Triphenyl phosphorothioate

A trisubstituted aromatic thiophosphoric ester used as a flame retardant additive and lubricant extreme pressure agent. Classified under HTS 2920.19.40.00 as an 'other' aromatic phosphorodithioate with three phenyl groups. Meets chapter 29 criteria for separate chemically defined organic phosphorus compounds.

Import Duty Rates by Country of Origin

Origin CountryMFN RateCh.99 SurchargesTotal Effective Rate
πŸ‡¨πŸ‡³China6.5%+35.0%41.5%
πŸ‡²πŸ‡½Mexico6.5%+10.0%16.5%
πŸ‡¨πŸ‡¦Canada6.5%+10.0%16.5%
πŸ‡©πŸ‡ͺGermany6.5%+10.0%16.5%
πŸ‡―πŸ‡΅Japan6.5%+10.0%16.5%

Alternative Classifications

This product could be classified differently depending on its characteristics or intended use.

2909.60.20Lower: 40.5% vs 41.5%

If classified primarily by alcohol component rather than phosphorus function

Chapter notes prioritize classification by ester component occurring last numerically, potentially shifting to alcohol-derived esters.

3812Lower: 15% vs 41.5%

If when imported pre-mixed as prepared rubber accelerator

Mixtures containing this compound for specific rubber industry use fall under prepared chemical additives of heading 3812.

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Import Tips & Compliance

β€’ Verify purity exceeds 98% to qualify as chemically defined compound per chapter notes; include REACH/ TSCA compliance docs; avoid bulk packaging that suggests mixtures under heading 3824

Related Products under HTS 2920.19.40.00

O,O-Diethyl S-(2-chlorophenyl) phosphorothioate

This aromatic thiophosphoric ester, known as Tolylfluanid intermediate, is a phosphorodithioate derivative used in pesticide synthesis. It falls under HTS 2920.19.40.00 as an 'other' aromatic thiophosphoric ester with halogenated substitution on the phenyl ring. The chemical structure features phosphorus-sulfur bonds characteristic of this subheading.

O,O-Dimethyl S-phenyl phosphorothioate

Simple aromatic phosphorodithioate ester serving as intermediate for insecticide synthesis and analytical standards. Falls under HTS 2920.19.40.00 as 'other' aromatic thiophosphoric ester without additional heteroatoms. The phenyl-thiophosphoryl structure defines its chapter 29 classification.

Cresyl diphenyl phosphorothioate

Mixed aryl thiophosphoric ester used in hydraulic fluids and as antioxidant in petroleum additives. HTS 2920.19.40.00 classification applies to this aromatic 'other' phosphorodithioate with cresyl (methylphenyl) substitution. Exceeds purity threshold for separate chemical compound status.

O-Ethyl O-(4-nitrophenyl) phosphorothioate

Nitrosated aromatic thiophosphoric ester used in pharmaceutical intermediate synthesis and as analytical reagent. Classified HTS 2920.19.40.00 due to nitro-substituted phenyl ring on phosphorodithioate core. Chapter notes explicitly include nitrated derivatives in this heading.

Diphenyl phosphorochloridothioate

Aromatic thiophosphoric ester chloride intermediate for agricultural chemical synthesis. HTS 2920.19.40.00 covers this 'other' bis-aryl phosphorodithioate derivative. Acid halide functionality remains classified with parent thiophosphoric acid ester per chapter note (E).

O,O-Diethyl S-(4-methylphenyl) phosphorothioate

Para-tolyl substituted aromatic phosphorodithioate used in acaricide formulations. Falls under HTS 2920.19.40.00 as 'other' thiophosphoric ester with methyl-substituted phenyl ring. Chemically defined structure excludes mixture classification.