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03971

Sigma-Aldrich

Hematoxylin solution according to Delafield

for microscopy

Synonym(s):

Delafield’s hematoxylin

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About This Item

Beilstein:
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.

Signal Word

Danger

Hazard Statements

Hazard Classifications

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

Target Organs

Eyes,Central nervous system

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

107.6 °F - closed cup

Flash Point(C)

42 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 2 petroleums
Hazardous rank III
Water insoluble liquid

ISHL Indicated Name

Substances Subject to be Indicated Names

ISHL Notified Names

Substances Subject to be Notified Names

JAN Code

03971-VAR:
03971-250ML:4548173101354
03971-BULK:


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Lijun Dong et al.
Inflammation, 40(6), 1944-1958 (2017-09-04)
T cells are involved in chronic inflammation of adipose tissue in obese conditions. However, the impact of age on the adipose T cells remains unknown. In this study, we investigated T cells in the white adipose tissue of young and
Niina Vuokila et al.
Cellular and molecular life sciences : CMLS, 75(24), 4557-4581 (2018-08-30)
Traumatic brain injury (TBI) initiates molecular and cellular pathologies that underlie post-injury morbidities, including hippocampus-related memory decline and epileptogenesis. Non-coding small RNAs are master regulators of gene expression with the potential to affect multiple molecular pathways. To evaluate whether hippocampal
Hongling Zhu et al.
Experimental and therapeutic medicine, 14(4), 3609-3615 (2017-10-19)
Basic fibroblast growth factor (bFGF), a known angiogenic factor, may provide a potential strategy for the treatment of myocardial infarction (MI), but it is limited by a relatively short half-life. Dex-PCL-HEMA/PNIPAAm hydrogel provides a reservoir for the controlled release of
Wen-Chen Ji et al.
Neurological research, 42(5), 361-371 (2020-03-10)
Objectives: Spinal cord injury (SCI) is a most debilitating traumatic injury, and cytotherapy is a promising alternative treatment strategy. Here we investigated the effect and mechanism of adipose-derived stem/stromal cells (ASCs) with overexpressing brain-derived neurotrophic factor (BDNF) and neurotrophin-3 (NT3)
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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