Pararosaniline Acetate CAS: 6035-94-5 | MF: C19H17N3€š¬¢C2H4O2 | MW: 347.41S10143, Part Number S10143, Buy Histological Stains & Dyes for Histology, Cytology, Microbiology, Hematology & Biology Lab from TriStains at Chemical World.
.Pararosaniline Acetate is a member of the triphenylmethane dye family and is a synthetic dye derived from pararosaniline. It is a key component of basic fuchsin and is also referred to as Basic Parafuchsin, Basic Red 9, and Magenta‚¬ž¢ O. With a chemical formula of C21H21N3O2, this compound is widely utilized in biological and histological staining techniques due to its affinity for binding to nucleic acids and proteins, resulting in a distinctive coloration of cellular components.
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Application :
- Pararosaniline Acetate is widely used in histology and microbiology for staining tissues and microorganisms. It is particularly effective for staining bacterial cell walls and fungal structures.
- It is used as a primary stain in Gram staining procedures to differentiate between Gram-positive and Gram-negative bacteria.
- It is utilized in molecular biology for staining nucleic acids, making it valuable for various research applications involving DNA and RNA visualization.
Benefits :
- Provides clear and distinct staining of cellular structures
- Gives reliable and reproducible staining results
- Versatile and cost-effective
Alternate Names | Basic Parafuchsin; Basic Red 9 |
Application | Pararosaniline acetate is a pure, principal component of Pararosaniline hydrochloride |
CAS Number | 6035-94-5 |
Molecular Weight | 347.41 |
Molecular Formula: | C19H17N3C2H4O2 |
Pararosaniline acetate is the pure, principal component of Pararosaniline hydrochloride (sc-203751).
Appearance | Powder |
Physical State | Solid |
Solubility | Soluble in 95% ethanol (0.1%), and water. |
Storage | Store at 4° C |
Melting Point | 203° C (lit.)(dec.) |
Boiling Point | 568.2° C at 760 mmHg (Predicted) |
SAFETY INFORMATION
WGK Germany | 3 |
PubChem CID | 735112 |
MDL Number | MFCD00012570 |
EC Number | 227-918-6 |
SMILES : | CC(=O)[O-].C1=CC(=[NH2+])C=CC1=C(C2=CC=C(C=C2)N)C3=CC=C(C=C3)N |
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