GB732139A - Manufacture and application of new derivatives of 4:4-diaminostilbene disulphonic acid-(2:2) - Google Patents

Manufacture and application of new derivatives of 4:4-diaminostilbene disulphonic acid-(2:2)

Info

Publication number
GB732139A
GB732139A GB22763/52A GB2276352A GB732139A GB 732139 A GB732139 A GB 732139A GB 22763/52 A GB22763/52 A GB 22763/52A GB 2276352 A GB2276352 A GB 2276352A GB 732139 A GB732139 A GB 732139A
Authority
GB
United Kingdom
Prior art keywords
compound
mols
amine
hydroxyethylamino
ammonia
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
GB22763/52A
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.)
BASF Schweiz AG
Original Assignee
Ciba AG
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 Ciba AG filed Critical Ciba AG
Publication of GB732139A publication Critical patent/GB732139A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D251/00Heterocyclic compounds containing 1,3,5-triazine rings
    • C07D251/02Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
    • C07D251/12Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D251/26Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hetero atoms directly attached to ring carbon atoms
    • C07D251/40Nitrogen atoms
    • C07D251/54Three nitrogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D251/00Heterocyclic compounds containing 1,3,5-triazine rings
    • C07D251/02Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
    • C07D251/12Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D251/26Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hetero atoms directly attached to ring carbon atoms
    • C07D251/40Nitrogen atoms
    • C07D251/54Three nitrogen atoms
    • C07D251/70Other substituted melamines

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Coloring (AREA)

Abstract

Cellulosic textile fibres are brightened by treating them, with or without a washing agent and whether dyed, printed or not, with a blue-fluorescent compound of the general formula <FORM:0732139/IV (c)/1> or a salt thereof, in which V, W and Z indicate -NH2 or the residue of a primary or secondary amine, and X and Y are of the same kind as W and Z or are chlorine, or an aryl-O-, aryl-S- or alkyl-S-residue. Many such compounds are specified. In examples, (11) undyed cotton yarn is treated in a bath containing 0.01 g. per 1. of the compound <FORM:0732139/IV (c)/2> (12) undyed cellulosic material is washed with a mixture of sodium 2-heptadecyl-N-benzylbenz-imidazyl-disulphonate with the compound <FORM:0732139/IV (c)/3> and (13) cotton is washed in a bath containing soap, sodium carbonate, sodium pyrophosphate, sodium borate, magnesium silicate and the compound specified in (11) above, or the compound <FORM:0732139/IV (c)/4>ALSO:The invention comprises 4,41-diaminostilbene-2,21-disulphonic acid derivatives of the general formula <FORM:0732139/IV (b)/1> and salts thereof, in which V, W and Z indicate -NH2 or the residue of a primary or secondary amine, and X and Y are of the same kind as W and Z, or are chlorine, or an aryl-O-, aryl-S-, or alkyl-S-residue. The compounds are prepared by a sequence of known methods from 2 mols. of 4-aminostilbene-2,21, disulphonic acid containing in the 41-position a group convertible into an amino group, 3 mols. of cyanuric chloride and either 3-5 mols. of ammonia or an amine, or 2 mols. of an aromatic hydroxyl or mercapto compound or aliphatic mercapto compound and 3 mols. of ammonia or an amine, the convertible group being converted into an amino group at an intermediate stage. The methods described are (a) reducing to amino groups the nitro groups in the compound <FORM:0732139/IV (b)/2> and condensing in any sequence 2 mols. of cyanuric chloride with 1 mol. of the reduction product and with 2-4 mols. of ammonia or amine, or with 2 mols. of aromatic hydroxyl or mercapto compound or aliphatic mercapto compound and 2 mols. of ammonia or amine; (b) reducing the nitro group in the compound <FORM:0732139/IV (b)/3> and condensing in any sequence 1 mol. of cyanuric chloride with 2 mols. of the reduction product and 1 mol. of ammonia or an amine; (c) the condensing compound <FORM:0732139/IV (b)/4> with the compound <FORM:0732139/IV (b)/5> and reacting the product with 1 mol. of ammonia or an amine; and (d) reducing the nitro group in the compound <FORM:0732139/IV (b)/6> and reacting 1 mol. of cyanuric chloride in any sequence with 1 mol. of the reduction product and with 1-2 mols. of ammonia or an amine or 1 mol. of an aromatic hydroxyl or mercapto compound or aliphatic mercapto compound and 1 mol. of ammonia or an amine. Examples are given of the preparation of compounds in which (1) X, Y = Cl; W, Z = ethylamino; and V = morpholino, by method (a). (2) X, Y = b -hydroxyethylamino; W, Z = anilino; and V = morpholino, by method (a). (3) X, Y, W, Z = ethylamino; V = morpholino, by the action of ethylamine on the product of (1). (4) X, Y = b -hydroxyethylamino; V, W, Z = anilino, by method (b). (5) X, Y, V, W, Z = b -hydroxyethylamino, by method (b). (6) X = b -hydroxyethylamino; Y, Z = ethylamino; V, W = anilino, by method (c). (7) X = ethylamino; Y, Z = b -hydroxyethylamino; W = anilino; V = morpholino, by method (c). (8) X, Y = p-methylphenoxy; W, Z = b -hydroxyethylamino; V = ethylamino, by method (a). (9) X = phenoxy; Y, Z = ethylamino; V, W = b -hydroxyethylamino, by method (c); and (10) X = anilino; V, W, Z = b -hydroxyethylamino; Y = p-methylphenylmercapto, by method (d). Many other similar products are specified.ALSO:Washing compositions comprise soap or other washing agent together with a blue-fluorescent compound of the general formula <FORM:0732139/III/1> or a salt thereof, in which V, W and Z indicate -NH2 or the residue of a primary or secondary amine, and X and Y are of the same kind as W and Z or are chlorine, or an aryl-O-, aryl-S- or alkyl-S-residue. Many such compounds are specified. Examples include compositions comprising (12) a mixture of sodium 2-heptadecyl-N-benzylbenzimidazyl disulphonate and the compound <FORM:0732139/III/2> and (13) a composition comprising soap, sodium carbonate, sodium pyrophosphate, sodium borate, magnesium silicate and the compound <FORM:0732139/III/3> or the compound <FORM:0732139/III/4>
GB22763/52A 1951-09-13 1952-09-10 Manufacture and application of new derivatives of 4:4-diaminostilbene disulphonic acid-(2:2) Expired GB732139A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH732139X 1951-09-13

Publications (1)

Publication Number Publication Date
GB732139A true GB732139A (en) 1955-06-22

Family

ID=4532442

Family Applications (1)

Application Number Title Priority Date Filing Date
GB22763/52A Expired GB732139A (en) 1951-09-13 1952-09-10 Manufacture and application of new derivatives of 4:4-diaminostilbene disulphonic acid-(2:2)

Country Status (1)

Country Link
GB (1) GB732139A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE102004031101B4 (en) * 2004-06-28 2010-04-08 Kemira Oyj Use of Triazinylflavonataufhellern
CN109311826A (en) * 2016-05-17 2019-02-05 布兰科福有限责任两合公司 Fluorescent whitening agent and its mixture
CN114058079A (en) * 2021-12-23 2022-02-18 中交第一公路勘察设计研究院有限公司 Asphalt light stabilizer with strong ultraviolet absorption function and preparation method thereof

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE102004031101B4 (en) * 2004-06-28 2010-04-08 Kemira Oyj Use of Triazinylflavonataufhellern
CN109311826A (en) * 2016-05-17 2019-02-05 布兰科福有限责任两合公司 Fluorescent whitening agent and its mixture
CN114058079A (en) * 2021-12-23 2022-02-18 中交第一公路勘察设计研究院有限公司 Asphalt light stabilizer with strong ultraviolet absorption function and preparation method thereof

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