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[ CAS No. 18472-51-0 ] {[proInfo.proName]}

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Chemical Structure| 18472-51-0
Chemical Structure| 18472-51-0
Structure of 18472-51-0 * Storage: {[proInfo.prStorage]}
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Product Details of [ 18472-51-0 ]

CAS No. :18472-51-0 MDL No. :MFCD00083599
Formula : C34H54Cl2N10O14 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 897.76 Pubchem ID :-
Synonyms :
Chlorhexidine (digluconate)
Chemical Name :1,1'-Hexamethylenebis[5-(p-chlorophenyl)biguanide] (2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanoic acid(1:2)

Safety of [ 18472-51-0 ]

Signal Word:Danger Class:9
Precautionary Statements:P273-P280-P305+P351+P338+P310-P391-P501 UN#:3082
Hazard Statements:H318-H400-H411 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 18472-51-0 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 18472-51-0 ]

[ 18472-51-0 ] Synthesis Path-Downstream   1~9

  • 1
  • [ 3380-34-5 ]
  • [ 18472-51-0 ]
  • chlorohexidine triclosan complex [ No CAS ]
YieldReaction ConditionsOperation in experiment
Example 7. Preparation of Chlorohexidine <strong>[3380-34-5]Triclosan</strong> Complex (1 : 1)[0073] <strong>[3380-34-5]Triclosan</strong> (5.8g) was added to sodium hydroxide solution (5M, 4ml, 0.02mol), stirred and heated until a light yellow solution obtained. This solution was then added to chloro- hexidine digluconate solution (20%>, 45ml), mixed well and stirred. A white precipitate was formed, filtered, washed with water and air-dried. Weight: 1 l .lg (102%). 1H NMR (500MHz, d-DMSO) delta: 7.56(1H), 7.23(4H), 7.21(1H), 7.03(4H), 7.12 (1H), 6.88(1H), 6.64 (1H), 6.44 (1H), 3.08 (4H), 1.45 (4H), 1.28 (4H).
YieldReaction ConditionsOperation in experiment
With titanium(IV) oxide In water UV-irradiation;
  • 3
  • [ 18472-51-0 ]
  • [ 1638214-13-7 ]
YieldReaction ConditionsOperation in experiment
With Sodium tripolyphosphate In water at 20℃; 3 Examp1es 1-6 ; C.omparative Examp1es 1-3 : Elution of CHX from functionalised borosilicate glass surfaces General procedure: Chlorhexidine based salts were prepared by combining, at room temperature and under rapid stirring, 100 mLchlorhexidine (as the digluconate salt in aqueous solution at a concentration of 10 mM) and 100 mL of one of a range of anions in aqueous solution, also at an initial concentration of 10 mM, to effect final total concentrations of 5 mM of each. The anions used are shown in Table 1. Table 1 The precipitate was then allowed to adhere on borosilicate glass coverslips .
  • 4
  • [ 18472-51-0 ]
  • [ 1638214-12-6 ]
YieldReaction ConditionsOperation in experiment
With sodium pyrophosphate In water at 20℃; 2 Examp1es 1-6 ; C.omparative Examp1es 1-3 : Elution of CHX from functionalised borosilicate glass surfaces General procedure: Chlorhexidine based salts were prepared by combining, at room temperature and under rapid stirring, 100 mLchlorhexidine (as the digluconate salt in aqueous solution at a concentration of 10 mM) and 100 mL of one of a range of anions in aqueous solution, also at an initial concentration of 10 mM, to effect final total concentrations of 5 mM of each. The anions used are shown in Table 1. Table 1 The precipitate was then allowed to adhere on borosilicate glass coverslips .
  • 5
  • [ 18472-51-0 ]
  • [ 72099-49-1 ]
YieldReaction ConditionsOperation in experiment
With calcium(II) nitrate tetrahydrate In water at 20℃; 6 Examp1es 1-6 ; C.omparative Examp1es 1-3 : Elution of CHX from functionalised borosilicate glass surfaces General procedure: Chlorhexidine based salts were prepared by combining, at room temperature and under rapid stirring, 100 mLchlorhexidine (as the digluconate salt in aqueous solution at a concentration of 10 mM) and 100 mL of one of a range of anions in aqueous solution, also at an initial concentration of 10 mM, to effect final total concentrations of 5 mM of each. The anions used are shown in Table 1. Table 1 The precipitate was then allowed to adhere on borosilicate glass coverslips .
  • 6
  • [ 18472-51-0 ]
  • [ 954118-20-8 ]
YieldReaction ConditionsOperation in experiment
With calcium carbonate In water at 20℃; 5 Examp1es 1-6 ; C.omparative Examp1es 1-3 : Elution of CHX from functionalised borosilicate glass surfaces General procedure: Chlorhexidine based salts were prepared by combining, at room temperature and under rapid stirring, 100 mLchlorhexidine (as the digluconate salt in aqueous solution at a concentration of 10 mM) and 100 mL of one of a range of anions in aqueous solution, also at an initial concentration of 10 mM, to effect final total concentrations of 5 mM of each. The anions used are shown in Table 1. Table 1 The precipitate was then allowed to adhere on borosilicate glass coverslips .
  • 7
  • [ 18472-51-0 ]
  • [ 95774-24-6 ]
YieldReaction ConditionsOperation in experiment
With disodium hydrogenphosphate In water at 20℃; 1 Examp1es 1-6 ; C.omparative Examp1es 1-3 : Elution of CHX from functionalised borosilicate glass surfaces General procedure: Chlorhexidine based salts were prepared by combining, at room temperature and under rapid stirring, 100 mLchlorhexidine (as the digluconate salt in aqueous solution at a concentration of 10 mM) and 100 mL of one of a range of anions in aqueous solution, also at an initial concentration of 10 mM, to effect final total concentrations of 5 mM of each. The anions used are shown in Table 1. Table 1 The precipitate was then allowed to adhere on borosilicate glass coverslips .
  • 8
  • [ 18472-51-0 ]
  • [ 1638214-14-8 ]
YieldReaction ConditionsOperation in experiment
With sodium hexametaphosphate In water at 20℃; 4 Examp1es 1-6 ; C.omparative Examp1es 1-3 : Elution of CHX from functionalised borosilicate glass surfaces General procedure: Chlorhexidine based salts were prepared by combining, at room temperature and under rapid stirring, 100 mLchlorhexidine (as the digluconate salt in aqueous solution at a concentration of 10 mM) and 100 mL of one of a range of anions in aqueous solution, also at an initial concentration of 10 mM, to effect final total concentrations of 5 mM of each. The anions used are shown in Table 1. Table 1 The precipitate was then allowed to adhere on borosilicate glass coverslips .
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Similar Product of
[ 18472-51-0 ]

Chemical Structure| 55-56-1

A814733[ 55-56-1 ]

1,1'-Hexamethylenebis[5-(p-chlorophenyl)biguanide]

Reason: Free-salt