JP2008156332A5 - - Google Patents

Info

Publication number

JP2008156332A5

JP2008156332A5 JP2007150109A JP2007150109A JP2008156332A5 JP 2008156332 A5 JP2008156332 A5 JP 2008156332A5 JP 2007150109 A JP2007150109 A JP 2007150109A JP 2007150109 A JP2007150109 A JP 2007150109A JP 2008156332 A5 JP2008156332 A5 JP 2008156332A5

Authority

JP

Japan

Prior art keywords

group

ester compound

liquid

reaction

active microorganism

Prior art date

2007-06-06

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.)

Granted

Links

• Espacenet
• Global Dossier
• Discuss

• -1 ester compound Chemical class 0.000 claims 33
• 239000007788 liquid Substances 0.000 claims 15
• 244000005700 microbiome Species 0.000 claims 15
• 238000002360 preparation method Methods 0.000 claims 11
• 241000607479 Yersinia pestis Species 0.000 claims 9
• WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims 8
• 235000014113 dietary fatty acids Nutrition 0.000 claims 8
• 229930195729 fatty acid Natural products 0.000 claims 8
• 239000000194 fatty acid Substances 0.000 claims 8
• 230000000361 pesticidal effect Effects 0.000 claims 8
• 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 6
• 239000004094 surface-active agent Substances 0.000 claims 6
• FWMNVWWHGCHHJJ-SKKKGAJSSA-N 4-amino-1-[(2r)-6-amino-2-[[(2r)-2-[[(2r)-2-[[(2r)-2-amino-3-phenylpropanoyl]amino]-3-phenylpropanoyl]amino]-4-methylpentanoyl]amino]hexanoyl]piperidine-4-carboxylic acid Chemical compound C([C@H](C(=O)N[C@H](CC(C)C)C(=O)N[C@H](CCCCN)C(=O)N1CCC(N)(CC1)C(O)=O)NC(=O)[C@H](N)CC=1C=CC=CC=1)C1=CC=CC=C1 FWMNVWWHGCHHJJ-SKKKGAJSSA-N 0.000 claims 5
• 241000233866 Fungi Species 0.000 claims 5
• 229940105990 diglycerin Drugs 0.000 claims 5
• GPLRAVKSCUXZTP-UHFFFAOYSA-N diglycerol Chemical compound OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 claims 5
• LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 4
• 235000011037 adipic acid Nutrition 0.000 claims 4
• 239000001361 adipic acid Substances 0.000 claims 4
• GHVNFZFCNZKVNT-UHFFFAOYSA-N decanoic acid Chemical compound CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 claims 4
• 150000004665 fatty acids Chemical class 0.000 claims 4
• 238000009472 formulation Methods 0.000 claims 4
• 230000000813 microbial effect Effects 0.000 claims 4
• 239000000203 mixture Substances 0.000 claims 4
• QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 claims 4
• 150000005846 sugar alcohols Polymers 0.000 claims 4
• 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims 3
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 3
• 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims 3
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 3
• 239000002736 nonionic surfactant Substances 0.000 claims 3
• OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 claims 3
• OBETXYAYXDNJHR-SSDOTTSWSA-M (2r)-2-ethylhexanoate Chemical compound CCCC[C@@H](CC)C([O-])=O OBETXYAYXDNJHR-SSDOTTSWSA-M 0.000 claims 2
• YEGNTQBFSQBGJT-UHFFFAOYSA-N 2-heptylundecan-1-ol Chemical compound CCCCCCCCCC(CO)CCCCCCC YEGNTQBFSQBGJT-UHFFFAOYSA-N 0.000 claims 2
• 239000005632 Capric acid (CAS 334-48-5) Substances 0.000 claims 2
• 241000193160 Isaria tenuipes Species 0.000 claims 2
• 229920003171 Poly (ethylene oxide) Polymers 0.000 claims 2
• 239000003905 agrochemical Substances 0.000 claims 2
• 150000005215 alkyl ethers Chemical class 0.000 claims 2
• OBETXYAYXDNJHR-UHFFFAOYSA-N alpha-ethylcaproic acid Natural products CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 claims 2
• 150000001875 compounds Chemical class 0.000 claims 2
• 238000004945 emulsification Methods 0.000 claims 2
• 238000000034 method Methods 0.000 claims 2
• SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 claims 2
• WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 claims 2
• 239000000575 pesticide Substances 0.000 claims 2
• 108020005096 28S Ribosomal RNA Proteins 0.000 claims 1
• 108020004565 5.8S Ribosomal RNA Proteins 0.000 claims 1
• 241001236817 Paecilomyces <Clavicipitaceae> Species 0.000 claims 1
• ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical class CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 claims 1
• 238000004519 manufacturing process Methods 0.000 claims 1
• SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 claims 1