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Key Documents

439223

Sigma-Aldrich

Diclorometano

suitable for HPLC, ≥99.9%, contains 40-150 ppm amylene as stabilizer

Sinonimo/i:

Cloruro di metilene

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About This Item

Formula empirica (notazione di Hill):
CH2Cl2
Numero CAS:
Peso molecolare:
84.93
Beilstein:
1730800
Numero CE:
Numero MDL:
Codice UNSPSC:
12190000
ID PubChem:
NACRES:
NA.21

Densità del vapore

2.9 (vs air)

Livello qualitativo

Tensione di vapore

24.45 psi ( 55 °C)
6.83 psi ( 20 °C)

Saggio

≥99.9%

Forma fisica

liquid

Temp. autoaccensione

1223 °F

contiene

40-150 ppm amylene as stabilizer

Limite di esplosione

22 %

tecniche

HPLC: suitable

Impurezze

Free halogens, passes test
≤0.0003 meq/g Titr. acid
≤0.02% water

Residuo dopo evaporazione

<0.0003%

Colore

APHA: ≤10
clear

Indice di rifrazione

n20/D 1.424 (lit.)

P. eboll.

39.8-40 °C (lit.)

Punto di fusione

−95 °C (lit.)

Densità

1.325 g/mL at 25 °C (lit.)

λ

H2O reference

Assorbanza UV

λ: 235 nm Amax: 1.00
λ: 240 nm Amax: 0.20
λ: 250 nm Amax: 0.05
λ: 260 nm Amax: 0.02
λ: 340-400 nm Amax: 0.01

Compatibilità

passes test for HPLC

Stringa SMILE

ClCCl

InChI

1S/CH2Cl2/c2-1-3/h1H2
YMWUJEATGCHHMB-UHFFFAOYSA-N

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Descrizione generale

Dichloromethane (DCM) is a chlorinated organic solvent with a wide range of industrial applications. It has C2v symmetry, low boiling point, high density and is immiscible in water. Degradation of DCM by various methods has been reported. Ultrasonic absorption studies of liquid DCM shows strong relaxation effect. A study reports the dielectric characteristics of DCM over a wide frequency range. DCM is susceptible to degradation with time, which can be suppressed by adding amylene as a stabilizer.

Applicazioni

Dichloromethane (Methylene chloride) may be used in the following processes:
  • To compose ultrasonic baths for cleaning and protection of aluminum coating over atactic-PMMA (poly(methyl methacrylate)) for dielectric studies.
  • Preparation of AMBF3 (ammoniomethyltrifluoroborate)-conjugated biomolecules.
  • Sample preparation for GC-MS (Gas Chromatography-Mass Spectrometry) analysis.
  • Preparation of ammonium acetate solvent mixture in combination with isopropanol, acetonitrile and water for mass spectral analysis of neutral lipids.
  • Quantification of glutathione (GSH) and glutathione disulfide (GSSG) in biological samples by HPLC and spectrophotometry.
  • As an extractant for 2,2-dithioethyl-4-(2′-pyridyl)-4-butyro-γ-lactone.
Meets ACS specifications

Nota sulla preparazione

Product filtered through a 0.2 μm filter

Pittogrammi

Health hazardExclamation mark

Avvertenze

Warning

Indicazioni di pericolo

Classi di pericolo

Carc. 2 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Organi bersaglio

Central nervous system

Codice della classe di stoccaggio

6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

does not flash

Punto d’infiammabilità (°C)

does not flash

Dispositivi di protezione individuale

Eyeshields, Faceshields, Gloves


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Daniela Giustarini et al.
Nature protocols, 8(9), 1660-1669 (2013-08-10)
This protocol describes a procedure for determining glutathione (GSH) and glutathione disulfide (GSSG) concentrations in blood and other tissues. Artifactual oxidation to GSSG of 5-15% of the GSH found in a sample can occur during deproteination of biological samples with
Rodney C Baker et al.
Methods in enzymology, 538, 89-105 (2014-02-18)
Mass spectrometry technology has enabled significant advances in detailing the alterations of the lipidome in response to pathological conditions or experimental manipulations. Lipids comprise a wide range of compounds with functions that include structural, intracellular signaling, trafficking, and storage. Characterization
Jane A Mullaney et al.
Journal of agricultural and food chemistry, 61(12), 3039-3046 (2013-03-07)
Glucosinolates from the genus Brassica can be converted into bioactive compounds known to induce phase II enzymes, which may decrease the risk of cancers. Conversion via hydrolysis is usually by the brassica enzyme myrosinase, which can be inactivated by cooking
Vitamin B12-mediated hydrodechlorination of dichloromethane by bimetallic Cu/Al particles.
Huang CC, et al.
Chemical Engineering Journal, 273, 413-420 (2015)
Dichloromethane Detection Based on Near-Infrared Absorptive Sensing.
Han JH and Yoon SM
IEEE Journal of Selected Topics in Quantum Electronics, 18(5), 1547-1552 (2012)

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