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N,N'-???????

N,N'-???????
N,N'-??????? ??? ???
?? ??:
102-08-9
???:
N,N'-???????
???(??):
N,N'-???????;?????????
???:
1,3-Diphenyl-2-thiourea
???(??):
1,3-DIPHENYLTHIOUREA;DPTU;DFT;Diphenylthiourea;N,N'-Diphenylthiourea;N,N'-Diphenylthiourea;Activit;noccelerc;N,N´Anchoracel
CBNumber:
CB9324569
???:
C13H12N2S
??? ??:
228.31
MOL ??:
102-08-9.mol
MSDS ??:
SDS

N,N'-??????? ??

???
152-155 °C(lit.)
?? ?
50℃
??
1.32
?? ??
400kg/m3
???
0.001Pa at 25℃
???
1.5700 (estimate)
?? ??
Store below +30°C.
?? ?? (pKa)
12.68±0.70(Predicted)
??? ??
??? ??
??
???? ?? ???
???
19&C?? <0.01g/100mL
Merck
14,3333
BRN
644277
???
????. ?? ??. ?? ???? ???? ????.
InChI
1S/C13H12N2S/c16-13(14-11-7-3-1-4-8-11)15-12-9-5-2-6-10-12/h1-10H,(H2,14,15,16)
InChIKey
FCSHMCFRCYZTRQ-UHFFFAOYSA-N
SMILES
S=C(Nc1ccccc1)Nc2ccccc2
LogP
3.6
CAS ??????
102-08-9(CAS DataBase Reference)
NIST
Thiourea, n,n'-diphenyl-(102-08-9)
EPA
Diphenylthiourea (102-08-9)
??
  • ?? ? ?? ??
  • ?? ? ???? ?? (GHS)
??? ?? T
?? ???? ?? 25
????? 36/37/39-45-24/25
????(UN No.) UN 2811 6.1/PG 2
WGK ?? 3
RTECS ?? FE1225000
TSCA TSCA listed
?? ?? 6.1
???? II
HS ?? 29309070
???? ??? 11 - Combustible Solids
Hazard Classifications Aquatic Chronic 2
Repr. 2
Skin Sens. 1
STOT RE 2
?? ?? ??? 102-08-9(Hazardous Substances Data)
?? MLD orally in rabbits: 1.5 g/kg (Hanzlik, Irvine)
???? ?? KE-12102
????(GHS): Exclamation Mark (GHS07)Health Hazard (GHS08)Environment (GHS09)
?? ?: Warning
??·?? ??:
?? ??·?? ?? ?? ?? ?? ?? ? ?? ?? P- ??
H317 ????? ?? ??? ??? ? ?? ?? ??? ?? ?? 1 ?? P261, P272, P280, P302+P352,P333+P313, P321, P363, P501
H373 ??? ?? ?? ???? ??(??, ??? ?? ??? ?? ??? ??)? ??? ??? ? ?? ?? ???? ?? - ?? ?? ?? 2 ?? P260, P314, P501
H411 ??? ??? ?? ????? ??? ?? ????? ?? - ?? ?? 2
??????:
P201 ?? ? ?? ???? ?????.
P202 ?? ?? ?? ??? ?? ???? ??? ???? ???.
P273 ???? ???? ???.
P280 ????/???/???/?????? ?????.
P302+P352 ??? ??? ??? ?? ????.
P308+P313 ?? ?? ??? ???? ???? ??· ??? ????.
NFPA 704
1
3 0

N,N'-??????? MSDS


1,3-Diphenyl-2-thiourea

N,N'-??????? C??? ??, ??, ??

??

Diphenylthiourea is a rubber chemical used as an accelerator and stabilizer in neopren.

??? ??

white powder

??

Vulcanizing accelerator; sulfur dyes.

?? ??

White to off-white powder.

??? ?? ??

Insoluble in water.

?? ???

An organosulfide amide. Organosulfides are incompatible with acids, diazo and azo compounds, halocarbons, isocyanates, aldehydes, alkali metals, nitrides, hydrides, and other strong reducing agents. Reactions with these materials generate heat and in many cases hydrogen gas. Many of these compounds may liberate hydrogen sulfide upon decomposition or reaction with an acid. Organic amides/imides react with azo and diazo compounds to generate toxic gases. Flammable gases are formed by the reaction of organic amides/imides with strong reducing agents. Amides are very weak bases (weaker than water). Imides are less basic yet and in fact react with strong bases to form salts. That is, they can react as acids. Mixing amides with dehydrating agents such as P2O5 or SOCl2 generates the corresponding nitrile. The combustion of these compounds generates mixed oxides of nitrogen (NOx).

????

ACUTE/CHRONIC HAZARDS: When heated to decomposition 1,3-Diphenyl-2-thiourea emits highly toxic fumes.

????

Flash point data for 1,3-Diphenyl-2-thiourea are not available. 1,3-Diphenyl-2-thiourea is probably combustible.

?? ??

Thiocarbanilide (diphenyl thiourea) is a crystalline compound, only marginally soluble in water. In solution, it can assume a tautomeric form, typical of thiocarbanilide.
The first tautomer has acidic characteristics. The hydrogen can easily react with cations from the mineral surface and therefore can act as a collector. The second form (II) does not have collecting properties. Thiocarbanilide is a very effective and selective collector for galena. Diphenylthiocarbazide (C6H5–NH–NH)2–C=S. This collector also appears in two forms; in the active form the hydrogen is connected to sulfur. This reagent can be both anionic and cationic. This collector can be utilized for flotation of nickel and cobalt minerals after treatment of the pulp with copper sulfate.

?? ?? ??

It is a rubber chemical used as an accelerator and stabilizing agent in neoprene

Safety Profile

Moderately toxic by ingestion and intraperitoneal routes. Experimental reproductive effects. When heated to decomposition it emits highly toxic fumes of SOx, and NOx,.

Purification Methods

Crystallise the thiourea from boiling EtOH by adding hot water and allowing to cool. [Beilstein 12 H 394, 12 IV 810.]

N,N'-??????? ?? ?? ? ???

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N,N'-??????? ?? ??

???( 360)?? ??
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