************FEATURED NEWS***********
Flavor-Base
2004
- A major upgrade to the
world's most extensive database on flavoring materials and
food additives is now available for Windows 95/98/Me/NT/XP
& 2000. Flavor-Base 2004 provides extensive flavor &
regulatory data relevant to the Flavor, Food, Beverage &
Tobacco industries. For more details and
demos - Click
HERE
Flavor
& Fragrance Industry Leaders
- See the Top Ten and their Sales
Volume. View charts on market segments.
For
past News visit our Archives
NEW - Download area for
Demos
Download Flavor-Base
2004
Demo
Download
"Beverage-Master 2000"
Demo for
Excel
Download
"Juice-Master 2000"
Demo for
Exce
Download
"Additive-Master"
for Free
Trial
Download
"VCF 2000 - Volatile Compounds in
Foods"
Demo
Download
FRM 2001 - Flavor Raw Materials
Demo
Download
ESO 2000 - Essential oils
Demo
Download
PMP 2001 - Perfumery Materials
Demo
Special Features on
this Site
Olfaction
- A Review in Progress
Odor and
Flavor Detection
Thresholds
Phytochemical
& Ethnobotanical Search
Page
Search
PubMed .... from
our site
Lycopene - An
Ultimate Phytochemical
Nutraceutical?
Carotenoid
Precursors of Aroma
Constituents
Boronia
- Aromas from
Carotenoids
Saffron
- Aromas from
Carotenoids
Rose -
Aromas from Carotenoids
Osmanthus
- Aromas from Carotenoids
Tobacco -
Aromas from Carotenoids
Aldehydes -
GRAS: Odor
Properties and Molecular
Visualization
Alkenols:
Odor Properties and Molecular
Visualization
Burnt
Sugar Notes: Odor Properties and Molecular
Visualization
delta-Lactones
- GRAS: Odor
Properties and Molecular
Visualization
Esters -
GRAS: Odor
Properties and Molecular
Visualization
gamma-Lactones
- GRAS: Odor
Properties and Molecular
Visualization
Pyrazines
- GRAS: Odor
Properties and Molecular
Visualization
GC-MS analysis
of hardwood smoke
flavor.
GC-MS
analysis of Dark Fire-cured
Tobacco
Visit Perfumer's
World and download the
Perfumer's
Workbook (free) to see the future
of computing in formulation
creativity.
|
Links
to
Takasago International - US
Patents,
1996-2005
as of January 17, 2006
PAT. NO.
|
Title
|
6,987,202
|
Phosphine
compounds, transition metal complexes with the
compounds contained as ligands therein, and
asymmetric synthesis catalysts containing the
complexes
|
6,960,350
|
Antifungal
fragrance composition
|
6,956,139
|
(1R,
2S, 5R)-3-1-menthoxyalkan-1-OL cooling
sensate
|
6,932,986
|
Essential
oil mixture for miticide, miticide composition,
and spray for miticide
|
6,930,083
|
Isomer
composition excellent in chemical resistance
containing optically active
trans-1-(2,2,6-trimethylcyclohexyl)-2-buten-1-one
and fragrance compositions containing the isomer
composition
|
6,903,233
|
Process
for producing optically active
3-halogenocarboxylic acid ester and
3-azidocarboxylic acid ester
|
6,903,067
|
Fragrance
composition containing
3-(3-hexenyl)-2-cyclopentenone
|
6,899,901
|
Sensate
composition imparting initial sensation upon
contact
|
6,890,567
|
Sensate
composition imparting initial sensation upon
contact
|
6,887,820
|
Method
for producing optically active compounds
|
6,855,847
|
Process
for producing optically active amide from
.alpha. .beta.- unsaturated amide derivative in
the presence of transition metal complex
containing phosphine-phosphorane compound and
transition metal
|
6,838,106
|
Warming
composition for food and drink or for oral care
preparation
|
6,838,103
|
Deterioration
preventive agent for milk-containing foods
|
6,833,481
|
Process
for producing 2-alkyl-2cyclopentenones
|
6,822,121
|
Production
process of cyclohexenyl ketones
|
6,811,789
|
Fragrant
composition having mosquito-repelling effect
|
6,805,920
|
Polymerizable
liquid crystal compound and optical film
|
6,794,328
|
Diphosphine
compound, production intermediate thereof,
transition metal complex containing the compound
as ligand and asymmetric hydrogenation catalyst
containing the complex
|
6,780,443
|
Sensate
composition imparting initial sensation upon
contact
|
6,774,269
|
Process
for producing isopulegol
|
6,770,618
|
(1S,6R)-2,2,6-Trimethylcyclohexyl
methyl ketone and/or
(1R,6S)-2,2,6-trimethylcyclohexyl methyl ketone,
process for producing the same, and perfume
composition containing the same
|
6,759,557
|
Melanin
production inhibitors and skincare products
containing such inhibitors
|
6,752,862
|
Color
fading/discoloration preventive agent
|
6,730,629
|
Asymmetric
phosphine ligand
|
6,723,871
|
Process
for producing optically active alcohol
|
6,723,501
|
Methods
of judging mouth odor
|
6,720,016
|
Flavor
composition and stable transparent drink
containing the same
|
6,717,016
|
Phosphine
compound, transition metal complex containing
the same phosphine compound as ligand and
asymmetric synthesis catalyst containing the
complex
|
PAT. NO.
|
Title
|
6,673,844
|
Warming
composition
|
6,645,254
|
Aromatic
bleaching agent composition
|
6,624,320
|
Asymmetric
phosphine ligand
|
6,608,214
|
Process
for producing optically active
.gamma.-butyrolactone
|
6,596,887
|
Process
for producing an optically active
ruthenium-phosphine complex and process for
producing an optically active alcohol by using
the complex
|
6,570,035
|
Process
for producing pivaloyl-acetic acid ester
|
6,570,010
|
Inclusion
compounds of vanillyl alcohol derivative in
cyclodextrin and compositions containing the
same
|
6,548,711
|
Process
for producing 2-vinylcyclododecanone
|
6,548,474
|
Disubstituted
cycloalkanones as fragrance materials
|
6,545,112
|
Process
for producing .beta.-butyrolactone homopolymer
or copolymer
|
6,544,535
|
Composition
for improving cooling sensation effects
|
6,528,074
|
Lipid
composition containing a liquid crystal
structure
|
6,515,188
|
Method
for producing 3-l-menthoxypropane-1,2-diol
|
6,515,156
|
METHOD
FOR PRODUCING AXIAL ASYMMETRIC COMPOUNDS,
INTERMEDIATES FOR PRODUCING THE SAME, COMPLEXES
OF TRANSITION METALS WITH NOVEL AXIAL ASYMMETRIC
COMPOUNDS AS THE LIGANDS, CATALYSTS FOR
ASYMMETRIC HYDROGENATION, AND CATALYSTS FOR
FORMING ASYMMETRIC CARBON-CARBON BONDS
|
6,495,193
|
Citrus
flavor having high stability, method of
preparation thereof and food and drink product
containing said flavor
|
6,492,545
|
Process
for producing optically active alcohol
|
6,489,522
|
Process
for producing optically active
3,7-dimethyl-6-octenol and process for producing
intermediate therefor
|
6,489,273
|
Fragrance
compositions containing
2-cyclohexyl-1,1-dimethyl ethanol esters
|
6,486,353
|
Process
for producing optically active
3,7-dimethyl-6-octenol and process for producing
intermediate therefor
|
6,476,278
|
Processes
for the preparation of alcohols
|
6,475,544
|
Anti-deterioration
agent for food flavors, method for preventing
deterioration of food flavors, and foods
containing anti-deterioration agent for food
flavors
|
6,472,539
|
Production
process of diphosphine oxide and diphosphonate
|
6,465,594
|
Phosphine
derivative and polymer thereof and transition
metal complex comprising the same
|
6,455,720
|
2,2(diarlyl)vinylphosphine
compound, palladium catalyst thereof, and
process for producing arylamine, diaryl, or
arylalkyne with the catalyst
|
6,440,400
|
Trimethylcylohexane
derivatives and melanin-formation inhibitors and
perfumeholding agents with the use of the same
|
6,420,027
|
Biodegradable
complex fiber and method for producing the same
|
6,410,034
|
Dermal
absorption-promoting agent
|
6,407,293
|
Process
for producing 3-1-menthoxypropane-1,2-diol
|
6,403,804
|
Process
for preparing optically active oxazolidinone
derivative
|
6,388,130
|
Method
for producing axial asymmetric compounds, and
intermediates for producing the same
|
6,384,074
|
Cell
growth activating composition containing
compound having labdane structure
|
6,379,735
|
Method
of sugar-like flavorous component and method of
preparation of perfumery composition or beverage
using the resulting flavorous component
|
6,379,659
|
Keratin
fiber strengthening agent and method for
strengthening keratin fiber
|
6,365,776
|
Process
for producing aromatic amines
|
6,365,755
|
Ammonium
3,5,6-trihydroxyhexanoate derivatives and
preparation process thereof
|
6,355,627
|
Branched
cyclodextrin clathrate compound of hinokitiols
and composition containing the same
|
6,355,232
|
Agent
for protecting skin and hair moisture
|
6,342,644
|
Method
for producing 1-menthol
|
6,340,751
|
Process
for the preparation of 4-substituted azetidinone
derivatives
|
6,333,291
|
Optically
active diphosphine compound, production
intermediate thereof, transition metal complex
containing the compound as ligand and asymmetric
hydrogenation catalyst containing the complex
|
6,328,982
|
Cool
feeling composition
|
6,323,353
|
Complexes
of transition metals with novel axial asymmetric
compounds as the ligands
|
6,323,174
|
Diene
compound and process for producing the same
|
6,313,365
|
Ruthenium
metathesis catalyst and method for producing
olefin reaction product by metathesis reaction
using the same
|
6,313,317
|
Ruthenium-phosphine
complex and method for producing the same
|
6,313,214
|
Melanin
inhibiting and cell growth activating
compositions containing compounds having labdane
structure
|
6,294,161
|
Deodorant
composition
|
6,287,618
|
Method
of production of citrus concentrated aroma and
method of preparation of flavorous composition
or drink using the resulting flavorous component
|
6,280,754
|
Dermal
topical formulations
|
6,268,333
|
Sedative
effect-providing fragrance modifier
|
6,248,848
|
Optically
active phosphine derivative having at least two
vinyl groups, polymer produced using the same as
monomer, and transition metal complexes of these
|
6,239,324
|
Diene
compound and process for producing the same
|
6,235,393
|
Biodegradable
complex fiber and method for producing the same
|
6,228,547
|
Bis(3,4-methylenedioxyphenylamino)
derivatives and electrophotographic
photoreceptor containing the derivatives
|
RE37,159
|
Propanol
derivatives and perfumes containing the same
|
6,200,254
|
Macrocyclic
ketones as fragrance materials and methods for
making same
|
6,197,996
|
Process
for preparing optically active carnitine ester
|
6,194,468
|
Hair
growth stimulants
|
6,175,047
|
Ruthenium
metathesis catalyst and method for producing
olefin reaction product by metathesis reaction
using the same
|
6,172,264
|
Triphenylamine
derivative, charge-transporting material
comprising the same, and electrophotographic
photoreceptor
|
6,169,211
|
Process
and apparatus for production of
5-cyclohexadecen-1-one
|
6,169,179
|
Method
for manufacturing
(3S,4R)-4-[(R)-1'-formylethyl]azetidin-2-one
derivatives
|
6,165,615
|
Gradual-releasing
capsule and method for manufacturing the same
|
6,162,470
|
Method
for reducing or eliminating the odor of animal
excreta, compounding ingredient to be used in
the method and feeds, pet foods or foods
containing the compounding ingredient
|
6,150,409
|
Adjuvants
and methods for raising intracellular calcium
ion concentration
|
6,150,065
|
Electrophotographic
photoreceptor
|
6,143,834
|
Optically
active phosphine derivative having at least two
vinyl groups, polymer produced using the same as
monomer, and transition metal complexes of these
|
6,123,945
|
Water-soluble
anti-oxidation agents
|
6,121,343
|
Perfume-containing
controlled release biodegradable resin
composition
|
6,110,888
|
Substituted
phenols as fragrance, flavor and antimicrobial
compounds
|
6,093,345
|
Optically
active compound, liquid crystal composition
containing the same, and liquid crystal
electro-optic element using the same
|
6,086,644
|
Scented
candle and manufacturing method for same
|
6,084,138
|
(E)-(R)-2-alkyl-4-(2,2,3-trimethylcyclopent-3-en-1-yl)-2-buten-1-ol,
process for preparing the same, and use thereof
|
6,083,651
|
Phenothiazine
or phenoxazine derivative, charge-transporting
material comprising the same, and
electrophotographic photoreceptor
|
6,075,154
|
Method
of preparation of
2,2'-bis(diarylphosphino)-6,6'-bis(trifluoromethyl)-1,1'-biphenyl,
transition metal complex using it as ligand, and
optically active 3-hydroxybutanoic acid ester
derivative or .beta.-butyrolactone
|
PAT. NO.
|
Title
|
6,043,380
|
Ruthenium-I0D0-optically
active phosphine complex
|
6,040,465
|
Process
for producing optically active .beta.-lactones
|
6,025,503
|
Process
for producing optically active titanium alkoxide
complexes
|
6,022,936
|
Optically
active phosphine derivative having vinyl group,
polymer produced using the same as monomer, and
transition metal complexes of these
|
6,010,701
|
Cell
proliferator and applications thereof
|
6,008,358
|
Process
for the preparation of piperidinylidene
derivative
|
5,998,668
|
Optically
active compound and process for producing the
same
|
5,998,635
|
Process
for producing a .beta.-lactone derivative
|
5,994,291
|
(E)-(R)-2-alkyl-4-(2,2,3,-Trimethylcyclopent-3-en-1-yl)-2-buten-1-ol,
process for preparing the same, and use thereof
|
5,989,765
|
Triphenylamine
derivative, charge-transporting material
comprising the same, and electrophotographic
photoreceptor
|
5,981,782
|
Ruthenium-optically
active phosphine complex, process for the
preparation thereof and process for the
preparation of optically active
4-methyl-2-oxetanone using same
|
5,981,771
|
Ruthenium-optically
active phosphine complex, process for the
preparation thereof and process for the
preparation of optically active
4-methyl-2-oxetanone using same
|
5,965,803
|
Odor
collection apparatus
|
5,965,059
|
Optically
active compound, antiferroelectric liquid
crystal composition containing the same, process
for producing the same and process for producing
an optically active carboxylic acid
|
5,959,161
|
Method
for producing para-menthane-3,8-diol
|
5,948,460
|
Flavored
product additive and method for using same
|
5,945,559
|
Process
for producing 3-oxocarboxylic acid esters
|
5,942,629
|
Process
for producing optically active pyrrolidine
derivatives
|
5,942,615
|
Phenothiazine
or phenoxazine derivative, charge-transporting
material comprising the same, and
electrophotographic photoreceptor
|
5,925,792
|
Process
for preparing 2-amino-1,3-alkanediol or
derivative thereof, process for preparing
optically active dihydrosphingosine derivative,
and intermediates for optically active
dihydrosphingosine derivative
|
5,922,918
|
Method
for making an optically active diphosphine
ligand
|
5,919,962
|
Process
for preparing ruthenium-phosphine complex
|
5,916,578
|
Lipid
composition containing a liquid crystal phase
|
5,910,610
|
Triphenylamine
derivative, charge-transporting material
comprising the same, and electrophotographic
photoreceptor
|
5,892,133
|
Repellent
agent against harmful insects and perfume
composition containing the same
|
5,882,813
|
Electrophotographic
photoreceptor
|
5,872,273
|
Chiral
diphosphine compound intermediate for preparing
the same transition metal complex having the
same diphosphine compound as ligand and
asymmetric hydrogenation catalyst
|
5,859,249
|
2-phenyl-2-(2'-piperidinylidene)acetate
derivative, process for manufacturing the same,
and process for manufacturing optically active
2-phenyl-2-(2'-piperidinyl)acetate derivative by
asymmetrically hydrogenating the same
|
5,858,348
|
Perfume
composition containing
(4R)-cis-4-methyl-2-substituted-tetrahydro-2H-pyran
derivative and method for improving fragrance by
using
(4R)-cis-4-methyl-2-substituted-tetrahydro-2H-pyran
derivative
|
5,856,590
|
Process
for producing cis-4-t-butylcyclohexanol
|
5,849,961
|
Optically
active 1,1'-biphenanthryl-2,2'-diol, process for
preparing the same, and resolving reagent
comprising the same
|
5,847,222
|
Optically
active diphosphine compound, method for making
the compound, transition metal complex having
the compound as ligand and method for making
optically active substance by use of the complex
|
5,840,811
|
Optically
active block polyester copolymer and method for
production thereof
|
5,837,877
|
Process
for preparing optically active
4-hydroxy-2-pyrrolidone
|
5,831,125
|
Method
of making primary amide derivative
|
5,824,830
|
Ruthenium-phosphine
complex
|
5,824,822
|
Phospphine-phosinite
compound and process for preparing
4-(R)-1'-formylethyl!-azetidin-2-one
derivatives using the same
|
5,824,751
|
Biodegradable
high molecular composition
|
5,820,782
|
Optically
active compound and antiferroelectric liquid
crystal composition containing the same
|
5,808,162
|
Chiral
unsymmetric diphosphine compound and transition
metal complex containing the same as ligand
|
5,804,170
|
Deodorant
composition
|
5,801,271
|
7-(n-substituted
amino)-2-phenylheptanoic acid derivative and
process for manufacturing the same
|
5,789,609
|
Optically
active diphosphine, transition metal complex
containing the same, and process for producing
optically active compound using the complex
|
5,786,386
|
Antibacterial
and fungicidal agent
|
5,780,692
|
Process
for producing optically active benzhydrol
compounds
|
5,780,649
|
Process
for preparing optically active cyclic compounds
|
5,777,103
|
Process
for producing cyclohexylazetidinone
|
5,773,410
|
Method
for purifying (-)-N-isopulegol and citrus
perfume composition containing (-)-N-isopulegol
obtained by the method
|
5,756,863
|
Process
for preparing optically active cyclohexanol
derivatives
|
5,756,760
|
1-substituted-2-diphenylphosphinonaphthalene
and transition metal complex comprising the same
as a ligand
|
PAT. NO.
|
Title
|
5,756,134
|
Process
for producing fruit flavor
|
5,753,610
|
Perfume
containing (6E) -2,3-dihydrofarnesol
|
5,753,609
|
Fragrance
composition containing
4-(1-menthoxymethyl)-2-phenyl-1,3-dioxolane or
its derivatives
|
5,750,804
|
Process
for producing trans-3-isocamphylcyclohexanol
|
5,750,785
|
1,4-bis(2',
2'-diphenylvinyl)benzene derivative and charge
transporting material and electrophotographic
photoreceptor using the same
|
5,736,284
|
Carbazole
derivative charge transporting material using
the same and electrophotographic photoreceptor
|
5,725,894
|
Coccidiosis-relieving
agent and feed containing the same
|
5,716,542
|
Liquid
crystal compound and liquid crystal composition
containing the same
|
5,714,624
|
Oxotitanium
complex, asymmetric hydrogenation catalyst
comprising the complex, and process for
producing .beta.-hydroxy ketone or
.alpha.-hydroxy carboxylic acid ester using the
complex
|
5,712,388
|
Method
of preparing a derivative of optically active
azetidin-2-one
|
5,709,895
|
Process
for producing flavor-containing capsule
|
5,705,678
|
Oxotitanium
complex, asymmetric hydrogenation catalyst
comprising the complex, and process for
producing .beta.-hydroxy ketone or
.alpha.-hydroxy carboxylic acid ester using the
complex
|
5,693,868
|
Method
for producing optically active diphosphine
compounds
|
5,688,985
|
Process
for producing keto nitrile derivative
|
5,686,616
|
Process
for preparing an optically active amine
|
5,672,783
|
Method
for producing 3,7-dimethyl-5,7-octadiene-1-ol or
rose oxide
|
5,667,722
|
Antiferroelectric
liquid crystal compound and antiferroelectric
liquid crystal composition containing the same
|
5,663,460
|
Liquid
l-n-menthol composition and process for
preparing the same
|
5,658,584
|
Antimicrobial
compositions with hinokitiol and citronellic
acid
|
5,648,548
|
Optically
active asymmetric diphosphine and process for
producing optically active substance in its
presence
|
5,631,397
|
Process
for producing optically active diaminohexanone
derivative
|
5,631,345
|
Process
for producing optically active polyketone
|
5,631,344
|
Block
copolymer of polyesters and polycarbonates and
process for preparation thereof
|
5,629,420
|
Substituted
acetoxyazetidinone derivatives and process for
preparing 4-acyloxyazetidinone derivatives
|
5,626,852
|
Composition
containing body activated fragrance for
contacting the skin and method of use
|
5,616,751
|
Oxotitanium
complex, asymmetric hydrogenation catalyst
comprising the complex, and process for
producing .beta.-hydroxy ketone or
.alpha.-hydroxy carboxylic acid ester using the
complex
|
5,608,119
|
(2S)-3-[(1R,
2S,
5R)-[5-methyl-2-(1-methylethyl)-cyclohexyl]oxy]-1,
2-propanediol, process for producing the same,
and compositions containing the same
|
5,606,052
|
Substituted
acetoxyazetidinone derivatives and process for
preparing 4-acyloxyazetidinone derivatives
|
5,599,954
|
N-substituted-7-amino-5-hydroxy-3-oxoheptanoic
acid derivatives and method for producing the
same
|
5,587,510
|
(S)-2-aralkyl-3-chloropropionic
acid and process for the preparation thereof
|
5,581,007
|
Process
for preparing optically active
allophenylnorstatin derivatives
|
5,574,152
|
4-(1,1-dialkoxycarbonylalkyl)
azetidin-2-one derivative and process for
producing 4-(1-carboxyalkyl) azetidin-2-one
derivative using the same
|
5,573,878
|
Triphenylamine
derivative, charge-transporting material
comprising the same, and electrophotographic
photoreceptor
|
5,567,560
|
Triphenylamine
derivative charge-transporting material
containing electrophotographic photoreceptor
|
5,563,295
|
Process
for producing optically active carboxylic acid
|
5,556,998
|
Transition
metal complex, process for the preparation of
the same, and asymmetric hydrogenation catalyst
comprising the same
|
5,545,424
|
4-(1-menthoxymethyl)-2-phenyl-1,3-dioxolane
or its derivatives and flavor composition
containing the same
|
5,532,402
|
Process
for producing optically active
hydroxyalkylphosphonates
|
5,530,150
|
Phosphine
compound, complex containing the phosphine
compound as ligand, process for producing
optically active aldehyde using the phosphine
compound or the complex, and
4-[(R)-1'-formylethyl]azetidin-2-one
derivatives
|
5,523,458
|
Process
for producing optically active diaminohexanone
derivative
|
5,521,042
|
1,4-bis(2',2'-diphenylvinyl)benzene
derivative and charge transporting material and
electrophotographic photoreceptor using the same
|
5,516,883
|
Biodegradable
optically active copolymer and process for
producing the same
|
5,502,221
|
Process
for producing cyclohexylbutyric acid derivative
|
5,496,580
|
Method
for improving flavor of food or drink
|
5,486,441
|
Electrophotographic
photoreceptor containing
1,4-bis(4,4-diphenyl-1,3-butadienyl)benzene
derivative
|
All
Patent Links are USPTO-provided content
For patents prior to 1976 click HERE
Please email us to suggest a link or other suggestion
at leffingwell@mindspring.com
Copyright
© 2000-2001 by Leffingwell &
Associates
|