| Identification | Back Directory | [Name]
DULCIN | [CAS]
150-69-6 | [Synonyms]
Sucrol
Valzin
DULCIN
Dulein
Dulcine
NSC 1839
D-DULCINE
Suesstoff
GLYCOSINE
NCI-C02073
AKOS B029772
PHENETYL UREA
P-PHENETYLUREA
p-Phenethylurea
Phenethylcarbamid
Phenetolcarbamide
4-Ureidophenetole
ETHOXYPHENYL UREA
Dulcin (sweetener)
p-Phenetolcarbamid
4-Ethoxyphenylurea
P-ETHOXYPHENYLUREA
p-Phenetolcarbamide
p-ethoxyphyenylurea
P-PHENETOLECARBAMIDE
(p-ethoxyphenyl)-ure
PARA-ETHOXYPHENYLUREA
p-Phenethyl carbamide
p-Ethoxyfenylmocovina
1-(4-Ethoxyphenyl)urea
N-(4-ETHOXYPHENYL)UREA
Urea, (4-ethoxyphenyl)-
Urea, (p-ethoxyphenyl)-
Urea,N-(4-ethoxyphenyl)-
p-Aethoxyphenylharnstoff
Dulcin=4-Ethoxyphenylurea
4-Ureidophenetole, 4-(Carbamoylamino)phenetole | [EINECS(EC#)]
205-767-7 | [Molecular Formula]
C9H12N2O2 | [MDL Number]
MFCD00025431 | [MOL File]
150-69-6.mol | [Molecular Weight]
180.2 |
| Chemical Properties | Back Directory | [Melting point ]
160-161℃ | [Boiling point ]
313.03°C (rough estimate) | [density ]
1.199 | [refractive index ]
1.5373 (estimate) | [storage temp. ]
0-6°C | [solubility ]
DMSO (Slightly), Methanol (Slightly) | [form ]
Solid | [color ]
White to Off-White | [Water Solubility ]
1.21g/L(21 ºC) | [λmax]
289nm(EtOH)(lit.) | [Merck ]
14,3464 | [LogP]
1.005 (est) | [CAS DataBase Reference]
150-69-6 | [IARC]
3 (Vol. 12, Sup 7) 1987 | [EPA Substance Registry System]
Dulcin (150-69-6) |
| Hazard Information | Back Directory | [Chemical Properties]
Off-White Solid | [Uses]
Dulcin is a non-nutritive sweetener. Dulcin is a sweet analgesic for use in medical procedures or treatments. | [Uses]
Non-nutritive sweetener. | [General Description]
White crystals. | [Air & Water Reactions]
Partially decomposes on heating in water; hydrolyzes in 0.1 N acetic acid. Slightly water soluble . | [Reactivity Profile]
DULCIN is an example of an amide. Amides react with azo and diazo compounds to generate toxic gases. Flammable gases are formed by the reaction of organic amides 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). | [Definition]
ChEBI:Dulcin is a member of ureas. | [Production Methods]
4-Ethoxyphenylurea, dulcin, is produced from the addition of potassium cyanate to p-phenetidine hydrochloride in aqueous solution at room temperature or from mixing urea and p-phenetidine hydrochloride to a mixture of hydrochloric acid and glacial acetic acid. |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [RTECS ]
YT2275000 | [Hazard Note ]
Irritant | [HS Code ]
2924190090 | [Safety Profile]
Human poison by
ingestion. Moderately toxic experimentally
by ingestion. Human systemic effects by
ingestion: somnolence, hallucinations,
distorted perceptions, and changes in motor
activity. In adults 20 to 40 g produces
dizziness, nausea, methemoglobinemia,
cyanosis, and hypotension. Questionable
carcinogen with experimental tumorigenic
data. When heated to decomposition it
emits toxic fumes of NOx. | [Hazardous Substances Data]
150-69-6(Hazardous Substances Data) |
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