NAMES AND DATABASE IDS
NAMES AND DATABASE IDS
Names Database IDs
IUPAC name
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4-[(4-aminophenyl)(4-iminocyclohexa-2,5-dien-1-ylidene)methyl]aniline hydrochloride
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IUPAC Traditional name
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pararosaniline hydrochloride
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Synonyms
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Basic Fuchsin
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Pararosaniline hydrochloride
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Parafuchsin hydrochloride
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Paramagenta hydrochloride
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Pararosaniline chloride
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Basic Parafuchsin
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BASIC FUCHSIN HYDROCHLORIDE
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C.I. 42500
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Parafuchsin
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Basic Red 9
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PARAROSANILINE
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Basic Fuchsin
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Magenta™ O
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Pararosaniline hydrochloride
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4,4'-((4-Iminocyclohexa-2,5-dien-1-ylidene)methylene)dianiline hydrochloride
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碱性副品红
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碱性红 9
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CAS Number
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EC Number
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MDL Number
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Beilstein Number
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PubChem SID
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PubChem CID
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Color Index Number
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DATA SOURCES
DATA SOURCES
All Sources Commercial Sources Non-commercial Sources
CALCULATED PROPERTIES
CALCULATED PROPERTIES
JChem
H Acceptors
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3
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H Donor
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3
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LogD (pH = 5.5)
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-0.5890857
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LogD (pH = 7.4)
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0.039863743
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Log P
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2.8143616
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Molar Refractivity
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115.9541 cm3
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Polarizability
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34.50045 Å3
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Polar Surface Area
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75.89 Å2
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Rotatable Bonds
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2
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Lipinski's Rule of Five
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true
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PROPERTIES
PROPERTIES
Physical Property
Safety Information
Product Information
Bioassay(PubChem)
Apperance
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metallic green
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data source
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Melting Point
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240°C
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data source
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268- 270°C
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data source
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268-270 °C (dec.)(lit.)
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data source
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Absorption Wavelength
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λmax 544 nm
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data source
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λmax 545 nm
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data source
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Storage Condition
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Room Temperature (15-30°C)
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data source
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RTECS
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CX9850100
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data source
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European Hazard Symbols
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Toxic (T)
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data source
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MSDS Link
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German water hazard class
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3
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data source
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Risk Statements
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45
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data source
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R:45
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data source
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Safety Statements
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53-45
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data source
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S:45-53
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data source
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GHS Pictograms
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data source
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GHS Signal Word
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Danger
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Show
data source
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GHS Hazard statements
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H350
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data source
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GHS Precautionary statements
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P201-P308 + P313
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data source
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Personal Protective Equipment
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Eyeshields, full-face particle respirator type N100 (US), Gloves, respirator cartridge type N100 (US), type P1 (EN143) respirator filter, type P3 (EN 143) respirator cartridges
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data source
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Purity
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95+%
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Grade
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certified by the Biological Stain Commission
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data source
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for microscopy (Bact., Bot., Hist.)
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data source
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Compostion
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Dye content, >85%
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data source
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Dye content, >88%
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Show
data source
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Dye content, ≥88%
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Show
data source
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Certificate of Analysis
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pH Range
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1.0 - 3.1, purple to red
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Show
data source
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Linear Formula
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C19H18N3Cl
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data source
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Empirical Formula (Hill Notation)
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C19H17N3 · HCl
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Show
data source
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DETAILS
DETAILS
MP Biomedicals
Sigma Aldrich
MP Biomedicals -
02151800
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C.I. 42500 Free Base Purple crystals |
MP Biomedicals -
02150423
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C.I. 42500 Hydrochloride Biological stain for Gomori's aldehyde-fuchsin method, periodic acid Schiff method, and in Endo medium for distinguishing coli and aerogene bacteria. Dye content: ~ 88% min. SUSPECTED CANCER AGENT! |
Sigma Aldrich -
76250
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Other Notes This is the pure, principal component of mixtures commonly referred to as Basic Fuchsin. Reagent for the colorimetric determination of sulfite in foods1 Legal Information Magenta is a trademark of Magenta Corp. |
Sigma Aldrich -
P1528
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Other Notes This is the pure, principal component of mixtures commonly referred to as Basic Fuchsin. 包装 25, 100 g in glass bottle Suitability Certified for use in acid-fast staining procedures utilizing carbol-fuchsin; Endo medium; as Schiff′s reagent in the Periodic Acid Schiff (PAS) and Feulgen techniques; Gomori′s aldehyde fuchsin method for pancreatic B cells and hepatitis B surface antigen. 法律信息 Magenta 商标 Magenta Corp. |
Sigma Aldrich -
215597
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Packaging 25 g in glass bottle Legal Information Magenta is a trademark of Magenta Corp. |
Sigma Aldrich -
P3750
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Other Notes This is the pure, principal component of mixtures commonly referred to as Basic Fuchsin. 包装 25 g in glass bottle 法律信息 Magenta 商标 Magenta Corp. |
Sigma Aldrich -
857343
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Packaging 25, 100 g in glass bottle Suitability Certified for use for acid-fast staining with carbol-fuchsin, as ENDO medium, and as Schiff′s reagent in the Periodic Acid Schiff (PAS) and Feulgen techniques. Legal Information Magenta is a trademark of Magenta Corp. |
PATENTS
PATENTS
PubChem Patent
Google Patent