CAS No.3050-88-2,Phenol, 4-nonyl-,phosphite (3:1) Suppliers

Detail of "3050-88-2"

CAS Number:

3050-88-2

Name:

Phenol, 4-nonyl-,phosphite (3:1)

Superlist Name:

Tris(4-nonylphenyl) phosphite

Molecular Structure:

Formula:

C₄₅H₆₉O₃P

Molecular Weight:

689.00

Deleted CAS:

221229-36-3

Synonyms:

Phenol,p-nonyl-, phosphite (3:1) (8CI);Phenol, p-nonyl-, phosphite (6CI,7CI);4-Nonylphenol phosphite (3:1);Alkanox TNPP;Anullex TNPP;Phos 1;Tri(4-n-nonylphenyl) phosphite;Tri(p-nonylphenyl) phosphite;Tris(p-nonylphenyl) phosphite;p-Nonylphenolphosphite (3:1);p-Nonylphenyl phosphite;Tris-(4-nonylphenyl)-phosphite;

Density:

0.99 g/mL at 25 °C(lit.)

Boiling Point:

687.5 °C at 760 mmHg

Flash Point:

467 °C

Transport Information:

UN 3082

Reference

Masses based on acrylic acid esters, polymerizable by UV-light: Masses based on acrylic acid esters, polymerizable by UV-light. Schmitt, Werner; Purrmann, Robert (ESPE Fabrik Pharmazeutischer Praeparate G.m.b.H., Austria). Ger. Offen. DE 2646416 26 May 1977, 25 pp. (German). (Germany). CODEN: GWXXBX. CLASS: IC: C08L033-08. PRIORITY: CH 75-15138 21 Nov 1975. DOCUMENT TYPE: Patent CA Section: 35 (Synthetic High Polymers) Phosphite esters were used to accelerate the hardening of methacrylate compds., such as the dimethacrylate ester of 2,2-bis[4-(3-hydroxypropoxy)phenyl]propane (I), contg. benzoin or a benzoin deriv. during exposure to UV light. The hardened resins were useful as dental fillings, ink binders, coatings, etc. Thus, I stabilized with 200 ppm p-methoxyphenol and 200 ppm Ionol and contg. 2% benzoin Me ether and 5% tris(4-nonylphenyl phosphite (II) [3050-88-2] hardened during 11 s in UV light, compared with 22 s without II.

Processing stabilizers for polypropylene: Processing stabilizers for polypropylene.Several substances are used for example 38613-77-3 and 3050-88-2 which are their cas registry numbers. Mitterhofer, F. (Basel, Switz.). Kunststoffe, 67(3), 151-3 (German) 1977. CODEN: KUNSAV. DOCUMENT TYPE: Journal CA Section: 36 (Plastics Manufacture and Processing) The increase in stability of polypropylene (I) [9003-07-0] during processing and use by sterically hindered phenols was increased by addn. of org. phosphites and phosphonites and further increased by addn. of Ca stearate [1592-23-0], whereas dilauryl thiodipropionate [123-28-4] with distearyl pentaerythritol diphosphite [3806-34-6] did not increase the processing stability of unstabilized I. .

Detail of "3050-88-2"

Phenol, 4-nonyl-,phosphite (3:1)

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CAS No.3050-88-2 Tris(4-nonylphenyl) phosphite

CAS No.3050-88-2 Tris(4-nonylphenyl) phosphite

CAS No.3050-88-2 Tris(4-nonylphenyl) phosphite

CAS No.3050-88-2 Tris(4-nonylphenyl) phosphite

CAS No.3050-88-2 Tris(4-nonylphenyl) phosphite

CAS No.3050-88-2 Tris(4-nonylphenyl) phosphite

CAS No.3050-88-2 Tris(4-nonylphenyl) phosphite

CAS No.3050-88-2 Tris(4-nonylphenyl) phosphite

CAS No.3050-88-2 Tris(4-nonylphenyl) phosphite

CAS No.3050-88-2 Tris(4-nonylphenyl) phosphite

CAS No.3050-88-2 Tris(4-nonylphenyl) phosphite

CAS No.3050-88-2 Tris(4-nonylphenyl) phosphite

Reference