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3082-03-9

"3,7,13,17-tetramethyl-21H,23H-Porphine-2,8,12,18-tetrapropanoic acid" is a complex organic compound with a molecular formula of C36H40N4O4. It is a derivative of porphyrin, a large heterocyclic macrocycle that is an essential component of hemoglobin, chlorophyll, and many other biological molecules. This specific compound features four methyl groups at positions 3, 7, 13, and 17, and four propanoic acid groups at positions 2, 8, 12, and 18. The structure of 3,7,13,17-tetramethyl-21H,23H-Porphine-2,8,12,18-tetrapropanoic acid is characterized by its 21H,23H-Porphine core, which is a type of porphyrin with two hydrogen atoms at positions 21 and 23. The tetrapropanoic acid groups give 3,7,13,17-tetramethyl-21H,23H-Porphine-2,8,12,18-tetrapropanoic acid its acidic properties, making it a potential candidate for various applications in chemistry and biology, such as in the study of metal complexes, drug design, or as a building block for more complex molecules.

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  • 3,7,13,17-tetramethyl-21H,23H-Porphine-2,8,12,18-tetrapropanoic acid

    Cas No: 3082-03-9

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  • 3082-03-9 Structure

  • Basic information

    1. Product Name: 3,7,13,17-tetramethyl-21H,23H-Porphine-2,8,12,18-tetrapropanoic acid
    2. Synonyms: 3,7,13,17-tetramethyl-21H,23H-Porphine-2,8,12,18-tetrapropanoic acid;Coproporphyrin II
    3. CAS NO:3082-03-9
    4. Molecular Formula: C36H38N4O8
    5. Molecular Weight: 654.70892
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 3082-03-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 1264.7°Cat760mmHg
    3. Flash Point: 718.7°C
    4. Appearance: /
    5. Density: 1.366g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3,7,13,17-tetramethyl-21H,23H-Porphine-2,8,12,18-tetrapropanoic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,7,13,17-tetramethyl-21H,23H-Porphine-2,8,12,18-tetrapropanoic acid(3082-03-9)
    11. EPA Substance Registry System: 3,7,13,17-tetramethyl-21H,23H-Porphine-2,8,12,18-tetrapropanoic acid(3082-03-9)

  • 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: 3082-03-9(Hazardous Substances Data)

3082-03-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3082-03-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,8 and 2 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3082-03:
(6*3)+(5*0)+(4*8)+(3*2)+(2*0)+(1*3)=59
59 % 10 = 9
So 3082-03-9 is a valid CAS Registry Number.

3082-03-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[8,12,18-tris(2-carboxyethyl)-3,7,13,17-tetramethyl-21,22-dihydroporphyrin-2-yl]propanoic acid

1.2 Other means of identification

Product number -
Other names Coproporphyrin III

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:3082-03-9 SDS

3082-03-9Upstream product

3082-03-9Downstream Products

3082-03-9Relevant articles and documents

Biosynthesis of Porphyrins and Related Macrocycles. Part 15. Chemical and Enzymic Formation of Uroporphyrinogen Isomers from Unrearranged Aminomethylpyrromethane: Separation of Isomeric Coproporphyrin Esters

Battersby, Alan R.,Buckley, Dennis G.,Johnson, Dawid W.,Mander, Lewis N.,McDonald, Edward,Williams, D. Clive

, p. 2779 - 2785 (2007/10/02)

The unrearranged pyrromethane (1) is transformed chemically mainly into uro'gen-I with a smaller amount of uro'gen-IV but only traces of uro'gen-III are formed.Uro'gen-I is produced via a tetrapyrrolic (bilane) intermediate and when the diaminase-cosynthetase enzyme system from Euglena gracilis is present, this intermediate is converted into uro'gen-III.The rearrangement step for this conversion has the same characteristics found earlier for the natural biosynthetic process from porphobilinogen.Pyrromethane (1) is not a direct biosynthetic precursor of uro'gen-III and reasons are advanced why this is understandable.Methods are developed based on high pressure liquid chromatography for the separation of all four isomeric coproporphyrin esters.

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