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D9154

Sigma-Aldrich

o-Dianisidine dihydrochloride

tablet

Sinonimo/i:

3,3′-Dimethoxybenzidine dihydrochloride, Fast Blue B

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About This Item

Formula empirica (notazione di Hill):
C14H16N2O2 · 2HCl
Numero CAS:
20325-40-0
Peso molecolare:
317.21
Beilstein:
3917996
Numero CE:
243-737-5
Numero MDL:
MFCD00012488
Codice UNSPSC:
12352204
ID PubChem:
24894263
NACRES:
NA.83

product name

o-Dianisidine dihydrochloride, tablet, 10 mg substrate per tablet

Forma fisica

tablet

Solubilità

water: 1 tablet/10 mL, clear, colorless

Temperatura di conservazione

2-8°C

Stringa SMILE

Cl.Cl.COc1cc(ccc1N)-c2ccc(N)c(OC)c2

InChI

1S/C14H16N2O2.2ClH/c1-17-13-7-9(3-5-11(13)15)10-4-6-12(16)14(8-10)18-2;;/h3-8H,15-16H2,1-2H3;2*1H
UXTIAFYTYOEQHV-UHFFFAOYSA-N

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Specificità

o-Dianisidine (3,3′-dimethoxybenzidine) is a peroxidase substrate suitable for use in ELISA procedures. This substrate produces a soluble end product that is yellow-orange in color and can be read spectrophotometrically at 405 nm. The reaction may be stopped with 5 M HCl.

Attenzione

Probably carcinogenic.

Ricostituzione

Dissolve one tablet in 60 ml of 50 mM phosphate-citrate buffer, pH 5.0. Add 12 μl of fresh 30% hydrogen peroxide immediately before to use.

Avvertenze

Danger

Indicazioni di pericolo

H302,H314,H350

Classi di pericolo

Acute Tox. 4 Oral - Carc. 1B - Eye Dam. 1 - Skin Corr. 1

Codice della classe di stoccaggio

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

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges

Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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Sigma-Aldrich

G7141

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Supelco

G3293

Reagente per saggio del glucosio

D-(+)-Glucosio ≥99.5% (GC)

Sigma-Aldrich

G8270

D-(+)-Glucosio

Rémy Ricoux et al.
Bioconjugate chemistry, 19(4), 899-910 (2008-03-08)
To develop artificial hemoproteins that could lead to new selective oxidation biocatalysts, a strategy based on the insertion of various iron-porphyrin cofactors into Xylanase A (Xln10A) was chosen. This protein has a globally positive charge and a wide enough active
Cathrine Nordgaard et al.
International journal of molecular sciences, 22(17) (2021-09-11)
p38 and c-Jun N-terninal kinase (JNK) are activated in response to acute stress and inflammatory signals. Through modification of a plethora of substrates, these kinases profoundly re-shape cellular physiology for the optimal response to a harmful environment and/or an inflammatory
Uta Merle et al.
Journal of hepatology, 51(5), 925-930 (2009-09-02)
A low serum ceruloplasmin concentration is considered diagnostic for Wilson's disease. We aimed to evaluate an enzymatic test for ceruloplasmin oxidase activity and to compare it with the routinely used immunological ceruloplasmin measurement. Serum ceruloplasmin was measured enzymatically with o-dianisidine
Iain S MacPherson et al.
Protein engineering, design & selection : PEDS, 23(3), 137-145 (2010-01-20)
Directed evolution methods were developed for Cu-containing nitrite reductase (NiR) from Alcaligenes faecalis S-6. The PCR cloning strategy allows for the efficient production of libraries of 100 000 clones by a modification of a megaprimer-based whole-plasmid synthesis reaction. The high-throughput
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The International journal of developmental biology, 54(4), 573-583 (2009-09-17)
The insulin-like growth factor (IGF) family is essential for normal embryonic growth and development and it is highly conserved through vertebrate evolution. However, the roles that the individual members of the IGF family play in embryonic development have not been
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