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Merck
모든 사진(5)

주요 문서

185361

Sigma-Aldrich

Terephthalic acid

greener alternative

98%

동의어(들):

Benzene-1,4-dicarboxylic acid

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About This Item

Linear Formula:
C6H4-1,4-(CO2H)2
CAS Number:
Molecular Weight:
166.13
Beilstein:
1909333
EC Number:
MDL number:
UNSPSC 코드:
12162002
eCl@ss:
39024105
PubChem Substance ID:
NACRES:
NA.23

vapor pressure

<0.01 mmHg ( 20 °C)

Quality Level

분석

98%

형태

powder

autoignition temp.

925 °F

환경친화적 대안 제품 특성

Design for Energy Efficiency
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

mp

>300 °C (lit.)

solubility

water: ~0.017 g/L at 25 °C

density

1.58 g/cm3 at 25 °C

환경친화적 대안 카테고리

SMILES string

OC(=O)c1ccc(cc1)C(O)=O

InChI

1S/C8H6O4/c9-7(10)5-1-2-6(4-3-5)8(11)12/h1-4H,(H,9,10)(H,11,12)

InChI key

KKEYFWRCBNTPAC-UHFFFAOYSA-N

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일반 설명

Terephthalic acid belongs to the class of monomers known as aromatic dicarboxylic acids. It is primarily used as a key monomer in the production of a high-performance polymer known as polyethylene terephthalate (PET). It is also used to prepare other polymers such as polybutylene terephthalate (PBT), polymer blends, and alloys. Terephthalic acid-based polymers are widely used in various industries including, packaging, textile fibers, polyester resins, polyurethane coatings, polyurethane foams, protective coatings, electrical components, and automotive applications due to their excellent properties such as high thermal stability, chemical resistance, lightweight, transparency, high strength, and durability. In the medical industry, terephthalic acid-based polymers may be used in the production of medical devices and equipment such as surgical sutures, tissue engineering scaffolds, and vascular grafts due to their biocompatibility, chemical resistance, and ease of processing.

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for energy efficiency. Find details here.

애플리케이션

Terephthalic acid can be used:
  • As a monomer in the synthesis of poly(butylene terephthalate) (PBT), a type of polyester, that is used in various fields including Automotive components, textile Industry, packaging materials, electrical and electronic components.
  • As an organic ligand in the synthesis of the cobalt(II) metal–organic framework (MOFs), which finds applications in electrochemical energy storage, catalysis, optoelectronics, and water treatment.
  • Terephthalic acid (TPA) can be synthesized from bio-based materials for a variety of applications, which include the production of polyester fiber, non-fiber field, PET bottles, synthetic perfumes and medicines.
  • Terephthalic acid is used as a linker molecule in the preparation of metal-organic frameworks (MOFs).

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves


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문서 라이브러리 방문

이미 열람한 고객

Photocatalytic degradation of terephthalic acid using titania and zinc oxide photocatalysts: Comparative study
Shafaei A, et al.
Desalination, 252(1-3), 8-16 (2010)
Biobased terephthalic acid technologies: a literature review
Collias DI, et al.
Industrial Biotechnology (New Rochelle, N.Y.), 10(2), 91-105 (2014)
Synthesis of ethylene glycol and terephthalic acid from biomass for producing PET
Pang J, et al.
Green Chemistry, 18(2), 342-359 (2016)
Jingqi Tian et al.
Biosensors & bioelectronics, 71, 1-6 (2015-04-17)
Considerable recent attention has been paid to homogeneous fluorescent DNA detection with the use of nanostructures as a universal "quencher", but it still remains a great challenge to develop such nanosensor with the benefits of low cost, high speed, sensitivity
Akram Hijazi et al.
Dalton transactions (Cambridge, England : 2003), 42(14), 4848-4858 (2013-02-01)
We report the syntheses and characterizations, in the solid state and in solution, of three new cyclic polyoxothiomolybdates self-assembled around 2,5-dimethylterephthalate (DMT) and 2,5-bis(trifluoromethyl)terephthalate (DFMT) ligands, namely [Mo12DMT](2-), [Mo12DFMT](2-) and [Mo16DFMT](2-). A series of these two Mo12-compounds completed by the

문서

Metal-organic frameworks offer high surface area materials for alternative energy applications through simple synthetic strategies.

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