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16536-89-3

L-ADRENALINE BITARTRATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 16536-89-3 Structure

  • Basic information

    1. Product Name: L-ADRENALINE BITARTRATE
    2. Synonyms: (-)-3,4-Dihydroxy-a-((methylamino)methyl)benzyl Alcohol (+)-Tartrate (1:1) Salt; (2R,3R)-2,3-Dihydroxybutandis?ure--4-[(1R)-1-hydroxy-2-(methylamino)ethyl]benzol-1,2-diol(1:1); (2R,3R)-2,3-Dihydroxysuccinic acid - 4-[(1R)-1-hydroxy-2-(methylamino)ethyl]-1,2-benzenediol (1:1); (2R,3R)-2,3-Dihydroxysuccinic acid - 4-[(1R)-1-hydroxy-2-(methylamino)ethyl]benzene-1,2-diol (1:1); (R)-4-(1-Hydroxy-2-(methylamino)ethyl)-1,2-benzenediol (R-(R*,R*))-2,3-Dihydroxybutanedioate (1:1) (Salt); 4-[(1R)-1-hydroxy-2-(methylamino)ethyl]benzene-1,2-diol 2,3-dihydroxybutanedioate (salt); acide (2R,3R)-2,3-dihydroxybutanedio?que - 4-[(1R)-1-hydroxy-2-(méthylamino)éthyl]benzène-1,2-diol (1:1); butanedioic acid, 2,3-dihydroxy-, (2R,3R)-, compd. with 4-[(1R)-1-hydroxy-2-(methylamino)ethyl]-1,2-benzenediol (1:1); 4-[(1R)-1-hydroxy-2-(methylamino)ethyl]benzene-1,2-diol 2,3-dihydroxybutanedioate (1:1)
    3. CAS NO:16536-89-3
    4. Molecular Formula: MW:
    5. Molecular Weight: 0
    6. EINECS: 200-097-1
    7. Product Categories: N/A
    8. Mol File: 16536-89-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 413.1°Cat760mmHg
    3. Flash Point: 207.9°C
    4. Appearance: /
    5. Density: g/cm3
    6. Vapor Pressure: 1.45E-07mmHg at 25°C
    7. Refractive Index: N/A
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: L-ADRENALINE BITARTRATE(CAS DataBase Reference)
    11. NIST Chemistry Reference: L-ADRENALINE BITARTRATE(16536-89-3)
    12. EPA Substance Registry System: L-ADRENALINE BITARTRATE(16536-89-3)

  • 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: 16536-89-3(Hazardous Substances Data)

16536-89-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16536-89-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,5,3 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 16536-89:
(7*1)+(6*6)+(5*5)+(4*3)+(3*6)+(2*8)+(1*9)=123
123 % 10 = 3
So 16536-89-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H13NO3.C4H6O6/c1-10-5-9(13)6-2-3-7(11)8(12)4-6;5-1(3(7)8)2(6)4(9)10/h2-4,9-13H,5H2,1H3;1-2,5-6H,(H,7,8)(H,9,10)/t9-;1-,2-/m01/s1

16536-89-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R,3R)-2,3-dihydroxybutanedioic acid,4-[(1R)-1-hydroxy-2-(methylamino)ethyl]benzene-1,2-diol

1.2 Other means of identification

Product number -
Other names Asthmahaler

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:16536-89-3 SDS

16536-89-3Downstream Products

16536-89-3Relevant articles and documents

PROCESS FOR THE SYNTHESIS OF OPTICALLY ACTIVE BETA-AMINO ALCOHOLS

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Page/Page column 17-18, (2019/11/04)

Subject-matter of the present invention is a process for the preparation of optically active phenyl-beta-amino alcohols by means of a specific reduction of the corresponding phenyl-beta-amino ketones. Further subject-matter of the invention are said novel synthesis intermediates and their use for the preparation of active pharmaceutical ingredients.

PROCESS FOR THE PREPARATION OF OPTICALLY ENRICHED ADRENALINE

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Paragraph 0039-0043, (2016/06/01)

A process for the production of (-)-adrenaline and (-)-adrenaline-L-tartrate is provided. The process provides for a new, efficient and commercially feasible process for the optical resolution of racemic adrenaline. In one aspect, a one pot process for the synthesis of (-)-adrenaline is provided. The process provides a simple and less expensive 5 process that can be used to prepare commercial scale batches of (-)-adrenaline and (-)-adrenaline-L-tartrate of API quality. The process avoids the use of expensive and unpredictable chiral catalysts.

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