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聚[[6-[(1,1,3,3-四甲基丁基)氨基]-1,3,5-三嗪-2,4-二基][(2,2,6,6-四甲基-4-哌啶基)亚氨基]-1,6-己二基[(2,2,6,6-四甲基-4-哌啶基)亚氨]] | 71878-19-8

中文名称
聚[[6-[(1,1,3,3-四甲基丁基)氨基]-1,3,5-三嗪-2,4-二基][(2,2,6,6-四甲基-4-哌啶基)亚氨基]-1,6-己二基[(2,2,6,6-四甲基-4-哌啶基)亚氨]]
中文别名
光稳定剂LQ-944;紫外吸收剂783;聚{[6-[(1,1,3,3-四甲基丁基)氨基]]-1,3,5-三嗪-2,4-[(2,2,6,6,-四甲基-哌啶基)亚氨基]-1,6-己二撑[(2,2,6,6-四甲基-4-哌啶基)亚氨基]};聚-{[6-[(1,1,3,3-四甲基丁基)-亚氨基]-1,3,5-三嗪-2,4-二基][2-(2,2,6,6-四甲基哌啶基)-氨基]-亚己基-[4-(2,2,6,6-四甲基哌啶基)-亚氨基]};光稳定剂783;光稳定剂UV-944;受阻胺光稳定剂HS-944;聚[[6-[(1,1,3,3-四甲基丁基)胺]-1,3,5-三嗪-2,4-二基][(2,2,6,6-四甲基-4-哌啶)亚胺]-1,6-二己二基[(2,2,6,6-四甲基-4-哌啶)亚胺]]];光稳定剂TH-944;N,N'-双-(2,2,6,6-四甲基-4-哌啶基)-1,6-己二胺与2,4,6-三氯-1,3,5-三嗪的聚合物和1,1,3,3-四甲基丁胺的反应产物;光稳定剂944;聚-{[6-[(1,1,3,3,-四甲基丁基)-胺基]1,3,5,-三嗪-2,4-二基][(2,2,6,6-四甲基哌啶基)-亚胺基]-1,6-己烷二基-[(2,2,6,6-四甲基哌啶基)-亚胺基]};光稳定剂 TH-944
英文名称
Chimassorb LS 944LD
英文别名
N,N'-bis(2,2,6,6-tetramethylpiperidin-4-yl)hexane-1,6-diamine;2,4,6-trichloro-1,3,5-triazine;2,4,4-trimethylpentan-2-amine
聚[[6-[(1,1,3,3-四甲基丁基)氨基]-1,3,5-三嗪-2,4-二基][(2,2,6,6-四甲基-4-哌啶基)亚氨基]-1,6-己二基[(2,2,6,6-四甲基-4-哌啶基)亚氨]]化学式
CAS
71878-19-8
化学式
C35H69Cl3N8
mdl
——
分子量
708.3
InChiKey
ORECYURYFJYPKY-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 熔点:
    136-140 °C(lit.)
  • 物理描述:
    DryPowder, PelletsLargeCrystals

计算性质

  • 辛醇/水分配系数(LogP):
    8.34
  • 重原子数:
    46
  • 可旋转键数:
    11
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.91
  • 拓扑面积:
    113
  • 氢给体数:
    5
  • 氢受体数:
    8

安全信息

  • 危险品标志:
    T+
  • 安全说明:
    S26,S36/37,S45
  • 危险类别码:
    R26,R36/37
  • WGK Germany:
    3
  • RTECS号:
    TR7755000
  • 危险品运输编号:
    UN 2811

制备方法与用途

光稳定剂 TH-944简介

光稳定剂 TH-944挥发性低,稳定性好,能有效保护高分子材料免受紫外光照射和长期热老化引起的光降解和热降解。

理化性质
特征 参数
外观 白色粉末或淡黄色颗粒
透光率 425nm: ≥93%
450nm: ≥95%
挥发分 ≤1%
灰 分 ≤0.1%
熔点 110℃ - 130℃
堆积密度 548-646 g/L
相对密度 20℃: 1.01
失重温度 ≥270℃
溶解性 可溶于丙酮、甲苯、二甲苯、苯、乙酸乙酯、乙烷、氯仿等有机溶剂,微溶于甲醇,不溶于水。
毒性 无毒
应用

光稳定剂 TH-944广泛应用于低密度聚乙烯薄膜、聚丙烯纤维、聚丙烯胶带、EVA薄膜、ABS、聚苯乙烯及食品包装中,以提高塑料制品的稳定性。

特点与用途

聚合型高效受阻胺类光稳定剂,具有低挥发性和低迁移性。它不仅能提供热稳定效果和抗氧化效果,还能与抗氧剂和紫外线吸收剂产生协同作用。适用于聚烯烃、烯烃共聚物以及聚苯醚复合物、聚甲醛、酰氨酯、软硬PVC及PVC共混物等。

储存

应避免阳光直射、潮湿环境和高温,同时要避开含硫或卤族元素的稳定剂、阻燃剂或杀虫剂。

适用范围

适用于聚烯烃塑料(如PP,PE),烯烃共聚物(如EVA)以及聚丙烯与弹性体的共混物。此外,还可以有效用于聚甲醛(POM)、聚酰胺(PA)、聚氨酯(PU),软硬PVC及PVC共混物,并对苯乙烯类弹性体和胶粘体也有良好的功效。

用途

适用于低密度聚乙烯薄膜、聚丙烯纤维、聚丙烯胶带、EVA薄膜、ABS、聚苯乙烯及食品包装中。

文献信息

  • [EN] USE OF 4-CYANO-NAPHTHALENE-1, 8-DICARBOXIMIDE DERIVATIVES AND RELATED COMPOUNDS TO PROTECT ORGANIC MATERIAL FROM THE DAMAGING EFFECTS OF LIGHT<br/>[FR] UTILISATION DE DERIVES 4-CYANO-NAPHTHALENE-1, 8-DICARBOXIMIDE ET COMPOSES ASSOCIES POUR LA PROTECTION DE MATIERE ORGANIQUE CONTRE LES EFFETS NUISIBLES DE LA LUMIERE
    申请人:BASF AG
    公开号:WO2005047265A1
    公开(公告)日:2005-05-26
    A description is given of the use of naphthalene-1,8-dicarboxylic monoimides of the formula (I), in which R1 is hydrogen, alkyl, alkenyl, cycloalkyl, cycloalkenyl, heterocycloalkyl, aryl or heteroaryl and R2 is a radical containing at least one π electron system containing a carbon atom and at least one further atom selected from carbon, oxygen, and nitrogen, with the proviso that the radical contains at least one atom other than carbon; to protect organic material from the damaging effects of light, of compositions which comprise at least one naphthalene-1,8-dicarboxylic monoimide of the formula (I) in an amount which provides protection from the damaging effects of light, and at least one organic material, and of new naphthalene-1,8-dicarboxylic monoimides (I).
    描述了使用式(I)的萘-1,8-二羧酸单亚胺,其中R1是氢、烷基、烯基、环烷基、环烯基、杂环烷基、芳基或杂芳基,R2是一个含有至少一个π电子体系的基团,其中包含一个碳原子和至少一个来自碳、氧和氮的其他原子,但基团至少包含一个碳以外的原子;用于保护有机材料免受光的破坏作用的组合物的描述,该组合物包括至少一种式(I)的萘-1,8-二羧酸单亚胺,其含量提供了对光的破坏作用的保护,以及至少一种有机材料,以及新的萘-1,8-二羧酸单亚胺(I)。
  • Stabilization of iodine biocides
    申请人:Uhr Hermann
    公开号:US20090036555A1
    公开(公告)日:2009-02-05
    2-(2-Hydroxyphenyl)benzotriazoles are outstandingly suitable for stabilizing iodine-containing biocides in industrial materials, more particularly in paints based on alkyd resin.
    2-(2-羟基苯基)苯并三唑在工业材料中稳定含碘生物杀菌剂方面特别适用,尤其是在基于醇酸树脂的油性漆中。
  • STABLE COMPOSITIONS OF THIABENDAZOLE AND IODINE-CONTAINING FUNGICIDES
    申请人:LANXESS Deutschland GmbH
    公开号:US20150051279A1
    公开(公告)日:2015-02-19
    The present invention relates to stable compositions for the fungicidal equipment of thermoplastic polymers, in particular PVC, comprising thiabendazole, at least one iodine-containing fungicide and at least one epoxide and optionally further fungicidally active compounds, and also to methods for preparing these formulations and to uses thereof for the protection of thermoplastic polymers against attack and destruction by microorganisms. Moreover, the invention relates to mold-resistant PVC materials equipped with the compositions according to the invention.
    本发明涉及用于热塑性聚合物的抗真菌设备的稳定组合物,特别是PVC,包括噻苯唑、至少一种含碘真菌剂和至少一种环氧化物,以及可选的其他具有抗真菌活性的化合物,以及制备这些配方的方法和用途,用于保护热塑性聚合物免受微生物的侵害和破坏。此外,该发明涉及配备了根据本发明的组合物的耐霉PVC材料。
  • Oligomeric hindered amine light stabilizers based on multi-functional carbonyl compounds and methods of making same
    申请人:——
    公开号:US20020087000A1
    公开(公告)日:2002-07-04
    Oligomeric compounds and methods of making the compound having the formula: T&Parenopenst;E-F&Parenclosest; i &Parenopenst;E-F′&Parenclosest; j &Parenopenst;E′-F&Parenclosest; k &Parenopenst;E′-F′&Parenclosest; l S  (II) wherein i, j, k, and l are integers from about 0 to 300 and the sum of i, j, k, and l is greater than 2, wherein the units F, F′ and T are derived from one or more multi-functional carbonyl compounds of general structure DO—CO—CR a R b —(—CR c R d —) n —NH—(Y) m —CO—OD  (IV) wherein n is an integer from 1 to 15, m is either 0 or 1; R a , R b , R c , and R d , are each a hydrogen or a hydrocarbyl group; Y is CO—(CR e R f ) p , wherein R e and R f are each a hydrogen or hydrocarbyl group and p is zero or an integer from 1 to 20 or CO—C 6 H 4 —, wherein the substitution pattern on the phenylene group is an ortho, meta, or para substitution pattern, and one or more of the hydrogens of the phenylene group may be substituted by a hydrocarbyl group or a functional group; and D is a hydrocarbyl group and the units E, E′ and S are derived from one or more 1-substituted piperidin-4-ol or 4-aminopiperidines of general structure 1 wherein Z is OH or NHG, wherein G is H or C 1 -C 12 alkyl, R 1 is —(CH 2 ) s —OH, —(CH 2 ) s —NH 2 , C 1 -C 18 hydroxyalkoxy or C 5 -C 12 hydroxycycloalkoxy; wherein s is an integer from 1 to 10; R 2 represents hydrogen, C 1 -C 8 alkyl, or benzyl; R 3 , R 4 , R 5 , and R 6 are each a hydrogen, C 1 -C 8 alkyl, benzyl or phenethyl, or two geminal R moieties, which together with the carbon to which they are attached form a C 5 -C 10 cycloalkyl. The compounds are useful for stabilizing polymer compositions against photo- and thermal degradation.
    含有以下公式的化合物的寡聚体化合物及其制备方法:T&Parenopenst;E-F&Parenclosest;i&Parenopenst;E-F′&Parenclosest;j&Parenopenst;E′-F&Parenclosest;k&Parenopenst;E′-F′&Parenclosest;lS  (II),其中i、j、k和l为约0至300的整数,且i、j、k和l的总和大于2,其中单位F、F′和T来源于一个或多个具有一般结构DO—CO—CRaRb—(—CRcRd—)n—NH—(Y)m—CO—OD  (IV)的多功能羰基化合物,其中n为1至15的整数,m为0或1;Ra、Rb、Rc和Rd分别为氢或烃基团;Y为CO—(CReRf)p,其中Re和Rf分别为氢或烃基团,p为0或1至20的整数,或CO—C6H4—,苯环基上的取代模式为邻位、间位或对位取代模式,苯环基的一个或多个氢原子可被烃基团或功能基团取代;D为烃基团,单位E、E′和S来源于一个或多个具有一般结构1的1-取代哌啶-4-醇或4-氨基哌啶,其中Z为OH或NHG,G为H或C1-C12烷基,R1为—(CH2)s—OH、—(CH2)s—NH2、C1-C18羟基烷氧基或C5-C12羟基环烷氧基,其中s为1至10的整数;R2代表氢、C1-C8烷基或苄基;R3、R4、R5和R6分别为氢、C1-C8烷基、苄基或苯乙基,或两个伪生R基团,它们与它们附着的碳形成C5-C10环烷基。这些化合物可用于稳定聚合物组合物对光和热降解的作用。
  • Hindered amine light stabilizers based on multi-functional carbonyl compounds and methods of making same
    申请人:——
    公开号:US20020099218A1
    公开(公告)日:2002-07-25
    Compounds and methods of preparing compounds of the formula: RZ—CO—CR a R b —(CR c R d ) n —NH—(Y) m —CO—A  (I) wherein n is an integer from 1 to 15, m is either 0 or 1; R a , R b , R c , and R d are each a hydrogen or a hydrocarbyl group; Y is CO—(CR e R f ) p , wherein R e and R f are each a hydrogen or hydrocarbyl group and p is zero or an integer from 1 to 20 or CO—C 6 H 4 —, wherein the substitution pattern on the phenylene group is an ortho, meta, or para substitution pattern and one or more of the hydrogens of the phenylene group may be substituted by a hydrocarbyl group or a functional group; Z is —O— or —NG—, wherein G is H, C 1 -C 12 alkyl or the radical R; wherein R is 1 wherein R 1 is hydrogen, C 1 -C 18 alkyl, O, OH, CH 2 CN, C 1 -C 18 alkoxy, C-C 18 hydroxyalkoxy, C 5 -C 12 cycloalkoxy, C 5 -C 12 hydroxycycloalkoxy, C 3 -C 6 alkenyl, C 1 -C 18 alkynyl, C 7 -C 9 phenylalkyl, unsubstituted or substituted on the phenyl with 1, 2 or 3 C 1 -C 4 alkyls, or an aliphatic C 1 -C 8 acyl; R 2 is hydrogen, C 1 -C 8 alkyl, or benzyl; R 3 , R 4 , R 5 , and R 6 are each a hydrogen, C 1 -C 8 alkyl, benzyl or phenethyl, or two geminal R moieties, which together with the carbon to which they are attached form a C 5 -C 10 cycloalkyl; and A is either ZR or a hydrocarbyl group, which are useful for stabilizing polymer compositions against photo- and thermal degradation.
    该公式的化合物及其制备方法:RZ—CO—CRaRb—(CRcRd)n—NH—(Y)m—CO—A(I)其中n是1到15之间的整数,m为0或1;Ra、Rb、Rc和Rd分别是氢或烃基团;Y是CO—(CReRf)p,其中Re和Rf分别是氢或烃基团,p为0或1到20之间的整数,或CO—C6H4—,其中苯环上的取代模式为邻位、间位或对位取代模式,苯环的一个或多个氢原子可能被烃基团或功能基团取代;Z是—O—或—NG—,其中G是H、C1-C12烷基或基团R;其中R是1其中R1是氢、C1-C18烷基、O、OH、CH2CN、C1-C18甲氧基、C-C18羟基甲氧基、C5-C12环氧基、C5-C12羟基环氧基、C3-C6烯基、C1-C18炔基、C7-C9苯基烷基,苯基上未取代或取代1、2或3个C1-C4烷基,或脂肪族C1-C8酰基;R2是氢、C1-C8烷基或苄基;R3、R4、R5和R6分别是氢、C1-C8烷基、苄基或苯乙基,或两个共轭的R基,与它们附着的碳形成C5-C10环烷基;A是ZR或烃基团,可用于稳定聚合物组合物对光和热降解的影响。
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