Food acidulant chemistry
Malic acid is used in acidulant and flavor formulation contexts. [3]
CHEMICAL PROFILE CAS 6915-15-7
Properties, Uses, pKa, Safety,
Comparisons & Suppliers
Malic acid combines two carboxyl groups with one hydroxyl on a four-carbon chain. The molecule is chiral, so the general name needs a DL, L, or D specification when buying. [1]
Identity focus: Solid · DL identity. Aqueous pKa values depend on conditions; product assay is a separate measurement.
THE ESSENTIALS
Two –COOH groups give two acid–base steps. The separate hydroxyl adds another functional group and a chiral center.
Malic acid combines two carboxyl groups with one hydroxyl on a four-carbon chain. The molecule is chiral, so the general name needs a DL, L, or D specification when buying. [1] [3]
Condensed connectivity schematic; see the specified stereochemical identity below. [1]
Malic acid is used in acidulant and flavor formulation contexts. [3]
Its acidity and complexing chemistry are used in specified formulations. [3]
A hydroxyl-bearing diacid starting material for specified ester and polymer chemistry.. [3]
The supplier section separates package size, assay, grade, and market context for three named products. [4]
GO A LITTLE DEEPER
Two –COOH groups give two acid–base steps. The separate hydroxyl adds another functional group and a chiral center. [1]
The L form encountered in biochemical discussion and the DL products in this table should not be treated as the same stereochemical supply. This page’s principal identity and supplier set describe DL-malic acid. [1] [4] [5] [6]
DL-malic acid uses CAS 6915-15-7. L-malic acid is CAS 97-67-6. A ≥99% chemical assay is not a claim of ≥99% enantiomeric purity. The pKa values shown retain the compiled OECD 112 test conditions. [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 | Malic Acid | Citric Acid |
|---|---|---|
| Molecular formula | C₄H₆O₅ [1] | C₆H₈O₇ [7] |
| Molecular weight | 134.09 g/mol [1] | 192.12 g/mol [7] |
| Carbon atoms | 4 [1] | 6 [7] |
| Carboxyl groups | 2 [1] | 3 [7] |
| Structure | HOOC–CH₂–CH(OH)–COOH [1] | HOOC–CH₂–C(OH)(COOH)–CH₂–COOH [7] |
| Chemical family | Hydroxydicarboxylic acid [1] | Hydroxytricarboxylic acid [7] |
| Identity focus | Solid · DL identity [1] | Solid · anhydrous identity [7] |
| pKa context | 3.51 / 5.03 (20 °C; OECD 112) [2] | 3.13 / 4.76 / 6.4 (supplier reference) [11] |
Use the specified malic stereoisomer in a malate-based procedure. Use citrate in a citrate-based formulation. Food or polymer development requires matching the application specification, not merely choosing the cheaper acid. [1] [3] [7]
Match HOOC–CH₂–CH(OH)–COOH and the method’s required chemical form.
Match HOOC–CH₂–C(OH)(COOH)–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
Malic acid is used in acidulant and flavor formulation contexts. Verify stereochemistry and the required food-use specification separately from reagent assay. [3]
Its acidity and complexing chemistry are used in specified formulations. Performance depends on chemical form and conditions. [3]
A hydroxyl-bearing diacid starting material for specified ester and polymer chemistry. [3]
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. Specify DL, L, or D form and require stereochemical evidence when relevant.
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-AldrichMalic Acid | Check supplier · DL formM0875-100G | ≥98% (capillary GC) | 100 g | $53.40USD · US public price | Not comparedGrades, assay bases, or forms differ | COA lookup on product page (opens new tab)SDSCheck supplierCOO lookup on product page (opens new tab) Document notes: Sigma-Aldrich
| View Product: Sigma-Aldrich, M0875-100G (opens new tab) | |
| Check supplier · DL formM0875-500G | ≥98% (capillary GC) | 500 g | $68.10USD · US public price | Not comparedGrades, assay bases, or forms differ | View Product: Sigma-Aldrich, M0875-500G (opens new tab) | |||
| TCIMalic Acid | Check supplierM0020DL form · CAS 6915-15-7 | >99.0% (titration) | 25 g | $25.00USD · US public price | Not comparedGrades, assay bases, or forms differ | Document notes: TCI
| View Product: TCI, M0020 (opens new tab) | |
| Check supplierM0020DL form · CAS 6915-15-7 | >99.0% (titration) | 500 g | $32.00USD · US public price | Not comparedGrades, assay bases, or forms differ | View Product: TCI, M0020 (opens new tab) | |||
| FUJIFILM WakoMalic Acid | Wako Special Grade · DL form135-00562 | ≥99.0% (titration) | 25 g | $18.00USD · US list price | Not comparedGrades, assay bases, or forms differ | Document notes: FUJIFILM Wako
| View Product: FUJIFILM Wako, 135-00562 (opens new tab) | |
| Wako Special Grade · DL form139-00565 | ≥99.0% (titration) | 500 g | $24.00USD · US list price | Not comparedGrades, assay bases, or forms differ | View Product: FUJIFILM Wako, 139-00565 (opens new tab) |
Malic Acid
Check supplier · DL form
Last checked:
Malic Acid
Check supplier
DL form · CAS 6915-15-7
Last checked:
Malic Acid
Wako Special Grade · DL form
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]
General “malic acid” naming can conceal stereochemistry. Do not compare a dissolution test with a saturation-solubility value.
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
Turn your requirements into a clear supplier brief.
A BUYER’S CHECKLIST
Selections remain only while this page is open.
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]
TCI reports a solid melting at 130 °C and water solubility 558 g/L at 20 °C. Sigma’s 50 mg/mL entry is a dissolution test, not a maximum-solubility measurement. [4] [5] [6]
Hydrate, concentration, stereoisomer, and temperature can change the relevant specification. Product reference data are not a reviewed lot certificate.
Reference pKa: 3.51 / 5.03 (20 °C; OECD 112). [2]
General “malic acid” naming can conceal stereochemistry. Do not compare a dissolution test with a saturation-solubility value.
Temperature, ionic strength, and the use of activities versus concentrations matter in quantitative work. These reference values are not buffer recipes.
Match chemical form, concentration, region, and product code. Use its handling, storage, incompatibility, first-aid and disposal guidance alongside the workplace risk assessment.
A current regional SDS remains to be verified; the supplier documentation field says Check supplier. This profile is not a substitute for that document.
Review supplier documentationCOMMON QUESTIONS
Two –COOH groups give two acid–base steps. The separate hydroxyl adds another functional group and a chiral center. [1]
Citric acid adds a third carboxyl group and has a different six-carbon framework. Malic acid has a stereocenter; its product form matters even when both acids are considered as acidulants. [7]
Specify DL, L, or D form and require stereochemical evidence when relevant. [4]
No. The table retains differing grades, assay bases, forms, and markets. No normalized ranking or currency conversion is applied. [5]
General “malic acid” naming can conceal stereochemistry. Do not compare a dissolution test with a saturation-solubility value. [6]
The RFQ is a prototype that prepares an on-screen brief. Nothing is sent to suppliers. Confirm actual bulk terms directly with the supplier. [4]
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.
Compiled reference entries; their methods and conditions matter. Citric acid’s displayed stepwise values are from the linked Sigma specification.
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.
Direct product listing checked October 3, 2026. Product-specific grade, assay, package, public price and documentation retrieval evidence.
Direct product listing checked October 3, 2026. Product-specific grade, assay, package, public price and documentation retrieval evidence.
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.
General “malic acid” naming can conceal stereochemistry. Do not compare a dissolution test with a saturation-solubility value.
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.