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1. Bardac 22
2. Deciquam 222
3. Didecyldimethylammonium
4. Didecyldimethylammonium Bromide
1. 7173-51-5
2. Didecyl Dimethyl Ammonium Chloride
3. N-decyl-n,n-dimethyldecan-1-aminium Chloride
4. Ddac
5. Quaternium 12
6. Quaternium-12
7. Arquad 10
8. Bardac 22
9. Didecyl(dimethyl)azanium;chloride
10. Bardac 2250
11. 1-decanaminium, N-decyl-n,n-dimethyl-, Chloride
12. Didecyl Dimethylammonium Chloride
13. N-decyl-n,n-dimethyl-1-decanaminium Chloride
14. Didecyldimonium Chloride
15. Jxn40o9y9b
16. Chebi:79935
17. Astop
18. Didecyl Dimethyl Ammonium Chloride, 80% Aqueous Solution
19. 1-decanaminium, N-decyl-n,n-dimethyl-, Chloride (1:1)
20. Britewood Q
21. Dimethyldidecylammonium Chloride
22. Bio-dac
23. N-decyl-n,n-dimethyldecan-1-aminium (chloride)
24. Odex Q
25. Quartamin D 10e
26. Quartamin D 10p
27. Nissan Cation 2db
28. Timbercote 2000
29. Slaoff 91
30. Aliquat 203
31. Querton 210cl
32. Dodigen 1881
33. Bardac 2270e
34. Calgon H 130
35. Caswell No. 331a
36. Maquat 4480e
37. Acticide
38. Bardac 2280
39. Sporekill
40. Kleengrow
41. H 130 (molluscicide)
42. Arquad 210-50
43. Bio-dac 50-22
44. Britewood Xl
45. Acticide Ddq
46. Catiogen Ddm
47. Tret-o-lite Xc 507
48. Cation Ddc
49. Catiogen Ddm-pg
50. Asepas 3
51. Didecyldimethylammoniumchloride
52. Septapav Khs 70
53. Acticide Ddq 40
54. Microbiocide B 74
55. Btc 99
56. Ddc 80
57. Stenquat 1010
58. Arquad 210
59. Cation Ddc 50
60. Cation Ddc-80
61. Macrotrol Mt 200
62. Microbiocide N 750
63. Btco 1010
64. New Des 50
65. Bardac 2240
66. Kamin Rm 2d50a
67. D 10p
68. K-sanit Bp 80
69. Btc 1010
70. Arquad 210-50e
71. Arquad 210-80e
72. Arquad 210-85e
73. Fentacare 1021-80
74. Ammonium, Didecyldimethyl-, Chloride
75. Einecs 230-525-2
76. Arquad 210-80
77. Nissan Cation 2db500e
78. Nissan Cation 2db800e
79. Unii-jxn40o9y9b
80. Epa Pesticide Chemical Code 069149
81. Dairyland Brand Chg Teat Dip
82. Didecyldimethylammounium Chloride
83. Didecyl(dimethyl)azanium Chloride
84. Hsdb 7611
85. 2db500e
86. Didecyl(dimethyl)ammonium Chloride
87. Btc 2250
88. Aq 210
89. Bardac-22
90. Alfa Bergamon (tn)
91. Calgon H130
92. Querton 2100l
93. Didecyl(dimethyl)ammonium
94. H 130
95. Ec 230-525-2
96. Dsstox_cid_12537
97. Dsstox_rid_78974
98. Dsstox_gsid_32537
99. M 21080
100. N,n-didecyl-n,n-dimethylammonium Chloride
101. Schembl20265
102. Maquat 4450-e
103. Chembl224987
104. Dicapryldimonium Chloride
105. Dtxsid9032537
106. Tox21_300598
107. Didecyldimethylammonium Chlorid
108. Mfcd00066262
109. Akos015901447
110. Cs-w022921
111. Didecyldimonium Chloride [inci]
112. Hy-w042181
113. Didecyldimethyl Ammonium Chloride
114. Ncgc00254240-01
115. Da-17489
116. Cas-7173-51-5
117. N-decyl-n,n-dimethyldecan-1-aminiumchloride
118. Didecyldimethylammonium Chloride [mi]
119. Ft-0629457
120. N-decyl-n,n-dimethyl 1-decanaminium Chloride
121. 1-decanaminium,n-decyl-n,n-dimethyl-,chloride
122. D07822
123. Didecyldimethylammonium Chlorid [who-dd]
124. Didecyldimethylammonium Chloride [mart.]
125. N-decyl-n,n-dimethyldecan-1-ammonium Chloride
126. Didecyl Dimethyl Ammonium Chloride [hsdb]
127. A837307
128. Q418930
129. Didecyldimethylammonium Chloride, Analytical Standard
130. W-104509
131. Didecyldimethylammonium Chloride 100 Microg/ml In Acetonitrile
| Molecular Weight | 362.1 g/mol |
|---|---|
| Molecular Formula | C22H48ClN |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 18 |
| Exact Mass | 361.3475282 g/mol |
| Monoisotopic Mass | 361.3475282 g/mol |
| Topological Polar Surface Area | 0 Ų |
| Heavy Atom Count | 24 |
| Formal Charge | 0 |
| Complexity | 200 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 2 |
EXPL THER A double blind trial with 2 concentrations of the combination didecyl dimethyl ammonium chloride (Hoe S-2922, Bardac-22) with prednicarbate for the treatment of impetiginized eczema in 30 hospitalized patients is described. The study did not reveal any significant differences in effectiveness, although a trend in favor of the higher concentration was apparent.
Wolbling RH, Schafer V; Arzneim. Forsch.; 37 (2): 218-220 (1987)
D - Dermatologicals
D08 - Antiseptics and disinfectants
D08A - Antiseptics and disinfectants
D08AJ - Quaternary ammonium compounds
D08AJ06 - Didecyldimethylammonium chloride
DDAC (40% aqueous in both radiolabled (14C) and nonradiolabled form), used in a definitive pharmacokinetic study to determine absorption, distribution and excretion and was administered orally (single dose), by gavage, to Charles River CD Rats (Crl CD(SD)Br--5/sex/group) in 3 dose regimens: 1) A single low dose (5 mg/kg), 2) a repeated low dose in diet containing 34 ppm "cold" in the feed daily for 14 days, followed by a 5 mg/kg dose of (14C)]-DDCA (9.01 mCi/mmole, and 99% radiochemical purity) or 3) a single high dose of 50 mg/kg. Excretion of radioactivity was shown to occur primarily in the feces (89-99%), some in urine (<2.5%), and an insignificant amount was expired. Highly ionic DDAC is not readily absorbed from the GI tract...
California Environmental Protection Agency/Department of Pesticide Regulation; Toxicology Data Review Summaries: on Didecyldimethylammoniumchlorid. Available from, as of July 4, 2008: https://www.cdpr.ca.gov/docs/risk/toxsums/toxsumlist.htm
DDAC (40% aqueous in both radiolabled (14C) and nonradiolabled form), used in a definitive pharmacokinetic study to determine absorption, distribution and excretion and was administered orally (single dose), by gavage, to Charles River CD (Crl CD(SD)Br--5/sex/group) ... . In the addendum the metabolic profile was determined in a 2 step experiment. First, another group of rats (10 male Charles River CD (Crl CD(SD)Br) were treated with (14C)-DDAC at 50 mg/kg in order to obtain enough (14C) residues to use as standards. The (14C) metabolites were characterized by TLC, HPLC and MS. The second part of the experiment involved using the "standard" metabolic profiles to analyze the metabolites from feces samples obtained in the initial study. It was shown that metabolism tends to be sex specific. Females metabolize the parent compound more so than males. Metabolism, which may be microbial in nature, involved the oxidation of the 2 decyl side chains to form hydroxy and hydroxyketo derivatives. Modification of methyl substituents was not evident.
California Environmental Protection Agency/Department of Pesticide Regulation; Toxicology Data Review Summaries. Available from: https://www.cdpr.ca.gov/docs/risk/toxsums/toxsumlist.htm on Didecyldimethylammoniumchloride as of July 4, 2008.
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