ-Butyrolactone; 2-Acetyl-1-methylpyrrole; Furfuryl alcohol; 2-Acetylpyrrole; Pyrrole-2-carboxaldehyde

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