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4810-42-8

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4810-42-8 Usage

Description

N,N-diethylpyridine-3-sulfonamide, commonly known as DEET, is a widely used insect repellent that offers effective protection against mosquito and tick bites. It operates by blocking the insects' olfactory receptors, which makes it challenging for them to locate and feed on the skin. DEET is available in various forms, including lotions, sprays, and wipes, and is considered safe for use when following label instructions. Although there have been concerns regarding its potential health and environmental effects, studies have demonstrated that DEET is generally safe for human use and does not present significant risks when used in the recommended doses. DEET is a valuable resource for preventing insect-borne diseases and ensuring protection in outdoor settings.

Uses

Used in Insect Repellent Applications:
N,N-diethylpyridine-3-sulfonamide is used as an insect repellent for preventing mosquito and tick bites. It serves to block the insects' olfactory receptors, making it difficult for them to locate and feed on the skin, thereby providing protection against insect-borne diseases.
Used in Outdoor Protection:
N,N-diethylpyridine-3-sulfonamide is used as a protective agent in outdoor settings to safeguard individuals from the bites of insects that may carry diseases. By applying DEET in the recommended forms such as lotions, sprays, and wipes, people can enjoy outdoor activities with reduced risk of insect bites.

Check Digit Verification of cas no

The CAS Registry Mumber 4810-42-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,1 and 0 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4810-42:
(6*4)+(5*8)+(4*1)+(3*0)+(2*4)+(1*2)=78
78 % 10 = 8
So 4810-42-8 is a valid CAS Registry Number.

4810-42-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-diethylpyridine-3-sulfonamide

1.2 Other means of identification

Product number -
Other names N,N-diethyl-3-pyridinesulfonamide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4810-42-8 SDS

4810-42-8Downstream Products

4810-42-8Relevant articles and documents

Nucleophilic C-H Etherification of Heteroarenes Enabled by Base-Catalyzed Halogen Transfer

Puleo, Thomas R.,Klaus, Danielle R.,Bandar, Jeffrey S.

supporting information, p. 12480 - 12486 (2021/08/24)

We report a general protocol for the direct C-H etherification of N-heteroarenes. Potassium tert-butoxide catalyzes halogen transfer from 2-halothiophenes to N-heteroarenes to form N-heteroaryl halide intermediates that undergo tandem base-promoted alcohol substitution. Thus, the simple inclusion of inexpensive 2-halothiophenes enables regioselective oxidative coupling of alcohols with 1,3-azoles, pyridines, diazines, and polyazines under basic reaction conditions.

Efficient and scalable synthesis of pyridine sulfonamides

Emura, Takashi,Yoshino, Hitoshi,Tachibana, Kazutaka,Shiraishi, Takuya,Honma, Akie,Mizutani, Akemi,Muraoka, Terushige

experimental part, p. 1117 - 1120 (2011/06/20)

Short-step and scalable transformations from 2,6-dibromopyridine to 6-bromopyridine-2-sulfonamide by means of halogen-metal exchange and subsequent reaction with sulfuryl chloride followed by amidation are established. Application of the method for the synthesis of various pyridine sulfonamides is also described. Georg Thieme Verlag Stuttgart - New York.

Facile one-pot synthesis of aromatic and heteroaromatic sulfonamides

Pandya, Rina,Murashima, Takashi,Tedeschi, Livio,Barrett, Anthony G. M.

, p. 8274 - 8276 (2007/10/03)

A series of arene and heteroarene sulfonamides were prepared in one vessel from aryl and heteroaryl bromides via conversion into the corresponding Grignard reagents using either magnesium or isopropylmagnesium chloride and subsequent reaction with sulfur dioxide, sulfuryl chloride, and an amine.

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