33040
2,5-Diaminohydroquinone dihydrochloride
technical, ≥90% (AT)
Synonym(s):
2,5-Diamino-1,4-benzenediol dihydrochloride, 2,5-Diamino-1,4-dihydroxybenzene dihydrochloride
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About This Item
Empirical Formula (Hill Notation):
C6H8N2O2 · 2HCl
CAS Number:
Molecular Weight:
213.06
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
5795549
Assay:
≥90% (AT)
Form:
powder
InChI
1S/C6H8N2O2.2ClH/c7-3-1-5(9)4(8)2-6(3)10;;/h1-2,9-10H,7-8H2;2*1H
SMILES string
Cl.Cl.Nc1cc(O)c(N)cc1O
InChI key
NILKAWPWTYPHAH-UHFFFAOYSA-N
grade
technical
assay
≥90% (AT)
form
powder
Quality Level
Related Categories
Application
2,5-Diaminohydroquinone dihydrochloride was used in the preparation of polymers. It was also used in the preparation of chemically cross-linked polyimide and silica hybrid films.
Disclaimer
may discolor to black-violet on storage
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Synthesis and characterization of chemically cross-linked polyimide-siloxane hybrid films.
Ahmad Z, et al.
Journal of Non-Crystalline Solids, 355(8), 507-517 (2009)
Polymers derived from 2, 5-diamino-p-benzoquinone-diimide and related compounds.
Szita J and Marvel CS.
Journal of Polymer Science Part A: Polymer Chemistry, 7(11), 3203-3217 (1969)
A H-bond stabilized quinone electrode material for Li-organic batteries: the strength of weak bonds.
Louis Sieuw et al.
Chemical science, 10(2), 418-426 (2019-02-13)
Small organic materials are generally plagued by their high solubility in battery electrolytes. Finding approaches to suppress solubilization while not penalizing gravimetric capacity remains a challenge. Here we propose the concept of a hydrogen bond stabilized organic battery framework as
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