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DL-2,4-Diaminoglutaric acid, a chemical compound with the molecular formula C5H10N2O4, is a derivative of the amino acid glutamic acid. It features a central carbon atom bonded to two amino groups, a carboxylic acid group, and a hydrogen atom. DL-2,4-Diaminoglutaric acid has garnered interest due to its potential therapeutic applications and contributions to organic synthesis and pharmaceutical research.

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  • 1421-04-1 Structure
  • Basic information

    1. Product Name: DL-2,4-Diaminoglutaric acid
    2. Synonyms: DL-2,4-Diaminoglutaric acid;2,4-bis(azanyl)pentanedioic acid;2,4-diaminopentanedioic acid
    3. CAS NO:1421-04-1
    4. Molecular Formula: C5H10N2O4
    5. Molecular Weight: 162.1439
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1421-04-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 391.2 °C at 760 mmHg
    3. Flash Point: 190.4 °C
    4. Appearance: /
    5. Density: 1.495 g/cm3
    6. Vapor Pressure: 3.28E-07mmHg at 25°C
    7. Refractive Index: 1.565
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: DL-2,4-Diaminoglutaric acid(CAS DataBase Reference)
    11. NIST Chemistry Reference: DL-2,4-Diaminoglutaric acid(1421-04-1)
    12. EPA Substance Registry System: DL-2,4-Diaminoglutaric acid(1421-04-1)
  • 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: 1421-04-1(Hazardous Substances Data)

1421-04-1 Usage

Uses

Used in Pharmaceutical Research:
DL-2,4-Diaminoglutaric acid is used as a research compound for its potential role in the treatment of neurodegenerative disorders such as amyotrophic lateral sclerosis (ALS). Its study is crucial for understanding its therapeutic effects and mechanisms of action in these conditions.
Used in Organic Synthesis:
In the field of organic synthesis, DL-2,4-Diaminoglutaric acid serves as a valuable intermediate or building block for the development of new organic compounds and pharmaceuticals. Its unique structure allows for various chemical reactions that can lead to the creation of novel molecules with potential applications in medicine and other industries.
While the provided materials do not specify different applications across various industries, the general uses outlined above encompass the primary areas where DL-2,4-Diaminoglutaric acid is currently being explored. As research progresses, additional applications may be discovered, further expanding the utility of this compound.

Check Digit Verification of cas no

The CAS Registry Mumber 1421-04-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,2 and 1 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1421-04:
(6*1)+(5*4)+(4*2)+(3*1)+(2*0)+(1*4)=41
41 % 10 = 1
So 1421-04-1 is a valid CAS Registry Number.
InChI:InChI=1/C5H10N2O4/c6-2(4(8)9)1-3(7)5(10)11/h2-3H,1,6-7H2,(H,8,9)(H,10,11)

1421-04-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name DL-2,4-Diaminoglutaric acid

1.2 Other means of identification

Product number -
Other names threo-2,4-diaminopentanedioic acid

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:1421-04-1 SDS

1421-04-1Relevant articles and documents

Synthesis of stereoisomers of 2,4-diaminoglutaric and 2,5-diaminoadipic acids

Krasnov, V. P.,Zhdanova, E. A.,Korolyova, M. A.,Bukrina, I. M.,Kodess, M. I.,et al.

, p. 319 - 323 (1997)

Stereoisomers of 2,4-diaminoglutaric and 2,5-diaminoadipic acids were synthesized from glutamic and 2-aminoadipic acids, respectively.The stereochemistry of the products was established by 1H NMR spectroscopy and X-ray analysis. - Keywords: 2,4-diaminoglutaric acid; 2,5-diaminoadipic acid; nucleophilic substitution; stereoisomers; racemization

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