BACKGROUND OF THE INVENTION
[0001] Our invention relates to the field of perfumery and, more particularly, to improved
fragranced detergents and fabric softeners.
[0002] The use of enzymes in fabric detergents in order to improve their efficiency has
been known for a number of years. Among such enzymes, lipases are particularly preferred
as a result of the capacity to hydrolyze the fat materials on the dirty linen and
thus to facilitate its cleaning. However, it is known that malodor problems can occasionally
occur after certain application conditions and in order to solve these malodor problems,
techniques exist for carefully choosing the perfume ingredients incorporated in the
detergents and which, following a washing, are deposited on the fabrics, for example,
European Patent No. 430,315. Accordingly, appropriate perfuming of such detergents
appears to be extremely important.
[0003] A substantive fragrance ingredient that is desired to be incorporated into such fabric
detergents for fragrancing same and such fabric softeners for fragrancing same is
the tricyclic isochroman known as GALAXOLIDE® (trademark of International Flavors
& Fragrances Inc. of New York, New York) which is a mixture of compounds having the
structures:

with the majority of the isomers being the compound having the structure:

However, in very high concentrations (e.g., greater than 50%), GALAXOLIDE® has extremely
high viscosity and at lower temperatures exists in the crystalline state making it
difficult for incorporation into fragrances. In the prior art, the GALAXOLIDE® has
been combined with other materials in order to form "eutectic" compositions containing
GALAXOLIDE® and other materials, for example, benzophenone.
[0004] However, a need exists for creating a low viscosity, high concentration form of GALAXOLIDE®
in fragrances which are used in fabric detergents and fabric softeners, particularly
where the detergent and softener systems involve the use of enzymes such as lipase.
[0005] There is a need for such detergents and fabric softeners to be able to impart to
the fabrics a long lasting odor as stated, supra, such the user perceives this odor
for a considerable time after the textiles have been washed and subsequently dried.
To this end, it has been known to use in the fabric detergents and softeners perfuming
ingredients which have a good tenacity on the fabric, i.e., ingredients whose odor
once imparted to the textiles upon the washing can be perceived by the consumer for
several days. However, there are many perfuming substances known for their extremely
pleasant odors and, namely, a quality of "freshness" often associated with the notion
of cleanliness, which substances are unfortunately not very tenacious or even not
tenacious at all on fabrics such as their perfuming effect can only be perceived very
briefly, at the most, for a few hours following the washing and drying operations.
In general, U.S. Letters Patent No. 5,649,979 issued on July 22, 1997 indicates that
the fragrance effect of such substances is prolonged and thus the "freshness" of the
fabrics has been prolonged. Thus, U.S. Letters Patent No. 5,649,979 indicates that
a "novel" solution to the problem has been achieved where a process for perfuming
textiles washed with detergents containing lipases has been discovered. U.S. Letters
Patent No. 5,649,979 establishes that by adding particular ingredients to the fabric
detergent and/or fabric softener that is subsequently applied, one could distinctly
improve the odor of the fabrics treated with these products and prolong the fragrance
of the fabrics after drying.
[0006] U.S. Letters Patent No. 5,649,979 provides a process for perfuming fabrics washed
in the presence of a lipase-containing detergent and, optionally, subsequently treated
with a fabric softener with the process being characterized in that the detergent
and/or fabric softener contains a compound of the formula:

wherein:
(a) R represents a radical derived from a fragrant alcohol of formula ROH and Y represents a C7 to C24 linear or branched, saturated or unsaturated alkyl radical, or a ―(CH2)nCOOR group wherein R is defined as above and n is an integer from 0 to 6; or
(b) Y represents a C7 to c24 linear or branched, saturated or unsaturated alkyl radical and R represents a group of the formula:

wherein either R1 represents hydrogen and R2 represents an alkylidene radical derived from a fragrant aldehyde of the formula:

or R2 represents an alkylidene radical and R1 an alkyl radical, R1 and R2 being then derived from a fragrant ketone of the formula:

and, optionally, being part of a ring such as indicated by the dashed line which
contains 5 to 18 carbon atoms and can be substituted.
Examples relevant to our invention as set forth in U.S. Letters Patent No. 5,649,979
are:
the compound having the structure:

(at column 12, line 3) and the compound having the structure:

(at column 12, line 57), both compounds being adipic acid esters.
[0007] However, nothing in U.S. Letters Patent No. 5,649,979 and nothing in the prior art
indicates the creation of the synergistic effect of formation of the mixture of the
two fragrant materials in situ, 2-ethyl hexanol and the mixture of tricyclic isochromans
having the structures:

(GALAXOLIDE®) as a result of admixing in proportions of from about 1:1 up to about
3:1 (weight:weight) of di(2-ethyl hexyl) adipate and GALAXOLIDE® and nothing in the
prior art indicates that as a result of the discovery of such a mixture the concentration
of pure GALAXOLIDE® can be greatly increased, particularly when used with fabric detergent
and fabric softener systems which use enzymes.
THE INVENTION
[0008] Our invention concerns a process for the creation of a liquid fragrance composition
that is easily used in forming still further liquid fragrance compositions, containing
GALAXOLIDE®, a mixture of compounds having the structures:

comprising the steps of admixing a sufficient quantity of di(2-ethyl hexyl) adipate
with substantially pure GALAXOLIDE®, thereby creating a composition in the liquid
phase having a viscosity in the range of from about 180 centipoises (cps) up to about
250 cps at 25°C.
[0009] More specifically, our invention is directed to a mixture consisting essentially
of:
(i) tricyclic isochroman compounds having the structures:

(ii) di(2-ethyl hexyl) adipate having the structure:

with the range of weight raios of tricyclic isochroman:di(2-ethyl hexyl) adipate
being from about 1:1 up to about 3:1.
More preferably, the foregoing mixture of tricyclic isochroman and di(2-ethyl hexyl)
adipate is 2:1 and the viscosity thereof is about 210 cps at 25°C.
[0010] Our invention is further directed to a laundry detergent or fabric softener comprising
the above-identified perfuming composition as an active perfume ingredient. Our invention
is further directed to a method for perfuming fabrics which comprises washing the
fabrics in the presence of a lipase-containing detergent and, optionally, subsequently
treating the fabric with a fabric softener wherein the detergent or fabric softener
comprises as an active perfume ingredient the above-identified range of mixtures of
tricyclic isochroman compounds having the structures:

and di(2-ethyl hexyl) adipate having the structure:

with the range of weight ratios of tricyclic isochroman:di(2-ethyl hexyl) adipate
being from about 1:1 up to about 3:1.
[0011] Relevant to the uniqueness of the mixture of GALAXOLIDE® and the di(2-ethyl hexyl)
adipate of our invention is the fact that the calculated log
10[n-octanol/water partition coefficient] (hereinafter referred to as "C log
10P" is in the range of from about 4.4 up to about 7.0 with the low part of the C log
10P range being for the mixture have the ratio of GALAXOLIDE®:di(2-ethyl hexyl) adipate
of 3:1, and the high part of the range (7.0) being for the ratio of GALAXOLIDE®:di(2-ethyl
hexyl) adipate of 1:1. Accordingly, for the di(2-ethyl hexyl) adipate - GALAXOLIDE®
compositions of matter of our invention, the following inequality applies:

The C log
10P of the most preferred composition of our invention, the composition wherein the
ratio of GALAXOLIDE®:di(2-ethyl hexyl) adipate is 2:1, is 6.61.
[0012] The standard for the optimum GALAXOLIDE® aroma is for the main peak of the GALAXOLIDE®
(that is for the presence of the compound having the structure:

to be between 52% and 56% by weight of all components obtained in a GLC (liquid chromatography)
sample. Thus, when using a diethyl phthalate solvent (with diethyl phthalate having
the structure:

the equation of
G vs.
W is:

. On the other hand, when using in place of the di(2-ethyl hexyl) adipate, octyl benzoate
having the structure:

the equation of
G vs.
W is:

.
[0013] When using di(2-ethyl hexyl) adipate (the mixture of our invention), the equation
is:

.
[0014] Thus, the mixture of GALAXOLIDE® and di(2-ethyl hexyl) adipate in combination provides
a new aroma containing notes of both 2-ethyl hexanol and GALAXOLIDE®, but also enables
the GALAXOLIDE® to be used in much greater proportions than has been used before,
for example, with diethyl phthalate.
[0015] In addition, the process of our invention is advantageous whenever other fragrance
compounds are also used which show a weak tenacity on fabrics and which are compatible
from an olfactory standpoint with GALAXOLIDE® and 2-ethyl hexanol.
[0016] The GALAXOLIDE® - di(2-ethyl hexyl) adipate of our invention can be added to detergents
and fabric softeners either as such or in admixture with other perfuming ingredients,
solvents or adjuvants of current use in perfumery. The concentrations in which they
can be added to the detergents and fabric softeners according to the inventions have
the values usual in the art for this type of product. The skilled person in the art
is quite able to select such values as a function of the nature of the product to
be perfumed and of the desired olfactive effect. By way of example, concentrations
of the order of from about 0.005 up to about 7% by weight of the mixture of GALAXOLIDE®
and di(2-ethyl hexyl) adipate relative to the weight of detergent and/or fabric softener
composition are useful.
[0017] The fabric detergents and softeners, according to our invention, can take the form
of powders or granular solids, bars, pastes as well as aqueous or non-aqueous liquids
and contain the usual ingredients for this type of product. Thus the detergents can
typically contain, in addition to the lipase enzyme (as specifically disclosed in
European Patent No. 430,315) active anionic, cationic, nonionic or zwitterionic surfactants
as well as filling agents, bleaching agents, confining agents and other ingredients
of current use in the detergent bases intended for washing cloth such as linen. Many
examples of such compositions are found in the art and in literature, for example,
European Patent No. 397,245. By way of example, a base detergent of this type to which
there is added the lipase in the desired concentrations can have the following composition
(origin: Henkel KGaA of Düsseldorf, Germany):
| Ingredients |
Parts by Weight |
| Linear sodium alkyl benzene sulfonate (average length of the alkyl chain: C11.5) |
8.0 |
| Ethoxylated tallow alcohol |
2.9 |
| Sodium triphosphate |
43.8 |
| Sodium silicate |
7.5 |
| Magnesium silicate |
1.9 |
| Carboxymethylcellulose |
1.2 |
| Sodium ethylenediaminetetraacetate |
0.2 |
| Sodium sulfate |
21.2 |
| Water |
13.3 |
| Total |
100.0 |
[0018] Similar considerations apply to the fabric softener bases useful in the practice
in our invention which typically contain cationic softening ingredients as cited in
European Patent No. 397, 245.
BRIEF DESCRIPTION OF THE DRAWINGS
[0019]
Figure 1 is the GLC profile for a mixture of two parts GALAXOLIDE® (a mixture of compounds
having the structures:

and one part di(2-ethyl hexyl) adipate having the structure:

(conditions: 250 mm capillary silica column programmed from 50 up to 250°C at 10°C
per minute).
Figure 2 is another GLC profile for the 2:1 mixture of GALAXOLIDE® di(2-ethyl hexyl) adipate
(conditions: 200 mm CARBOWAX® 20M column programmed from 50 up to 250°C at 10°C per
minute).
Figure 3 is a graph showing on the Y axis the GLC percent main peak for GALAXOLIDE® (the main peak being for the compound
having the structure:

vs. weight percent GALAXOLIDE® undiluted in the mixture on the X axis.
DETAILED DESCRIPTION OF THE DRAWINGS
[0020] Referring to Figure 1, the peak indicated by reference numeral
10 is the peak for the compound having the structure:

The peak indicated by reference numeral
12 is the peak for the di(2-ethyl hexyl) adipate.
[0021] Referring to Figure 2, the peak indicated by reference numeral
20 is the peak for the compound having the structure:

The peak indicated by reference numeral
22 is the peak for the di(2-ethyl hexyl) adipate

[0022] Referring to Figure 3, the
Y axis for the GLC percent for the main peak of GALAXOLIDE® is indicated by reference
numeral
36 and the weight percent GALAXOLIDE® (undiluted) on the
X axis is indicated by reference numeral
35. The graph indicated by reference numeral
30 is the graph for the mixtures of GALAXOLIDE® and diethyl phthalate having the structure:

The graph indicated by reference numeral
32 is the graph for mixtures of GALAXOLIDE® and di(2-ethyl hexyl) adipate. The graph
indicated by reference numeral
34 is the graph for mixtures of GALAXOLIDE® and 2-ethyl hexyl benzoate having the structure:

[0023] The use of the di(2-ethyl hexyl) adipate with the tricyclic isochroman:
(iv) enables the creation of novel mixtures of the fragrance material, 2-ethyl hexanol
and the tricyclic isochroman mixture defined according to the three structures:

when using an enzyme detergent via control release mechanisms for the fragrance composition.
(i) enables the concentration of the initial tricyclic isochroman to be substantially
increased (and still be useful in conjunction with the mixing of same with other fragrances);
(ii) significantly eliminates any adverse viscosity problem caused by the increasing
concentration of the tricyclic isochroman;
(iii) facilitates the use of high concentrations of tricyclic isochroman in connection
with fabric softeners and detergents; and
EXAMPLE I
TEST ON FABRICS
[0024] A number of tests were carried out on fabrics under a variety of conditions, with
the fabrics having been treated according to the following method:
[0025] A standard cotton swatch of 32 grams is placed in a LINITEST® type vessel containing
1.3 grams of a standard powder detergent base comprising 1% by weight of lipase (LIPOLASE®
100T manufactured by Novo Nordisk S.A. of Denmark) and 260 ml water. The cotton swatch
is washed for 30 minutes at 40°C. It is then taken out of the vessel and rinsed with
3 x 200 ml portions of water. It is then plunged for 5 minutes in 200 ml water containing
0.6 grams of a fabric softener base which contains a certain percentage by weight
comprised between 0.5 and 1% of a mixture of GALAXOLIDE® and di(2-ethyl hexyl) adipate
or, when applicable, of the corresponding alcohol which is 2-ethyl hexanol-1. The
cotton swatch is then spin-dried without having been used and dried on a clothes line.
[0026] This method is equivalent to a washing in a real machine for washing 5 kg of linen
in approximately 20 liters of water with a rinsing of 4 x 20 liters of water, the
fabric softener being applied in the last rinsing water. The fabric softener base
used has the following compositions:
| Ingredients |
Parts by Weight |
| ARQUAD® 2HT (75%) (trademark of Akzo Corporation of the Netherlands) |
5.00 |
| Formalin (40%) |
0.20 |
| Demineralized water |
94.80 |
| Total |
100.00 |
[0027] In two separate tests, the cotton swatches were treated according to this general
method, using as an additive to the fabric softener, respectively, (i) a 2:1 mixture
of GALAXOLIDE®:di(2-ethyl hexyl) adipate, 1% in test
A; and (ii) a 2:1 weight:weight mixture of GALAXOLIDE®:2-ethyl hexanol-1 in test
B.
[0028] The two swatches were submitted for a blind panel test evaluation 24 hours after
having been taken out of the LINITEST® apparatus. Each member of the panel is then
requested to smell a strip which had been dipped into 2-ethyl hexanol-1 in order to
cause them to be familiar with the odor of this particular component. Each member
of the panel was then asked to smell the two cotton swatches as set forth above and
state whether they detect the nuances of (i) 2-ethyl hexanol-1 and (ii) GALAXOLIDE®.
[0029] With the swatches of tests
A and
B, all members of the panel detected all nuances of GALAXOLIDE®.
[0030] Seventy percent of the panel members detected all of the nuances of 2-ethyl hexanol-1
in test
A. Twenty-five percent of the panel members detected all of the nuances of 2-ethyl
hexanol-1 in test
B.
[0031] A further evaluation of the two swatches was carried out by the same panel under
identical conditions 24 hours later, that is, 48 hours after taking the swatches out
of the LINITEST® apparatus. None of the panel members could identify the aroma of
2-ethyl hexanol-1 on the swatch of test
B, whereas 50% of the panel members identified all of the nuances of 2-ethyl hexanol-1
on the swatch coming out of test
A.
[0032] Similar results are obtained when the above-mentioned mixture of GALAXOLIDE® and
di(2-ethyl hexyl) adipate were present in the fabric softener at a rate of 0.5% by
weight.
EXAMPLE II
FABRICS TREATED IN A WASHING MACHINE
[0033] A base perfume composition is prepared by admixing the following ingredients:
| Ingredients |
Percent by Weight |
| Vetiver Venezuela |
30 |
| Phenylethyl alcohol |
25 |
| Benzylpropionate |
20 |
| 10-Undecenal |
8 |
| Hexylcinnamic aldehyde |
80 |
| Methyl anthranilate |
20 |
| Verdyl acetate |
30 |
| Trans, trans-δ-damascone |
12 |
| Eugenol |
8 |
| Isoeugenol |
20 |
| Orange essential oil |
25 |
| Benzylsalicylate |
40 |
| Phenylsalicylate |
25 |
| α-Terpeniol |
20 |
[0034] Two compositions are prepared with the aforementioned base as follows:
Composition A:
500 parts by weight of fragrance composition and 150 parts by weight of the mixture
of GALAXOLIDE®:di(2_ethyl hexyl) adipate, in a weight ratio of 2:1; and
Composition B:
500 parts by weight of the fragrance as set forth, supra, and 150 parts by weight
of a 2:1 mixture of GALAXOLIDE® (100%) and 2-ethyl hexanol-1 (2:1).
[0035] The resulting compositions are then each added at the rate of 0.7% by weight to a
non-perfumed fabric softener base to prepare two samples:
A and
B of a perfumed softener.
[0036] In two identical washing machines, two standard batches of 1,400 grams each of cotton
textiles were treated. Each machine was charged with 130 grams of a standard, unperfumed
detergent base containing 1% of lipase (LIPOLASE® 100T of the Novo Nordisk S.A. of
Denmark).
[0037] To one machine, 100 grams of the perfumed softener
A was added. To the second machine, 100 grams of the perfumed softener
B was added.
[0038] After washing, each batch of textiles was sampled by a blind panel of 25 individuals.
Each member of the blind panel identified the aroma of the batch treated with perfumed
softener samples
A and
B.
[0039] As a result of this test, 20 panelists indicated a distinct difference between the
quality, intensity and substantivity of the aroma created in a textile batch when
using sample
A compared to using sample
B as follows (on a scale of 1-100):
| Sample |
Intensity |
Substantivity |
Quality |
| A |
8 |
9 |
9 |
| B |
3 |
4 |
8 |
[0040] When the evaluation was repeated after 48 hours of air drying, 50% of the panelists
detected a distinction and that distinction is as follows:
| Sample |
Intensity |
Substantivity |
Quality |
| A |
6 |
8 |
9 |
| B |
1 |
2 |
7 |
[0041] The features disclosed in the foregoing description, in the following claims and/or
in the accompanying drawings may, both separately and in any combination thereof,
be material for realising the invention in diverse forms thereof.
[0042] In the present specification "comprise" means "includes or consists of" and "comprising"
means "including or consisting of".
1. A mixture consisting essentially of (i) tricyclic isochroman compounds having the
structures:

and (ii) di(2-ethyl hexyl) adipate having the structure:

with the range of weight ratios of tricyclic isochroman:di(2-ethyl hexyl) adipate
being from about 1:1 up to about 3:1.
2. The mixture of Claim 1 wherein the weight ratio of tricyclic isochroman:di(2-ethyl
hexyl) adipate is 2:1 and the viscosity thereof is about 210 centipoises (cps) at
25°C.
3. A laundry detergent or fabric softener composition comprising a perfuming composition
comprising as an active perfuming ingredient, the composition of Claim 1.
4. A laundry detergent or fabric softener composition comprising a perfuming composition
comprising as an active perfuming ingredient, the composition of Claim 2.
5. A method for perfuming fabric which comprises washing said fabric in the presence
of a lipase-containing detergent and, optionally, subsequently treating said fabric
with a fabric softener wherein said detergent and said fabric softener each comprise
as an active perfuming ingredient the mixture of Claim 1.
6. A method according to Claim 5 wherein said fabrics, after the washing cycle, are treated
with a fragrance composition containing a mixture of (i) tricyclic isochromans having
the structures:

and (ii) di(2-ethyl hexyl) adipate having the structure:

with the range of weight ratios of tricyclic isochroman:di(2-ethyl hexyl) adipate
being from about 1:1 up to about 3:1 and, in addition, a fragrance composition containing
components other than tricyclic isochromans, 2-ethyl hexanol-1 or di(2-ethyl hexyl)
adipate.
7. A method for perfuming fabric which comprises washing said fabric in the presence
of a lipase-containing detergent and, optionally, subsequently treating said fabric
with a fabric softener wherein said detergent and said fabric softener each comprise
as an active perfuming ingredient the mixture or Claim 2.
8. A method according to Claim 5 wherein said fabrics, after the washing cycle, are treated
with a fabric softener composition containing a mixture of (i) tricyclic isochroman
compounds having the structures:

and (ii) di(2-ethyl hexyl) adipate having the structure:

with the range of weight ratios of tricyclic isochroman:di(2-ethyl hexyl) adipate
being 2:1 and the viscosity of the tricyclic isochroman:di(2-ethyl hexyl) adipate
being about 210 cps at 25°C.
9. A fragrance composition consisting essentially of 2-ethyl hexanol-1 and the tricyclic
isochroman composition containing the compounds having the structures:

wherein the weight ratio of tricyclic isochroman:2-ethyl hexanol-1 is in the range
of from about 1:1 up to about 3:1.
10. A process for creation of a liquid fragrance composition Containing a mixture of compounds
having the structures:

and 2-ethyl hexanol-1 comprising the steps of admixing a sufficient quantity of di(2-ethyl
hexyl) adipate with a substantially pure mixture of the compounds having the structures:
11. A mixture or composition according to any one of Claims 1 to 4 or Claim 9 having a
C log10 P range defined according to the inequality 4.4 ≤ log10P≤ 7.0.
12. A method for perfuming fabric which comprises washing said fabric in the presence
of a detergent and, optionally, subsequently treating said fabric with a fabric softener
wherein said detergent and said fabric softener each comprise as an active perfuming
ingredient the fragrance composition of Claim 9.
13. A process according to Claim 10 further comprising the step of admixing a lipase.
14. A process according to Claim 10 or Claim 13 wherein the liquid fragrance composition
has a viscosity in the range of from about 180 cps up to about 250 cps at 25°C.
15. A process according to Claim 10, 13 or 14 wherein the liquid fragrance composition
has a C log10P range defined according to the inequality 4.4 ≤ log10P≤ 7.0.