CAS: 26636-01-1; 6-Methylheptyl 2-[dimethyl-[2-(6-Methylheptoxy)-2-Oxoethyl]Sulfanylstannyl]Sulfanylacetate
该化合物是一种化学化合物,具有有机锡和硫醚两种功能的复杂结构,其特征是有机锡和硫醚,其有机物运动特征一般会增强其在各种化学工艺中的稳定性和反应性,硫醚组的存在表明,在化学和材料科学协调方面,特别是在聚合聚合聚合物或配方稳定剂方面,可能具有潜在应用.二氨基酯成分表明,该化合物具有疏水性特征,可能影响其溶解性以及与其他物质的相互作用.此外,含有有机锡的化合物经常因其生物活动和环境影响而进行研究,因为有机锡化合物可能对水生生物产生毒性.
- 英文名称6-Methylheptyl 2-[dimethyl-[2-(6-Methylheptoxy)-2-Oxoethyl]Sulfanylstannyl]Sulfanylacetate
- 中文名称2,2-[(二甲基亚锡)双(硫代)]双乙酸二异辛酯
- IUPAC名称6-methylheptyl 2-[dimethyl-[2-(6-methylheptoxy)-2-oxoethyl]sulfanylstannyl]sulfanylacetate
- 其它别名Aceticacid, 2,2'-[(dimethylstannylene)bis(thio)]bis-, diiso°Ctyl ester (9CI); Tin,bis[(carboxymethyl)thio]dimethyl-, diiso°Ctyl ester (7CI); Bis[[[(iso°Ctyloxy)carbonyl]methyl]thio]dimethyltin; Diiso°Ctyl [(dimethylstannylene)dithio]diacetate; Dimethyltin S,S'-bis(iso°Ctylmercaptoacetate); Dimethyltin bis(iso°Ctyl mercaptoacetate); Dimethyltinbis(iso°Ctyl thioglycolate); Dimethyltin di(iso°Ctyl thioglycolate); T 40(ester)
- CAS编号26636-01-1
- MFCD编号:MFCD00077999
- EINECS号:247-862-6
- FDA UNII编号:9AFG988025
- 分子式:C22H44O4S2Sn
- 分子量:555.42
- 产品CID: 1244440
- 产品分类有机原料 → 有机金属类化合物 → 有机锡
物理性质
MSDS等安全信息
- GHS象形图
- GHS符号GHS08 & GHS07;
注释: Health hazard & Exclamation mark - 危险类别生殖毒性 类别2
急性毒性 类别4(经口)
特定目标器官毒性-重复接触 类别1
皮肤致敏 类别1
水生慢性毒性 类别3 - 警示词Danger(危险)
- 危险描述H361 |怀疑对生育能力或胎儿造成损害.
H302 |吞咽有害.
H372 |长期或反复接触损害器官.
H317 |可能引起皮肤过敏反应.
H412 |对水生生物有害并具有长期持续影响. - 防范说明P201-P202-P281-P308+P313-P405-P501-P261-P272-P280-P302+P352-P333+P313-P321-P363-P501-P273-P501-P264-P270-P301+P312-P330-P501-P260-P264-P270-P314-P501
- UN编号2788
- 安全声明Organotin compounds produce neurotoxic and immunotoxic effects. Organotins may directly activate glial cells contributing to neuronal cell degeneration by local release of pro-inflammatory cytokines, tumor necrosis factor-_, and/or interleukins. They may also induce apoptosis by direct action on neuronal cells. Organotin compounds stimulate the neuronal release of and/or decrease of neuronal cell uptake of neurotransmitters in brain tissue, including aspartate, GABA, glutamate, norepinephrine, and serotonin. This may be either a contributing factor to or result of the neuronal cell loss. The immunotoxic effects of organotins are characterized by thymic atrophy caused by the suppression of proliferation of immature thymocytes and apoptosis of mature thymocytes. Organotin compounds are believed to exert these effects by suppressing DNA and protein synthesis, inducing the expression of genes involved in apoptosis (such as nur77), and disrupting the regulation of intracellular calcium levels, giving rise to the uncontrolled production of reactive oxygen species, release of cytochrome c to the cytosol, and the proteolytic and nucleolytic cascade of apoptosis. The suppression of proliferation of immature thymocytes further results in the suppression of T-cell-mediated immune responses. Organotins are also endocrine disruptors and are believed to contribute to obesity by inappropriate receptor activation, leading to adipocyte differentiation. Inorganic tin triggers eryptosis, contributing to tin-induced anemia. (L308, A182, A184)
- 危险类别码Caused skin irritation in rabbits, but no eye irritation; Oral LD50 (rat) = 1380 mg/kg; [HSDB] See Tin, organic compounds.
欧盟法规
ECHA物质ECHA物质C&L通报REACH预注册合成工艺路线路线简述
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2905130000-正丁醇
2909110000-乙醚
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摘要:USEPA/Office of Water; Federal-State Toxicology and Risk Analysis Committee (FSTRAC). Summary of State and Federal Drinking Water Standards and Guidelines (11/93) To Present
摘要:Lewis, R.J. Sax's Dangerous Properties of Industrial Materials. 9th ed. Volumes 1-3. New York, NY: Van Nostrand Reinhold, 1996., p. 467
摘要:40 CFR 716.120 (7/1/2000)
参考文献:10.1155/bca.2005.191
摘要:Bychkov PV, Shekhovtsova TN, Milaeva ER. Inhibition of Horse Liver Alcohol Dehydrogenase byMethyltin Compounds. Bioinorganic Chemistry and Applications. 2005 Jan;3(3-4):191–9. doi: 10.1155/bca.2005.191.
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