3,3-Dimethylglutaric acid

• Catalog No.: 40340
• CAS Number: 4839-46-7
• M. F.: C7H12O4
• M. W.: 160.16778
• Purity: ≥98.0% (GC)

SYNONYMS

• Title: 3,3-二甲基戊二酸
• IUPAC name: 3,3-dimethylpentanedioic acid
• IUPAC Traditional name: β,β-dimethylglutaric acid
• Synonyms: NSC 14987; 二甲基谷氨酸; NSC 49114; 3,3-Dimethylpentanedioic acid

DATABASE IDS

• MDL Number: MFCD00002716
• Beilstein Number: 1765439
• CAS Number: 4839-46-7
• PubChem SID: 24865190
• EC Number: 225-425-0

PROPERTIES

• Grade: purum
• Linear Formula: HOOCCH2C(CH3)2CH2COOH
• Purity: ≥98.0% (GC)
• Melting Point: 100-102 °C(lit.)
• Melting Point: 100-102 °C
• GHS Signal Word: Warning
• GHS Hazard statements: H315-H319-H335
• European Hazard Symbols: Irritant (Xi)
• Personal Protective Equipment: dust mask type N95 (US), Eyeshields, Gloves
• GHS Precautionary statements: P261-P305 + P351 + P338
• Risk Statements: 36/37/38
• Safety Statements: 26-36
• German water hazard class: 3

DETAILS

Description (English)

Application
Reactant involved in:
• Cyclodehydration of diols1
• Synthesis of conjugates of betulin derivatives used as anti-HIV agents2
• Preparation of dimeric peptide antagonists of IgG-FcRn interaction3
• Microwave-assisted protection of glutaraldehyde4
• Synthesis of glycyrrhetinic acid derivatives for proteasome inhibition5
• Catalytic, asymmetric transannular aldolizations6

Description (简体中文)

Application
Reactant involved in:
• Cyclodehydration of diols1
• Synthesis of conjugates of betulin derivatives used as anti-HIV agents2
• Preparation of dimeric peptide antagonists of IgG-FcRn interaction3
• Microwave-assisted protection of glutaraldehyde4
• Synthesis of glycyrrhetinic acid derivatives for proteasome inhibition5
• Catalytic, asymmetric transannular aldolizations6