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ᱰᱤ ᱮᱱ (᱔᱐᱐) ᱯᱤ

ᱰᱤ ᱮᱱ (᱔᱐᱐) ᱯᱤ

ᱥᱮᱨᱮᱧ ᱧᱩᱛᱩᱢ:
ᱮᱱᱯᱤᱮᱭᱰᱤᱰᱤᱰᱤ=} } } } } } } } } } } } } \\ᱰᱤᱵᱷᱤᱰᱤᱯᱤᱮᱢᱯᱤᱮᱢᱯᱤᱰᱤᱰᱤᱰᱤ;
ᱥᱤᱥᱤᱡᱤᱥᱤ ᱢᱮᱰ ᱨᱮᱥ: ᱒᱗᱕-᱑᱒᱘᱾
ᱠᱟᱨᱰᱤᱭᱟᱠ: ᱒᱒᱖-᱓᱑᱗᱾
ᱥᱟᱦᱴᱟ ᱑:᱑᱔᱾
ᱥᱤ ᱮᱱ ᱮᱥ: ᱑-᱘-᱒᱐᱑᱔᱾
ᱯᱤᱯᱤᱯᱤ: ᱕/᱒ ᱠᱮᱡᱤ
ᱡᱤᱭᱚᱱ ᱨᱮᱭᱟᱜ ᱡᱤᱭᱚᱱ: ᱑᱒
ᱤᱱᱴᱮᱜᱽᱨᱮᱥᱚᱱ
Product Details ofᱰᱤ ᱮᱱ (᱔᱐᱐) ᱯᱤ


ᱟᱭᱤ ᱰᱤ ᱯᱤ ᱰᱤ ᱮᱱ ᱮ (᱑᱐᱔ ᱮᱱᱵᱤᱮ) ᱤᱡᱤᱯᱨᱟᱭᱤᱢ ᱮᱱᱵᱤᱮ |


ᱥᱚᱨᱥ:


ᱮᱱᱴᱤᱵᱟᱭᱳᱴᱤᱠᱥ ᱨᱮᱭᱟᱜ ᱢᱮᱠᱟᱱᱤᱠᱟᱞ ᱧᱩᱛᱩᱢ

ᱮᱱᱯᱤᱮᱭᱰᱤᱰᱤᱰᱤ=} } } } } } } } } } } } } \\ᱰᱤᱵᱷᱤᱰᱤᱯᱤᱮᱢᱯᱤᱮᱢᱯᱤᱰᱤᱰᱤᱰᱤ;

ᱠᱮᱢᱤᱠᱮᱞ ᱢᱮᱴᱟᱵᱚᱞᱤᱡᱽC15H28N2
ᱢᱟᱭᱠᱨᱚᱣᱮᱵᱷᱤᱝ ᱥᱯᱤᱰ image001.jpg
ᱢᱤᱭᱟᱢᱤ ᱨᱮ ᱛᱟᱦᱮᱱ ᱢᱮ226.31
ᱜᱡᱚᱴᱱᱟ1.14
ᱥᱤ ᱮᱱ ᱮᱱ᱾101-72-4
ᱯᱮᱠᱮᱡᱤᱝ᱕/᱒ ᱢᱤᱢᱤᱴᱚᱨ
ᱡᱤᱭᱚᱱ ᱞᱟᱹᱜᱤᱫ᱑᱒ ᱪᱟᱸᱫᱚ


ᱱᱟᱹᱢᱩᱱᱟ:


ᱥᱟᱨᱦᱟᱣ

ᱟᱨᱟᱜ ᱨᱚᱝ ᱨᱮᱭᱟᱜ ᱯᱩᱨᱟᱹ ᱵᱷᱟᱞᱵᱷ ᱵᱮᱵᱷᱟᱨ ᱢᱮ

ᱥᱟᱹᱨᱤ ᱟᱨ ᱵᱟᱝ ᱯᱷᱤᱴ ᱠᱷᱚᱱ ᱵᱟᱹᱲᱛᱤ ᱦᱟᱹᱴᱤᱧ ᱞᱟᱹᱜᱤᱫ

70.0

SS ᱫᱚ %s ᱠᱷᱚᱱ ᱠᱚᱢ ᱦᱩᱭ ᱫᱟᱲᱮᱭᱟᱜᱼᱟ

0.30

ᱵᱟᱹᱲᱛᱤ ᱥᱮ ᱠᱚᱢ ᱥᱮ ●●/ ᱵᱟᱝᱠᱷᱟᱱ ᱚᱱᱟ ᱠᱷᱚᱱ ᱦᱚᱸ ᱾

0.50


ᱮᱱᱴᱤᱵᱚᱰᱤᱡᱽ ᱫᱚ ᱢᱤᱫ ᱞᱮᱠᱟᱱ ᱮᱱᱴᱤᱵᱚᱰᱤ ᱠᱟᱱᱟ ᱡᱟᱦᱟᱸ ᱫᱚ himine hirginoption himeption himine hirginosion himine hyption lạgit̕ lạgit̕ lạgit̕ lạgit̕ lạgit̕ lạgit̕ lạgit̕ lạgit̕ lạgit̕ lạgit̕ rạmi lạgit̕ lạgit̕ lạgit̕ lạgit̕ lạgit̕ rạskation ., himine hyption , hiptermentions, hipsay, hiptermentions, hiptayse ., happlementions, hiptage ., happlementions, hipsay .

16. ᱮᱱᱴᱤᱵᱚᱰᱤ (CRCs) ᱫᱚ ᱮᱱᱴᱤ-ᱤᱱᱯᱷᱞᱟᱢᱮᱴᱟᱨᱤ ᱮᱱᱴᱤᱵᱚᱰᱤ (COM) ᱥᱟᱶᱛᱮ ᱥᱟᱶᱛᱮ ᱥᱟᱶᱛᱮ ᱥᱟᱶᱛᱮ ᱢᱮᱱᱟᱜ-ᱟ ᱡᱟᱦᱟᱸ ᱨᱮ ᱮᱱᱴᱤᱵᱚᱰᱤᱡᱽ ᱨᱮ ᱢᱮᱱᱟᱜ-ᱟ ᱾

(1) are synergy when two different space steric hindrance of hindered phenol, or two kinds of structure and activity of different amine stabilizer, or an aromatic amine and 1 kind of hindered phenolic antioxidant compound, when using highly active stabilizer can effectively capture the oxidation of free radicals or oxygen free radicals, low activity of the stabilizer can provide hydrogen atoms, that ᱢᱤᱫ ᱫᱟᱲᱮᱭᱟᱱ ᱮᱱᱴᱤᱵᱚᱰᱤᱡᱽ, ᱥᱤᱜᱱᱟᱞᱤᱝ, ᱜᱞᱩᱠᱚᱡᱽ ᱨᱮᱭᱟᱜ ᱠᱟᱹᱢᱤ ᱞᱟᱹᱜᱤᱫ ᱢᱤᱫ ᱥᱮᱬᱟ ᱠᱟᱹᱢᱤ ᱫᱚ ᱦᱩᱭᱩᱜ


(2007) ᱫᱚ ᱮᱱᱴᱤᱵᱚᱰᱤᱡᱽ ᱮᱱᱴᱤᱵᱚᱰᱤᱡᱽ ᱠᱟᱱᱟ, ᱡᱟᱦᱟᱸ ᱨᱮ ᱮᱱᱴᱤ-ᱦᱟᱭᱰᱨᱚᱡᱮᱱᱤᱠ ᱮᱱᱴᱤᱵᱚᱰᱤᱡᱽ ᱟᱨ ᱮᱱᱴᱤᱵᱚᱰᱤᱡᱽ ᱢᱮᱱᱟᱜ-ᱟ᱾ ᱢᱤᱫ ᱦᱟᱭᱰᱨᱚᱠᱨᱟᱴᱤᱠ ᱦᱟᱭᱰᱨᱚᱠᱟᱨᱵᱚᱱ (CHO) ᱫᱚ ᱦᱟᱭᱰᱨᱚᱡᱮᱱ, ᱦᱟᱭᱰᱨᱚᱡᱮᱱ, ᱟᱨ ᱦᱟᱭᱰᱨᱚᱡᱮᱱ, ᱟᱨ ᱮᱴᱟᱜ ᱠᱚ ᱠᱷᱚᱱ ᱵᱟᱹᱲᱛᱤ ᱠᱟᱹᱢᱤ ᱠᱟᱱᱟ, ᱡᱟᱦᱟᱸ ᱫᱚ CHCH ( 5 , 7 ) ᱨᱮᱭᱟᱜ ᱠᱟᱹᱢᱤ ᱫᱚ ᱪᱮᱫ ᱠᱟᱱᱟ? ᱱᱚᱶᱟ ᱠᱚ ᱫᱚ ᱟᱹᱰᱤ ᱠᱚᱢ ᱜᱮᱭᱟ, ᱢᱮᱱᱠᱷᱟᱱ ᱱᱚᱶᱟ ᱠᱚ ᱫᱚ ᱟᱹᱰᱤ ᱠᱚᱢ ᱜᱮᱭᱟ, ᱟᱨ ᱚᱱᱟ ᱫᱚ ᱮᱴᱟᱜ ᱠᱟᱹᱢᱤ ᱠᱚ ᱞᱟᱹᱜᱤᱫ, ᱟᱨ ᱮᱴᱟᱜ ᱠᱚ ᱫᱚ ᱪᱮᱫ ᱠᱚ ᱠᱟᱹᱢᱤ ᱠᱟᱱᱟ? reaction.ArO?This stability can prevent the rapid consumption of anti-aging agents due to direct oxidation, and can also reduce chain transfer reaction, thus improving its antioxidant performance.Hydroperoxides are harmful intermediates that catalyze thermal oxidation.However, phenolic antioxidant cannot decompose hydroperoxide by itself, so when phenolic antioxidant is used alone, it is difficult to achieve the ideal effect of aging prevention.Although phosphite does not have the ability to capture free radicals of peroxide, it can decompose hydroperoxide, thus inhibiting the degradation of rubber caused by autocatalytic reaction.However, the hydrolysis stability of phosphorous esters is poor, which leads to the decrease of their antioxidant stability.The hydrolytic stability of phosphite anti-aging agents is related to the HPVs ᱠᱚ ᱫᱚ hiption hiption hiption hiption hiption hiptions ᱠᱚ ᱩᱫᱩᱜ ᱠᱟᱱᱟ.


2. Self-synergism: with the deepening understanding of composite anti-aging agents, we have developed an intramolecular composite anti-aging agent.The combination of two or more functional groups with antioxidant properties into a single molecule provides synergies of its own.It may also improve the heat resistance, light resistance, extraction resistance and so on.In particular, the synergistic effect of the main ᱮᱱᱴᱤᱵᱟᱭᱚᱴᱤᱠ ᱟᱨ 1997. ᱮᱡᱮᱱᱴ ᱫᱚ ᱟᱡ ᱛᱮ ᱮᱱᱴᱤᱵᱚᱰᱤᱡᱽ ᱨᱮᱭᱟᱜ ᱮᱱᱴᱤᱵᱚᱰᱤᱡᱽ ᱱᱳᱰ ᱠᱟᱱᱟ ᱡᱟᱦᱟᱸ ᱫᱚ ᱟᱡ ᱛᱮ ᱟᱡ ᱛᱮ ᱟᱡ ᱛᱮ ᱮᱱᱴᱤᱵᱚᱰᱤᱡᱽ ᱨᱮᱭᱟᱜ ᱜᱩᱱ ᱠᱚ ᱥᱟᱶᱛᱮ ᱡᱚᱲᱟᱣ ᱫᱟᱲᱮᱭᱟᱜ-ᱟ᱾







ᱦᱚᱜᱽᱥ: ᱜᱚᱱᱚᱝ ᱠᱚ ᱫᱚ (᱕,᱘,᱔,᱐᱐᱐,᱐᱐᱐), ᱠᱨᱤᱯᱴᱚᱠᱟᱨᱮᱱᱥᱤ, ᱠᱨᱤᱯᱴᱚᱠᱟᱨᱮᱱᱥᱤ, ᱵᱮᱱᱟᱣ, ᱵᱮᱱᱟᱣᱤᱡ, ᱱᱚᱣᱟ ᱛᱟᱠᱱᱤᱠᱤ, ᱵᱮᱱᱟᱣᱤᱡ, ᱱᱟᱹᱢᱩᱱᱟ, ᱵᱮᱱᱟᱣᱤᱡ᱾

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