19213-70-8

• 

• Basic information

  1. Product Name: acetyltaurine
  2. Synonyms: acetyltaurine
  3. CAS NO:19213-70-8
  4. Molecular Formula: C₄H₉NO₄S
  5. Molecular Weight: 167.18
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 19213-70-8.mol
  9. Article Data: 1

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: N/A
  3. Flash Point: N/A
  4. Appearance: /
  5. Density: 1.404g/cm³
  6. Refractive Index: 1.494
  7. Storage Temp.: Refrigerator
  8. Solubility: Methanol (Slightly), Water (Slightly)
  9. CAS DataBase Reference: acetyltaurine(CAS DataBase Reference)
  10. NIST Chemistry Reference: acetyltaurine(19213-70-8)
  11. EPA Substance Registry System: acetyltaurine(19213-70-8)

• Safety Data

  1. Hazard Codes: N/A
  2. Statements: N/A
  3. Safety Statements: N/A
  4. WGK Germany:
  5. RTECS:
  6. HazardClass: N/A
  7. PackingGroup: N/A
  8. Hazardous Substances Data: 19213-70-8(Hazardous Substances Data)

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• Ethanesulfonic acid,2-(acetylamino)-

  Cas No: 19213-70-8

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• Suzhou Health Chemicals Co., Ltd.
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19213-70-8 Usage

Definition

ChEBI: An amino sulfonic acid that is taurine substituted by an acetyl group at the N atom.

Check Digit Verification of cas no

The CAS Registry Mumber 19213-70-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,2,1 and 3 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 19213-70:
(7*1)+(6*9)+(5*2)+(4*1)+(3*3)+(2*7)+(1*0)=98
98 % 10 = 8
So 19213-70-8 is a valid CAS Registry Number.

InChI:InChI=1/C4H9NO4S/c1-4(6)5-2-3-10(7,8)9/h2-3H2,1H3,(H,5,6)(H,7,8,9)

19213-70-8Upstream product

• 1190-73-4 2-(acetylamino)ethanethiol 

19213-70-8Downstream Products

• 107-35-7 Tau 

19213-70-8Relevant articles and documents

Efficient synthesis of taurine and structurally diverse substituted taurines from aziridines

Hu, Libo,Zhu, Hui,Du, Da-Ming,Xu, Jiaxi

, p. 4543 - 4546 (2008/02/05)

(Chemical Equation Presented) Taurine and substituted taurines were synthesized efficiently from aziridines via ring-opening reaction with thioacetic acid, oxidation with performic acid, and hydrolysis in hydrochloric acid. The current method shows more benefit in purification and efficiency in the preparation of taurine and structurally diverse 2-substituted, 2,2-disubstituted, and 1,2-, 2,2-, and 2,N-alkylene taurines.

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