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Merck

02473

2-Hexanon

analytical standard

Synonym(e):

Butyl-methylketon

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5 ML

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Über diesen Artikel

Lineare Formel:
CH3(CH2)3COCH3
CAS-Nummer:
Molekulargewicht:
100.16
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
209-731-1
Beilstein/REAXYS Number:
1737676
MDL number:

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Produktname

2-Hexanon, analytical standard

InChI key

QQZOPKMRPOGIEB-UHFFFAOYSA-N

InChI

1S/C6H12O/c1-3-4-5-6(2)7/h3-5H2,1-2H3

SMILES string

CCCCC(C)=O

grade

analytical standard

vapor pressure

10 mmHg ( 39 °C)

assay

≥99.5% (GC)

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

refractive index

n20/D 1.401 (lit.)
n20/D 1.401

bp

127 °C (lit.)

mp

−57 °C (lit.)

density

0.812 g/mL at 25 °C (lit.)

application(s)

cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

Quality Level

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Dieser Artikel
PHR3502W32900247733-U
2-Hexanon analytical standard

Supelco

02473

2-Hexanon

application(s)

cleaning products
cosmetics
environmental
food and beverages
personal care

application(s)

pharmaceutical small molecule

application(s)

flavors and fragrances

application(s)

cleaning products
cosmetics
food and beverages
personal care
petroleum

grade

analytical standard

grade

certified reference material, pharmaceutical secondary standard

grade

-

grade

analytical standard

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

technique(s)

-

technique(s)

-

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

assay

≥99.5% (GC)

assay

-

assay

≥97%

assay

-

format

neat

format

-

format

-

format

neat

vapor pressure

10 mmHg ( 39 °C)

vapor pressure

10 mmHg ( 39 °C)

vapor pressure

-

vapor pressure

10 mmHg ( 39 °C)

Application

2-Hexanone may be used as an analytical standard for the determination of the analyte in biological samples, starch-based polymers, moldy building materials, and alcoholic matrices by various chromatography techniques.[1][2][3][4][5]

General description

2-Hexanone (MBK, 2-Oxohexane) is a volatile organic compound, that exists as a clear, colorless liquid with a sharp odor. It dissolves very easily in water, and can evaporate easily into the air as a vapor. It is occasionally found as a volatile component of normal human biofluids. It was used as an industrial hexacarbon solvent, but is no longer used or made owing to its neurotoxic nature leading to various human diseases.[6]

signalword

Danger

Hazard Classifications

Flam. Liq. 3 - Repr. 2 - STOT RE 1 - STOT SE 3

target_organs

Central nervous system

Lagerklasse

3 - Flammable liquids

wgk

WGK 1

flash_point_f

73.4 °F - closed cup

flash_point_c

23 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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Die Dokumentenbibliothek aufrufen

E L White et al.
Biomedical mass spectrometry, 6(4), 169-172 (1979-04-01)
A quantitative method is reported for the determination of n-hexane, 2-hexanone and 2,5-hexanedione in biological tissues by stable isotope dilution using gas chromatography mass spectrometry. n-[2H14]Hexane, 2-[2H5]hexanone and 2,5-[2H10]hexanedione are used as the isotopic diluents. After tissue homogenization and extraction
T.S.S. Dikshith
Handbook of Chemicals and Safety, 19-Apr, 228-228 (2016)
Solid-phase extraction and subsequent gas chromatography-mass spectrometry analysis for identification of complex mixtures of degradation products in starch-based polymers
Hakkarainen M, et al.
Journal of Chromatography A, 741(2), 251-263 (1996)
P Manini et al.
Rapid communications in mass spectrometry : RCM, 12(21), 1615-1624 (1998-11-10)
A liquid chromatography atmospheric pressure electrospray mass spectrometry (ESI-LC/MS) system was evaluated for the identification and characterization of n-hexane conjugated metabolites (glucuronides) in untreated urine samples. Chromatography of glucuronides was obtained under ion-suppressed reversed-phase conditions, by using high-speed (3 cm
Takaya Hoshikawa et al.
Chemical & pharmaceutical bulletin, 60(4), 548-553 (2012-04-03)
Intramolecular [2+2] cycloaddition of γ,δ-unsaturated ketenes derived from hex-5-enoyl chloride derivatives gave bicyclo[2.1.1]hexan-5-ones with complete regioselectivity.

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