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17691-19-9

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17691-19-9 Usage

Chemical Properties

SLIGHTLY YELLOW CRYSTALLINE POWDER

Flammability and Explosibility

Notclassified

Check Digit Verification of cas no

The CAS Registry Mumber 17691-19-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,6,9 and 1 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 17691-19:
(7*1)+(6*7)+(5*6)+(4*9)+(3*1)+(2*1)+(1*9)=129
129 % 10 = 9
So 17691-19-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H4ClNO5S/c7-5-2-1-4(14(11,12)13)3-6(5)8(9)10/h1-3H,(H,11,12,13)/p-1

17691-19-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name sodium,4-chloro-3-nitrobenzenesulfonate

1.2 Other means of identification

Product number -
Other names 4-chloro-3-nitrobenzenesulphonic acid sodium salt

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:17691-19-9 SDS

17691-19-9Upstream product

17691-19-9Relevant articles and documents

Method for preparing sodium 3-nitrobenzene sulfonate and derivative thereof through chlorosulfonic acid sulfonation

-

Paragraph 0067; 0068; 0069; 0070; 0071, (2019/01/07)

The invention discloses a method for preparing sodium 3-nitrobenzene sulfonate and a derivative thereof through chlorosulfonic acid sulfonation. The method comprises the following steps: 1) putting anitrobenzene raw material and chlorosulfonic acid into a reaction container, heating to 90-150 DEG C, keeping the temperature, carrying out a sulfonation reaction, and discharging a hydrogen chloridegas generated in the reaction process outside the reaction system in time, wherein the mole ratio of the nitrobenzene raw material to the chlorosulfonic acid is 1:(0.4-0.6); 2) carrying out aftertreatment on the reaction liquid obtained in the step 1) by using soda, thereby obtaining the sodium 3-nitrobenzene sulfonate or the derivative thereof. By adopting the method, a reverse thinking mode is adopted, the amount of the chlorosulfonic acid is reduced till being smaller than that of the nitrobenzene, and then the small amount of the chlorosulfonic acid can be converted by using the excessiveamount of the nitrobenzene; therefore, the method disclosed by the invention has no problem of treating residual chlorosulfonic acid; in addition, the excessive nitrobenzene can be easily recycled andcirculated, the hydrogen chloride as a byproduct can be also easily separated and recycled.

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