InChI key
POULHZVOKOAJMA-UHFFFAOYSA-N
InChI
1S/C12H24O2/c1-2-3-4-5-6-7-8-9-10-11-12(13)14/h2-11H2,1H3,(H,13,14)
SMILES string
CCCCCCCCCCCC(O)=O
vapor pressure
1 mmHg ( 121 °C), 50 mmHg ( 210 °C)
assay
≥99.5%
bp
225 °C/100 mmHg (lit.)
mp
44-46 °C (lit.)
density
0.883 g/mL at 25 °C (lit.)
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Isaac Levy et al.
The Journal of clinical endocrinology and metabolism, 100(11), 4106-4113 (2015-09-01)
Adults with hypoparathyroidism have significant rates of nephrocalcinosis and impaired renal function. Little is known about the impact of hypoparathyroidism treatment on renal function in children. To determine the prevalence and predictors for renal abnormalities (nephrocalcinosis and decreased estimated glomerular
M T Ryan et al.
Biochimica et biophysica acta, 427(1), 337-349 (1976-03-18)
Careful investigation of the influence of palmitic and lauric acid on the interaction of progesterone and testosterone with several batches of untreated and defatted bovine and human serum albumins have revealed that, by contrast with published data for studies with
Juliette Lambert et al.
Oncotarget, 5(15), 6280-6288 (2014-07-16)
We analysed the prognostic significance of minimal residual disease (MRD) level in adult patients with acute myeloid leukemia (AML) treated in the randomized gemtuzumab ozogamicin (GO) ALFA-0701 trial. Levels of WT1 and NPM1 gene transcripts were assessed using cDNA-based real-time
Meng-Meng Bai et al.
Journal of agricultural and food chemistry, 63(8), 2198-2205 (2015-02-14)
Eucommia ulmoides leaves have been used as a functional food and drink in China. The purpose of this study was to identify the bioactive constituents with soluble epoxide hydrolase (sEH) inhibitory activity and anti-inflammatory properties. Twenty-seven known compounds (1-27) were
M Schmidt et al.
Leukemia, 28(12), 2292-2299 (2014-09-13)
To study clonal evolution in chronic myeloid leukemia (CML), we searched for BCR-ABL-independent gene mutations in both Philadelphia chromosome (Ph)-negative and Ph-positive clones in 29 chronic-phase CML patients by targeted deep sequencing of 25 genes frequently mutated in myeloid disorders.
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