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hydroxymethylbilane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 3-[5-[[3-(2-carboxyethyl)-5-[[3-(2-carboxyethyl)-5-[[3-(2-carboxyethyl)-4-(carboxymethyl)-5-(hydroxymethyl)-1H-pyrrol-2-yl]methy

    Cas No: 71861-60-4

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  • 71861-60-4 Structure
  • Basic information

    1. Product Name: hydroxymethylbilane
    2. Synonyms: 21H-Biline-2,7,12,17-tetrapropanoic acid, 3,8,13,18-tetrakis(carboxymethyl)-5,10,15,22,23,24-hexahydro-19-(hydroxymethyl)-;Preuroporphyrinogen
    3. CAS NO:71861-60-4
    4. Molecular Formula: C40H46N4O17
    5. Molecular Weight: 854.81
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 71861-60-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 1135.6°C at 760 mmHg
    3. Flash Point: 640.6°C
    4. Appearance: /
    5. Density: 1.582g/cm3
    6. Vapor Pressure: 0mmHg at 25°C
    7. Refractive Index: 1.687
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: hydroxymethylbilane(CAS DataBase Reference)
    11. NIST Chemistry Reference: hydroxymethylbilane(71861-60-4)
    12. EPA Substance Registry System: hydroxymethylbilane(71861-60-4)
  • 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: 71861-60-4(Hazardous Substances Data)

71861-60-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71861-60-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,8,6 and 1 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 71861-60:
(7*7)+(6*1)+(5*8)+(4*6)+(3*1)+(2*6)+(1*0)=134
134 % 10 = 4
So 71861-60-4 is a valid CAS Registry Number.
InChI:InChI=1/C40H46N4O17/c45-17-32-25(12-40(60)61)21(4-8-36(52)53)29(44-32)15-31-24(11-39(58)59)20(3-7-35(50)51)28(43-31)14-30-23(10-38(56)57)19(2-6-34(48)49)27(42-30)13-26-22(9-37(54)55)18(16-41-26)1-5-33(46)47/h16,41-45H,1-15,17H2,(H,46,47)(H,48,49)(H,50,51)(H,52,53)(H,54,55)(H,56,57)(H,58,59)(H,60,61)

71861-60-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name preuroporphyrinogen

1.2 Other means of identification

Product number -
Other names Methylol-bilan

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:71861-60-4 SDS

71861-60-4Relevant articles and documents

Handling heme: The mechanisms underlying the movement of heme within and between cells

Donegan, Rebecca K.,Moore, Courtney M.,Hanna, David A.,Reddi, Amit R.

, p. 88 - 100 (2018/08/21)

Heme is an essential cofactor and signaling molecule required for virtually all aerobic life. However, excess heme is cytotoxic. Therefore, heme must be safely transported and trafficked from the site of synthesis in the mitochondria or uptake at the cell surface, to hemoproteins in most subcellular compartments. While heme synthesis and degradation are relatively well characterized, little is known about how heme is trafficked and transported throughout the cell. Herein, we review eukaryotic heme transport, trafficking, and mobilization, with a focus on factors that regulate bioavailable heme. We also highlight the role of gasotransmitters and small molecules in heme mobilization and bioavailability, and heme trafficking at the host-pathogen interface.

Biosynthesis of Porphyrins and Related Macrocycles. Part 18. Proof by Spectroscopy and Synthesis that Unrearranged Hydroxymethylbilane is the Product from Deaminase and the Substrate for Cosynthetase in the Biosynthesis of Uropophyrinogen-III

Battersby, Alan R.,Fookes, Christopher J. R.,Gustafson-Potter, Kerstin E.,McDonald, Edward,Matcham, George W. J.

, p. 2427 - 2444 (2007/10/02)

When the enzyme deaminase acts alone on porphobilinogen, it releases a tarnsient intermediate into the medium which is unaffected by further treatment with a large excess of deaminase.The intermediate undergoes rapid ring-closure chemically (t1/2/su

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