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Hidrato de diclorhidrato de 3,3',5,5'-tetrametilbencidina, + 99 %, Thermo Scientific Chemicals
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Hidrato de diclorhidrato de 3,3',5,5'-tetrametilbencidina, + 99 %, Thermo Scientific Chemicals
Hidrato de diclorhidrato de 3,3',5,5'-tetrametilbencidina, + 99 %, Thermo Scientific Chemicals
Hidrato de diclorhidrato de 3,3',5,5'-tetrametilbencidina, + 99 %, Thermo Scientific Chemicals
Thermo Scientific Chemicals

Hidrato de diclorhidrato de 3,3',5,5'-tetrametilbencidina, + 99 %, Thermo Scientific Chemicals

CAS: 207738-08-7 | C16H22Cl2N2 | 313.27 g/mol
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Número de catálogoCantidad
J60332.88
también denominado J60332-88
2.5 g
Número de catálogo J60332.88
también denominado J60332-88
Precio (USD)
-
Cantidad:
2.5 g
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Identificadores químicos
CAS207738-08-7
IUPAC Name3,3',5,5'-tetramethyl-[1,1'-biphenyl]-4,4'-diamine dihydrochloride
Molecular FormulaC16H22Cl2N2
InChI KeyNYNRGZULARUZCC-UHFFFAOYSA-N
SMILESCl.Cl.CC1=CC(=CC(C)=C1N)C1=CC(C)=C(N)C(C)=C1
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EspecificacionesSpecification SheetHoja de especificaciones
Appearance (Color)White
Assay (unspecified)≥97.5%
Ash≤0.1%
Heavy Metals≤5ppm
FormPowder
3,3',5,5'-Tetramethylbenzidine dihydrochloride hydrate is a chromophore substrate in ELISA assays. It is a noncarcinogenic substitute for benzidine.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Aplicaciones
El hidrato de diclorhidrato de 3,3′,5,5′-tetrametilbencidina es un sustrato cromóforo en los ensayos ELISA. Es un sustituto no cancerígeno de la bencidina.

Solubilidad
Soluble en DMSO (aprox. 1,7 mg/ml), y 1:300 DMSO:PBS (pH 7,2) (0,03 mg/ml).

Notas
Sensible a la humedad y a la luz. Almacenar alejado de agentes oxidantes, calor, luz, ácidos y agua/humedad.
RUO – Research Use Only

General References:

  1. Sarah Gerlo; Peggy Verdood; Birgit Gellersen; Elisabeth L. Hooghe-Peters and Ron Kooijman. Mechanism of Prostaglandin (PG)E2-Induced Prolactin Expression in Human T Cells: Cooperation of Two PGE2 Receptor Subtypes, E-Prostanoid (EP) 3 and EP4, Via Calcium- and Cyclic Adenosine 5'-Monophosphate-Mediated Signaling Pathways. The Journal of Immunology.2004, 173 (10), 5952-5962.
  2. Evemie Schutyser; Sofie Struyf; Patricia Menten; Jean-Pierre Lenaerts; René Conings; Willy Put; Anja Wuyts; Paul Proost and Jo Van Damme. Regulated Production and Molecular Diversity of Human Liver and Activation-Regulated Chemokine/Macrophage Inflammatory Protein-3α from Normal and Transformed Cells. The Journal of Immunology. 1973, 165 (8), 4470-4477.