Derived in whole or in part from aromatic hydrocarbons

Polycarboxylic acids, their anhydrides, halides, peroxides and peroxyacids; their halogenated, sulfonated, nitrated or nitrosated derivatives: > Acyclic polycarboxylic acids, their anhydrides, halides, peroxides, peroxyacids and their derivatives: > Other: > Fumaric acid: > Derived in whole or in part from aromatic hydrocarbons

Duty Rate (from China)

41.5%
MFN Base Rate6.5%

Except for products described in headings 9903.03.02–9903.03.11, articles the product of any country, as provided for in subdivision (aa) of U.S. note 2 to this subchapter

Except as provided in headings 9903.88.13, 9903.88.18, 9903.88.33, 9903.88.34, 9903.88.35, 9903.88.36, 9903.88.37, 9903.88.38, 9903.88.40, 9903.88.41, 9903.88.43, 9903.88.45, 9903.88.46, 9903.88.48, 9903.88.56, 9903.88.64, 9903.88.66, 9903.88.67, 9903.88.68, or 9903.88.69, articles the product of China, as provided for in U.S. note 20(e) to this subchapter and as provided for in the subheadings enumerated in U.S. note 20(f)

Total Effective Rate41.5%

Products classified under HTS 2917.19.15.00

Aromatic-Derived Fumaric Acid

Fumaric acid produced through chemical processes involving aromatic hydrocarbons like benzene or toluene derivatives, used primarily in resins and polymer production. Classified under HTS 2917.19.1500 as an acyclic polycarboxylic acid derived in whole or part from aromatic hydrocarbons. Meets chapter 29 requirements for chemically defined organic compounds with specified oxygen functions.

Phthalic Anhydride Fumaric Coproduct

Fumaric acid obtained as byproduct from phthalic anhydride production via aromatic hydrocarbon oxidation processes. Falls under 2917.19.1500 due to aromatic derivation and acyclic polycarboxylic acid structure. Used in unsaturated polyester resins and food acidulant applications.

Xylene Oxidation Fumaric Acid

Fumaric acid synthesized via partial oxidation of mixed xylenes (aromatic hydrocarbons), purified for industrial use in alkyd resins. HTS 2917.19.1500 classification reflects aromatic derivation and acyclic nature per chapter 29 definitions. Excludes cyclic aromatic acids like phthalic.

Toluene-Derived Trans-Butenedioic Acid

High-purity trans-butenedioic acid (fumaric acid) from toluene oxidation processes, used in beverage acidulation and bioplastics. Derived from aromatic hydrocarbons qualifying for 2917.19.1500. Meets chemical purity standards of chapter 29 note (a).

Benzene Process Fumaric Acid

Fumaric acid isolated from benzene partial oxidation routes, primarily for unsaturated polyester resin manufacture. Aromatic hydrocarbon derivation confirmed by carbon isotope analysis. Classified 2917.19.1500 excluding cyclic byproducts like maleic anhydride.

Mixed Aromatics Fumaric Acid

Fumaric acid from coker light oil (mixed aromatics) processing, used in paper sizing and food preservation. HTS 2917.19.1500 applies due to partial aromatic hydrocarbon derivation meeting chapter specificity. Exceeds 99% purity for technical grade.

Cumene Oxidation Fumaric Byproduct

Fumaric acid recovered from cumene (isopropylbenzene) oxidation process streams, repurposed for polymer applications. Aromatic derivation via cumene qualifies for 2917.19.1500. Separated from primary acetone/phenol products.

Coal Tar Fumaric Acid Derivative

Fumaric acid extracted from coal tar light oil fractionation and oxidation, traditional aromatic source for specialty resins. Meets 2917.19.1500 criteria as aromatic-derived acyclic polycarboxylic acid. Historical production method still used in some regions.

Styrene Coproduct Fumaric Acid

Fumaric acid isolated from styrene oxidation process side streams, used in food coating applications. Aromatic hydrocarbon styrene derivation qualifies for specific 2917.19.1500 tariff treatment. High purity grade meeting FCC specifications.

Pseudocumene Route Fumaric Acid

Fumaric acid manufactured via pseudocumene (1,2,4-trimethylbenzene) selective oxidation technology. Advanced aromatic hydrocarbon derivation for electronic grade resins. Precise 2917.19.1500 classification per acyclic structure and chapter notes.