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71878-19-8

71878-19-8 Structure

71878-19-8 Structure
IdentificationMore
[Name]

Chimassorb 944
[CAS]

71878-19-8
[Synonyms]

CHIMASSORB 944
Poly[[6-[(1,1,3,3-tetramethylbutyl)amino]-s-triazine-2,4-diyl]-[(2,2,6,6-tetramethyl-4-piperidyl)imino]-hexamethylene-[(2,2,6,6-tetramethyl-4-piperidyl)imino]]
UV 944
1,3,3-tetramethylbutyl)amino)-"poly(6-((
Cr-144
Hals3
poly((6-((1,1,3,3-tetramethylbutyl)amino)-1,3,5-triazine-2,4-diyl)((2,2,6,6-te
Poly[[6-[(1,1,3,3-tetramethylbutyl)amino]-1,3,5-triazine-2,4-diyl][(2,2,6,6-tetramethyl-4-piperidinyl)imino]-1,6-hexanediyl[(2,2,6,6-tetramethyl-4-piperidinyl)imino]]
Previouscas:70624-18-9
tramethyl-4-piperidinyl)imino)-1,6-hexanediyl((2,2,6,6-tetramethyl-4-piperidin
yl)imino))
"
LS 944
poly(6-((1,1,3,3-tetramethylbutyl)amino)-
POLY(TETRAMEBUAMINO)-TRIAZ-DIYLTETRAME-P
POLY6-(1,1,3,3-TETRAMETHYLBUTYL)AMINO-S-TRIAZINE-2,4-DIYL-(2,2,6,6-TETRAMETHYL-4-PIPERIDYL)IMINO-HEXAMETHYLENE-(2,2,6,6-TETRAMETHYL-4-PIPERIDYL)IMINO
Poly6-(1,1,3,3-tetramethylbutyl)amino-1,3,5-triazine-2,4-diyl(2,2,6,6-tetramethyl-4-piperidinyl)imino-1,6-hexanediyl(2,2,6,6-tetramethyl-4-piperidinyl)imino
Hindered Amine Light Stabilizer 944 (HALS 944)
LIGHT STABILIZER UV 944 (CHEMISORB 944)
Poly-{-(-6-1,1,3,3-tetramethylbutylamino)-1,3,5-triazine-2,4-diyl}-2,26,6-t
[EINECS(EC#)]

615-678-9
[Molecular Formula]

(C35H68N8)n
[MDL Number]

MFCD00134710
[MOL File]

71878-19-8.mol
[Molecular Weight]

708.335
Chemical PropertiesBack Directory
[Melting point ]

136-140 °C(lit.)
[λmax]

240 nm
[InChIKey]

ORECYURYFJYPKY-UHFFFAOYSA-N
[SMILES]

N1=C(Cl)N=C(N=C1Cl)Cl.N1C(C)(C)CC(CC1(C)C)NCCCCCCNC1CC(C)(C)NC(C)(C)C1.C(C)(C)(N)CC(C)(C)C
[CAS DataBase Reference]

71878-19-8(CAS DataBase Reference)
[EPA Substance Registry System]

71878-19-8(EPA Substance)
Safety DataBack Directory
[Symbol(GHS) ]

Skull and Crossbones (GHS06)
GHS06
[Signal word ]

Danger
[Hazard statements ]

H319-H330-H335
[Precautionary statements ]

P260-P264-P271-P280-P304+P340+P310-P305+P351+P338
[Hazard Codes ]

T+
[Risk Statements ]

R26:Very Toxic by inhalation.
R36/37:Irritating to eyes and respiratory system .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37:Wear suitable protective clothing and gloves .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) .
[RIDADR ]

UN 2811 6.1/PG 2
[WGK Germany ]

3
[RTECS ]

TR7755000
[Storage Class]

6.1A - Combustible acute toxic Cat. 1 and 2
very toxic hazardous materials
[Hazard Classifications]

Acute Tox. 2 Inhalation
Eye Irrit. 2
STOT SE 3
Questions And AnswerBack Directory
[Characterization]

Chimassorb 944 is a high molecular weight hindered amine light stabilizer (HALS). It shows excellent compatibility, good resistance to extraction and low volatility.
[Applications]

Chimassorb 944 areas of application include polyolefins (PP, PE), olefin copolymers such as EVA as well as blends of polypropylene with elastomers.
In addition in certain instances Chimassorb 944 is highly effective in polyacetals, polyamides, polyurethanes, flexible and rigid PVC, as well as PVC blends, and in certain styrenic elastomer and adhesive specialty applications.
[Features/benefits]

Chimassorb 944 imparts excellent light stability to thin articles, particularly fibers and films. In thick cross sections it is specifically suitable for polyethylene articles.
Chimassorb 944 is highly effective as a long-term thermal stabilizer in thin and thick articles and shows good extraction resistance.
[Physical properties]

Solubility (20 °C)
% w/w
Acetone
> 50
Chloroform
> 30
Ethanol
< 0.1
Ethyl acetate
> 50
n-Hexane
41
Methanol
3
Dichloromethane
> 50
Toluene
> 50
Water
< 0.01
 
Hazard InformationBack Directory
[Uses]

Hindered amine UV light stabilizer for polyolefins.
[General Description]

Poly[[6-[(1,1,3,3-tetramethylbutyl)amino]-s-triazine-2,4-diyl]-[(2,2,6,6-tetramethyl-4-piperidyl)imino]-hexamethylene-[(2,2,6,6-tetramethyl-4-piperidyl)imino](HAS) is an amine hindered light stabilizer that can be used as an antioxidant by attaching the nitroxyl radical with the surface atoms.
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