1962-75-0

  • Product Name:dibutyl terephthalate
  • Molecular Formula:C16H22 O4
  • Molecular Weight:278.348
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Product Details

pd_meltingpoint:16℃

Purity:99%

Manufacturer Supply Best Quality dibutyl terephthalate 1962-75-0 with Efficient Transportation

  • Molecular Formula:C16H22 O4
  • Molecular Weight:278.348
  • Vapor Pressure:7.84E-05mmHg at 25°C 
  • Melting Point:16℃ 
  • Refractive Index:1.463 (45 oC) 
  • Boiling Point:341.8°Cat760mmHg 
  • Flash Point:180.2°C 
  • PSA:52.60000 
  • Density:1.053g/cm3 
  • LogP:3.60040 

dibutyl terephthalate(Cas 1962-75-0) Usage

General Description

Dibutyl terephthalate is a chemical compound commonly used as a plasticizer and fragrance ingredient. It is derived from terephthalic acid and is used to enhance the flexibility and durability of various materials such as polymers, resins, and adhesives. Dibutyl terephthalate is also utilized in the production of personal care products, including cosmetics and perfumes, to impart a pleasant scent and improve the texture of the final product. However,

InChI:InChI=1/C16H22O4/c1-3-5-11-19-15(17)13-7-9-14(10-8-13)16(18)20-12-6-4-2/h7-10H,3-6,11-12H2,1-2H3

1962-75-0 Relevant articles

Mechanistic insight into the synergistic Cu/Pd-catalyzed carbonylation of aryl iodides using alcohols and dioxygen as the carbonyl source

Li, Junxuan,Zhou, Jinlei,Wang, Yumei,Yu, Yue,Liu, Qiang,Yang, Tilong,Chen, Huoji,Cao, Hua

, p. 68 - 74 (2021/11/16)

Pd-catalyzed carbonylation, as an effici...

Palladium-Catalyzed Butoxycarbonylation of Polybromo(hetero)arenes: A Practical Method for the Preparation of (Hetero)arenepolycarboxylates and -carboxylic Acids

Wu, Weilong,Jing, Yongkang,Zhang, Deyi,Yan, Xianghe,Liang, Rong,Lu, Zhiqiang,Ji, Baoming

, p. 403 - 410 (2021/10/12)

The palladium-catalyzed alkoxycarbonylat...

PLASTICIZER COMPOSITION AND RESIN COMPOSITION INCLUDING THE SAME

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Paragraph 0068, (2021/05/07)

A plasticizer composition and a resin co...

A METHOD FOR MANUFACTURING TEREPHTHALATE-BASED COMPOSITION COMPRISING APPLYING PRESSURE

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Page/Page column title page; 2; 3, (2021/10/15)

Provided is a method for manufacturing a...

1962-75-0 Process route

2-Ethylhexyl alcohol
104-76-7

2-Ethylhexyl alcohol

terephthalic acid
100-21-0

terephthalic acid

butan-1-ol
71-36-3

butan-1-ol

di-n-butyl terephthalate
1962-75-0

di-n-butyl terephthalate

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

di(2-ethylhexyl)terephthalate

1-butyl 4-(2-ethylhexyl)terephthalate

1-butyl 4-(2-ethylhexyl)terephthalate

Conditions
Conditions Yield
With methanesulfonic acid; at 210 ℃; for 4h; under 760.051 Torr; Inert atmosphere;
1,4-benzenedicarboxylic acid dimethyl ester
120-61-6

1,4-benzenedicarboxylic acid dimethyl ester

2-methyl-propan-1-ol
78-83-1

2-methyl-propan-1-ol

butan-1-ol
71-36-3

butan-1-ol

n-butyl isobutyl terephthalate
1020110-91-1

n-butyl isobutyl terephthalate

di-n-butyl terephthalate
1962-75-0

di-n-butyl terephthalate

diisobutyl terephthalate
18699-48-4

diisobutyl terephthalate

methyl isobutyl terephthalate

methyl isobutyl terephthalate

Conditions
Conditions Yield
With Amberlyst 35 resin; at 120 - 140 ℃; Overall yield = 92.2 %; Overall yield = 76.987 g;

1962-75-0 Upstream products

  • 100-20-9
    100-20-9

    terephthaloyl chloride

  • 71-36-3
    71-36-3

    butan-1-ol

  • 120-61-6
    120-61-6

    1,4-benzenedicarboxylic acid dimethyl ester

  • 100-21-0
    100-21-0

    terephthalic acid

1962-75-0 Downstream products

  • 5547-49-9
    5547-49-9

    6,6′-(1,4-phenylene)bis(1,3,5-triazine-2,4-diamine)

  • 6422-86-2
    6422-86-2

    di(2-ethylhexyl)terephthalate

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