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Chlorosulfuric acid (IUPAC name: sulfurochloridic acid) is the inorganic compound with the formula HSO 3 Cl. Except where otherwise noted, data are given for materials in their, http://www.newenv.com/resources/nfpa_chemicals, https://en.wikipedia.org/w/index.php?title=Chlorosulfuric_acid&oldid=973610687, Pages using collapsible list with both background and text-align in titlestyle, Articles containing unverified chemical infoboxes, Creative Commons Attribution-ShareAlike License, 151 to 152 °C (304 to 306 °F; 424 to 425 K) (755 mmHg or 100.7 kPa), This page was last edited on 18 August 2020, at 05:58. Industry: Dyestuff, Pharmaceutical Recent References to Chlorosulfonic Acid. Chlorosulphonic acid An intermediate used to produce sulphates, sulphonates, sulphonyl chlorides with organic compounds like hydrocarbons, alcohols, phenols and amines. Chlorosulfuric acid is a tetrahedral molecule. I agree to receive commercial messages from GlobalSpec including product announcements and event invitations, saccharin and cyclamate; long chain alkyl and alkylarylsulfonates as detergents; sulfonyl polymers, sulfonyl azides and hydrazides as blowing agents used in the preparation of foam plastics; sulfonyl dyes and pigments (see Chapter 1, p 5). The formula is more descriptively written SO2(OH)Cl, but HSO3Cl is traditional.

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WORLD'S Chlorosulfonic acid mixed with sulfur trioxide is also used as a chemical smoke in warfare (see Chapter 7, ref. UNLIMITED

It is an intermediate, chemically and conceptually, between sulfuryl chloride (SO2Cl2) and sulfuric acid (H2SO4).

IEEE GlobalSpec may share your personal information and website activity with our clients for which you express explicit interest, or with vendors looking to reach people like you. The antibacterial action was found to be generally confined to derivatives of sulfanilamide ( p-aminobenzenesulfonamide) of the type depicted by structure 1 with variations in R 1 and R 2; in the majority of the sulfa drugs the substituent R 1 = H, but there is considerable variation in the other substituent, R 2.

ClSO3H reacts violently with water to yield sulfuric acid and hydrogen chloride, commonly seen as vapors fuming from the liquid: Precautions, such as proper ventilation, associated with HCl should be observed. as well as subscriptions and other promotional notifications. : 7790-94-5 MSDS SECTION 1: Identification of the substance/mixture and of the company/undertaking 1.1. Reaction of Chlorosulfonic Acid with Elements and Inorganic Compounds, Chapter 8: By submitting your registration, you agree to our Privacy Policy. Product identifier Product form : Substance: EC Index-No. Chlorosulfonic acid has been used as an anti-contrail agent in Ryan Model 147 reconnaissance drones,[5] and to produce smoke screens.[6][7]. COMMERCIAL USES OF CHLOROSULFONIC ACID, Industrial Computers and Embedded Systems, Material Handling and Packaging Equipment, Electrical and Electronic Contract Manufacturing, Chapter 2: <>/XObject<>>>/Group <>/Annots[13 0 R 14 0 R ]>> Sulfanilamides are synthezised by reaction of the appropriate substituted aniline 2 with excess chlorosulfonic acid to yield the sulfonyl chloride 3 and subsequent condensation with the amine gives the corresponding sulfanilamide 1.

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: 232-234-6 CAS-No. [3] The compound is rarely obtained pure. ��M�G��4��Li$rk�6�&��dZ{&���Z� Ӵ�c��7/=��N�u�K6�f����e�0я Q(&��U�u�4L{�D�! Probably this is caused by corrosion of the bottle caps which often cannot resist for a longer period of time. 4 0 obj

33). An invaluable text for synthetic chemists in the pharmaceutical, agrochemical, plastic and detergent industries, this book provides a detailed, up-to-date account of the reactions of chlorosulfonic acid with aliphatic, aromatic and heterocyclic compounds. Companies affiliated with GlobalSpec can contact me when I express interest in their product or service.

Upon standing with excess sulfur trioxide, it decomposes to pyrosulfuryl chlorides:[4], The industrial synthesis entails the reaction of hydrogen chloride with a solution of sulfur trioxide in sulfuric acid:[4]. Sulfonation and Chlorosulfonation of Aromatic Compounds using Chlorosulfonic Acid, 9: Copyright The Royal Society of Chemistry 2002 under license agreement with Books24x7, FDA Approval Fluoroelastomer for Food Contact. (���. An error occurred while processing the form. Include me in professional surveys and promotional announcements from GlobalSpec.

: 016-017-00-1 EC-No. Use of this website signifies your agreement to our Terms of Use. ClSO2OH is used to prepare alkyl sulfates, which are useful as detergents and as chemical intermediates: An early synthesis of saccharin begins with the reaction of toluene with ClSO2OH to give the ortho- and para-toluenesulfonyl chloride derivatives: Oxidation of the ortho isomer gives the benzoic acid derivative that then is cyclized with ammonia and neutralized with base to afford saccharin. D��B�J���4��5sJ�;MMI�rc|7��oRT?<9;�8�����������i���}pxzA7���|���/�/Z�t0�)jd���������Ȟ3�wN��#3��9T� 6�#dpx���uI.�� tb�\���^��q"r��G��кA�� �(���kZ��h�=�Tk��u�s�=v����N+*���&%�%s�=L��.���_͈�#�u% ��dG� ��x��e$�d��� 3.X��}�iL O��k�I��iKp�oJz��\^�ٷQ6�f�Y�w�NMp|��@G�,ʍ��n�Ѧ� � �K�r��u�}�Q�N�~�d��h�� '%��V V5fӋ͋+�ʴ1`� Ί�$ܫ>bf%#'ӤJ���wū0$��1�C�%�]O�_%�b�Ӝ���� .

: 7790-94-5 Product code : 02771 Formula : HClO3S Synonyms : Sulphuric chlorohydrin,Chlorosulphuric acid 1.2.

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During this reaction a lot of hydrogenchloride gas is formed. Salts and esters of chlorosulfuric acid are known as chlorosulfates. It is also known as chlorosulfonic acid, being the sulfonic acid of chlorine.It is a distillable, colorless liquid which is hygroscopic and a powerful lachrymator.. Salts and esters of chlorosulfuric acid are known as chlorosulfates Many important industrial chemicals are manufactured by procedures involving chlorosulfonic acid. Old charges are often coloured brownish.

It is also known as chlorosulfonic acid, being the sulfonic acid of chlorine.

Miscellaneous Reactions of Chlorosulfonic Acid, Chapter 10: Reactions of Chlorosulfonic Acid with Heterocyclic Compounds, Chapter 7: IEEE GlobalSpec collects only the personal information you have entered above, your device information, and location data.

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Chlorosulfonic acid mixed with sulfur trioxide is also used as a chemical smoke in warfare (see Chapter 7, ref. '�l��ꉲ!��V�N'�d�� ү�����Ӄ����e{��� ��Gb���˃��_�� ���zZ��Z�ǕW#��0c Zփ�'dPZ��Z_ｼ���p�.1���Ԣpv�9ʮR�n&%%���ST��5�Z--��`�(�g�4wI4�u�6M� ��� ����\�T8V���2��m�i�IǮ������t�&]7����7�Xc���� ACCESS

Difference Between Dynamic & Kinematic Viscosity? BEST IDEAS. • To attach sulfate group to silk fibroin for improving its anticoagulant ability. CHAPTER 8: <>stream

rY':�B~��!z����D�n���8�? It can also be prepared by chlorination of sulfuric acid, written here for pedagogical purposes as HSO3(OH), vs. the usual format H2SO4: The latter method is more suited for laboratory-scale operations. Examples include: medicinal agents such as sulfonamide antibacterials and diuretics; disinfectants (chloramine and dichloramine T); pesticides like sulfonylurea; carbamate herbicides and aryl sulfone acaricides; synthetic sweeteners, e.g.

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Sulfonation and Chlorosulfonation of Organic Compounds, Chapter 3: These high temperature chlorinations are probably homolytic reactions.

CHLOROSULFONIC ACID FOR SYNTHESIS MSDS CAS-No. Aromatic Amines and Related Compounds, Chapter 5:

Since the discovery of the antibacterial activity of sulfonamides in 1935, some 15 000 derivatives of sulfanilamide ( 1; R 1 = R 2 = H) have been synthezised1 (see also Chapter 6, ref. It is a distillable, colorless liquid which is hygroscopic and a powerful lachrymator.[2]. Chlorosulfonic acid may be used in the following processes: • Synthesis of di-n-butyl ammonium chlorosulfonate, a secondary amine ionic liquid. 1 Medicinal Agents. They were the first synthetic antibacterial agents to be widely effective in humans. endobj

:�6��Zxೋ�Ü�CX��J���l�f�� ����30�P�z��� h�9����C�U�E���b�4�J1�*]l!� ݷM��,@�w8{�#�Ku Chlorosulfonic acid may function as a chlorinating agent for aromatic substrates at high temperatures, thus p-dichlorobenzene, by heating with excess of the reagent at 140 C, yields 1,2,4,5-tetrachlorobenzene while at higher temperatures (210 220 C), the reaction gives hexachlorobenzene (Chapter 6, ref. O1G(Q��(j{,G�R��hhk+�)t(o|�����d��!�%s0}R�v�þ��{���m/�I�0:T�R��d � ������?�'L��L! • To prepare sulfonated polyethersulfone (SPES) with enhanced hydrophilic property. If R 1 is an acyl... © Copyright 2020 GlobalSpec - All rights reserved. Preparation, Manufacture and Properties of Chlorosulfonic Acid, Appendix A:

Commercial Uses of Chlorosulfonic Acid, Chapter 9: Since the discovery of the antibacterial activity of sulfonamides in 1935, some 15 000 derivatives of sulfanilamide ( 1; R 1 = R 2 = H) have been synthezised1 (see also Chapter 6, ref. The Reaction of Chlorosulfonic Acid with Aliphatic Compounds, Chapter 6:



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