Author: claimsbot

1-15. (canceled)
16. A method for combating phytopathogenic fungi comprising treating the fungi or the materials, plants, the soil or seeds to be protected against fungal attack with an effective amount of a composition comprising a compound of the formula I
wherein:
R1 is selected from the group consisting of C2-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, C3-C8-cycloalkyl, C3-C8-cycloalkyl-C1-C4-alkyl;
wherein the aliphatic groups R1 are unsubstituted or carry 1, 2, 3 or 4 CN substituents;
wherein the cycloalkyl moieties of R1 are unsubstituted or carry 1, 2, 3 or up to the maximum number of identical or different groups Rb which independently of one another are selected from:
Rb is selected from the group consisting of halogen, CN, nitro, C1-C4-alkyl, C1-C4-alkoxy, C1-C4-halogenalkyl and C1-C4-halogenalkoxy;
or an N-oxide or an agriculturally acceptable salt thereof.
17. The method of claim 16, wherein R1 is C2-C6-alkyl, C2-C6-alkenyl or C2-C6-alk-1-ynyl.
18. The method of claim 17, wherein R1 is C2-C4-alkyl.
19. The method of claim 16, wherein R1 is C2-C6-alkenyl or C2-C6-alk-1-ynyl.
20. The method of claim 16, wherein R1 is C3-C8-cycloalkyl or C3-C8-cycloalkyl-C1-C4-alkyl.
21. The method of claim 16, wherein R1 is selected from the group consisting of ethyl, n-propyl, isopropyl, n-butyl, tert.-butyl, allyl, ethynyl, prop-1-ynyl; but-1-ynyl, cyclopropyl and cyclopropylmethyl.
22. A method for protecting plant propagation material and seedlings’ roots and shoots from infestation by harmful fungi comprising contacting the plant propagation material with a composition comprising a compound of claim 16.
23. A seed coated with at least one compound of formula I as defined in claim 16, in an amount of from 0.1 g to 10 kg per 100 kg of seed.
24. A compound of formula I
wherein:
R1 is selected from the group consisting of C2-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, C3-C8-cycloalkyl and C3-C8-cycloalkyl-C1-C4-alkyl;
wherein the aliphatic groups R1 are unsubstituted or carry 1, 2, 3 or 4 CN substituents;
wherein the cycloalkyl moieties of R1 are unsubstituted or carry 1, 2, 3 or up to the maximum number of identical or different groups Rb which independently of one another are selected from:
Rb is selected from the group consisting of halogen, CN, nitro, C1-C4-alkyl, C1-C4-alkoxy, C1-C4-halogenalkyl and C1-C4-halogenalkoxy;
or an N-oxide or an agriculturally acceptable salt thereof,
except for 2-2-chloro-4-(4-chloro-phenoxy)-phenyl-1-1,2,4triazol-1-yl-pent-4-yn-2-ol.
25. The compound of claim 20, wherein R1 is C2-C6-alkyl, C2-C6-alkenyl or C2-C6-alk-1-ynyl.
26. The compound of claim 21, wherein R1 is C2-C4-alkyl.
27. The compound of claim 20, wherein R1 is C2-C6-alkenyl or C2-C6-alk-1-ynyl.
28. The compound of claim 20, wherein R1 is C3-C8-cycloalkyl or C3-C8-cycloalkyl-C1-C4-alkyl.
29. The compound of claim 20, wherein R1 is selected from the group consisting of ethyl, n-propyl, isopropyl, n-butyl, tert.-butyl, allyl, ethynyl, prop-1-ynyl; but-1-ynyl, cyclopropyl and cyclopropylmethyl.
30. A process for preparing the compound of claim 20, comprising reacting a compound of formula III
wherein Y is F or Cl,
with 4-chlorophenole of formula II
under basic conditions;
and reacting the resulting compound of formula IV
in the presence of a catalyst with isopropylmagnesium bromide followed by a reaction with acetyl chloride;
halogenating the resulting compound of formula V
with bromine;
reacting the resulting compound of formula VI
under basic conditions with 1H-1,2,4-triazole;
and reacting the resulting compound of formula VII
with a compound of formula VIII R1-M,
wherein R1 is selected from the group consisting of C2-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, C3-C8-cycloalkyl and C3-C8-cycloalkyl-C1-C4-alkyl;
wherein the aliphatic groups R1 are unsubstituted or carry 1, 2, 3 or 4 CN substituents;
wherein the cycloalkyl moieties of R1 are unsubstituted or carry 1, 2, 3 or up to the maximum number of identical or different groups Rb which independently of one another are selected from:
Rb is selected from the group consisting of halogen, CN, nitro, C1-C4-alkyl, C1-C4-alkoxy, C1-C4-halogenalkyl and C1-C4-halogenalkoxy
and M is selected from the group consisting of MgBr, MgCl, Li and Na, to obtain compounds I.
31. A process for preparing the compound of claim 20, comprising reacting a compound of formula III
wherein Y is F or Cl,
in presence of a catalyst with isopropylmagnesium halide followed by a reaction with a compound of formula IX R1\u2014COCl,
wherein R1 is selected from the group consisting of C2-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, C3-C8-cycloalkyl or C3-C8-cycloalkyl-C1-C4-alkyl;
wherein the aliphatic groups R1 are unsubstituted or carry 1, 2, 3 or 4 CN substituents;
wherein the cycloalkyl moieties of R1 are unsubstituted or carry 1, 2, 3 or up to the maximum number of identical or different groups Rb which independently of one another are selected from:
Rb is selected from the group consisting of halogen, CN, nitro, C1-C4-alkyl, C1-C4-alkoxy, C1-C4-halogenalkyl and C1-C4-halogenalkoxy;
and the N-oxides and the agriculturally acceptable salts thereof,
converting the resulting compound of formula X
wherein Y is F or Cl;
under basic conditions with 4-chlorophenole of formula II
and reacting the resulting compound of formula Va
with trimethylsulf(ox)onium halide;
and reacting the resulting compound of formula XI
under basic conditions with 1H-1,2,4-triazole,
to obtain compounds of formula I.
32. A compound of formula XI
wherein R1 is C2-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, C3-C8-cycloalkyl and C3-C8-cycloalkyl-C1-C4-alkyl;
wherein the aliphatic groups R1 are unsubstituted or carry 1, 2, 3 or 4 CN substituents;
wherein the cycloalkyl moieties of R1 are unsubstituted or carry 1, 2, 3 or up to the maximum number of identical or different groups Rb which independently of one another are selected from:
Rb is selected from the group consisting of halogen, CN, nitro, C1-C4-alkyl, C1-C4-alkoxy, C1-C4-halogenalkyl and C1-C4-halogenalkoxy.
33. An agrochemical composition wherein said composition comprises an auxiliary and at least one compound of formula I, as defined in claim 20, an N-oxide or an agriculturally acceptable salt thereof.
34. The composition of claim 29, further comprising an additional active compound.

The claims below are in addition to those above.
All refrences to claim(s) which appear below refer to the numbering after this setence.

1. A method for obtaining site-specific recombination in a eukaryotic cell, the method comprising:
a. providing the eukaryotic cell
wherein
the eukaryotic cell comprises a polynucleotide that encodes a prokaryotic Bxb1 recombinase polypeptide,

wherein
the eukaryotic cell comprises a first site-specific recombination site and a second site-specific recombination site, wherein the first site-specific recombination site is a substrate for recombination with the second site-specific recombination site; and
b. contacting the first site-specific recombination site and second site-specific recombination site with a prokaryotic Bxb1 recombinase polypeptide, resulting in recombination between the first site-specific recombination site and second site-specific recombination site. The method of claim 1, wherein the eukaryotic cell is a plant cell.
2. The method of claim 1, wherein the eukaryotic cell is a yeast cell.
3. The method of claim 1, wherein the eukaryotic cell is an animal cell.
4. The method of claim 1, wherein the polynucleotide that encodes the prokaryotic Bxb1 recombinase polypeptide comprises SEQ ID NO:1.
5. The method of claim 1, wherein the polynucleotide that encodes the prokaryotic Bxb1 recombinase polypeptide encodes a recombinase polypeptide comprising SEQ ID NO:2.
6. The method of claim 1, wherein the prokaryotic Bxb1 recombinase polypeptide causes a site-specific excision of DNA,
wherein
the excision of the DNA is a result of recombination between the first site-specific recombination site and the second site-specific recombination site, and

wherein
the DNA that is excised is located between the first site-specific recombination site and the second site-specific recombination site on the same DNA molecule.
7. The method of claim 1, wherein the prokaryotic Bxb1 recombinase polypeptide causes a site-specific inversion of DNA
wherein
the inversion of the DNA is a result of recombination between the first site-specific recombination site and the second site-specific recombination site, and

wherein
the DNA that is inverted is located between the first site-specific recombination site and the second site-specific recombination site on the same DNA molecule.
8. The method of claim 1, wherein the prokaryotic Bxb1 recombinase polypeptide causes a site-specific integration of DNA
wherein
the integration of the DNA is a result of recombination between the first site-specific recombination site and the second site-specific recombination site, and

wherein
the DNA that is integrated is located between the first site-specific recombination site and the second site-specific recombination site on the same DNA molecule.
9. A method for obtaining site-specific recombination in a eukaryotic cell, the method comprising:
a. providing the eukaryotic cell
wherein
the eukaryotic cell comprises a polynucleotide that encodes a prokaryotic U153 recombinase polypeptide,

wherein
the eukaryotic cell comprises a first site-specific recombination site and a second site-specific recombination site, wherein the first site-specific recombination site is a substrate for recombination with the second site-specific recombination site; and
b. contacting the first site-specific recombination site and second site-specific recombination site with a prokaryotic U153 recombinase polypeptide, resulting in recombination between the first site-specific recombination site and second site-specific recombination sites.
10. The method of claim 9, wherein the eukaryotic cell is a plant cell.
11. The method of claim 9, wherein the eukaryotic cell is a yeast cell.
12. The method of claim 9, wherein the eukaryotic cell is an animal cell.
13. The method of claim 9, wherein the polynucleotide that encodes the prokaryotic U153 recombinase polypeptide comprises SEQ ID NO:19.
14. The method of claim 9, wherein the polynucleotide that encodes the prokaryotic U153 recombinase polypeptide encodes a recombinase polypeptide comprising SEQ ID NO:20.
15. The method of claim 9, wherein the prokaryotic U153 recombinase polypeptide causes a site-specific excision of DNA,
wherein
the excision of the DNA is a result of recombination between the first site-specific recombination site and the second site-specific recombination site, and

wherein
the DNA that is excised is located between the first site-specific recombination site and the second site-specific recombination site on the same DNA molecule.
16. The method of claim 9, wherein the prokaryotic U153 recombinase polypeptide causes a site-specific inversion of DNA,
wherein
the inversion of the DNA is a result of recombination between the first site-specific recombination site and the second site-specific recombination site, and

wherein
the DNA that is inverted is located between the first site-specific recombination site and the second site-specific recombination site on the same DNA molecule.
17. The method of claim 9, wherein the prokaryotic U153 recombinase polypeptide causes a site-specific integration of DNA,
wherein
the integration of the DNA is a result of recombination between the first site-specific recombination site and the second site-specific recombination site, and

wherein
the DNA that is integrated is located between the first site-specific recombination site and the second site-specific recombination site on the same DNA molecule.
18. A method for obtaining a eukaryotic cell having a stably integrated transgene, the method comprising:
a. introducing a first nucleic acid into a eukaryotic cell that comprises a first recombination site,
b. introducing a second nucleic acid comprising a transgene and a second recombination site, which second recombination site can serve as a substrate for recombination with the first recombination site; and
c. contacting the first and the second recombination sites with a recombinase polypeptide, wherein the recombinase polypeptide catalyzes recombination between first and second recombination sites, resulting in integration of the second nucleic acid at the first recombination site(s), thereby forming two hybrid sites flanking the inserted DNA.
19. The method of claim 18, wherein the recombinase polypeptide can mediate site-specific recombination between the first and second recombination sites, but cannot mediate recombination between the hybrid sites in the absence of an additional factor that is not present in the eukaryotic cell.
20. The method of claim 18, wherein the recombination sites and recombinase polynucleotide are selected from the group consisting of a bacteriophage Bxb1 recombination system, and a bacteriophage U153 recombination system.

1. A method for generating seismic fluid prediction data for a subsurface region, comprising:
preconditioning seismic data for amplitude-versus-offset (AVO) analysis;
generating seismic AVO attribute data for the subsurface region, including creating intercept (A) and gradient (B) seismic data using two or more angle stacks of seismic data;
generating lithology prediction data with the intercept (A) and gradient (B) seismic data;
generating an AVO crossplot for fluids to identify an initial AVO anomaly; and
generating seismic fluid prediction data based on the generated AVO crossplot and lithology prediction data.
2. The method of claim 1, further comprising acquiring seismic data representative of the subsurface region.
3. The method of claim 1, further comprising processing two or more angle-stacks of seismic data.
4. The method of claim 1, wherein preconditioning seismic data comprises:
spectral broadening the seismic data; and
amplitude scaling the seismic data to fit an AVO model of interest.
5. The method of claim 4, wherein preconditioning seismic data further comprises rotating the seismic data to quadrature phase.
6. The method of claim 1, wherein preconditioning seismic data further comprises spectral shaping the seismic data.
7. The method of claim 6, wherein spectral shaping the seismic data comprises spectral shaping the seismic data to boost the low frequency content, including:
estimating a seismic wavelet of the seismic data; and
applying a filter to move the amplitude spectrum of the seismic data to an earth model.
8. The method of claim 6, wherein preconditioning seismic data further comprises:
amplitude scaling the seismic data for each angle stack to fit an AVO model of interest; and
rotating the seismic data to quadrature phase.
9. The method of claim 8, wherein amplitude scaling the seismic data for each angle stack comprises generating a synthetic well-tie to the seismic data using an AVO model for each angle stack and scaling the seismic data to match synthetic amplitude for each angle stack.
10. The method of claim 1, wherein preconditioning seismic data further comprises spectrally whitening the seismic data to equalize amplitudes of the seismic data at all frequencies.
11. The method of claim 10, wherein spectrally whitening the seismic data comprises:
estimating a seismic wavelet of the seismic data; and
applying a filter to equalize amplitudes of the seismic data at all frequencies.
12. The method of claim 10, wherein preconditioning seismic data further comprises:
integrating the spectrally whitened data along time domain or depth domain for each trace; and
amplitude scaling the seismic data for each angle stack to fit an AVO model of interest.
13. The method of claim 12, wherein preconditioning further comprises removing a background trend in amplitude from the integrated data by applying a filter to remove the background trend.
14. The method of claim 1, wherein generating AVO data comprises formulating the intercept (A) and gradient (B) seismic data using a Shuey multi-term approximation, or Zoeppritz equations.
15. The method of claim 1, wherein generating the AVO crossplot for fluids to highlight the initial AVO anomaly comprises crossplotting the intercept (A) and gradient (B) seismic data at a well or other chosen hydrocarbon location within the subsurface region.
16. The method of claim 15, wherein the other chosen hydrocarbon location comprises one or more seismic traces for analysis.
17. The method of claim 15, further comprising:
providing a fluid line on the AVO crossplot; and
designating data on the AVO crossplot as anomalous or non-anomalous features with respect to the fluid line.
18. The method of claim 17, wherein the fluid line comprises one or more fluid lines separating anomalous and non-anomalous hydrocarbon bearing features from other hydrocarbon bearing features or non-hydrocarbon bearing features.
19. The method of claim 18, wherein the non-hydrocarbon bearing features are wet sands andor wet shales and the hydrocarbon bearing features are hydrocarbon bearing sands.
20. The method of claim 1, wherein generating the seismic fluid prediction data based on the generated AVO crossplot and lithology prediction data comprises:
creating fluid prediction data comprising an initial seismic dataset including non-anomalous reference points of seismic data for the subsurface region;
analyzing each point of the seismic data, trace-by-trace, to determine if each point falls within an anomalous zone for a hydrocarbon bearing feature on the AVO crossplot;
assigning a hydrocarbon value for each point determined to fall within the anomalous zone; and
expanding the fluid prediction data along the seismic trace for each point determined to fall within the anomalous zone.
21. The method of claim 20, wherein expanding the fluid prediction data comprises
identifying one or more hydrocarbon-water contacts with an individual time sample prior to creating the fluid prediction data; and
inputting hydrocarbon-water contacts as horizons that limit the expansion of the fluid prediction data.
22. The method of claim 20, wherein assigning the hydrocarbon value for each point and expanding the fluid prediction model are iteratively performed in a forward and a reverse direction with respect to the seismic trace.
23. The method of claim 18, wherein generating the seismic fluid prediction data based on the generated AVO crossplot and lithology prediction data comprises:
creating a fluid prediction data comprising an initial seismic dataset including non-anomalous reference points of seismic data for the subsurface region;
analyzing each point of the seismic data, trace-by-trace, to determine if each point falls within an anomalous zone for a hydrocarbon bearing feature on the AVO crossplot;
assigning a hydrocarbon value for each point determined to fall within the anomalous zone; and
expanding the fluid prediction data along the seismic trace for each point determined to fall within the anomalous zone.
24. The method of claim 23, wherein expanding the fluid prediction data comprises
identifying one or more hydrocarbon-water contacts with an individual time sample prior to creating the fluid prediction data; and
inputting hydrocarbon-water contacts as horizons that limit the expansion of the fluid prediction data.
25. The method of claim 24, wherein assigning the hydrocarbon value for each point and expanding the fluid prediction model are each iteratively performed in a forward and a reverse direction with respect to the seismic trace.
26. A tangible computer-readable storage medium having embodied thereon a computer program configured to, when executed by a processor, for generating seismic fluid prediction data for a subsurface region, the medium comprising one or more code segments configured to:
precondition seismic data for amplitude-versus-offset (AVO) analysis;
generate seismic AVO attribute data for the subsurface region, including creating intercept (A) and gradient (B) seismic data using two or more angle stacks of seismic data;
generate lithology prediction data with the intercept (A) and gradient (B) seismic data;
generate an AVO crossplot for fluids to identify an initial AVO anomaly; and
generate seismic fluid prediction data based on the generated AVO crossplot and lithology prediction data.
27. The tangible computer-readable storage medium of claim 26, further comprising one or more code segments configured to process two or more angle-stacks of seismic data.
28. The tangible computer-readable storage medium of claim 26, wherein the one or more code segments configured to precondition seismic data comprises one or more code segments configured to:
spectral broaden the seismic data;
amplitude scale the seismic data to fit an AVO model of interest; and
rotate the seismic data to quadrature phase.
29. The tangible computer-readable storage medium of claim 26, wherein the one or more code segments configured to precondition seismic data comprises one or more code segments configured to:
spectral shape the seismic data, wherein spectral shaping the seismic data comprises spectral shaping the seismic data to boost the low frequency content, including:
estimating a seismic wavelet of the seismic data; and
applying a filter to move the amplitude spectrum of the seismic data to an earth model; and

amplitude scale the seismic data for each angle stack to fit an AVO model of interest; and
rotate the seismic data to quadrature phase.
30. The tangible computer-readable medium of claim 26, wherein the one or more code segments configured to precondition seismic data further comprises one or more code segments configured to:
spectrally whiten the seismic data to equalize amplitudes of the seismic data at all frequencies, wherein spectrally whitening the seismic data comprises:
estimating a seismic wavelet of the seismic data; and
applying a filter to equalize amplitudes of the seismic data at all frequencies; and

integrate the spectrally whitened data along time domain or depth domain for each trace; and
amplitude scaling the seismic data for each angle stack to fit an AVO model of interest.
31. The tangible computer-readable medium of claim 26, wherein the one or more code segments configured to generate the AVO crossplot for fluids to identify the initial AVO anomaly comprises one or more code segments configured to crossplot the intercept (A) and gradient (B) seismic data at a well or other chosen hydrocarbon location within the subsurface region.
32. The tangible computer-readable medium of claim 31, further comprising one or more code segments configured to:
provide a fluid line on the AVO crossplot; and
designate data on the AVO crossplot as anomalous or non-anomalous features with respect to the fluid line.
33. The tangible computer-readable medium of claim 32, wherein the fluid line comprises one or more fluid lines separating anomalous and non-anomalous hydrocarbon bearing features from other hydrocarbon bearing features or non-hydrocarbon bearing features.
34. The tangible computer-readable medium of claim 33, wherein the non-hydrocarbon bearing features are wet sands andor wet shales and the hydrocarbon bearing features are hydrocarbon bearing sands.
35. The tangible computer-readable medium of claim 26, wherein the one or more code segments to generate the seismic fluid prediction data based on the generated AVO crossplot and lithology prediction data comprises one or more code segments configured to:
create fluid prediction data comprising an initial seismic dataset including non-anomalous reference points of seismic data for the subsurface region;
analyze each point of the seismic data, trace-by-trace, to determine if each point falls within an anomalous zone for a hydrocarbon bearing feature on the AVO crossplot;
assign a hydrocarbon value for each point determined to fall within the anomalous zone; and
expand the fluid prediction data along the seismic trace for each point determined to fall within the anomalous zone.
36. The tangible computer readable medium of claim 35, wherein assigning the hydrocarbon value for each point and expanding the fluid prediction model are iteratively performed in a forward and a reverse direction with respect to the seismic trace.
37. The tangible computer readable medium of claim 35, wherein expanding the fluid prediction data comprises identifying one or more hydrocarbon-water contacts with an individual time sample prior to creating the fluid prediction data; and inputting hydrocarbon-water contacts as horizons that limit the expansion of the fluid prediction data.
38. A method for producing hydrocarbons from a subsurface region, comprising:
generating seismic fluid prediction data for a subsurface region, wherein generating seismic fluid prediction data includes:
preconditioning seismic data for amplitude-versus-offset (AVO) analysis;
generating seismic AVO attribute data for the subsurface region, including creating intercept (A) and gradient (B) seismic data using two or more angle stacks of seismic data;
generating lithology prediction data with the intercept (A) and gradient (B) seismic data;
generating an AVO crossplot for fluids to identify an initial AVO anomaly; and
generating seismic fluid prediction data based on the generated AVO crossplot and lithology prediction data; and

controlling production of a hydrocarbon bearing asset within the subsurface region based on the seismic fluid prediction data; and
producing hydrocarbons from the hydrocarbon bearing asset.
39. The method of claim 38, wherein controlling production of the hydrocarbon bearing asset includes optimizing well location or well production.
40. The method of claim 38, further comprising using the seismic fluid prediction data for spatially identifying fluids for transformation with one or more equations in a seismic reflectivity and rock physics inversion to determine rock properties.

The claims below are in addition to those above.
All refrences to claim(s) which appear below refer to the numbering after this setence.

1. A cloth, comprising a water-insoluble nonwoven, which has been moistened with an impregnation solution comprising an oil-in-water emulsion having a viscosity of less than 2000 mPa\xb7s, and comprising:
one or more partially neutralized glyceride esters selected from the group consisting of monoglyceride and diglyceride esters of saturated fatty acids with citric acid and
one or more fatty alcohols selected from the group consisting of branched and unbranched alkyl alcohols with 10 to 40 carbon atoms.
2. The cloth as claimed in claim 1, wherein the weight ratio of the unimpregnated cloth to the impregnation solution is from 1:1 to 1:5.
3. The cloth as claimed in claim 1, wherein the one or more partially neutralized glyceride esters include glyceryl stearate citrate.
4. The cloth as claimed in claim 1, wherein the one or more fatty alcohols include cetyl alcohol, stearyl alcohol, or a mixture thereof.
5. The cloth as claimed in claim 1, wherein the one or more fatty alcohols include cetyl stearyl alcohol.
6. The cloth as claimed in claim 1, wherein the total amount of the one or more partially neutralized glyceride esters in the impregnation solution is from 0.1 to 10.0% by weight, based on the total weight of the impregnation solution.
7. The cloth as claimed in claim 6, wherein the total amount of the one or more partially neutralized glyceride esters in the impregnation solution is from 0.5 to 6.0% by weight, based on the total weight of the impregnation solution.
8. The cloth as claimed in claim 1, wherein the total amount of the one or more fatty alcohols in the impregnation solution is from 0.1 to 10.0% by weight, based on the total weight of the impregnation solution.
9. The cloth as claimed in claim 1, wherein the total amount of the one or more fatty alcohols in the impregnation solution is from 0.5 to 6.0% by weight, based on the total weight of the impregnation solution.
10. The cloth as claimed in claim 1, wherein the weight ratio of the one or more partially neutralized glyceride esters to the one or more fatty alcohols is from 7:3 to 3:7.
11. The cloth as claimed in claim 10, wherein the weight ratio of the one or more partially neutralized glyceride esters to the one or more fatty alcohols is from 2:1 to 1:2.
12. The cloth as claimed in claim 11, wherein the weight ratio of the one or more partially neutralized glyceride esters to the one or more fatty alcohols is about 1:1.
13. The cloth as claimed in claim 1, wherein the impregnation solution includes an oil phase and an aqueous phase, wherein the oil phase is present in the impregnation solution in an amount from 5 to 40% by weight, based on the total weight of the impregnation solution.
14. The cloth as claimed in claim 1, wherein the impregnation solution further comprises one or more auxiliaries, additives or active ingredients selected from the group consisting of moisturizers, waxes, surfactants, preservatives, antioxidants, dyes, plant extracts, UV filters, pigments, deodorant and antiperspirant active ingredients, dermatological active ingredients and perfumes.
15. The cloth as claimed in claim 1, wherein the oil-in-water emulsion comprises one or more fatty alcohols selected from the group consisting of branched and unbranched alkyl alcohols with 10 to 30 carbon atoms.
16. A cloth, comprising a water-insoluble nonwoven, which has been moistened with an impregnation solution comprising an oil-in-water emulsion having a viscosity of less than 2000 mPa\xb7s, and comprising:
one or more partially neutralized glyceride esters selected from the group consisting of monoglyceride and diglyceride esters of saturated fatty acids with citric acid;
one or more fatty alcohols selected from the group consisting of branched and unbranched alkyl alcohols with 10 to 40 carbon atoms; and
one or more washing-acting surfactants having a HLB greater than about 25.
17. The cloth as claimed in claim 16, wherein the amount of water in the impregnation solution is less than about 80.0% by weight, based on the total weight of the impregnation solution.
18. The cloth as claimed in claim 16, wherein the weight ratio of the unimpregnated cloth to the impregnation solution is from 1:1 to 1:5.
19. The cloth as claimed in claim 16, wherein the one or more partially neutralized glyceride esters include glyceryl stearate citrate.
20. The cloth as claimed in claim 16, wherein the one or more fatty alcohols include cetyl alcohol, stearyl alcohol, or a mixture thereof.
21. The cloth as claimed in claim 16, wherein the total amount of the one or more partially neutralized glyceride esters in the impregnation solution is from 0.1 to 10.0% by weight, based on the total weight of the impregnation solution.
22. The cloth as claimed in claim 16, wherein the total amount of the one or more fatty alcohols in the impregnation solution is from 0.1 to 10.0% by weight, based on the total weight of the impregnation solution.
23. The cloth as claimed in claim 16, wherein the weight ratio of the one or more partially neutralized glyceride esters to the one or more fatty alcohols is from 7:3 to 3:7.
24. The cloth as claimed in claim 16, wherein the impregnation solution includes an oil phase and an aqueous phase, wherein the oil phase is present in the impregnation solution in an amount from 5 to 40% by weight, based on the total weight of the impregnation solution.
25. The cloth as claimed in claim 16, wherein the impregnation solution further comprises one or more auxiliaries, additives or active ingredients selected from the group consisting of moisturizers, waxes, preservatives, antioxidants, dyes, plant extracts, UV filters, pigments, deodorant and antiperspirant active ingredients, dermatological active ingredients and perfumes.