AT69359B - Process for producing colorations on vegetable fibers. - Google Patents
Process for producing colorations on vegetable fibers.Info
- Publication number
- AT69359B AT69359B AT69359DA AT69359B AT 69359 B AT69359 B AT 69359B AT 69359D A AT69359D A AT 69359DA AT 69359 B AT69359 B AT 69359B
- Authority
- AT
- Austria
- Prior art keywords
- sep
- vegetable fibers
- colorations
- producing
- aminonaphtol
- Prior art date
Links
- 239000000835 fiber Substances 0.000 title 1
- 235000013311 vegetables Nutrition 0.000 title 1
- DPJCXCZTLWNFOH-UHFFFAOYSA-N 2-nitroaniline Chemical compound NC1=CC=CC=C1[N+]([O-])=O DPJCXCZTLWNFOH-UHFFFAOYSA-N 0.000 description 2
- PZDXDOLQKQBWJV-UHFFFAOYSA-N 4-(nitromethoxy)aniline Chemical compound NC1=CC=C(OC[N+]([O-])=O)C=C1 PZDXDOLQKQBWJV-UHFFFAOYSA-N 0.000 description 2
- COHYTHOBJLSHDF-UHFFFAOYSA-N Indigo Chemical compound N1C2=CC=CC=C2C(=O)C1=C1C(=O)C2=CC=CC=C2N1 COHYTHOBJLSHDF-UHFFFAOYSA-N 0.000 description 2
- KHUFHLFHOQVFGB-UHFFFAOYSA-N 1-aminoanthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2N KHUFHLFHOQVFGB-UHFFFAOYSA-N 0.000 description 1
- XOGPDSATLSAZEK-UHFFFAOYSA-N 2-Aminoanthraquinone Chemical compound C1=CC=C2C(=O)C3=CC(N)=CC=C3C(=O)C2=C1 XOGPDSATLSAZEK-UHFFFAOYSA-N 0.000 description 1
- JRBJSXQPQWSCCF-UHFFFAOYSA-N 3,3'-Dimethoxybenzidine Chemical compound C1=C(N)C(OC)=CC(C=2C=C(OC)C(N)=CC=2)=C1 JRBJSXQPQWSCCF-UHFFFAOYSA-N 0.000 description 1
- XWPDPFLBSAPRCO-UHFFFAOYSA-N 4-(chloromethoxy)aniline Chemical compound NC1=CC=C(OCCl)C=C1 XWPDPFLBSAPRCO-UHFFFAOYSA-N 0.000 description 1
- TYMLOMAKGOJONV-UHFFFAOYSA-N 4-nitroaniline Chemical compound NC1=CC=C([N+]([O-])=O)C=C1 TYMLOMAKGOJONV-UHFFFAOYSA-N 0.000 description 1
- QPQKUYVSJWQSDY-UHFFFAOYSA-N 4-phenyldiazenylaniline Chemical compound C1=CC(N)=CC=C1N=NC1=CC=CC=C1 QPQKUYVSJWQSDY-UHFFFAOYSA-N 0.000 description 1
- RGCKGOZRHPZPFP-UHFFFAOYSA-N alizarin Chemical compound C1=CC=C2C(=O)C3=C(O)C(O)=CC=C3C(=O)C2=C1 RGCKGOZRHPZPFP-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- QFCSRGLEMDRBMN-UHFFFAOYSA-N n-(2-methylphenyl)nitramide Chemical compound CC1=CC=CC=C1N[N+]([O-])=O QFCSRGLEMDRBMN-UHFFFAOYSA-N 0.000 description 1
- RCTGMCJBQGBLKT-PAMTUDGESA-N scarlet red Chemical compound CC1=CC=CC=C1\N=N\C(C=C1C)=CC=C1\N=N\C1=C(O)C=CC2=CC=CC=C12 RCTGMCJBQGBLKT-PAMTUDGESA-N 0.000 description 1
- 229960005369 scarlet red Drugs 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
<Desc/Clms Page number 1>
EMI1.1
EMI1.2
<Desc/Clms Page number 2>
EMI2.1
<tb>
<tb> Diawoverblundung <SEP> von <SEP> Endkomponente <SEP> Nuance
<tb> o-Nitranilin <SEP> 2.6-Dichlorbenzoyl-1.7-aminonaphtol <SEP> gelblich-scharlach
<tb> p-Nitranilin <SEP> 2.4-Dichlorbenzoyl-1.7-aminonaphtol <SEP> scharlach
<tb> Nitrotoluidin
<tb> o-Chlorbenzoyl-1.7-aminonaphtol <SEP> rot
<tb> (CH2:NH2:NO2=1:4:3)
<tb> Nitroauisidin
<tb> o-Chlorbenzoyl-1.7-aminonaphtol <SEP> blaustichig-rot
<tb> (OCH2:NH2:NO2=1:2:5)
<tb> Nitroanisidin
<tb> p-Chlorbenzoyl-1.7-aminonaphtol <SEP> blaustichig-rot
<tb> (OCH2:NH2:NO2=1:2:5)
<tb> Nitroanisidin
<tb> m-Nitrobenzoyl-1.7-aminonaphtol <SEP> bordeaux
<tb> (OCH2:NH2:NO2=1:2:5)
<tb> Chloranisidin
<tb> 2.4-Dichlorbenzoyl-1.7-aminonaphtol <SEP> alizarinrot
<tb> (OCH2:NH2:Cl=1:2:
4)
<tb> Aminoazobenzol <SEP> Benzoyl-1.7-aminonaphtol <SEP> korinth
<tb> o-Dianisidin <SEP> m-itrobenzoyl-1.7-aminonaphtol <SEP> indigoblau
<tb> o-Chlor- <SEP> oder
<tb> α-Aminoanthrachinon <SEP> rot
<tb> o.p-Dichlorbenzoyl-1.7-aminonaphtol
<tb> o-Chlor- <SEP> oder
<tb> ss-Aminoanthrachinon <SEP> boideaux
<tb> o.p-Dichlorbenzoyl-1.7-aminonaphtol
<tb> o-Nitranilin <SEP> p-Toluolsulfo-1.7-aminonaphtol <SEP> scharlachrot
<tb>
EMI2.2
EMI2.3
<Desc / Clms Page number 1>
EMI1.1
EMI1.2
<Desc / Clms Page number 2>
EMI2.1
<tb>
<tb> Diawo blending <SEP> of <SEP> end component <SEP> Nuance
<tb> o-Nitraniline <SEP> 2.6-dichlorobenzoyl-1.7-aminonaphtol <SEP> yellowish-scarlet
<tb> p-Nitraniline <SEP> 2.4-dichlorobenzoyl-1.7-aminonaphtol <SEP> scarlet
<tb> nitrotoluidine
<tb> o-chlorobenzoyl-1.7-aminonaphtol <SEP> red
<tb> (CH2: NH2: NO2 = 1: 4: 3)
<tb> nitroauisidine
<tb> o-chlorobenzoyl-1.7-aminonaphtol <SEP> bluish-red
<tb> (OCH2: NH2: NO2 = 1: 2: 5)
<tb> nitroanisidine
<tb> p-chlorobenzoyl-1.7-aminonaphtol <SEP> bluish-red
<tb> (OCH2: NH2: NO2 = 1: 2: 5)
<tb> nitroanisidine
<tb> m-nitrobenzoyl-1.7-aminonaphtol <SEP> bordeaux
<tb> (OCH2: NH2: NO2 = 1: 2: 5)
<tb> chloranisidine
<tb> 2.4-dichlorobenzoyl-1.7-aminonaphtol <SEP> alizarin red
<tb> (OCH2: NH2: Cl = 1: 2:
4)
<tb> Aminoazobenzene <SEP> Benzoyl-1.7-aminonaphtol <SEP> korinth
<tb> o-Dianisidine <SEP> m-itrobenzoyl-1.7-aminonaphtol <SEP> indigo blue
<tb> o-chlorine- <SEP> or
<tb> α-Aminoanthraquinone <SEP> red
<tb> o.p-dichlorobenzoyl-1,7-aminonaphtol
<tb> o-chlorine- <SEP> or
<tb> ss-aminoanthraquinone <SEP> boideaux
<tb> o.p-dichlorobenzoyl-1,7-aminonaphtol
<tb> o-Nitraniline <SEP> p-Toluenesulfo-1.7-aminonaphtol <SEP> scarlet red
<tb>
EMI2.2
EMI2.3
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AT69359T | 1914-06-19 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AT69359B true AT69359B (en) | 1915-07-10 |
Family
ID=30119769
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT69359D AT69359B (en) | 1914-06-19 | 1914-06-19 | Process for producing colorations on vegetable fibers. |
Country Status (1)
| Country | Link |
|---|---|
| AT (1) | AT69359B (en) |
-
1914
- 1914-06-19 AT AT69359D patent/AT69359B/en active
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