Jalaric acid

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

MedKoo CAT#: 596100

CAS#: 24205-55-8

Description: Jalaric acid is a bioactive chemical.

Chemical Structure

Jalaric acid
CAS# 24205-55-8

Theoretical Analysis

MedKoo Cat#: 596100
Name: Jalaric acid
CAS#: 24205-55-8
Chemical Formula:
Exact Mass:
Molecular Weight:
Elemental Analysis:

Price and Availability

This product is not in stock, which may be available by custom synthesis. For cost-effective reason, minimum order is 1g (price is usually high, lead time is 2~3 months, depending on the technical challenge). Quote less than 1g will not be provided. To request quote, please email to sales @medkoo.com or click below button.
Note: Price will be listed if it is available in the future.

Request quote for custom synthesis

Synonym: Jalaric acid;

IUPAC/Chemical Name: (3S,3aS,4S,7R,8S,8aS)-3-formyl-4-hydroxy-8-(hydroxymethyl)-8-methyl-2,3,4,7,8,8a-hexahydro-1H-3a,7-methanoazulene-6-carboxylic acid


InChi Code: InChI=1S/C15H20O5/c1-14(7-17)10-5-15(8(6-16)2-3-11(14)15)12(18)4-9(10)13(19)20/h4,6,8,10-12,17-18H,2-3,5,7H2,1H3,(H,19,20)/t8-,10+,11+,12+,14-,15-/m1/s1

SMILES Code: O=C(C1=C[C@H](O)[C@]23[C@@H](C=O)CC[C@@]2([H])[C@](C)(CO)[C@@]1([H])C3)O

Appearance: Solid powder

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: Soluble in DMSO

Shelf Life: >2 years if stored properly

Drug Formulation: This drug may be formulated in DMSO

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 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

Molarity Calculator

Calculate the mass, volume, or concentration required for a solution.

*When preparing stock solutions always use the batch-specific molecular weight of the product found on the vial label and SDS / CoA (available online).

Reconstitution Calculator

The reconstitution calculator allows you to quickly calculate the volume of a reagent to reconstitute your vial. Simply enter the mass of reagent and the target concentration and the calculator will determine the rest.


Dilution Calculator

Calculate the dilution required to prepare a stock solution.

1: Roth T, Beer B, Pick A, Sieber V. Thermostabilization of the uronate dehydrogenase from Agrobacterium tumefaciens by semi-rational design. AMB Express. 2017 Dec;7(1):103. doi: 10.1186/s13568-017-0405-2. Epub 2017 May 23. PubMed PMID: 28545260; PubMed Central PMCID: PMC5442039.

2: Enomoto-Rogers Y, Masaki H, Ito T, Furihata K, Iwata T. Conformation analysis of d-glucaric acid in deuterium oxide by NMR based on its JHH and JCH coupling constants. Magn Reson Chem. 2016 Jul;54(7):561-7. doi: 10.1002/mrc.4396. Epub 2016 Jan 8. PubMed PMID: 26749401.

3: Mehtiö T, Toivari M, Wiebe MG, Harlin A, Penttilä M, Koivula A. Production and applications of carbohydrate-derived sugar acids as generic biobased chemicals. Crit Rev Biotechnol. 2016 Oct;36(5):904-16. doi: 10.3109/07388551.2015.1060189. Epub 2015 Jul 15. Review. PubMed PMID: 26177333.

4: Pick A, Schmid J, Sieber V. Characterization of uronate dehydrogenases catalysing the initial step in an oxidative pathway. Microb Biotechnol. 2015 Jul;8(4):633-43. doi: 10.1111/1751-7915.12265. Epub 2015 Apr 17. PubMed PMID: 25884328; PubMed Central PMCID: PMC4476818.

5: Martin AA, Tomasini M, Kholodovych V, Gu L, Sommerfeld SD, Uhrich KE, Murthy NS, Welsh WJ, Moghe PV. Carbohydrate-derived amphiphilic macromolecules: a biophysical structural characterization and analysis of binding behaviors to model membranes. J Funct Biomater. 2015 Apr 8;6(2):171-91. doi: 10.3390/jfb6020171. PubMed PMID: 25855953; PubMed Central PMCID: PMC4493506.

6: Mehtiö T, Nurmi L, Rämö V, Mikkonen H, Harlin A. Synthesis and characterization of copolyanhydrides of carbohydrate-based galactaric acid and adipic acid. Carbohydr Res. 2015 Jan 30;402:102-10. doi: 10.1016/j.carres.2014.07.009. Epub 2014 Jul 19. PubMed PMID: 25497340.

7: Mangiameli MF, González JC, Bellú S, Bertoni F, Sala LF. Redox and complexation chemistry of the CrVI/CrV-D-glucaric acid system. Dalton Trans. 2014 Jun 28;43(24):9242-54. doi: 10.1039/c4dt00717d. PubMed PMID: 24816781.

8: van der Klis F, Frissen AE, van Haveren J, van Es DS. Waste not, want not: mild and selective catalytic oxidation of uronic acids. ChemSusChem. 2013 Sep;6(9):1640-5. doi: 10.1002/cssc.201300367. Epub 2013 Aug 12. PubMed PMID: 23940072.

9: Ruiz A, Mardones C, Vergara C, Hermosín-Gutiérrez I, von Baer D, Hinrichsen P, Rodriguez R, Arribillaga D, Dominguez E. Analysis of hydroxycinnamic acids derivatives in calafate (Berberis microphylla G. Forst) berries by liquid chromatography with photodiode array and mass spectrometry detection. J Chromatogr A. 2013 Mar 15;1281:38-45. doi: 10.1016/j.chroma.2013.01.059. Epub 2013 Jan 23. PubMed PMID: 23398997.

10: Callahan DL, Roessner U, Dumontet V, Perrier N, Wedd AG, O'Hair RA, Baker AJ, Kolev SD. LC-MS and GC-MS metabolite profiling of nickel(II) complexes in the latex of the nickel-hyperaccumulating tree Sebertia acuminata and identification of methylated aldaric acid as a new nickel(II) ligand. Phytochemistry. 2008 Jan;69(1):240-51. Epub 2007 Sep 4. PubMed PMID: 17765935.

11: Denton TT, Joyce AS, Kiely DE. Preparation of N-alkylbis(3-aminopropyl)amines by the catalytic hydrogenation of N-alkylbis(cyanoethyl)amines. J Org Chem. 2007 Jun 22;72(13):4997-5000. Epub 2007 May 31. PubMed PMID: 17536864.

12: Dornyei A, Garribba E, Jakusch T, Forgo P, Micera G, Kiss T. Vanadium(IV,V) complexes of D-saccharic and mucic acids in aqueous solution. Dalton Trans. 2004 Jun 21;(12):1882-91. Epub 2004 May 25. PubMed PMID: 15381996.

13: Gonzalez JC, Daier V, Garcia S, Goodman BA, Atria AM, Sala LF, Signorella S. Redox and complexation chemistry of the Cr(VI)/Cr(V)-D-galacturonic acid system. Dalton Trans. 2004 Aug 7;(15):2288-96. Epub 2004 Jun 24. PubMed PMID: 15278120.

14: Libkind D, Brizzio S, van Broock M. Rhodotorula mucilaginosa, a carotenoid producing yeast strain from a Patagonian high-altitude lake. Folia Microbiol (Praha). 2004;49(1):19-25. PubMed PMID: 15143736.

15: Ono H, Kuwahara Y, Nishida R. Hydroxybenzoic acid derivatives in a nonhost rutaceous plant, Orixajaponica, deter both oviposition and larval feeding in a rutaceae-feeding swallowtail butterfly, Papilio xuthus L. J Chem Ecol. 2004 Feb;30(2):287-301. PubMed PMID: 15112725.

16: Lakatos A, Bertani R, Kiss T, Venzo A, Casarin M, Benetollo F, Ganis P, Favretto D; Solution and Solid-State Study. AlIII ion complexes of saccharic acid and mucic acid: a solution and solid-state study. Chemistry. 2004 Mar 5;10(5):1281-90. PubMed PMID: 15007818.

17: Takenaka M, Yan X, Ono H, Yoshida M, Nagata T, Nakanishi T. Caffeic acid derivatives in the roots of yacon (Smallanthus sonchifolius). J Agric Food Chem. 2003 Jan 29;51(3):793-6. PubMed PMID: 12537459.

18: Fonseca A. Utilization of tartaric acid and related compounds by yeasts: taxonomic implications. Can J Microbiol. 1992 Dec;38(12):1242-51. PubMed PMID: 1288842.

19: Wang J, Taha Z. Catalytic oxidation and flow detection of carbohydrates at ruthenium dioxide modified electrodes. Anal Chem. 1990 Jul 15;62(14):1413-6. PubMed PMID: 2382839.

20: Elliger CA, Wong Y, Chan BG, Waiss AC Jr. Growth inhibitors in tomato (Lycopersicon) to tomato fruitworm (Heliothis zea). J Chem Ecol. 1981 Jul;7(4):753-8. doi: 10.1007/BF00990307. PubMed PMID: 24420689.