H4398
DL-β-Hydroxypalmitic acid
≥98%
Synonym(s):
3-Hydroxyhexadecanoic acid
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About This Item
Empirical Formula (Hill Notation):
C16H32O3
CAS Number:
Molecular Weight:
272.42
MDL number:
UNSPSC Code:
12352211
PubChem Substance ID:
NACRES:
NA.25
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Assay
≥98%
form
powder
functional group
carboxylic acid
lipid type
saturated FAs
shipped in
ambient
storage temp.
2-8°C
SMILES string
CCCCCCCCCCCCCC(O)CC(O)=O
InChI
1S/C16H32O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-15(17)14-16(18)19/h15,17H,2-14H2,1H3,(H,18,19)
InChI key
CBWALJHXHCJYTE-UHFFFAOYSA-N
Biochem/physiol Actions
DL-β-Hydroxypalmitic acid is a mixture of D- and L-β-hydroxypalmitic (3-hydroxyhexadecanoic) acids. 3-hydroxyhexadecanoic [C16:0(3-OH)] may be used in studies that involve the lipid structures of endotoxin lipid A molecules.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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David W Johnson et al.
Rapid communications in mass spectrometry : RCM, 17(2), 171-175 (2003-01-04)
Acetyl trimethylaminoethyl ester iodide derivatives have been used to selectively analyze isomeric long-chain hydroxy fatty acids by electrospray ionization tandem mass spectrometry (ESI-MS/MS). The binary derivatives of 2-, 3-, 12- and 16-hydroxypalmitic acids afford remarkably different product ion spectra. Further
O Sebolai et al.
Antonie van Leeuwenhoek, 80(3-4), 311-315 (2002-02-06)
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M Fodorová et al.
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Bacteria show distinct and characteristic fatty acid (FA) patterns which can be modified by environmental conditions. In this study, we cultivated six plant-pathogenic bacteria of agricultural concern and performed a detailed analysis of the fatty acid composition. The study covered
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