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Disodium3-[(2,4-dimethyl-6-sulfonatophenyl)hydrazinylidene]-4-oxonaphthalene-1-sulfonate

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Name

Disodium3-[(2,4-dimethyl-6-sulfonatophenyl)hydrazinylidene]-4-oxonaphthalene-1-sulfonate

EINECS N/A
CAS No. 4548-53-2 Density g/cm3
PSA 176.11000 LogP 5.54740
Solubility 130.4g/L at 30℃ Melting Point >300℃
Formula C18H16 N2 O7 S2 . 2 Na Boiling Point °Cat760mmHg
Molecular Weight 480.44 Flash Point °C
Transport Information N/A Appearance N/A
Safety Low toxicity by ingestion. Questionable carcinogen with experimental carcinogenic and tumorigenic data. When heated to decomposition it emits toxic fumes of NOx and SOx. Risk Codes N/A
Molecular Structure Molecular Structure of 4548-53-2 (PONCEAU SX) Hazard Symbols N/A
Synonyms

1-Naphthalenesulfonicacid, 3-[(2,4-dimethyl-5-sulfophenyl)azo]-4-hydroxy-, disodium salt (9CI); C.I.Food Red 1 (7CI); C.I. Food Red 1, disodium salt (8CI); Ponceau SX (6CI); 12101Red; 1306 Red; C.I. 14700; Certicol Ponceau SXS; D and C Red No. 4; EdicolSupra Ponceau SX; FD and C Red No. 4; FD&C Red No. 4; FDC Red 4; Food Red1; Food Red 4; Hexacol Ponceau SX; Japan Red 4; Japan Red 504; Japan Red No. 4;Japan Red No. 504; Red 4; Red No. 1; Red No. 504; Usacert Red No. 4

 

Disodium3-[(2,4-dimethyl-6-sulfonatophenyl)hydrazinylidene]-4-oxonaphthalene-1-sulfonate Chemical Properties

IUPAC Name: Disodium3-[(2,4-dimethyl-6-sulfonatophenyl)hydrazinylidene]-4-oxonaphthalene-1-sulfonate
CAS: 4548-53-2
The Molecular formula of Disodium3-[(2,4-dimethyl-6-sulfonatophenyl)hydrazinylidene]-4-oxonaphthalene-1-sulfonate (CAS NO.4548-53-2): C18H14N2Na2O7S2
The Molecular Weight of Disodium3-[(2,4-dimethyl-6-sulfonatophenyl)hydrazinylidene]-4-oxonaphthalene-1-sulfonate (CAS NO.4548-53-2): 480.42
The Molecular Structure of Disodium3-[(2,4-dimethyl-6-sulfonatophenyl)hydrazinylidene]-4-oxonaphthalene-1-sulfonate (CAS NO.4548-53-2):

Appearance: red crystals

Disodium3-[(2,4-dimethyl-6-sulfonatophenyl)hydrazinylidene]-4-oxonaphthalene-1-sulfonate Toxicity Data With Reference

1.    

orl-rat LD50:>2 g/kg

    MEIEDD    Merck Index. 11 (1989),1209.
2.    

CONSENSUS REPORTS: IARC Cancer Review: Group 3 ; Animal Sufficient Evidence . Reported in EPA TSCA Inventory.

    IMEMDT    IARC Monographs on the Evaluation of Carcinogenic Risk of Chemicals to Man . 7 (1987),p. 56.(World Health Organization, Internation Agency for Research on Cancer,Lyon, France.: ) (Single copies can be ordered from WHO Publications Centre U.S.A., 49 Sheridan Avenue, Albany, NY 12210) IMEMDT    IARC Monographs on the Evaluation of Carcinogenic Risk of Chemicals to Man . 8 (1975),p. 207.(World Health Organization, Internation Agency for Research on Cancer,Lyon, France.: ) (Single copies can be ordered from WHO Publications Centre U.S.A., 49 Sheridan Avenue, Albany, NY 12210)

Disodium3-[(2,4-dimethyl-6-sulfonatophenyl)hydrazinylidene]-4-oxonaphthalene-1-sulfonate Safety Profile

Low toxicity by ingestion. Questionable carcinogen with experimental carcinogenic and tumorigenic data. When heated to decomposition it emits toxic fumes of NOx and SOx.
Safety Information about Disodium3-[(2,4-dimethyl-6-sulfonatophenyl)hydrazinylidene]-4-oxonaphthalene-1-sulfonate (CAS NO.4548-53-2):
Safety Statements about Disodium3-[(2,4-dimethyl-6-sulfonatophenyl)hydrazinylidene]-4-oxonaphthalene-1-sulfonate (CAS NO.4548-53-2):
S22: Do not breathe dust.
S24/25: Avoid contact with skin and eyes.
RTECS: QK2705000

Disodium3-[(2,4-dimethyl-6-sulfonatophenyl)hydrazinylidene]-4-oxonaphthalene-1-sulfonate Specification

  Disodium3-[(2,4-dimethyl-6-sulfonatophenyl)hydrazinylidene]-4-oxonaphthalene-1-sulfonatewith CAS number of 4548-53-2 is also known as Ponceau SX ; 12101Red ; 1306Red ; 2-(6-Sulfo-2,4-xylylazo)-1-naphthol-4-sulfonicacid,disodiumsalt ; 2-(6-sulpho-2,4-xylylazo)-1-naphthol-4-sulphonicacid,disodiumsalt ; 3-((2,4-dimethyl-5-sulfophenyl)azo)-4-hydroxy-1-naphthalenesulfonicacid,dis ; 3-((2,4-dimethyl-5-sulphophenyl)azo)-4-hydroxy-1-naphthalenesulphonicacid,d ; 3-[(2,4-dimethyl-5-sulfophenyl)azo]-4-hydroxy-1-naphthalenesulfonicacidis . Ponceau SX is an azo compound. Azo, diazo, azido compounds can detonate. This applies in particular to organic azides that have been sensitized by the addition of metal salts or strong acids. Toxic gases are formed by mixing materials of this class with acids, aldehydes, amides, carbamates, cyanides, inorganic fluorides, halogenated organics, isocyanates, ketones, metals, nitrides, peroxides, phenols, epoxides, acyl halides, and strong oxidizing or reducing agents. Flammable gases are formed by mixing materials in this group with alkali metals.

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