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74886-57-0

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74886-57-0 Usage

Type of compound

Quaternary ammonium salt

Components

Trimethylammonium cation and bromoethoxy anion

Use

Pesticide and insecticide

Effective against

Aphids, mites, and whiteflies

Target crops

Cotton, fruits, and vegetables

Mode of action

Contact and stomach poison, disrupting the nervous system of insects

Outcome

Paralysis and eventual death of insects

Concerns

Toxicity to non-target organisms and potential for environmental accumulation

Regulations

Limited use and regulated in many countries

Check Digit Verification of cas no

The CAS Registry Mumber 74886-57-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,8,8 and 6 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 74886-57:
(7*7)+(6*4)+(5*8)+(4*8)+(3*6)+(2*5)+(1*7)=180
180 % 10 = 0
So 74886-57-0 is a valid CAS Registry Number.

74886-57-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-bromoethoxy)ethyl-trimethylazanium,bromide

1.2 Other means of identification

Product number -
Other names -

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:74886-57-0 SDS

74886-57-0Downstream Products

74886-57-0Relevant articles and documents

Facile synthesis of (ω-bromoalkyl)trimethylammonium bromides

Bartsch, Richard A.,Zhao, Wenyi,Zhang, Zhi-Yi

, p. 2393 - 2398 (2007/10/03)

Reaction of a 1,ω-dibromoalkane with trimethylamine in THF at room temperature precipitates the corresponding (ω-bromoalkyl)trimethylammonium bromide to cleanly form the mono-substituted product in the absence of the bis-quat salt.

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