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Wednesday, July 29, 2020 | History

2 edition of toxicity of diallyl phthalate found in the catalog.

toxicity of diallyl phthalate

William Arthur McOmie

toxicity of diallyl phthalate

by William Arthur McOmie

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  • 12 Currently reading

Published by Univ. of California Press in Berkeley .
Written in English

    Subjects:
  • Diallyl phthalate.

  • Edition Notes

    Statementby W.A. McOmie and Hamilton H. Anderson.
    SeriesUniversity of California publications in pharmacology,, v. 2, no. 16
    ContributionsAnderson, Hamilton Holland, 1902- joint author.
    Classifications
    LC ClassificationsRM300 .C32a vol. 2, no. 16
    The Physical Object
    Pagination205-215 p.
    Number of Pages215
    ID Numbers
    Open LibraryOL192156M
    LC Control Numbera 47005916

    OSAKA SODA CO., LTD. -Something Better with Chemicals-"Global Niche Top" thermosetting resin. Diallyl Phthalate(DAP) resin is a thermosetting resin with a lot of excellent physical properties such as electrical insulation properties, heat resistance, water resistance, chemical resistance, and molding.   The aquatic toxicity of Phthalate esters is discussed in this chapter. This chapter begins with an examination of the physico-chemical properties of phthalate esters that have a significant influence on toxicity. Acute and chronic toxicity are then reviewed with a focus on chronic effects.

    Diallyl Phthalate (DAP) Characteristics: Diallyl phthalate(DAP) is a colorless or light yellow transparent liquid. Each molecule contains two allyloxy groups, it is stable at room temperature, but if under heating and adding some initiator, it will be very reactive, and can . TOXICITY REVIEW FOR DIETHYL PHTHALATE (DEP, CASRN ) 1. INTRODUCTION This report summarizes available data on the identity, physicochemical properties, manufacture, supply, use, toxicity, and exposure associated with diethyl phthalate (DEP). This assessment was prepared from a variety of review articles (NICNAS, ; EPA, ; ECB.

    Basis for revised IDLH: The revised IDLH for dibutyl phthalate is 4, mg/m 3 based on acute inhalation toxicity data in animals [Izmerov et al. ]. [Note: Due to its low volatility, this concentration could only be reached at elevated temperatures or if the liquid droplets become airborne as in a mist.]. Other names: 1,2-Benzenedicarboxylic acid, dipropenyl ester; Phthalic acid, diallyl ester; Allyl phthalate; Dapon R; o-Phthalic acid, diallyl ester; Dapon 35; NCI-C; Diallylester kyseliny ftalove; Diallyl ester of phthalic acid; DAP monomer; Diallyl ester o-phthalic acid; Diallylester phthalic acid; 1,2-Benzenedicarboxylic acid, 1,2-di.


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Toxicity of diallyl phthalate by William Arthur McOmie Download PDF EPUB FB2

Diallyl phthalate (DAP) is more hepatotoxic to rats than to mice, and demonstrated the same species difference in toxicity for allyl alcohol (AA). The data suggest that the toxicity of diallyl phthalate probably results from allyl alcohol cleaved from diallyl phthalate.

To determine if the species difference in susceptibility to hepatotoxicity. Di-n-pentyl phthalate was the most potent in producing testicular toxicity. Phthalates of one to three carbons (methyl, ethyl, andn-propyl) did not produce testicular toxicity when given at a dose equimolar with DBP at 2 g/kg-d.

Similarly, linear-chain phthalates. Phthalates, or phthalate esters, are a group of chemicals often included in the production of plastics, such as serving as plasticizer to enhance the flexibility of polyvinyl chloride (NTP-CERHR, ).An important source of human exposure to phthalate is food, especially fatty and processed food.

Human is also exposed to phthalates which are released from phthalates-containing. Diallyl phthalate Revision Date Apr Hazardous Polymerization No information available. Hazardous Reactions None under normal processing. Toxicological information Acute Toxicity Product Information Component Information Component LD50 Oral LD50 Dermal LC50 Inhalation Diallyl phthalate LD50 = mg/kg (Rat)LD50 = mg/kg (Rabbit).

Reference substance name: Diallyl phthalate EC Number: EC Name: Diallyl phthalate CAS Number: Molecular formula: C14H14O4 IUPAC Name. Phthalates are a ubiquitous class of compounds [18, 19] used most commonly as a softener for products made with polyvinyl chloride (PVC).

The term “phthalate” refers to the di-ester derivatives of phthalic acid and thus represents a group of different, though structurally related compounds.

Phthalates have diverse uses in modern commerce. Phthalates are also found in modern electronics and medical applications such as catheters and blood transfusion devices. The most widely used phthalates are di(2-ethylhexyl) phthalate (DEHP), diisodecyl phthalate (DIDP), and diisononyl phthalate (DINP).

DEHP was the dominant plasticizer used globally in PVC due to its low cost. Benzylbutylphthalate (BBP) is used in the manufacture of foamed. ACUTE/CHRONIC HAZARDS: This compound is toxic by ingestion.

It may cause irritation of the eyes, skin and mucous membranes. It is also a lacrimator. It can be absorbed through the skin. diallyl phthalate to be between 50 million and million pounds inand 1to10 million pounds in the surveys conducted every four years from – (U.S.

EPA ). Because its production exceeds one million pounds per year, diallyl phthalate qualifies as a High Production Volume material according to the EPA. Exposure. Diallyl phthalate Acute Tox. 4; Aquatic Acute 1; Aquatic Chronic 1; H, HHazardous ingredients according to Directive /45/EC Component Classification Concentration Diallyl phthalate Xn, N, R22 - R50/53 - Formula: C14H14O4: Molecular Weight (g/mol) CAS-No.

FIRST AID MEASURES: Description of first aid measures. Diallyl phthalate is an organic compound with the formula C 14 H 14 O 4, and its systematic name is the same with the product the CAS registry numberit is also named as 1,2-Benzenedicarboxylic acid, dipropenyl ester. DIALLYL PHTHALATE (DAP) The term DAP is used both for the monomeric and polymeric forms.

The monomer is used as a cross-linking agent in unsaturated polyester resins. As a polymer, it is used in the production of thermosetting molding powders, casting resins and laminates. This is the material of choice for critical, high-performance military.

Diallyl phthalate inhibits algae growth. MedKoo Biosciences, Inc. Leading supplier of anticancer chemical reagents and kinase inhibitors Tel: + Fax: + Email. Overview of materials for Diallyl Phthalate (DAP) Molding Compound, Short Glass Fiber Filled, This property data is a summary of similar materials in the MatWeb database for the category "Diallyl Phthalate (DAP) Molding Compound, Short Glass Fiber.

DIALLYL PHTHALATE COMPRESSION MOUNTING COMPOUND Page 1 Section 1: Identification PRODUCT INDENTIFIER: DIALLYL PHTHALATE COMPRESSION MOUNTING COMPOUND CHEMICAL FAMILY: EPOXY MOLDING COMPOUND EMERGENCY PHONE: CHEMTREC (US) Day or night Customer No.

MANUFACTURER: PACE Technologies E. 34th. Mono-(2-ethylhexyl) phthalate (MEHP) is a well-characterized Sertoli cell toxicant and is the active toxic metabolite of di-(2-ethylhexyl) phthalate (DEHP).

DEHP is widely dispersed throughout the environment due to its use for the production of plastic products (Thomas and Thomas, ; Albro, ; Boekelheide, ).

According to the harmonised classification and labelling (CLP00) approved by the European Union, this substance is very toxic to aquatic life, is very toxic to aquatic life with long lasting effects and is harmful if swallowed.

n (diallyl o-phthalate, DAP). In the monomeric form, DAP is a colorless liquid ester with a viscosity about equal to that of kerosene, widely used as a crosslinking monomer for unsaturated polyester resins, and as a polymerizable plasticizer for many resins.

Diallyl isophthalate | C14H14O4 | CID - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more.

COVID is an emerging, rapidly evolving situation. Get the latest public health information from CDC: https. Diallyl phthalate is a chemical compound from the group of phthalic acid esters.

Diallyl phthalate is a flammable, difficult to ignite, oily, colorless to yellowish liquid with a pleasant odor that is very negligibly soluble in water. Diallyl phthalate can be used to make allyl resins by means of peroxide catalysts.

Because existing toxicity information was considered inadequate, the effects of exposure to dibutyl phthalate were examined in male and female F/N rats and B6C3F. 1. mice in week feed studies. Furthermore, due to concern over the potential for pervasive exposure of humans to dibutyl phthalate, additional perinatal studies examined rats.The imprinting factors of diallyl phthalate (DAP), DBP and diethylhexyl phthalate (DEHP) were 1.

53, 2. 21 and 1. 39 respectively, showing that MMIPs had better recognition performance for DBP. The experiment of regeneration recycles with five times showed the regeneration ability of DBP was only reduced by 3%.Diallyl ISO Phthalate: Short Glass: Yes: Granules: GET A QUOTE. Name * First Last.

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