Environmental occurrence, human exposure,
- Classification:Chemical Auxiliary Agent, Chemical Auxiliary Agent
- CAS No.:28553-12-0
- Other Names:Di-isononyl phthalate
- MF:C26H42O4 Diisononyl Phthalate
- EINECS No.:271-090-9
- Purity:99%, 99%
- Type:DINP
- Usage:Coating Auxiliary Agents, Leather Auxiliary Agents, Plastic Auxiliary Agents, Rubber Auxiliary Agents, Textile Auxiliary Agents
- MOQ:1000KG
- Package:25kg/drum
- Storage:Dry Place
Di-iso-nonyl phthalate (DINP) and di-iso-decyl phthalate (DIDP) have been employed increasingly as plasticizers to replace di-(2-ethylhexyl) phthalate (DEHP), a hormonal disruptor. Through this systematic review, we
Di-isononyl phthalate (DiNP) is a high-molecular-weight phthalate commonly used as a plasticizer for polyvinyl chloride and other end products, such as medical devices and
Human Biological Monitoring of Diisononyl Phthalate
- Classification:Chemical Auxiliary Agent
- CAS No.:68515-48-0
- Other Names:DINP
- MF:C26H42O4
- EINECS No.:249-079-5
- Purity:99.6%
- Type:PVC resin plasticizer
- Usage:Petroleum Additives, Plastic Auxiliary Agents, Rubber Auxiliary Agents
- MOQ:1000KG
- Package:25kg/drum
- Model Number:DINP
2.1. Production and Composition of DINP. Commercially available DINP is a complex mixture of diesters of o-phthalic acid containing C8–C10 (C9 rich) alkyl side chains.In
di-‘isononyl’ phthalate (DINP) CAS NO 28553-12-0 AND 68515-48-0 EINECS NO 249-079-5 AND 271-090-9 REVIEW REPORT JULY 2010 2 1. Introduction Entries 51 and 52 of Annex
Diisononyl phthalate C26H42O4 CID 590836 PubChem
- Classification:Chemical Auxiliary Agent
- CAS No.:28553-12-0
- Other Names:DINP
- MF:C26H42O4 Diisononyl Phthalate
- EINECS No.:271-090-9
- Purity:>99.5%
- Type:plasticizer
- Usage:Coating Auxiliary Agents, Leather Auxiliary Agents, Paper Chemicals, Plastic Auxiliary Agents, Rubber Auxiliary Agents
- MOQ:200kgs
- Package:200kgs/battle
- Storage:Dry Place
Diisononyl phthalate (DINP) has been widely used in polyvinyl chloride (PVC) products and is ubiquitous as a substitute; however, its toxicity due to exposure remains to be determined.
Di-isononyl phthalate (DiNP), a common plasticizer used in polyvinyl chloride products, exhibits endocrine-disrupting capabilities. It is also toxic to the brain, reproductive
Di-isononyl phthalate (DINP) ECPI January 2015
- Classification:Chemical Auxiliary Agent
- CAS No.:68515-48-0
- Other Names:Di-isononyl phthalate
- MF:C26H42O4, C26H42O4
- EINECS No.:249-079-5
- Purity:99.5% Diisononyl Phthalate
- Type:New Type Environment DINP Plasticizer
- Usage:Coating Auxiliary Agents, Electronics Chemicals, Leather Auxiliary Agents, Paper Chemicals, Petroleum Additives, Plastic Auxiliary Agents, Rubber Auxiliary Agents, Surfactants, Textile Auxiliary Agents, Water Treatment Chemicals
- MOQ:200kgs
- Package:200kgs/battle
- Shelf life:2 Years
Di-isononyl phthalate (DINP) is an oily colourless liq-uid with a slight ester odour. Production Process Di-isononyl phthalate is produced by one-step ester-ification of phthalic anhydride
DINP is a general purpose plasticizer for PVC in many applications and has replaced use of DEHP as a plasticizer in many applications except for medical supplies (Ullmann's 2017,
Comparative analysis of diisononyl phthalate and di(isononyl
- Classification:Chemical Auxiliary Agent, Chemical Auxiliary Agent
- CAS No.:68515-48-0
- Other Names:Di-isononyl phthalate
- MF:C26H42O4 Diisononyl Phthalate
- EINECS No.:249-079-5
- Purity:99.5% Diisononyl Phthalate
- Type:PVC resin plasticizer
- Usage:Coating Auxiliary Agents, Leather Auxiliary Agents, Plastic Auxiliary Agents, Rubber Auxiliary Agents, Textile Auxiliary Agents
- MOQ:1000KG
- Package:25kg/drum
- Function:PVC Plasticizer
Diisononyl phthalate (DINP) is a large molecular weight phthalate which is primarily used in the production of polymers and commercial plastic products. 20 DINP has become one
Diisononyl phthalate (DINP) is one of the widely used dialkyl phthalate (DAPs) softeners in the production of flexible polyvinyl chloride (PVC) plastics, copolymers, and resins. Unpublished final report submitted to Nissan Chemical Industries, August 29, 1980, cited from Exxon Biomedical Sciences Inc. (1997). Google Scholar