n n diethyl toluamide

Pseudomonas putida DTB grew aerobically with N N -diethyl- m -toluamide (DEET) as a sole carbon source initially breaking it down into 3-methylbenzoate and diethylamine The former was further metabolized via 3-methylcatechol and meta ring cleavage A gene from DTB dthA was heterologously expressed and shown to encode the ability to hydrolyze DEET into 3-methylbenzoate and diethylamine Category : Adhesives and Sealants: CAS NO : 134-62-3: EC NO : 205-149-7: MF : C 12 H 17 NO: MW : 191 2695: Product description : REGISTRATION NO:WP20080181 PERMIT NO:HNP43064-I1787 Introduction Chemical Name: N N —diethyl—m—toluamide Diethyl toluamide Registered Trade Name: DEET or DETA Molecular Formula: C12H17NO Molecular Weight: 191 3 Molecular Structural

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N N-diethyl-m-toluamide Insect-Repellents B V 17-01-2020 17-01-2020 17-01-2020 NL-0012011-0000 Mugga Anti-Insect Roller N N-diethyl-m-toluamide Insect-Repellents B V 17-01-2020 17-01-2020 17-01-2020 NL-0013481-0000 Insect repellents spray 30% DEET N N-diethyl-m-toluamide Insect-Repellents B V 17-01-2020 17-01-2020 17-01-2020

By using the N N-Diethyl-m-toluamide (DEET) is the active ingredient in many insect-repellent preparations and synthesize this substance from m-bromotoluene Explanation of Solution The reaction involve nucleophile acyl substitution using SOCl 2 to convert the leaving group €"OH to a

N N-diethyl-m-toluamide is a monocarboxylic acid amide resulting from the formal condensation of the carboxy group of m-toluic acid with the nitrogen of diethylamine First developed by the U S Army in 1946 for use by military personnel in insect-infested areas it is the most widely used insect repellent worldwide

N N-Diethyl-m-toluamide m-Toluic acid diethylamide 3-methyl-2-deutero-N N-diethylbenzamide 3-Methyl-N N-diethylbenzamide A I 3-22542 AI 3-22542 ai3-22542 amincenec-em Autan Baker'S antifol N N-diethyl-3-methyl-Benzamide n n-diethyl-m-toluamid 2 4-diethyl-3-methylbenzamide Diethyl-3-methylbenzamide benzamide N N-diethyl-3-methyl

The molecule diagram of DEET represents the chemical name For example the amide in Toluamide are the nitrogens Diethyl means that there are two carbon groups coming off of the nitrogen Meta means that there are two nitrogens that are two carbons away from the H 3 C The N n

DEET Technical Fact Sheet

DEET is an insect and acarid repellent The International Union of Pure and Applied Chemistry (IUPAC) name for DEET is N N-diethyl-m-toluamide and other isomers and it is a member of the N N-dialkylamide family of chemicals The Chemical Abstracts Service (CAS) registry number for

The NADPH- and oxygen-dependent metabolism of N N-diethyl-m-toluamide (deet insect repellent) has been studied at 37 degrees C in suspensions of liver microsomes from phenobarbital-pretreated male Wistar rats In pH 8 Tris-HCl buffer and at a substrate concentration of 200 microM metabolic reactions corresponded to benzylic hydroxylation and N-deethylation and to combinations of these

Pseudomonas putida DTB grew aerobically with N N -diethyl- m -toluamide (DEET) as a sole carbon source initially breaking it down into 3-methylbenzoate and diethylamine The former was further metabolized via 3-methylcatechol and meta ring cleavage A gene from DTB dthA was heterologously expressed and shown to encode the ability to hydrolyze DEET into 3-methylbenzoate and diethylamine

The manufacturing process for DEET (N N-diethyl-m-toluamide) technical active ingredient typically results in a mixture of N N-diethyl-m-toluamide other related toluamides (e g ortho and para isomers) as well as impurities The re-evaluation of DEET published in Re-evaluation Decision Document RRD2002-01 Personal insect repellents containing DEET (N N-diethyl-m-toluamide and related

DEET is an insect and acarid repellent The International Union of Pure and Applied Chemistry (IUPAC) name for DEET is N N-diethyl-m-toluamide and other isomers and it is a member of the N N-dialkylamide family of chemicals The Chemical Abstracts Service (CAS) registry number for

3-3-2011DEET is a chemical (N N-diethyl-meta-toluamide) used as the active ingredient in many insect repellent products DEET was developed by the U S Army in 1946 and was registered for use by the general public in 1957 It is now widely used with approximately 30% of the U S population using DEET repellents each year DEET products are currently available in a variety of forms: liquids lotions

As a member of the wwPDB the RCSB PDB curates and annotates PDB data according to agreed upon standards The RCSB PDB also provides a variety of tools and resources Users can perform simple and advanced searches based on annotations relating to sequence structure and function These molecules are visualized downloaded and analyzed by users who range from students to specialized scientists

The photocatalysis of N N-diethyl-meta-toluamide (DEET) was examined using aqueous Degussa P-25 TiO2 dispersions and a 350 nm high pressure Hg lamp UV reactor Various concentrations of humic acid (HA) were added to the photocatalytic sample matrix in order to simulate the influence of natural organic matter (NOM) present during water treatment

N N

N N-Diethyl-m-toluamide (DEET/OFF) CAS# 134-62-3 Catalog Number # BIOC-196N-10MG CRM RM Certified Reference Material Number of Components Comps 1 Unit 10 mg Price(USD) Price $12 00 Compare Email Add to Cart Add Additional Information Storage Condition Storage Ambient (5 C) Safety Data Sheet SDS

N N-Diethyl-m-toluamide 134-62-3 Suppliers provide N N-Diethyl-m-toluamide 134-62-3 product and the products related with China (Mainland) N N-Diethyl-m-toluamide 134-62-3 Hunan chemfish Pharmaceutical co Ltd China (Mainland) Hunan chemfish Pharmaceutical co Ltd Alkylated aniline series Salicylic acid Sulphonic

N N-diethyl-m-toluamide an insect repellent by sulfate radical In this experiment sulfate radical was generated using peroxymonosulfate with iron(II) and cobalt(II) as activator The second-order rate constant for the reaction of the sulfate radical with N N-diethyl-m-toluamide was found

The permeation behaviours of the insect repellent N N‐diethyl‐m‐toluamide (DEET) and the sunscreen oxybenzone were assessed in a series of in‐vitro diffusion studies using piglet skin and poly (dimethylsiloxane) (PDMS) membrane

As a member of the wwPDB the RCSB PDB curates and annotates PDB data according to agreed upon standards The RCSB PDB also provides a variety of tools and resources Users can perform simple and advanced searches based on annotations relating to sequence structure and function These molecules are visualized downloaded and analyzed by users who range from students to specialized scientists

3-7-2000Reported adverse side effects after using N N-diethyl-m-toluamide (DEET)-containing mosquito repellent products appear to be the result of significant absorption of DEET through human skin The overall objective was to develop formulations of DEET with significantly reduced permeation using the basic principles and model of skin permeation based on Fick's laws of diffusion at steady state

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