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9-SAHSA

9-SAHSA Structure
9-SAHSA structure
CAS No.
1895916-79-6
Chemical Name:
9-SAHSA
Synonyms
9-SAHSA;NQJLCZWOOVLQNP-UHFFFAOYSA-N;9-[(1-oxooctadecyl)oxy]-octadecanoicacid;Octadecanoic acid, 9-[(1-oxooctadecyl)oxy]-
CBNumber:
CB13152530
Molecular Formula:
C36H70O4
Molecular Weight:
566.94
MDL Number:
MOL File:
1895916-79-6.mol
Last updated:2023-05-04 17:34:35
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9-SAHSA Properties

Boiling point 640.1±38.0 °C(Predicted)
Density 0.912±0.06 g/cm3(Predicted)
solubility DMF: 20 mg/ml; DMSO: 15 mg/ml; Ethanol: 20 mg/ml; Ethanol:PBS(pH 7.2) (1:1): 0.5 mg/ml
pka 4.78±0.10(Predicted)

9-SAHSA price More Price(4)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 17109 9-SAHSA ≥95% 1895916-79-6 1mg $62 2024-03-01 Buy
Cayman Chemical 17109 9-SAHSA ≥95% 1895916-79-6 5mg $270 2024-03-01 Buy
Cayman Chemical 17109 9-SAHSA ≥95% 1895916-79-6 10mg $477 2024-03-01 Buy
AK Scientific 0429DW 9-Octadecanoyloxy-octadecanoicacid 1895916-79-6 1mg $166 2021-12-16 Buy
Product number Packaging Price Buy
17109 1mg $62 Buy
17109 5mg $270 Buy
17109 10mg $477 Buy
0429DW 1mg $166 Buy

9-SAHSA Chemical Properties,Uses,Production

Description

Branched fatty acid esters of hydroxy fatty acids (FAHFAs) are newly identified endogenous lipids regulated by fasting and high-fat feeding and associated with insulin sensitivity.1 Structurally, these esters are comprised of a C-16 or C-18 fatty acid (e.g., palmitoleic, palmitic, oleic, or stearic acid) linked to either a C-16 or C-18 hydroxy substituent. 9-SAHSA is a FAHFA in which stearic acid is esterified at the 9th carbon of hydroxy stearic acid. The levels of SAHSA are moderately elevated in the serum of glucose tolerant AG4OX mice, which overexpress the Glut4 glucose transporter specifically in adipose tissue.1

Definition

ChEBI: 9-(octadecanoyloxy)octadecanoic acid is a fatty acid ester obtained by formal condensation of the carboxy group of octadecanoic acid with the hydroxy group of 9-hydroxyoctadecanoic acid. It is a fatty acid ester and a monocarboxylic acid. It is functionally related to an octadecanoic acid and a 9-hydroxyoctadecanoic acid. It is a conjugate acid of a 9-(octadecanoyloxy)octadecanoate.

References

1. Yore, M.M., Syed, I., Moraes-Vieira, P.M., et al. Discovery of a class of endogenous mammalian lipids with anti-diabetic and anti-inflammatory effects Cell 159(2),318-332(2014).

9-SAHSA Preparation Products And Raw materials

Raw materials

Preparation Products

9-SAHSA Suppliers

Global( 18)Suppliers
Supplier Tel Email Country ProdList Advantage
Shanghai Hongye Biotechnology Co. Ltd 400-9205774 sales@glpbio.cn China 6870 58
ChemeGen(Shanghai) Biotechnology Co.,Ltd. 18818260767 sales@chemegen.com China 11289 58
MedBioPharmaceutical Technology Inc 021-69568360 18916172912 order@med-bio.cn China 8141 58
Shanghai Yifei Biotechnology Co. , Ltd. 021-65675885 18964387627 customer_service@efebio.com China 8740 58
Supplier Advantage
Shanghai Hongye Biotechnology Co. Ltd 58
ChemeGen(Shanghai) Biotechnology Co.,Ltd. 58
MedBioPharmaceutical Technology Inc 58
Shanghai Yifei Biotechnology Co. , Ltd. 58
9-SAHSA NQJLCZWOOVLQNP-UHFFFAOYSA-N Octadecanoic acid, 9-[(1-oxooctadecyl)oxy]- 9-[(1-oxooctadecyl)oxy]-octadecanoicacid 1895916-79-6