Atlas of Polymers

The Engineering Polymers Era (1961-1979)

1968

Polybutylene Terephthalate (PBT)

The Electric Insulator

“How a New Polyester Powered the Electronic Age”·thermoplastic·polyester·Celanese Corporation, General Electric

For eight months of 1968, Czechoslovakia ran an experiment in how much a rigid system could be allowed to bend. Alexander Dubček, installed as First Secretary in January, spent the spring loosening censorship, rehabilitating political prisoners, and promising what he called “socialism with a human face”, reform from inside the structure, not a break from it. On the night of 20 August, the answer came back: two thousand Warsaw Pact tanks and two hundred thousand troops crossed the border and occupied the country in a matter of days. The structure, it turned out, had less give in it than Dubček had hoped.

Plate I

Two young men walk along a cobbled Prague street past a burning tank wreathed in smoke, one of them carrying a Czechoslovak flag, as onlookers watch from the pavement and soldiers stand atop a second armoured vehicle behind it.
Prague, August 1968: a burning tank during the Warsaw Pact invasion that ended the Prague Spring reforms within days of the Soviet response.Wikimedia Commons

Two months later, in Mexico City, a much smaller question of “how much can be pushed further” produced a very different answer. The 1968 Olympics were run at altitude, on the first synthetic all-weather track any Games had used, and the thin air and the new surface combined to shatter records across the sprints and the jumps. On 18 October, Bob Beamon took off in the long jump and landed 8.90 metres away, 55 centimetres beyond the existing world record, a margin so large that the measuring equipment at trackside couldn’t reach it and had to be fetched by hand. The record stood for almost twenty-three years.

Plate II

A close-up action photograph of an athlete in mid-air during a long jump, knees drawn up toward his chest, arms trailing behind, with a blurred stadium crowd in the background.
Bob Beamon in flight at the 1968 Mexico City Olympics, seconds before landing a world record that would stand until 1991.Wikimedia Commons

Neither event has anything directly to do with plastics, but 1968 was, in both cases, a year spent testing how far a known, proven structure could be pushed before it stopped behaving the way everyone expected. Chemists at the Celanese Corporation were quietly running a molecular version of the same experiment. Polyethylene terephthalate, PET, had been a proven fiber and film polymer for two decades by then, but it made a poor injection-molding resin: left to cool in a mold, it crystallized so slowly and reluctantly that parts came out warped, weak, or barely solid at all. Celanese’s chemists asked what would happen if they replaced PET’s short, two-carbon ethylene glycol with 1,4-butanediol, a diol with two extra carbons of length. Unlike Czechoslovakia’s experiment, this one didn’t get crushed by adding too much give; it worked better than the original. The longer, more flexible unit let the chain fold on itself and crystallize far faster than PET ever had, and polybutylene terephthalate went from laboratory curiosity to a workable injection-molding resin because of it.

Two Extra Carbons

The chemistry of PBT is almost identical to PET’s: the same terephthalic acid unit, rigid and flat, alternating along the chain with a flexible diol segment. The only real difference is the length of that flexible piece: four carbons instead of two. That small addition changes how quickly the chain can arrange itself into an ordered, crystalline structure once it starts cooling in a mold. PET needs a hot mold and a long cycle to crystallize at all, which suits it to blown bottles and film but frustrates anyone trying to mold a part in a few seconds. PBT crystallizes readily at ordinary mold temperatures, fast enough to suit the high-volume injection-molding cycles that electrical and automotive manufacturers were already running for other materials. Celanese introduced the first PBT resin for injection molding, a glass-reinforced grade sold as Celanex, in 1969; General Electric followed in 1972 with its own line, sold as Valox, aimed squarely at the same electrical and electronic connector market.

A Rigid, Well-Insulated Solid

PBT crystallizes to a genuinely useful degree straight out of the mold, without the extra heat treatment PET often needs, which is why it holds dimensions so reliably once it cools. It stays rigid and dimensionally stable well past the temperature of boiling water, absorbs very little moisture even after prolonged immersion, and its electrical properties (resistance to current flow, resistance to voltage breakdown) are strong enough that it remains one of the standard resins for anything that has to keep electricity where it belongs. Mechanically it strikes a genuinely useful balance: stiff enough to hold a connector’s shape under repeated insertion and removal, yet able to absorb an impact and flex before it cracks, rather than shattering the way a more brittle engineering plastic would. Chemically, it tolerates dilute acids, alcohols, and everyday oils and greases comfortably, and it holds up well through years of outdoor UV exposure with only minor discoloration, but concentrated acids, strong alkalis, and prolonged exposure to hot water attack the ester linkages directly, which is why a PBT part is not the one to specify for a dishwasher or a caustic wash-down line.

From Reaction Flask to Resin Pellet

PBT is built the same way PET is: either by transesterifying dimethyl terephthalate with 1,4-butanediol, or by esterifying terephthalic acid with the same diol directly, then driving the polycondensation forward under heat and vacuum with a titanium or tin catalyst, distilling off the excess butanediol as the chain lengthens. The resin that results is dried carefully before use (like most polyesters, PBT will hydrolyze in its own melt if processed wet) and is then injection-molded, extruded, or blow-molded into its final shape.

Where the Extra Speed Went

PBT’s first market was exactly the one it was built for: electrical connectors, switches, terminal blocks, and the insulating housings around anything that carries current, where its combination of fast molding, dimensional stability, and electrical resistance let manufacturers turn out complex, tightly toleranced parts at high volume. Automotive electronics followed close behind, and PBT is still the resin behind a great many sensor housings, ignition components, and the connectors that link a modern car’s wiring harness together. Away from wiring altogether, PBT fiber shows up in keyboard keycaps prized for resisting the shine that builds up on cheaper plastic over years of typing, and in toothbrush bristles and false eyelashes, applications with nothing to do with electricity at all but that depend on the same crystallinity that gives the material its stiffness and wear resistance.

Plates III & IV

A close-up view of a mechanical keyboard's function-row and number-row keycaps in matte dark grey, with a single red Escape key at the left edge.
PBT keycaps on a mechanical keyboard, valued for keeping their matte finish and printed legends far longer than cheaper keycap plastics.Wikimedia Commons
A close-up of a black, threaded, cylindrical electrical connector plug with nine gold pins set into a red insert, attached to a thick coiled cable.
A heavy-duty vehicle wiring connector, the class of rigid, weatherproof, precisely molded part that engineering polyesters like PBT were built to fill.Wikimedia Commons

One further application deserves its own mention: General Electric later blended PBT with polycarbonate to create Xenoy, a material that combined PBT’s toughness and chemical resistance with polycarbonate’s impact strength even in cold weather. The result was flexible enough to survive a low-speed impact and spring back into shape, which is exactly why the 1984 Ford Taurus and Mercury Sable used it for a genuinely new kind of part: an all-plastic bumper system, front and rear, on volume-production cars.

values with [n] cite the numbered references·estimates are flagged·“not yet available” and “N/A” are honest states, not gaps

polybutylene terephthalate repeat unit O O O O n

Polybutylene Terephthalate repeat unit

Abbreviation
PBT
Type
polymer family (hub)
CAS number
24968-12-5
Resin ID code
none assigned
Formula
(C12H12O4)n
Repeat unit (BigSMILES)
{[][>]OCCCCOC(=O)c1ccc(cc1)C(=O)[<][]}
IUPAC name
—
Synonyms
Novaduran; Celanex; Crastin; Ultradur
Also known as
NovaduranCelanexUltradur

Chemical family
polyester
Backbone class
heterochain
Polymerization mechanism
step-growth-condensation
Polymer class
thermoplastic

Year of origin
1968
Era
The Engineering Polymers Era (1961-1979)
Key figures
Celanese Corporation · General Electric
Events referenced
Prague Spring and the Warsaw Pact invasion of Czechoslovakia (1968) · Bob Beamon's long jump world record at the 1968 Mexico City Olympics

Polymerization type
step-growth condensation
Common monomers (feedstocks)
1,4-butanediol, terephthalic acid
Catalysts
not yet available

Developed by Imperial Chemical Industries (ICI); shares terephthalic acid chemistry with PET but uses a 4-carbon diol rather than ethylene glycol. Compared to PET, PBT crystallizes faster, has slightly lower strength/rigidity, but superior impact resistance.

Tacticity
not yet available
Crystal structure
Triclinic, two allomorphs (α: a≈0.486, b≈0.596, c≈1.165 nm; β: a≈0.472, b≈0.579, c≈1.300 nm), 1 chain per unit cell; nearly planar chain conformation.
Typical crystallinity
35.25 (27.8–42.7) %[2]

Molecular weight

Number average (Mn)
19850 (5600–34100) g/mol[2]
Mass average (Mw)
75500 (26000–125000) g/mol[2]Mark's Polymer Data Handbook reports a narrower 30,000–80,000 g/mol range by light scattering.
Dispersity (Mw/Mn)
2.59 (2–3.18)[2]
Mark-Houwink constants: [η] = K · Ma
SolventTM rangeKa
unspecified (solution viscometry)[3]303 K—0.0117 mL/g0.87

Faster crystallization rate than PET makes PBT better suited to short injection-molding cycle times.

Density
1.29 (1.24–1.34) g/cm³[2]At 20°C, unfilled resin. Mark's Polymer Data Handbook reports measured densities of 1.33–1.34 g/cm³.
Melt flow index
34 (18–50) g/10min[2]250°C/2.16 kg
Refractive index
not yet available
Transmittance
not yet available
Haze
not yet available
Gloss
not yet available
Water absorption
0.3 (0.1–0.5) %[2]Equilibrium, immersion in water at 23°C; equilibrium at 23°C/50% RH: 0.2–0.25%.
Dielectric constant
3.25 (3.2–3.3)[2]1 MHz
Dielectric strength
77.5 (15–140) kV/mm[2]Film, d = 0.6–0.8 mm. Mark's Polymer Data Handbook reports 15.8 kV/mm (ASTM D149).
Electrical conductivity
2.5 × 10⁻¹⁵–1 × 10⁻¹³ S/m[2]Reciprocal of reported volume resistivity range (~1×10¹³–4×10¹⁴ Ω·m).

Glass transition (Tg)
46 (31–60) °C[2]DSC value 46°C; wider reported range 31–60°C. Mark's Polymer Data Handbook reports 30–60°C (ASTM D3418).
Melting temperature (Tm)
215.15 (208.3–222) °C[2]Mark's Polymer Data Handbook reports 222–232°C (ASTM D3418).
Crystallization (Tc)
not yet available
Heat deflection (HDT)
57.5 (50–65) °C[2]1.8 MPa, unfilled resin; at 0.45 MPa: 130–165°C. Replaces an earlier unsourced figure that conflated the two test loads.
Decomposition onset
288 °C[2]
Thermal conductivity
not yet available

Tensile modulus
2300 (2000–2600) MPa[2]Mark's Polymer Data Handbook reports 2,600 MPa (ASTM D638).
Yield strength
53 (47–59) MPa[2]Tensile stress at yield.
Tensile strength at break
53.5 (50–57) MPa[2]Unqualified 'tensile strength' row, distinct from reported yield stress (47–59 MPa). Mark reports 55 MPa breaking strength.
Elongation at break
167.5 (35–300) %[2]
Impact strength (Izod)
53 J/m[2]23°C, notched. Mark's Polymer Data Handbook reports the same value (ASTM D256-86).
Impact strength (Charpy)
6.5 (4–9) kJ/m²[2]23°C, notched
Hardness
72 Rockwell M[2]
Flexural modulus
2200 (2000–2400) MPa[2]Mark's Polymer Data Handbook reports 2,300 MPa (3-point flexure, ASTM D790).
Poisson's ratio
not yet available
Coefficient of friction
0.45 (0.3–0.6)[2]

Solvent: dilute acids
good[2]
Solvent: concentrated acids
poor[2]
Solvent: alcohols
good[2]
Solvent: alkalis
poor[2]
Solvent: aliphatic hydrocarbons
good[2]
Solvent: aromatic hydrocarbons
good[2]
Solvent: esters
good to fair[2]
Solvent: greases & oils
very good[2]
Solvent: halogenated hydrocarbons
poor[2]
Solvent: ketones
poor[2]
Weathering / UV
Good outdoor weathering resistance: 3-year exposure in Central Europe caused only slight color change; 90% tensile strength retained after 3,600 h in Xenotest accelerated weathering.[2]
Hydrolysis resistance
Sensitive to hot water above 60°C[1]
Flammability (UL94)
HB[2]Unfilled resin; V-0 achievable with flame-retardant grades.
Limiting oxygen index
22.1 (22–22.2) %[2]
Solubility parameter (δ)
not yet available

Gas permeability

not yet available

Polymer-solvent interaction parameter (χ)

not yet available

Processing methods
injection moldingextrusion
Drying required
Yes
Processing temperature
252.5 (235–270) °C[2]Injection molding; other methods (coating, pipe extrusion) 230–290°C.
Shrinkage rate
1.55 (0.9–2.2) %[2]

  • Electrical & electronicselectrical connector/housing insulation
  • Automotiveplug connectors
  • Consumer goodsshowerheads · irons · keyboard keycaps · toothbrush fibers · false eyelashes

Recyclable
Yes
Biodegradable
No
Degradation pathway
not yet available

LD50 (oral, rat)
not yet available
NFPA health
1[2]HMIS rating, 0–4 scale
NFPA flammability
1[2]HMIS rating, 0–4 scale
NFPA reactivity
0[2]HMIS rating, 0–4 scale
Carcinogenic classification
not listed by ACGIH, NIOSH, NTP[2]

TLV (ACGIH): 3 mg/m³ (respirable), 10 mg/m³ (total). OSHA exposure limit: 5 mg/m³ (respirable), 15 mg/m³ (total).

  1. [1]Polybutylene terephthalateWikipediaAccessed 2026-07-14https://en.wikipedia.org/wiki/Polybutylene_terephthalate[wiki-pbt]
  2. [2]Handbook of PolymersChemTec Publishinghttps://www.worldcat.org/isbn/9781895198928[handbook-wypych-2016]
  3. [3]Polymer Data HandbookOxford University Presshttps://search.worldcat.org/search?q=Polymer+Data+Handbook+Mark+1999[handbook-mark-1999]

Illustrations

  1. Plate IPrague, August 1968: a burning tank during the Warsaw Pact invasion that ended the Prague Spring reforms within days of the Soviet response.The Central Intelligence Agency · Public domainWikimedia Commons
  2. Plate IIBob Beamon in flight at the 1968 Mexico City Olympics, seconds before landing a world record that would stand until 1991.Unknown author · CC0Wikimedia Commons
  3. Plate IIIPBT keycaps on a mechanical keyboard, valued for keeping their matte finish and printed legends far longer than cheaper keycap plastics.Brett Spangler from Austin, US · CC BY-SA 2.0Wikimedia Commons
  4. Plate IVA heavy-duty vehicle wiring connector, the class of rigid, weatherproof, precisely molded part that engineering polyesters like PBT were built to fill.Florian-schäffer · CC BY-SA 3.0Wikimedia Commons