Synonym
Anisoin; NSC-8504; NSC8504; NSC 8504;
IUPAC/Chemical Name
2-hydroxy-1,2-bis(4-methoxyphenyl)ethan-1-one
InChi Key
LRRQSCPPOIUNGX-UHFFFAOYSA-N
InChi Code
1S/C16H16O4/c1-19-13-7-3-11(4-8-13)15(17)16(18)12-5-9-14(20-2)10-6-12/h3-10,15,17H,1-2H3
SMILES Code
COC1=CC=C(C=C1)C(O)C(=O)C2=CC=C(OC)C=C2
Appearance
To be determined
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 -4 C for short term (days to weeks) or -20 C for long term(months to years).
Solubility
To be determined
Shelf Life
>2 years if stored properly
Drug Formulation
To be determined
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
Preparing Stock Solutions
The following data is based on the
product
molecular weight
272.30
Batch specific molecular weights may vary
from batch to batch
due to the degree of hydration, which will
affect the solvent
volumes required to prepare stock solutions.
Concentration / Solvent Volume / Mass |
1 mg |
5 mg |
10 mg |
1 mM |
1.15 mL |
5.76 mL |
11.51 mL |
5 mM |
0.23 mL |
1.15 mL |
2.3 mL |
10 mM |
0.12 mL |
0.58 mL |
1.15 mL |
50 mM |
0.02 mL |
0.12 mL |
0.23 mL |
1: Gatti R, Gioia MG. Anisoin: a useful pre-chromatographic derivatization fluorogenic reagent for LC analysis of guanidino compounds. J Pharm Biomed Anal. 2006 Sep 11;42(1):11-6. doi: 10.1016/j.jpba.2005.12.035. Epub 2006 Feb 3. PMID: 16460903.
2: González B, Olave I, Calderón I, Vicuña R. Degradation of diarylethane structures by Pseudomonas fluorescens biovar I. Arch Microbiol. 1988;149(5):389-94. doi: 10.1007/BF00425576. PMID: 3132905.
3: Jackson CA, Couger MB, Prabhakaran M, Ramachandriya KD, Canaan P, Fathepure BZ. Isolation and characterization of Rhizobium sp. strain YS-1r that degrades lignin in plant biomass. J Appl Microbiol. 2017 Apr;122(4):940-952. doi: 10.1111/jam.13401. Epub 2017 Feb 27. PMID: 28092137.
4: Gruseck R, Palatinszky M, Wagner M, Hofmann T, Zumstein M. Quantification of guanidine in environmental samples using benzoin derivatization and LC-MS analysis. MethodsX. 2024 Sep 24;13:102972. doi: 10.1016/j.mex.2024.102972. PMID: 39435044; PMCID: PMC11492725.
5: Gonzalez B, Merino A, Almeida M, Vicña R. Comparative growth of natural bacterial isolates on various lignin-related compounds. Appl Environ Microbiol. 1986 Dec;52(6):1428-32. doi: 10.1128/aem.52.6.1428-1432.1986. PMID: 16347250; PMCID: PMC239249.
6: Rhoads TL, Mikell AT Jr, Eley MH. Investigation of the lignin-degrading activity of Serratia marcescens: biochemical screening and ultrastructural evidence. Can J Microbiol. 1995 Jul;41(7):592-600. doi: 10.1139/m95-079. PMID: 7641141.
7: González B, Vicuña R. Benzaldehyde lyase, a novel thiamine PPi-requiring enzyme, from Pseudomonas fluorescens biovar I. J Bacteriol. 1989 May;171(5):2401-5. doi: 10.1128/jb.171.5.2401-2405.1989. PMID: 2496105; PMCID: PMC209914.
8: Vicuña R, Gonzalez B, Ruttimann C, Sapag A, Seelenfreund D. Biochemical and genetic studies of bacteria metabolizing lignin-related compounds. Arch Biol Med Exp. 1988 Jun;21(1):247-55. PMID: 3154864.
9: Sabbah DA, Ibrahim AH, Talib WH, Alqaisi KM, Sweidan K, Bardaweel SK, Sheikha GA, Zhong HA, Al-Shalabi E, Khalaf RA, Mubarak MS. Ligand-Based Drug Design: Synthesis and Biological Evaluation of Substituted Benzoin Derivatives as Potential Antitumor Agents. Med Chem. 2019;15(4):417-429. doi: 10.2174/1573406414666180912111846. PMID: 30207238.
10: TADROS W, EKLADIUS L. Preparation of deoxyanisoin and some stilbenes: reducing action of sodium glycollate in glycols. Nature. 1950 Sep 23;166(4221):525. doi: 10.1038/166525a0. PMID: 14780130.