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03973

Sigma-Aldrich

Hematoxylin solution A according to Weigert

for microscopy

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About This Item

Beilstein/REAXYS Number:
91401
MDL number:
MFCD00078111
UNSPSC Code:
12171500
PubChem Substance ID:
329747851

grade

for microscopy

concentration

100 g/L

impurities

ethanol

density

0.84 g/mL at 20 °C

suitability

suitable for microscopy

SMILES string

[H][C@]12c3cc(O)c(O)cc3C[C@@]1(O)COc4c(O)c(O)ccc24

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

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pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Danger

hcodes

H225,H319

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 2

Storage Class

3 - Flammable liquids

wgk_germany

WGK 1

flash_point_f

57.2 °F

flash_point_c

14 °C

ppe

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

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Harris Hematoxylin Solution, Modified

Sigma-Aldrich

HHS32

Harris Hematoxylin Solution, Modified

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
Li-Gen Lin et al.
Journal of medicinal chemistry, 51(15), 4419-4429 (2008-07-10)
Protein tyrosine kinase (PTK) inhibitors represent emerging therapeutics for cancer chemoprevention. In our study, hematoxylin (26) was identified as one of the most remarkable c-Src inhibitors in an orthogonal compound-mixing library (32200 compounds) by using an ELISA-based automated high-throughput screening

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