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Para Amino Azobenzene

Para Amino Azobenzene Suppliers list
Company Name: TCI AMERICA
Tel: 800-4238616
Email: sales@tciamerica.com
Products Intro: Cas:103-33-3
ProductName:Azobenzene
Brand:TCIChemical | Product Number:A0565 | Purity:min.98.0%
Company Name: Apollo Scientific Ltd.  
Tel: 44 161 406 0505
Email: sales@apolloscientific.co.uk
Products Intro: Cas:103-33-3
ProductName:Azobenzene
Brand: Apollo Scientific | Product Number: OR315219
Company Name: Alfa Aesar  
Tel: 1 888 343-8025 Specialty/Bulk
Email: tech@alfa.com
Products Intro: Cas:103-33-3
ProductName:Azobenzene
Brand: Alfa Aesar | Product Number: A10425
Company Name: Ultra Pure Lab Chem Industries LLP  
Tel: 08046077962
Email:
Products Intro: Cas:60-09-3
ProductName:p-Amino Azobenzene
Company Name: NINGBO JL NEW MATERIAL CO.,LTD  
Tel: 0574 88552216 18969899212
Email: sales@chematerials.cn
Products Intro: Cas:104-23-4
ProductName:PARA AMINO AZOBENZENE 4 SULPHONIC ACID
Purity: 98% | Package: 25KG;1KGS

Para Amino Azobenzene manufacturers

  • Azobenzene
  • Azobenzene pictures
  • $100.00
  • 2026-09-02
  • CAS:103-33-3
  • Min. Order: 1KG
  • Purity: 99%
  • Azobenzene
  • Azobenzene pictures
  • $10.00
  • 2026-03-20
  • CAS:103-33-3
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: 10 mt
  • AZOBENZENE
  • AZOBENZENE pictures
  • $2.00
  • 2019-07-06
  • CAS:103-33-3
  • Min. Order: 1kg
  • Purity: 99%
  • Supply Ability: 100kg
Para Amino Azobenzene Basic information
Product Name:Para Amino Azobenzene
Synonyms:4-Aminoazobenzene,CI 11000;4-Aminoazobenzol;AAB;4-Aminoazobenzene, AR,98%;4-(2-PHENYLDIAZ-1-ENYL)ANILINE;4-BENZENEAZOANILINE;4-(PHENYLDIAZENYL)ANILINE;4-PHENYLAZO-PHENYLAMINE
CAS:60-09-3
MF:C12H11N3
MW:197.24
EINECS:200-453-6
Product Categories:Intermediates of Dyes and Pigments;Solvent Dyestuff
Mol File:60-09-3.mol
Para Amino Azobenzene Structure
Para Amino Azobenzene Chemical Properties
Melting point 123-126 °C(lit.)
Boiling point >360 °C(lit.)
density 1.2828 (rough estimate)
refractive index 1.6500 (estimate)
storage temp. 2-8°C
solubility Chloroform (Slightly), Methanol (Slightly)
Colour Index 11000
pka2.82(at 25℃)
color Yellow crystals or orange needles with blue case from EtOH
Water Solubility 29.59mg/L(25 ºC)
Merck 14,419
BRN 1913042
Henry's Law Constant1.1×105 mol/(m3Pa) at 25℃, HSDB (2015)
Stability:Stable. Incompatible with strong oxidizing agents.
Major Applicationcleaning products
cosmetics
environmental
food and beverages
personal care
InChI1S/C12H11N3/c13-10-6-8-12(9-7-10)15-14-11-4-2-1-3-5-11/h1-9H,13H2/b15-14+
InChIKeyQPQKUYVSJWQSDY-CCEZHUSRSA-N
SMILESNc1ccc(cc1)\N=N/c2ccccc2
CAS DataBase Reference60-09-3(CAS DataBase Reference)
NIST Chemistry ReferenceBenzenamine, 4-(phenylazo)-(60-09-3)
IARC2B (Vol. 8, Sup 7) 1987
EPA Substance Registry System4-Aminoazobenzene (60-09-3)
Safety Information
Hazard Codes T,N,Xi
Risk Statements 45-50/53-36/37/38-20/21/22-46
Safety Statements 53-45-60-61-36/37/39-26-22
RIDADR UN 3077 9/PG 3
WGK Germany 3
RTECS BY8225000
TSCA TSCA listed
HazardClass IRRITANT
PackingGroup III
HS Code 29270000
Storage Class6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
Hazard ClassificationsAcute Tox. 4 Oral
Aquatic Acute 1
Aquatic Chronic 1
Carc. 1B
Skin Sens. 1
Hazardous Substances Data60-09-3(Hazardous Substances Data)
ToxicityLD50 intraperitoneal in mouse: 200mg/kg
MSDS Information
ProviderLanguage
SigmaAldrich English
Para Amino Azobenzene Usage And Synthesis
DescriptionThis azoic coloring can be reduced in paraphenylenediamine (PPD). It ean be found in some semipermanent hair dyes, and patch tests are frequently positive (about 30%) in hairdressers with hand dermatitis. Because of cross-sensitivity, the detection of sensitization to p-aminoazobenzene may be assumed by a PPD test.
Chemical Properties4-Aminoazobenzene forms yellow to tan crystals or orange needles.
Chemical Propertiespowder
UsesIn form of its salts in dyeing; intermediate in manufacture of Acid Yellow, diazo dyes and indulines.
Usesas a dye for lacquer, varnish, wax products, oi! stains and styrene res ins; in insecticides; used as an intermediate in the manufacture of Acid Yellow, diazo dyes and indulines.
Preparationcommonly known as Aniline Yellow. (a) anilinehydrochloride solution added to a anilinediazonium salt, and slowly, until anilinediazonium salt salt disappear so far. Then in contain a small amount of anilinehydrochloride anilinesolution will product (Diazoaminobenzene) 30 ~ 40 ℃ heating 2 ~ 3 hours,acidified to form 4-(Phenyldiazenyl)benzenaminehydrochloride and crystalline precipitates. In order to obtain 4-(Phenyldiazenyl)benzenaminetimes the company, and then 4-(Phenyldiazenyl)benzenamine hydrochloride dissolved in water and mercerized. (B) anilinediazotization and coupling anilino-methanesulfonic acid, sodium hydroxide solution and then with boiled together, hydrolyzed mesylate.
DefinitionChEBI: Azobenzene substituted at one of the 4-positions by an amino group.
General DescriptionOdorless brownish-yellow needles with bluish coating, or an orange powder.
Air & Water ReactionsDust may form an explosive mixture in air. Insoluble in water.
Reactivity Profile4-AMINOAZOBENZENE can detonate, particularly if sensitized by the presence of metal salts or strong acids. May form toxic gases 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. May form flammable gases with alkali metals. May react explosively with strong oxidizing agents, metal salts, peroxides, and sulfides. Emits toxic fumes of oxides of nitrogen when heated to decomposition (over 350°C) [Sax, 2nd ed., 1965, p. 417].
HazardPossible carcinogen.
Fire HazardFlash point data for 4-AMINOAZOBENZENE are not available; however, 4-AMINOAZOBENZENE is probably combustible.
Contact allergensThis azoic coloring can be reduced in para-phenylenediamine (PPD). It can be found in some semi-permanent hair dyes and patch tests are frequently positive (about 30%) in hairdressers with hand dermatitis. Because of hydrolysis of the azo bond, the detection of sensitization to p-aminoazobenzene may be assumed by a PPD test.
Safety ProfileConfirmed carcinogen with experimental neoplastigenic and tumorigenic data. Poison by intraperitoneal route. An experimental teratogen. Mutation data reported. Used as a dye for lacquer, varnish, wax products, oil stains, and styrene resins. When heated to decomposition it emits toxic fumes of NOx. See also AMINES
Potential ExposureAn azo compound used in form of salts in dyeing; used as intermediate in manufacture of acid yellow and diazo dyes; in insecticides, waxes, lacquers, varnishes, stains, styrene resins
ShippingUN2811 Toxic solids, organic, n.o.s., Hazard Class: 6.1; Labels: 6.1-Poisonous materials, Technical Name Required. UN3143 Dyes, solid, toxic, n.o.s. or Dye intermediates, solid, toxic, n.o.s., Hazard Class: 6.1; Labels: 6.1-Poisonous materials, Technical Name Required
Properties and Applicationsgreen light yellow to red light yellow. Melting point is 127.5 ℃, its hydrochloride for blue crystal. Soluble in ethanol, slightly soluble in water for yellow. In concentrated sulfuric acid for brown, red after diluted solution; In hydrochloric acid solution for red, boil color disappear. Used for alcohol soluble paint, varnish, paraffin wax, oil, synthetic resin coloring.
Standard Light Fastness Heat-resistant(℃) Water Sodium Carbonate(5%) Hydrochloric acid(5%)
Melting point Stable
ISO Good 125 140 Good Good Good
Purification MethodsCrystallise this dye from EtOH, CCl4, pet ether/*C6H6, or a MeOH/H2O mixture. [Beilstein 16 IV 445.]
IncompatibilitiesDust may form explosive mixture with air. Azo 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. This chemicalis sensitive to prolonged exposure to heat. This chemical is incompatible with strong oxidizing agents
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