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MilliporeSigma

03971

Sigma-Aldrich

Hematoxylin solution according to Delafield

for microscopy

Sinónimos:

Delafield’s hematoxylin

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About This Item

Beilstein/REAXYS Number:
91401
MDL number:
UNSPSC Code:
12171500
PubChem Substance ID:
NACRES:
MA.02

grade

for microscopy

Quality Level

product line

BioChemika

form

liquid

technique(s)

microbe id | staining: suitable

impurities

ammonium alum
methanol

density

0.950-1.044 g/mL at 20 °C

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

room temp

suitability

Chlamydia spp.
Histoplasma spp.
Plasmodium spp.
Trichomonas spp.
bacteria
protozoa
spirochetes

SMILES string

Oc1cc2C[C@@]3(O)COc4c(O)c(O)ccc4[C@H]3c2cc1O

InChI

1S/C16H14O6/c17-10-2-1-8-13-9-4-12(19)11(18)3-7(9)5-16(13,21)6-22-15(8)14(10)20/h1-4,13,17-21H,5-6H2/t13-,16+/m0/s1

InChI key

WZUVPPKBWHMQCE-XJKSGUPXSA-N

General description

Hematoxylin solution according to Delafield is a naturally ripened alum hematoxylin with potassium alum or ammonium alum as the mordant. It is used when the counterstain doesn′t possess any acid content in it. It is suitable to be used as a nuclear stain with eosin.

Application

Hematoxylin solution according to Delafield has been used to stain the nuclei of different sections of adipose tissue for its histochemical analysis. It is suitable for staining thick or thin blood films. It is also frequently used to stain and study the visibility of microfilariae.

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Flam. Liq. 3 - STOT SE 1

target_organs

Eyes,Central nervous system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

107.6 °F - closed cup

flash_point_c

42 °C - closed cup

ppe

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


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Hideki Ishii et al.
Bioorganic & medicinal chemistry letters, 22(3), 1469-1474 (2012-01-17)
SAR studies for the exploration a novel class of anti-human immunodeficiency virus type 1 (HIV-1) agents based on the hematoxylin structure (1) are described. The systematic deoxygenations of 1 including asymmetric synthesis were conducted to obtain a compound showing high

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