6422-86-2

Usage

Chemical Properties

Clear colorless liquid

Uses

Different sources of media describe the Uses of 6422-86-2 differently. You can refer to the following data:
1. It is used primarily as a plasticizer for polyvinyl chloride and other polymers.
2. DOTP can form a composite blend with polyaniline (PANI)-ethyene dimethacrylate (EDMA), which can be used in the fabrication of conductive films. It may also be used as a plasticizer with polyvinyl chloride (PVC) to form solutions for artificial intravessel plaque.

Production Methods

DEHT is manufactured by the esterification of terephthalic acid and 2-ethylhexanol.

General Description

Dioctyl terephthalate (DOTP) is a plasticizer that can be prepared by alcoholysis of polyethylene terephthalate (PET) with isooctyl alcohol.

Carcinogenicity

The carcinogenic potential of DEHT was evaluated in a 2-year study in which male and female rats were given diets containing 1500, 6000, or 12,000 ppm. There was no effect on tumor incidence, and therefore, the NOEL for tumorigenicity was at least 12,000 ppm (equivalent to 666 mg/kg/day in males and 901 mg/kg/day in females).

InChI:InChI=1/C24H38O4/c1-5-9-11-19(7-3)17-27-23(25)21-13-15-22(16-14-21)24(26)28-18-20(8-4)12-10-6-2/h13-16,19-20H,5-12,17-18H2,1-4H3/t19-,20-/m1/s1

Synthetic route

2-Ethylhexyl alcohol (104-76-7) + terephthalic acid (100-21-0) → di(2-ethylhexyl)terephthalate (6422-86-2)

Conditions	Yield
With phenol and titanium tetraisopropoxide resin at 200℃; for 4h; Reagent/catalyst; Dean-Stark; Inert atmosphere;	99.5%
With titanium(IV) isopropylate at 170 - 200℃; Inert atmosphere; Large scale;	99%
With titanium(IV) isopropylate at 170 - 220℃; under 760.051 Torr; for 4.5h; Inert atmosphere; Large scale;	99%

2-Ethylhexyl alcohol (104-76-7) + polyethylene terephthalate → di(2-ethylhexyl)terephthalate (6422-86-2)

Conditions	Yield
With choline chloride; zinc diacetate at 185℃; for 1h; Kinetics; Reagent/catalyst; Temperature; Time; Green chemistry;	84.2%
With titanium(IV) isopropylate at 180 - 225℃; for 5h; Inert atmosphere;

terephthalic acid (100-21-0) + (+-)-2-ethyl-hexanol → di(2-ethylhexyl)terephthalate (6422-86-2)

2-Ethylhexyl alcohol (104-76-7) + terephthalic acid (100-21-0) + butan-1-ol (71-36-3) → di-n-butyl terephthalate (1962-75-0) + di(2-ethylhexyl)terephthalate (6422-86-2) + 1-butyl 4-(2-ethylhexyl)terephthalate

Conditions	Yield
With methanesulfonic acid at 210℃; under 760.051 Torr; for 4h; Inert atmosphere;

2-Ethylhexyl alcohol (104-76-7) + di-n-butyl terephthalate (1962-75-0) → di(2-ethylhexyl)terephthalate (6422-86-2) + 1-butyl 4-(2-ethylhexyl)terephthalate

Conditions	Yield
at 140℃; for 5h; Inert atmosphere;

di(2-ethylhexyl)terephthalate (6422-86-2) → bis(2-ethylhexyl)cyclohexane-1,4-dicarboxylate (84731-70-4)

Conditions	Yield
With hydrogen at 150℃; under 60006 Torr; for 3h;	99%
With hydrogen; alumina substrate/0.05 wtpercent Ru at 140℃; under 150015 Torr; for 3.5h;	97%

di(2-ethylhexyl)terephthalate (6422-86-2) + butan-1-ol (71-36-3) → di-n-butyl terephthalate (1962-75-0) + 1-butyl 4-(2-ethylhexyl)terephthalate

Conditions	Yield
With titanium tetraisopropoxide at 160℃; for 4h; Reagent/catalyst; Temperature; Concentration; Inert atmosphere; Large scale;
at 160℃; for 2h; Inert atmosphere;
at 160℃; for 2h; Inert atmosphere;

2-Ethylhexyl alcohol (104-76-7) + terephthalic acid (100-21-0) → di(2-ethylhexyl)terephthalate (6422-86-2)

Conditions	Yield
With phenol and titanium tetraisopropoxide resin at 200℃; for 4h; Reagent/catalyst; Dean-Stark; Inert atmosphere;	99.5%
With titanium(IV) isopropylate at 170 - 200℃; Inert atmosphere; Large scale;	99%
With titanium(IV) isopropylate at 170 - 220℃; under 760.051 Torr; for 4.5h; Inert atmosphere; Large scale;	99%

2-Ethylhexyl alcohol (104-76-7) + polyethylene terephthalate → di(2-ethylhexyl)terephthalate (6422-86-2)

Conditions	Yield
With choline chloride; zinc diacetate at 185℃; for 1h; Kinetics; Reagent/catalyst; Temperature; Time; Green chemistry;	84.2%
With titanium(IV) isopropylate at 180 - 225℃; for 5h; Inert atmosphere;

terephthalic acid (100-21-0) + (+-)-2-ethyl-hexanol → di(2-ethylhexyl)terephthalate (6422-86-2)

2-Ethylhexyl alcohol (104-76-7) + terephthalic acid (100-21-0) + butan-1-ol (71-36-3) → di-n-butyl terephthalate (1962-75-0) + di(2-ethylhexyl)terephthalate (6422-86-2) + 1-butyl 4-(2-ethylhexyl)terephthalate

Conditions	Yield
With methanesulfonic acid at 210℃; under 760.051 Torr; for 4h; Inert atmosphere;

2-Ethylhexyl alcohol (104-76-7) + di-n-butyl terephthalate (1962-75-0) → di(2-ethylhexyl)terephthalate (6422-86-2) + 1-butyl 4-(2-ethylhexyl)terephthalate

Conditions	Yield
at 140℃; for 5h; Inert atmosphere;

2-Ethylhexyl alcohol (104-76-7) + bis(2-propylheptyl)terephthalate → di(2-ethylhexyl)terephthalate (6422-86-2) + 2-propylheptyl 2-ethylhexyl terephthalate

Conditions	Yield
With titanium tetraisopropoxide at 160℃; for 5h; Inert atmosphere;

terephthalic acid (100-21-0) → di(2-ethylhexyl)terephthalate (6422-86-2) + 1-butyl 4-(2-ethylhexyl)terephthalate

Conditions	Yield
Multi-step reaction with 2 steps 1: methanesulfonic acid / 4 h / 210 °C / 760.05 Torr / Inert atmosphere 2: 5 h / 140 °C / Inert atmosphere View Scheme

1,4-benzenedicarboxylic acid dimethyl ester (120-61-6) + 2-Ethylhexyl alcohol (104-76-7) → di(2-ethylhexyl)terephthalate (6422-86-2)

Conditions	Yield
With titanium(IV) isopropylate; 2-(Ethylamino)ethanol for 1.4h; Heating;

2-Ethylhexyl alcohol (104-76-7) + isophthalic acid (121-91-5) + terephthalic acid (100-21-0) → Bis(2-ethylhexyl) isophthalate (137-89-3) + di(2-ethylhexyl)terephthalate (6422-86-2)

Conditions	Yield
With titanium(IV) tetraethanolate at 220℃; for 5h; Concentration; Inert atmosphere;

2-propylheptan-1-ol (10042-59-8) + 2-Ethylhexyl alcohol (104-76-7) + terephthalic acid (100-21-0) → di(2-ethylhexyl)terephthalate (6422-86-2) + bis(2-propylheptyl)terephthalate + 2-propylheptyl 2-ethylhexyl terephthalate

Conditions	Yield
With titanium(IV) isopropylate at 235℃; for 4h; Temperature; Inert atmosphere;

2-Ethylhexyl alcohol (104-76-7) + 2-isononyl alcohol (66793-83-7) + terephthalic acid (100-21-0) → di(2-ethylhexyl)terephthalate (6422-86-2) + diisononyl terephthalate + ethylhexyl isononyl terephthalate

Conditions	Yield
With titanium(IV) isopropylate at 220℃; for 9h;	A 10 %Chromat. B 36 %Chromat. C 54 %Chromat.

6-methylheptanol (1653-40-3) + terephthalic acid (100-21-0) → di(2-ethylhexyl)terephthalate (6422-86-2)

Conditions	Yield
With titanium(IV) isopropylate; monobutyltin triisooctanoate at 150 - 230℃; for 2h; Reagent/catalyst; Temperature;

2-Ethylhexyl alcohol (104-76-7) + 7-methyl-1-octanol (2430-22-0) + terephthalic acid (100-21-0) → diisononyl terephthalate + di(2-ethylhexyl)terephthalate (6422-86-2) + (2-ethylhexyl) isononyl terephthalate

Conditions	Yield
With titanium(IV) isopropylate at 170 - 220℃; for 4.5h; Inert atmosphere;

di(2-ethylhexyl)terephthalate (6422-86-2) → bis(2-ethylhexyl)cyclohexane-1,4-dicarboxylate (84731-70-4)

Conditions	Yield
With hydrogen at 150℃; under 60006 Torr; for 3h;	99%
With hydrogen; alumina substrate/0.05 wtpercent Ru at 140℃; under 150015 Torr; for 3.5h;	97%

di(2-ethylhexyl)terephthalate (6422-86-2) + butan-1-ol (71-36-3) → di-n-butyl terephthalate (1962-75-0) + 1-butyl 4-(2-ethylhexyl)terephthalate

Conditions	Yield
With titanium tetraisopropoxide at 160℃; for 4h; Reagent/catalyst; Temperature; Concentration; Inert atmosphere; Large scale;
at 160℃; for 2h; Inert atmosphere;
at 160℃; for 2h; Inert atmosphere;

2-propylheptan-1-ol (10042-59-8) + di(2-ethylhexyl)terephthalate (6422-86-2) → bis(2-propylheptyl)terephthalate

Conditions	Yield
With titanium tetraisopropoxide at 160℃; for 5h; Inert atmosphere;

di(2-ethylhexyl)terephthalate (6422-86-2) → 2-propylheptyl 2-ethylhexyl terephthalate

Conditions	Yield
Multi-step reaction with 2 steps 1: titanium tetraisopropoxide / 5 h / 160 °C / Inert atmosphere 2: titanium tetraisopropoxide / 5 h / 160 °C / Inert atmosphere View Scheme

di(2-ethylhexyl)terephthalate (6422-86-2) → di-n-butyl terephthalate (1962-75-0)

Conditions	Yield
Multi-step reaction with 3 steps 1: titanium tetraisopropoxide / 5 h / 160 °C / Inert atmosphere 2: titanium tetraisopropoxide / 5 h / 160 °C / Inert atmosphere 3: titanium tetraisopropoxide / 4 h / 160 °C / Inert atmosphere; Large scale View Scheme

di(2-ethylhexyl)terephthalate (6422-86-2) → bis(2-propylheptyl)terephthalate

Conditions	Yield
Multi-step reaction with 3 steps 1: titanium tetraisopropoxide / 4 h / 160 °C / Inert atmosphere; Large scale 2: 5 h / 140 °C / Inert atmosphere 3: titanium tetraisopropoxide / 5 h / 160 °C / Inert atmosphere View Scheme

di(2-ethylhexyl)terephthalate (6422-86-2) → C24H44O4 + C24H44O4

Conditions	Yield
With hydrogen at 120℃; under 150015 Torr; for 12h; Reagent/catalyst;
With Rh/Al2O3; hydrogen at 155 - 165℃; under 112511 Torr; Temperature; Industrial scale; stereoselective reaction;

2-methyl-propan-1-ol (78-83-1) + di(2-ethylhexyl)terephthalate (6422-86-2) → diisobutyl terephthalate (18699-48-4) + isobutyl(2-ethylhexyl) terephthalate

Conditions	Yield
at 160℃; for 2h; Inert atmosphere;

di-n-butyl terephthalate (1962-75-0) + di(2-ethylhexyl)terephthalate (6422-86-2) + 1-butyl 4-(2-ethylhexyl)terephthalate → bis(2-ethylhexyl)cyclohexane-1,4-dicarboxylate (84731-70-4) + 1,4-DBCH + 1,4-BEHCH

Conditions	Yield
With hydrogen at 150℃; under 60006 Torr; for 3h;

di(2-ethylhexyl)terephthalate (6422-86-2) → 1,4-BEHCH

Conditions	Yield
Multi-step reaction with 2 steps 1: 2 h / 160 °C / Inert atmosphere 2: hydrogen / 3 h / 150 °C / 60006 Torr View Scheme

Upstream product

• 104-76-7 2-Ethylhexyl alcohol 
• 100-21-0 terephthalic acid 
• 71-36-3 butan-1-ol 
• 1962-75-0 di-n-butyl terephthalate 
• 103-11-7 2-Ethylhexyl acrylate 
• 2430-22-0 7-methyl-1-octanol 
• 1653-40-3 6-methylheptanol 
• 66793-83-7 7-methyloctan-2-ol 
• 10042-59-8 2-propylheptan-1-ol 
• 121-91-5 isophthalic acid 
• 120-61-6 1,4-benzenedicarboxylic acid dimethyl ester 

Downstream Products

• 1962-75-0 di-n-butyl terephthalate 
• 84731-70-4 bis(2-ethylhexyl)cyclohexane-1,4-dicarboxylate 
• 93158-39-5 1,4-DBCH 
• 18699-48-4 diisobutyl terephthalate 

Relevant academic research and scientific papers

Alcoholysis of polyethylene terephthalate to produce dioctyl terephthalate using choline chloride-based deep eutectic solvents as efficient catalysts

Dioctyl terephthalate (DOTP) is a new kind of green and non-toxic plasticizer. The traditional process to prepare DOTP is costly and complicated, thus it is very necessary to find an efficient and environmentally-friendly way to obtain DOTP. In this study, we prepared DOTP from the alcoholysis of polyethylene terephthalate (PET) by using 2-ethyl-1-hexanol (2-EH) as the solvent, and used choline chloride-based deep eutectic solvents (ChCl-based DESs) as the catalysts due to their cheapness, low toxicity and ease of preparation. Under the optimized conditions (ChCl/Zn(Ac)2 1:1, 5 wt%, 180 °C, 60 min, PET:2-EH 1:5 molar ratio), the conversion of PET and the yield of DOTP were 100% and 84.7%, respectively. Furthermore, the possible mechanism was proposed through density functional theory (DFT) calculations and experimental results. It revealed that the hydrogen bonds (H-bonds) formed between 2-EH and DESs played a key role in accelerating the degradation process. Furthermore, the kinetics of the reaction was also investigated, and the results indicated that the alcoholysis of PET is a first-order reaction with an activation energy of 95.05 kJ mol-1. This work confirmed that ChCl-based DESs are favorable for the degradation of PET to prepare DOTP under mild conditions, which can also be used for other polymer degradation strategies.

Production of Copolyester Monomers from Plant-Based Acrylate and Acetaldehyde

PCTA is an important copolyester that has been widely used in our daily necessities. Currently, its monomers are industrially produced from petroleum-derived xylene. To reduce the reliance on fossil energy, we herein disclose an alternative route to acces

A Method for Manufacturing Diester-based Composition

A method for preparing a diesterase-based composition is provided to improve energy usage and economics of a reaction process by maintaining a portion of alcohol re-fed into a reactor before a reaction completion time.

ESTER COMPOUNDS AND THEIR APPLICATION AS PLASTICISER

The present invention relates to a novel ester-based compound and a use thereof and, especially, to a use of a novel ester-based compound as a plasticizer to improve heat resistance and compatibility. The use of the ester-based compound according to the present invention as a plasticizer for a heat-resistant resin composition can contribute to the improvement in properties of a molded product by offering synergistic effects in the improvement of properties, such as migration resistance and a weight loss on heating, and can improve the processability of a heat-resistant resin composition through a fast absorption rate and a short melting time.

METHOD FOR PREPARING PLASTICZER OF LOW MIGRATION DIOCTYL TEREPHTHALATE

A method for preparing a plasticzer of low migration di-2-ethylhexyl terephthalate includes, in the esterification reaction between terephthalic acid (PTA) and 2-ethyl-hexanol (2-EH), adding at least one short-chain alcohol and at least one long-chain alcohol to graft-modify di-2-ethylhexyl terephthalate. The reaction temperature is between 30 oC and 225 oC, and the reaction pressure is between 80 mbar and 1033 mbar. The modified di-2-ethylhexyl terephthalate prepared by the method can serve as an environmentally friendly plasticizer and have low migration and good processing characteristics.

METHODS FOR MANUFACTURING AND DECOLORIZING DIOCTYL TEREPHTHALATE

A method for manufacturing and a method for decolorizing dioctyl terephthalate are provided. The decolorizing dioctyl terephthalate includes: providing an unpurified dioctyl terephthalate; mixing the unpurified dioctyl terephthalate with a reducing agent and an adsorption medium to obtain a first decolorizing product; and mixing the first decolorizing product with a decolorizing adsorbent material to obtain a second decolorizing product. The method for manufacturing dioctyl terephthalate includes: a transesterification step, an alkaline washing and neutralization step, a redox step, a decolorization step and a stripping step; the decolorizing adsorbent material has an acid value between 0.1 and 2 mg KOH/g, a relative humidity between 2 and 10%, and a fineness between 80 and 100 cm2 /g.

A Method for Manufacturing Dialkyl Terephthalate-based Composition

The present invention relates to a process for preparing dialkyl terephtalate based compositions. To the present invention, the temperature of 1 st alcohol re-fed is kept relatively high, thereby reducing energy consumption which is additionally consumed for heating the alcohol. (by machine translation)

Synthesis method of plasticizer

The invention discloses a synthesis method of a plasticizer. By taking terephthalic acid and isooctyl alcohol as raw materials and taking one of imidazole ionic liquids such as 1-methyl-3-butylimidazole nitrate, 4-methyl-5-hydroxymethyl imidazole hydrochloride, 1-dodecyl-3-methylimidazole nitrate, 4-amino-5-formamide imidazole hydrochloride, 1,5-dimethyl-4-amino imidazole hydrochloride and the like as an ionic liquid catalyst, and esterifying is carried out to synthesize diisooctyl terephthalate. The synthesis method disclosed by the invention has the advantages of high conversion rate, high catalyst recycling frequency, simple process, environmental friendliness and the like.

Method for synthesizing dioctyl terephthalate through rapid esterification without alkali washing and water washing

The invention discloses a method for synthesizing dioctyl terephthalate through rapid esterification without alkali washing and water washing. According to the method, dioctyl terephthalate is synthesized from terephthalic acid and 2-ethylhexanol through esterification by taking polystyrene-supported 1-methylene-3-butylimidazolium chloride stannate ionic liquid as a catalyst. The method has the characteristics that the acid value of a product can be directly lower than the national standard, namely 1mgKOH/g, the alkali washing and the water washing are not required, the reaction speed is high,the conversion rate is high, the catalyst can be repeatedly used, the emission of wastewater is avoided, and the method is environment-friendly.

PLASTICIZER COMPOSITION AND RESIN COMPOSITION INCLUDING THE SAME

The present invention relates to a plasticizer composition and a resin composition including the same, and can provide a plasticizer composition in which three types of terephthalate-based materials and three types of cyclohexane 1,4-diester-based materials are mixed, and by which environmental friendliness can be secured, mechanical properties such as tensile strength and an elongation rate, physical properties such as migration properties and volatile loss can be improved to levels equal to or higher than those of existing products, and effects of improving processability and plasticizing efficiency can be expected, and a resin composition including the same.