MedKoo Cat#: 145819 | Name: Anisoin

Description:

WARNING: This product is for research use only, not for human or veterinary use.

Anisoin is a biochemical compound that belongs to the class of esters, typically synthesized from anisic acid (an aromatic compound) and alcohol. It has a characteristic fragrant, sweet aroma and is primarily used in the flavoring and fragrance industry.

Chemical Structure

Anisoin
Anisoin
CAS#119-52-8

Theoretical Analysis

MedKoo Cat#: 145819

Name: Anisoin

CAS#: 119-52-8

Chemical Formula: C16H16O4

Exact Mass: 272.1000

Molecular Weight: 272.30

Elemental Analysis: C, 70.58; H, 5.92; O, 23.50

Price and Availability

This product is currently not in stock but may be available through custom synthesis. To ensure cost efficiency, the minimum order quantity is 1 gram. The estimated lead time is 2 to 4 months, with pricing dependent on the complexity of the synthesis (typically high for intricate chemistries). Quotes for quantities below 1 gram will not be provided. To request a quote, please click the button below. Note: If this product becomes available in stock in the future, pricing will be listed accordingly.
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Related CAS #
No Data
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
More Info

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.

Recalculate based on batch purity %
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.