Loading…
Replacement of carcinogenic solvent HMPA by DMI in insect sex pheromone synthesis
Hexamethylphosphoric triamide (HMPA) is a good solvent for the alkylation of terminal acetylenes; however, it has been proven to be a carcinogen towards rats and should be considered as a serious risk to man when a large-scale synthesis is involved. Thus the search for a safe alternative is importan...
Saved in:
Published in: | Journal of chemical ecology 1990-12, Vol.16 (12), p.3245-3253 |
---|---|
Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c430t-18de9314f84c6c34f3d389f969622ceb2c5ed956805cd972d0291ebfef5c92993 |
---|---|
cites | cdi_FETCH-LOGICAL-c430t-18de9314f84c6c34f3d389f969622ceb2c5ed956805cd972d0291ebfef5c92993 |
container_end_page | 3253 |
container_issue | 12 |
container_start_page | 3245 |
container_title | Journal of chemical ecology |
container_volume | 16 |
creator | Lo, C.C. (TACTRI, Taiwan, R.O.C.) Chao, P.M |
description | Hexamethylphosphoric triamide (HMPA) is a good solvent for the alkylation of terminal acetylenes; however, it has been proven to be a carcinogen towards rats and should be considered as a serious risk to man when a large-scale synthesis is involved. Thus the search for a safe alternative is important. The physical properties of 1,3-dimethyl-2-imidazolidinone (DMI) are similar to DMPU (1,3-dimethyl-2-oxo-hexahydropyrimidine) and HMPA, but the potential toxicological risk of DMI is less than DMPU and HMPA. When used in the alkylation of terminal acetylenes, DMI is comparable with HMPA, thus it is a good alternative solvent to the carcinogen HMPA in the alkylation because it provides a safer working environment than DMPU and HMPA |
doi_str_mv | 10.1007/bf00982095 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_15820468</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>15820468</sourcerecordid><originalsourceid>FETCH-LOGICAL-c430t-18de9314f84c6c34f3d389f969622ceb2c5ed956805cd972d0291ebfef5c92993</originalsourceid><addsrcrecordid>eNo90M9LwzAUB_Agis7pxaMHyUE8CNX8aNLm6K-5wYY_dy5p-qKVtqlJJ-6_t2ObkEfg8eHx3hehE0quKCHJdW4JUSkjSuygARUJj6iQdBcNVu2IcE4P0GEIX4QQJlOxjw5YzCTva4BeXqGttIEamg47i432pmzcBzSlwcFVP6v-ePZ8g_Mlvp9NcNn0L4DpcIBf3H6Cd7VrAIdl031CKMMR2rO6CnC8-YdoPnp4vxtH06fHyd3NNDIxJ11E0wIUp7FNYyMNjy0veKqskkoyZiBnRkChhEyJMIVKWEGYopBbsMIophQfoov13Na77wWELqvLYKCqdANuETIq-khimfbwcg2NdyF4sFnry1r7ZUZJtgowux1tA-zx2WbqIq-h-KfbxHpwvgE6GF1ZrxtThn8nKJFCrrY7XTOrXaY_fE_mb_29UqYJ_wODo37s</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>15820468</pqid></control><display><type>article</type><title>Replacement of carcinogenic solvent HMPA by DMI in insect sex pheromone synthesis</title><source>Springer Nature - Connect here FIRST to enable access</source><creator>Lo, C.C. (TACTRI, Taiwan, R.O.C.) ; Chao, P.M</creator><creatorcontrib>Lo, C.C. (TACTRI, Taiwan, R.O.C.) ; Chao, P.M</creatorcontrib><description>Hexamethylphosphoric triamide (HMPA) is a good solvent for the alkylation of terminal acetylenes; however, it has been proven to be a carcinogen towards rats and should be considered as a serious risk to man when a large-scale synthesis is involved. Thus the search for a safe alternative is important. The physical properties of 1,3-dimethyl-2-imidazolidinone (DMI) are similar to DMPU (1,3-dimethyl-2-oxo-hexahydropyrimidine) and HMPA, but the potential toxicological risk of DMI is less than DMPU and HMPA. When used in the alkylation of terminal acetylenes, DMI is comparable with HMPA, thus it is a good alternative solvent to the carcinogen HMPA in the alkylation because it provides a safer working environment than DMPU and HMPA</description><identifier>ISSN: 0098-0331</identifier><identifier>EISSN: 1573-1561</identifier><identifier>DOI: 10.1007/bf00982095</identifier><identifier>PMID: 24263426</identifier><identifier>CODEN: JCECD8</identifier><language>eng</language><publisher>New York, NY: Springer</publisher><subject>ADOXOPHYES ; AMIDAS ; AMIDE ; Animal, plant and microbial ecology ; Biological and medical sciences ; COMPOSE HETEROCYCLIQUE ; COMPOSE ORGANOAZOTE ; COMPUESTO ORGANICO DEL NITROGENO ; COMPUESTOS HETEROCICLICOS ; CONTROL DE INSECTOS ; FEROMONAS ; Fundamental and applied biological sciences. Psychology ; General aspects. Techniques ; Invertebrates ; Lepidoptera ; LUTTE ANTIINSECTE ; Methods and techniques (sampling, tagging, trapping, modelling...) ; NEOPLASMAS ; NEOPLASME ; PHEROMONE ; SEXE ; SEXO ; SOLVANT ; SOLVENTES ; Tortricidae ; TOXICIDAD ; TOXICITE</subject><ispartof>Journal of chemical ecology, 1990-12, Vol.16 (12), p.3245-3253</ispartof><rights>1992 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c430t-18de9314f84c6c34f3d389f969622ceb2c5ed956805cd972d0291ebfef5c92993</citedby><cites>FETCH-LOGICAL-c430t-18de9314f84c6c34f3d389f969622ceb2c5ed956805cd972d0291ebfef5c92993</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=5106569$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24263426$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lo, C.C. (TACTRI, Taiwan, R.O.C.)</creatorcontrib><creatorcontrib>Chao, P.M</creatorcontrib><title>Replacement of carcinogenic solvent HMPA by DMI in insect sex pheromone synthesis</title><title>Journal of chemical ecology</title><addtitle>J Chem Ecol</addtitle><description>Hexamethylphosphoric triamide (HMPA) is a good solvent for the alkylation of terminal acetylenes; however, it has been proven to be a carcinogen towards rats and should be considered as a serious risk to man when a large-scale synthesis is involved. Thus the search for a safe alternative is important. The physical properties of 1,3-dimethyl-2-imidazolidinone (DMI) are similar to DMPU (1,3-dimethyl-2-oxo-hexahydropyrimidine) and HMPA, but the potential toxicological risk of DMI is less than DMPU and HMPA. When used in the alkylation of terminal acetylenes, DMI is comparable with HMPA, thus it is a good alternative solvent to the carcinogen HMPA in the alkylation because it provides a safer working environment than DMPU and HMPA</description><subject>ADOXOPHYES</subject><subject>AMIDAS</subject><subject>AMIDE</subject><subject>Animal, plant and microbial ecology</subject><subject>Biological and medical sciences</subject><subject>COMPOSE HETEROCYCLIQUE</subject><subject>COMPOSE ORGANOAZOTE</subject><subject>COMPUESTO ORGANICO DEL NITROGENO</subject><subject>COMPUESTOS HETEROCICLICOS</subject><subject>CONTROL DE INSECTOS</subject><subject>FEROMONAS</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>General aspects. Techniques</subject><subject>Invertebrates</subject><subject>Lepidoptera</subject><subject>LUTTE ANTIINSECTE</subject><subject>Methods and techniques (sampling, tagging, trapping, modelling...)</subject><subject>NEOPLASMAS</subject><subject>NEOPLASME</subject><subject>PHEROMONE</subject><subject>SEXE</subject><subject>SEXO</subject><subject>SOLVANT</subject><subject>SOLVENTES</subject><subject>Tortricidae</subject><subject>TOXICIDAD</subject><subject>TOXICITE</subject><issn>0098-0331</issn><issn>1573-1561</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1990</creationdate><recordtype>article</recordtype><recordid>eNo90M9LwzAUB_Agis7pxaMHyUE8CNX8aNLm6K-5wYY_dy5p-qKVtqlJJ-6_t2ObkEfg8eHx3hehE0quKCHJdW4JUSkjSuygARUJj6iQdBcNVu2IcE4P0GEIX4QQJlOxjw5YzCTva4BeXqGttIEamg47i432pmzcBzSlwcFVP6v-ePZ8g_Mlvp9NcNn0L4DpcIBf3H6Cd7VrAIdl031CKMMR2rO6CnC8-YdoPnp4vxtH06fHyd3NNDIxJ11E0wIUp7FNYyMNjy0veKqskkoyZiBnRkChhEyJMIVKWEGYopBbsMIophQfoov13Na77wWELqvLYKCqdANuETIq-khimfbwcg2NdyF4sFnry1r7ZUZJtgowux1tA-zx2WbqIq-h-KfbxHpwvgE6GF1ZrxtThn8nKJFCrrY7XTOrXaY_fE_mb_29UqYJ_wODo37s</recordid><startdate>19901201</startdate><enddate>19901201</enddate><creator>Lo, C.C. (TACTRI, Taiwan, R.O.C.)</creator><creator>Chao, P.M</creator><general>Springer</general><scope>FBQ</scope><scope>IQODW</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QR</scope><scope>7SS</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>19901201</creationdate><title>Replacement of carcinogenic solvent HMPA by DMI in insect sex pheromone synthesis</title><author>Lo, C.C. (TACTRI, Taiwan, R.O.C.) ; Chao, P.M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c430t-18de9314f84c6c34f3d389f969622ceb2c5ed956805cd972d0291ebfef5c92993</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1990</creationdate><topic>ADOXOPHYES</topic><topic>AMIDAS</topic><topic>AMIDE</topic><topic>Animal, plant and microbial ecology</topic><topic>Biological and medical sciences</topic><topic>COMPOSE HETEROCYCLIQUE</topic><topic>COMPOSE ORGANOAZOTE</topic><topic>COMPUESTO ORGANICO DEL NITROGENO</topic><topic>COMPUESTOS HETEROCICLICOS</topic><topic>CONTROL DE INSECTOS</topic><topic>FEROMONAS</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>General aspects. Techniques</topic><topic>Invertebrates</topic><topic>Lepidoptera</topic><topic>LUTTE ANTIINSECTE</topic><topic>Methods and techniques (sampling, tagging, trapping, modelling...)</topic><topic>NEOPLASMAS</topic><topic>NEOPLASME</topic><topic>PHEROMONE</topic><topic>SEXE</topic><topic>SEXO</topic><topic>SOLVANT</topic><topic>SOLVENTES</topic><topic>Tortricidae</topic><topic>TOXICIDAD</topic><topic>TOXICITE</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lo, C.C. (TACTRI, Taiwan, R.O.C.)</creatorcontrib><creatorcontrib>Chao, P.M</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Chemoreception Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Journal of chemical ecology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lo, C.C. (TACTRI, Taiwan, R.O.C.)</au><au>Chao, P.M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Replacement of carcinogenic solvent HMPA by DMI in insect sex pheromone synthesis</atitle><jtitle>Journal of chemical ecology</jtitle><addtitle>J Chem Ecol</addtitle><date>1990-12-01</date><risdate>1990</risdate><volume>16</volume><issue>12</issue><spage>3245</spage><epage>3253</epage><pages>3245-3253</pages><issn>0098-0331</issn><eissn>1573-1561</eissn><coden>JCECD8</coden><abstract>Hexamethylphosphoric triamide (HMPA) is a good solvent for the alkylation of terminal acetylenes; however, it has been proven to be a carcinogen towards rats and should be considered as a serious risk to man when a large-scale synthesis is involved. Thus the search for a safe alternative is important. The physical properties of 1,3-dimethyl-2-imidazolidinone (DMI) are similar to DMPU (1,3-dimethyl-2-oxo-hexahydropyrimidine) and HMPA, but the potential toxicological risk of DMI is less than DMPU and HMPA. When used in the alkylation of terminal acetylenes, DMI is comparable with HMPA, thus it is a good alternative solvent to the carcinogen HMPA in the alkylation because it provides a safer working environment than DMPU and HMPA</abstract><cop>New York, NY</cop><pub>Springer</pub><pmid>24263426</pmid><doi>10.1007/bf00982095</doi><tpages>9</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0098-0331 |
ispartof | Journal of chemical ecology, 1990-12, Vol.16 (12), p.3245-3253 |
issn | 0098-0331 1573-1561 |
language | eng |
recordid | cdi_proquest_miscellaneous_15820468 |
source | Springer Nature - Connect here FIRST to enable access |
subjects | ADOXOPHYES AMIDAS AMIDE Animal, plant and microbial ecology Biological and medical sciences COMPOSE HETEROCYCLIQUE COMPOSE ORGANOAZOTE COMPUESTO ORGANICO DEL NITROGENO COMPUESTOS HETEROCICLICOS CONTROL DE INSECTOS FEROMONAS Fundamental and applied biological sciences. Psychology General aspects. Techniques Invertebrates Lepidoptera LUTTE ANTIINSECTE Methods and techniques (sampling, tagging, trapping, modelling...) NEOPLASMAS NEOPLASME PHEROMONE SEXE SEXO SOLVANT SOLVENTES Tortricidae TOXICIDAD TOXICITE |
title | Replacement of carcinogenic solvent HMPA by DMI in insect sex pheromone synthesis |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T14%3A34%3A26IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Replacement%20of%20carcinogenic%20solvent%20HMPA%20by%20DMI%20in%20insect%20sex%20pheromone%20synthesis&rft.jtitle=Journal%20of%20chemical%20ecology&rft.au=Lo,%20C.C.%20(TACTRI,%20Taiwan,%20R.O.C.)&rft.date=1990-12-01&rft.volume=16&rft.issue=12&rft.spage=3245&rft.epage=3253&rft.pages=3245-3253&rft.issn=0098-0331&rft.eissn=1573-1561&rft.coden=JCECD8&rft_id=info:doi/10.1007/bf00982095&rft_dat=%3Cproquest_cross%3E15820468%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c430t-18de9314f84c6c34f3d389f969622ceb2c5ed956805cd972d0291ebfef5c92993%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=15820468&rft_id=info:pmid/24263426&rfr_iscdi=true |