418943
2,2′-[4-(2-Hydroxyethylamino)-3-nitrophenylimino]diethanol
98%
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About This Item
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assay
98%
mp
108-111 °C (lit.)
solubility
water: soluble(lit.)
SMILES string
OCCNc1ccc(cc1[N+]([O-])=O)N(CCO)CCO
InChI
1S/C12H19N3O5/c16-6-3-13-11-2-1-10(9-12(11)15(19)20)14(4-7-17)5-8-18/h1-2,9,13,16-18H,3-8H2
InChI key
MIWUTEVJIISHCP-UHFFFAOYSA-N
General description
2,2′-[4-(2-Hydroxyethylamino)-3-nitrophenylimino]diethanol (HC Blue No.2) is a water-soluble purple dye.
Application
2,2′-[4-(2-Hydroxyethylamino)-3-nitrophenylimino]diethanol may be employed to improve the visibility of self-healing ureidopyrimidinone (UPy) hydrogel (poly(ethylene glycol) containing bifunctional UDP groups).
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk_germany
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Species comparisons regarding comparative metabolism of two structurally similar phenylenediamines (HC Blue 1 and HC Blue 2).
Progress in clinical and biological research, 340D, 305-314 (1990-01-01)
Self-Healing Supramolecular Polymers In Action.
Macromolecular Chemistry and Physics, 213(2), 234-242 (2012)
HC Blue No. 2.
IARC monographs on the evaluation of carcinogenic risks to humans, 57, 143-151 (1993-01-01)
Cell biology and toxicology, 6(2), 139-155 (1990-04-01)
Previous studies indicated that HC Blue 1 induced heptocellular carcinomas in B6C3F1 mice whereas the structurally similar nitroaromatic amine HC Blue 2 did not. In an attempt to elucidate the biochemical mechanisms responsible for their different carcinogenic potencies, comparative metabolism
Mutation research, 241(2), 145-150 (1990-06-01)
2 hair dyes, HC Blue No. 1 and HC Blue No. 2, were evaluated for the in vitro induction of unscheduled DNA synthesis (UDS) in primary hepatocytes of rat, mouse, hamster, rabbit and monkey. NC Blue No. 1, which is
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