USPP12213P2 - Hop plant named ‘YCR Accession No. 14’ - Google Patents
Hop plant named ‘YCR Accession No. 14’ Download PDFInfo
- Publication number
- USPP12213P2 USPP12213P2 US09/287,403 US28740399V USPP12213P2 US PP12213 P2 USPP12213 P2 US PP12213P2 US 28740399 V US28740399 V US 28740399V US PP12213 P2 USPP12213 P2 US PP12213P2
- Authority
- US
- United States
- Prior art keywords
- new
- variety
- hop plant
- hop
- methyl
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired - Lifetime
Links
- 244000025221 Humulus lupulus Species 0.000 title description 18
- 241000218228 Humulus Species 0.000 claims abstract 2
- 241000221785 Erysiphales Species 0.000 abstract description 2
- 241000579741 Sphaerotheca <fungi> Species 0.000 abstract description 2
- 125000003118 aryl group Chemical group 0.000 abstract description 2
- ZAJNGDIORYACQU-UHFFFAOYSA-N decan-2-one Chemical compound CCCCCCCCC(C)=O ZAJNGDIORYACQU-UHFFFAOYSA-N 0.000 description 8
- 229930004725 sesquiterpene Natural products 0.000 description 8
- 150000004354 sesquiterpene derivatives Chemical class 0.000 description 8
- WWZKQHOCKIZLMA-UHFFFAOYSA-N Caprylic acid Natural products CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 5
- 239000002253 acid Substances 0.000 description 5
- 150000003505 terpenes Chemical class 0.000 description 5
- 235000007586 terpenes Nutrition 0.000 description 5
- LSKONYYRONEBKA-UHFFFAOYSA-N 2-Dodecanone Chemical compound CCCCCCCCCCC(C)=O LSKONYYRONEBKA-UHFFFAOYSA-N 0.000 description 4
- CJPNOLIZCWDHJK-UHFFFAOYSA-N 2-Pentadecanone Chemical compound CCCCCCCCCCCCCC(C)=O CJPNOLIZCWDHJK-UHFFFAOYSA-N 0.000 description 4
- GLZPCOQZEFWAFX-UHFFFAOYSA-N Geraniol Chemical compound CC(C)=CCCC(C)=CCO GLZPCOQZEFWAFX-UHFFFAOYSA-N 0.000 description 4
- 150000007513 acids Chemical class 0.000 description 4
- YRHYCMZPEVDGFQ-UHFFFAOYSA-N methyl decanoate Chemical compound CCCCCCCCCC(=O)OC YRHYCMZPEVDGFQ-UHFFFAOYSA-N 0.000 description 4
- XPQPWPZFBULGKT-UHFFFAOYSA-N methyl undecanoate Chemical compound CCCCCCCCCCC(=O)OC XPQPWPZFBULGKT-UHFFFAOYSA-N 0.000 description 4
- CYIFVRUOHKNECG-UHFFFAOYSA-N tridecan-2-one Chemical compound CCCCCCCCCCCC(C)=O CYIFVRUOHKNECG-UHFFFAOYSA-N 0.000 description 4
- KYWIYKKSMDLRDC-UHFFFAOYSA-N undecan-2-one Chemical compound CCCCCCCCCC(C)=O KYWIYKKSMDLRDC-UHFFFAOYSA-N 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 235000008694 Humulus lupulus Nutrition 0.000 description 3
- FAMPSKZZVDUYOS-UHFFFAOYSA-N alpha-Caryophyllene Natural products CC1=CCC(C)(C)C=CCC(C)=CCC1 FAMPSKZZVDUYOS-UHFFFAOYSA-N 0.000 description 3
- DQKNHNPHGVWPJF-UHFFFAOYSA-N heptadeca-1,3,5-triene Chemical compound CCCCCCCCCCCC=CC=CC=C DQKNHNPHGVWPJF-UHFFFAOYSA-N 0.000 description 3
- VEGYMPQCXPVQJY-UHFFFAOYSA-N (10ξ)-eudesma-4,6-diene Chemical compound C1CCC2(C)CCC(C(C)C)=CC2=C1C VEGYMPQCXPVQJY-UHFFFAOYSA-N 0.000 description 2
- RKQDKXOBRXTSFS-PIHCAMFYSA-N (4e,7e)-3,3,7,11-tetramethyl-12-oxabicyclo[9.1.0]dodeca-4,7-diene Chemical compound C1C(C)(C)\C=C\CC(/C)=C/CCC2(C)OC21 RKQDKXOBRXTSFS-PIHCAMFYSA-N 0.000 description 2
- GYSCBCSGKXNZRH-UHFFFAOYSA-N 1-benzothiophene-2-carboxamide Chemical compound C1=CC=C2SC(C(=O)N)=CC2=C1 GYSCBCSGKXNZRH-UHFFFAOYSA-N 0.000 description 2
- PVYFCGRBIREQLL-UHFFFAOYSA-N 2-Methylbutyl 2-methylbutanoate Chemical compound CCC(C)COC(=O)C(C)CC PVYFCGRBIREQLL-UHFFFAOYSA-N 0.000 description 2
- POQLVOYRGNFGRM-UHFFFAOYSA-N 2-Tetradecanone Chemical compound CCCCCCCCCCCCC(C)=O POQLVOYRGNFGRM-UHFFFAOYSA-N 0.000 description 2
- SEPQTYODOKLVSB-UHFFFAOYSA-N 3-methylbut-2-enal Chemical compound CC(C)=CC=O SEPQTYODOKLVSB-UHFFFAOYSA-N 0.000 description 2
- NVEQFIOZRFFVFW-UHFFFAOYSA-N 9-epi-beta-caryophyllene oxide Natural products C=C1CCC2OC2(C)CCC2C(C)(C)CC21 NVEQFIOZRFFVFW-UHFFFAOYSA-N 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- GHVNFZFCNZKVNT-UHFFFAOYSA-N Decanoic acid Natural products CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 2
- YWHLKYXPLRWGSE-UHFFFAOYSA-N Dimethyl trisulfide Chemical compound CSSSC YWHLKYXPLRWGSE-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- CYHBDKTZDLSRMY-UHFFFAOYSA-N Hexyl 2-methylpropanoate Chemical compound CCCCCCOC(=O)C(C)C CYHBDKTZDLSRMY-UHFFFAOYSA-N 0.000 description 2
- RKQDKXOBRXTSFS-FTFIOASISA-N Humulene epoxide Natural products C[C@]12O[C@@H]1CC(C)(C)/C=C/C/C(/C)=C\CC2 RKQDKXOBRXTSFS-FTFIOASISA-N 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- YWSDDOFJTUOVMX-VAWYXSNFSA-N Methyl (E)-2-dodecenoate Chemical compound CCCCCCCCC\C=C\C(=O)OC YWSDDOFJTUOVMX-VAWYXSNFSA-N 0.000 description 2
- 239000005640 Methyl decanoate Substances 0.000 description 2
- KGEKLUUHTZCSIP-HOSYDEDBSA-N [(1s,4s,6r)-1,7,7-trimethyl-6-bicyclo[2.2.1]heptanyl] acetate Chemical compound C1C[C@]2(C)[C@H](OC(=O)C)C[C@H]1C2(C)C KGEKLUUHTZCSIP-HOSYDEDBSA-N 0.000 description 2
- QMAYBMKBYCGXDH-UHFFFAOYSA-N alpha-amorphene Natural products C1CC(C)=CC2C(C(C)C)CC=C(C)C21 QMAYBMKBYCGXDH-UHFFFAOYSA-N 0.000 description 2
- XUEHVOLRMXNRKQ-KHMAMNHCSA-N alpha-cubebene Chemical compound CC(C)[C@@H]([C@H]12)CC[C@@H](C)[C@]32[C@@H]1C(C)=CC3 XUEHVOLRMXNRKQ-KHMAMNHCSA-N 0.000 description 2
- OBETXYAYXDNJHR-UHFFFAOYSA-N alpha-ethylcaproic acid Natural products CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 description 2
- UAHWPYUMFXYFJY-UHFFFAOYSA-N beta-myrcene Chemical compound CC(C)=CCCC(=C)C=C UAHWPYUMFXYFJY-UHFFFAOYSA-N 0.000 description 2
- NVEQFIOZRFFVFW-RGCMKSIDSA-N caryophyllene oxide Chemical compound C=C1CC[C@H]2O[C@]2(C)CC[C@H]2C(C)(C)C[C@@H]21 NVEQFIOZRFFVFW-RGCMKSIDSA-N 0.000 description 2
- MNWFXJYAOYHMED-UHFFFAOYSA-N heptanoic acid Chemical compound CCCCCCC(O)=O MNWFXJYAOYHMED-UHFFFAOYSA-N 0.000 description 2
- JARKCYVAAOWBJS-UHFFFAOYSA-N hexanal Chemical compound CCCCCC=O JARKCYVAAOWBJS-UHFFFAOYSA-N 0.000 description 2
- QTGAEXCCAPTGLB-UHFFFAOYSA-N humulene epoxide II Natural products C1CC(C)=CCC(C)(C)C=CCC2(C)OC21 QTGAEXCCAPTGLB-UHFFFAOYSA-N 0.000 description 2
- KQNPFQTWMSNSAP-UHFFFAOYSA-N isobutyric acid Chemical compound CC(C)C(O)=O KQNPFQTWMSNSAP-UHFFFAOYSA-N 0.000 description 2
- GWYFCOCPABKNJV-UHFFFAOYSA-N isovaleric acid Chemical compound CC(C)CC(O)=O GWYFCOCPABKNJV-UHFFFAOYSA-N 0.000 description 2
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 2
- CDOSHBSSFJOMGT-UHFFFAOYSA-N linalool Chemical compound CC(C)=CCCC(C)(O)C=C CDOSHBSSFJOMGT-UHFFFAOYSA-N 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- QIYDQYBDGDYJKD-UHFFFAOYSA-N methyl 6-methylheptanoate Chemical compound COC(=O)CCCCC(C)C QIYDQYBDGDYJKD-UHFFFAOYSA-N 0.000 description 2
- IJXHLVMUNBOGRR-UHFFFAOYSA-N methyl nonanoate Chemical compound CCCCCCCCC(=O)OC IJXHLVMUNBOGRR-UHFFFAOYSA-N 0.000 description 2
- JGHZJRVDZXSNKQ-UHFFFAOYSA-N methyl octanoate Chemical compound CCCCCCCC(=O)OC JGHZJRVDZXSNKQ-UHFFFAOYSA-N 0.000 description 2
- VKCYHJWLYTUGCC-UHFFFAOYSA-N nonan-2-one Chemical compound CCCCCCCC(C)=O VKCYHJWLYTUGCC-UHFFFAOYSA-N 0.000 description 2
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- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 2
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- 229940023569 palmate Drugs 0.000 description 2
- HGBOYTHUEUWSSQ-UHFFFAOYSA-N pentanal Chemical compound CCCCC=O HGBOYTHUEUWSSQ-UHFFFAOYSA-N 0.000 description 2
- XNGKCOFXDHYSGR-UHFFFAOYSA-N perillene Chemical compound CC(C)=CCCC=1C=COC=1 XNGKCOFXDHYSGR-UHFFFAOYSA-N 0.000 description 2
- 238000002798 spectrophotometry method Methods 0.000 description 2
- 239000000341 volatile oil Substances 0.000 description 2
- GRWFGVWFFZKLTI-UHFFFAOYSA-N α-pinene Chemical compound CC1=CCC2C(C)(C)C1C2 GRWFGVWFFZKLTI-UHFFFAOYSA-N 0.000 description 2
- OZQAPQSEYFAMCY-QLFBSQMISA-N α-selinene Chemical compound C1CC=C(C)[C@@H]2C[C@H](C(=C)C)CC[C@]21C OZQAPQSEYFAMCY-QLFBSQMISA-N 0.000 description 2
- YHQGMYUVUMAZJR-UHFFFAOYSA-N α-terpinene Chemical compound CC(C)C1=CC=C(C)CC1 YHQGMYUVUMAZJR-UHFFFAOYSA-N 0.000 description 2
- NPNUFJAVOOONJE-ZIAGYGMSSA-N β-(E)-Caryophyllene Chemical compound C1CC(C)=CCCC(=C)[C@H]2CC(C)(C)[C@@H]21 NPNUFJAVOOONJE-ZIAGYGMSSA-N 0.000 description 2
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- WTARULDDTDQWMU-IUCAKERBSA-N (-)-Nopinene Natural products C1[C@@H]2C(C)(C)[C@H]1CCC2=C WTARULDDTDQWMU-IUCAKERBSA-N 0.000 description 1
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- 239000001490 (3R)-3,7-dimethylocta-1,6-dien-3-ol Substances 0.000 description 1
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- 238000013465 asexual reproduction Methods 0.000 description 1
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- 235000019253 formic acid Nutrition 0.000 description 1
- 229910052949 galena Inorganic materials 0.000 description 1
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- 238000002290 gas chromatography-mass spectrometry Methods 0.000 description 1
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- 230000010354 integration Effects 0.000 description 1
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- -1 isoprenoid compound Chemical class 0.000 description 1
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- 239000003921 oil Substances 0.000 description 1
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Images
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01H—NEW PLANTS OR NON-TRANSGENIC PROCESSES FOR OBTAINING THEM; PLANT REPRODUCTION BY TISSUE CULTURE TECHNIQUES
- A01H5/00—Angiosperms, i.e. flowering plants, characterised by their plant parts; Angiosperms characterised otherwise than by their botanic taxonomy
- A01H5/08—Fruits
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01H—NEW PLANTS OR NON-TRANSGENIC PROCESSES FOR OBTAINING THEM; PLANT REPRODUCTION BY TISSUE CULTURE TECHNIQUES
- A01H6/00—Angiosperms, i.e. flowering plants, characterised by their botanic taxonomy
- A01H6/28—Cannabaceae, e.g. cannabis
Definitions
- This invention relates to a new and distinct variety of hop plant, and more particularly to a new hop plant variety of unknown parentage which was discovered among plants created as part of a controlled breeding program.
- the new variety has been stably reproduced over successive generations. Discovery of the new variety and initial reproduction by root cuttings was carried out in a research nursery in Prosser, Wash., U.S.A. Subsequent asexual reproduction took place in Granger, Wash., U.S.A.
- FIG. 1 shows a hop cone of the new hop plant variety
- FIG. 2 shows a cluster of hop cones of the new hop variety
- FIG. 3 shows a cluster of hop cones of the new hop variety
- FIG. 4 shows a blossom and leaf of the new hop plant variety
- FIG. 5 shows a bine of the new hop plant variety
- FIG. 6 shows a hop plant of the new variety.
- the new hop plant variety is a cultivar of recent origin, used for its bittering and aromatic properties.
- the new variety is moderately tolerant to powdery mildew and Sphaerotheca.
- the new variety produces a medium size compact cone with good pickability (similar to Cascade, unpatented) and storageability (25% to 30% alpha loss after 6 months common storage).
- the cones mature medium early (about September 1 in Granger, Wash., and yield a crop of 2650 to 2880 pounds per acre (2970 to 3230 kg/ha).
- Beta acids 4.0%-5.0% of cone weight (ASBC Spectrophotometric method).
- Aroma. Sharp, floral with spicy notes.
- Analytical data Essential oil profile of YCR Accession No. 14: 110 mg of 10% Adsorbate/150C/5 Min. by DTD-GC-MS.
- sesquiterpene 200 m.w. 0.139 157 base peak 1308 10505 dodecatrienoic acid 0.129 1318 12734 tetradecadienol 0.157 1332 1349 caryophyllyl alcohol 0.017 1342 19979 caryophyllene oxide 0.246 1348 2006 methyltridecadienoate 0.025 1356 12300 2-tetradecanone + methyl- 0.151 tridecenoate + humulene epoxide 1367 2300 methyltridecenoate 0.028 1373 34158 humulene epoxide 0.420 1379 247 0.003 1384 2559 ? sesquiterpene m/z 204/179 0.031 1390 231 ?
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Physiology (AREA)
- Botany (AREA)
- Developmental Biology & Embryology (AREA)
- Environmental Sciences (AREA)
- Natural Medicines & Medicinal Plants (AREA)
- Breeding Of Plants And Reproduction By Means Of Culturing (AREA)
- Detergent Compositions (AREA)
Abstract
A new hop plant variety is disclosed. The new variety is used for its bittering and aromatic properties. The new variety is moderately tolerant to powdery mildew and Sphaerotheca. The new variety produces a medium size compact cone with good pickability and storageability. The cones mature early, and yield a crop of 2650 to 2880 pounds per acre (2970 to 3230 kg/ha).
Description
This invention relates to a new and distinct variety of hop plant, and more particularly to a new hop plant variety of unknown parentage which was discovered among plants created as part of a controlled breeding program. The new variety has been stably reproduced over successive generations. Discovery of the new variety and initial reproduction by root cuttings was carried out in a research nursery in Prosser, Wash., U.S.A. Subsequent asexual reproduction took place in Granger, Wash., U.S.A.
FIG. 1 shows a hop cone of the new hop plant variety;
FIG. 2 shows a cluster of hop cones of the new hop variety;
FIG. 3 shows a cluster of hop cones of the new hop variety;
FIG. 4 shows a blossom and leaf of the new hop plant variety;
FIG. 5 shows a bine of the new hop plant variety; and
FIG. 6 shows a hop plant of the new variety.
The new hop plant variety is a cultivar of recent origin, used for its bittering and aromatic properties. The new variety is moderately tolerant to powdery mildew and Sphaerotheca. The new variety produces a medium size compact cone with good pickability (similar to Cascade, unpatented) and storageability (25% to 30% alpha loss after 6 months common storage). The cones mature medium early (about September 1 in Granger, Wash., and yield a crop of 2650 to 2880 pounds per acre (2970 to 3230 kg/ha).
The following is a detailed botanical description of the new and distinct variety of Humulus lupulus, based on observations of specimens grown in Granger, Wash. during the 1998 growing season. All colors are described according to The Royal Horticultural Society Colour Chart. It should be understood that the botanical and analytical chemical characteristics described will vary somewhat depending upon cultural practices and climate conditions and can vary with location and season.
Bine:
Color.—Yellow green (146C).
Stripe.—Greyed purple (183A).
Stipule color.—Light green.
Stipule direction.—Up, forked.
Diameter.—0.80 cm (measurement taken at 2.75 m).
Shoot emergence.—Medium early to medium; similar to Galena.
Leaves:
Leaf arrangement.—Opposite.
Leaf shape.—Cordate to palmate.
Average length.—17.3 cm.
Average width.—17 cm.
Color — upper surface, mature.—Green (139A).
Color — lower surface, mature.—Green (137B).
Color — upper surface, immature.—Green (137A).
Color — lower surface, immature.—Green (137C).
Number of leaf lobes.—1-5.
Margin.—Serrate.
Serrations per inch.—4 min., 7 max.
Pose.—Downward.
Average petiole length.—8.0 cm.
Petiole color at base.—Greyed purple (183A).
Venation.—Palmate.
Vein color.—Yellow green (146C).
Cones:
Average length.—2.8 cm.
Average diameter.—1.5 cm.
Color.—Bract: Yellow green (144A). Bracteole: Yellow green (145C).
Shape.—Ovoid.
Bract shape.—Ovate.
Bract tip shape.—Acute.
Bract tip position.—Appressed.
Bracteole shape.—Lanceolate.
Shattering potential at harvest average for commercial varieties.—Similar to Cascade.
% Alpha acids.—12.0%-14.0% of cone weigh (ASBC Spectrophotometric method).
% Beta acids.—4.0%-5.0% of cone weight (ASBC Spectrophotometric method).
% Cohumulone.—15.0%-20.0% of alpha acids.
Total oils.—2.0-2.5 mL/100 g.
Aroma.—Sharp, floral with spicy notes.
Analytical data: Essential oil profile of YCR Accession No. 14: 110 mg of 10% Adsorbate/150C/5 Min. by DTD-GC-MS.
MS | Area | Area | |
Spec # | Integration | Peak Assignment | % |
77-246 | 39360 | acetone + isoprene | 0.484 |
306-322 | 7766 | 2-methyl-3-buten-1-ol | 0.096 |
336 | 1454 | pentanal ? | 0.018 |
352 | 266 | hexene | 0.003 |
389 | 850 | formic acid | 0.010 |
396 | 6832 | acetic acid | 0.084 |
422 | 488 | methylpentanone | 0.006 |
430 | 932 | ? m/z 56, 70 peaks | 0.011 |
457 | 2767 | 3-methyl-2-butenal | 0.034 |
471 | 1795 | hexanal | 0.022 |
478 | 3315 | isobutyric acid | 0.041 |
489 | 3359 | n-octane | 0.041 |
539 | 11204 | 3-methylbutyric acid | 0.138 |
545 | 2082 | 2-methylbutyric acid | 0.026 |
548 | 972 | 2-methyl-2-butanol acetate | 0.012 |
555 | 301 | ? m/z 82/81/67 peaks | 0.004 |
561 | 245 | ? m/z 81 peak | 0.003 |
565 | 738 | propanoic acid | 0.009 |
579 | 26435 | 4-penten-2-ol + | 0.325 |
2,6-dimethyl-2,4-heptadiene | |||
592 | 4135 | 5,5-dimethyl-2(5H)-furanone | 0.051 |
603 | 980 | alpha-pinene | 0.012 |
611 | 128 | propylisobutyrate | 0.002 |
617 | 1236 | dimethyltrisulfide | 0.015 |
626 | 9978 | 2-methylbutylpropanoate | 0.123 |
634 | 235 | 6-methyl-5-heptene-2-one | 0.003 |
638 | 15055 | beta-pinene + hexanoic acid | 0.185 |
652 | 1521624 | myrcene | 18.728 |
655 | 9934 | 2,7-dimethyl-2,6-octadiene | 0.122 |
663 | 26663 | isobutyl-2-methylbutyrate | 0.328 |
667 | 31112 | 3-methylbutylisobutyrate | 0.383 |
671 | 19675 | methylheptanoate | 0.242 |
674 | 200 | alpha-terpinene | 0.002 |
677 | 418 | p-cymene | 0.005 |
685 | 10340 | limonene + beta-phellandrene | 0.127 |
690 | 244 | ? terpene | 0.003 |
698 | 4618 | beta-oclmene + | 0.057 |
pentyl-2-methylpropanoate | |||
712 | 584 | gamma-terpinene | 0.007 |
717 | 1726 | Isooctanol | 0.021 |
728 | 8437 | heptanoic acid | 0.104 |
733 | 31157 | methyl-6-methylheptanoate + | 0.383 |
2-nonanone | |||
738 | 1362 | linalool oxide | 0.017 |
747 | 34668 | linalool + nonanal + | 0.427 |
3-(4-methyl-3-pentenyl)-furan | |||
752 | 8440 | 2-methylbutyl-2-methylbutyrate | 0.104 |
756 | 9488 | pentyl-3-methylbutyrate | 0.117 |
762 | 292 | ? terpene | 0.004 |
769 | 34847 | methyloctanoate | 0.429 |
775 | 1026 | 0.013 | |
779 | 3860 | 2,3-dihydro-3,5-dihydroxy-6-methyl- | 0.048 |
4(H)-pyran-4-one | |||
790 | 5801 | octanoic acid (branched isomer) | 0.071 |
797 | 1219 | hexylisobutyrate | 0.015 |
800 | 312 | cis-3-hexenylisobutyrate | 0.004 |
802 | 614 | 2-decanone (branched isomer) | 0.006 |
806 | 220 | 2-decanone (branched isomer) | 0.003 |
815 | 492 | ? terpene m/z 41/69 peaks | 0.006 |
829 | 27744 | ? 130 m.w.branched alcohol m/z | 0.341 |
59 base peak + octanoic acid | |||
836 | 1313 | ? terpene m/z 41/69/152 peaks | 0.016 |
841 | 13019 | 2-decanone | 0.160 |
846 | 6935 | methyl-4-octenoate | 0.065 |
852 | 241 | 0.003 | |
858 | 1223 | heptylpropanoate | 0.015 |
864 | 4438 | methylnonenoate | 0.055 |
881 | 24061 | methylnonanoate | 0.296 |
886 | 2321 | nerol | 0.029 |
892 | 460 | 0.006 | |
899 | 235 | 0.003 | |
904 | 531 | 0.007 | |
910 | 2019 | 2-methylheptylpropanoate | 0.025 |
915 | 66621 | geraniol | 0.820 |
918 | 18565 | 2-undecanone (branched isomer) | 0.228 |
925 | 1264 | ? terpene m/z 41/69 peaks | 0.016 |
939 | 20854 | undecenyl alcohol | 0.257 |
950 | 1126 | octenyl acetate | 0.014 |
955 | 166 | ? 180 m.w., 95 base peak, | 0.002 |
possibly bornylformate | |||
963 | 101264 | methyldecanoate (branched isomer) + | 1.246 |
2-undecanone | |||
978 | 920 | octylpropanoate | 0.011 |
963 | 160309 | methyl-4-decenoate + | 1.973 |
methyl-4,8-decadienoate | |||
996 | 51491 | methylgeranate | 0.634 |
1004 | 40310 | methyldecanoate | 0.496 |
1016 | 1736 | decanoic acid (branched isomer) | 0.021 |
1034 | 6140 | octyl-2-methylpropanoate | 0.076 |
1039 | 958 | ? unsaturated alcohol or aldehyde | 0.012 |
1050 | 14056 | 2-dodecanone (branched isomer) | 0.173 |
1057 | 6412 | alpha-cubebene | 0.079 |
1064 | 6428 | decanoic acid | 0.079 |
1073 | 3240 | geranyl acetate | 0.040 |
1078 | 1933 | ? acetate | 0.024 |
1082 | 23 | possibly bornylacetate | 0.000 |
1087 | 6203 | alpha-ylangene + methylundecanoate | 0.076 |
(branched isomer) | |||
1092 | 29196 | alpha-copaene + 2-dodecanone | 0.359 |
1107 | 2850 | ? 204 m.w. sesquiterpene | 0.035 |
1113 | 3500 | methylundecadienoate | 0.043 |
1123 | 1495 | methyl -10-undecenoate | 0.018 |
1129 | 1024 | ? sesquiterpene 206 m.w. | 0.013 |
163 base peak | |||
1135 | 2161 | methylundecanoate | 0.027 |
1151 | 1612921 | caryophyllene | 19.852 |
1159 | 33311 | beta-cubebene | 0.410 |
1164 | 835 | 0.010 | |
1169 | 1805 | ? sesquiterpene 206 m.w. | 0.022 |
163 base peak | |||
1180 | 5290 | 2-tridecanone (branched isomer) | 0.065 |
1196 | 3160413 | humulene | 38.898 |
1200 | 2148 | ? 204 m.w. | 0.026 |
sesquiterpene 161 base peak | |||
1204 | 350 | methyldodecenoate | 0.004 |
1215 | 67631 | gamma-muurolene | 0.832 |
1224 | 45481 | 2-tridecanone | 0.560 |
1230 | 24862 | metyldodecenoate (branched isomer) | 0.306 |
1238 | 176494 | methyl-3,6-decadienoate | 2.172 |
1246 | 53191 | geranyl isobutyrate + | 0.655 |
alpha-selinene (scan 1242) | |||
1251 | 20079 | methyldodecenoate + delta-cadinene | 0.247 |
1262 | 64843 | alpha-muurolene | 0.798 |
1266 | 2064 | calamenene | 0.025 |
1273 | 95640 | beta-cardinene | 1.177 |
1276 | 1865 | delta-selinene | 0.023 |
1285 | 10335 | sesquiterpene w/no common name | 0.127 |
CAS#16728-99-7, cadinene-type | |||
1292 | 11255 | ? sesquiterpene 200 m.w. | 0.139 |
157 base peak | |||
1308 | 10505 | dodecatrienoic acid | 0.129 |
1318 | 12734 | tetradecadienol | 0.157 |
1332 | 1349 | caryophyllyl alcohol | 0.017 |
1342 | 19979 | caryophyllene oxide | 0.246 |
1348 | 2006 | methyltridecadienoate | 0.025 |
1356 | 12300 | 2-tetradecanone + methyl- | 0.151 |
tridecenoate + humulene epoxide | |||
1367 | 2300 | methyltridecenoate | 0.028 |
1373 | 34158 | humulene epoxide | 0.420 |
1379 | 247 | 0.003 | |
1384 | 2559 | ? sesquiterpene m/z 204/179 | 0.031 |
1390 | 231 | ? 222 m.w. sesquiterpene | 0.003 |
1399 | 11574 | globutol | 0.142 |
1411 | 15578 | delta-cadinol | 0.192 |
1429 | 35634 | pentadecatrienol | 0.439 |
1436 | 821 | 2-pentadecanone (branched isomer) | 0.010 |
1445 | 12234 | pentadecadienol | 0.151 |
1451 | 5168 | heptadecatriene | 0.064 |
1463 | 770 | heptadecatriene | 0.009 |
1467 | 1248 | heptadecatriene | 0.015 |
1481 | 1416 | 2-pentadecanone | 0.017 |
1499 | 968 | caryophyllyl acetate | 0.012 |
1580 | 2392 | ? 250 m.w. w/115 base peak | 0.029 |
1772 | 703 | ? long chain isoprenoid compound | 0.009 |
1944-1995 | 337102 | mix of hop acid analogues (lupulon, | |
humulon + dihydro derivatives) | |||
8124778 | Total Essential Oil Components | 100.000 | |
(minus hop acids) | |||
Claims (1)
1. A new variety of hop plant, substantially as herein shown and
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US09/287,403 USPP12213P2 (en) | 1999-04-06 | 1999-04-06 | Hop plant named ‘YCR Accession No. 14’ |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US09/287,403 USPP12213P2 (en) | 1999-04-06 | 1999-04-06 | Hop plant named ‘YCR Accession No. 14’ |
Publications (1)
Publication Number | Publication Date |
---|---|
USPP12213P2 true USPP12213P2 (en) | 2001-11-20 |
Family
ID=23102751
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US09/287,403 Expired - Lifetime USPP12213P2 (en) | 1999-04-06 | 1999-04-06 | Hop plant named ‘YCR Accession No. 14’ |
Country Status (1)
Country | Link |
---|---|
US (1) | USPP12213P2 (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20040202760A1 (en) * | 2003-04-11 | 2004-10-14 | Dewis Mark L. | Alkyldienamides exhibiting taste and sensory effect in flavor compositions |
US7141686B2 (en) | 2003-07-10 | 2006-11-28 | International Flavors & Fragrances Inc. | E2, E4, Z8-undecatrienoic acid and ester and carboxamide derivatives thereof, organoleptic uses thereof and processes for preparing same |
US7632531B2 (en) | 2003-04-11 | 2009-12-15 | International Flavors & Fragnances Inc. | Alkyldienamides exhibiting taste and sensory effect in flavor compositions |
US8007839B2 (en) | 2003-10-03 | 2011-08-30 | International Flavors & Fragrances | Conjugated dienamides, methods of production thereof, compositions containing same and uses thereof |
-
1999
- 1999-04-06 US US09/287,403 patent/USPP12213P2/en not_active Expired - Lifetime
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20040202760A1 (en) * | 2003-04-11 | 2004-10-14 | Dewis Mark L. | Alkyldienamides exhibiting taste and sensory effect in flavor compositions |
US7361376B2 (en) | 2003-04-11 | 2008-04-22 | International Flavors & Fragrances Inc. | Alkyldienamides exhibiting taste and sensory effect in flavor compositions |
US7632531B2 (en) | 2003-04-11 | 2009-12-15 | International Flavors & Fragnances Inc. | Alkyldienamides exhibiting taste and sensory effect in flavor compositions |
US7141686B2 (en) | 2003-07-10 | 2006-11-28 | International Flavors & Fragrances Inc. | E2, E4, Z8-undecatrienoic acid and ester and carboxamide derivatives thereof, organoleptic uses thereof and processes for preparing same |
EP2112135A2 (en) | 2003-07-10 | 2009-10-28 | INTERNATIONAL FLAVORS & FRAGRANCES INC. | E2, E4,Z8-undecatrienoic acid and ester and carboxamide derivatives thereof, organoleptic uses thereof and processes for preparing same |
US8007839B2 (en) | 2003-10-03 | 2011-08-30 | International Flavors & Fragrances | Conjugated dienamides, methods of production thereof, compositions containing same and uses thereof |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
AS | Assignment |
Owner name: YAKIMA CHIEF RANCHES, INC., WASHINGTON Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:ZIMMERMANN, CHARLES E.;REEL/FRAME:010065/0893 Effective date: 19990621 |