The Experts below are selected from a list of 297 Experts worldwide ranked by ideXlab platform
Atri D. Tripathi - One of the best experts on this subject based on the ideXlab platform.
-
excess molar enthalpies of 1 1 2 2 tetrachloroethane 2 methylfuran tetrahydrofuran 1 4 dioxane and Cyclopentanone at 308 15 and 318 15 k
Journal of Chemical & Engineering Data, 1995Co-Authors: Renu Chadha, Atri D. TripathiAbstract:Excess molar enthalpies at 308.15 and 318.15 K have been determined for 1,1,2,2-tetrachloroethane with 2-methylfuran, tetrahydrofuran, 1,4-dioxane, and Cyclopentanone. All four systems are exothermic. The excess enthalpies (in absolute values) decrease in the order tetrahydrofuran > Cyclopentanone > 1,4-dioxane > 2-methylfuran
-
Excess Molar Enthalpies of 1,1,2,2-Tetrachloroethane + 2-Methylfuran, + Tetrahydrofuran, + 1,4-Dioxane, and + Cyclopentanone at 308.15 and 318.15 K
Journal of Chemical & Engineering Data, 1995Co-Authors: Renu Chadha, Atri D. TripathiAbstract:Excess molar enthalpies at 308.15 and 318.15 K have been determined for 1,1,2,2-tetrachloroethane with 2-methylfuran, tetrahydrofuran, 1,4-dioxane, and Cyclopentanone. All four systems are exothermic. The excess enthalpies (in absolute values) decrease in the order tetrahydrofuran > Cyclopentanone > 1,4-dioxane > 2-methylfuran
-
Enthalpies of mixing of tetrachloroethane with furan, methylfuran, tetrahydrofuran, Cyclopentanone and 1,4-dioxane
Thermochimica Acta, 1995Co-Authors: Gopal Pathak, Atri D. Tripathi, U.d. Phalgune, Shirish D PradhanAbstract:Abstract Enthalpies of mixing of furan, methylfuran, tetrahydrofuran (THF), 1,4-dioxane and Cyclopentanone with tetrachloroethane (TCE) were determined by microcalorimetry. All the systems were exothermic in nature, showing the following trend: THF > Cyclopentanone > 1,4-dioxane > methylfuran > furan. Saturation of the ring led to a marked increase in the energy of intermolecular interaction. This was attributed to the specific interactions between oxygen and the H of TCE, oxygen and the Cl of TCE, and between the CH 2 group and the Cl of TCE. This hypothesis was confirmed by a downfield shift in the NMR spectra on addition of TCE to pure THF, 1,4-dioxane and Cyclopentanone.
A M Api - One of the best experts on this subject based on the ideXlab platform.
-
Fragrance material review on 2-hexylidene Cyclopentanone.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 2012Co-Authors: J Scognamiglio, L Jones, C S Letizia, A M ApiAbstract:A toxicologic and dermatologic review of 2-hexylidene Cyclopentanone when used as a fragrance ingredient is presented. 2-Hexylidene Cyclopentanone is a member of the fragrance structural group ketones alkyl cyclic. The common characteristic structural element of the group members is a Cyclopentanone or cyclopentenone ring with a straight or branched chain alkane or alkene substituent. This review contains a detailed summary of all available toxicology and dermatology papers that are related to this individual fragrance ingredient and is not intended as a stand-alone document. Available data for 2-hexylidene Cyclopentanone were evaluated then summarized and includes physical properties, acute toxicity, skin irritation, mucous membrane (eye) irritation, skin sensitization, elicitation, phototoxicity, photoallergy, toxicokinetics, repeated dose, and genotoxicity data. A safety assessment of the entire ketones alkyl cyclic will be published simultaneously with this document; please refer to Belsito et al. (2012) for an overall assessment of the safe use of this material and all ketones alkyl cyclic in fragrances.
-
Fragrance material review on methyl jasmonate.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 2012Co-Authors: J Scognamiglio, L Jones, C S Letizia, A M ApiAbstract:A toxicologic and dermatologic review of methyl jasmonate when used as a fragrance ingredient is presented. Methyl jasmonate is a member of the fragrance structural group Ketones Cyclopentanones and Cyclopentenones. The common characteristic structural element of the group members is a Cyclopentanone or cyclopentenone ring with a straight or branched chain alkane or alkene substituent. This review contains a detailed summary of all available toxicology and dermatology papers that are related to this individual fragrance ingredient and is not intended as a stand-alone document. Available data for methyl jasmonate were evaluated then summarized and includes physical properties, acute toxicity, skin irritation, mucous membrane (eye) irritation, skin sensitization, phototoxicity, and photoallergy data. A safety assessment of the entire Ketones Cyclopentanones and Cyclopentenones will be published simultaneously with this document; please refer to Belsito et al. (2012) for an overall assessment of the safe use of this material and all Ketones Cyclopentanones and Cyclopentenones in fragrances.
-
Fragrance material review on methyl hexyl oxo Cyclopentanone carboxylate.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 2012Co-Authors: J Scognamiglio, L Jones, C S Letizia, A M ApiAbstract:A toxicologic and dermatologic review of methyl hexyl oxo Cyclopentanone carboxylate when used as a fragrance ingredient is presented. Methyl hexyl oxo Cyclopentanone carboxylate is a member of the fragrance structural group ketones Cyclopentanones and cyclopentenones. The common characteristic structural element of the group members is a Cyclopentanone or cyclopentenone ring with a straight or branched chain alkane or alkene substituent. This review contains a detailed summary of all available toxicology and dermatology papers that are related to this individual fragrance ingredient and is not intended as a stand-alone document. Available data for methyl hexyl oxo Cyclopentanone carboxylate were evaluated then summarized and includes physical properties, acute toxicity, skin irritation, skin sensitization, and genotoxicity data. A safety assessment of the entire ketones Cyclopentanones and cyclopentenones will be published simultaneously with this document; please refer to Belsito et al. (this issue) for an overall assessment of the safe use of this material and all ketones Cyclopentanones and cyclopentenones in fragrances.
-
Fragrance material review on cis-jasmone.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 2012Co-Authors: J Scognamiglio, L Jones, C S Letizia, A M ApiAbstract:A toxicologic and dermatologic review of cis-jasmone when used as a fragrance ingredient is presented. cis-Jasmone is a member of the fragrance structural group ketones Cyclopentanones and cyclopentenones. The common characteristic structural element of the group members is a Cyclopentanone or cyclopentenone ring with a straight or branched chain alkane or alkene substituent. This review contains a detailed summary of all available toxicology and dermatology papers that are related to this individual fragrance ingredient and is not intended as a stand-alone document. Available data for cis-jasmone were evaluated then summarized and includes physical properties, acute toxicity, skin irritation, mucous membrane (eye) irritation, skin sensitization, phototoxicity, photoallergy, and genotoxicity data. A safety assessment of the entire ketones Cyclopentanones and cyclopentenones will be published simultaneously with this document; please refer to Belsito et al. (2012) for an overall assessment of the safe use of this material and all ketones Cyclopentanones and cyclopentenones in fragrances.
-
Fragrance material review on Cyclopentanone.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 2012Co-Authors: J Scognamiglio, L Jones, C S Letizia, A M ApiAbstract:A toxicologic and dermatologic review of Cyclopentanone when used as a fragrance ingredient is presented. Cyclopentanone is a member of the fragrance structural group ketones Cyclopentanones and Cyclopentanones. The common characteristic structural element of the group members is a Cyclopentanone or Cyclopentanone ring with a straight or branched chain alkane or alkene substituent. This review contains a detailed summary of all available toxicology and dermatology papers that are related to this individual fragrance ingredient and is not intended as a stand-alone document. Available data for Cyclopentanone were evaluated then summarized and includes physical properties, acute toxicity, skin irritation, mucous membrane (eye) irritation, skin sensitization, repeated dose, reproductive toxicity, and genotoxicity data. A safety assessment of the entire ketones Cyclopentanones and cyclopentenones will be published simultaneously with this document; please refer to Belsito et al. (2012) for an overall assessment of the safe use of this material and all ketones Cyclopentanones and cyclopentenones in fragrances.
J Scognamiglio - One of the best experts on this subject based on the ideXlab platform.
-
Fragrance material review on 2-hexylidene Cyclopentanone.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 2012Co-Authors: J Scognamiglio, L Jones, C S Letizia, A M ApiAbstract:A toxicologic and dermatologic review of 2-hexylidene Cyclopentanone when used as a fragrance ingredient is presented. 2-Hexylidene Cyclopentanone is a member of the fragrance structural group ketones alkyl cyclic. The common characteristic structural element of the group members is a Cyclopentanone or cyclopentenone ring with a straight or branched chain alkane or alkene substituent. This review contains a detailed summary of all available toxicology and dermatology papers that are related to this individual fragrance ingredient and is not intended as a stand-alone document. Available data for 2-hexylidene Cyclopentanone were evaluated then summarized and includes physical properties, acute toxicity, skin irritation, mucous membrane (eye) irritation, skin sensitization, elicitation, phototoxicity, photoallergy, toxicokinetics, repeated dose, and genotoxicity data. A safety assessment of the entire ketones alkyl cyclic will be published simultaneously with this document; please refer to Belsito et al. (2012) for an overall assessment of the safe use of this material and all ketones alkyl cyclic in fragrances.
-
Fragrance material review on methyl jasmonate.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 2012Co-Authors: J Scognamiglio, L Jones, C S Letizia, A M ApiAbstract:A toxicologic and dermatologic review of methyl jasmonate when used as a fragrance ingredient is presented. Methyl jasmonate is a member of the fragrance structural group Ketones Cyclopentanones and Cyclopentenones. The common characteristic structural element of the group members is a Cyclopentanone or cyclopentenone ring with a straight or branched chain alkane or alkene substituent. This review contains a detailed summary of all available toxicology and dermatology papers that are related to this individual fragrance ingredient and is not intended as a stand-alone document. Available data for methyl jasmonate were evaluated then summarized and includes physical properties, acute toxicity, skin irritation, mucous membrane (eye) irritation, skin sensitization, phototoxicity, and photoallergy data. A safety assessment of the entire Ketones Cyclopentanones and Cyclopentenones will be published simultaneously with this document; please refer to Belsito et al. (2012) for an overall assessment of the safe use of this material and all Ketones Cyclopentanones and Cyclopentenones in fragrances.
-
Fragrance material review on methyl hexyl oxo Cyclopentanone carboxylate.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 2012Co-Authors: J Scognamiglio, L Jones, C S Letizia, A M ApiAbstract:A toxicologic and dermatologic review of methyl hexyl oxo Cyclopentanone carboxylate when used as a fragrance ingredient is presented. Methyl hexyl oxo Cyclopentanone carboxylate is a member of the fragrance structural group ketones Cyclopentanones and cyclopentenones. The common characteristic structural element of the group members is a Cyclopentanone or cyclopentenone ring with a straight or branched chain alkane or alkene substituent. This review contains a detailed summary of all available toxicology and dermatology papers that are related to this individual fragrance ingredient and is not intended as a stand-alone document. Available data for methyl hexyl oxo Cyclopentanone carboxylate were evaluated then summarized and includes physical properties, acute toxicity, skin irritation, skin sensitization, and genotoxicity data. A safety assessment of the entire ketones Cyclopentanones and cyclopentenones will be published simultaneously with this document; please refer to Belsito et al. (this issue) for an overall assessment of the safe use of this material and all ketones Cyclopentanones and cyclopentenones in fragrances.
-
Fragrance material review on cis-jasmone.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 2012Co-Authors: J Scognamiglio, L Jones, C S Letizia, A M ApiAbstract:A toxicologic and dermatologic review of cis-jasmone when used as a fragrance ingredient is presented. cis-Jasmone is a member of the fragrance structural group ketones Cyclopentanones and cyclopentenones. The common characteristic structural element of the group members is a Cyclopentanone or cyclopentenone ring with a straight or branched chain alkane or alkene substituent. This review contains a detailed summary of all available toxicology and dermatology papers that are related to this individual fragrance ingredient and is not intended as a stand-alone document. Available data for cis-jasmone were evaluated then summarized and includes physical properties, acute toxicity, skin irritation, mucous membrane (eye) irritation, skin sensitization, phototoxicity, photoallergy, and genotoxicity data. A safety assessment of the entire ketones Cyclopentanones and cyclopentenones will be published simultaneously with this document; please refer to Belsito et al. (2012) for an overall assessment of the safe use of this material and all ketones Cyclopentanones and cyclopentenones in fragrances.
-
Fragrance material review on Cyclopentanone.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 2012Co-Authors: J Scognamiglio, L Jones, C S Letizia, A M ApiAbstract:A toxicologic and dermatologic review of Cyclopentanone when used as a fragrance ingredient is presented. Cyclopentanone is a member of the fragrance structural group ketones Cyclopentanones and Cyclopentanones. The common characteristic structural element of the group members is a Cyclopentanone or Cyclopentanone ring with a straight or branched chain alkane or alkene substituent. This review contains a detailed summary of all available toxicology and dermatology papers that are related to this individual fragrance ingredient and is not intended as a stand-alone document. Available data for Cyclopentanone were evaluated then summarized and includes physical properties, acute toxicity, skin irritation, mucous membrane (eye) irritation, skin sensitization, repeated dose, reproductive toxicity, and genotoxicity data. A safety assessment of the entire ketones Cyclopentanones and cyclopentenones will be published simultaneously with this document; please refer to Belsito et al. (2012) for an overall assessment of the safe use of this material and all ketones Cyclopentanones and cyclopentenones in fragrances.
Renu Chadha - One of the best experts on this subject based on the ideXlab platform.
-
excess molar enthalpies of 1 1 2 2 tetrachloroethane 2 methylfuran tetrahydrofuran 1 4 dioxane and Cyclopentanone at 308 15 and 318 15 k
Journal of Chemical & Engineering Data, 1995Co-Authors: Renu Chadha, Atri D. TripathiAbstract:Excess molar enthalpies at 308.15 and 318.15 K have been determined for 1,1,2,2-tetrachloroethane with 2-methylfuran, tetrahydrofuran, 1,4-dioxane, and Cyclopentanone. All four systems are exothermic. The excess enthalpies (in absolute values) decrease in the order tetrahydrofuran > Cyclopentanone > 1,4-dioxane > 2-methylfuran
-
Excess Molar Enthalpies of 1,1,2,2-Tetrachloroethane + 2-Methylfuran, + Tetrahydrofuran, + 1,4-Dioxane, and + Cyclopentanone at 308.15 and 318.15 K
Journal of Chemical & Engineering Data, 1995Co-Authors: Renu Chadha, Atri D. TripathiAbstract:Excess molar enthalpies at 308.15 and 318.15 K have been determined for 1,1,2,2-tetrachloroethane with 2-methylfuran, tetrahydrofuran, 1,4-dioxane, and Cyclopentanone. All four systems are exothermic. The excess enthalpies (in absolute values) decrease in the order tetrahydrofuran > Cyclopentanone > 1,4-dioxane > 2-methylfuran
C S Letizia - One of the best experts on this subject based on the ideXlab platform.
-
Fragrance material review on 2-hexylidene Cyclopentanone.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 2012Co-Authors: J Scognamiglio, L Jones, C S Letizia, A M ApiAbstract:A toxicologic and dermatologic review of 2-hexylidene Cyclopentanone when used as a fragrance ingredient is presented. 2-Hexylidene Cyclopentanone is a member of the fragrance structural group ketones alkyl cyclic. The common characteristic structural element of the group members is a Cyclopentanone or cyclopentenone ring with a straight or branched chain alkane or alkene substituent. This review contains a detailed summary of all available toxicology and dermatology papers that are related to this individual fragrance ingredient and is not intended as a stand-alone document. Available data for 2-hexylidene Cyclopentanone were evaluated then summarized and includes physical properties, acute toxicity, skin irritation, mucous membrane (eye) irritation, skin sensitization, elicitation, phototoxicity, photoallergy, toxicokinetics, repeated dose, and genotoxicity data. A safety assessment of the entire ketones alkyl cyclic will be published simultaneously with this document; please refer to Belsito et al. (2012) for an overall assessment of the safe use of this material and all ketones alkyl cyclic in fragrances.
-
Fragrance material review on methyl jasmonate.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 2012Co-Authors: J Scognamiglio, L Jones, C S Letizia, A M ApiAbstract:A toxicologic and dermatologic review of methyl jasmonate when used as a fragrance ingredient is presented. Methyl jasmonate is a member of the fragrance structural group Ketones Cyclopentanones and Cyclopentenones. The common characteristic structural element of the group members is a Cyclopentanone or cyclopentenone ring with a straight or branched chain alkane or alkene substituent. This review contains a detailed summary of all available toxicology and dermatology papers that are related to this individual fragrance ingredient and is not intended as a stand-alone document. Available data for methyl jasmonate were evaluated then summarized and includes physical properties, acute toxicity, skin irritation, mucous membrane (eye) irritation, skin sensitization, phototoxicity, and photoallergy data. A safety assessment of the entire Ketones Cyclopentanones and Cyclopentenones will be published simultaneously with this document; please refer to Belsito et al. (2012) for an overall assessment of the safe use of this material and all Ketones Cyclopentanones and Cyclopentenones in fragrances.
-
Fragrance material review on methyl hexyl oxo Cyclopentanone carboxylate.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 2012Co-Authors: J Scognamiglio, L Jones, C S Letizia, A M ApiAbstract:A toxicologic and dermatologic review of methyl hexyl oxo Cyclopentanone carboxylate when used as a fragrance ingredient is presented. Methyl hexyl oxo Cyclopentanone carboxylate is a member of the fragrance structural group ketones Cyclopentanones and cyclopentenones. The common characteristic structural element of the group members is a Cyclopentanone or cyclopentenone ring with a straight or branched chain alkane or alkene substituent. This review contains a detailed summary of all available toxicology and dermatology papers that are related to this individual fragrance ingredient and is not intended as a stand-alone document. Available data for methyl hexyl oxo Cyclopentanone carboxylate were evaluated then summarized and includes physical properties, acute toxicity, skin irritation, skin sensitization, and genotoxicity data. A safety assessment of the entire ketones Cyclopentanones and cyclopentenones will be published simultaneously with this document; please refer to Belsito et al. (this issue) for an overall assessment of the safe use of this material and all ketones Cyclopentanones and cyclopentenones in fragrances.
-
Fragrance material review on cis-jasmone.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 2012Co-Authors: J Scognamiglio, L Jones, C S Letizia, A M ApiAbstract:A toxicologic and dermatologic review of cis-jasmone when used as a fragrance ingredient is presented. cis-Jasmone is a member of the fragrance structural group ketones Cyclopentanones and cyclopentenones. The common characteristic structural element of the group members is a Cyclopentanone or cyclopentenone ring with a straight or branched chain alkane or alkene substituent. This review contains a detailed summary of all available toxicology and dermatology papers that are related to this individual fragrance ingredient and is not intended as a stand-alone document. Available data for cis-jasmone were evaluated then summarized and includes physical properties, acute toxicity, skin irritation, mucous membrane (eye) irritation, skin sensitization, phototoxicity, photoallergy, and genotoxicity data. A safety assessment of the entire ketones Cyclopentanones and cyclopentenones will be published simultaneously with this document; please refer to Belsito et al. (2012) for an overall assessment of the safe use of this material and all ketones Cyclopentanones and cyclopentenones in fragrances.
-
Fragrance material review on Cyclopentanone.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 2012Co-Authors: J Scognamiglio, L Jones, C S Letizia, A M ApiAbstract:A toxicologic and dermatologic review of Cyclopentanone when used as a fragrance ingredient is presented. Cyclopentanone is a member of the fragrance structural group ketones Cyclopentanones and Cyclopentanones. The common characteristic structural element of the group members is a Cyclopentanone or Cyclopentanone ring with a straight or branched chain alkane or alkene substituent. This review contains a detailed summary of all available toxicology and dermatology papers that are related to this individual fragrance ingredient and is not intended as a stand-alone document. Available data for Cyclopentanone were evaluated then summarized and includes physical properties, acute toxicity, skin irritation, mucous membrane (eye) irritation, skin sensitization, repeated dose, reproductive toxicity, and genotoxicity data. A safety assessment of the entire ketones Cyclopentanones and cyclopentenones will be published simultaneously with this document; please refer to Belsito et al. (2012) for an overall assessment of the safe use of this material and all ketones Cyclopentanones and cyclopentenones in fragrances.
