US627642A - Manufacture of ointments. - Google Patents

Manufacture of ointments. Download PDF

Info

Publication number
US627642A
US627642A US69443998A US1898694439A US627642A US 627642 A US627642 A US 627642A US 69443998 A US69443998 A US 69443998A US 1898694439 A US1898694439 A US 1898694439A US 627642 A US627642 A US 627642A
Authority
US
United States
Prior art keywords
manufacture
formaldehyde
excess
ointments
lanolin
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US69443998A
Inventor
Thomas George Fermor Hesketh
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to US69443998A priority Critical patent/US627642A/en
Application granted granted Critical
Publication of US627642A publication Critical patent/US627642A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/56Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
    • A61K31/565Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids not substituted in position 17 beta by a carbon atom, e.g. estrane, estradiol
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J9/00Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of more than two carbon atoms, e.g. cholane, cholestane, coprostane

Definitions

  • This invention relates to the production of soaps, ointments, embrocations, and similar preparations having antiseptic and medicinal properties and depends upon the property possessed by formaldehyde of forming con: densation products.
  • oily or fatty substances are treated at suitable temperatures with formaldehyde or its solutions un der a reflux condenser at normal atmospheric pressure or in aclosed vessel at increased pressure.
  • Any quantity of lanolin is mixed with an several hours, according to the quantity of material being manufactured. On the small scale five to six hours is found sufficient. The excess of formaldehyde solution is then removed, and the resulting compound is found to have a higher.melting-point than lanolin and when hot to smell offormaldehyde.
  • This compound is found to exercise most beneficial action upon the skins of man and animals and maybe applied directly or incorporated with various well-known substances-such as vaselin, olive-oil, cold cream, and the like-to render its application easy and pleasant or may be mixed with lanolin.
  • W'hen soap is requirecha condensation procluct, as above described, may be incorporated with the soap mass before pouring into the cooling-frames, or part of the fatty substance of the soap may be previously treated with formaldehyde, as described, and the condensation product added toward the end of the saponification, the manufacture being then proceeded with in the usual manner.
  • condensation compounds of formaldehyde with lanolin consisting in mixing lanolin with an excess of formaldehyde solution, then heating the mixture to about 100 centigrade for several hours, and afterward removing the excess of formaldehyde solution, substantially as described.
  • condensation compounds of formaldehyde with an oily or fatty substance consisting in mixing the oily or fatty substance with an excess of formaldehyde, then heating the mixture to a suitable temperature, and afterward removing the excess of formaldehyde, substantially as described.

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Preparation (AREA)

Description

UNITED STATES PATENT OFFICE.
THOMAS GEORGE FERMOR HESKETH, OF TOWOESTER, ENGLAND.
MANUFACTURE OF OINTMENTS.
SPECIFICATION forming part of Letters Patent No. 627,642, dated June 2'7, 1899.
' Application filed October 24, 1898. Serial No. 694A39- (No specimens.)
Northampton, England, have invented certain new and useful Improvements in the Manufacture of Ointments, (for which application for Letters Patent of Great Britain was filed on March 24, 1898,.No. 7,169,) of which the following is a full, clear, and exact description.
This invention relates to the production of soaps, ointments, embrocations, and similar preparations having antiseptic and medicinal properties and depends upon the property possessed by formaldehyde of forming con: densation products.
In carrying out my invention oily or fatty substances are treated at suitable temperatures with formaldehyde or its solutions un der a reflux condenser at normal atmospheric pressure or in aclosed vessel at increased pressure.
In order to make my invention clear, I will describe the production of the condensation compound of lanolin.
Any quantity of lanolin is mixed with an several hours, according to the quantity of material being manufactured. On the small scale five to six hours is found sufficient. The excess of formaldehyde solution is then removed, and the resulting compound is found to have a higher.melting-point than lanolin and when hot to smell offormaldehyde. This compound is found to exercise most beneficial action upon the skins of man and animals and maybe applied directly or incorporated with various well-known substances-such as vaselin, olive-oil, cold cream, and the like-to render its application easy and pleasant or may be mixed with lanolin.
W'hen soap is requirecha condensation procluct, as above described, may be incorporated with the soap mass before pouring into the cooling-frames, or part of the fatty substance of the soap may be previously treated with formaldehyde, as described, and the condensation product added toward the end of the saponification, the manufacture being then proceeded with in the usual manner.
Having fully described my invention, what I claim, and desire to secure by Letters Patent, is
1. The manufacture of condensation compounds of formaldehyde with lanolin consisting in mixing lanolin with an excess of formaldehyde solution, then heating the mixture to about 100 centigrade for several hours, and afterward removing the excess of formaldehyde solution, substantially as described.
2. The manufacture of condensation compounds of formaldehyde with an oily or fatty substance consisting in mixing the oily or fatty substance with an excess of formaldehyde, then heating the mixture to a suitable temperature, and afterward removing the excess of formaldehyde, substantially as described.
3. The manufacture of medicinal and antiseptic ointment, embrocation and the like from condensation compounds, consisting in mixing lanolin with an excess of formaldehyde solution, then heating the mixture to about 100 centigrade for several hours, then removing the excess of formaldehyde solution, and incorporating said compounds with an ointment vehicle, substantially as described.
4. The manufacture of medicinal and antiseptic ointment, embrocation and the like from condensation compounds, consisting in mixing an oily or fatty substance with an excess of formaldehyde, then heating the mixture to a suitable temperature, and afterward removing the excess of formaldehyde, and incorporating said compounds with an oint ment-vehicle such as described.
In testimony that I claim the foregoing as my invention 1 have signed my name in presence of two subscribing witnesses.
THOMAS GEORGE FERMOR HESKET Witnesses:
FRED. FALLS, JOHN MOPADDEN.
US69443998A 1898-10-24 1898-10-24 Manufacture of ointments. Expired - Lifetime US627642A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US69443998A US627642A (en) 1898-10-24 1898-10-24 Manufacture of ointments.

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US69443998A US627642A (en) 1898-10-24 1898-10-24 Manufacture of ointments.

Publications (1)

Publication Number Publication Date
US627642A true US627642A (en) 1899-06-27

Family

ID=2696240

Family Applications (1)

Application Number Title Priority Date Filing Date
US69443998A Expired - Lifetime US627642A (en) 1898-10-24 1898-10-24 Manufacture of ointments.

Country Status (1)

Country Link
US (1) US627642A (en)

Similar Documents

Publication Publication Date Title
US922692A (en) Thermoplastic keratin composition.
JPS60209537A (en) Hydroxyl derivative of camphorenic aldehyde and perfume composition, perfume base and perfumed product containing same
DE918747C (en) Process for the production of artificial musk fragrances from m- and p-cymene
US627642A (en) Manufacture of ointments.
US3258400A (en) Isopropyl and diisopropyl-3, 4-dihydrocoumarins in perfume compositions
US1699245A (en) Production of condensation products of methylol compounds of a urea
US1029737A (en) Fusible phenol resin and method of forming same.
US2476815A (en) Method for the preparation of 1-alkoxy-2, 4-dinitro-6-tertiary-butyl-benzenes
US2997503A (en) Process of preparing substituted tetrahydronaphthalenes
US2105792A (en) Unsaturated ketones
US690848A (en) Toilet cream.
Smith et al. Vitamin E. XLVII. 1 The Coumaran Isomer of α-Tocopherol
US1124611A (en) Dry fat and oil compounds.
US1028074A (en) Ortho-oxalic-acid ester of meta-cresol and process for the manufacture of the same.
US2572563A (en) Aromatic compositions and process of treating lactone material to prepare them
US647075A (en) Process of making compounds of paraphenetidin.
US652969A (en) Process of making ionone.
US750213A (en) Cozchjco chscilceucplcach
US610361A (en) Otto manasse
US988733A (en) Formaldehyde compound and process of making same.
US775251A (en) Process of making homologues of ionone.
US762765A (en) Homologues of isoionone and process of making same.
US991735A (en) Octenediones.
JPS5862111A (en) Perfume composition containing one or more tetramethyl-tricycloundecyl-alkyl ketones as perfume base and perfumed products
US1670825A (en) Unsaturated aldehydes and in the manufacture thereof