GB1273986A - Bi- and ter-thienyl compounds and their use as optical brighteners - Google Patents

Bi- and ter-thienyl compounds and their use as optical brighteners

Info

Publication number
GB1273986A
GB1273986A GB4104168A GB4104168A GB1273986A GB 1273986 A GB1273986 A GB 1273986A GB 4104168 A GB4104168 A GB 4104168A GB 4104168 A GB4104168 A GB 4104168A GB 1273986 A GB1273986 A GB 1273986A
Authority
GB
United Kingdom
Prior art keywords
bithienyl
nylon
alkyl
acetyl
aug
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
GB4104168A
Inventor
Ronald Edward Atkinson
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.)
Procter and Gamble Ltd
Original Assignee
Procter and Gamble Ltd
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 Procter and Gamble Ltd filed Critical Procter and Gamble Ltd
Priority to GB4104168A priority Critical patent/GB1273986A/en
Publication of GB1273986A publication Critical patent/GB1273986A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D333/00Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/02Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • C07D333/04Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
    • C07D333/26Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D333/38Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D333/00Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/02Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • C07D333/04Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
    • C07D333/06Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
    • C07D333/24Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals

Abstract

1,273,986. Optical brightening of macromolecular materials. PROCTOR & GAMBLE Ltd. 27 Aug., 1969 [23 Aug., 1968], No. 41041/ 68. Heading D1P. [Also in Divisions C2 and C5] Macromolecular and polymeric organic materials, such as nylon and wool, are brightened by incorporating or applying thereto a polythienyl compound of the general formula: wherein X represents R, OR, OM or NRR', (R and R' each represent an alkyl, substituted alkyl radical or H atom and M is a cation) Y is H, halogen, alkyl or substituted alkyl and n is 2 or 3. In the Example pieces of Nylon 6 and Nylon 66 material were washed with a detergent composition containing Na dodecyl benzene sulphonate, Na toluene sulphonate, Na tripolyphosphate, Na silicate, coconut ethanolamide, Na carboxymethyl cellulose, Na sulphate and Na perlaurate together with the optical brightener 5-propionyl-2, 2'-bithienyl, 5-acetyl-2, 2'-bithienyl, 5-methyl-5'-formyl-2, 2'- bithienyl, or 5-ethyl-5'-acetyl-2, 2'-bithienyl.
GB4104168A 1968-08-28 1968-08-28 Bi- and ter-thienyl compounds and their use as optical brighteners Expired GB1273986A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB4104168A GB1273986A (en) 1968-08-28 1968-08-28 Bi- and ter-thienyl compounds and their use as optical brighteners

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB4104168A GB1273986A (en) 1968-08-28 1968-08-28 Bi- and ter-thienyl compounds and their use as optical brighteners

Publications (1)

Publication Number Publication Date
GB1273986A true GB1273986A (en) 1972-05-10

Family

ID=10417841

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4104168A Expired GB1273986A (en) 1968-08-28 1968-08-28 Bi- and ter-thienyl compounds and their use as optical brighteners

Country Status (1)

Country Link
GB (1) GB1273986A (en)

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Legal Events

Date Code Title Description
PS Patent sealed
PLNP Patent lapsed through nonpayment of renewal fees