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Aromatic Diester · CAS 120-61-6

Dimethyl Terephthalate

C6H4(COOCH3)2 Molar mass 194.18 g/mol

The dimethyl ester of terephthalic acid supplied by Chelora Chemicals — the original industrial raw material for PET polyester and still used for polyester film and specialty resin grades — exported from Indonesia as white crystalline flake with full batch documentation on every shipment.

Identification Sheet REP.
IUPAC nameDimethyl benzene-1,4-dicarboxylate
CAS number120-61-6
Molecular formulaC₁₀H₁₀O₄
Molar mass194.18 g/mol
AppearanceWhite crystalline solid / flake
Common synonymsDimethyl Terephthalate, DMT, Dimethyl 1,4-Benzenedicarboxylate
Melting Point140 – 142 °Clit.
Boiling Point288 °Cat 1 atm, with some decomposition
Specific Gravity1.20solid, 20 °C
Flash Point146 °Cclosed cup, approx.
AppearanceWhite crystalline solid / flakepractically odourless
Purity Offered99.9%+ (fibre/film grade)crystalline flake
01 / PRODUCT DOSSIER

What Dimethyl Terephthalate is, and why buyers source it

A working overview of the compound's chemistry, its historical and continuing role in polyester manufacture, and the grade Chelora Chemicals keeps in regular supply.

Dimethyl Terephthalate is the dimethyl ester of terephthalic acid: the same symmetric, para-substituted benzene ring as purified terephthalic acid, but with each carboxylic acid group capped as a methyl ester rather than left free. That esterified form is considerably more soluble and easier to purify by distillation and crystallisation than the free diacid, which is precisely why DMT was the industry's original route to high-purity polyester feedstock, before terephthalic acid purification technology advanced enough to make the PTA route commercially dominant.

At room temperature it is a white, odourless crystalline solid or flake, melting to a clear liquid well above its melting point and only sparingly soluble in cold water, though it dissolves more readily in many organic solvents. It reacts with glycols by transesterification, releasing methanol rather than the water that the free diacid route releases.

Where it fits in the value chain

Dimethyl Terephthalate's defining end use is transesterification with monoethylene glycol to produce polyethylene terephthalate (PET), historically the dominant industrial route to PET and still used today for certain film grades (including high-clarity polyester film) and in regions and plants built around DMT-based infrastructure. It is also transesterified with 1,4-butanediol to give polybutylene terephthalate (PBT) engineering resin, and with other polyols in specialty polyester and alkyd resin formulations where its high purity and ease of handling as a melt or solid are valued.

Grade we supply

Chelora Chemicals offers Dimethyl Terephthalate in fibre/film grade (99.9%+ purity) as crystalline flake, suited to transesterification for PET film and fibre, PBT manufacture, and specialty polyester resin production. The grade is supplied with a batch-wise certificate of analysis.

02 / MANUFACTURING ROUTE

How Dimethyl Terephthalate is made

An overview of the production route for orientation purposes. Our manufacturing partners' own process parameters and in-process controls are proprietary and are not disclosed beyond what is needed to interpret the certificate of analysis.

Dimethyl Terephthalate is manufactured by the combined oxidation and esterification of para-xylene with methanol, in what is widely known as the Witten process. Para-xylene is oxidised with air, and the resulting intermediate acids and partial esters are esterified with methanol as the sequence proceeds, passing through methyl p-toluate as a key intermediate, until both ring substituents have been fully oxidised and esterified to give dimethyl terephthalate directly, without isolating the free diacid at any stage.

The crude DMT is purified by fractional distillation and recrystallisation, which is comparatively straightforward given the ester's higher solubility in organic solvents and its clean, sharp melting point relative to the free diacid, and is what originally made the DMT route commercially attractive before PTA purification technology (notably catalytic hydrogenation of the 4-CBA impurity) matured enough to allow the simpler, more direct PTA process to take over as the industry's dominant route.

03 / APPLICATIONS

Industries and processes that use it

Dimethyl Terephthalate is consumed across PET film and fibre manufacture, PBT engineering resin, and specialty polyester and alkyd resin formulations. The fields below account for most of the demand we see through our export desk.

Field 01

PET Film Manufacture

Transesterified with monoethylene glycol to produce high-clarity PET film, including biaxially oriented film used in packaging, electrical insulation and imaging media.

Field 02

PET Fibre (DMT Route)

Transesterified to produce PET resin for textile fibre manufacture in plants built around DMT-based process infrastructure.

Field 03

Polybutylene Terephthalate (PBT)

Transesterified with 1,4-butanediol to give PBT, an engineering thermoplastic used in electrical connectors and automotive components.

Field 04

Specialty Polyester & Alkyd Resins

Transesterified with other polyols in specialty polyester coil-coating resins and alkyd resin formulations that value its high purity and ease of handling.

04 / REACTION CHEMISTRY

How the molecule is typically carried forward

The two methyl ester groups on the symmetric aromatic ring govern almost all of this molecule's further reaction chemistry. Reaction classes below account for most of the ways Dimethyl Terephthalate is converted into a finished polyester.

Transesterification

Each methyl ester reacts with a glycol hydroxyl under catalysis, releasing methanol, to form a new glycol ester linkage — the defining first step of DMT-route polyester manufacture.

Polycondensation

The resulting bis(glycol ester) is further polymerised under vacuum and heat, releasing excess glycol and building the long PET or PBT polymer chain.

Methanol Recovery & Recycle

The methanol released during transesterification is recovered by distillation and recycled, both as a process economy and because residual methanol must be removed before polycondensation proceeds.

Alkyd Resin Incorporation

Reaction with polyol and fatty-acid components under esterification conditions incorporates the terephthalate unit into alkyd coating-resin formulations.

05 / RELATED BUILDING BLOCKS

Dimethyl Terephthalate against other polyester intermediates we supply

Buyers sourcing DMT for polyester manufacture often also consider the now-dominant PTA direct-esterification route, or the nylon-chain intermediates for comparison. A quick reference to what else is on our regular supply list.

ProductCAS NumberCategoryNotes
Dimethyl Terephthalate120-61-6Aromatic diesterThe product on this page — the original ester-route raw material for PET and PBT.
Purified Terephthalic Acid100-21-0Aromatic dicarboxylic acidThe now-dominant direct-esterification alternative raw material for PET — see its product page.
Adipic Acid124-04-9Aliphatic dicarboxylic acidA related dicarboxylic acid, the co-monomer of nylon 66 — see its product page.
Caprolactam105-60-2Cyclic lactamThe single-monomer feedstock for nylon 6, a related condensation-polymer chain — see its product page.

Exact physical constants and purity specifications are confirmed per batch on the certificate of analysis — treat the notes above as a sourcing guide, not a specification sheet, for products other than Dimethyl Terephthalate.

06 / HAZARD & HANDLING

Safety classification at a glance

Based on GHS classification as commonly listed for this substance. This is a summary for orientation only — always work from the current safety data sheet supplied with your specific batch.

H319

Causes serious eye irritation.

H315

Causes skin irritation.

Low Acute Toxicity

Comparatively low acute oral and dermal toxicity relative to many industrial organic esters.

Dust Control

Handled as crystalline flake; minimise airborne dust during transfer and packing.

PPE Standard

Chemical-resistant gloves and safety goggles are the baseline for routine handling.

Thermal Handling

Handled molten above its melting point in some dosing systems; standard hot-material handling precautions apply.

Combustible Solid

Combustible as a fine dust under specific conditions; avoid dust accumulation and ignition sources.

Signal word

Warning — GHS07 harmful pictogram applies.

This compound causes skin and eye irritation and has a comparatively low acute toxicity profile among industrial esters. It should be handled with chemical-resistant gloves, eye protection and dust control during milling and packing, and with standard hot-material precautions where handled molten. Full first-aid, storage, spill and PPE guidance is in the MSDS issued with every shipment, and should be read in full before this material is handled.

07 / STORAGE & SHELF LIFE

Keeping it on spec between delivery and use

General storage guidance for this grade. Site-specific storage rules, segregation requirements and re-test intervals should follow your own EHS procedures and the MSDS issued with your batch.

Storage TemperatureCool, ambient (solid) or heated (molten)
ContainerSealed bags / drums / heated tank
Typical Shelf Life36 months, unopened
Keep Away FromStrong oxidizers, moisture ingress
Beyond Shelf LifeRe-assay before use

Store in a cool, dry area away from strong oxidising agents, in tightly closed original packaging, protected from moisture. If handled molten, maintain even heating to avoid localised degradation and colour development. Re-check assay, colour and melting point on a batch held past its retest date before use.

08 / PACKING & EXPORT

How it ships from Indonesia

Standard packing and export terms for this product. Confirm exact figures against your order — they vary slightly by destination and quantity.

Standard Packing25 kg bags (flake) / 1,000 kg jumbo bags
Bulk PackingHeated bulk tanker on request
Min. OrderFrom 1 tonne
Lead Time2 – 3 weeks
Export TermsFOB · CFR · CIF
09 / QUALITY & DOCUMENTATION

What travels with every batch

Specification is agreed before the purchase order, not discovered on arrival. Every shipment of Dimethyl Terephthalate leaves with a documented, checkable paper trail.

Doc 01

Certificate of Analysis

Batch-wise assay, colour and key physical constants, issued against the agreed specification so your QC team can check it, not just file it.

Doc 02

Safety Data Sheet

GHS-format SDS in English covering hazard classification, handling, storage, first-aid and spill response for the exact grade shipped.

Doc 03

Technical Data Sheet

Reference physical and chemical properties, recommended storage and typical applications, for internal circulation to your process or R&D teams.

Doc 04

Certificate of Origin

Confirms Indonesian origin for customs clearance and any preferential-duty claim at your destination port.

Doc 05

Dangerous Goods Declaration

UN packing group, classification and shipper's declaration prepared ahead of loading so documentation never holds up customs.

Doc 06

Third-Party Inspection

Independent pre-shipment inspection and re-sampling can be arranged on request, at your cost, for buyers who require it as a matter of policy.

10 / FAQ

Frequently asked questions

What buyers most often ask our sales desk about this grade.

01What is Dimethyl Terephthalate used for?+
Predominantly as the ester-route raw material for PET film and fibre manufacture, transesterified with monoethylene glycol; it is also transesterified with 1,4-butanediol to give PBT, and used in specialty polyester and alkyd resin formulations.
02What is the CAS number of Dimethyl Terephthalate?+
Its CAS Registry Number is 120-61-6, with molecular formula C₁₀H₁₀O₄ and a molar mass of 194.18 g/mol.
03How is Dimethyl Terephthalate made?+
By the combined oxidation and esterification of para-xylene with methanol (the Witten process), passing through methyl p-toluate as an intermediate, giving DMT directly without isolating the free diacid.
04What purity grade does Chelora Chemicals supply?+
We supply fibre/film grade (99.9%+ purity) as crystalline flake, suited to transesterification for PET film and fibre, PBT manufacture, and specialty polyester resin production. Each batch ships with a certificate of analysis.
05Is Dimethyl Terephthalate hazardous?+
It has a comparatively low acute toxicity profile but causes skin and eye irritation. It should be handled with the PPE and precautions specified in the MSDS supplied with each shipment, particularly during milling and packing.
06Why was DMT the original industrial route to PET before PTA became dominant?+
As a methyl ester rather than a free acid, DMT is markedly more soluble in organic solvents and purifies to a sharp, consistent melting point by straightforward distillation and recrystallisation, which made it achievable with the purification technology available when PET was first commercialised; PTA only became the preferred route once catalytic hydrogenation technology was developed to remove the 4-carboxybenzaldehyde impurity that otherwise limited free-acid purity.
07What packing options are available?+
Standard packing is 25 kg bags for the flake grade or 1,000 kg jumbo bags, with heated bulk tanker shipment available on request.
08How long does delivery take?+
Typical lead time is two to three weeks plus transit, depending on whether the grade is ex-stock or made to order and your destination port. A firm date is confirmed in the written quotation.
09Can I get a sample before placing a bulk order?+
Yes. Pre-shipment samples and a batch certificate of analysis can be arranged so your QC team can verify the specification before committing to volume.
10Do you supply the direct-esterification alternative as well?+
Yes, we also supply Purified Terephthalic Acid, the now-dominant direct-esterification alternative raw material for PET.
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