Polymer intermediates
Used in unsaturated polyester and alkyd-related chemistry. [3]
CHEMICAL PROFILE CAS 110-17-8
Properties, Uses, pKa, Safety,
Comparisons & Suppliers
Fumaric acid is a four-carbon diacid with a trans carbon–carbon double bond. That unsaturation distinguishes it from succinic acid and from its cis isomer, maleic acid. [1]
Identity focus: Solid. Aqueous pKa values depend on conditions; product assay is a separate measurement.
THE ESSENTIALS
The molecule has two carboxyl groups and a double bond in the middle. “Trans” means the carboxyl groups lie on opposite sides of that double bond.
Fumaric acid is a four-carbon diacid with a trans carbon–carbon double bond. That unsaturation distinguishes it from succinic acid and from its cis isomer, maleic acid. [1] [3]
Safety at a glance — The listed Sigma fumaric-acid product 800269 (US listing) is classified as causing serious eye irritation (H319). This is not a serious-eye-damage classification; confirm the classification of the exact product being handled. [4]
A condensed structural formula keeps the functional groups visible. [1]
Used in unsaturated polyester and alkyd-related chemistry. [3]
Fumarate participates in cellular metabolism. [12]
The supplier section separates package size, assay, grade, and market context for three named products. [4] [5] [6]
GO A LITTLE DEEPER
The molecule has two carboxyl groups and a double bond in the middle. “Trans” means the carboxyl groups lie on opposite sides of that double bond. [1]
The E configuration is part of fumaric acid’s identity. Maleic acid has the cis arrangement and is a separate substance. Fumarate salts also differ from the free acid sold here. [1] [4] [5] [6]
The compiled pKa values are 3.03 and 4.54 at 25 °C. A different reference gives 3.03 and 4.44 at 18 °C. The source and temperature differences are retained; temperature alone has not been established as the cause of the difference. [1] [2] [4] [5] [6]
Acid–base reference values describe equilibria under specified conditions. They are not a substitute for a validated formulation or an assay on the purchased lot.
MAKE THE CONNECTION
Similar names and functional groups do not mean interchangeable chemicals.
SIDE-BY-SIDE COMPARISON
Fixed comparison for this prototype. Acid selectors are disabled; additional comparisons are coming later.
| Property | Fumaric Acid | Succinic Acid |
|---|---|---|
| Molecular formula | C₄H₄O₄ [1] | C₄H₆O₄ [7] |
| Molecular weight | 116.07 g/mol [1] | 118.09 g/mol [7] |
| Carbon atoms | 4 [1] | 4 [7] |
| Carboxyl groups | 2 [1] | 2 [7] |
| Structure | HOOC–CH=CH–COOH · E (trans) [1] | HOOC–CH₂–CH₂–COOH [7] |
| Chemical family | Unsaturated dicarboxylic acid [1] | Dicarboxylic acid [7] |
| Identity focus | Solid [1] | Solid [7] |
| pKa context | 3.03 / 4.54 (25 °C) [2] | 4.207 / 5.635 (25 °C) [11] |
Choose fumaric acid when the procedure requires the trans unsaturated diacid. Choose succinic acid for the saturated four-carbon framework. For biological work, distinguish fumarate and succinate salts from the free acids. [1] [3] [7]
Match HOOC–CH=CH–COOH · E (trans) and the method’s required chemical form.
Match HOOC–CH₂–CH₂–COOH; verify the identity before substituting a related acid.
Before choosing: match the reaction or formulation, then verify the exact form, grade, assay basis, and impurities. These contexts do not establish suitability for an industrial or regulated application.
FROM STRUCTURE TO APPLICATION
Used in unsaturated polyester and alkyd-related chemistry. The resulting resin is a derivative with its own specification. [3]
Fumaric acid is used in food formulation contexts. Solubility, process conditions, and the applicable grade must be validated. For the US uses covered by 21 CFR 172.350, fumaric acid must contain at least 99.5% by weight on an anhydrous basis and meet the other applicable requirements. The laboratory products shown are not demonstrated to meet that requirement solely from their displayed minimum assays; this does not establish that a particular lot fails. [3] [14]
Fumarate participates in cellular metabolism. That biological role does not establish a particular experimental use for purchased free fumaric acid; free acid and salts must be distinguished. [12]
SOURCE WITH CONTEXT
Compare specific products and package options. Listings are not ranked recommendations.
Package sizes stay grouped under the supplier product. Assay methods, product forms, and regional markets remain visible. Confirm fumaric E/trans identity rather than maleic cis form or a fumarate salt.
Scroll horizontally if needed. Supplier and package identity stay visible.
| Supplier | Product / Grade | Purity / Assay | Package Size | Public Price | Normalized Price | Documentation | Last Checked | Action |
|---|---|---|---|---|---|---|---|---|
| Sigma-AldrichFumaric Acid | For synthesis8002690100 | ≥99.0% (acidimetric) | 100 g | $48.80USD · US public price | Not comparedGrades, assay bases, or forms differ | Document notes: Sigma-Aldrich
| View Product: Sigma-Aldrich, 8002690100 (opens new tab) | |
| For synthesis8002691000 | ≥99.0% (acidimetric) | 1 kg | $69.90USD · US public price | Not comparedGrades, assay bases, or forms differ | View Product: Sigma-Aldrich, 8002691000 (opens new tab) | |||
| For synthesis8002699050 | ≥99.0% (acidimetric) | 50 kg | $923.00USD · US public price | Not comparedGrades, assay bases, or forms differ | View Product: Sigma-Aldrich, 8002699050 (opens new tab) | |||
| TCIFumaric Acid | Check supplierF0067Catalog headline >99.0% (GC)(T); separate specification minima are shown. | ≥99.0% — GC specification ≥99.0% — neutralization titration specification | 25 g | $20.00USD · US public price | Not comparedGrades, assay bases, or forms differ | Document notes: TCI
| View Product: TCI, F0067 (opens new tab) | |
| Check supplierF0067Catalog headline >99.0% (GC)(T); separate specification minima are shown. | ≥99.0% — GC specification ≥99.0% — neutralization titration specification | 500 g | $25.00USD · US public price | Not comparedGrades, assay bases, or forms differ | View Product: TCI, F0067 (opens new tab) | |||
| FUJIFILM WakoFumaric Acid | Wako Special Grade069-00652 | ≥98.0% (titration) | 25 g | $21.00USD · US list price | Not comparedGrades, assay bases, or forms differ | Document notes: FUJIFILM Wako
| View Product: FUJIFILM Wako, 069-00652 (opens new tab) | |
| Wako Special Grade063-00655 | ≥98.0% (titration) | 500 g | $25.00USD · US list price | Not comparedGrades, assay bases, or forms differ | View Product: FUJIFILM Wako, 063-00655 (opens new tab) |
Fumaric Acid
For synthesis
Last checked:
Fumaric Acid
Check supplier
Catalog headline >99.0% (GC)(T); separate specification minima are shown.
Last checked:
Fumaric Acid
Wako Special Grade
Last checked:
COA = Certificate of Analysis · SDS = Safety Data Sheet · COO = Certificate of Origin.
Lookup means a retrieval option was visible, not that a lot certificate was reviewed. Check supplier means availability or the applicable document was not verified.
Prices may vary by quantity, account, contract, geography, and availability. These products have different grades, assay bases, or forms; no normalized comparison is shown. Foreign-market prices are reference listings only. No currency conversion, mass-to-volume conversion, or ranking is applied. Confirm equivalent specifications and a current quote before comparison. [4] [5] [6]
Compiled pKa references and supplier solubility entries are not fully comparable. Use stated conditions and confirm a suitable experimental reference for quantitative work. A 50 kg package is listed, but current availability and bulk terms are unverified.
Only the displayed identity, specification, packages, public prices and stated documentation evidence were reviewed. Current stock, lead times, shipping eligibility, contract pricing, lot certificates, and regulatory suitability are unverified.
There are no paid placements. Future paid listings will show “Sponsored” in both views; payment will not determine chemistry interpretation or imply a ranking.
PLAN A LARGER ORDER
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A BUYER’S CHECKLIST
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FOR YOUR REFERENCE
Identity, product reference properties, and handling context.
Connectivity SMILES describes connectivity; it is not an independent stereochemical assignment. CAS and product-form distinctions are supported by the supplier listings. [1] [4] [5] [6]
Thermal behavior is reported around 287 °C with decomposition; the observed range depends on measurement method (PubChem compiled references). TCI reports water solubility 6.3 g/L at 25 °C. Sigma lists 4.9 g/L with incompletely specified conditions. The discrepancy is unresolved; temperature alone has not been shown to explain it. [13] [5] [4]
Hydrate, concentration, stereoisomer, and temperature can change the relevant specification. Product reference data are not a reviewed lot certificate.
Reference pKa: 3.03 / 4.54 (25 °C). [2]
Compiled pKa references and supplier solubility entries are not fully comparable. Use stated conditions and confirm a suitable experimental reference for quantitative work. A 50 kg package is listed, but current availability and bulk terms are unverified.
Temperature, ionic strength, and the use of activities versus concentrations matter in quantitative work. These reference values are not buffer recipes.
The listed Sigma fumaric-acid product 800269 (US listing) is classified as causing serious eye irritation (H319). This is not a serious-eye-damage classification; confirm the classification of the exact product being handled. [4]
Hazard classifications can vary by concentration, formulation, supplier and jurisdiction. Review the SDS for the exact product before handling. This summary does not replace the SDS.
Supplier safety information and SDS retrieval (opens new tab)
A product-page safety classification is not verification of every regional SDS. Confirm product code, chemical form and current local document.
Review supplier documentationCOMMON QUESTIONS
The molecule has two carboxyl groups and a double bond in the middle. “Trans” means the carboxyl groups lie on opposite sides of that double bond. [1]
Succinic acid has a saturated CH₂–CH₂ segment; fumaric acid has a trans CH=CH segment. The double bond introduces reaction and polymer possibilities absent from the saturated structure. [7]
Confirm fumaric E/trans identity rather than maleic cis form or a fumarate salt. [4]
No. The table retains differing grades, assay bases, forms, and markets. No normalized ranking or currency conversion is applied. [5]
Compiled pKa references and supplier solubility entries are not fully comparable. Use stated conditions and confirm a suitable experimental reference for quantitative work. A 50 kg package is listed, but current availability and bulk terms are unverified.
The RFQ is a prototype that prepares an on-screen brief. Nothing is sent to suppliers. Confirm actual bulk terms directly with the supplier.
TRACE THE INFORMATION
Identity and compiled reference values are separated from supplier-specific specifications. Structural comparisons and buyer guidance are editorial interpretation. Sources were checked October 3, 2026; supplier information can change.
Official PUG REST identity record: formula, molecular weight, IUPAC name, and connectivity SMILES.
Fumaric Acid compiled dissociation values; stated temperature and medium are retained. Unspecified conditions are not inferred.
Compiled application references; uses of derivatives are distinguished from direct use of the acid.
Direct product listing checked October 3, 2026. Product-specific grade, assay, package, public price and documentation retrieval evidence. Product-page safety information applies to the identified product and regional listing, not every grade or jurisdiction.
Direct product listing checked October 3, 2026. Product-specific grade, assay, package, public price and documentation retrieval evidence. Product-page safety information applies to the identified product and regional listing, not every grade or jurisdiction.
Direct product listing checked October 3, 2026. Product-specific grade, assay, package, public price and documentation retrieval evidence. Product-page safety information applies to the identified product and regional listing, not every grade or jurisdiction.
Primary comparison identity. Explanations of structural differences are editorial interpretation of verified identities.
Related chemical identity; relevance is based on structure or the stated application relationship.
Related chemical identity; relevance is based on structure or the stated application relationship.
Related chemical identity; relevance is based on structure or the stated application relationship.
The primary comparison’s pKa source; reference conditions are preserved.
Succinate and fumarate in the citric acid cycle; salts/ions are distinguished from purchased free acids.
Compiled thermal observations include decomposition and measurement-dependent ranges, rather than a clean equilibrium melting point.
US food-use conditions include at least 99.5% fumaric acid by weight on an anhydrous basis; a laboratory listing alone does not establish compliance.
Compiled pKa references and supplier solubility entries are not fully comparable. Use stated conditions and confirm a suitable experimental reference for quantitative work. A 50 kg package is listed, but current availability and bulk terms are unverified.
This informational prototype is not a supplier, quotation service, or endorsement of a product’s fitness for an application. Buyers should verify the applicable specification, certification, and regulatory requirements for their intended use.