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线性分子式:
CH3(CH2)6COONa
化学文摘社编号:
分子量:
166.19
UNSPSC Code:
12352107
NACRES:
NA.25
PubChem Substance ID:
EC Number:
217-850-5
Beilstein/REAXYS Number:
3597723
MDL number:
InChI key
BYKRNSHANADUFY-UHFFFAOYSA-M
InChI
1S/C8H16O2.Na/c1-2-3-4-5-6-7-8(9)10;/h2-7H2,1H3,(H,9,10);/q;+1/p-1
SMILES string
[Na+].CCCCCCCC([O-])=O
biological source
synthetic
description
anionic
assay
≥99% (capillary GC)
form
powder
mol wt
166.19 g/mol
mp
240.3 °C ((lit.))
solubility
water: 50 mg/mL
functional group
ester
shipped in
ambient
storage temp.
room temp
Quality Level
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Application
辛酸钠可在热灭菌条件下用作白蛋白和纤维蛋白原等分子的蛋白质稳定剂。
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
存储类别
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Nina Dinjaski et al.
Biomaterials, 35(1), 14-24 (2013-10-08)
Biomaterial-associated infections represent a significant clinical problem, and treatment of these microbial infections is becoming troublesome due to the increasing number of antibiotic-resistant strains. Here, we report a naturally functionalized bacterial polyhydroxyalkanoate (PHACOS) with antibacterial properties. We demonstrate that PHACOS
Rosario Pignatello et al.
Materials (Basel, Switzerland), 12(6) (2019-03-17)
A biodegradable poly(3-R-hydroxyalkanoate) synthesized by Pseudomonas mediterranea was investigated as a biomaterial to obtain colloidal drug delivery systems. Using a nanoprecipitation method, nanoparticles with a mean size of 155 nm and a negative surface charge were formed. They can be
Makoto Anraku et al.
Biochimica et biophysica acta, 1702(1), 9-17 (2004-09-29)
The capability of octanoate, N-acetyl-L-tryptophanate (N-AcTrp) and other ions of fatty acids and amino acids to stabilize human serum albumin (HSA) against thermal and oxidative stress was studied. Native-PAGE showed that octanoate, and more hydrophobic fatty acids anions, stabilizes the
Andrea S Pereyra et al.
Journal of lipid research, 62, 100069-100069 (2021-03-25)
Long-chain fatty acid oxidation is frequently impaired in primary and systemic metabolic diseases affecting the heart; thus, therapeutically increasing reliance on normally minor energetic substrates, such as ketones and medium-chain fatty acids, could benefit cardiac health. However, the molecular fundamentals
Mengqing Gao et al.
Cell reports, 36(4), 109460-109460 (2021-07-29)
In addition to acetylation, histones are modified by a series of competing longer-chain acylations. Most of these acylation marks are enriched and co-exist with acetylation on active gene regulatory elements. Their seemingly redundant functions hinder our understanding of histone acylations'
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