WO2012138049A1 - Non-aqueous fluid marker containing n-benzyl-n-ethylaniline and method for preparing the same - Google Patents

Non-aqueous fluid marker containing n-benzyl-n-ethylaniline and method for preparing the same Download PDF

Info

Publication number
WO2012138049A1
WO2012138049A1 PCT/KR2012/000990 KR2012000990W WO2012138049A1 WO 2012138049 A1 WO2012138049 A1 WO 2012138049A1 KR 2012000990 W KR2012000990 W KR 2012000990W WO 2012138049 A1 WO2012138049 A1 WO 2012138049A1
Authority
WO
WIPO (PCT)
Prior art keywords
group
aqueous fluid
marker
acid
benzyl
Prior art date
Application number
PCT/KR2012/000990
Other languages
French (fr)
Other versions
WO2012138049A4 (en
Inventor
Seung Rim Shin
Kun Jun
Seong Wook Kong
Original Assignee
Korea Research Institute Of Chemical Technology
Inwoo Corporation
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=46969406&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=WO2012138049(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Korea Research Institute Of Chemical Technology, Inwoo Corporation filed Critical Korea Research Institute Of Chemical Technology
Publication of WO2012138049A1 publication Critical patent/WO2012138049A1/en
Publication of WO2012138049A4 publication Critical patent/WO2012138049A4/en

Links

Images

Classifications

    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B29/00—Monoazo dyes prepared by diazotising and coupling
    • C09B29/0025—Monoazo dyes prepared by diazotising and coupling from diazotized amino heterocyclic compounds
    • C09B29/0074—Monoazo dyes prepared by diazotising and coupling from diazotized amino heterocyclic compounds the heterocyclic ring containing nitrogen and sulfur as heteroatoms
    • C09B29/0077—Monoazo dyes prepared by diazotising and coupling from diazotized amino heterocyclic compounds the heterocyclic ring containing nitrogen and sulfur as heteroatoms containing a five-membered heterocyclic ring with one nitrogen and one sulfur as heteroatoms
    • C09B29/0085—Thiazoles or condensed thiazoles
    • C09B29/0088—Benzothiazoles
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N31/00—Investigating or analysing non-biological materials by the use of the chemical methods specified in the subgroup; Apparatus specially adapted for such methods
    • G01N31/22—Investigating or analysing non-biological materials by the use of the chemical methods specified in the subgroup; Apparatus specially adapted for such methods using chemical indicators
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C245/00—Compounds containing chains of at least two nitrogen atoms with at least one nitrogen-to-nitrogen multiple bond
    • C07C245/02—Azo compounds, i.e. compounds having the free valencies of —N=N— groups attached to different atoms, e.g. diazohydroxides
    • C07C245/06—Azo compounds, i.e. compounds having the free valencies of —N=N— groups attached to different atoms, e.g. diazohydroxides with nitrogen atoms of azo groups bound to carbon atoms of six-membered aromatic rings
    • C07C245/08—Azo compounds, i.e. compounds having the free valencies of —N=N— groups attached to different atoms, e.g. diazohydroxides with nitrogen atoms of azo groups bound to carbon atoms of six-membered aromatic rings with the two nitrogen atoms of azo groups bound to carbon atoms of six-membered aromatic rings, e.g. azobenzene
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B29/00—Monoazo dyes prepared by diazotising and coupling
    • C09B29/0003—Monoazo dyes prepared by diazotising and coupling from diazotized anilines
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B29/00—Monoazo dyes prepared by diazotising and coupling
    • C09B29/06—Monoazo dyes prepared by diazotising and coupling from coupling components containing amino as the only directing group
    • C09B29/08—Amino benzenes
    • C09B29/0805—Amino benzenes free of acid groups
    • C09B29/0807—Amino benzenes free of acid groups characterised by the amino group
    • C09B29/0809—Amino benzenes free of acid groups characterised by the amino group substituted amino group
    • C09B29/081—Amino benzenes free of acid groups characterised by the amino group substituted amino group unsubstituted alkylamino, alkenylamino, alkynylamino, cycloalkylamino, aralkylamino or arylamino
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B67/00—Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
    • C09B67/0071—Process features in the making of dyestuff preparations; Dehydrating agents; Dispersing agents; Dustfree compositions
    • C09B67/0083—Solutions of dyes
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/75—Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated
    • G01N21/77—Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated by observing the effect on a chemical indicator
    • G01N21/78—Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated by observing the effect on a chemical indicator producing a change of colour
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/26—Oils; Viscous liquids; Paints; Inks

Definitions

  • the present invention relates to an azo dye represented by the following Formula 1, which can be used as a marker for a non-aqueous fluid product, and a method for preparing the same.
  • Recently, extensive research aimed at developing a novel azo dye suitable for a variety of applications by adding functionality to the dyes has continued to progress.
  • a heteroazo disperse dye using N -benzyl- N -ethylaniline as a coupler exhibits solvatochromism.
  • a maximum absorption wavelength ( ⁇ max ) of a compound represented by the following Formula 2 was 503 nm in a chloroform, but it shifted to a longer wavelength of 614 nm in a glacial acetic acid by 111 nm.
  • the methods for identifying the non-aqueous fluid products are as follows ; a method for exhibiting a color by adding a marker to a non-aqueous fluid product and then adding an acid or a base as a developing agent thereto, a quantitative measurement using a dye absorbing in a near infrared region, etc., are used.
  • these methods have some problems in that the color may not be detected as the effect of the marker is lost over time, the developing agent used to develop a detectable color of markers may be difficult to handle as it is easily decomposed, and the good quantitative measurement may not perform as the components of the marker are slowly decomposed in water or organic solvent.
  • U.S. Patent No. 6,514,917 discloses that a variety of azo dyes, which are easily handled and have high storage stability, can be used as markers to label petroleum products by reaction with an organic or inorganic acid.
  • US Patent No. 6,514,917 discloses a method for quantifying a marker using an organic phosphoric or sulfonic acid as a developing agent miscible with petroleum products without extraction to an aqueous phase from the petroleum products.
  • the materials to be useful as markers for non-aqueous fluid products must have high solubility in a target product, have excellent storage stability, be detected even in a small amount, be easily detected, and be used in various non-aqueous fluid products.
  • it is very difficult to use the existing azo dyes as a marker in terms of solubility and coloration in some non-aqueous fluid products such as petroleum products, solvents, inks, lubricants, etc.
  • an object of the present invention is to provide a novel yellow azo disperse dye for identifying a non-aqueous fluid product, and a method for preparing the same.
  • the present invention provides a non-aqueous fluid marker containing N -benzyl- N -ethylaniline represented by the following Formula 1:
  • R is a C 1 to C 12 alkyl group, a C 1 to C 12 alkoxy group, a C 1 to C 12 hydroxyalkyl group, a C 1 to C 12 hydroxyalkoxyalkyl group, a C 1 to C 12 alkylphenyl group, a C 1 to C 12 alkoxyphenyl group, a nitro group, a cyano group or a halogen atom.
  • the present invention provides a method for preparing a non-aqueous fluid marker, comprising: diazotizing an aniline derivative represented by the following Formula 3; and reacting N -benzyl- N -ethylaniline represented by the following Formula 4 with the diazotized aniline derivative:
  • R is a C 1 to C 12 alkyl group, a C 1 to C 12 alkoxy group, a C 1 to C 12 hydroxyalkyl group, a C 1 to C 12 hydroxyalkoxyalkyl group, a C 1 to C 12 alkylphenyl group, a C 1 to C 12 alkoxyphenyl group, a nitro group, a cyano group or a halogen atom.
  • the present invention provides a method for identifying a non-aqueous fluid product, comprising: dissolving a non-aqueous fluid marker, which contains N -benzyl- N -ethylaniline represented by the above Formula 1, in a target product; and developing a color of the target product with an acid developer.
  • FIG. 1 is a graph illustrating a change in UV-VIS absorption spectra before and after addition of an acid developer to a marker solution containing an azo disperse dye prepared in Example 1, in which a change in maximum absorption wavelength is shown.
  • the present invention provides a non-aqueous fluid marker containing N -benzyl- N -ethylaniline represented by the following Formula 1:
  • R is a C 1 to C 12 alkyl group, a C 1 to C 12 alkoxy group, a C 1 to C 12 hydroxyalkyl group, a C 1 to C 12 hydroxyalkoxyalkyl group, a C 1 to C 12 alkylphenyl group, a C 1 to C 12 alkoxyphenyl group, a nitro group, a cyano group or a halogen atom.
  • alkyl group refers to a linear or branched aliphatic saturated hydrocarbon group having 1 to 12 carbon atoms. More particularly, the alkyl group may include a methyl group, an ethyl group, a n -propyl group, an i -propyl group, a n -butyl group, an i -butyl group, a t -butyl group, an n -pentyl group, an i -pentyl group, a n -hexyl group, an i -hexyl group, a n -heptyl group, an i -heptyl group, a n -octyl group, an i -octyl group, a n -nonyl group, an i -nonyl group, a n -dodecyl group, an i -dodecyl group,
  • alkoxy group refers to a linear or branched aliphatic alkoxy group having 1 to 12 carbon atoms. More particularly, the alkyl group may include a methoxy group, an ethoxy group, a n -propyloxy group, an i -propyloxy group, an n -butoxy group, an i -butoxy group, a t -butoxy group, an n -pentoxy group, an i -pentoxy group, etc.
  • hydroxyalkyl group refers to a OH-alkyl group in which a hydroxyl group is bound to the aforementioned alkyl group. More particularly, the hydroxyalkyl group may include a hydroxymethyl group, a hydroxyethyl group, a hydroxy- n -propyl group, a hydroxy- n -butyl group, a hydroxy- i -butyl group, a hydroxy- n -pentyl group, a hydroxy- i -pentyl group, a hydroxy- n -hexyl group, a hydroxy- i -hexyl group, etc.
  • hydroxyalkoxyalkyl group refers to a hydroxyalkyl-O-alkyl group in which an alkoxy group is bound to the hydroxyalkyl group. More particularly, the hydroxyalkoxyalkyl group may include a hydroxyethoxymethyl group, a hydroxyethoxyethyl group, a hydroxymethoxypropyl group, a hydroxyethoxypropyl group, a hydroxyethoxybutyl group, a hydroxyethoxypentyl group, a hydroxyethoxyhexyl group, etc.
  • alkylphenyl group may include a methylphenyl group, an ethylphenyl group, a n -propylphenyl group, an n -butylphenyl group, etc.
  • alkoxyphenyl group may include a methoxyphenyl group, an ethoxyphenyl group, a n -propyloxyphenyl group, a n -butoxyphenyl group, etc.
  • halogen atom is a fluorine atom, a chlorine atom, a bromine atom or an iodine atom.
  • a particularly preferred the oil marker is a compound in which R in Formula 1 is a C 1 to C 12 alkyl group or a C 1 to C 12 alkoxy group.
  • the present invention provides a method for preparing a non-aqueous fluid marker containing N -benzyl- N -ethylaniline represented by the Formula 1.
  • the non-aqueous fluid marker may be prepared by diazotizing an aniline derivative represented by the following Formula 3 and reacting the diazotized aniline derivative with N -benzyl- N -ethylaniline represented by the following Formula 4.
  • R has the same meaning as defined above.
  • the diazotization is performed by dispersing an aniline derivative in water or acetic acid or in a mixed solution of acetic acid and propionic acid at 0-10 °C and adding concentrated hydrochloric acid and NaNO 2 or HO 3 SONO to react with each other.
  • the mixed solution of the acetic acid and propionic acid may be mixed in a volume ratio of 5:1.
  • the diazotized aniline derivative may be reacted with the N -benzyl- N -ethylaniline represented by the above Formula 4 to give a yellow azo disperse dye represented by the above Formula 1.
  • the N -benzyl- N -ethylaniline may be dissolved in acetic acid or in a mixed solution of acetic acid and propionic acid in a separate container and maintained at 0-10 °C, and the prepared solution may then be added to the diazotized solution to carry out a coupling reaction at 0-10 °C.
  • the acetic acid and propionic acid may be mixed in a volume ratio of 5:1.
  • the present invention provides a method for identifying a target product using a non-aqueous fluid marker containing N -benzyl- N -ethylaniline represented by the above Formula 1.
  • the non-aqueous fluid marker containing the N -benzyl- N -ethylaniline represented by the above Formula 1 according to the present invention shows a purple color by reacting with acid developer when the non-aqueous fluid marker is dissolved in a target product. That is, when the marker according to the present invention reacts with the acid developer in the non-aqueous fluid product, a maximum absorption wavelength of the non-aqueous fluid product shifts from 410 nm to a longer wavelength of 560 nm. Therefore, the color of the non-aqueous fluid product is changed from its own color (i.e., yellow) to purple. Accordingly, it is possible to distinguish the non-aqueous fluid product including the marker according to the present invention from marker-free products.
  • the non-aqueous fluid manufacturer dissolves the marker according to the present invention in the non-aqueous fluid product, it is possible to easily distinguish the product from other companies’ products using the acid developer. Therefore, it is possible to control the quality of the product in the distribution process.
  • the type of non-aqueous fluids to be distinguished is not particularly limited, and the non-aqueous fluid may include gasoline, diesel, kerosene, biodiesel, bioethanol, xylene, ink, non-aqueous lubricant, solvent, and mixtures thereof.
  • the acid developer may include an organic acid such as dodecyl sulfonic acid, and an inorganic acid such as sulfuric acid or phosphoric acid.
  • the dodecyl sulfonic acid may be used as the acid developer.
  • N -benzyl- N -ethylaniline as a coupler was dissolved in 20 ml of an acid mixture (where the volume ratio of acetic acid to propionic acid was 5:1) and maintained at 5-10 °C. Then, the prepared solution was slowly added to the diazotized solution and stirred at 5-10 °C for 3.5 hours. 25 g of sodium acetate (NaOAc) was added to the reaction solution and stirred at room temperature for 30 minutes. The reaction mixture was poured into 250 g of ice-water, stirred for 1 hour to produce a solid product, and filtered.
  • NaOAc sodium acetate
  • the isolated product was dispersed in 100 ml of isopropyl alcohol, stirred at room temperature for 30 minutes, filtered, and then dried, thereby obtaining a marker according to the present invention as a yellow solid azo disperse dye represented by the following Formula 5.
  • non-aqueous fluid markers containing N -benzyl- N -ethylaniline according to the present invention were prepared in the same manner as in Example 1, except that aniline derivatives as listed in the following Table 1 were used.
  • Example 1 4-C 4 H 9 5.36 76.3
  • Example 2 4-tert-C 4 H 9 5.36 78.2
  • Example 3 4-C 12 H 25 9.40 41.4
  • Example 4 4-CH 3 3.85 69.9
  • Example 5 4-OCH 3 4.43 17.3
  • N -benzyl- N -ethylaniline as a coupler was dissolved in 10 ml of an acid mixture (where the volume ratio of acetic acid to propionic acid was 5:1) and maintained at 5-10 °C. Then, the prepared solution was slowly added to the diazotized solution and stirred at 0-5 °C for 2 hours. 2.5 g of NaOAc was added to the reaction mixture and stirred at room temperature for 30 minutes. The reaction mixture was poured into 50 g of ice-water, stirred for 1 hour to produce a solid product, and filtered.
  • Example 1 371 A; 0.92(3H, t), 1.25(3H, t), 1.36(2H, sextet), 1.62(2H, qt), 2.66(2H, t), 3.64(2H, q), 4.70(2H, s), 6.84(2H, d), 7.23-7.35(7H, m), 7.73(2H, d), 7.78(2H, d)
  • Example 2 371 C; 1.26(3H, t), 1.33(9H, s), 3.56(2H, q), 4.61(2H, s), 6.75(2H, d), 7.20-7.34(5H, m), 7.45(2H, d), 7.74(2H, d), 7.81(2H, d)
  • Example 3 483 C 0.86(3H, t), 1.24-1.28(20H, m), 1.57-1.64(4H,
  • Example 1 402 A 1.30(3H, t), 3.72(2H, q), 3.89(3H, s), 4.81 (2H, s), 6.94(2H, d), 7.09(1H, dd), 7.26-7.37(5H, m), 7.50(1H, d), 7.83-7.90(3H, m)
  • Example 2 320 A 1.27(3H, t), 2.44(3H, s), 3.68(2H, q), 4.76 (2H, s), 6.36(1H, s), 6.87(2H, d), 7.24-7.36(5H, m), 7.80(2H, d) * Solvent for 1 H NMR ; CDCl 3 (C), Acetone- d 6 (A)
  • Test Example 1 Test for acid reactivity of yellow azo disperse dyes
  • UV-VIS molar absorption coefficients ( ⁇ ) and maximum absorption wavelengths ( ⁇ max ) of the samples prepared in (1) were measured. Then, 10 ⁇ l of the acid developer solution prepared in (2) was added to each sample and stirred for 1 minute. Then, the UV-VIS molar absorption coefficient ( ⁇ ) and maximum absorption wavelength ( ⁇ max ) of each sample were measured to observe a change in color.
  • the UV-VIS molar absorption coefficient and maximum absorption wavelength were measured using a UV-VIS-NIR spectrophotometer (UV-3101 PC, SHIMADZU). The measurement results are listed in the following Table 3 and shown in FIG. 1.
  • the alkyl group-substituted yellow azo disperse dyes prepared in Examples 1 -4 showed a distinct purple color and a maximum absorption wavelength was shifted to a longer wavelength by 150 nm or more when the dodecylbenzene sulfonic acid solution was added to the marker solution.
  • the methoxy group-substituted yellow azo disperse dye prepared in Example 5 had a higher absorbance at 476 nm than at 565 nm as shown in the above Table 3, when the dodecylbenzene sulfonic acid solution was added to the marker solution. The color change of the marker solution could be observed, however the appearance of color was not distinctive.
  • alkyl group-substituted yellow azo disperse dyes prepared in Examples 1-4 which exhibits their distinct colors by addition of dodecylbenzene sulfonic acid solution as the acid developer, can be more effectively used as an acid-reactive marker.
  • the marker containing N -benzyl- N -ethylaniline according to the present invention exhibits high solubility in non-aqueous fluid products, has excellent storage stability, can be detected even in a small amount, and can develop a distinct color by reaction with an organic acid such as dodecylbenzene sulfonic acid and an inorganic acid such as sulfuric acid or phosphoric acid in the non-aqueous fluid product. Therefore, when the marker is added to a product, the product can be easily distinguished from other companies’ products containing no marker or illegally distributed products such as adulterated gasoline, which makes it possible to easily control the quality of the product in the distribution process.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Biochemistry (AREA)
  • Pathology (AREA)
  • Analytical Chemistry (AREA)
  • Immunology (AREA)
  • General Health & Medical Sciences (AREA)
  • General Physics & Mathematics (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Biophysics (AREA)
  • Molecular Biology (AREA)
  • Food Science & Technology (AREA)
  • Medicinal Chemistry (AREA)
  • Plasma & Fusion (AREA)
  • Investigating Or Analyzing Non-Biological Materials By The Use Of Chemical Means (AREA)

Abstract

The present invention provides an azo dye which can be used as a marker for a non-aqueous fluid product containing N-benzyl-N-ethylaniline, and a method for preparing the same. The marker containing N-benzyl-N-ethylaniline according to the present invention exhibits high solubility in non-aqueous fluid products, has excellent storage stability, can be detected even in a small amount, and can exhibit a distinct color by reaction with an acid developer in the non-aqueous fluid product. Therefore, when the marker is added to a non-aqueous fluid product, the product can be easily distinguished from other companies' products containing no marker, which makes it possible to easily control the quality of the non-aqueous fluid product in the distribution process.

Description

NON-AQUEOUS FLUID MARKER CONTAINING N-BENZYL-N-ETHYLANILINE AND METHOD FOR PREPARING THE SAME
The present invention relates to an azo dye represented by the following Formula 1, which can be used as a marker for a non-aqueous fluid product, and a method for preparing the same.
Formula 1
Figure PCTKR2012000990-appb-I000001
A dye containing an azo group (-N=N-) as a chromophore is called an azo dye, and the azo dyes account for 50 % or more of the currently used dyes. Recently, extensive research aimed at developing a novel azo dye suitable for a variety of applications by adding functionality to the dyes has continued to progress.
According to a recent report (M. R. Yazdanbakhsh. et. al., J. Mol. Liquid. 151: 107-112 (2010)), a heteroazo disperse dye using N-benzyl-N-ethylaniline as a coupler exhibits solvatochromism. For example, a maximum absorption wavelength (λmax) of a compound represented by the following Formula 2 was 503 nm in a chloroform, but it shifted to a longer wavelength of 614 nm in a glacial acetic acid by 111 nm.
Formula 2
Figure PCTKR2012000990-appb-I000002
At present, the methods for identifying the non-aqueous fluid products are as follows ; a method for exhibiting a color by adding a marker to a non-aqueous fluid product and then adding an acid or a base as a developing agent thereto, a quantitative measurement using a dye absorbing in a near infrared region, etc., are used. However, these methods have some problems in that the color may not be detected as the effect of the marker is lost over time, the developing agent used to develop a detectable color of markers may be difficult to handle as it is easily decomposed, and the good quantitative measurement may not perform as the components of the marker are slowly decomposed in water or organic solvent.
U.S. Patent No. 6,514,917, U.S. Patent No. 5,737,871, U.S. Patent No. 5,490,872, WO 1995-017483, and WO 1999-067346 disclose that a variety of azo dyes, which are easily handled and have high storage stability, can be used as markers to label petroleum products by reaction with an organic or inorganic acid. In particular, US Patent No. 6,514,917 discloses a method for quantifying a marker using an organic phosphoric or sulfonic acid as a developing agent miscible with petroleum products without extraction to an aqueous phase from the petroleum products.
The materials to be useful as markers for non-aqueous fluid products must have high solubility in a target product, have excellent storage stability, be detected even in a small amount, be easily detected, and be used in various non-aqueous fluid products. However, it is very difficult to use the existing azo dyes as a marker in terms of solubility and coloration in some non-aqueous fluid products such as petroleum products, solvents, inks, lubricants, etc.
As a result of continuous studies to develop a compound which can exhibit a distinct color in a non-aqueous fluid product and facilitate quantitative measurement without extraction to an aqueous phase, the present inventors completed this invention by synthesizing several types of yellow azo disperse dyes containing N-benzyl-N-ethylaniline and these dyes could be effectively used as markers for non-aqueous fluid products.
Accordingly, an object of the present invention is to provide a novel yellow azo disperse dye for identifying a non-aqueous fluid product, and a method for preparing the same.
In one aspect, the present invention provides a non-aqueous fluid marker containing N-benzyl-N-ethylaniline represented by the following Formula 1:
Formula 1
Figure PCTKR2012000990-appb-I000003
wherein R is a C1 to C12 alkyl group, a C1 to C12 alkoxy group, a C1 to C12 hydroxyalkyl group, a C1 to C12 hydroxyalkoxyalkyl group, a C1 to C12 alkylphenyl group, a C1 to C12 alkoxyphenyl group, a nitro group, a cyano group or a halogen atom.
In another aspect, the present invention provides a method for preparing a non-aqueous fluid marker, comprising: diazotizing an aniline derivative represented by the following Formula 3; and reacting N-benzyl-N-ethylaniline represented by the following Formula 4 with the diazotized aniline derivative:
Figure PCTKR2012000990-appb-I000004
wherein R is a C1 to C12 alkyl group, a C1 to C12 alkoxy group, a C1 to C12 hydroxyalkyl group, a C1 to C12 hydroxyalkoxyalkyl group, a C1 to C12 alkylphenyl group, a C1 to C12 alkoxyphenyl group, a nitro group, a cyano group or a halogen atom.
In still another aspect, the present invention provides a method for identifying a non-aqueous fluid product, comprising: dissolving a non-aqueous fluid marker, which contains N-benzyl-N-ethylaniline represented by the above Formula 1, in a target product; and developing a color of the target product with an acid developer.
The above and other features of the present invention will now be described in detail with reference to certain exemplary embodiments thereof illustrated the accompanying drawings which are given hereinbelow by way of illustration only, and thus are not limitative of the present invention, and wherein:
FIG. 1 is a graph illustrating a change in UV-VIS absorption spectra before and after addition of an acid developer to a marker solution containing an azo disperse dye prepared in Example 1, in which a change in maximum absorption wavelength is shown.
Hereinafter, preferred embodiments of the present invention will be described in detail with reference to the accompanying drawings.
The present invention provides a non-aqueous fluid marker containing N-benzyl-N-ethylaniline represented by the following Formula 1:
Formula 1
Figure PCTKR2012000990-appb-I000005

wherein R is a C1 to C12 alkyl group, a C1 to C12 alkoxy group, a C1 to C12 hydroxyalkyl group, a C1 to C12 hydroxyalkoxyalkyl group, a C1 to C12 alkylphenyl group, a C1 to C12 alkoxyphenyl group, a nitro group, a cyano group or a halogen atom.
The above-described substituents will be described in detail below.
The term “alkyl group” refers to a linear or branched aliphatic saturated hydrocarbon group having 1 to 12 carbon atoms. More particularly, the alkyl group may include a methyl group, an ethyl group, a n-propyl group, an i-propyl group, a n-butyl group, an i-butyl group, a t-butyl group, an n-pentyl group, an i-pentyl group, a n-hexyl group, an i-hexyl group, a n-heptyl group, an i-heptyl group, a n-octyl group, an i-octyl group, a n-nonyl group, an i-nonyl group, a n-dodecyl group, an i-dodecyl group, etc.
The term “alkoxy group” refers to a linear or branched aliphatic alkoxy group having 1 to 12 carbon atoms. More particularly, the alkyl group may include a methoxy group, an ethoxy group, a n-propyloxy group, an i-propyloxy group, an n-butoxy group, an i-butoxy group, a t-butoxy group, an n-pentoxy group, an i-pentoxy group, etc.
The term “hydroxyalkyl group” refers to a OH-alkyl group in which a hydroxyl group is bound to the aforementioned alkyl group. More particularly, the hydroxyalkyl group may include a hydroxymethyl group, a hydroxyethyl group, a hydroxy-n-propyl group, a hydroxy-n-butyl group, a hydroxy-i-butyl group, a hydroxy-n-pentyl group, a hydroxy-i-pentyl group, a hydroxy-n-hexyl group, a hydroxy-i-hexyl group, etc.
The term “hydroxyalkoxyalkyl group” refers to a hydroxyalkyl-O-alkyl group in which an alkoxy group is bound to the hydroxyalkyl group. More particularly, the hydroxyalkoxyalkyl group may include a hydroxyethoxymethyl group, a hydroxyethoxyethyl group, a hydroxymethoxypropyl group, a hydroxyethoxypropyl group, a hydroxyethoxybutyl group, a hydroxyethoxypentyl group, a hydroxyethoxyhexyl group, etc.
The term “alkylphenyl group” may include a methylphenyl group, an ethylphenyl group, a n-propylphenyl group, an n-butylphenyl group, etc.
The term “alkoxyphenyl group” may include a methoxyphenyl group, an ethoxyphenyl group, a n-propyloxyphenyl group, a n-butoxyphenyl group, etc.
The term “halogen atom” is a fluorine atom, a chlorine atom, a bromine atom or an iodine atom.
According to the present invention, a particularly preferred the oil marker is a compound in which R in Formula 1 is a C1 to C12 alkyl group or a C1 to C12 alkoxy group.
Moreover, the present invention provides a method for preparing a non-aqueous fluid marker containing N-benzyl-N-ethylaniline represented by the Formula 1. The non-aqueous fluid marker may be prepared by diazotizing an aniline derivative represented by the following Formula 3 and reacting the diazotized aniline derivative with N-benzyl-N-ethylaniline represented by the following Formula 4.
Figure PCTKR2012000990-appb-I000006
In the above Formulas 1 and 3, R has the same meaning as defined above.
In more detail, in the step of diazotizing an aniline derivative represented by the above Formula 3, the diazotization is performed by dispersing an aniline derivative in water or acetic acid or in a mixed solution of acetic acid and propionic acid at 0-10 °C and adding concentrated hydrochloric acid and NaNO2 or HO3SONO to react with each other. Preferably, in the mixed solution of the acetic acid and propionic acid may be mixed in a volume ratio of 5:1.
Then, the diazotized aniline derivative may be reacted with the N-benzyl-N-ethylaniline represented by the above Formula 4 to give a yellow azo disperse dye represented by the above Formula 1. The N-benzyl-N-ethylaniline may be dissolved in acetic acid or in a mixed solution of acetic acid and propionic acid in a separate container and maintained at 0-10 °C, and the prepared solution may then be added to the diazotized solution to carry out a coupling reaction at 0-10 °C. Preferably, in the mixed solution of acetic acid and propionic acid, the acetic acid and propionic acid may be mixed in a volume ratio of 5:1.
Furthermore, the present invention provides a method for identifying a target product using a non-aqueous fluid marker containing N-benzyl-N-ethylaniline represented by the above Formula 1.
The non-aqueous fluid marker containing the N-benzyl-N-ethylaniline represented by the above Formula 1 according to the present invention shows a purple color by reacting with acid developer when the non-aqueous fluid marker is dissolved in a target product. That is, when the marker according to the present invention reacts with the acid developer in the non-aqueous fluid product, a maximum absorption wavelength of the non-aqueous fluid product shifts from 410 nm to a longer wavelength of 560 nm. Therefore, the color of the non-aqueous fluid product is changed from its own color (i.e., yellow) to purple. Accordingly, it is possible to distinguish the non-aqueous fluid product including the marker according to the present invention from marker-free products. That is, when the non-aqueous fluid manufacturer dissolves the marker according to the present invention in the non-aqueous fluid product, it is possible to easily distinguish the product from other companies’ products using the acid developer. Therefore, it is possible to control the quality of the product in the distribution process. The type of non-aqueous fluids to be distinguished is not particularly limited, and the non-aqueous fluid may include gasoline, diesel, kerosene, biodiesel, bioethanol, xylene, ink, non-aqueous lubricant, solvent, and mixtures thereof. Moreover, the acid developer may include an organic acid such as dodecyl sulfonic acid, and an inorganic acid such as sulfuric acid or phosphoric acid. Preferably, the dodecyl sulfonic acid may be used as the acid developer.
Next, the present invention will be described in detail with reference to Examples, but the present invention is not limited by the following Examples.

EXAMPLES
Example 1
5.37 g (0.036 mol) of 4-butylaniline as a diazo compound was added to 70 ml ; of an acid mixture (where the volume ratio of acetic acid to propionic acid was 5: 1) and stirred at room temperature for about 20 minutes. Then, 7.7 ml (0.089 mol) of 35% hydrochloric acid was added to the resulting reactant and then maintained at 5-10 °C. Thereafter, 13 ml (0.039 mol) of 3N NaNO2 was slowly added thereto so that the reaction temperature would not rise and stirred at 5-10 °C for 1.5 hours, thereby completing diazotization. Finally, a small amount of sulfamic acid was added to remove excess nitrous acid.
Meanwhile, 7.6 g (0.036 mol) of N-benzyl-N-ethylaniline as a coupler was dissolved in 20 ml of an acid mixture (where the volume ratio of acetic acid to propionic acid was 5:1) and maintained at 5-10 °C. Then, the prepared solution was slowly added to the diazotized solution and stirred at 5-10 °C for 3.5 hours. 25 g of sodium acetate (NaOAc) was added to the reaction solution and stirred at room temperature for 30 minutes. The reaction mixture was poured into 250 g of ice-water, stirred for 1 hour to produce a solid product, and filtered. In order to purify the product, the isolated product was dispersed in 100 ml of isopropyl alcohol, stirred at room temperature for 30 minutes, filtered, and then dried, thereby obtaining a marker according to the present invention as a yellow solid azo disperse dye represented by the following Formula 5.
Formula 5
Figure PCTKR2012000990-appb-I000007

Examples 2-5
As yellow solid azo disperse dyes, non-aqueous fluid markers containing N-benzyl-N-ethylaniline according to the present invention were prepared in the same manner as in Example 1, except that aniline derivatives as listed in the following Table 1 were used.
The aniline derivatives represented by the above Formula 3 prepared in Examples 1-5, the amounts of aniline derivatives used, and their synthesis yields are listed in the following Table 1.
Figure PCTKR2012000990-appb-I000008
R Amount of diazo compound used (g) Yield (%)
Example 1 4-C4H9 5.36 76.3
Example 2 4-tert-C4H9 5.36 78.2
Example 3 4-C12H25 9.40 41.4
Example 4 4-CH3 3.85 69.9
Example 5 4-OCH3 4.43 17.3

Comparative Example 1
0.9 g (0.005 mol) of 2-amino-6-methoxybenzothiazole as a diazo compound was added to 10 ml of an acid mixture (where the volume ratio of acetic acid to propionic acid was 5:1) and stirred at room temperature for about 20 minutes. Then, the resulting reactant was maintained at 5-10 °C. Thereafter, 1.05 ml (0.0053 mol) of 40% HO3SONO was slowly added thereto so that the reaction temperature would not rise, and the resulting reactant was stirred at 5-10 °C for 1.5 hours, thereby completing diazotization. Finally, a small amount of sulfamic acid was added to remove excess nitrous acid.
Meanwhile, 1.05 g (0.005 mol) of N-benzyl-N-ethylaniline as a coupler was dissolved in 10 ml of an acid mixture (where the volume ratio of acetic acid to propionic acid was 5:1) and maintained at 5-10 °C. Then, the prepared solution was slowly added to the diazotized solution and stirred at 0-5 °C for 2 hours. 2.5 g of NaOAc was added to the reaction mixture and stirred at room temperature for 30 minutes. The reaction mixture was poured into 50 g of ice-water, stirred for 1 hour to produce a solid product, and filtered. In order to purify the product, the isolated product was dispersed 20 ml of isopropyl alcohol, stirred at room temperature for 30 minutes, filtered, and then dried, thereby obtaining 1.78 g of a red solid azo disperse dye represented by the following Formula 2 (yield = 88.6 %).
Formula 2
Figure PCTKR2012000990-appb-I000009

Comparative Example 2
The compound of Formula 6 was prepared according to the method described in Comparative Example 1 using 0.49 g (0.005 mol) of 3-amino-5-methylisoxazole as diazo compound, thereby obtaining 1.20 g of a yellow solid azo disperse dye (yield = 75 %) represented by the following Formula 6.
Formula 6
Figure PCTKR2012000990-appb-I000010
The mass spectra (m/e) and 1H NMR spectra data for confirming the respective structures of the azo disperse dyes containing N-benzyl-N-ethylaniline prepared in Examples 1-5 and Comparative Examples 1 and 2 are listed in the following Table 2.
m/e 1H NMR* (δ ppm )
Example 1 371 A; 0.92(3H, t), 1.25(3H, t), 1.36(2H, sextet), 1.62(2H, qt), 2.66(2H, t), 3.64(2H, q), 4.70(2H, s), 6.84(2H, d), 7.23-7.35(7H, m), 7.73(2H, d), 7.78(2H, d)
Example 2 371 C; 1.26(3H, t), 1.33(9H, s), 3.56(2H, q), 4.61(2H, s), 6.75(2H, d), 7.20-7.34(5H, m), 7.45(2H, d), 7.74(2H, d), 7.81(2H, d)
Example 3 483 C; 0.86(3H, t), 1.24-1.28(20H, m), 1.57-1.64(4H, m), 2.63(2H, t), 3.56(2H, q), 4.62(2H, s), 6.75(2H, d), 7.20-7.34(7H, m), 7.73(2H, d), 7.81(2H, d)
Example 4 329 C; 1.25(3H, t), 2.38(3H, s), 3.55(2H, q), 4.61(2H, s), 6.75(2H, d), 7.20-7.31(7H, m), 7.72(2H, d), 7.80(2H, d)
Example 5 345 A; 1.25(3H, t), 3.63(2H, q), 3.86(3H, s), 4.70 (2H, s), 6.83(2H, d), 7.03(2H, d), 7.21-7.35(7H, m), 7.74(2H, d), 7.78(2H, d)
Comp.
Example 1		 402 A; 1.30(3H, t), 3.72(2H, q), 3.89(3H, s), 4.81 (2H, s), 6.94(2H, d), 7.09(1H, dd), 7.26-7.37(5H, m), 7.50(1H, d), 7.83-7.90(3H, m)
Comp.
Example 2		 320 A; 1.27(3H, t), 2.44(3H, s), 3.68(2H, q), 4.76 (2H, s), 6.36(1H, s), 6.87(2H, d), 7.24-7.36(5H, m), 7.80(2H, d)
* Solvent for 1H NMR ; CDCl3(C), Acetone-d6 (A)

Test Example 1: Test for acid reactivity of yellow azo disperse dyes
(1) Preparation of marker solution
A proper amount of each of the azo disperse dyes prepared in Examples 1-5 and Comparative Examples 1 and 2 was taken and diluted with xylene in a 25 ml volumetric flask, and 1 ml of the azo disperse dye solution was taken and diluted with xylene in a 10 ml volumetric flask to prepare a marker solution. Concentrations of the marker solutions are listed in the following Table 3.
(2) Preparation of acid developer solution
3 g of xylene was added to 7 g of dodecylbenzene sulfonic acid to prepare a coloring agent solution.
(3) Measurement of UV-VIS molar absorption coefficients and maximum absorption wavelength
The UV-VIS molar absorption coefficients (ε) and maximum absorption wavelengths (λmax) of the samples prepared in (1) were measured. Then, 10 μl of the acid developer solution prepared in (2) was added to each sample and stirred for 1 minute. Then, the UV-VIS molar absorption coefficient (ε) and maximum absorption wavelength (λmax) of each sample were measured to observe a change in color. The UV-VIS molar absorption coefficient and maximum absorption wavelength were measured using a UV-VIS-NIR spectrophotometer (UV-3101 PC, SHIMADZU). The measurement results are listed in the following Table 3 and shown in FIG. 1.
Concentration
(mg /L)		 Before addition
of developing agent		 After addition
of developing agent		 Wavelength
shift (nm)
λmax * εmax/
Lmol-1cm-1 		λmax * εmax/
Lmol-1cm-1
Example 1 17.12 410 3.261 x 104 562 4.537 x 104 152
542 4.507 x 104
Example 2 14.84 409 3.235 x 104 563 4.633 x 104 154
542 4.590 x 104
Example 3 16.64 410 3.086 x 104 562 4.488 x 104 152
542 4.464 x 104
Example 4 15.00 409 3.216 x 103 562 4.464 x 104 153
539 4.424 x 104
Example 5 16.04 409 2.850 x 104 565 1.693 x 104 67
476 2.089 x 104
Comp. Example 1 15.40 489 4.252 x 104 512 3.310 x 104 23
Comp. Example 2 17.28 408 3.152 x 104 451 2.052 x 104 43
* Solvent for UV measurement: Xylene

The alkyl group-substituted yellow azo disperse dyes prepared in Examples 1 -4 showed a distinct purple color and a maximum absorption wavelength was shifted to a longer wavelength by 150 nm or more when the dodecylbenzene sulfonic acid solution was added to the marker solution.
The methoxy group-substituted yellow azo disperse dye prepared in Example 5 had a higher absorbance at 476 nm than at 565 nm as shown in the above Table 3, when the dodecylbenzene sulfonic acid solution was added to the marker solution. The color change of the marker solution could be observed, however the appearance of color was not distinctive.
In Comparative Example 1 using 2-amino-6-methoxybenzothiazole as the diazo compound, when the dodecylbenzene sulfonic acid solution was added to the marker solution, a maximum absorption wavelength of the azo disperse dye was shifted to a longer wavelength by 23 nm, and thus the color change of the marker solution was insignificant. Moreover, the compound of Formula 2 prepared in Comparative Example 1 was not suitable for use as a marker since the compound itself exhibited a red visible color in the xylene.
In Comparative Example 2 using 3-amino-5-methylisoxazole as the diazo compound, when the dodecylbenzene sulfonic acid solution was added to the marker solution, a maximum absorption wavelength of the azo disperse dye was shifted to a longer wavelength by 43 nm, and thus the color change of the marker solution was insignificant. The azo disperse dye was not suitable for use as a marker since the azo disperse dye exhibited a dark yellow visible color even when the acid developer was added to the marker solution.
Therefore, it is considered that the alkyl group-substituted yellow azo disperse dyes prepared in Examples 1-4, which exhibits their distinct colors by addition of dodecylbenzene sulfonic acid solution as the acid developer, can be more effectively used as an acid-reactive marker.
As described above, the marker containing N-benzyl-N-ethylaniline according to the present invention exhibits high solubility in non-aqueous fluid products, has excellent storage stability, can be detected even in a small amount, and can develop a distinct color by reaction with an organic acid such as dodecylbenzene sulfonic acid and an inorganic acid such as sulfuric acid or phosphoric acid in the non-aqueous fluid product. Therefore, when the marker is added to a product, the product can be easily distinguished from other companies’ products containing no marker or illegally distributed products such as adulterated gasoline, which makes it possible to easily control the quality of the product in the distribution process.
The invention has been described in detail with reference to preferred embodiments thereof. However, it will be appreciated by those skilled in the art that changes may be made in these embodiments without departing from the principles and spirit of the invention, the scope of which is defined in the appended claims and their equivalents.

Claims (6)

  1. A non-aqueous fluid marker comprising N-benzyl-N-ethylaniline represented by the following Formula 1:
    Formula 1
    Figure PCTKR2012000990-appb-I000011

    wherein R is a C1 to C12 alkyl group, a C1 to C12 alkoxy group, a C1 to C12 hydroxyalkyl group, a C1 to C12 hydroxyalkoxyalkyl group, a C1 to C12 alkylphenyl group, a C1 to C12 alkoxyphenyl group, a nitro group, a cyano group or a halogen atom.
  2. The non-aqueous fluid marker according to claim 1, wherein R is a methyl group, a n-butyl group, a t-butyl group, an n-dodecyl group or a methoxy group.

  3. A method for preparing a non-aqueous fluid marker, comprising:
    diazotizing an aniline derivative represented by the following Formula 3; and
    reacting N-benzyl-N-ethylaniline represented by the following Formula 4 with the diazotized aniline derivative:
    Figure PCTKR2012000990-appb-I000012

    wherein R is a C1 to C12 alkyl group, a C1 to C12 alkoxy group, a C1 to C12 hydroxyalkyl group, a C1 to C12 hydroxyalkoxyalkyl group, a C1 to C12 alkylphenyl group, a C1 to C12 alkoxyphenyl group, a nitro group, a cyano group or a halogen atom.

  4. A method for identifying a non-aqueous fluid product, comprising:
    dissolving a non-aqueous fluid marker, which contains N-benzyl-N-ethylaniline represented by the following Formula 1, in a target product; and developing a detectable color of the target product with an acid developer:
    Formula 1
    Figure PCTKR2012000990-appb-I000013

    wherein R is a C1 to C12 alkyl group, a C1 to C12 alkoxy group, a C1 to C12 hydroxyalkyl group, a C1 to C12 hydroxyalkoxyalkyl group, a C1 to C12 alkylphenyl group, a C1 to C12 alkoxyphenyl group, a nitro group, a cyano group or a halogen atom.

  5. The method according to claim 4, wherein the target product is at least one selected from the group consisting of gasoline, diesel, kerosene, biodiesel, bioethanol, xylene, ink, and non-aqueous lubricant.

  6. The method according to claim 4, wherein the acid developer is dodecylbenzene sulfonic acid, sulfuric acid or phosphoric acid.

PCT/KR2012/000990 2011-04-07 2012-02-10 Non-aqueous fluid marker containing n-benzyl-n-ethylaniline and method for preparing the same WO2012138049A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
KR10-2011-0032329 2011-04-07
KR1020110032329A KR101300673B1 (en) 2011-04-07 2011-04-07 Nonaqueous fluid marker having N-benzyl-N-ethylaniline and Preparing method thereof

Publications (2)

Publication Number Publication Date
WO2012138049A1 true WO2012138049A1 (en) 2012-10-11
WO2012138049A4 WO2012138049A4 (en) 2012-12-13

Family

ID=46969406

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/KR2012/000990 WO2012138049A1 (en) 2011-04-07 2012-02-10 Non-aqueous fluid marker containing n-benzyl-n-ethylaniline and method for preparing the same

Country Status (2)

Country Link
KR (1) KR101300673B1 (en)
WO (1) WO2012138049A1 (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103242249A (en) * 2013-05-30 2013-08-14 杨文龙 Compound capable of identifying dodecylbenzene sulfonic acid ions as well as preparation method and application thereof
CN105859576A (en) * 2016-05-05 2016-08-17 成都中恒华铁科技有限公司 Method for synthesizing phenylbutazone drug intermediate azobenzene
CN107421899A (en) * 2017-06-28 2017-12-01 重庆市宇驰检测技术有限公司 Determine the detection method of water quality aniline, formaldehyde simultaneously based on ultraviolet-visible absorption spectroscopy
CN112051224A (en) * 2020-08-12 2020-12-08 昆明理工大学 Method for detecting blending ratio of biodiesel blending fuel based on ultraviolet-visible spectrophotometry

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20220118077A (en) 2021-02-18 2022-08-25 한국화학연구원 Azo based compound for detecting hazardous acids and detection method using the same

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7101983B2 (en) * 2001-04-03 2006-09-05 Clariant Finance (Bvi) Limited Azo dyes
EP1820537A1 (en) * 2006-02-18 2007-08-22 Wella Aktiengesellschaft Agents for coloring keratin fibers
US20070218206A1 (en) * 2004-08-11 2007-09-20 Hans Reichert Method of Printing a Time-Temperature Indicator Based on Azo Coupling Reactions onto a Susbtrate
EP1471117B1 (en) * 2003-04-24 2008-07-09 Xerox Corporation Azo dyes with a polyoxyalkylene moiety and inks containing them

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6514917B1 (en) * 2001-08-28 2003-02-04 United Color Manufacturing, Inc. Molecular tags for organic solvent systems
CN101981167B (en) * 2008-03-25 2014-08-13 卢布里佐尔公司 Marker dyes for petroleum products

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7101983B2 (en) * 2001-04-03 2006-09-05 Clariant Finance (Bvi) Limited Azo dyes
EP1471117B1 (en) * 2003-04-24 2008-07-09 Xerox Corporation Azo dyes with a polyoxyalkylene moiety and inks containing them
US20070218206A1 (en) * 2004-08-11 2007-09-20 Hans Reichert Method of Printing a Time-Temperature Indicator Based on Azo Coupling Reactions onto a Susbtrate
EP1820537A1 (en) * 2006-02-18 2007-08-22 Wella Aktiengesellschaft Agents for coloring keratin fibers

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
YAZDANBAKHSH, M. R. ET AL., JOURNAL OF MOLECULAR LIQUIDS, vol. 151, 4 December 2010 (2010-12-04), pages 107 - 112 *

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103242249A (en) * 2013-05-30 2013-08-14 杨文龙 Compound capable of identifying dodecylbenzene sulfonic acid ions as well as preparation method and application thereof
CN105859576A (en) * 2016-05-05 2016-08-17 成都中恒华铁科技有限公司 Method for synthesizing phenylbutazone drug intermediate azobenzene
CN107421899A (en) * 2017-06-28 2017-12-01 重庆市宇驰检测技术有限公司 Determine the detection method of water quality aniline, formaldehyde simultaneously based on ultraviolet-visible absorption spectroscopy
CN112051224A (en) * 2020-08-12 2020-12-08 昆明理工大学 Method for detecting blending ratio of biodiesel blending fuel based on ultraviolet-visible spectrophotometry
CN112051224B (en) * 2020-08-12 2021-08-06 昆明理工大学 Method for detecting blending ratio of biodiesel blending fuel based on ultraviolet-visible spectrophotometry

Also Published As

Publication number Publication date
KR101300673B1 (en) 2013-08-28
WO2012138049A4 (en) 2012-12-13
KR20120114663A (en) 2012-10-17

Similar Documents

Publication Publication Date Title
WO2012138049A1 (en) Non-aqueous fluid marker containing n-benzyl-n-ethylaniline and method for preparing the same
JP2008255358A (en) Colorant compound
JP2009280691A (en) Azo compound and salt of the same
Geng et al. 2-Amino-4-chloro-5-formylthiophene-3-carbonitrile derived azo dyes
CN105038316A (en) Heterocyclic-ring disperse azo dye and preparation method thereof
JP2009013290A (en) Azo compound or its salt
Geng et al. From heterocyclic hydrazone to hydrazone-azomethine dyes: Solvent and pH induced hydrazone and azo-keto transformation for a family of pyrazolone-based heterocyclic dyes
Zhao et al. Construction of benzothiazole/pyridone based bi-heterocyclic dyes and their NiII and CuII complexes
Qian et al. Visualized fabric discoloration of bi-heterocyclic hydrazone dyes
CN111896536A (en) Benzothiazole azo acid-base indicator and synthesis method thereof
KR101521141B1 (en) Azo compound or its salt
EP0553858B1 (en) Monoazo compound and dense solution thereof
Yen Synthesis and solvatochromism of heterocyclic bichromophoric dyes derived from 2‐aminothiazole
KR20220118077A (en) Azo based compound for detecting hazardous acids and detection method using the same
Lee et al. Synthesis of quenchers to control the fluorescence of Rhodamine B and improve the contrast ratio of blue filters for LCDs
Seferoĝlu et al. Hetarylazoindoles 1. Synthesis, characterization, and spectroscopic properties of new hetarylazoindole dyes
CN109988118B (en) Heterocyclic azo compound and synthesis method and application thereof
CN105820596A (en) Tetrahydroquinoline dye, ink and electrowetting display
KR100891000B1 (en) Azo yellow pigments comprising N-substituted benzamide type and its process
Shan et al. A new highly sensitive and colorimetric pH indicator derived from 2-amino-5-nitrothiazole and H-acid
CN101337942A (en) Azo compound or salts thereof
RU2273652C1 (en) Dyes based on 3,5-dinitroaniline and 2-amino-4,6-dinitrotoluene
CN115073934A (en) Benzisothiazole heterocyclic azo dye and preparation method thereof
KR20090004762A (en) Azo compound or its salt
CN113388261A (en) Synthetic method of dye for polarizer

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 12767892

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 12767892

Country of ref document: EP

Kind code of ref document: A1