GB472624A - Improvements in or relating to preservatives, antiseptics, germicides and the like - Google Patents

Improvements in or relating to preservatives, antiseptics, germicides and the like

Info

Publication number
GB472624A
GB472624A GB35765/35A GB3576535A GB472624A GB 472624 A GB472624 A GB 472624A GB 35765/35 A GB35765/35 A GB 35765/35A GB 3576535 A GB3576535 A GB 3576535A GB 472624 A GB472624 A GB 472624A
Authority
GB
United Kingdom
Prior art keywords
salts
oils
acids
hydroxy
acid
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
Application number
GB35765/35A
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
Publication of GB472624A publication Critical patent/GB472624A/en
Expired legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N37/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
    • A01N37/36Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
    • A01N37/38Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids having at least one oxygen or sulfur atom attached to an aromatic ring system
    • A01N37/40Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids having at least one oxygen or sulfur atom attached to an aromatic ring system having at least one carboxylic group or a thio analogue, or a derivative thereof, and one oxygen or sulfur atom attached to the same aromatic ring system

Abstract

The calcium salts of hydroxy - methyl - isopropyl-benzene-carboxylic acids, such as o-carracrotic acid, are prepared by heating a suspension in water of the acid and calcium carbonate, cooling and filtering the mixture, and crystallizing out the salt. Hydroxyquinoline-carboxylic acids or their esters or ethers are rendered water-soluble by admixture with acids or acid salts, such as citric, tartaric or lactic acids or potassium bisulphate, whereby salts or double salts are obtained.ALSO:Carboxylic groups may be introduced into essential oils by treatment of the oils or their solutions at elevated temperature with metallic sodium whilst passing carbon dioxide, or by treatment of the oils with potassium permanganate. Hydroxyl groups may be introduced by treating the oils with caustic soda and formaldehyde. The products are used as germicides.ALSO:Antiseptics, preservatives and fungicides, for the treatment of foods, medicines, adhesives, oils, tannin extracts, inks, sizes and other substances, comprise one or more of the following compounds, viz. hydroxy benzene carboxylic acids containing at least two alkyl groups as nuclear substituents or in which the benzene nucleus is fused with a further iso- or hetero-cyclic ring; salts, esters or ethers of these acids; halogen derivatives of the foregoing compounds; substances produced by subjecting essential oils or their constituents to chemical treatment whereby carboxyl or hydroxyl groups or both are introduced. The salts used may be those of alkali or alkaline earth metals or magnesium or the active compounds may be used in conjunction with water-soluble alkaline earth or magnesium salts of inorganic or organic acids. In the case of hydroxy quinoline carboxylic acids, these may be used in aqueous solution in admixture with citric, tartaric or lactic acid or potassium bisulphate. The preservatives may be used in solid or liquid form or as solutions, colloidal solutions, or emulsions made with fatty alcohol sulphonates or other emulsifying agents, and they may be incorporated with the substances to be treated, or applied externally thereto, or dispersed in the atmosphere in which the substances are stored. Solutions are preferably used at pH 7 or less and the acidity may be adjusted to obtain selective action against particular micro-organisms. Active substances definitely specified include the following, viz.-thymotic, carvacrotic, 8-hydroxy-quinoline-7-carboxylic, b -naphthol-a -o-carboxylic, and dimethyl-hydroxy-benzene carboxylic acids, the methyl, propyl and isobutyl esters and sodium, calcium and magnesium salts of some of these, and the hydroxylated and carboxylated derivatives of various specified essential oils. Carboxyl groups may be introduced into essential oils by treatment of the oils or their solutions at elevated temperature with metallic sodium whilst passing carbon dioxide, or by treatment of the oils with potassium permanganate. Hydroxyl groups may be introduced by treating the oils with caustic soda and formaldehyde. The calcium salts of hydroxy - methyl-isopropyl-benzene carboxylic acids, such as o-carvacrotic acid, are prepared by heating a suspension in water of the acid and calcium carbonate, cooling and filtering the mixture, and crystallizing out the salt. Hydroxy-quinoline carboxylic acids or their esters or ethers are rendered water-soluble by admixture with acids or acid salts, such as citric, tartaric or lactic acids or potassium bisulphate whereby salts or double salts are obtained.
GB35765/35A 1935-03-26 1935-12-24 Improvements in or relating to preservatives, antiseptics, germicides and the like Expired GB472624A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE472624X 1935-03-26

Publications (1)

Publication Number Publication Date
GB472624A true GB472624A (en) 1937-09-27

Family

ID=6541457

Family Applications (1)

Application Number Title Priority Date Filing Date
GB35765/35A Expired GB472624A (en) 1935-03-26 1935-12-24 Improvements in or relating to preservatives, antiseptics, germicides and the like

Country Status (1)

Country Link
GB (1) GB472624A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20150102037A (en) * 2012-12-27 2015-09-04 킴벌리-클라크 월드와이드, 인크. Water soluble essential oils and their use
US10532124B2 (en) 2012-12-27 2020-01-14 Kimberly-Clark Worldwide, Inc. Water soluble farnesol analogs and their use

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20150102037A (en) * 2012-12-27 2015-09-04 킴벌리-클라크 월드와이드, 인크. Water soluble essential oils and their use
US20150329798A1 (en) * 2012-12-27 2015-11-19 Kimberly-Clark Worldwide, Inc. Water Soluble Essential Oils and Their Use
US10532124B2 (en) 2012-12-27 2020-01-14 Kimberly-Clark Worldwide, Inc. Water soluble farnesol analogs and their use
KR102079990B1 (en) 2012-12-27 2020-05-27 킴벌리-클라크 월드와이드, 인크. Water soluble essential oils and their use
US10717946B2 (en) * 2012-12-27 2020-07-21 Kimberly-Clark Worldside, Inc. Water soluble essential oils and their use
US11383003B2 (en) 2012-12-27 2022-07-12 Kimberly-Clark Worldwide, Inc. Water soluble farnesol analogs and their use

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