GLYCIDYL NEODECANOATE, MIXTURE OF BRANCHED ISOMERS
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GLYCIDYL NEODECANOATE, MIXTURE OF BRANCHED ISOMERS
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CAS No:
26761-45-5
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Formula:
C13H24O3
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Chemical Name:
GLYCIDYL NEODECANOATE, MIXTURE OF BRANCHED ISOMERS
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Synonyms:
oxiran-2-ylmethyl 2-ethyl-2,5-dimethylhexanoate;GLYCIDYL NEODECANOATE, MIXTURE OF BRANCHED ISOMERS;glycidylesterofneodecanoicacid;glycidylneodecanoate;glycidylneodecanoate,mixtureofbranchedisome;glydexxn10;Neodecanoicacid,2,3-epoxypropylester;Neodecanoicacid,oxiranylmethylester
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CAS No:
Description
Liquid
yellow liquid
The mutagenic activity of glycidyl ester of neodecanoic acid was investigated in cultures of S. typhimutium TA98, TA100, TA102, TA1535, TA1537, and TA1538; E. coli WP2 and WP2 uvr A; and in cultures of S. cerevisiae JD1, both with and without the incorporation of rat liver microsomal enzymes. The results indicated that glycidyl ester of neodecanoic acid induced an increase in mutation frequency only after metabolic activation in Salmonella strains TA100, TA1535, and TA1538. The mutation frequency was within the spontaneous frequency range in the absence of S9 fractions for these strains; however, in some experiments weak responses were observed in the absence of S9. In TA98, TA102, TA1537, and TA1538, there was no increase in mutation frequency either with or without S9. There was no increase in gene mutation and frequency in either of the E. coli strains with or without activation. Similarly, in Saccharomyces no changes in gene conversion frequency were reported. In general, no significant effects were detected below 100mg of material per plate, suggesting that the mutagenic activity was relatively weak. The bacterial results indicate thatmutagenicity was expressed by both base-pair substitution and frameshift mechanisms.In other studies, monolayer slides of cultures of rat liver (RL1) cells were exposed to culture medium containing glycidyl ester of neodecanoic acid, and after 24 h incubation, the slides were processed for metaphase chromosome analysis . In the RL1 cells, NAGE induced a low frequency of chromatid aberrations at concentrations just below the cytotoxic dose (50 mg/mL).
GLYCIDYL NEODECANOATE, MIXTURE OF BRANCHED ISOMERS Basic Attributes
228.32786
228.17254462 g/mol
247-979-2
TSCA listed
DTXSID20275056
Colorless to pale yellow
Characteristics
38.8 Ų
0.966 g/mL at 25 °C(lit.)
310.14°C (rough estimate)
n20/D 1.444(lit.)
70mg/L at 20℃
1.5Pa at 24.85℃
Mild odor
Insoluble in water.
GLYCIDYL NEODECANOATE, MIXTURE OF BRANCHED ISOMERS reacts vigorously with strong oxidizing agents and strong Lewis and mineral acids. Reacts with considerable heat release with many curing agents.
Safety Information
Xi
26-36
QO7800000
36/37/38
GLYCIDYL NEODECANOATE, MIXTURE OF BRANCHED ISOMERS is probably combustible.
GLYCIDYL NEODECANOATE, MIXTURE OF BRANCHED ISOMERS Use and Manufacturing
Heat Stablilizers
Building/construction materials not covered elsewhere
This material may be used as an epoxy resin reactive diluent, as a component of epoxy coating systems, and as an ingredient in alkyl resins to modify film properties. Improved chemical resistance, weatherability, film hardness, and acid number control are the properties enhanced in epoxy resin applications by the use of this material.
1,000,000 - 10,000,000 lb
The glycidyl ester of neodecanoic acid (NAGE) is produced by the reaction of neodecanoic acid with epichlorohydrin in the presence of base.
All other chemical product and preparation manufacturing|Neodecanoic acid, 2-oxiranylmethyl ester: ACTIVE|TP - indicates a substance that is the subject of a proposed TSCA section 4 test rule.
Computed Properties
Molecular Weight:228.33
XLogP3:3.7
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:9
Exact Mass:228.17254462
Monoisotopic Mass:228.17254462
Topological Polar Surface Area:38.8
Heavy Atom Count:16
Complexity:223
Undefined Atom Stereocenter Count:1
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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