Glyoxal trimer dihydrate

• Catalog No.: 50655
• CAS Number: 4405-13-4
• M. F.: C6H10O8
• M. W.: 210.1388
• Purity: ≥95% (T)

SYNONYMS

• Title: 乙二醛三聚物 二水合物
• IUPAC name: hexahydro-[1,4]dioxino[2,3-b][1,4]dioxine-2,3,6,7-tetrol
• IUPAC Traditional name: hexahydro-[1,4]dioxino[2,3-b][1,4]dioxine-2,3,6,7-tetrol
• Synonyms: Ethanedial trimer dihydrate; Hexahydro[1,4]dioxino[2,3-b]-1,4-dioxin-2,3,6,7-tetrol; 乙二醛

DATABASE IDS

• CAS Number: 4405-13-4
• PubChem SID: 24873389
• MDL Number: MFCD00010556
• Beilstein Number: 3542160
• EC Number: 224-551-3

PROPERTIES

• Linear Formula: (HC(O)C(O)H)3 · 2H2O
• Purity: ≥95% (T)
• Purity: ≥95%
• 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
• RTECS: JH5380000
• Safety Statements: 26-36
• German water hazard class: 3

DETAILS

Description (English)

Other Notes
This form of glyoxal is composed of 3 moles of glyoxal and 2 moles of water in a relatively stable configuration.
Application
Reactant involved in the synthesis of:
• Aza-analogs of 1,4-naphthoquinones as effectors of plasmodial thioredoxin and glutathione reductase1
• Substituted side-bridged cyclam derivatives2
• Furandicarboxylic acid di-methyl ester derivatives3

Description (简体中文)

Other Notes
这种形式的乙二醛是由 3mol 乙二醛 和 2mol 水组成的相对稳定的溶液。
Application
Reactant involved in the synthesis of:
• Aza-analogs of 1,4-naphthoquinones as effectors of plasmodial thioredoxin and glutathione reductase1
• Substituted side-bridged cyclam derivatives2
• Furandicarboxylic acid di-methyl ester derivatives3