1-Docosanol-d45

CAS: 661-19-8

Ref. TR-D678857

Product Information

• Name: 1-Docosanol-d45
• Synonyms: 1-Docosonol-d45, Abreva-d45, Behenic-d45 Alcohol, Behenyl-d45 80 Alcohol, Behenyl-d45 Alc. 80, Behenyl-d45 Alcohol, Conol-d45 2265, Conol-d45 2280, Docosanol-d45, Docosyl-d45 Alcohol, Hainol-d45 22S, IK-d45 2, IK 2-d45 (alcohol), Kalcohl-d45 220, Kalcohl-d45 22080, Kalcol-d45 22080, Lanette-d45 22, NAA-d45 422, NSC-d45 8407, Nacol-d45 22-97, Nacol-d45 22-98, Nacol-d45 C 22, Stenol-d45 1822, Stenol-d45 1822A, Tadenan-d45, Toho-d45 BH 65, n-Docosanol-d45, 1-Docosonol, Abreva, Behenic Alcohol, Behenyl 80 Alcohol, Behenyl alc. 80, Behenyl alcohol, Behenyl alcohol 65, Conol 2265, Conol 2280, Docosan-1-ol, Docosane-1-Ol, Docosanol, Docosyl alcohol, Ginol 22, Hainol 22 S, Hainol 22S, IK 2 (alcohol), Ik 2, Kalcohl 220, Kalcohl 22080, Kalcol 22080, Kalkol 220-80, Lanette 22, Naa 422, Nacol 22-97, Nacol 22-98, Nacol C 22, Nikkol Behenyl Alcohol 65, Nikkol Behenyl Alcohol 80, Nsc 8407, Ranette 22, Stenol 1822, Stenol 1822A, Tadenan, Toho BH 65, n-Docosanol
• CAS: 661-19-8

Description

Applications 1-Docosanol-d45 is the labelled form of 1-Docosanol (D678855). 1-Docosanol works as a surfactant in cosmetics. 1-Docosanol cream has also been approved by the US Food and Drug Administration as a safe and effective topical treatment for herpes labialis.
References Noweck, K., et al.: Ullmann's Encyclopedia of Industrial Chemistry (2006); McKeough, M., et al.: Arch. Dermatol., 137, 1153 (2001)

• Brand: TRC

Chemical properties

• Molecular weight: 371.88
• Formula: C₂₂HD₄₅O
• Color/Form: Neat
• InChI: InChI=1S/C22H46O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23/h23H,2-22H2,1H3/i1D3,2D2,3D2,4D2,5D2,6D2,7D2,8D2,9D2,10D2,11D2,12D2,13D2,14D2,15D2,16D2,17D2,18D2,19D2,20D2,21D2,22D2
• InChI key: InChIKey=NOPFSRXAKWQILS-DXXJCQCKSA-N
• SMILES: [2H]C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])O