Isobutyramide - ≥98%(GC) , CAS No.563-83-7

Name: Isobutyramide - ≥98%(GC) , CAS No.563-83-7
SKU: I157612
Availability: InStock

CAS: 563-83-7 Cat. No.: I157612 Formule: C₄H₉NO Poids moléculaire: 87.12 Beilstein Registry Number: 2293 Numéro CE: 209-265-9

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Isobutyramide - ≥98%(GC) CAS No(563-83-7) by Aladdin Scientific

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DISPONIBLE À COMMANDE

GRADE & PURITY ≥98%(GC)

Synonyms

W-105521 | AKOS001084432 | NSC8423 | NSC-8423 | Isobutyrimidic acid | SY015332 | isobutyric acid amide | 2-Methylpropanamide | 2-methyl-propanamide | I0102 | Q10859786 | NSC 8423 | dimethylacetoamide | 4-02-00-00852 (Beilstein Handbook Reference) | IBO |

Storage

Room temperature

Shipped In

Normal

Vue d’ensemble Specifications Noms et identifiants Documentation Advanced Data Taxonomic Classification Structure 3D Cibles associées (humaines) Cibles associées (non humaines) Mécanismes d'action Certificats (CoA, COO, BSE/TSE et tableau d'analyse) Propriétés chimiques et physiques Citations of This Product Calculateurs de solution Avis

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Why this grade

≥98%(GC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Room temperature Ships Normal Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Vue d’ensemble

In the process of synthesis, isobutylamide was used to assemble protein capsules by chemical grafting sequence of human serum albumin.

Specifications

Synonymes

Spécifications et pureté

≥98%(GC)

Mécanismes biochimiques et physiologiques

Isobutylamide activates the transcription of human gamma globin gene and mouse embryonic epsilon (y) - globin gene. It can be used to treat β - thalassemia and sickle cell disease.

Conditions de stockage de stockage

Room temperature

Expédié en

Normal

Pureté

≥98%(GC)

Noms et identifiants

Pubchem Sid

488184139

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/488184139

Sourires canoniques

CC(C)C(=O)N

IUPAC Name

2-methylpropanamide

InChIKey

WFKAJVHLWXSISD-UHFFFAOYSA-N

INCHI

1S/C4H9NO/c1-3(2)4(5)6/h3H,1-2H3,(H2,5,6)

Isomères SMILES

CC(C)C(=O)N

WGK Allemagne

RTECS

TX1475000

Poids moléculaire

87.12

Beilstein

2293

Reaxy-Rn

1737615

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1737615&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organic acids and derivatives
  - Classe Carboxylic acids and derivatives
    - Subclass Carboxylic acid derivatives
      - Level5 Carboxylic acid amides
        Level6 Primary carboxylic acid amides

Kingdom	Organic compounds
Superclass	Organic acids and derivatives
Classe	Carboxylic acids and derivatives
Subclass	Carboxylic acid derivatives
Intermediate Tree Nodes	Carboxylic acid amides
Direct Parent	Primary carboxylic acid amides
Alternative Parents	Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework	Aliphatic acyclic compounds
Substituents	Primary carboxylic acid amide - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - Aliphatic acyclic compound
Description	This compound belongs to the class of organic compounds known as primary carboxylic acid amides. These are compounds comprising primary carboxylic acid amide functional group, with the general structure RC(=O)NH2.
External Descriptors	a small molecule
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Structure 3D

Cibles associées (humaines)

ACHN (49357 Activities)

Lot Number	Certificate Type	Date	Article
L2215578	Certificate of Analysis	Sep 07, 2026	I157612
L2215579	Certificate of Analysis	Sep 07, 2026	I157612
L2215586	Certificate of Analysis	Sep 07, 2026	I157612
L2215598	Certificate of Analysis	Sep 07, 2026	I157612
L2215681	Certificate of Analysis	Sep 07, 2026	I157612
K2113018	Certificate of Analysis	Aug 13, 2025	I157612
K2113019	Certificate of Analysis	Aug 13, 2025	I157612
K1722009	Certificate of Analysis	Jun 12, 2025	I157612
E2430450	Certificate of Analysis	Apr 16, 2024	I157612
E2430478	Certificate of Analysis	Apr 16, 2024	I157612
I2511005	Certificate of Analysis	Nov 21, 2022	I157612
L2215583	Certificate of Analysis	Nov 21, 2022	I157612
D2315712	Certificate of Analysis	May 13, 2021	I157612

Solubilité	Soluble in water.
Point d'ébullition (°C)	216-220°C
Point de fusion (°C)	128 °C
Poids moléculaire	87.120 g/mol
XLogP3	0.200
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	1
Rotatable Bond Count	1
Exact Mass	87.0684 Da
Monoisotopic Mass	87.0684 Da
Topological Polar Surface Area	43.100 Å²
Heavy Atom Count	6
Formal Charge	0
Complexity	58.600
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

Isobutyramide - ≥98%(GC) , CAS No.563-83-7

Storage & shipping

Quality documents

Literature proof

Vue d’ensemble

Specifications

Documentation

📋 Safety Data Sheet (SDS)

✅ Certificate of Analysis (COA)

📊 Datasheet

🔬 Specification Sheet

Advanced Data

Molarity Calculator

Dilution Calculator

Reconstitution Calculator

Avis des clients

📚 Citations by Application

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