Aromatic

Organic derivatives of hydrazine or of hydroxylamine: > Other: > Aromatic

Duty Rate (from China)

31.5%
MFN Base Rate6.5%

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)

Articles the product of any country, as provided for in subdivision (aa)(ii) of U.S. note 2 to this subchapter

Total Effective Rate31.5%

Products classified under HTS 2928.00.25.00

Phenylhydrazine Hydrochloride

Phenylhydrazine hydrochloride is an aromatic derivative of hydrazine, featuring a phenyl group attached to the hydrazine moiety with a hydrochloride salt form. It falls under HTS 2928.00.25.00 as an aromatic organic derivative of hydrazine, consistent with Chapter 29 notes for chemically defined organic compounds. Commonly used in organic synthesis and analytical chemistry for derivative formation.

2,4-Dinitrophenylhydrazine

2,4-Dinitrophenylhydrazine (DNPH) is an aromatic hydrazine derivative with nitro groups on the phenyl ring, used primarily for carbonyl compound identification. Classified under HTS 2928.00.25.00 as an aromatic derivative of hydrazine per Chapter 29 scope for separate chemically defined compounds. Its structure maintains the hydrazine parent with aromatic substitution.

4-Nitrophenylhydrazine

4-Nitrophenylhydrazine is a chemically defined aromatic derivative featuring a nitro-substituted phenyl ring linked to hydrazine. It qualifies for HTS 2928.00.25.00 under Chapter 29 as a separate organic hydrazine derivative, not covered by exclusions like coloring matters. Used in pharmaceutical intermediates and dye synthesis.

Acetylphenylhydrazine

Acetylphenylhydrazine is an N-acetyl derivative of phenylhydrazine, retaining its aromatic hydrazine core structure. It is classified under HTS 2928.00.25.00 as an aromatic hydrazine derivative, where the acetyl group is a substituent on the nitrogen per Chapter 29 rules for derivatives. Applied in organic synthesis and as a reagent.

1-Phenyl-3-pyrazolidinone (Phenidone)

Phenidone, or 1-phenyl-3-pyrazolidinone, is a cyclic hydrazine derivative with an aromatic phenyl substituent. It falls under HTS 2928.00.25.00 as an aromatic derivative of hydrazine, chemically defined and within Chapter 29 scope excluding only specific forms. Used as a photographic developer and antioxidant.

p-Toluenesulfonylhydrazide

p-Toluenesulfonylhydrazide (TSH) is an aromatic sulfonyl hydrazide with a tosyl group attached to hydrazine. Classified in HTS 2928.00.25.00 as an aromatic hydrazine derivative; sulfonated forms remain here unless organo-sulfur dominates per notes. Widely used as a foaming agent in plastics.

Benzylideneacetone Tosylhydrazone

Benzylideneacetone tosylhydrazone is a condensation product of an aromatic aldehyde, ketone, and tosylhydrazine, retaining hydrazine derivative character. It qualifies under HTS 2928.00.25.00 as aromatic per Chapter 29 for chemically defined hydrazine derivatives. Used in organic synthesis like Shapiro reaction.

N-Aminopiperidine Hydrochloride

N-Aminopiperidine hydrochloride features a hydrazine-like amino group on a heterocyclic ring with aromatic impurities qualifying it as aromatic mixture. However, primarily classified under HTS 2928.00.25.00 if aromatic character dominates per Chapter notes on mixtures of isomers.

Girard's Reagent T

Girard's Reagent T (trimethylacetylhydrazide trimethylammonium chloride) is an aromatic-capable hydrazide used for carbonyl isolation, classified as aromatic derivative under HTS 2928.00.25.00 when phenyl-substituted variants imported.

Semicarbazide Hydrochloride

Semicarbazide hydrochloride, 1-aminourea HCl, is a hydrazine derivative with aromatic applications, classified under HTS 2928.00.25.00 for aromatic forms used in pharma synthesis.