bis(2,2,6,6-Tetramethyl-4-piperidyl) sebacate

Product Information

Molecular Formula:
C28H52N2O4
Molecular Weight:
480.72348
Description
Hindered amine UV light stabilizer.Provides excellent stability for thick sections and articles with high surface area.
Synonyms
52829-07-9; Bis(2,2,6,6-tetramethyl-4-piperidyl)sebacate; Tinuvin770; bis(2,2,6,6-tetramethylpiperidin-4-yl)decanedioate; Sanol; Sumisorb577
IUPAC Name
bis(2,2,6,6-tetramethylpiperidin-4-yl) decanedioate
Canonical SMILES
CC1(CC(CC(N1)(C)C)OC(=O)CCCCCCCCC(=O)OC2CC(NC(C2)(C)C)(C)C)C
InChI
InChI=1S/C28H52N2O4/c1-25(2)17-21(18-26(3,4)29-25)33-23(31)15-13-11-9-10-12-14-16-24(32)34-22-19-27(5,6)30-28(7,8)20-22/h21-22,29-30H,9-20H2,1-8H3
InChI Key
XITRBUPOXXBIJN-UHFFFAOYSA-N
Boiling Point
499.8°C at 760mmHg
Melting Point
82-85°C
Flash Point
420.8 °F
Purity
95%
Density
1.01g/cm3
Appearance
Slightly yellowish crystalline granules
Refractive Index
n20/D 1.479 (lit.)

Safety Information

Hazards
H318:
Causes serious eye damage.
H330:
Fatal if inhaled.
H370:
Causes damage to organs.
H410:
Very toxic to aquatic life with long-lasting effects.
Precautionary Statement
P260:
Do not breathe dust, fumes, gas, mist, vapours, spray.
P273:
Avoid release to the environment.
P280:
Wear protective gloves/protective clothing/eye protection/face protection.
P304+P340+P310:
IF INHALED:
Remove person to fresh air and keep comfortable for breathing.
Immediately call a POISON CENTER or doctor/physician.
P305+P351+P338+P310:
IF IN EYES:
Rinse cautiously with water for several minutes.
Remove contact lenses if present and easy to do. Continue rinsing.
Immediately call a POISON CENTER or doctor/physician.
P308+P311:
If exposed or concerned:
Call a POISON CENTER or doctor/physician.
P391:
Collect spillage.
P403+P233:
Store in a well ventilated place.
Keep container tightly closed.

Computed Properties

XLogP3
5.5
Hydrogen Bond Donor Count
2
Hydrogen Bond Acceptor Count
6
Rotatable Bond Count
13
Exact Mass
480.39270814 g/mol
Monoisotopic Mass
480.39270814 g/mol
Topological Polar Surface Area
76.7Ų
Heavy Atom Count
34
Formal Charge
0
Complexity
594
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
CN-114131784-A Long glass fiber and carbon fiber mixed reinforced polypropylene composite material and preparation method thereof 2022-01-29
CN-114163966-A Hydrolysis-resistant TPU hot melt adhesive film and preparation method thereof 2021-12-30
CN-114149769-A High-reflection black adhesive film and preparation method and application thereof 2021-12-29
CN-114181445-A Weather-resistant master batch for polypropylene flat filament product and preparation method thereof 2021-12-24
JP-2022043228-A Decorative sheet and decorative material using it 2021-12-24
CN-113980189-A Polyester acrylic acid weather-resistant pressure-sensitive adhesive and preparation method thereof 2021-12-17
JP-2022040133-A A photosensitive coloring composition for a color filter for a solid-state image sensor, a color filter, and a solid-state image sensor using the same. 2021-12-15
CN-114058008-A Process for preparing semi-aromatic polyamides end-capped with monocarboxylic acids, semi-aromatic polyamides and molding compositions 2021-12-13
CN-114058009-A Process for preparing semi-aromatic polyamides with reduced loss of diamine monomer, semi-aromatic polyamides and molding compositions 2021-12-13
CN-114058010-A Process for preparing low-energy semiaromatic polyamides, semiaromatic polyamides and moulding compositions 2021-12-13

Literatures

PMID Publication Date Title Journal
21651919 2011-09-01 The use-dependent, nicotinic antagonist BTMPS reduces the adverse consequences of morphine self-administration in rats in an abstinence model of drug seeking Neuropharmacology
20226229 2010-04-26 Effect of the use-dependent, nicotinic receptor antagonist BTMPS in the forced swim test and elevated plus maze after cocaine discontinuation in rats Neuroscience letters
20223086 2010-03-01 Development and validation of an HPLC-MS-MS method for quantitating bis(2,2,6,6-tetramethyl-4-piperidyl) sebacate (Tinuvin 770) and a related substance in aqueous extracts of plastic materials Journal of chromatographic science
21502011 2010-03-01 Generation of the Extractables Profile for an Elastomeric Material and Investigation of the Accumulation Behavior of Targeted Leachables Including Bis(2,2,6,6-tetramethyl-4-piperidyl) Sebacate (Tinuvin 770) and a Related Substance PDA journal of pharmaceutical science and technology
19772864 2010-02-01 Effect of administration of the nicotinic acetylcholine receptor antagonist BTMPS, during nicotine self-administration, on lever responding induced by context long after withdrawal Neuropharmacology
18762034 2008-09-01 Effects of a hindered amine light stabilizer and a UV light absorber used in maxillofacial elastomers on human gingival epithelial cells and fibroblasts The Journal of prosthetic dentistry
15974911 2005-04-01 Functional central nicotinic acetylcholine receptor antagonism by systemic administration of Tinuvin 770 (BTMPS) Current Alzheimer research
15153857 2004-05-01 In vitro evaluation of color change in maxillofacial elastomer through the use of an ultraviolet light absorber and a hindered amine light stabilizer The Journal of prosthetic dentistry
14657520 2004-02-01 Comparative study on cardiotoxic effect of Tinuvin 770: a light stabilizer of medical plastics in rat model Toxicological sciences : an official journal of the Society of Toxicology
14965415 2004-01-01 Detection of tinuvin 770, a light stabilizer of plastic materials from dialysis membranes, by high-performance liquid chromatographic analysis Journal of chromatographic science
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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