1. Home
  2. 1,3-Benzenediol, 4,6-diamino-, dihydrochloride

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

1,3-Benzenediol, 4,6-diamino-, dihydrochloride

Oc1cc(O)c(cc1N)N.Cl.Cl Request for Quotation
Chemical Name: 1,3-Benzenediol, 4,6-diamino-, dihydrochloride
CAS Number: 16523-31-2
Product Number: AG001W00(AGN-PC-0Q8P0A)
Synonyms:
MDL No:
Molecular Formula: C6H10Cl2N2O2
Molecular Weight: 213.0618

Identification/Properties

Properties
MP:
254 °C (dec.)(lit.)
BP:
430.1°C at 760 mmHg
Storage:
Light sensitive;Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
213.058g/mol
Hydrogen Bond Donor Count:
6
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
0
Exact Mass:
212.012g/mol
Monoisotopic Mass:
212.012g/mol
Topological Polar Surface Area:
92.5A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
108
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
3
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


4,6-Diaminobenzene-1,3-diol dihydrochloride, also known as quinizarin dihydrochloride, is a versatile compound used in chemical synthesis for its unique properties. This compound is commonly employed as a chemical reagent in various organic reactions due to its ability to participate in redox and condensation reactions.One of the key applications of 4,6-diaminobenzene-1,3-diol dihydrochloride in chemical synthesis is in the preparation of azo dyes. Its reactivity allows it to undergo diazo coupling reactions with diazonium salts, resulting in the formation of colored azo compounds widely used in the textile and dye industries. Additionally, this compound serves as a valuable building block for the synthesis of other organic compounds, such as pharmaceuticals and agrochemicals.Furthermore, 4,6-diaminobenzene-1,3-diol dihydrochloride is utilized in the development of complex coordination compounds and metal complexes. Its chelating properties enable it to form stable complexes with a variety of metal ions, making it a crucial component in the field of coordination chemistry.Overall, the application of 4,6-diaminobenzene-1,3-diol dihydrochloride in chemical synthesis plays a significant role in various industries, contributing to the production of a wide range of important materials and compounds.