Browse
Submit Data
Databases
API
Help

Dataset Information

0 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Bis(1,2,2,6,6-penta-methyl-piperidin-4-yl) 2-butyl-2-(3,5-di-tert-butyl-4-hydroxy-benz-yl)malonate (Tinuvin 144).

ABSTRACT: The title compound, C(42)H(72)N(2)O(5), a hindered amine light stabiliser (HALS) with the trade name Tinuvin 144 was prepared from bis-(1,2,2,6,6-penta-methyl-piperidin-4-yl) 2-butyl-malonate and 2,6-di-tert-butyl-4-[(dimethyl-amino)meth-yl]phenol using lithium amide as a catalyst. In the mol-ecule, both piperidine rings adopt chair conformations. In the crystal, inversion dimers linked by pairs of O-H?O hydrogen bonds occur.

SUBMITTER: Zeng T

PROVIDER: S-EPMC2970408 | biostudies-other | 2009

REPOSITORIES: biostudies-other

ACCESS DATA

Json Xml

Publications

Bis(1,2,2,6,6-penta-methyl-piperidin-4-yl) 2-butyl-2-(3,5-di-tert-butyl-4-hydroxy-benz-yl)malonate (Tinuvin 144).

Zeng Tao T Ren Wan-Zhong WZ

Acta crystallographica. Section E, Structure reports online 20090905 Pt 10

The title compound, C(42)H(72)N(2)O(5), a hindered amine light stabiliser (HALS) with the trade name Tinuvin 144 was prepared from bis-(1,2,2,6,6-penta-methyl-piperidin-4-yl) 2-butyl-malonate and 2,6-di-tert-butyl-4-[(dimethyl-amino)meth-yl]phenol using lithium amide as a catalyst. In the mol-ecule, both piperidine rings adopt chair conformations. In the crystal, inversion dimers linked by pairs of O-H⋯O hydrogen bonds occur. ...[more]

PMID: 21577826

Similar Datasets

Dimethyl 2-butyl-2-(3,5-di-tert-butyl-4-hydroxy-benz-yl)malonate.

Project description:The title compound, C(25)H(38)O(5), was formed by the reaction of dimethyl 2-butyl-malonate and 2,6-di-tert-butyl-4-[(dimethyl-amino)meth-yl]phenol. In the crystal structure, mol-ecules are linked by inter-molecular O-H?O hydrogen bonds into chains along [010].

| S-EPMC2970493 | biostudies-other

Diethyl 2,2-bis-(3,5-di-tert-butyl-4-hy-droxy-benz-yl)malonate.

Project description:The title mol-ecule, C(37)H(56)O(6), possesses twofold symmetry, with the twofold axis passing through the quaternary C atom. In the crystal, neighbouring mol-ecules are linked via O-H?O hydrogen bonds involving the phenol OH group and the carbonyl O atom, forming chains propagating in [101]. Within these chains, rings are formed with an R(2) (2)(20) motif. There are also C-H?O inter-actions present within the rings.

| S-EPMC3275203 | biostudies-literature

2-[(3,5-Di-tert-butyl-4-hydroxy-benz-yl)-sulfan-yl]-N'-isopropyl-ideneaceto-hydrazide.

Project description:The title compound, C(20)H(32)N(2)O(2)S, the condensation product of a thio-acetohydrazine and acetone, has a two-coordinate S atom and the angle at this atom is 100.7 (1)°. The (CH(3))C=N-NH-C(O)- substituent engages in N-H⋯O hydrogen-bonding inter-actions with the substituent of an adjacent mol-ecule across a center of inversion, generating a dimeric structure.

| S-EPMC2968854 | biostudies-literature

Di-n-butyl-ammonium 2-[(3,5-di-tert-butyl-4-hy-droxy-benz-yl)sulfan-yl]benzoate.

Project description:The title salt, C(8)H(20)N(+)·C(22)H(27)O(3)S(-), is a proton-transfer compound derived from the recently reported parent carb-oxy-lic acid [Alhadi et al. (2010). Acta Cryst. E66, o1787] by the addition of a second equivalent of di-n-butyl-amine, yielding the di-n-butyl-ammonium carboxyl-ate salt. The structure of the carboxyl-ate anion resembles that of the parent carb-oxy-lic acid. The main difference lies in the position of the H atom in the 4-hy-droxy group. In the anion the O-H bond is perpendicular, rather than parallel, to the benzyl ring. This position appears to facilitate hydrogen bonding to an O atom of the carboxyl-ate group of a symmetry-related anion. In addition, there are three N-H⋯O hydrogen bonds. In contrast, the neutral species hydrogen bonds via a carboxylic acid dimer. The dihedral angle between the benzene rings in the anion is 79.19 (7)°.

| S-EPMC3007956 | biostudies-literature

catena-Poly[[triphenyl-tin(IV)]-?-2-[(3,5-di-tert-butyl-4-hydroxy-benz-yl)sulfan-yl]acetato-?O:O'].

Project description:The title compound, [Sn(C(6)H(5))(3)(C(17)H(25)O(3)S)](n), comprises two symmetry-independent five-coordinated triphenyl-tin mol-ecules which are linked by carboxyl-ate bridges into a polymeric chain. The Sn(IV) atom is in a distorted trans-C(3)SnO(2) trigonal-bipyramidal geometry. The presence of two bulky tert-butyl groups on the benzene ring prevents any hydrogen-bonding inter-actions involving the hydroxyl substituents.

| S-EPMC2969233 | biostudies-literature

Di-n-butyl-ammonium 2-(3,5-di-tert-butyl-4-hydroxy-benzyl-sulfan-yl)nicotinate.

Project description:The asymmetric unit of the title compound, C(8)H(20)N(+)·C(21)H(26)NO(3)S(-), contains two indpendent ion pairs which are disposed about a psuedo-inversion center, generating an ammonium-carboxylate N-H?O hydrogen-bonded four-component cluster. In the crystal structure, adjacent clusters are linked by hydr-oxy-carboxylate O-H?O hydrogen bonds, forming a chain.

| S-EPMC2960651 | biostudies-literature

Bis[1-(3,5-di-tert-butyl-2-hydroxy-benz-yl)-3-isopropyl-imidazolium] penta-chlorido(tetra-hydro-furan)samarate(III)-tetrahydrofuran-toluene (1/1/1).

Project description:The title compound, (C(21)H(33)N(2)O)(2)[SmCl(5)(C(4)H(8)O)]·C(7)H(8)·C(4)H(8)O, has a layered structure in which each distorted octa-hedral [SmCl(5)(THF)](2-) unit (THF is tetra-hydro-furan) is capped by two cations. The central metal Sm(III) atom of the [SmCl(5)(THF)](2-) anionic unit is coordinated by five Cl atoms and one THF O atom, forming a distorted octa-hedral geometry. The crystal structure displays C-H?Cl and O-H?Cl hydrogen bonding. The structure exhibits disorder of the solvent.

| S-EPMC2979468 | biostudies-literature

2,4-Di-tert-butyl-6-[1-(3,5-di-tert-butyl-2-hydroxy-phen-yl)eth-yl]phenyl 4-methyl-benzene-sulfonate.

Project description:The title compound, C(37)H(52)O(4)S, was obtained by the reaction of 6,6'-(ethane-1,1-di-yl)bis-(2,4-di-tert-butyl-phenol) and 4-methyl-benzene-1-sulfonyl chloride. The mol-ecular conformation is stabilized by an intra-molecular O-H?O hydrogen bond. Two of the tert-butyl groups are disordered over two sets of sites with occupancies 0.530?(15)/0.470?(15) and 0.615?(11)/0.385?(11).

| S-EPMC2968069 | biostudies-literature

2-(3,5-Di-tert-butyl-4-hydroxy-benzyl-sulfan-yl)nicotinic acid.

Project description:Two mol-ecules of the title compound, C(21)H(27)NO(3)S, are disposed about a center of inversion, generating an O-H⋯O hydrogen-bonded dimer.

| S-EPMC2960523 | biostudies-literature

Ethyl 4-[(3,5-di-tert-butyl-2-hy-droxy-benz-yl)amino]-benzoate.

Project description:The title amine, C(24)H(33)NO(3), has two substituted aromatic rings at either end of the -CH(2)NH- linkage [C(ar-yl)-CH(2)-NH-C(ar-yl) torsion angle = 77.4 (3)°]. The amino and hy-droxy groups are hydrogen-bond donors to the carbonyl O atom of an adjacent mol-ecule. These hydrogen bonds give rise to a chain that runs along the b axis. One of the tert-butyl groups is disordered over two positions with a site-occupation factor of 0.834 (6) for the major occupied site.

| S-EPMC3009098 | biostudies-literature

OmicsDI is part of the ELIXIR infrastructure

OmicsDI is an Elixir interoperability service. Learn more ›

Tweets

OmicsDI Databases

PRIDE
PeptideAtlas
MassIVE
JPOST Repository
Physiome Model Repository

EGA
EVA
ENA
LINCS
PAXDB
Cell Collective

MetaboLights
Metabolomics Workbench
MetabolomeExpress
GNPS
BioModels
FAIRDOMHub

ArrayExpress
dbGaP
ExpressionAtlas
GEO
NODE

Information

Databases
Help
API
Contact us
Code on GitHub
Terms of use
Submit Data