Atlas of Polymers

The Wartime Innovation Period (1939-1945)

1941

Styrene-Acrylonitrile (SAN)

The Clear, Tough Cousin That Paved the Way

thermoplastic·styrenic · acrylic

On 7 December 1941, Japanese aircraft sank or damaged eight battleships at Pearl Harbor, and the United States entered the war it had spent two years supplying from the sidelines. The consequences reached the rest of the world within weeks. Japanese forces swept down through Malaya and the Dutch East Indies, and by the time Singapore fell in February 1942, the United States had lost something like nine-tenths of its natural rubber supply, the material behind every tire, hose, and gasket in the country, almost none of which grew on American soil.

Plate I

A warship listing and burning at anchor, engulfed in a vast column of black smoke, photographed from water level with a smaller vessel spraying firefighting water in the foreground.
Pearl Harbor, 7 December 1941. Within ten weeks, Japan's advance through Southeast Asia would cut off nearly all of America's natural rubber.Wikimedia Commons

Washington had already seen the shortage coming. A government rubber-stockpiling agency had been created in 1940, and by 1941 it was underwriting a crash effort to build a synthetic rubber industry that barely existed in the United States at all. On the home front that meant scrap drives: every worn tire, hose, and rubber boot was suddenly worth collecting, down to whatever a farmer could load onto a cart.

Plate II

A donkey pulling a two-wheeled cart heaped with old tires past a filling station, with two men seated among the load.
Old tires collected for a wartime scrap rubber drive: the shortage reached rural roads as well as city streets.Wikimedia Commons

Behind the scrap drives sat a much bigger industrial push. In 1941, B.F. Goodrich was already turning out sheets of a homegrown synthetic rubber called Ameripol at its Akron plant, and the rest of the rubber industry was racing to scale up variants of its own, including one built from butadiene and a nitrogen-bearing chemical called acrylonitrile, which until then had barely been made in the United States at industrial volume. The war didn’t just demand rubber. It demanded that America build, almost overnight, a domestic supply of chemicals it had previously had little reason to produce at scale.

Plate III

Two factory workers in overalls bent over a rolling mill, guiding a thick, damp white sheet of rubber crumb between heavy rollers.
Synthetic rubber coming off the rolling mill at B.F. Goodrich's Akron plant in 1941, part of the wartime buildup that made acrylonitrile a bulk American chemical for the first time.Wikimedia Commons

Plate IV

A four-panel wartime poster illustrating a gas mask, a life raft, a scout car and a heavy bomber, each labelled with the pounds of rubber it required, above the headline 'America needs your scrap rubber'.
A 1942 War Production Board poster spelling out, item by item, just how much of the war effort ran on rubber. That shortage pushed acrylonitrile into bulk American production in the first place.Wikimedia Commons

Acrylonitrile suddenly being cheap and abundant is the reason SAN exists. Somewhere in that same wartime chemistry, a researcher tried copolymerizing acrylonitrile with styrene and left out the butadiene that would have made it a rubber. What came out was not elastic at all: it was a hard, clear plastic, tougher and more heat-resistant than styrene alone. Styrene-acrylonitrile (SAN) reached the patent literature and small-scale commercial production in the early 1940s, a direct byproduct of a crisis that had nothing to do with plastics at all.

A Polar Partner

SAN is a random copolymer, typically around three-quarters styrene to one-quarter acrylonitrile, the two monomers strung together along a single amorphous chain with no regular pattern to the sequence. The styrene units contribute the clarity and easy processing familiar from plain polystyrene; the acrylonitrile units contribute something styrene alone cannot. Their polar nitrile groups attract one another strongly across neighbouring chains, pulling the whole structure tighter and making it harder for heat, stress, or a solvent to pull the chains apart. Push the acrylonitrile content higher and the material gets tougher and more chemically resistant, but also more prone to a yellow tint and harder to mold; SAN’s commercial grades sit at the balance point of that trade-off.

The improvement over polystyrene shows up directly where it matters. SAN survives a dip in boiling water that would visibly deform plain polystyrene, and it takes a sharp knock without shattering the way an unmodified polystyrene part would. It gives up very little of polystyrene’s clarity to get there; light still passes through it with barely any of the scattering that would cloud a lesser plastic. The trade is not free: SAN absorbs a little more moisture than polystyrene and remains just as unable to shrug off oils, greases, or common solvents, which still attack it about as readily as they attack its parent. What it resists far better are the mild acids and alkalis in ordinary cleaning products, which makes it useful in a kitchen or bathroom even though, like polystyrene, it has no real defense against a splash of solvent or cooking oil left standing.

From Two Monomers to a Resin

SAN is made by copolymerizing its two monomers through any of the standard routes (bulk, solution, suspension, or emulsion polymerization), each giving different control over molecular weight and how evenly the two monomers end up distributed along the chain. Because styrene and acrylonitrile do not add to a growing chain at exactly the same rate, keeping the feed composition steady through the reaction takes real care; get it wrong and the copolymer’s properties drift from batch to batch.

Commercial SAN stayed a specialty material through the 1940s; production was small and the price was high enough to confine it to applications that could justify the cost. As output scaled up and prices fell in the following decades, it settled into a durable niche: valued anywhere polystyrene’s clarity was wanted but its fragility could not be tolerated. Its most consequential role, though, turned out to be as a starting point rather than a finished product.

The Quiet Parent of a Superstar

SAN’s own applications lean on exactly the combination its chemistry provides: clear, rigid housewares and cosmetic packaging that need to survive daily handling without crazing, battery cases and appliance housings that need dimensional stability, even plastic optical fibers that put its transparency to work in a way few people ever notice. None of that made SAN famous. What did was what happened when a third monomer, butadiene rubber, was blended into the same styrene-acrylonitrile matrix: the product was ABS, the tough, glossy plastic behind LEGO bricks, car dashboards, and a great many appliance housings besides. SAN is the resin ABS is built on, and without the wartime scramble for a domestic acrylonitrile supply, neither one arrives when it did.

The Enduring Middle Ground

SAN never won the fame of its offspring or the ubiquity of the polystyrene it improved on, and it never needed to. It occupies a specific middle ground (clearer than ABS, tougher than polystyrene), and modern grades, along with weather-resistant relatives like ASA, still fill exactly that gap decades later. It is a reminder that not every advance in materials arrives with a name attached: this one arrived out of a shortage, quietly solved a problem nobody had asked it to solve, and then spent the rest of the century being the unglamorous, dependable answer to it.

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

styrene acrylonitrile repeat unit N ran ran

Styrene-Acrylonitrile repeat unit

Abbreviation
SAN
Type
polymer family (hub)
CAS number
9003-54-7
Resin ID code
none assigned
Formula
(C8H8)x·(C3H3N)yA statistical (random) copolymer, typically 70–80% styrene by weight; the two brackets show the two monomer units and their approximate ratio, not a block sequence, since the two are mixed at random along the chain.
Repeat unit (BigSMILES)
{[][$]CC(c1ccccc1)[$],[$]CC(C#N)[$][]}
IUPAC name
—
Synonyms
—
Also known as
—

Chemical family
styrenicacrylic
Backbone class
carbon-chain
Polymerization mechanism
free-radical
Constitutional monomer
StyreneAcrylonitrile
Polymer class
thermoplastic

Year of origin
1941
Era
The Wartime Innovation Period (1939-1945)
Key figures
—

Polymerization type
free-radical chain-growth copolymerization
Common monomers (feedstocks)
styrene, acrylonitrile
Catalysts
not yet available

Random copolymerization of styrene (70–80 wt%) and acrylonitrile (20–30 wt%). Higher acrylonitrile content improves mechanical strength and chemical resistance but introduces a yellowish tint. SAN itself later became the base resin for ABS, when polybutadiene rubber particles (10–20 micrometers) are dispersed/grafted into it to add toughness.

Tacticity
not yet available
Crystal structure
not yet available
Typical crystallinity
0 %estimate[1]Amorphous, transparent random copolymer.

Molecular weight

Number average (Mn)
not yet available
Mass average (Mw)
175000 (165000–185000) g/mol[2]
Dispersity (Mw/Mn)
not yet available

Mark-Houwink constants

not yet available

Brittle relative to rubber-toughened ABS, which is precisely why ABS was later developed by adding polybutadiene to a SAN-like matrix.

Density
1.08 (1.07–1.09) g/cm³[2]20 °C.
Melt flow index
7.5 g/10min[2]230 °C/3.8 kg.
Refractive index
1.57[2]20 °C.
Transmittance
88.5 (85–92) %[2]
Haze
not yet available
Gloss
not yet available
Water absorption
0.3 (0.25–0.35) %[2]Equilibrium, immersed in water at 23 °C.
Dielectric constant
2.85 (2.7–3)[2]100 Hz to 1 MHz.
Dielectric strength
not yet available
Electrical conductivity
[2]Upper bound; reciprocal of reported volume resistivity (>1×10¹³ Ω·m).

Glass transition (Tg)
107.5 (103–112) °C[2]Experimental range; giving SAN boiling-water resistance that plain polystyrene lacks.
Melting temperature (Tm)
Not applicableAmorphous; no true melting point.
Crystallization (Tc)
Not applicable
Heat deflection (HDT)
95 (86–104) °C[2]1.8 MPa.
Decomposition onset
260 °C[2]Reported as 'decomposition temperature' (onset not separately specified).
Thermal conductivity
not yet available

Tensile modulus
3750 (3600–3900) MPa[2]
Yield strength
Not applicableRigid, brittle copolymer with no distinct yield region reported (low elongation at break, 2.5–4%); see tensile_strength_at_break.
Tensile strength at break
70 (61–79) MPa[2]Source reports unqualified 'tensile strength'.
Elongation at break
3.25 (2.5–4) %[2]
Impact strength (Izod)
25.35 (24–26.7) J/m[3]ASTM D256Two named commercial grades (Lustran-35, Tyril-880).
Impact strength (Charpy)
2 (1.5–2.5) kJ/m²[2]Notched, 23 °C.
Hardness
not yet available
Flexural modulus
not yet available
Poisson's ratio
0.366[2]
Coefficient of friction
not yet available

Solvent: acids
good[2]
Solvent: alcohols
good[2]
Solvent: alkalis
very good[2]
Solvent: aliphatic hydrocarbons
good[2]
Solvent: aromatic hydrocarbons
poor[2]
Solvent: esters
poor[2]
Solvent: greases & oils
poor[2]
Solvent: halogenated hydrocarbons
poor[2]
Solvent: ketones
poor[2]
Weathering / UV
not yet available
Hydrolysis resistance
Resistant to boiling water (unlike plain polystyrene)[1]
Flammability (UL94)
HB[2]1.6/0.8 mm specimen thickness.
Limiting oxygen index
18 %[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
240 (220–260) °C[2]Injection molding; extrusion runs 220–240 °C.
Shrinkage rate
0.5 (0.3–0.7) %[2]

  • Food & consumerfood containers · water bottles · kitchenware · cosmetic jars
  • Electronicscomputer product housings · battery cases
  • Opticalplastic optical fibers

Recyclable
Yes
Biodegradable
No
Degradation pathway
not yet available

LD50 (oral, rat)
1800 mg/kg[2]
NFPA health
0[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]

Skin (rabbit) LD50: 2,000 mg/kg. Aquatic toxicity (48 h LC50): Daphnia magna 13 mg/L, bluegill sunfish 28 mg/L, fathead minnow 10 mg/L.

  1. [1]Styrene-acrylonitrile resinWikipediaAccessed 2026-07-14https://en.wikipedia.org/wiki/Styrene-acrylonitrile_resin[wiki-san-resin]
  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 IPearl Harbor, 7 December 1941. Within ten weeks, Japan's advance through Southeast Asia would cut off nearly all of America's natural rubber.U.S. Navy · Public domainWikimedia Commons
  2. Plate IIOld tires collected for a wartime scrap rubber drive: the shortage reached rural roads as well as city streets.Unknown author · Public domainWikimedia Commons
  3. Plate IIISynthetic rubber coming off the rolling mill at B.F. Goodrich's Akron plant in 1941, part of the wartime buildup that made acrylonitrile a bulk American chemical for the first time.Alfred T. Palmer · Public domainWikimedia Commons
  4. Plate IVA 1942 War Production Board poster spelling out, item by item, just how much of the war effort ran on rubber. That shortage pushed acrylonitrile into bulk American production in the first place.Boston Public Library · CC BY 2.0Wikimedia Commons