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CHEMICAL PROFILE CAS 87-69-4

Tartaric Acid

Properties, Uses, pKa, Safety,
Comparisons & Suppliers

Tartaric acid has two carboxyl groups and two hydroxyl-bearing carbons. Its stereochemistry makes L, D, DL, and meso forms an essential distinction; this page focuses on L-(+)-tartaric acid. [1]

At a glance

Quick reference
Molecular formula
C₄H₆O₆ [1]
CAS number
87-69-4 [4]
Molecular weight
150.09 g/mol [1]
IUPAC name
(2R,3R)-2,3-dihydroxybutanedioic acid [1]
Chemical family
Dihydroxydicarboxylic acid [1]
Carbon atoms
4 [1]
Carboxyl groups
2 [1]
pKa reference
3.036 / 4.366 (25 °C, water, zero ionic strength; L-(+) form) [2]

Identity focus: Solid · L-(+) identity. Aqueous pKa values depend on conditions; product assay is a separate measurement.

01

THE ESSENTIALS

Tartaric Acid in 30 Seconds

There are two acidic ends and two hydroxyl groups in the middle. The same connectivity can describe different three-dimensional forms.

Tartaric acid has two carboxyl groups and two hydroxyl-bearing carbons. Its stereochemistry makes L, D, DL, and meso forms an essential distinction; this page focuses on L-(+)-tartaric acid. [1] [3]

Safety at a glance — The listed Sigma L-(+)-tartaric acid product 251380 (US listing) is classified as causing serious eye damage (H318). Supplier classifications differ; this must not be generalized to every tartaric-acid product. [4]

Tartaric Acid condensed structure: HOOC–CH(OH)–CH(OH)–COOHHOOC–CH(OH)–CH(OH)–COOHConnectivity schematic · stereochemistry specified separately

Condensed connectivity schematic; see the specified stereochemical identity below. [1]

01

Chiral synthesis and resolution

Tartaric-acid chemistry is used in chiral work. [3] [4]

02

Acidulant formulations

Used in food and formulation contexts. [3] [4]

03

Tartrate derivatives

A precursor for tartrate salts and esters. [3] [4]

04

Commercial availability

The supplier section separates package size, assay, grade, and market context for three named products. [4] [5] [6]

02

GO A LITTLE DEEPER

Understanding Tartaric Acid

THE SIMPLE EXPLANATION

The functional groups

There are two acidic ends and two hydroxyl groups in the middle. The same connectivity can describe different three-dimensional forms. [1]

A LITTLE DEEPER

What the structure changes

The L form shown here has the (2R,3R) configuration. A condensed connectivity drawing does not establish that configuration by itself. Product labels, CAS identity, and optical specifications must agree. [1] [4] [5] [6]

Technical detail Identity, dissociation & specification

All three selected products use L-tartaric acid CAS 87-69-4. TCI separately reports chemical assay >99.0% by titration and optical purity ≥99.5% ee by LC. Enantiomeric excess (ee) is a stereochemical measurement and is not the same quantity as chemical assay. The aqueous pKa reference is for the L-(+) identity at 25 °C and zero ionic strength. [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.

03

MAKE THE CONNECTION

How Tartaric Acid Compares

Similar names and functional groups do not mean interchangeable chemicals.

SIDE-BY-SIDE COMPARISON

Tartaric Acid vs Malic Acid

Dihydroxydicarboxylic acid
versus
Hydroxydicarboxylic acid

Fixed comparison for this prototype. Acid selectors are disabled; additional comparisons are coming later.

Tartaric Acid compared with Malic Acid
PropertyTartaric AcidMalic Acid
Molecular formulaC₄H₆O₆ [1]C₄H₆O₅ [7]
Molecular weight150.09 g/mol [1]134.09 g/mol [7]
Carbon atoms4 [1]4 [7]
Carboxyl groups2 [1]2 [7]
StructureHOOC–CH(OH)–CH(OH)–COOH [1]HOOC–CH₂–CH(OH)–COOH [7]
Chemical familyDihydroxydicarboxylic acid [1]Hydroxydicarboxylic acid [7]
Identity focusSolid · L-(+) identity [1]Solid · DL identity [7]
pKa context3.036 / 4.366 (25 °C, water, zero ionic strength; L-(+) form) [2]3.51 / 5.03 (20 °C; OECD 112) [11]
Chemical identities are compared here; supplier grades, concentrations, and stereochemical specifications are separate purchasing attributes. pKa values retain their stated conditions; no quantitative solubility ranking is implied. The structure schematic does not encode stereochemistry.

When Might You Choose One Instead of the Other?

Use L-tartaric acid when a resolution or formulation method explicitly calls for that form. Use the specified malic stereoisomer for a malate-based method. A generic “tartaric acid” quote should be clarified before comparing prices. [1] [3] [7]

Specified starting material

Tartaric Acid

Match HOOC–CH(OH)–CH(OH)–COOH and the method’s required chemical form.

Malic Acid

Match HOOC–CH₂–CH(OH)–COOH; verify the identity before substituting a related acid.

Sources: [1] [7]

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.

04

FROM STRUCTURE TO APPLICATION

What Is Tartaric Acid Used For?

01

Chiral synthesis and resolution

Tartaric-acid chemistry is used in chiral work. The specific stereoisomer and optical specification are part of the reagent identity. [3] [4]

02

Acidulant formulations

Used in food and formulation contexts. A reagent-grade assay does not establish the required application specification. [3] [4]

03

Tartrate derivatives

A precursor for tartrate salts and esters. Counterion and ester form must be specified separately from the free acid. [3] [4]

05

CHOOSE THE RIGHT SPECIFICATION

Buying Tartaric Acid

Selecting tartaric acid involves more than the lowest price. Start with your application, then define purity, grade, quantity, documentation, and packaging.

1

What Are You Buying It For?

Intended use
Research / Synthesis

Require L-(+) identity, stereochemical specification, and separate chemical and optical assay. Match the procedure’s identity and impurity specification; request a lot COA and current regional SDS.

2

Define Your Requirements

These are requirements you can request, not a list of guaranteed available combinations. Confirm each product’s actual specification.

Set your requirements to prepare a sourcing brief.
06

SOURCE WITH CONTEXT

Tartaric Acid Suppliers

Compare specific products and package options. Listings are not ranked recommendations.

3 suppliers · 3 products · 6 package listingsLatest supplier check: October 3, 2026

Package sizes stay grouped under the supplier product. Assay methods, product forms, and regional markets remain visible. Require L-(+) identity, stereochemical specification, and separate chemical and optical assay.

Scroll horizontally if needed. Supplier and package identity stay visible.

6 package listings grouped under three supplier products
SupplierProduct / GradePurity / AssayPackage SizePublic PriceNormalized PriceDocumentationLast CheckedAction
Sigma-AldrichTartaric AcidACS reagent · L form251380-100G≥99.5%100 g$61.30USD · US public priceNot comparedGrades, assay bases, or forms differ
Document notes: Sigma-Aldrich
  • A product-specific certificate retrieval option was visible; no lot certificate was reviewed. Open the product page and use its certificate section.
  • A current regional SDS was not verified in this pass.
  • A product-specific Certificate of Origin retrieval option was visible; no origin certificate was reviewed. Country of origin is unverified and is not inferred.
View Product: Sigma-Aldrich, 251380-100G (opens new tab)
ACS reagent · L form251380-500G≥99.5%500 g$144.00USD · US public priceNot comparedGrades, assay bases, or forms differView Product: Sigma-Aldrich, 251380-500G (opens new tab)
TCITartaric AcidCheck supplierT0025L form; optical purity ≥99.5% ee (LC) is a separate specification.>99.0% (titration)25 g$17.00USD · US public priceNot comparedGrades, assay bases, or forms differ
COA lookup on product page (opens new tab)SDSCheck supplierCOOCheck supplier
Document notes: TCI
  • A product-specific certificate retrieval option was visible; no lot certificate was reviewed. Open the product page and use its certificate section.
  • A current regional SDS was not verified in this pass.
  • Origin-document availability was not verified. Country of origin is unverified and is not inferred.
View Product: TCI, T0025 (opens new tab)
Check supplierT0025L form; optical purity ≥99.5% ee (LC) is a separate specification.>99.0% (titration)500 g$47.00USD · US public priceNot comparedGrades, assay bases, or forms differView Product: TCI, T0025 (opens new tab)
FUJIFILM WakoTartaric AcidGuaranteed Reagent · L form203-00052≥99.5% (mass/mass, titration)25 g$32.00USD · US list priceNot comparedGrades, assay bases, or forms differ
COA lookup on product page (opens new tab)SDSCheck supplierCOOCheck supplier
Document notes: FUJIFILM Wako
  • A product-specific certificate retrieval option was visible; no lot certificate was reviewed. Open the product page and use its certificate section.
  • A current regional SDS was not verified in this pass.
  • Origin-document availability was not verified. Country of origin is unverified and is not inferred.
View Product: FUJIFILM Wako, 203-00052 (opens new tab)
Guaranteed Reagent · L form207-00055≥99.5% (mass/mass, titration)500 g$49.00USD · US list priceNot comparedGrades, assay bases, or forms differView Product: FUJIFILM Wako, 207-00055 (opens new tab)

Sigma-Aldrich

Tartaric Acid

≥99.5%

ACS reagent · L form

100 g

251380-100G
Public price
$61.30USD · US public price
Normalized price
Not comparedGrades, assay bases, or forms differ
View Product: Sigma-Aldrich, 251380-100G (opens new tab)

500 g

251380-500G
Public price
$144.00USD · US public price
Normalized price
Not comparedGrades, assay bases, or forms differ
View Product: Sigma-Aldrich, 251380-500G (opens new tab)

Documentation

Document notes: Sigma-Aldrich
  • A product-specific certificate retrieval option was visible; no lot certificate was reviewed. Open the product page and use its certificate section.
  • A current regional SDS was not verified in this pass.
  • A product-specific Certificate of Origin retrieval option was visible; no origin certificate was reviewed. Country of origin is unverified and is not inferred.

Last checked:

TCI

Tartaric Acid

>99.0% (titration)

Check supplier
L form; optical purity ≥99.5% ee (LC) is a separate specification.

25 g

T0025
Public price
$17.00USD · US public price
Normalized price
Not comparedGrades, assay bases, or forms differ
View Product: TCI, T0025 (opens new tab)

500 g

T0025
Public price
$47.00USD · US public price
Normalized price
Not comparedGrades, assay bases, or forms differ
View Product: TCI, T0025 (opens new tab)

Documentation

COA lookup on product page (opens new tab)SDSCheck supplierCOOCheck supplier
Document notes: TCI
  • A product-specific certificate retrieval option was visible; no lot certificate was reviewed. Open the product page and use its certificate section.
  • A current regional SDS was not verified in this pass.
  • Origin-document availability was not verified. Country of origin is unverified and is not inferred.

Last checked:

FUJIFILM Wako

Tartaric Acid

≥99.5% (mass/mass, titration)

Guaranteed Reagent · L form

25 g

203-00052
Public price
$32.00USD · US list price
Normalized price
Not comparedGrades, assay bases, or forms differ
View Product: FUJIFILM Wako, 203-00052 (opens new tab)

500 g

207-00055
Public price
$49.00USD · US list price
Normalized price
Not comparedGrades, assay bases, or forms differ
View Product: FUJIFILM Wako, 207-00055 (opens new tab)

Documentation

COA lookup on product page (opens new tab)SDSCheck supplierCOOCheck supplier
Document notes: FUJIFILM Wako
  • A product-specific certificate retrieval option was visible; no lot certificate was reviewed. Open the product page and use its certificate section.
  • A current regional SDS was not verified in this pass.
  • Origin-document availability was not verified. Country of origin is unverified and is not inferred.

Last checked:

Documentation evidence

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]

Verification limits & placement policy

NIST provides condition-defined pKa values for L-(+)-tartaric acid. A properly specified L-form quantitative saturation value is still needed for solution design. Optical purity and chemical assay remain separate specifications.

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.

07

PLAN A LARGER ORDER

Need Tartaric Acid in Bulk?

Turn your requirements into a clear supplier brief.

RFQ PROTOTYPE
Bulk RFQ feature — coming soon. Prototype form: submissions are not currently sent to suppliers. Use sample details to prepare an on-screen brief.
Prepare a bulk request Prototype form

The prefilled CAS identifies this profile’s principal form. Confirm or edit it for the requested product, especially a hydrate, stereoisomer, or salt. State the exact form and concentration before using the brief.

Prototype only · No request will be sent
08

A BUYER’S CHECKLIST

Before You Buy Tartaric Acid

Selections remain only while this page is open.

09

FOR YOUR REFERENCE

Tartaric Acid Technical Reference

Identity, product reference properties, and handling context.

Identification Names, formula & identifiers
Principal CAS
87-69-4
Identity focus
Solid · L-(+) identity
Formula
C₄H₆O₆
Molecular weight
150.09 g/mol
IUPAC name
(2R,3R)-2,3-dihydroxybutanedioic acid
Connectivity SMILES
C(C(C(=O)O)O)(C(=O)O)O
PubChem CID
444305

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]

Physical Properties Product references & conditions

L-(+)-tartaric acid is readily soluble in water (FAO/WHO reference). Sigma’s listed L-form product reports a melting range of 170–172 °C; this must not be replaced with a DL-tartaric value. No quantitative saturation concentration is recommended here. [13] [4]

Hydrate, concentration, stereoisomer, and temperature can change the relevant specification. Product reference data are not a reviewed lot certificate.

Acid/Base Properties Verified values & missing data

Reference pKa: 3.036 / 4.366 (25 °C, water, zero ionic strength; L-(+) form). [2]

NIST provides condition-defined pKa values for L-(+)-tartaric acid. A properly specified L-form quantitative saturation value is still needed for solution design. Optical purity and chemical assay remain separate specifications.

Temperature, ionic strength, and the use of activities versus concentrations matter in quantitative work. These reference values are not buffer recipes.

Safety at a Glance Product-specific hazards

The listed Sigma L-(+)-tartaric acid product 251380 (US listing) is classified as causing serious eye damage (H318). Supplier classifications differ; this must not be generalized to every tartaric-acid product. [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 documentation
10

COMMON QUESTIONS

Tartaric Acid FAQ

What distinguishes Tartaric Acid?

There are two acidic ends and two hydroxyl groups in the middle. The same connectivity can describe different three-dimensional forms. [1]

How does it differ from Malic Acid?

Malic acid has one hydroxyl-bearing stereocenter; tartaric acid has two hydroxyl-bearing carbons. Choosing between them changes both functional-group count and stereochemical requirements. [7]

What must a buyer specify?

Require L-(+) identity, stereochemical specification, and separate chemical and optical assay. [4]

Are the listed products directly price-comparable?

No. The table retains differing grades, assay bases, forms, and markets. No normalized ranking or currency conversion is applied. [5]

What reference data still need checking?

NIST provides condition-defined pKa values for L-(+)-tartaric acid. A properly specified L-form quantitative saturation value is still needed for solution design. Optical purity and chemical assay remain separate specifications.

Can I request a bulk quote here?

The RFQ is a prototype that prepares an on-screen brief. Nothing is sent to suppliers. Confirm actual bulk terms directly with the supplier.

11

TRACE THE INFORMATION

Sources & Editorial Notes

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.

  1. PubChem · chemical identity (opens new tab)

    Official PUG REST identity record: formula, molecular weight, IUPAC name, and connectivity SMILES.

  2. NIST · L-(+)-tartaric acid aqueous ionization (opens new tab)

    Goldberg, Kishore and Lennen (2002), table 7.63: evaluated aqueous pKa at 25 °C and zero ionic strength.

  3. PubChem · applications (opens new tab)

    Compiled application references; uses of derivatives are distinguished from direct use of the acid.

  4. Sigma-Aldrich · commercial product (opens new tab)

    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.

  5. TCI · commercial product (opens new tab)

    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.

  6. FUJIFILM Wako · commercial product (opens new tab)

    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.

  7. Malic Acid · identity (opens new tab)

    Primary comparison identity. Explanations of structural differences are editorial interpretation of verified identities.

  8. Citric Acid · identity (opens new tab)

    Related chemical identity; relevance is based on structure or the stated application relationship.

  9. Succinic Acid · identity (opens new tab)

    Related chemical identity; relevance is based on structure or the stated application relationship.

  10. Lactic Acid · identity (opens new tab)

    Related chemical identity; relevance is based on structure or the stated application relationship.

  11. Malic Acid · acid–base reference (opens new tab)

    The primary comparison’s pKa source; reference conditions are preserved.

  12. OpenStax · Citric acid cycle (opens new tab)

    Succinate and fumarate in the citric acid cycle; salts/ions are distinguished from purchased free acids.

  13. FAO/WHO · Tartaric acid (opens new tab)

    Authoritative description of water solubility. Used only qualitatively; its solvent-volume statement is not converted to a saturation concentration.

Review limits

NIST provides condition-defined pKa values for L-(+)-tartaric acid. A properly specified L-form quantitative saturation value is still needed for solution design. Optical purity and chemical assay remain separate specifications.

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.