I5133
咪唑烷基脲
别名:
N,N′′-亚甲基双[N′-[3-(羟甲基)-2,5-二氧基-4-咪唑烷]-尿素
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关于此项目
经验公式（希尔记法）:
C11H16N8O8
化学文摘社编号:
分子量:
388.29
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
EC Number:
254-372-6
MDL number:
Form:
powder
SMILES string
[OCN1C(NC(=O)NCNC(=O)NC2N(CO)C(=O)NC2=O)C(=O)NC1=O], OCN1C(NC(=O)NCNC(=O)NC2N(CO)C(=O)NC2=O)C(=O)NC1=O
InChI key
[ZCTXEAQXZGPWFG-UHFFFAOYSA-N], ZCTXEAQXZGPWFG-UHFFFAOYSA-N
InChI
[1S/C11H16N8O8/c20-2-18-4(6(22)16-10(18)26)14-8(24)12-1-13-9(25)15-5-7(23)17-11(27)19(5)3-21/h4-5,20-21H,1-3H2,(H2,12,14,24)(H2,13,15,25)(H,16,22,26)(H,17,23,27)], 1S/C11H16N8O8/c20-2-18-4(6(22)16-10(18)26)14-8(24)12-1-13-9(25)15-5-7(23)17-11(27)19(5)3-21/h4-5,20-21H,1-3H2,(H2,12,14,24)(H2,13,15,25)(H,16,22,26)(H,17,23,27)
form
powder
mp
240.5 °C
solubility
water: soluble 1 g/L at 20 °C
density
1.24 g/cm3 at 20 °C
storage temp.
2-8°C
Quality Level
Application
咪唑烷基脲可作为氢键增强剂，用于：
- 使用聚乙二醇(PEG)和二异氰酸酯制备聚合超分子水凝胶。
- 制备多功能聚丙烯酰胺水凝胶。
用于：
研究药物营养敏感筛选的药理学研究，即从线粒体呼吸到糖酵解的迁移能量代谢
涉及纳米结构植物载体局部活性分子递送的治疗研究
用作抗氧化剂的局部制剂
研究药物营养敏感筛选的药理学研究，即从线粒体呼吸到糖酵解的迁移能量代谢
涉及纳米结构植物载体局部活性分子递送的治疗研究
用作抗氧化剂的局部制剂
signalword
Warning
hcodes
Hazard Classifications
Skin Sens. 1B
存储类别
11 - Combustible Solids
wgk
WGK 2
ppe
dust mask type N95 (US), Eyeshields, Gloves
D Matosiuk et al.
European journal of medicinal chemistry, 36(10), 783-797 (2001-12-12)
The synthesis and physicochemical properties of new carbonyl derivatives of 1-aryl-2-iminoimidazolidine are presented. Isomeric 1-(1-arylimidazolidine-2-ylidene)-3-arylureas (series A) and 1-aryl-2-imine-3-arylaminocarbonylimidazolidines (series B) were obtained after the condensation reaction of 1-aryl-2-iminoimidazolidines and arylisocyanates. 1-Aryl-2-iminoimidazolidines were synthesised in a two-step reaction from the
Marléne Isaksson et al.
Contact dermatitis, 54(1), 29-34 (2006-01-24)
A topical corticosteroid preparation on the Swedish market, Flutivate cream, contains a fairly high concentration of formaldehyde (FA). In this study, we have investigated the clinical relevance of contact allergy to FA when treating an allergic eczema with Flutivate cream
Effects of Several Cosmetic Preservatives on ROS-Dependent Apoptosis of Rat Neural Progenitor Cells.
Onjeon Ryu et al.
Biomolecules & therapeutics, 26(6), 608-615 (2018-02-13)
Benzalkonium chloride, diazolidinyl urea, and imidazolidinyl urea are commonly used preservatives in cosmetics. Recent reports suggested that these compounds may have cellular and systemic toxicity in high concentration. In addition, diazolidinyl urea and imidazolidinyl urea are known formaldehyde (FA) releasers
T Agner et al.
Contact dermatitis, 45(1), 21-25 (2001-06-26)
The preservatives imidazolidinyl urea (IMID, Germall 115) and diazolidinyl urea (DU, Germall II) are commonly used in cosmetic products and are well-known sensitizers. The aim of the present study was to establish the optimal patch test concentration in hydrophilic dried-in
Robert L Rietschel et al.
Dermatitis : contact, atopic, occupational, drug, 18(3), 155-162 (2007-08-30)
To determine whether petrolatum or aqueous vehicles are more sensitive for detecting allergy to imidazolidinylurea (IU), diazolidinylurea (DU), and dimethylol dimethyl hydantoin (DM). The relationship of these allergens to formaldehyde sensitivity was also explored. Retrospective analysis of patients patch-tested by
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