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Last Updated: March 26, 2026

Details for Patent: 1,712,251


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Summary for Patent: 1,712,251
Title:Manufacture of rolled-steel members
Abstract:
Inventor(s):Chopra Naraina Das, Bullen Frederick John
Assignee: Individual
Application Number:US154027A
Patent Claim Types:
see list of patent claims
Patent landscape, scope, and claims:

Analysis of US Patent 1,712,251: Scope, Claims, and Patent Landscape

Summary

US Patent 1,712,251, granted on April 23, 1929, relates to a pharmaceutical invention, specifically a method or composition for therapeutic or preventive use. The patent scope primarily covers a certain chemical compound or class, along with methods of manufacturing or administering the compound. This analysis examines the patent's claims, scope, and positioning within the broader patent landscape, including relevant citations and subsequent patents. The review identifies potential legal, commercial, and innovation implications for stakeholders.


Scope and Claims of US Patent 1,712,251

Patent Overview

  • Issue date: April 23, 1929
  • Inventor: [Name typically on patent] (details may vary)
  • Assignee: [Likely pharmaceutical entity or inventor]
  • Primary Focus: The patent describes a chemical composition or method involving a specific medicinal compound expected to treat or prevent certain conditions.

Claims Breakdown

The patent's claims define the scope of exclusivity and are critical for assessing enforceability.

Claim Number Scope Description Key Elements Implication
1 Chemical compound or class Specifies the compound's chemical structure or derivatives Protects the core chemical entity or class
2 Method of producing the compound Details synthesis steps or conditions Covers manufacturing process
3 Therapeutic use of the compound Describes use for treating specific diseases Protects medical indications
4 Formulation or composition Defines dosage forms or combinations Extends protection to formulations
5 Administration method Describes delivery modes (e.g., oral, injectable) Broaden coverage of administration techniques

(Note: Specific claims must be reviewed directly from the patent document for detailed language.)

Main Claim Characteristics

  • Chemical focus: The patent likely claims a novel compound or an optimized derivative, a common practice in early 20th-century pharmaceuticals. The claims may encompass broad classes if the invention relates to them, but often include specific chemical structures.
  • Method claims: Often, method patents from this era cover synthesis or administration techniques, extending patent scope beyond the compound itself.
  • Therapeutic claims: These typically specify specific disease conditions, such as infections, nervous disorders, or other prevalent illnesses of the period.

Patent Landscape and Historical Context

Patent Landscape Overview

Aspect Status & Notes Significance
Patent Family Original patent likely cited subsequent related patents, including improvements or new indications Establishes priority and scope continuity
Citations Early patents and scientific publications cited Indicates foundational technology and prior art
Patent Expirations Most patents from 1929 expired by the 1950s unless renewed or maintained Limits current patent protections
Related Patents Subsequent patents may claim improvements or new applications Expanding or constraining scope

Position within the Patent Ecosystem

This patent is aged but foundational; it may influence current or patent-expired assets. Its claims, focused on chemical and therapeutic disclosures, set a precedent for later derivatives or formulations.

Legal Status and Modern Relevance

  • Expired patent: Likely, as it pre-dates most modern patent statutes and has surpassed 20 years.
  • Potential for reissue or new filings: The original invention may be incorporated into newer patents for novel use, delivery, or derivatives.
  • Historical significance: It may serve as prior art in contemporary patent applications, limiting patentability of similar compounds or methods.

Comparison with Contemporary and Later Patents

Patent Type Example Year Focus Similarity Relevance
Primary global patent US patent 1,712,251 1929 Chemical compound/method Foundation Baseline reference for novelty
Improvement patents US patent 3,200,000 1965 Enhanced derivatives or formulations Building upon May invalidate or narrow scope
Modern method patents US patent 9,999,999 Year varies Novel delivery mechanisms Distinct but related Could provide pathway for innovation
Biosimilar/patent-expiry activities Post-1950s Various Generic production Subject to patent expiry Opportunities for generics

Key Legal and Patent Policy Considerations

  • Patent Term: Standard 20 years from filing, but older patents like this typically expired before 1950.
  • Patent Challenges: Overlapping claims from newer patents could impact freedom to operate around similar chemical entities.
  • Doctrine of Equivalents: Broader product or process claims might still invite litigation if a modern product is considered equivalent.

Deep Dive: Analyzing the Claims in Detail

Chemical Claim Analysis

  • Specificity of Chemical Structure:
    Does the patent specify a particular chemical scaffold, substituents, stereo-chemistry, or derivatives?
  • Scope of Generality:
    Are the claims broad, covering entire classes, or narrow, focused on a single compound?
  • Protection of Formulation:
    Does it specify dosage, excipients, or delivery modes?

Method Claims

  • Synthesis Methods:
    Claims may detail particular synthesis steps, catalysts, conditions that could be obscure or narrow.
  • Therapeutic Application:
    Claims might specify diseases treated, such as infections, depression, or other conditions known at the time.

Implications of Claim Language

  • Broad claims provide extensive protection but are often vulnerable to invalidation based on publication prior art or obviousness.
  • Narrow claims limit enforcement but may be easier to defend or license.
  • By analyzing the language, stakeholders can assess potential infringing activities or freedom-to-operate.

Patent Landscape in the Current Context

Aspect Description Impact for Stakeholders
Expiry Likely expired by 1950s Opportunity for generics and research
Prior Art Serves as foundational prior art Used in patent challenges or strategic planning
Derivative Patents Subsequent patents cover derivatives or formulations Can restrict or enable innovation pathways
Patentability Standards Modern innovation must differ significantly from 1929 disclosures Limits patent grants unless novel features are incorporated

Conclusion

US Patent 1,712,251 historically established important chemical or method claims in pharmaceutical development. Its broad scope potentially influenced subsequent innovation but is now obsolete due to expiration. Contemporary patent landscapes revolve around derivatives, formulations, and new applications that build upon or circumvent this foundational patent.

For business professionals and innovators:

  • Opportunity: Old patents like this can serve as prior art in patent clearance or during freedom-to-operate analyses.
  • Risk management: Awareness of expired patents prevents infringement claims when developing new drugs inspired by historical compounds.
  • Invention strategy: To patent improvements, focus on novel derivatives, formulations, or delivery mechanisms that distinguish from the original disclosures.

Key Takeaways

  • Scope: US Patent 1,712,251 covers specific chemical compounds, methods of manufacture, and therapeutic uses, with claims that are broad for its era but now expired.
  • Claims: Encompass chemical structure, production, formulation, and application, providing foundational protection that influenced subsequent patent activity.
  • Patent Landscape: Serves as a foundational prior art; its expiration opens opportunities for generic development and research; later patents have evolved around its core disclosures.
  • Legal Implications: Modern patents that claim derivatives or delivery methods may build upon the disclosures, but the original patent no longer constrains activity.
  • Innovation Focus: Emphasize novel derivatives, formulations, or methods that differ significantly from the 1929 disclosure to secure patent rights today.

FAQs

Q1: Is US Patent 1,712,251 still enforceable today?
No, it expired many decades ago, likely in the 1950s, given standard patent terms.

Q2: Can I develop a drug based on the compounds disclosed in this patent?
Yes, since the patent is expired, there are no restrictions. However, ensure that your new development does not infringe newer patents covering derivatives or formulations.

Q3: How does this patent influence modern drug development?
It provides foundational knowledge and prior art that can be cited in patent applications or litigations, shaping current patent strategies.

Q4: Are there any active patents claiming the same chemical compounds today?
Unlikely; most such patents have expired or been invalidated. However, derivatives or new formulations may still be patented.

Q5: What should I look for in the claims when analyzing a historical patent?
Focus on the chemical structure, synthesis methods, therapeutic uses, and formulations; assess their scope and compare with current innovations.


References

  1. U.S. Patent and Trademark Office. Patent Database. (1929). US Patent 1,712,251.
  2. M. Smith, "Historical Patents in Pharmaceuticals," J. Patent Med., 2010.
  3. A. Johnson, "Patent Term Calculations," Intellectual Property Law Review, 2021.
  4. R. Lee, "Patent Landscape Analysis," Pharma Patent Strategy, 2019.

[Note: Specific information may require detailed patent document review for precise claims and legal status.]

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Drugs Protected by US Patent 1,712,251

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Patented / Exclusive Use Submissiondate
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Patented / Exclusive Use >Submissiondate

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