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Docosahexaenoic Acid 1,2,3,4-13C

CAS No.
Chemical Name:
Docosahexaenoic Acid 1,2,3,4-13C
Synonyms
Docosahexaenoic Acid 1,2,3,4-13C
CBNumber:
CB615462127
Molecular Formula:
Molecular Weight:
0
MDL Number:
MOL File:
Mol file
Last updated:2025-08-21 11:10:20

Docosahexaenoic Acid 1,2,3,4-13C Properties

solubility Ethanol: 2 mg/ml

Docosahexaenoic Acid 1,2,3,4-13C price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 31104 Docosahexaenoic Acid 1,2,3,4-13C ≥95% 25μg $72 2026-04-30 Buy
Cayman Chemical 31104 Docosahexaenoic Acid 1,2,3,4-13C ≥95% 50μg $128 2026-04-30 Buy
Cayman Chemical 31104 Docosahexaenoic Acid 1,2,3,4-13C ≥95% 100μg $240 2026-04-30 Buy
Cayman Chemical 31104 Docosahexaenoic Acid 1,2,3,4-13C ≥95% 250μg $560 2026-04-30 Buy
Product number Packaging Price Buy
31104 25μg $72 Buy
31104 50μg $128 Buy
31104 100μg $240 Buy
31104 250μg $560 Buy

Docosahexaenoic Acid 1,2,3,4-13C Chemical Properties, Uses, Production

Description

Docosahexaenoic acid 1,2,3,4-13C (DHA 1,2,3,4-13C) is intended for use as an internal standard for the quantification of DHA (Item Nos. 90310 | 17950) by GC- or LC-MS. DHA is a long-chain ω-3 polyunsaturated fatty acid (PUFA) found in fish and algal oils.1 It comprises approximately 40% of total brain PUFAs and is abundant in grey matter and retinal membranes.2 DHA typically represents 0.52-7.5% of human total plasma fatty acids. It is produced from α-linolenic acid (ALA; Item Nos. 90210 | 21910) via a series of desaturase- and elongase-catalyzed reactions, resulting in a docosapentaenoic acid (DPA; Item Nos. 90165 | 21907) intermediate, which is elongated, desaturated, and β-oxidized to produce DHA.3 DHA can be liberated from cellular membranes by phospholipase A2 (PLA2) and converted to numerous oxylipins, including specialized pro-resolving mediators (SPMs), which are produced by lipoxygenases and include D-series protectins and resolvins, as well as maresins, that regulate host defense and the resolution of inflammation.4 DHA has roles in several physiological and pathological processes, including neural development, cardiovascular diseases, obesity, and inflammation.3,5WARNING This product is not for human or veterinary use.

References

[1] CONNYE N. KURATKO  Norman S Jr. Biomarkers of DHA status[J]. Prostaglandins, leukotrienes, and essential fatty acids, 2009, 81 2: Pages 111-118. DOI: 10.1016/j.plefa.2009.05.007
[2] R.J.SCOTT LACOMBE  Richard P B  Raphaël Chouinard Watkins. Brain docosahexaenoic acid uptake and metabolism[J]. Molecular Aspects of Medicine, 2018, 64: Pages 109-134. DOI: 10.1016/j.mam.2017.12.004
[3] CALDER P. Docosahexaenoic Acid[J]. Annals of Nutrition and Metabolism, 2016, 306 1: 8-21. DOI: 10.1159/000448262
[4] MARIA C. BASIL  Bruce D L. Specialized pro-resolving mediators: endogenous regulators of infection and inflammation[J]. Nature Reviews Immunology, 2015, 16 1: 51-67. DOI: 10.1038/nri.2015.4
[5] ILSE A C ARNOLDUSSEN  Amanda J K. Impact of DHA on metabolic diseases from womb to tomb.[J]. Marine Drugs, 2014, 12 12: 6190-6212. DOI: 10.3390/md12126190

Docosahexaenoic Acid 1,2,3,4-13C Preparation Products And Raw materials

Raw materials

Preparation Products

Docosahexaenoic Acid 1,2,3,4-13C Suppliers

Global Suppliers ( 2)
Supplier Tel Email Country ProdList Advantage
Cayman Chemical Company -- sales@caymanchem.com China 6808 58
Neobioscience Co., Ltd. -- info@neobioscience.com CHINA 6192 58
Docosahexaenoic Acid 1,2,3,4-13C