462268
4,4′-二氨基二苯乙烯-2,2′-二磺酸
technical grade, 85%
别名:
水甘草酸
等级
technical grade
质量水平
方案
85%
mp
>300 °C (lit.)
官能团
sulfonic acid
SMILES字符串
Nc1ccc(\C=C\c2ccc(N)cc2S(O)(=O)=O)c(c1)S(O)(=O)=O
InChI
1S/C14H14N2O6S2/c15-11-5-3-9(13(7-11)23(17,18)19)1-2-10-4-6-12(16)8-14(10)24(20,21)22/h1-8H,15-16H2,(H,17,18,19)(H,20,21,22)/b2-1+
InChI key
REJHVSOVQBJEBF-OWOJBTEDSA-N
一般描述
4,4′-二氨基-2,2′-二苯乙烯二磺酸二钠盐可用于合成染料和光学增白剂或荧光增白剂。
Ahmed Mohamed El-Toni et al.
Journal of colloid and interface science, 293(2), 449-454 (2005-07-19)
Organic ultraviolet (UV) rays absorbents have been used as sunscreen materials, but they may pose a safety problem when used at high concentration. In order to prevent direct contact of organic UV rays absorbent to the human skin, a typical
G Yu et al.
Chemosphere, 37(3), 487-494 (1998-07-14)
Two advanced oxidation processes, Fenton's reagent oxidation and ozonation, were used for pretreatment of a 4,4'-diaminostilbene-2,2'-disulfonic acid (DSD-acid) manufacturing wastewater on a laboratory scale. The results showed that both methods are suitable for partial removal of chemical oxygen demand (COD)
Z Li et al.
Huan jing ke xue= Huanjing kexue, 22(6), 57-60 (2002-02-22)
H acid and DSD acid are two important substrate of dyes, which wastewater is treated more difficulty because of containing multi-component, with high chroma value and nonbiodegradability. A treatment way of this wastewater by extraction based on chemical association was
K A Hostetler et al.
Journal of toxicology and environmental health, 48(2), 141-149 (1996-06-07)
4,4'-Diamino-2,2'-stilbene disulfonic acid (DAS), a key intermediate in the synthesis of dyes and fluorescent whitening agents, has been purported to have weak estrogenic properties based on apparent structural similarity with diethylstibestrol (DES) and unsubstantiated reports of male reproductive dysfunction in
C J Venglarik et al.
Molecular and cellular biochemistry, 140(2), 137-146 (1994-11-23)
We showed previously that the disulfonic stilbene DNDS (4,4'-dinitrostilben-2,2'-disulfonic acid) was a potent blocker of outwardly rectifying chloride channels (ORCC). The studies reported here were designed to quantify the relationship between electron withdrawal by the 4,4'-substituents and blocker potency. Specifically
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