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553-79-7

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553-79-7 Usage

Chemical Properties

Artificial sweetener.

Uses

Food additive (prohibited).

Safety Profile

When heated to decompositionemits toxic fumes of NOx.

Purification Methods

Crystallise the aniline from n-propyl alcohol/pet ether or H2O (136mg/L at 20o). [Beilstein 13 III 878, 13 IV 897.]

Check Digit Verification of cas no

The CAS Registry Mumber 553-79-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,5 and 3 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 553-79:
(5*5)+(4*5)+(3*3)+(2*7)+(1*9)=77
77 % 10 = 7
So 553-79-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H12N2O3/c1-2-5-14-9-4-3-7(11(12)13)6-8(9)10/h3-4,6H,2,5,10H2,1H3

553-79-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-nitro-2-propoxyaniline

1.2 Other means of identification

Product number -
Other names Ultrasweet

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:553-79-7 SDS

553-79-7Relevant articles and documents

PARTIAL REDUCTION OF DINITROARENES TO NITROANILINES WITH HYDRAZINE HYDRATE.

Avyyangar,Kalkote,Lugade,Nikrad,Sharma

, p. 3159 - 3164 (2007/10/02)

Dinitroarenes containing substituents such as hydroxyl and amine groups could be conveniently reduced with 3 molar equivalents of hydrazine hydrate in presence of Raney nickel catalyst in ethanol/1,2-dichloro-ethane solvent mixture to give a product wherein one of the two nitro groups was reduced to the amino group. The yields of the partial reduction products are good. Under similar conditions alkoxyl substitutes in the o,p-position to the nitro groups were displaced by the hydrazine to give 2,4-dinitrophenyl-hydrazine as the main product. The details of the reduction reaction are described.

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