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Butanedinitrile, hydroxy-, also known as hydroxybutanedinitrile or 2,3-butanedione dioxime, is an organic compound with the chemical formula C4H6N2O2. It is a white crystalline solid that is soluble in water and various organic solvents. Butanedinitrile, hydroxy- is primarily used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. It is also employed as a reagent in analytical chemistry for the detection and determination of metal ions, particularly nickel and cobalt. Due to its potential applications in various industries, research and development efforts are ongoing to improve its synthesis methods and explore new uses for this versatile chemical.

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  • 4341-85-9 Structure
  • Basic information

    1. Product Name: Butanedinitrile, hydroxy-
    2. Synonyms:
    3. CAS NO:4341-85-9
    4. Molecular Formula: C4H4N2O
    5. Molecular Weight: 96.0886
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 4341-85-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Butanedinitrile, hydroxy-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Butanedinitrile, hydroxy-(4341-85-9)
    11. EPA Substance Registry System: Butanedinitrile, hydroxy-(4341-85-9)
  • 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: 4341-85-9(Hazardous Substances Data)

4341-85-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4341-85-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,4 and 1 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4341-85:
(6*4)+(5*3)+(4*4)+(3*1)+(2*8)+(1*5)=79
79 % 10 = 9
So 4341-85-9 is a valid CAS Registry Number.

4341-85-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-hydroxybutanedinitrile

1.2 Other means of identification

Product number -
Other names malic dinitrile

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:4341-85-9 SDS

4341-85-9Relevant articles and documents

Common origins of RNA, protein and lipid precursors in a cyanosulfidic protometabolism

Patel, Bhavesh H.,Percivalle, Claudia,Ritson, Dougal J.,Duffy, Colm D.,Sutherland, John D.

, p. 301 - 307 (2015/04/14)

A minimal cell can be thought of as comprising informational, compartment-forming and metabolic subsystems. To imagine the abiotic assembly of such an overall system, however, places great demands on hypothetical prebiotic chemistry. The perceived differences and incompatibilities between these subsystems have led to the widely held assumption that one or other subsystem must have preceded the others. Here we experimentally investigate the validity of this assumption by examining the assembly of various biomolecular building blocks from prebiotically plausible intermediates and one-carbon feedstock molecules. We show that precursors of ribonucleotides, amino acids and lipids can all be derived by the reductive homologation of hydrogen cyanide and some of its derivatives, and thus that all the cellular subsystems could have arisen simultaneously through common chemistry. The key reaction steps are driven by ultraviolet light, use hydrogen sulfide as the reductant and can be accelerated by Cu(I)-Cu(II) photoredox cycling.

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