In re Smith

148 F.2d 351, 32 C.C.P.A. 959, 65 U.S.P.Q. (BNA) 167, 1945 CCPA LEXIS 427
Court of Customs and Patent Appeals·Decided March 12, 1945·No. No. 4979·Published·Cited by 8 cases

Opinions

Bland, Judge,

delivered the opinion of the court:

This appeal involves a single claim numbered 7, the only claim in appellant’s application. It reads:

7. An insecticide containing as its essential active ingredient substantially pure gamma, gamma-dipyridyl.

[960] As indicated by the claim, the substance is for use in combating insect infestation on vegetation, and it appears that it may be applied in either liquid or dust form.

The applicant appears to be a scientist employed by the United States Department of Agriculture, and the application, filed March 31, 1941, was made under the provisions of law governing patent applications by Government employees.

The examiner rejected the claim as being unpatentable over the disclosure of a publication, issued by the Department of Agriculture in October 1926, entitled “Toxicity of Dipyridyls and Certain Other Organic Compounds as Contact Insecticides.” The Board of Appeals affirmed the decision of the examiner and the instant appeal to this court followed.

The publication cited appears to have been prepared by Charles H. Richardson and C. R. Smith, scientists in the employ of the department, and it is hereinafter referred to as the Richardson et al. article. It is identified in the statement of the examiner as appearing in the “Journal of Agriculture Research, Yol. 33, pages 597-609 (1926).”

Neither the examiner nor the board quoted the text of that part of the Richardson et al. article which was regarded as anticipatory In his statement following the appeal to the board the examiner said:

The claim is rejected as directly met by the Richardson et al. publication. Richardson et al. teach the use of dipyridyls generally and give specific attention to gamma, gamma-dipyridyl. Applicant urges that this is not a reference as Richardson et al. show that the gamma, gamma-dipyridyl is not as effective as the others, and will, in fact, dilute the toxic effect of the other dipyridyls. This teaches that the concept of using gamma, gamma-dipyridyl as an insecticide is old. It does not necessarily, as applicant urges,-show that gamma, gamma-dipyridyl is not useful as an insecticide. It simply shows that gamma, gamma-dipyridyl is not as toxic to the insects tested as the other dipyridyls. In regards to applicant’s ■ arguments that he has produced an invention by reversing the teaching of the prior art, attention is directed to In re Golin, 538 O. G. 5.

In the course of its decision tbe board said:

The subject matter in issue is an insecticide consisting mainly of gamma, gamma-dipyridyl. The appealed claim stands finally rejected on the publication cited above. There are six dipyridyls which are fully discussed in the article cited. The authors of this article made a general survey with regard to the use of these isomers as possible insecticides. Judging from the statements made at the bottom of page 599 and at the top of page 609 the gamma, gamma-dipyridyl was not considered as effective an insecticide as the others mentioned.

It is difficult to see wherein there could be any invention involved in the subsequent discovery that the gamma, gamma-dipyridyl was effective as an insecticide. The reference shows that the substance per se was old and well known and its use as an insecticide was clearly contemplated by the authors of the article. At best all that appellant has done was to discover that under certain conditions not specified in the appealed claim the material would be effective.

[961] In addition to the case of In Re Colin, 29 C. C. P. A. (Patents) 757, 124 F. (2d) 219, 52 USPQ 89, cited by the examiner, the board also directs attention to the case of In Re Thucm, 30 C. C. P., A. (Patents) 979, 135 F. (2d) 344, 57 USPQ 324, which was decided by ns subsequent to the decision of the examiner in the instant case, but prior to the decision of the board.

As stated in the board’s decision, six dipyridyls were discussed in the Richardson et al. article, one of them being the gamma, gamma-dipyridyls.

We have examined the article with much care in the effort to ascertain just what the experiments therein described disclose with respect to gamma, gamma-dipyridyl, and we here quote the statements deemed to be pertinent in this case. In the introduction it is said:

* * * A previous publication discussed the toxicity of some pyridine derivatives (8)2 and referred briefly to the compounds which form the subject of the present investigation. It was found in these experiments that impure yy dipyridyl was much more toxic than the purified substance, and it was later shown that these impurities consisted principally of isomeric dipyridyls. It is the purpose of this paper to report on the toxic value of these dipyridyls as contact insecticides. * * *

At a later point it is stated:

Oxidation of sodium dipyridine with moist air results in the formation of yy dipyridyl, the sodium atom and two hydrogen atoms being removed. Careful regulation of the temperature during the preliminary, sodiumpyridine digestion, followed by oxidation (with dry air or oxygen) of the sodium dipyridines thus formed, leads to the production of an oil which contains chiefly aa, pp, py, and yy dipyridyls. This crude dipyridyl oil, from which most of the yy dipyridyl was removed, was used in the experiments described below. * * *

Under the beading “PRELIMINARY EXPERIMENTS ON THE TOXICITY OF CRUDE -DIPYRIDYL OIL,” appears the following:

Studies on the toxicity of the dipyridyls as contact insecticides were begun'in August, 1920. The first indication of toxic action appeared when a crude mixture, the result of an attempt to produce yy dipyridyl, was found to be highly toxic to the bean aphis (Aphis rumiáis L.) at a concentration of 1 percent of the. mixture.3 Experiments soon demonstrated that purified yy dipyridyl was only slightly toxic, if at all, and that the mother liquor separated from it was even more poisonous to insects than the original mixture. * * *

Under the heading “METHODS OF APPLICATION OF CRUDE DIPYRIDYL OIL,” it is said: '

After a large number of preliminary experiments, a crude dipyridyl oil known to contain a variable mixture of aa, pp, and py dipyridyls was prepared for the toxicity experiments. * * *

Under the heading of “SUMMARY” the following statement appears:

[962] act, /3/3, py, and yy dipyridyls, which occur in the crude dipyridyl oil used in these tests, were not so toxic to Aphis rumiáis as the crude oil itself; yy dipyridyl is much less toxic than the other three compounds.

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In re Smith, 148 F.2d 351, 32 C.C.P.A. 959, 65 U.S.P.Q. (BNA) 167, 1945 CCPA LEXIS 427 (ccpa 1945).

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