75940
2-Oxooctanoic acid
≥99.0% (T)
Synonym(s):
α-Ketooctanoic acid, 2-Oxocaprylic acid
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About This Item
Linear Formula:
CH3(CH2)5COCOOH
CAS Number:
Molecular Weight:
158.19
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
206-331-9
Beilstein/REAXYS Number:
1757862
MDL number:
Assay:
≥99.0% (T)
Form:
flakes
Quality Level
assay
≥99.0% (T)
form
flakes
bp
82 °C/0.05 mmHg
mp
33-36 °C
functional group
carboxylic acid, ketone
storage temp.
2-8°C
SMILES string
CCCCCCC(=O)C(O)=O
InChI
1S/C8H14O3/c1-2-3-4-5-6-7(9)8(10)11/h2-6H2,1H3,(H,10,11)
InChI key
GPPUPQFYDYLTIY-UHFFFAOYSA-N
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Huifang Xu et al.
Journal of colloid and interface science, 509, 265-274 (2017-09-16)
Single-tailed short-chain alkyl keto-acids/salts, a class of fatty acid/salt derivatives, such as sodium 2-ketooctanate (KOCOONa), are a kind of weakly acid/salt type amphiphiles and plausible prebiotic molecules, and the current understanding of their aggregation behavior in aqueous solutions is still
Sarah A Almahboub et al.
Applied microbiology and biotechnology, 102(2), 789-799 (2017-11-28)
Terminal modification of peptides is frequently used to improve their hydrophobicity. While N-terminal modification with fatty acids (lipidation) has been reported previously, C-terminal lipidation is limited as it requires the use of linkers. Here we report the use of a
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 03970590-10MG | 04061838628558 |
| E4268-100MG | 04061833603581 |
| 93894-10MG | 04061833283394 |
| Y0001936 | 04061835123179 |
| E4143-50MG | 04061835544455 |
| 324880-10MG | 04055977196092 |
| 1236700-20MG | 04061838722508 |
| PHR1333-1G | 04061834415961 |
| 75940-1G | 04061825926414 |