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Type HazMat fee for 500 gram (Estimated)
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Chemical Structure| 107-36-8 Chemical Structure| 107-36-8
Chemical Structure| 107-36-8

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Isethionic acid (2-Hydroxyethanesulfonic acid) is an organic sulfur compound found in animals and some red algae. It can act as an anionic surfactant and exhibits antifouling activity against Balanus amphitrite.

Synonyms: 2-Hydroxyethanesulfonic acid

4.5 *For Research Use Only !

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Product Details of Isethionic acid

CAS No. :107-36-8
Formula : C2H6O4S
M.W : 126.13
SMILES Code : OCCS(=O)(O)=O
Synonyms :
2-Hydroxyethanesulfonic acid
MDL No. :MFCD00242599
InChI Key :SUMDYPCJJOFFON-UHFFFAOYSA-N
Pubchem ID :7866

Safety of Isethionic acid

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H302-H314
Precautionary Statements:P260-P264-P270-P280-P301+P310+P330+P331-P303+P361+P353+P310-P304+P340+P310-P305+P351+P338+P310-P363-P405-P501
Class:8
UN#:3265
Packing Group:

Application In Synthesis of Isethionic acid

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 107-36-8 ]

[ 107-36-8 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 6608-47-5 ]
  • [ 1184-84-5 ]
  • [ 107-36-8 ]
  • 2
  • [ 755037-03-7 ]
  • [ 107-36-8 ]
  • regorafenib isethionate salt [ No CAS ]
YieldReaction ConditionsOperation in experiment
In water; ethyl acetate; at 40℃; for 2h; 1.0 g of <strong>[755037-03-7]Regorafenib</strong> added into 10mL of ethyl acetate and 1ml of water and heated to 40 C to dissolve. The 0.33g of 2-hydroxyethyl sulfonate added into reaction solution and not less than 40 C keep the reaction for 2 hours. After cooling to room temperature, no precipitation, the reaction mixture was concentrated to dryness to obtain amorphous crystal form of <strong>[755037-03-7]Regorafenib</strong> isethionate
 

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