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Electronic G2Electronic G3Electronic G4Electronic G5Superior ReagentHigh-Purity & Specialty Solvents

Ethyl Acetate

CH₃COOC₂H₅ · CAS 141-78-6

Ethyl Acetate considered for pharmaceutical extraction, coatings, process work-up. Selection begins with the application, critical limits, destination, pack and qualification plan.

A common starting point

pharmaceutical extraction

Molecular weight

88.11 g/mol

Boiling point

77.1 °C

Density

0.902 g/mL

High-purity optionsBatch documentationFlexible packaging review
Ethyl Acetate manufacturing, filling and industrial supply environment

Product identity

CAS number
141-78-6
Formula
CH₃COOC₂H₅
Boiling point
77.1 °C
Density
0.902 g/mL

Product overview

A product route built around the application

Ethyl Acetate is considered for processes that need a consistent material, controlled critical impurities and a supply format that can move from qualification to routine use. The grade should be selected against the actual process—not a generic purity claim.

01

High-purity options

Compare listed grades and current product-specific limits.

02

Controlled attributes

Focus testing on the impurities and performance risks that matter.

03

Supply planning

Align sample, production pack, forecast and document route early.

Purification and controlled manufacturing route for Ethyl Acetate

Application fit

Qualify Ethyl Acetate around the process

The product name begins the discussion. Critical attributes, test methods, packaging and routine supply conditions determine whether a candidate is useful.

01

pharmaceutical extraction

Review the current specification and representative sample against the actual process and qualified baseline.

02

coatings

Review the current specification and representative sample against the actual process and qualified baseline.

03

process work-up

Review the current specification and representative sample against the actual process and qualified baseline.

Before you specify

A better enquiry starts with four answers

A higher grade is not automatically the better choice. The useful option fits the process, analytical method, packaging route and qualification plan without adding controls the application does not need.

01

What role does the material perform in the process?

02

Which limits and methods control customer acceptance?

03

What sample and production pack represent routine use?

04

Which destination, documents, annual demand and timing apply?

Specification data

Compare the listed grade columns

This table is an indicative product overview for initial screening. Confirm the current controlled specification, test methods, reporting limits and available lot documentation before qualification or purchase.

ParameterTest methodUnitG4HPLCAR
Assay (GC)GC-FID%≥99.99≥99.8≥99.5
Water Content (KF)Karl Fischerppm≤20≤50≤500
Acidity (as HAc)Titrationppm≤2≤5≤5
EthanolGC-FIDppm≤50≤200≤500
Residue on EvaporationGravimetricppm≤2≤2≤5

Website values do not replace a signed sales specification. The agreed specification and lot-specific Certificate of Analysis govern supplied material.

Electronic grade context

Use the grade scale as a first comparison

SEMI C1 describes liquid-chemical grades and analytical procedures. A grade name helps organise a discussion; your process specification still decides which limits and methods are acceptable.

Electronic Grade Purity Comparison — SEMI C1 StandardG1 → G5
GradePurity (GC)Metals (ICP)ParticlesWater (KF)Process Node
G2
≥99.9%
≤10 ppb≤100/mL≤50 ppm≥180nm Mature Node
G3
≥99.99%
≤2 ppb≤20/mL≤20 ppm45–180nm
G4
≥99.999%
≤0.5 ppb≤10/mL≤10 ppm7–45nm
G5
≥99.9999%
<0.1 ppb≤5/mL≤5 ppm<7nm / EUV / Marangoni

All grades tested by ICP-MS (28 elements), in-line LPC (ISO Class 3 fill), and Karl Fischer titration. G5 = SEMI C1 Tier D. Full CoA per lot.  Request CoA template →

Where this product is used

Application routes for Ethyl Acetate

These examples help with discovery. They are not claims of universal suitability; material compatibility, process performance and the controlled specification still need review.

Ethyl Acetate industrial and analytical application environment

Semiconductor & electronics

  • Photoresist formulation co-solvent
  • organic dielectric coating process
  • thin-film display buffer layer solvent

Laboratory & analytical

  • TLC & column chromatography (normal phase)
  • pharmaceutical API extraction
  • Fmoc peptide coupling solvent
  • flash chromatography

Industrial & other

  • Artificial fruit flavoring
  • nail polish formulation
  • printing inks
  • adhesives & sealants

Representative application cases

A practical evidence route for Ethyl Acetate

These are illustrative composite qualification scenarios, not named customer claims. Exact methods, limits and acceptance decisions belong to the customer’s controlled process.

CASE 01

European process qualification

A contamination-sensitive production team compares Ethyl Acetate (EtOAc) with its incumbent material using the agreed water, metals, organic-impurity, residue and particle controls.

Evidence route

Supplier CoA and specification data are evaluated alongside a representative process trial and incoming-control plan.

CASE 02

North American second-source review

A site qualifies Ethyl Acetate (EtOAc) for supply resilience without changing its approved process or dispensing route.

Evidence route

The review connects sample identity, production-pack compatibility, analytical comparison and documented change communication.

Purification, filtration, testing and clean filling for Ethyl Acetate

Manufacturing advantage

A controlled route from purification to final filling

The supply route for Ethyl Acetate connects incoming-material review, product-specific treatment, controlled transfer, testing, filling and lot documentation. Exact equipment and controls depend on the qualified product and grade.

01

Purification

Product-specific separation or treatment route.

02

Filtration

Compatible filtration and controlled transfer.

03

Testing

Release against the agreed specification.

04

Clean filling

Pack, closure and lot identification review.

Explore manufacturing →

Quality assurance & documentation

Evidence your quality team can review

Documents are matched to the supplied product, grade, lot and destination. The links below request the current controlled version; they are not static files with uncertain revision status.

Quality testing and controlled documentation for Ethyl Acetate

Packaging options

Choose the pack with the handling route in mind

Availability varies by grade and destination. Confirm container material, closure, headspace, connection, minimum order, dangerous-goods route and qualification-lot needs.

01

Qualification & laboratory packs

For evaluation, method work and lower-volume routine use.

500 mL2.5 L5 L25 L
02

Drums & production packs

For regular production consumption and controlled dispensing.

25 L200 L
03

IBC & bulk routes

For higher-volume programmes after site, grade and logistics review.

Confirm by grade

Technical resources

Continue the technical review

Use application notes for context, then confirm current product documents before qualification.

Knowledge centre →

Start a product review

Need a reliable supply route for Ethyl Acetate?

Send the application, current specification, critical limits, pack, destination and forecast so the response can be technically useful.