retinaldehyde

retinal structural formula

structural formula

business number 038n
molecular formula c20h28o
molecular weight 284.40
label

vitamin a aldehyde,

enzymes

numbering system

cas number:116-31-4

mdl number:mfcd00001550

einecs number:204-135-8

rtecs number:vh6407000

brn number:none

pubchem number:24899355

physical property data

1. character: undetermined

2. density (g/ml,25) : undetermined

3. relative vapor density (g/ml,air =1): undetermined

4. melting point ( ºc):64-65

5. boiling point (ºc,normal pressure): undetermined

6. boiling point (ºc, kpa): undetermined

7. refractive index: undetermined

8. flashpoint (ºc): undetermined

9. specific rotation (º): undetermined

10. autoignition point or ignition temperature (ºc): undetermined

11. vapor pressure (mmhg, ºc): undetermined

12. saturated vapor pressure (kpa, ºc): undetermined

13. heat of combustion (kj/mol): undetermined

14. critical temperature (ºc): undetermined

15. critical pressure (kpa): undetermined

16. oil and water (octanol/log value of the partition coefficient for water: undetermined

17. explosion upper limit (%,v/v): undetermined

18. 7. number of heavy atoms:21

8. surface charge :0

9. complexity :522

10. number of isotope atoms:0

11. determine the number of atomic stereocenters:0

12. uncertain number of atomic stereocenters:0

13. determine the number of stereocenters of chemical bonds:4

14. uncertain number of chemical bond stereocenters:0

15. number of covalent bond units: 1

properties and stability

none

storage method

none

synthesis method

vitamina after being catalyzed by alcohol dehydrogenase and coenzymes i and ii, cis and trans retinal are formed.

purpose

β-carotene intermediates .

ial”>4

14. uncertain number of chemical bond stereocenters:0

15. number of covalent bond units: 1

properties and stability

none

storage method

none

synthesis method

vitamina after being catalyzed by alcohol dehydrogenase and coenzymes i and ii, cis and trans retinal are formed.

purpose

β-carotene intermediates .

This article is from the Internet, does not represent the position of Toluene diisocyanate reproduced please specify the source.https://www.chemicalchem.com/archives/27862

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