389439
1-芘甲醇
98%
别名:
1-羟甲基芘, 1-（1-羟甲基）芘
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关于此项目
经验公式（希尔记法）:
C17H12O
化学文摘社编号:
分子量:
232.28
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
方案
98%
表单
solid
mp
123-126 °C (lit.)
官能团
hydroxyl
SMILES字符串
OCc1ccc2ccc3cccc4ccc1c2c34
InChI
1S/C17H12O/c18-10-14-7-6-13-5-4-11-2-1-3-12-8-9-15(14)17(13)16(11)12/h1-9,18H,10H2
InChI key
NGDMLQSGYUCLDC-UHFFFAOYSA-N
应用
1-芘乙醇可用于：
- 合成腺苷-5′ 的钳形苯桥接荧光选择性传感器-三磷酸盐 (ATP) 检测。
- 作为合成芘端聚甲基丙烯酸缩水甘油酯聚合物的起始原料。
- 作为合成芘核心星形聚合物的引发剂。
- 合成医药和农药领域的重要中间体 1-芘甲醛。
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
Thermal conductivity and structure of non-covalent functionalized graphene/epoxy composites.
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Carbon, 49(15), 5107-5116 (2011)
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Mutation research, 324(3), 111-114 (1994-07-01)
Previous studies demonstrated that the ion composition of the exposure medium may strongly influence the mutagenicity of many compounds in the liquid preincubation modification of the reversion assay with his- Salmonella typhimurium strains. Similar influences were now observed in the
Ronny Kollock et al.
Biochemical pharmacology, 75(2), 527-537 (2007-10-09)
Alkylated polycyclic aromatic hydrocarbons can be metabolically activated via benzylic hydroxylation and sulphation to electrophilically reactive esters. However, we previously found that the predominant biotransformation route for the hepatocarcinogen 1-hydroxymethylpyrene (1-HMP) in the rat in vivo is the oxidation of
C D Sherman et al.
Carcinogenesis, 16(10), 2499-2506 (1995-10-01)
The promotional effect of phenobarbital and 1-hydroxymethyl-pyren on enzyme altered lesions in the rat liver were quantified within the framework of two separate multipath/multistage models. The experiment analyzed followed an initiation-promotion protocol in which female Wistar rats were initiated with
Bernhard H Monien et al.
Toxicology, 262(1), 80-85 (2009-06-02)
1-Methylpyrene (1-MP), an abundant alkylated polycyclic aromatic hydrocarbon, is activated by side-chain hydroxylation to 1-hydroxymethylpyrene (1-HMP) and subsequent sulfo-conjugation to electrophilic 1-sulfooxymethylpyrene (1-SMP). In rats, this activation mainly occurs in liver. 1-SMP may react with hepatic DNA or be exported
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