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Dinatrium-5-[[4'-[(7-amino-1-hydroxy-3-sulfonato-2-naphthyl)azo][1,1'-biphenyl]-4-yl]azo]salicylat

Direct Brown 2

HCID 17067
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Grundinformationen

CAS
2429-82-5
Standard-SMILES
Nc1ccc2cc(S(=O)(=O)[O-])c(N=Nc3ccc(-c4ccc(N=Nc5ccc(O)c(C(=O)[O-])c5)cc4)cc3)c(O)c2c1.[Na+].[Na+]
InChIKey
CXAVOCVLMJULES-UHFFFAOYSA-L
Summenformel
C29H19N5Na2O7S
Durchschnittliche Molmasse
627,5 g/mol
Monoisotopische Masse
627,0800577

Überblick

Reddish-brown solid or dark brown powder. (NTP, 1992)

Namen und Bezeichner

Bevorzugter Name
Direct Brown 2
IUPAC
disodium;5-[[4-[4-[(7-amino-1-hydroxy-3-sulfonatonaphthalen-2-yl)diazenyl]phenyl]phenyl]diazenyl]-2-hydroxybenzoate
Lokaler Name
Dinatrium-5-[[4'-[(7-amino-1-hydroxy-3-sulfonato-2-naphthyl)azo][1,1'-biphenyl]-4-yl]azo]salicylat
Englischer Name
DIRECT FAST BROWN M
Summenformel
C29H22N5NaO7S
Molmasse
607.57

Namen und Synonyme

Direct Fast Brown M2429-82-5CI Direct Brown 2DIRECT BROWN 2Azocard Brown MUnion Brown DRC.I. Direct Brown 2Azocord Brown MAzomine Brown MDiamine Brown MDiazine Brown MFenamin Brown M
Weitere Namen anzeigen
brownmci22311NSC74701c.i.22311NSC 74701NSC-74701azinebrownmbenzobrownmbenzobrownmcdiazobrownmc
Fixanol Brown MJapanol Brown MDiazol Brown MDirect Brown MMahogany EMBLAmanil Brown MRAtlantic Brown MAzine Brown M

Datenbank-Bezeichner

CAS
2429-82-5
PubChem CID
17067
DTXSID
DTXSID6025199
UNII
35C7Y2E3X5

Eigenschaften

Berechnete Struktureigenschaften

Polarare Oberfläche (TPSA)
222 Ų
H-Brücken-Donoren
3
H-Brücken-Akzeptoren
12
Frei drehbare Bindungen
5
Schwere Atome
44
Formalladung
0
Komplexität
1.070

Experimentelle und physikochemische Eigenschaften

Chemical ClassesDyes -> Benzidine Dyes
Solubility1 to 10 mg/mL at 68 °F (NTP, 1992)
Physical Description · 2 Einträge

Reddish-brown solid or dark brown powder. (NTP, 1992)

Reddish-brown or dark brown solid; [CAMEO]

Physikochemische Eigenschaften

Aggregatzustand
powder to crystal
Farbe
Light yellow to Brown to Dark green
Stabilität
Stable. Incompatible with strong oxidizing agents.
InChIKey
LIZWXWTXUIJRIZ-KZIIJSKASA-N
SMILES
OC1=C(C(S(O)(=O)=O)=CC2=CC=C(N)C=C12)/N=N/C1C=CC(C2C=CC(/N=N/C3C=CC(O)=C(C(=O)O)C=3)=CC=2)=CC=1.[NaH]
CAS Datenbank
2429 · 2429-82-5
EPA chemische Informationen
2 · C.I. Direct Brown 2, disodium salt (2429-82-5)

Sicherheit und Regulatorisches

Sicherheitsangaben dienen nur zur Orientierung und ersetzen weder das Sicherheitsdatenblatt (SDB) des Lieferanten noch geltende Vorschriften oder eine fachliche Bewertung.

GHS-Klassifizierung

GHS Classification · 6 Einträge

Danger

H302 (97.5%): Harmful if swallowed [Warning Acute toxicity, oral]

P203, P264, P270, P273, P280, P301+P317, P318, P330, P391, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 40 reports by companies from 3 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Danger

H350: May cause cancer [Danger Carcinogenicity]

Gefahrenhinweise

Regulatory Information · 3 Einträge

Chemical: Benzoic acid, 5-[[4'-[(7-amino-1-hydroxy-3-sulfo-2-naphthalenyl)azo][1,1'-biphenyl]-4-yl]azo]-2-hydroxy-, disodium salt

S - indicates a substance that is identified in a final Significant New Use Rule.

Benzoic acid, 5-[[4'-[(7-amino-1-hydroxy-3-sulfo-2-naphthalenyl)azo][1,1'-biphenyl]-4-yl]azo]-2-hydroxy-, disodium salt: Does not have an individual approval but may be used as a component in a product covered by a group standard. It is not approved for use as a chemical in its own right.

Other Safety InformationIMAP assessments - Benzidine-based dyes: Human health tier II assessment
Fire HazardsFlash point data for this chemical are not available, however, it is probably combustible. (NTP, 1992)
Hazards SummaryNo information available on health hazards: [CAMEO] One of the azo dyes metabolized to benzidine--known to be a human carcinogen; [NTP] See C.I. Direct Brown 95.
Reactive GroupAzo, Diazo, Azido, Hydrazine, and Azide Compounds
Reactivity Alerts

Chemie und Industrie

Verwendung und Herstellung

Uses · 3 Einträge

Used as dye for cellulose and nylon fibers, silk, wool, paper, leather, and cosmetics; [HSDB]

Pulp and Paper Processing [Category: Industry]

DYE FOR COLORING AND PRINTING CELLULOSE AND NYLON FIBERS, FOR SILK, WOOL, PAPER, LEATHER, COSMETICS

U.S. Exports · 2 Einträge

(1977) No Data

(1979) No Data

U.S. Imports · 2 Einträge

(1977) 1.00X10+6 GRAMS (PRINCPL CUSTMS DISTS)

(1979) 6.00X10+6 GRAMS (PRINCPL CUSTMS DISTS)

U.S. Production · 2 Einträge

(1978) 1.26X10+7 GRAMS

(1979) PROBABLY GREATER THAN 2.27X10+6 GRAMS

Consumption PatternsESSENTIALLY 100% AS A DYE
Methods of ManufacturingCOUPLING OF TETRAZOTIZED BENZIDINE WITH SALICYCLIC ACID, THEN COUPLING WITH GAMMA ACID UNDER ALKALINE CONDITIONS
General Manufacturing Information · 2 Einträge

Benzoic acid, 5-[2-[4'-[2-(7-amino-1-hydroxy-3-sulfo-2-naphthalenyl)diazenyl][1,1'-biphenyl]-4-yl]diazenyl]-2-hydroxy-, sodium salt (1:2): INACTIVE

SOL DYE TAKEN UP DIRECTLY BY FIBERS, PRESUMABLY DUE TO SELECTIVE ADSORPTION. USUALLY APPLIED TO COTTON OR...(COTTON-WOOL MIXT). DYING ASSISTANTS...SODIUM CHLORIDE OR SODIUM SULFATE ARE USED TO OBTAIN HIGHER CONCN OF DYE ON FIBERS. /DIRECT DYE/

Anwendungen

VerwendenDirect Fast Brown M is a direct dye used with textiles. It is a water pollutant, removed from the environment via adsorption by magnetic nano cobalt ferrite doped Capra aegagrus hircus dung activated carbon composite.

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EC Number
219-391-6
Explosive
Reactivity Profile · 1 Eintrag

DIRECT BROWN 2 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. Explosive combination can occur with strong oxidizing agents, metal salts, peroxides, and sulfides.

Air and Water ReactionsAzo dyes can be explosive when suspended in air at specific concentrations. Slightly soluble in water.
Hazard Classes and Categories · 2 Einträge

Acute Tox. 4 (97.5%)

Carcinogenicity - category 1B

Sicherheit und Schutzausrüstung

Fire FightingFires involving this compound can be controlled with a dry chemical, carbon dioxide or Halon extinguisher. (NTP, 1992)
First Aid · 1 Eintrag

EYES: First check the victim for contact lenses and remove if present. Flush victim's eyes with water or normal saline solution for 20 to 30 minutes while simultaneously calling a hospital or poison control center. Do not put any ointments, oils, or medication in the victim's eyes without specific instructions from a physician. IMMEDIATELY transport the victim after flushing eyes to a hospital even if no symptoms (such as redness or irritation) develop.

Nonfire Spill Response · 1 Eintrag

SMALL SPILLS AND LEAKAGE: If you spill this chemical, you should dampen the solid spill material with water, then transfer the dampened material to a suitable container. Use absorbent paper dampened with water to pick up any remaining material. Seal your contaminated clothing and the absorbent paper in a vapor-tight plastic bag for eventual disposal. Wash all contaminated surfaces with a soap and water solution. Do not reenter the contaminated area until the Safety Officer (or other responsible person) has verified that the area has been properly cleaned.

Personal Protective Equipment (PPE) · 1 Eintrag

RECOMMENDED RESPIRATOR: Where the neat test chemical is weighed and diluted, wear a NIOSH-approved half face respirator equipped with an organic vapor/acid gas cartridge (specific for organic vapors, HCl, acid gas and SO2) with a dust/mist filter. (NTP, 1992)

Toxikologische Informationen

Adverse EffectsNTP Carcinogen - Known to be a human carcinogen.

Sicherheitsdaten

tsca
TSCA listed
RTECS-Nr.
DM2800435
Giftige Stoffe Daten
2429-82-5(Hazardous Substances Data)

Darstellung

synthetische4-(4-Aminophenyl)benzenamine double nitriding, first coupled with 2-Hydroxybenzoic acid, and then in alkaline conditions and 6-Amino-4-hydroxynaphthalene-2-sulfonic acid coupling.

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