Hematoxylin
Synonym(s):H&E Stain, Gill;Hematoxylin;Hematoxylin cryst. (C.I. 75290);Natural Black 1
- CAS NO.:517-28-2
- Empirical Formula: C16H14O6
- Molecular Weight: 302.28
- MDL number: MFCD00283323
- EINECS: 208-237-3
- SAFETY DATA SHEET (SDS)
- Update Date: 2024-11-01 18:09:03
What is Hematoxylin?
Chemical properties
light brown crystals or powder
The Uses of Hematoxylin
Hematoxylin and eosin together make up Hematoxylin and eosin stain, one of the most commonly used stains in histology. Metal-haematein complexes are used to stain cell nuclei prior to examination under a microscope. Structures that stain with iron- or aluminum-haematein are often called basophilic, even though the mechanism of the staining is different from that of staining with basic dyes.
The Uses of Hematoxylin
Colorant in inks, biological stains.
What are the applications of Application
Gill′s Hematoxylin Solution, No. 3 is a nuclei stain used in histology
What are the applications of Application
Gill′s Hematoxylin Solution, No. 1 is a chromatin stain used in cytology
What are the applications of Application
Gill′s Hematoxylin Solution, No. 2 is a chromatin stain of blue-violet color used for both cytology and histology
Definition
ChEBI: (+)-haematoxylin is a haematoxylin. It is an enantiomer of a (-)-haematoxylin.
General Description
White to yellowish crystals that redden on exposure to light.
Air & Water Reactions
Soluble in hot water, slightly water soluble in cold .
Reactivity Profile
Sensitive to light. .
Hazard
May be carcinogenic.
storage
Store at RT
Purification Methods
Hematoxylin recrystallises from H2O (as trihydrate) in white-yellow crystals which become red on exposure to light and then melt at 100-120o. It has been recrystallised from Me2CO/*C6H6. It has been recrystallised as well from dilute aqueous NaHSO3 until colourless and is soluble in alkali, borax and glycerol. Store it in the dark below 0o. [Morsingh & Robinson Tetrahedron 26 182 1970, Dann & Hofmann Chem Ber 98 1498 1955, Beilstein 17/8 V 469.]
Properties of Hematoxylin
Melting point: | 200 °C (dec.)(lit.) |
Boiling point: | 363.32°C (rough estimate) |
Density | 1.2514 (rough estimate) |
vapor pressure | 0-0Pa at 20-25℃ |
refractive index | 1.4600 (estimate) |
storage temp. | Keep in dark place,Inert atmosphere,Room temperature |
solubility | Soluble in 95% ethanol(1 mg/mL). |
form | Powder/Solid |
Colour Index | 75290 |
pka | 6.7(at 25℃) |
color | Yellow to Brown |
PH Range | Red (0.0) to yellow (1.0);Pale yellow (5.0) to violet (6.0) |
Water Solubility | SOLUBLE IN HOT WATER |
Sensitive | Light Sensitive |
λmax | 292nm, 445nm, 560nm |
Merck | 14,4637 |
BRN | 91399 |
Stability: | Stable, but may discolour on exposure to light. Incompatible with strong oxidizing agents. |
Major Application | Plasma displays, textiles, hair dyes, identifying fresh and stale rice, diag-nosing cancer progression, detecting nosing cancer progression, cervical disease, central nervous system malfunctions, detecting genes, breast cancer, collagen in a tissue sample, apoptosis, demyelinating diseases, antigens, treatment of age-related macular degeneration, burns, prostate cancer, diabetesand obesity, viral diseases, neoplasms, peripheral neural and vascular ailments, skin disorders, biotechnological applications, reference standard materials for cytology, histology andimmunohistochemistry |
CAS DataBase Reference | 517-28-2 |
EPA Substance Registry System | Hematoxylin (517-28-2) |
Safety information for Hematoxylin
Signal word | Warning |
Pictogram(s) |
Exclamation Mark Irritant GHS07 |
GHS Hazard Statements |
H319:Serious eye damage/eye irritation |
Precautionary Statement Codes |
P264:Wash hands thoroughly after handling. P264:Wash skin thouroughly after handling. P280:Wear protective gloves/protective clothing/eye protection/face protection. P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing. P337+P313:IF eye irritation persists: Get medical advice/attention. |
Computed Descriptors for Hematoxylin
InChIKey | WZUVPPKBWHMQCE-UHFFFAOYSA-N |
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