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Piperylene

What is Piperylene

Piperylene (systematic name: 1,3-pentadiene) is a conjugated diene hydrocarbon with the molecular formula C5H6, existing primarily as two geometric isomers: cis-1,3-pentadiene (cis-piperylene) and trans-1,3-pentadiene (trans-piperylene). It is a colorless, volatile, flammable liquid with a characteristic hydrocarbon odor, boiling near 42–44°C. Piperylene is obtained commercially as a co-product from the C5 fraction of naphtha steam cracking, where it is separated by extractive distillation or selective hydrogenation. It is a key monomer and intermediate in the production of petroleum resins (C5 hydrocarbon resins), copolymers, and specialty adhesives, and also serves as a reactive diene in Diels-Alder synthesis.

Analysts Sentiment

Bullish

35.4%

Neutral

19.9%

Bearish

44.7%

1-Week Outlook, Updated: June 8, 2026 | Next Update: June 15, 2026

What's driving sentiment this week:

Past Week (2026-06-01 to 2026-06-07) — Sentiment: Mixed

Supply side remains constrained as Japan’s naphtha imports recovered only partially to around 78-80% of pre-conflict levels by 2026-06-06, limiting cracker C5 yields and piperylene output.

Demand pressure surged in Japan due to ongoing plastic resin shortages and panic buying reported on 2026-06-05, pushing local piperylene-based resin prices higher.

Geopolitical tensions persist with Hormuz Strait disruptions despite the 2026-06-07 OPEC+ symbolic output increase, which only mildly eases upstream feedstock supply pressure, leaving crude and naphtha costs elevated.

This Week (2026-06-08 to 2026-06-14) — Outlook: Bearish

Tight crude supply and naphtha feedstock costs are expected to continue dominating piperylene production economics, maintaining upward pressure on margins and costs.

The key catalyst will be the upcoming EIA weekly crude oil inventory report on 2026-06-10 (expected), where any further inventory draws will reinforce the tight supply narrative.

A reversal in crude inventory trends or significant easing of geopolitical disruptions would undermine the current bearish cost pressures and potentially improve piperylene availability.

Key Market Impact

Upstream crude and naphtha feedstock tightness driven by geopolitical supply disruptions is the dominant force increasing piperylene production costs and constraining output.

Producers and buyers are responding with cautious procurement and production adjustments amid volatile cracker utilization and elevated feedstock prices.

How About the Price?

Monthly Piperylene Price History (USD/ton)
Month Price (USD/ton) Change Change Rate
2026-06-08 178.3 0 0%
2026-01 178.3 18.3 11.44%
2025-01 160 5 3.23%
2024-01 155 12.5 8.77%
2023-01 142.5 7.5 5.56%
2022-01 135 6.8 5.3%
2021-01 128.2 7.7 6.39%
2020-01 120.5 0 0%

Price Trajectory 2020–2026 (Brief Recap)

Phase 1 — Stable Base (2020): Prices started at $120.5/ton in January 2020 with no reported influencing factors recorded in the event log.

Phase 2 — Gradual Increase (2021–2023): Prices steadily rose from $128.2/ton in January 2021 to $142.5/ton in January 2023 amidst a persistent lack of documented market events impacting pricing.

Phase 3 — Accelerated Growth (2024–2026): Prices increased more strongly from $155.0/ton in January 2024 to $178.3/ton in January 2026 and remained flat through June 8, 2026, though no influencing factors were logged to explain this rise.

Supply-side factors

  • No supply-side factors reported in the monthly influence/events data from 2020 through 2026.

Demand-side factors

  • No demand-side factors reported in the monthly influence/events data from 2020 through 2026.

Substitutes & Alternatives

SubstituteReplacement Scenario / How It Substitutes
IsopreneIn C5 petroleum resin production, isoprene-based or mixed C5 streams can partially substitute piperylene as a co-monomer. In Diels-Alder reactions, isoprene is a direct diene substitute for piperylene when the methyl substitution pattern is acceptable. Requires reformulation of resin recipes to account for different reactivity and molecular weight distribution.
Dicyclopentadiene (DCPD)In hydrocarbon resin manufacturing, DCPD-based resins (C9 or DCPD resins) can substitute piperylene-derived C5 resins in adhesive, coating, and rubber compounding applications. Substitution is not drop-in and requires reformulation; DCPD resins typically have higher softening points and different compatibility profiles.
Butadiene (1,3-butadiene)In copolymer and elastomer applications where piperylene is used as a minor diene monomer, butadiene can serve as a functional substitute, offering similar conjugated diene reactivity. Widely used in SBR and other synthetic rubbers. Requires adjustment of polymerization conditions and monomer ratios.
2-Methyl-1,3-butadiene (Isoprene, synthetic)In specialty polymer and Diels-Alder synthesis applications, synthetic isoprene is a close structural analog to piperylene and can substitute in many diene chemistry contexts. Higher cost than piperylene but available in higher purity grades for demanding applications.
C9 Aromatic Petroleum ResinsIn hot-melt adhesive, pressure-sensitive adhesive, and road-marking paint formulations, C9 aromatic resins derived from the C9 fraction of steam crackers can substitute C5 piperylene-based resins. Substitution is feasible but alters tack, color, and compatibility with base polymers; typically requires reformulation and compatibility testing.
Terpene Resins (alpha-pinene, beta-pinene)In adhesive and sealant applications, terpene-based hydrocarbon resins derived from pine-derived feedstocks can substitute piperylene resins, particularly where bio-based or low-odor products are preferred. These are partial, application-specific substitutes and are generally higher cost.
Cyclopentadiene (CPD) / DCPD-modified resinsIn rubber compounding and tackifier resin applications, CPD/DCPD copolymer resins can replace piperylene-based tackifiers. The substitution is common when C5 piperylene supply is constrained, but requires adjustment of resin softening point and compatibility with styrene-block copolymers.

Regulatory Status

RegionRegulation / Policy NameIssuing AuthorityYear (enacted or latest revision)Key Requirement / ThresholdSource
United StatesTSCA InventoryU.S. Environmental Protection Agency (EPA)1977Inventory-listed active substance; subject to Chemical Data Reporting (CDR) for manufacturers/importers at >=25,000 lb/year (or 2,500 lb/year if subject to certain TSCA actions)U.S. EPA TSCA Inventory and 2024 CDR Instructions
United StatesRisk Management Program (RMP) under Section 112(r) of the Clean Air ActU.S. Environmental Protection Agency (EPA)1996Regulated substance; threshold quantity 10,000 lbU.S. EPA List of Regulated Substances under Risk Management Program (2024)
United StatesCERCLA Hazardous SubstancesU.S. Environmental Protection Agency (EPA)1980Reportable quantity: 100 lbU.S. EPA Consolidated List of Lists (2024)
United StatesRCRA Hazardous WasteU.S. Environmental Protection Agency (EPA)1976Hazardous waste code: U186U.S. EPA Consolidated List of Lists (2024)
United StatesDOT Hazardous Materials TransportationU.S. Department of Transportation (DOT)1960UN number: 1993; hazard class: 3; packing group: IICAMEO Chemicals / DOT ERG Guide 128
United StatesGHS Classification (OSHA Hazard Communication Standard)U.S. Occupational Safety and Health Administration (OSHA)2012Hazard statements: H225 (highly flammable liquid and vapor), H304 (may be fatal if swallowed and enters airways); Signal word: DangerGlobally Harmonized System (GHS) criteria as applied by OSHA
European UnionREACH RegistrationEuropean Chemicals Agency (ECHA)2006Registered substance (EC 207-995-2, CAS 504-60-9); pre-registration and registration requirements apply for manufacturers/importersECHA Substance Information (EC Inventory)
ChinaHazardous Chemicals Catalog (China MEE / SAWS)Ministry of Ecology and Environment (MEE) / State Administration for Market Regulation (SAWS)2015 (updated)Included in national hazardous chemicals list; subject to handling, storage, and transport controlsChina MEE / SAWS Hazardous Chemicals Catalog
Global TradeHarmonized Tariff Schedule (HTS) 2901.29.10U.S. International Trade Commission / U.S. Customs and Border Protection1988 (ongoing)Duty rate: 5% ad valoremU.S. HTS / CBP rulings

Key Influence Events

No influence events available.

Piperylene (systematic name: 1,3-pentadiene) is a conjugated diene hydrocarbon with the molecular formula C5H6, existing primarily as two geometric isomers: cis-1,3-pentadiene (cis-piperylene) and trans-1,3-pentadiene (trans-piperylene). It is a colorless, volatile, flammable liquid with a characteristic hydrocarbon odor, boiling near 42–44°C. Piperylene is obtained commercially as a co-product from the C5 fraction of naphtha steam cracking, where it is separated by extractive distillation or selective hydrogenation. It is a key monomer and intermediate in the production of petroleum resins (C5 hydrocarbon resins), copolymers, and specialty adhesives, and also serves as a reactive diene in Diels-Alder synthesis.

Top Countries Production Capacity

No capacity data available.

Production Process of Piperylene

Piperylene (systematic name: 1,3-pentadiene) is a conjugated diene hydrocarbon with the molecular formula C5H6, existing primarily as two geometric isomers: cis-1,3-pentadiene (cis-piperylene) and trans-1,3-pentadiene (trans-piperylene). It is a colorless, volatile, flammable liquid with a characteristic hydrocarbon odor, boiling near 42–44°C. Piperylene is obtained commercially as a co-product from the C5 fraction of naphtha steam cracking, where it is separated by extractive distillation or selective hydrogenation. It is a key monomer and intermediate in the production of petroleum resins (C5 hydrocarbon resins), copolymers, and specialty adhesives, and also serves as a reactive diene in Diels-Alder synthesis.

Specs & Grades

PropertyTypical Value / RangeUnitGrade / Note
Purity (total 1,3-pentadiene)≥ 95.0wt%Polymerization grade
Purity (total 1,3-pentadiene)≥ 85.0wt%Technical / resin grade
cis-1,3-Pentadiene content15–25wt%Typical in mixed piperylene
trans-1,3-Pentadiene content60–75wt%Dominant isomer in commercial product
1,2-Pentadiene (impurity)≤ 1.0wt%Polymerization grade
Cyclopentadiene (impurity)≤ 0.5wt%Polymerization grade
Isoprene (impurity)≤ 1.0wt%Polymerization grade
Inhibitor (TBC or equivalent)50–100ppmStabilized commercial product
Boiling point (cis isomer)44.1°CPure component
Boiling point (trans isomer)42.0°CPure component
Density at 20°C0.676–0.682g/cm³Mixed isomers
Color (APHA)≤ 10Polymerization grade
Water content≤ 100ppmPolymerization grade
Sulfur content≤ 5ppmPolymerization grade

Who are the Top Players?

CompanyHeadquartersKey Facilities
Dow ChemicalMidland, Michigan, USA
ExxonMobilSpring, Texas, USABaytown, Texas
LyondellBasellHouston, Texas, USA
ShellLondon, UKMoerdijk, Netherlands, Deer Park, Texas, Singapore
Zeon CorporationTokyo, JapanMizushima
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