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1,3,4,6-Tetrakis(butoxymethyl)glycoluril_Molecular_structure_CAS_15968-37-3)
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1,3,4,6-Tetrakis(butoxymethyl)glycoluril

Catalog No. 441724 Name Sigma Aldrich
CAS Number 15968-37-3 Website http://www.sigmaaldrich.com
M. F. C24H46N4O6 Telephone 1-800-521-8956
M. W. 486.64524 Fax
Purity Email
Storage Chembase ID: 137989

SYNONYMS

Title
1,3,4,6-四(丁氧基甲基)甘脲
IUPAC name
1,3,4,6-tetrakis(butoxymethyl)-octahydroimidazo[4,5-d]imidazolidine-2,5-dione
IUPAC Traditional name
1,3,4,6-tetrakis(butoxymethyl)-dihydroimidazo[4,5-d]imidazolidine-2,5-dione

DATABASE IDS

CAS Number 15968-37-3
EC Number 240-108-7
MDL Number MFCD00216661

PROPERTIES

Empirical Formula (Hill Notation) C24H46N4O6
Gardner-Holdt 22.7-36.2 stokes(25 °C)(lit.)
Grade technical grade
Mol. Weight average Mn 550
Boiling Point >204 °C(lit.)
Density 1.07 g/mL at 25 °C(lit.)
Flash Point 113 °C
Flash Point 235.4 °F
Refractive Index n20/D 1.4788(lit.)
Solubility polar organic solvents: soluble
GHS Pictograms GHS08
GHS Signal Word Danger
GHS Hazard statements H350
European Hazard Symbols Toxic Toxic (T)
MSDS Link Download
Personal Protective Equipment Eyeshields, Gloves, type P2 (EN 143) respirator cartridges
GHS Precautionary statements P201-P308 + P313
Risk Statements 45-46
Safety Statements 53-36/37/39-45
German water hazard class 3

DETAILS

Description (English)
Application
Cross-linking agent. Cross-linking agent for water- or solvent-based alkyd, epoxy, epoxy ester, polyester and vinyl polymers used in coatings, enamels and primers.
Features and Benefits
Improves adhesion of cured films, increases corrosion resistance and flexibility. Requires strong acid cross-linking catalyst. Low tendency to self-condense.
Description (简体中文)
Application
交联剂。 水或溶剂型醇酸树脂、环氧树脂、环氧酯、聚酯和乙烯基聚合物的交联剂,可用于涂料、搪瓷和引物。
Features and Benefits
提高固化膜的粘附力,增加耐腐蚀性和柔韧性。需要强酸型交联催化剂。自缩趋势低。

REFERENCES