Alle Fotos(1)

Dokumente

41097

Dibrommethan -Lösung

Name: Dibrommethan -Lösung
Brand: SUPELCO

5000 μg/mL in methanol, analytical standard

Anmeldenzur Ansicht organisationsspezifischer und vertraglich vereinbarter Preise

Alle Fotos(1)

About This Item

CAS-Nummer:

74-95-3

MDL-Nummer:

MFCD00000168

UNSPSC-Code:

41116105

PubChem Substanz-ID:

329756057

Qualität

analytical standard

Analysenzertifikat (CofA)

certificate of analysis is enclosed in each package.

Verpackung

ampule of 1 mL

Konzentration

5000 μg/mL in methanol

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Anwendung(en)

environmental

Format

single component solution

Lagertemp.

2-8°C

SMILES String

BrCBr

InChI

1S/CH2Br2/c2-1-3/h1H2

InChIKey

FJBFPHVGVWTDIP-UHFFFAOYSA-N

Suchen Sie nach ähnlichen Produkten? Aufrufen Leitfaden zum Produktvergleich

Anwendung

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

Piktogramme

GHS02,GHS06,GHS08

Signalwort

Danger

H-Sätze

H225,H301 + H311 + H331,H370

P-Sätze

P210 - P233 - P280 - P301 + P310 - P303 + P361 + P353 - P304 + P340 + P311

Gefahreneinstufungen

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2 - STOT SE 1

Zielorgane

Eyes,Central nervous system

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 2

Flammpunkt (°F)

51.8 °F - closed cup

Flammpunkt (°C)

11 °C - closed cup

Persönliche Schutzausrüstung

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

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number

Die passende Version wird nicht angezeigt?

Wenn Sie eine bestimmte Version benötigen, können Sie anhand der Lot- oder Chargennummer nach einem spezifischen Zertifikat suchen.

Suche nach COA

Besitzen Sie dieses Produkt bereits?

In der Dokumentenbibliothek finden Sie die Dokumentation zu den Produkten, die Sie kürzlich erworben haben.

Die Dokumentenbibliothek aufrufen

Time resolved polarization dependent single shot four wave mixing.

Andrey Shalit et al.

Physical chemistry chemical physics : PCCP, 14(40), 13989-13996 (2012-09-20)

Single shot time resolved four wave mixing is a powerful tool for the acquisition of dynamic and spectroscopic data from molecules susceptible to bleaching or other photo-induced damage. We add polarization dependence to single shot methods, and demonstrate how magic

Dimethylselenide as a probe for reactions of halogenated alkoxyl radicals in aqueous solution. Degradation of dichloro- and dibromomethane.

Oksana Makogon et al.

The journal of physical chemistry. A, 112(26), 5908-5916 (2008-06-11)

Using pulse radiolysis and steady-state gamma-radiolysis techniques, it has been established that, in air-saturated aqueous solutions, peroxyl radicals CH 2HalOO (*) (Hal = halogen) derived from CH 2Cl 2 and CH 2Br 2 react with dimethyl selenide (Me 2Se), with

Molecular interactions in crystalline dibromomethane and diiodomethane, and the stabilities of their high-pressure and low-temperature phases.

Marcin Podsiadło et al.

Acta crystallographica. Section B, Structural science, 62(Pt 6), 1090-1098 (2006-11-17)

Dibromomethane, CH2Br2, and diiodomethane, CH2I2, have been in situ pressure-crystallized in a diamond-anvil cell and their structures determined by single-crystal X-ray diffraction at 0.61 and 0.16 GPa, respectively. The pressure-frozen CH2Br2 crystal is isostructural with its C2/c phase obtained by

Xenon and halogenated alkanes track putative substrate binding cavities in the soluble methane monooxygenase hydroxylase.

D A Whittington et al.

Biochemistry, 40(12), 3476-3482 (2001-04-12)

To investigate the role of protein cavities in facilitating movement of the substrates, methane and dioxygen, in the soluble methane monooxygenase hydroxylase (MMOH), we determined the X-ray structures of MMOH from Methylococcus capsulatus (Bath) cocrystallized with dibromomethane or iodoethane, or

Formation and mass spectrometric analysis of DNA and nucleoside adducts by S-(1-acetoxymethyl)glutathione and by glutathione S-transferase-mediated activation of dihalomethanes.

Glenn A Marsch et al.

Chemical research in toxicology, 17(1), 45-54 (2004-01-20)

The dihalomethane CH(2)Cl(2) is an industrial solvent of potential concern to humans because of its potential genotoxicity and carcinogenicity. To characterize DNA damage by dihalomethanes, a rapid DNA digestion under acidic conditions was developed to identify alkali labile DNA-dihalomethane nucleoside

Alle zugehörigen Dokumente anzeigen

Unser Team von Wissenschaftlern verfügt über Erfahrung in allen Forschungsbereichen einschließlich Life Science, Materialwissenschaften, chemischer Synthese, Chromatographie, Analytik und vielen mehr..

Setzen Sie sich mit dem technischen Dienst in Verbindung.