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21410

癸酸

≥98.0% (GC)

别名:

C10:0, NSC 5025, 癸酸, 羊蜡酸

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关于此项目

线性分子式:
CH3(CH2)8COOH
化学文摘社编号:
334-48-5
分子量:
172.26
EC Number:
206-376-4
UNSPSC Code:
12352211
PubChem Substance ID:
329752154
Beilstein/REAXYS Number:
1754556
MDL number:
MFCD00004441
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biological source

plant

vapor pressure

15 mmHg ( 160 °C)

assay

≥98.0% (GC)

bp

123-124 °C/0.1 mmHg, 268-270 °C (lit.)

mp

27-32 °C (lit.)

density

0.893 g/mL at 25 °C (lit.)

functional group

carboxylic acid

SMILES string

CCCCCCCCCC(O)=O

InChI

1S/C10H20O2/c1-2-3-4-5-6-7-8-9-10(11)12/h2-9H2,1H3,(H,11,12)

InChI key

GHVNFZFCNZKVNT-UHFFFAOYSA-N

Biochem/physiol Actions

Decanoic acid, a medium chain fatty acid (10-carbon fatty acid), is a ligand for peroxisome proliferator activated receptor (PPAR) γ. . Decanoic acid binds and acttivates PPARγ without leading to adipogenesis .

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pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Aquatic Chronic 3 - Eye Irrit. 2 - Skin Irrit. 2

存储类别

11 - Combustible Solids

wgk

WGK 1

flash_point_f

296.6 °F - closed cup

flash_point_c

147 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Raghu R V Malapaka et al.
The Journal of biological chemistry, 287(1), 183-195 (2011-11-01)
Peroxisome proliferator-activated receptors (PPARα, -β/δ, and -γ) are a subfamily of nuclear receptors that plays key roles in glucose and lipid metabolism. PPARγ is the molecular target of the thiazolidinedione class of antidiabetic drugs that has many side effects. PPARγ
M Duran et al.
The Journal of pediatrics, 107(3), 397-404 (1985-09-01)
Five patients aged 7 to 21 months are described who developed attacks of coma after a short prodromal illness with diarrhea or vomiting or both. Four had concomitant hypoglycemia, and all had hypoketonemia, with excessive urinary excretion of medium-chain dicarboxylic
G Del Vecchio et al.
Molecular pharmaceutics, 9(9), 2523-2533 (2012-07-26)
Claudin-5 is a tight junction (TJ) protein which limits the diffusion of small hydrophilic molecules. Thus, it represents a potential pharmacological target to improve drug delivery to the tissues protected by claudin-5-dependent barriers. Sodium caprate is known as an absorption
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