Acidulant formulations
Citric acid is used to adjust acidity in food, beverage, and pharmaceutical formulation contexts. [3]
CHEMICAL PROFILE CAS 77-92-9
Properties, Uses, pKa, Safety,
Comparisons & Suppliers
Citric acid has three carboxyl groups and one hydroxyl group. Its acid–base and metal-complexing chemistry underlies uses ranging from formulation acidification to laboratory reagents. [1]
Identity focus: Solid · anhydrous identity. Aqueous pKa values depend on conditions; product assay is a separate measurement.
THE ESSENTIALS
This molecule has three acidic –COOH groups around a small carbon framework. It can lose those three acidic protons in separate steps.
Citric acid has three carboxyl groups and one hydroxyl group. Its acid–base and metal-complexing chemistry underlies uses ranging from formulation acidification to laboratory reagents. [1] [3]
Safety at a glance — The listed anhydrous Sigma product 818707 (US listing) is classified for serious eye irritation and possible respiratory irritation (H319/H335). This classification is product-specific; it is not an eye-damage classification or a universal classification for all citric-acid products. [4]
A condensed structural formula keeps the functional groups visible. [1]
Citric acid is used to adjust acidity in food, beverage, and pharmaceutical formulation contexts. [3]
Citrate chemistry is used in sequestration and formulation work. [3]
Citric acid is a precursor to citrate esters, including plasticizer applications. [3]
The supplier section separates package size, assay, grade, and market context for three named products. [4] [5] [6]
GO A LITTLE DEEPER
This molecule has three acidic –COOH groups around a small carbon framework. It can lose those three acidic protons in separate steps. [1]
The hydroxyl group is an additional –OH, distinct from the hydroxyls inside the carboxyl groups. Commercial citric acid can be anhydrous or a monohydrate; the monohydrate includes water in the crystal and has a different formula weight. [1] [4] [5] [6]
The page identity is anhydrous citric acid. Citric acid monohydrate is CAS 5949-29-1, C₆H₈O₇·H₂O, 210.14 g/mol. Citrate salts are separate products. A mass-based recipe must account for the chosen chemical form. [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 | Citric Acid | Malic Acid |
|---|---|---|
| Molecular formula | C₆H₈O₇ [1] | C₄H₆O₅ [7] |
| Molecular weight | 192.12 g/mol [1] | 134.09 g/mol [7] |
| Carbon atoms | 6 [1] | 4 [7] |
| Carboxyl groups | 3 [1] | 2 [7] |
| Structure | HOOC–CH₂–C(OH)(COOH)–CH₂–COOH [1] | HOOC–CH₂–CH(OH)–COOH [7] |
| Chemical family | Hydroxytricarboxylic acid [1] | Hydroxydicarboxylic acid [7] |
| Identity focus | Solid · anhydrous identity [1] | Solid · DL identity [7] |
| pKa context | 3.128 / 4.761 / 6.396 (25 °C, water, zero ionic strength) [2] | 3.51 / 5.03 (20 °C; OECD 112) [11] |
For a citrate-based buffer or a procedure specifying citrate complexation, use the prescribed citrate form. For a malate-based process, use the specified malic stereoisomer and grade. In formulation work, validate the actual performance rather than substitute by equal mass. [1] [3] [7]
Match HOOC–CH₂–C(OH)(COOH)–CH₂–COOH and the method’s required chemical form.
Match HOOC–CH₂–CH(OH)–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
Citric acid is used to adjust acidity in food, beverage, and pharmaceutical formulation contexts. The listed laboratory products do not establish suitability for those regulated uses. [3]
Citrate chemistry is used in sequestration and formulation work. Metal binding depends on pH, metal identity, and the citrate form. [3]
Citric acid is a precursor to citrate esters, including plasticizer applications. Ester properties must not be attributed to the free acid. [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 anhydrous or monohydrate, assay basis, and the required application specification.
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-AldrichCitric Acid | For synthesis · anhydrous8187071000 | ≥99% (alkalimetric) | 1 kg | $90.90USD · US public price | Not comparedGrades, assay bases, or forms differ | Document notes: Sigma-Aldrich
| View Product: Sigma-Aldrich, 8187071000 (opens new tab) | |
| For synthesis · anhydrous8187075000 | ≥99% (alkalimetric) | 5 kg | $342.00USD · US public price | Not comparedGrades, assay bases, or forms differ | View Product: Sigma-Aldrich, 8187075000 (opens new tab) | |||
| TCICitric Acid | Check supplierC1949Anhydrous · CAS 77-92-9 | >98.0% (neutralization titration) | 500 g | $34.00USD · US public price | Not comparedGrades, assay bases, or forms differ | Document notes: TCI
| View Product: TCI, C1949 (opens new tab) | |
| FUJIFILM WakoCitric Acid | Guaranteed Reagent · monohydrate031-03492CAS 5949-29-1 · C₆H₈O₇·H₂O · 210.14 g/mol | ≥99.5% (mass/mass, titration) | 25 g | ¥1,500JPY · Japan suggested price (tax excluded) | Not comparedDifferent currency / market | COA lookup on product page (opens new tab)SDS PDF · Japan/JIS English (opens new tab)COOCheck supplier Document notes: FUJIFILM Wako
| View Product: FUJIFILM Wako, 031-03492 (opens new tab) | |
| Guaranteed Reagent · monohydrate035-03495CAS 5949-29-1 · C₆H₈O₇·H₂O · 210.14 g/mol | ≥99.5% (mass/mass, titration) | 500 g | ¥2,500JPY · Japan suggested price (tax excluded) | Not comparedDifferent currency / market | View Product: FUJIFILM Wako, 035-03495 (opens new tab) | |||
| Guaranteed Reagent · monohydrate031-03497CAS 5949-29-1 · C₆H₈O₇·H₂O · 210.14 g/mol | ≥99.5% (mass/mass, titration) | 20 kg | Price on request | Not comparedDifferent currency / market | View Product: FUJIFILM Wako, 031-03497 (opens new tab) |
Citric Acid
For synthesis · anhydrous
Last checked:
Citric Acid
Check supplier
Anhydrous · CAS 77-92-9
Last checked:
Citric Acid
Guaranteed Reagent · monohydrate
CAS 5949-29-1 · C₆H₈O₇·H₂O · 210.14 g/mol
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]
Use the condition-defined NIST pKa values for this reference. Quantitative supplier solubility entries remain insufficiently characterized for solution design; confirm the measurement basis and conditions for the selected form.
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.
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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]
Citric acid is very soluble in water, but supplier quantitative values use differing or incompletely specified measurement bases and conditions. No recommended saturation concentration is derived from them. [4] [5]
Hydrate, concentration, stereoisomer, and temperature can change the relevant specification. Product reference data are not a reviewed lot certificate.
Reference pKa: 3.128 / 4.761 / 6.396 (25 °C, water, zero ionic strength). [2]
Use the condition-defined NIST pKa values for this reference. Quantitative supplier solubility entries remain insufficiently characterized for solution design; confirm the measurement basis and conditions for the selected form.
Temperature, ionic strength, and the use of activities versus concentrations matter in quantitative work. These reference values are not buffer recipes.
The listed anhydrous Sigma product 818707 (US listing) is classified for serious eye irritation and possible respiratory irritation (H319/H335). This classification is product-specific; it is not an eye-damage classification or a universal classification for all citric-acid products. [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) · FUJIFILM Wako SDS PDF · Japan/JIS English (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
This molecule has three acidic –COOH groups around a small carbon framework. It can lose those three acidic protons in separate steps. [1]
Citric acid has three carboxyl groups; malic acid has two and a different carbon skeleton. Their shared use as acidulants does not make their buffering, complexing, or sensory behavior identical. [7]
Specify anhydrous or monohydrate, assay basis, and the required application specification. [4]
No. The table retains differing grades, assay bases, forms, and markets. No normalized ranking or currency conversion is applied. [5]
Use the condition-defined NIST pKa values for this reference. Quantitative supplier solubility entries remain insufficiently characterized for solution design; confirm the measurement basis and conditions for the selected form.
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.
Goldberg, Kishore and Lennen (2002), table 7.22: evaluated aqueous pKa at 25 °C and zero ionic strength.
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.
Use the condition-defined NIST pKa values for this reference. Quantitative supplier solubility entries remain insufficiently characterized for solution design; confirm the measurement basis and conditions for the selected form.
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.