CAS 4196-99-0|Scarlet Red Sulfonate NF

Introduction:Basic information about CAS 4196-99-0|Scarlet Red Sulfonate NF, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common NameScarlet Red Sulfonate NF
CAS Number4196-99-0Molecular Weight556.479
Density/Boiling Point/
Molecular FormulaC22H14N4Na2O7S2Melting Point181-188ºC
MSDSChineseUSAFlash Point300°(572°F)

Names

NameBiebrich scarlet
SynonymMore Synonyms

Scarlet Red Sulfonate NF BiologicalActivity

DescriptionBiebrich scarlet is an azo organosulfur dyes.
Related CatalogResearch Areas >>Others

Chemical & Physical Properties

Melting Point181-188ºC
Molecular FormulaC22H14N4Na2O7S2
Molecular Weight556.479
Flash Point300°(572°F)
Exact Mass556.009949
PSA200.83000
LogP7.34600
InChIKeyVVAVKBBTPWYADW-UHFFFAOYSA-L
SMILESO=S(=O)([O-])c1ccc(N=Nc2ccc(N=Nc3c(O)ccc4ccccc34)c(S(=O)(=O)[O-])c2)cc1.[Na+].[Na+]
Storage conditionStore at +15°C to +30°C.
StabilityStable. Incompatible with strong oxidizing agents.
Water Solubilityethanol: 1 mg/mL

Safety Information

Personal Protective EquipmentEyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard CodesXi,Xn
Risk PhrasesR36/37/38
Safety Phrases37/39-26-36
RIDADRNONH for all modes of transport
WGK Germany3

Articles5

More Articles
Synthesis and characterization of pH-sensitive poly(organophosphazene) hydrogels.

Biomaterials 17(23) , 2295-302, (1996)

A new class of pH-sensitive hydrogels has been designed and synthesized. These are novel polyphosphazenes that bear various ratios of sodium oxybenzoate and methoxyethoxyethoxy side groups. These wate...

Non-covalent binding of azo compound to peptide chain: interactions of biebrich scarlet and naphthochrome green with four model proteins.

Amino Acids 36(2) , 251-60, (2009)

We studied the non-specific interactions of two azo compounds: biebrich scarlet (BS) and naphthochrome green (NG), with four model proteins: bovine serum albumin, ovalbumin, poly-L-lysine and hemoglob...

A histochemical examination of the staining of kainate-induced neuronal degeneration by anionic dyes.

Biotech. Histochem. 73(5) , 244-54, (1998)

Anionic dyes, notably acid fuchsine, strongly stain the nuclei and cytoplasm of neurons severely damaged by injury or disease. We provide detailed instructions for staining nervous tissue with toluidi...

Synonyms

Imperial Scarlet 3B
Fast Scarlet BA
Amacid Chrome Red 3B
Ponceau BS
Wool Scarlet BR
Benzenesulfonic acid, 2-[(E)-2-(2-hydroxy-1-naphthalenyl)diazenyl]-5-[(E)-2-(4-sulfophenyl)diazenyl]-, sodium salt (1:2)
abcolred3bconc
Acid Scarlet BA
Scarlet EC
Naphthazine Scarlet BI
MFCD00003891
Cloth Red G
Scarlet Red Sulfonate NF
Biebrich scarlet WS
Amacid Red 3B
Scarlet 3B
EINECS 224-084-5
biebrich scarlet red
PONCEAU B
Benzenesulfonic acid, 2-((2-hydroxy-1-naphthalenyl)azo)-5-((4-sulfophenyl)azo)-, disodium salt
6-(2-hydroxy-[1]naphthylazo)-3,4'-azo-bis-benzenesulfonic acid,sodium salt
PONCEAU 3RB
ACID RED 66
SCARLET B
CROCEINE SCARLET
Biebrich scarlet sodium salt
Fenazo Scarlet B
sodium 6-(2-hydroxynaphthylazo)-3,4'-azodibenzenesulfonate
Calcochrome Red 650
6-(2-Hydroxy-[1]naphthylazo)-3,4'-azo-bis-benzolsulfonsaeure,Natriumsalz
Biebrich Scarlet
Disodium 2-[(E)-(2-hydroxy-1-naphthyl)diazenyl]-5-[(E)-(4-sulfonatophenyl)diazenyl]benzenesulfonate
Red HM
BONCEAU BS
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