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70303-40-1

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70303-40-1 Usage

General Description

2-HEXYL-3,5-DIMETHYLPYRAZINE is a chemical compound with a strong, nutty, and earthy odor. It is commonly used as a fragrance ingredient in perfumes, colognes, and personal care products. It is also used as a flavor additive in food and beverages, providing a unique, savory, and roasted flavor profile. Additionally, it is utilized in the production of agricultural products, as an insect repellent to protect crops from pests. 2-HEXYL-3,5-DIMETHYLPYRAZINE is considered safe for use in controlled amounts and is regulated by various health and safety organizations.

Check Digit Verification of cas no

The CAS Registry Mumber 70303-40-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,3,0 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 70303-40:
(7*7)+(6*0)+(5*3)+(4*0)+(3*3)+(2*4)+(1*0)=81
81 % 10 = 1
So 70303-40-1 is a valid CAS Registry Number.

70303-40-1SDS

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-HEXYL-3,5-DIMETHYLPYRAZINE

1.2 Other means of identification

Product number -
Other names Pyrazine,2-hexyl-3,5-dimethyl

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:70303-40-1 SDS

70303-40-1Downstream Products

70303-40-1Relevant articles and documents

Facile regiocontrolled synthesis of trialkyl-substituted pyrazines

Elmaaty, Tarek Abou,Castle, Lyle W.

, p. 5529 - 5530 (2005)

(Chemical Equation Presented) α-Nitro ketones can be transformed selectively into trialkyl-substituted pyrazines via reaction with α-amino ketones using octyl viologen as an electron-transfer reagent. The new synthetic method, and the optimal reaction conditions that allow for the regiochemical control, are described.

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