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1H-Purine-2,6-dione, 3,7-dihydro-1,3-dimethyl-
Non-ionic surfactants-Amine
Molecular Formula & Molecular Weight
Molecular Formula: C7H8N4O2
Molecular Weight: 180.16
Structural Formula
Appearance: solid.
Solubility: soluble in water; 25℃, 7.36g/L[1].
Stability: stable.
Risk: irritation, irritation to skin, eye.
Animal toxicity[1]: guinea pig oral LD50: 183mg/Kg;
guinea pig subcutaneous LDLo: 170mg/Kg;
mouse intramuscular LD50: 271mg/Kg;
mouse intraperitoneal LD50: 70mg/Kg;
mouse intravenous LD50: 136mg/Kg;
mouse oral LD50: 235mg/Kg;
mouse rectal LD50: 166mg/Kg;
mouse subcutaneous LD50: 138mg/Kg;
rabbit intravenous LD50: 150mg/Kg;
rabbit oral LD50: 350mg/Kg;
rat intraperitoneal LD50: 150mg/Kg;
rat oral LD50: 225mg/Kg;
rat intravenous LDLo: 240mg/Kg;
rat subcutaneous LDLo: 325mg/Kg.
reproductive effect.
Human toxicity[1]: child intramuscular TDLo: 50mg/Kg;
child oral TDLo: 10mg/Kg;
human intravenous TDLo: 10mg/Kg/D;
human oral TDLo: 5mg/Kg;
human rectal TDLo: 6mg/Kg;
human subcutaneous TDLo: 3.5mg/Kg;
infant oral TDLo: 348mg/Kg/4D-I;
man intravenous LDLo: 3.429mg/Kg;
man parenteral LDLo: 12mg/Kg;
man oral TDLo: 66mg/Kg;
man oral TDLo: 86mg/Kg;
man oral TDLo: 129mg/Kg;
women oral LDLo: 130mg/Kg;
women intravenous TDLo: 120mg/Kg/3D-C;
women oral TDLo: 5mg/Kg;
women oral TDLo: 108mg/Kg;
women oral TDLo: 281mg/Kg/4W;
women oral TDLo: 388mg/Kg.
overall carcinogenic evaluation: Group 3.
Ecology: may be hazardous to environment. Water body should be given special attention.
Biodegradability: biodegradable.
Characteristics: excellent antistatic, dispersing, anticorrosive abilities.
Quality standards & test methods
physical and chemical indexes
test methods
Actives*, %, ≥
*: should be marked on molecular weight.
Major Uses
Use as pharmaceutical ingredient.
Use as intermediate in organic synthesis.
Use as antistatic agent.
Conditioning agent in personal care products.
[1]: 58-55-9

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