????
|
|
???? ??
- ???
- 170-176 °C (lit.)
- ?? ?
- 263.89°C (estimate)
- ??
- 1.405
- ?? ??
- 640kg/m3
- ???
- 1.5300 (estimate)
- ?? ??
- Store below +30°C.
- ???
- ?: 20°C?? ???137g/L
- ??? ??
- ????
- ?? ?? (pKa)
- -1.0(at 25℃)
- Specific Gravity
- 1.406
- ??
- ???? ?? ??
- ??????(pH)
- 6-8 (50g/l, H2O, 20℃)
- ??
- ?? ??
- pH ??
- 5 - 7
- ???
- 13.6g/100mL(20℃)
- Merck
- 14,9367
- BRN
- 605327
- Henry's Law Constant
- 5.0×103 mol/(m3Pa) at 25℃, Duchowicz et al. (2020)
- ???
- ????. ??, ???, ????, ???, ???, ????? ???? ????. ?????? ???? ??? ? ??.
- ??? ?? ??
- ??
???
- InChI
- 1S/CH4N2S/c2-1(3)4/h(H4,2,3,4)
- InChIKey
- UMGDCJDMYOKAJW-UHFFFAOYSA-N
- SMILES
- NC(N)=S
- LogP
- -1.050 (est)
- CAS ??????
- 62-56-6(CAS DataBase Reference)
- IARC
- 3 (Vol. Sup 7, 79) 2001
- NIST
- Thiourea(62-56-6)
??
- ?? ? ?? ??
- ?? ? ???? ?? (GHS)
| ??? ?? | Xn,N,Xi | ||
|---|---|---|---|
| ?? ???? ?? | 22-40-51/53-63-43-38 | ||
| ????? | 36/37-61 | ||
| ????(UN No.) | UN 2811 6.1/PG 3 | ||
| WGK ?? | 2 | ||
| RTECS ?? | YU2800000 | ||
| ?? ?? ?? | 440 °C Dust | ||
| TSCA | TSCA listed | ||
| ?? ?? | 6.1 | ||
| ???? | III | ||
| HS ?? | 29309070 | ||
| ???? ??? | 11 - Combustible Solids | ||
| Hazard Classifications | Acute Tox. 4 Oral Aquatic Chronic 2 Carc. 2 Repr. 2 |
||
| ?? ?? ??? | 62-56-6(Hazardous Substances Data) | ||
| ?? | LD50 orally in wild Norway rats: 1830 mg/kg (Dieke) | ||
| ???? ?? | KE-33805 |
???? C??? ??, ??, ??
??
Thiourea appears as white crystal/powder, is combustible, and on contact with fire, gives off irritating or toxic fumes/gases. Thiourea is a reducing agent used primarily in the production of bleached recycled pulp. In addition, it is also effective in the bleaching of stone groundwood, pressurised groundwood. Thiourea undergoes decomposition on heating and produces toxic fumes of nitrogen oxides and sulphur oxides. It reacts violently with acrolein, strong acids, and strong oxidants. The main application of thiourea is in textile processing and also is commonly employed as a source of sulphide. Thiourea is a precursor to sulphide to produce metal sulphides, for example, mercury sulphide, upon reaction with the metal salt in aqueous solution. The industrial uses of thiourea include production of flame-retardant resins and vulcanisation accelerators. Thiourea is used as an auxiliary agent in diazo paper, light-sensitive photocopy paper, and almost all other types of copy paper. Thiourea is used in many industrial applications, including as a chemical intermediate or catalyst, in metal processing and plating, and in photoprocessing.??? ??
Thiourea consists of colorless, lustrous crystals or powder with a bitter taste.??
The product is wildly used in pharmaceutical industry, agricultural, chemicals, metallurgical industry, petroleum and so on. It is also main material for producing thiourea dioxide(CH1N2O2S).?? ??
Thiourea is manufactured by heating ammonium thiocyanate at 140-145C for about 4 hours; equilibrium is established when about 25% of the thiocyanate is converted to thiourea.Thiourea may also be prepared by the interaction of cyanamide and hydrogen sulphide:
Thiourea closely resembles urea in that reaction with formaldehyde gives methylol derivatives and then resinous condensates which on continued heating yield network structures. Thiourea-formaldehyde resins are slower curing than urea-formaldehyde resins and the hardened products are more brittle and more water-resistant. At one time thiourea-formaldehyde resins were added to urea-formaldehyde resins to give mouldings and laminates with improved water-resistance. These mixed resins have now been largely superseded by melamine-formaldehyde resins which give products with better resistance to heat.
??
ChEBI: The simplest member of the thiourea class, consisting of urea with the oxygen atom substituted by sulfur.?? ??
Thiourea is formed by heating ammonium thiocyanate at 170 °C (338 °F). After about an hour, 25% conversion is achieved. With HCl, thiourea forms thiourea hydrochloride; with mercuric oxide, thiourea forms a salt; and with silver chloride, it forms a complex salt.?? ??
White or off-white crystals or powder. Sinks and mixes with water.??? ?? ??
Water soluble.?? ???
Thiocarbamide is a white crystalline material or powder, toxic, carcinogenic. When heated to decomposition Thiocarbamide emits very toxic fumes of oxides of sulfur and oxides of nitrogen. Violent exothermic polymerization reaction with acrylaldehyde (acrolein) [MCA SD-85, 1961], violent decomposition of the reaction product with hydrogen peroxide and nitric acid [Bjorklund G. H. et al., Trans. R. Soc. Can.,1950, 44, p. 28], spontaneous explosion upon grinding with potassium chlorate [Soothill, D., Safety Management, 1992, 8(6), p. 11].???
A questionable carcinogen. May not be used in food products (FDA); skin irritant (allergenic).????
The acute oral toxicity of thiourea in mostanimals is of low order. The oral LD50 values reported in the literature show variation.Symptoms of chronic effects in rats includebone marrow depression and goiters. Administration of 32.8 mol of thiourea in chickembryos on day 17 of incubation resultedin the accumulation of parabronchial liquidin those embryos (Wittman et al. 1987). Theinvestigators have attributed such changes tothe toxic effects of thiourea, rather to than aretardation of pulmonary development.Dedon and coworkers (1986) observed thepossible protective action of thiourea againstplatinum toxicity. Thiourea and other sulfur-containing nucleophiles have the ability tochelate and remove platinum from biochemical sites of toxicity.Oral administration of thiourea resultedin tumors in the liver and thyroid in rats.It is carcinogenic to animals and has shownsufficient evidence.????
Noncombustible solid. There is no report of any explosion resulting from reactions of thiourea. Small amounts of thiourea in contact with acrolein may polymerize acrolein, which is a highly exothermic reaction.???
Thiourea is a sulphur analogue of urea. It is a crystalline and colorless solid which is relatively insoluble in water. Thiourea, capable of breaking the dormancy of seeds, is used to stimulate seed germination. Seeds are soaked for less than 24 hours before planting.?? ?? ??
Thiourea is used as a cleaner agent for silver and cop- per, and as an antioxidant in diazo copy paper. It can induce (photo-) contact dermatitis.??? ??
Thiourea is used as rubber antiozonant, toning agent; corrosion inhibitor; and in pharmaceutical manufacture; in the manufacture of photosensitive papers; flame-retardant textile sizes; boiler water treatment. It is also used in photography; pesticide manufacture; in textile chemicals.Carcinogenicity
Thiourea is reasonably anticipated to be a human carcinogen based on sufficient evidence of carcinogenicity from studies in experimental animals.?? ??
UN2811 Toxic solids, organic, n.o.s., Hazard Class: 6.1; Labels: 6.1-Poisonous materials, Technical Name Required. UN3077 Environmentally hazardous substances, solid, n.o.s., Hazard class: 9; Labels: 9-Miscellaneous hazardous material, Technical Name Required.Purification Methods
Crystallise thiourea from absolute EtOH, MeOH, acetonitrile or water. Dry it under vacuum over H2SO4 at room temperature. [Beilstein 3 IV 342.]? ???
Dust may form explosive mixture with air. Reacts violently with acrolein, strong acids (nitric acid). Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides.??? ??
Consult with environmental regulatory agencies for guidance on acceptable disposal practices. Generators of waste containing this contaminant (≥100 kg/mo) must conform with EPA regulations governing storage, transportation, treatment, and waste disposal.???? ?? ?? ? ???
???
?? ??
2-???-5-??????
4-(4-CHLOROPHENYL)PYRIMIDINE-2-THIOL
1-???-2-????
2-AMINO-6-METHYL-PYRIMIDINE-4-THIOL
2-???-((1-????-1-?????)???)-4-???????
6-AMINO-2-METHYLTHIO-3-METHYLURACIL
4,6-Dimethyl-2-methylmercapyrimidine
2-???-4-??-5-??????
??2-???-4-??-1,3-???-5-???????
Ethyl 4-amino-2-(ethylthio)-5-pyrimidinecarboxylate
9,10-DIMETHYLANTHRACENE
4-AMINO-2-MERCAPTOPYRIMIDINE-5-CARBONITRILE
4,6-DIMETHYL-2-THIOPYRIMIDINE
??2-???-4-??-5-??????????
Oxfendazole
??????
ETHYL 2-(ETHYLTHIO)-4-HYDROXYPYRIMIDINE-5-CARBOXYLATE
??????????
??2-???-4-?????-5-???????
2-??????? ?
2-???-??-(??????)-4-?????? ?
2-Amino-5-methylthiazole
????????
?? 2-???-??-(????????)-4-???????
??2-???-4-??????????
2-???-2-???????
4-HYDROXY-6-MERCAPTOPYRAZOLO[3,4-D]PYRIMIDINE
4,6-DIAMINO-2-MERCAPTOPYRIMIDINE
??? ????????
N-??????
4-AMINO-2-(METHYLTHIO)-6-PYRIMIDINOL
4-Amino-6-hydroxy-2-mercaptopyrimidine monohydrate
???? ????
Prazosin
2-???-4-?????? ?
5-METHOXY-2-SULFANYL-4-PYRIMIDINOL
???????
2-thiouracil
n-???????
5-ETHYL-2-THIOURACIL
???? ?? ??
???( 640)?? ??
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???? ?? ??:
N,N'-??????? ?? ????-?? ????????? ??????? ??? ???????? N,N'-??????? 2-?????? ???????
Thiourea, N-[6-cyano-5-(trifluoromethyl)-3-pyridinyl]-
Thiourea, N-(2-aminoethyl)-N'-(5-bromo-6-quinoxalinyl)-
Thiophosgene
1-(2-Chlorophenyl)-2-thiourea
1-PHENYL-2-THIOUREA
N-METHYLTHIOUREA
4-METHYL-5-(TRIFLUOROMETHYL)-1,2,4-TRIAZOLIN-3(2H)-THIONE
1-BENZYL-3-METHYL-2-THIOUREA