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Weitere Dokumente

I5161

SAFC

Jodacetamid

Arzneimittelherstellung

Anmeldenzur Ansicht organisationsspezifischer und vertraglich vereinbarter Preise
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About This Item

Lineare Formel:
ICH2CONH2
CAS-Nummer:
144-48-9
Molekulargewicht:
184.96
Beilstein:
1739080
EG-Nummer:
205-630-1
MDL-Nummer:
MFCD00008028
UNSPSC-Code:
12352200
NACRES:
NA.21

Biologische Quelle

synthetic

Qualitätsniveau

400

Assay

≥99% (NMR)

Form

powder

mp (Schmelzpunkt)

92-95 °C (lit.)

Löslichkeit

H2O: 0.5 M, clear, colorless

Eignung

suitable for manufacturing use

Lagertemp.

2-8°C

SMILES String

NC(=O)CI

InChI

1S/C2H4INO/c3-1-2(4)5/h1H2,(H2,4,5)

InChIKey

PGLTVOMIXTUURA-UHFFFAOYSA-N

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Verwandte Kategorien

Allgemeine Beschreibung

Our SAFC® portfolio of high-quality raw materials for use in biopharmaceutical processing withstands strict quality control procedures plus the documentation and expertise to help our customers meet requirements as defined by the M-Clarity Program.

M-Clarity Program

Our comprehensive portfolio of upstream process chemicals not only provides biopharmaceutical manufacturers with high-quality raw materials for production of classical and novel therapies, but also helps them get to market faster and simplify regulatory challenges. Trust us to deliver supply chain transparency and reliable sourcing around the globe, streamlining your product qualification with best-in-class regulatory support and service.

Biochem./physiol. Wirkung

Iodacetamid dient als Alkylierungsreagens für Cysteinreste bei der Peptidsequenzierung. Es ist ein irreversibler Inhibitor von Enzymen mit Cystein im aktiven Zentrum. Mit Histidinresten reagiert es sehr viel langsamer, aber diese Aktivität ist für die Hemmung der Ribonuklease verantwortlich.

Rechtliche Hinweise

SAFC is a registered trademark of Merck KGaA, Darmstadt, Germany

Piktogramme

Skull and crossbonesHealth hazard
GHS06,GHS08

Signalwort

Danger

Gefahreneinstufungen

Acute Tox. 3 Oral - Aquatic Chronic 4 - Resp. Sens. 1 - Skin Sens. 1

Lagerklassenschlüssel

6.1C - Combustible, acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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DL-Dithiothreitol for molecular biology, ≥98% (HPLC), ≥99% (titration)

Sigma-Aldrich

D9779

DL-Dithiothreitol

DL-Dithiothreitol ≥98% (HPLC), ≥99.0% (titration)

Sigma-Aldrich

D0632

DL-Dithiothreitol

DL-Dithiothreitol -Lösung BioUltra, for molecular biology, ~1 M in H2O

Sigma-Aldrich

43816

DL-Dithiothreitol -Lösung

Guanidin -hydrochlorid -Lösung Colorless liquid, 7.8 - 8.3 M, pH- 4.5 - 5.5

Sigma-Aldrich

G9284

Guanidin -hydrochlorid -Lösung

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Valentina R Minciacchi et al.
Oncotarget, 6(13), 11327-11341 (2015-04-11)
Large oncosomes (LO) are atypically large (1-10 µm diameter) cancer-derived extracellular vesicles (EVs), originating from the shedding of membrane blebs and associated with advanced disease. We report that 25% of the proteins, identified by a quantitative proteomics analysis, are differentially
Jeremy Rouillon et al.
Neuromuscular disorders : NMD, 24(7), 563-573 (2014-05-13)
Diagnosis of muscular dystrophies is currently based on invasive methods requiring muscle biopsies or blood tests. The aim of the present study was to identify urinary biomarkers as a diagnostic tool for muscular dystrophies. Here, the urinary proteomes of Duchenne
Elena B Lugli et al.
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Smoking is a well-established risk factor for rheumatoid arthritis (RA), and it has been proposed that smoking-induced citrullination renders autoantigens immunogenic. To investigate this mechanism, we examined human lung tissue from 40 subjects with defined smoking status, with or without
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Kidney international, 86(4), 757-767 (2014-05-03)
Almost half of patients receiving lithium salts have nephrogenic diabetes insipidus. Chronic lithium exposure induces AQP2 downregulation and changes in the cellular composition of the collecting duct. In order to understand these pathophysiological events, we determined the earliest lithium targets
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