- 英文名称3H-Naphtho[1,2,3-De]Quinoline-2,7-Dione, 3-Methyl-6-[(4-Methylphenyl)Amino]-
- 中文名称荧光红H5B
- IUPAC名称3-methyl-6-(p-tolylamino)-3H-naphtho[1,2,3-de]quinoline-2,7-dione
- 其它别名3H-Naphtho1,2,3-Dequinoline-2,7-Dione, 3-Methyl-6-(4-Methylphenyl)Amino-; 3-Methyl-6-[(4-Methylphenyl)Amino]-3H-Dibenz[f,Ij]Isoquinoline-2,7-Dione; Abcol Red 5B; Solvent Red 52; 2,3-Dihydro-3-Methyl-6-(P-Toluidino)-7H-Dibenz[f,Ij]Isoquinoline-2,7-Dione; 3H-Dibenz(F,Ij)Isoquinoline-2,7-Dione, 3-Methyl-6-((4-Methylphenyl)Amino)-
- CAS编号81-39-0
- MFCD编号:MFCD00272416
- EINECS号:201-346-7
- 分子式:C24H18N2O2
- 分子量:366.42
- 产品CID: 1807602
- 产品分类染料及颜料 → 染料 → 溶剂染料
上下游产品
CAS号873418-99-6 3-methyl-6-nitr... | CAS号106-49-0 对甲苯胺 | CAS号81-85-6 6-溴-3-甲基-3H-二苯并... | CAS号75507-40-3 1-(acetyl-methy... | CAS号6535-64-4 N-(4-(p-toluidi... | CAS号128-85-8 1-甲氨基-4-对甲苯氨基蒽醌合成工艺路线路线简述
- 合成目标产物 Solvent Red 52 主要起始原料 Ethanamine, N-[(3,5-Dichlorophenyl)Methylene]-2,2-Diethoxy- And P-Toluidine
- 81-85-6 = 81-39-0
反应条件:1.1 Reagents: Sodium Carbonate; Rt -> 185 °C; 4 H,180 - 185 °C; 185 °C -> 80 °C1.2 Reagents: Methanol
标题:Synthesis Of Anthrapyridone Solvent Dyes And Their Solubility
作者:Yin,Yi; Et Al
参考文献:Ranliao Yu Ranse 日期:2003 卷标:40(4) 页码:191-192
N-Methylanthrapyridon置于水,硝酸,Copper Diacetate,Sodium Acetate体系中,化学反应生成 荧光红h5B
参考文献:Nitroanthrapyridones
标题:Nitroanthrapyridones
摘要:
DOI:10.1021/jo01182A016
海关参考信息
- 2912110000-甲醛
2912210000-苯甲醛
2933310010-吡啶
2921440000-二苯胺 - 💡 提示:海关信息按照顺序优先匹配,如需确认的海关信息,请参考相关资料。
- 详情请参考:📖 海关编码查询和海关进出口税则
专利信息
专利号:US-5866628-A
优先权日:1996-08-30
标题 :Ultraviolet and electron beam radiation curable fluorescent printing ink concentrates and printing inks
发明人:LIKAVEC WAYNE R; BRADLEY CURTIS RAY
权利人:DAY GLO COLOR CORP
摘要:The present invention provides ultraviolet curable or electron beam curable fluorescent inks and ink concentrates, which cure upon exposure to ultraviolet or electron beam radiation. The synthesis of the fluorescent ink and ink concentrates does not involve the use of volatile organic solvents, so removal of solvents is not necessary during the manufacturing process. The fluorescent inks and ink concentrates display minimal, consistent color shift when cured. The cured fluorescent inks and ink concentrates are solvent resistant, particularly to methyl ethyl ketone, methanol, nonane, and sec butyl alcohol. The fluorescent ink and ink concentrate is comprised of: from about 20 to 90%, preferably from about 30 to 70%, more preferably from about 30 to 60% by weight of an oligomer, which is either a formaldehyde oligomer or a cyclic-aliphatic oligomer; from about 0.1 to 15%, preferably about 1 to 10%, of fluorescent dye; and from about 10 to 80%, preferably from about 30 to 70%, more preferably from about 35 to 60% of a photopolymerizable vehicle. The oligomer preferably has a weight average molecular weight of at least 400 g/mole. Preferably the oligomer has a molecular weight of from about 400 to 50,000 g/mole. The formaldehyde oligomer embodiment of the fluorescent ink preferably contains from about from 45% to 60% photopolymerizable vehicle, and from about 30 to 45%, oligomer. The formaldehyde oligomer contains from about 5% to 60%, preferably from about 15 to 45 % polymerized units of formaldehyde monomer and from about 40 to 95%, preferably about 55 to about 85%, polymerized units of an aromatic amide monomer. The cyclic-aliphatic oligomer embodiment preferably contains from about from 35% to 55% photopolymerizable vehicle, and from about 40 to 60%, oligomer. The cyclic-aliphatic oligomer contains polar groups and is comprised of polymerized units of from about 20 to 80%, preferably from about 30 to, 50% of cyclic monomers, and from about 80 to 20%, preferably from about 50 to about 70%, aliphatic monomers.