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amicarbalide

Product Name
amicarbalide
CAS No.
3459-96-9
Chemical Name
amicarbalide
Synonyms
M&B 5062 A;amicarbalide;3,3'-Diamidinocarbanilide;3,3'-Ureylenebisbenzamidine;1,3-bis(3-amidinophenyl)urea;1,3-bis(3-carbamimidoylphenyl)urea;3,3'-carbonylbis(azanediyl)dibenzimidamide;3,3'-Carbonyldiiminobis(benzenecarboxamidine);3,3'-(Carbonyldiimino)bis(benzenecarbimidamide);Benzenecarboximidamide, 3,3'-(carbonyldiimino)bis-
CBNumber
CB9934450
Molecular Formula
C15H16N6O
Formula Weight
296.332
MOL File
3459-96-9.mol
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amicarbalide Property

Density 
1.40
pka
13.69±0.70(Predicted)
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

AK Scientific
Product number
X1078
Product name
Amicarbalide
Packaging
25mg
Price
$594
Updated
2021/12/16
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amicarbalide Chemical Properties,Usage,Production

Originator

Diampron,May and Baker

Manufacturing Process

m-Aminobenzonitrile (50 g) in anhydrous pyridine (200 ml) was treated with a solution of phosgene (15 ml) in anhydrous toluene (100 ml) over 10 min with mechanical stirring. The red solution was heated for 0.5 hour on the steam bath, cooled, and added to water (2 litres). The pale grey precipitate was filtered off, washed with ether, and crystallised from methanol (250 ml). N,N1- Di(m-cyanophenyl)urea separated as grey prisms, melting point 205-206°C.
A suspension of N,N1-di(m-cyanophenyl)urea (42 g) in anhydrous chloroform (420 ml), containing anhydrous ethanol (70 ml), was saturated with anhydrous hydrogen chloride at 0-5°C. After setting aside for 2 hours, a clear solution was obtained, which began to crystallise. After a week, the crystals were filtered off, washed well with anhydrous ether, and dried over calcium chloride. The iminoether hydrochloride so obtained (72 g) was added to saturated anhydrous ethanolic ammonia (720 ml), and the suspension heated at 55-60°C for 6 hours. After cooling to 20°C the crystals were filtered off, and recrystallized from 2 N hydrochloric add (300 ml). 3,31- Diamidinodiphenylurea dihydrochloride monohydrate separated as white prisms, melting point 286°C (decomp.).
In practice it is usually used as isethonate salt.

Therapeutic Function

Antiprotozoal

amicarbalide Preparation Products And Raw materials

Raw materials

Preparation Products

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amicarbalide Suppliers

Alfa Chemistry
Tel
1-516-6625404
Fax
1-516-927-0118
Email
support@alfa-chemistry.com
Country
United States
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9171
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TargetMol Chemicals Inc.
Tel
+1-781-999-5354 +1-00000000000
Email
marketing@targetmol.com
Country
United States
ProdList
32161
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TargetMol Chemicals Inc.
Tel
+8613564774135
Email
zijue.cai@tsbiochem.com
Country
United States
ProdList
19885
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58
Waterstone Technology, LLC
Tel
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Email
sales@waterstonetech.com
Country
United States
ProdList
6786
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3459-96-9, amicarbalideRelated Search:


  • amicarbalide
  • 3,3'-(Carbonyldiimino)bis(benzenecarbimidamide)
  • 3,3'-Carbonyldiiminobis(benzenecarboxamidine)
  • 3,3'-Ureylenebisbenzamidine
  • M&B 5062 A
  • 1,3-bis(3-amidinophenyl)urea
  • 1,3-bis(3-carbamimidoylphenyl)urea
  • 3,3'-Diamidinocarbanilide
  • 3,3'-carbonylbis(azanediyl)dibenzimidamide
  • Benzenecarboximidamide, 3,3'-(carbonyldiimino)bis-
  • 3459-96-9
  • C15H16N6O