Upjohn Co. v. United States

623 F. Supp. 1281, 9 Ct. Int'l Trade 600, 9 C.I.T. 600, 1985 Ct. Intl. Trade LEXIS 1512
CourtUnited States Court of International Trade
DecidedNovember 27, 1985
DocketCourt 81-8-01015
StatusPublished
Cited by3 cases

This text of 623 F. Supp. 1281 (Upjohn Co. v. United States) is published on Counsel Stack Legal Research, covering United States Court of International Trade primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Upjohn Co. v. United States, 623 F. Supp. 1281, 9 Ct. Int'l Trade 600, 9 C.I.T. 600, 1985 Ct. Intl. Trade LEXIS 1512 (cit 1985).

Opinion

Memorandum Opinion and Order

DiCARLO, Judge:

Plaintiff brings this action pursuant to 28 U.S.C. § 1581(a) challenging defendant’s classification of a single entry of chemicals under item 403.90 of the Tariff Schedules of the United States (TSUS), as “[mjixtures in whole or in part of any of the products *1282 provided for in [Subpart B].” 1 Plaintiff claims that the chemical is properly classified under item 800.00 TSUS, as American goods returned. The Court finds that the merchandise is a product of the Netherlands, and was properly classified under item 403.90, TSUS.

FACTS

The facts of this case as stipulated by the parties are as follows:

1. Plaintiff, the Upjohn Company (hereinafter “Upjohn”), manufactured at its plant in LaPorte, Texas, a chemical described by Upjohn for internal purposes as crude 390 HOP, which is also known generally in the trade as polymethylene polyphenyl isocyanate, and also as polymeric MDI. For purposes of convenience, this material will be referred to throughout this stipulation as crude 390 HOP.

2. The crude 390 HOP was exported from the United States to the Netherlands.

3. Upjohn produced the crude 390 HOP in the following manner: aniline was reacted with formaldehyde to form polymethyulene polydiphenyl polyamine. The polymethylene polydiphenyl polyamine was reacted with phosgene to produce the crude 390 HOP, which contains isocyanate functional groups.

4. Isocyanates are reactive chemical compounds, each composed of. a nitrogen atom bonded to a carbon atom bonded to an oxygen atom, hereinafter referred to as an -NCO group. Crude 390 HOP is a mixture of compounds of different molecular weights containing isocyanate groups. These compounds are: diphenylmethane diisocyanate, also known as methylene diphenyl diisocyanate (hereinafter referred to as “pure MDI”), triisocyanate, and other isocyanates of higher molecular weight, commonly referred to as “higher molecular weight structures.” The lightest of these isocyanates is the pure MDI. The pure MDI molecule consists of 2 benzene rings joined together. Each ring contains one NCO (isocyanate) group [see Attachment A]. 2 The triisocyanate molecule consists of 3 benzene rings joined together, with each ring containing one NCO group [see Attachment B]. The higher molecular weight structures consist of 4 or more benzene rings joined together, with each ring containing one NCO group [see Attachment C].

5. The crude 390 HOP described in paragraph 1 was sold by plaintiff to an affiliate, Upjohn Polymer B.V. (hereinafter “Upjohn B.V.”), in an intercompany sale for $.1962 per lb. and was exported to the Netherlands. The merchandise was described on the commercial invoice as “Crude 390 HOP (Polymethylene Polyphenylisocyanate).”

6. The exported crude 390 HOP was a mixture consisting of approximately 68.8 percent pure MDI, 13.1 percent triisocyanate and 18.1 percent higher molecular weight structures.

7. The exported crude 390 HOP was subjected to a treatment in the Netherlands by Upjohn B.V. by which heat was applied at low pressure causing a portion of the MDI contained in the crude 390 HOP to vaporize and separate from the remainder of the material. This process, known as evaporation, occurred in a vessel known as a thin film evaporator. The MDI which was thus separated exited through a duct at the top of the thin film evaporator. No changes in molecular structure resulted from this process.

8. The material that remained following separation exited through the bottom of the thin film evaporator, was cooled and sent to storage. . It was a mixture of approximately 34.4 percent pure MDI, 26.1 *1283 percent triisocyanate, and 39.5 percent higher molecular weight structures.

9. The pure MDI which was separated and exited the top of the thin film evaporator was immediately subjected to a series of processes which further purified it.

10. The material described in paragraph 8 that remained is sometimes described by Upjohn for internal purposes as crude BLD. It is known generally in the trade as polymethylene polyphenyl isocyanate and as polymeric MDI. For purposes of convenience, this material will be referred to throughout this stipulation as crude BLD.

11. The crude BLD was sold by Upjohn B.V. to Upjohn Company (Plaintiff) for $.1962 per lb., exported from the Netherlands and is the subject of this case. It was described on the commercial invoice as “Crude BLD (Polymethylene Polyphenylisocyanate).”

12. The properties of the crude 390 HOP, the pure MDI and the crude BLD are set forth on Schedule “A” attached hereto. 3

SCHEDULE “A”
Property Crude 390 HOP exported from U.S. Crude BLD Imported Pure MDI into U.S.
Isocyanate Equivalent (IE) 133.7 125.1 141.5
Acidity, % as HCI .065 .003 .13
Chloride, % Hydrolyzable Chloride, % Total Hydrolyzable .08 .27 .003 .010 .14 .56
Viscosity, cps @ 25 C. 35 25 1143
Pure MDI, % 68.8 100 34.4
Triisocyanate, % 13.1 0 26.1
Higher molecular structures, % 18.1 0 39.5
Specific gravity 1.2 1.2 1.2
Color * brown colorless brown
UV, % T, 500 nra 73 100 65
UV, % T, 400 nm 26.5 100 11
Form liquid liquid liquid
Flashpoint 435 375 425

13. The components of the crude 390 HOP and crude BLD are the same, namely: pure MDI, triisocyanate, and higher molecular weight structures. The relative proportion of triisocyanate and higher molecular weight structures in the crude BLD following separation of a portion of the pure MDI from the crude 390 HOP increased in direct proportion to the amount of pure MDI removed from the crude 390 HOP. The remaining pure MDI in the crude BLD decreased in direct proportion to the amount of pure MDI removed from the crude 390 HOP.

14. The crude BLD remaining after the process described in paragraph 7, following storage as described in paragraph 8, was returned to the United States and blended by Upjohn with other polymeric MDI. The resulting products were known by the Upjohn tradename PAPI. These products were combined with polyols [a chemical group having a chain-like molecule containing an available group composed of one oxygen atom and one hydrogen atom] and *1284

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Cite This Page — Counsel Stack

Bluebook (online)
623 F. Supp. 1281, 9 Ct. Int'l Trade 600, 9 C.I.T. 600, 1985 Ct. Intl. Trade LEXIS 1512, Counsel Stack Legal Research, https://law.counselstack.com/opinion/upjohn-co-v-united-states-cit-1985.