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D9015

Sigma-Aldrich

3,3′-Diaminobenzidine tetrahydrochloride hydrate

≥96% purity (TLC), powder

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About This Item

Formule linéaire :
C12H14N4 · 4HCl · xH2O
Numéro CAS:
868272-85-9
Numéro CE :
231-018-9
Numéro MDL:
MFCD08273058
Code UNSPSC :
12171500
ID de substance PubChem :
24894241
Nomenclature NACRES :
NA.47

product name

3,3′-Diaminobenzidine tetrahydrochloride hydrate, ISOPAC®

Niveau de qualité

100

Pureté

≥96% (TLC)

Forme

powder

Couleur

off-white to faint red, to beige

Pf

280 °C

Solubilité

water: 50 mg/mL, clear to slightly hazy

Application(s)

diagnostic assay manufacturing
hematology
histology

Température de stockage

room temp

Chaîne SMILES 

O.Cl.Cl.Cl.Cl.Nc1ccc(cc1N)-c2ccc(N)c(N)c2

InChI

1S/C12H14N4.4ClH.H2O/c13-9-3-1-7(5-11(9)15)8-2-4-10(14)12(16)6-8;;;;;/h1-6H,13-16H2;4*1H;1H2

Clé InChI

DXWSCXIZIHILNP-UHFFFAOYSA-N

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Application

3,3′-Diaminobenzidine tetrahydrochloride hydrate has been used in immunohistological staining procedure and in situ hybridization.

Actions biochimiques/physiologiques

DAB (3,3′-Diaminobenzidine) is utilized in many applications for the visualization of peroxidase activity. In the peroxidase reaction, DAB serves as a hydrogen donor in the presence of peroxide. The oxidized DAB forms an insoluble brown end-product for use in immunohistological and immunoblotting staining procedures.

Conditionnement

Weight approximate. Packaged in a 100 mL serum bottle with silicon/PTFE septum and aluminum tear seal.

Attention

Injecting a compatible solvent permits preparation of any desired strength solution without exposure.

Reconstitution

Dissolving the contents in 100 mL of solvent yields a 0.1% solution.

Informations légales

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

ISOPAC de

Réf. du produit
Description
Tarif

Pictogrammes

Health hazardExclamation mark
GHS08,GHS07

Mention d'avertissement

Danger

Mentions de danger

H302,H319,H341,H350

Classification des risques

Acute Tox. 4 Oral - Carc. 1B - Eye Irrit. 2 - Muta. 2

Code de la classe de stockage

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

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, type N95 (US)

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Certificats d'analyse (COA)

Lot/Batch Number
MKCW2098
MKCQ1964
MKCK6532
MKCC3553
MKBT9193V

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

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Elson DA, et al.
Cancer Research, 60, 1267-1267 (2000)
Proliferation of bone marrow-derived cells contributes to regeneration after folic acid-induced acute tubular injury.
Fang TC, et al.
Journal of the American Society of Nephrology, 16, 1723-1723 (2005)
M R Arnold et al.
Neuropharmacology, 148, 257-271 (2018-12-24)
Caffeine is the most commonly used drug in the world. However, animal studies suggest that chronic consumption of caffeine during adolescence can result in enhanced anxiety-like behavioral responses during adulthood. One mechanism through which chronic caffeine administration may influence subsequent
Haematopoietic lineage-committed bone marrow cells, but not cloned cultured mesenchymal stem cells, contribute to regeneration of renal tubular epithelium after HgCl2-induced acute tubular injury.
Fang TC, et al.
Cell Proliferation, 41, 575-591 (2008)
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