40227
6-ドデカノイル-N,N-ジメチル-2-ナフチルアミン
suitable for fluorescence, ≥97.0% (HPLC)
別名:
2-(ジメチルアミノ)-6-ドデカノイルナフタレン, N,N-ジメチル-6-ドデカノイル-2-ナフチルアミン, ラウルダン
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この商品について
実験式（ヒル表記法）:
C24H35NO
CAS番号:
分子量:
353.54
UNSPSC Code:
12352116
NACRES:
NA.32
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
7379104
Quality Level
assay
≥97.0% (HPLC)
mp
88 °C (lit.)
solubility
DMF: soluble, acetonitrile: soluble, methanol: soluble
fluorescence
λex 366 nm; λem 497 nm in methanol
suitability
suitable for fluorescence
SMILES string
CCCCCCCCCCCC(=O)c1ccc2cc(ccc2c1)N(C)C
InChI
1S/C24H35NO/c1-4-5-6-7-8-9-10-11-12-13-24(26)22-15-14-21-19-23(25(2)3)17-16-20(21)18-22/h14-19H,4-13H2,1-3H3
InChI key
JHDGGIDITFLRJY-UHFFFAOYSA-N
Application
6-ドデカノイル-N,N-ジメチル-2-ナフチルアミン（Laurdan）は、膜の構造、秩序、流動性などの動的プロセスの研究に使用される蛍光プローブです。
Packaging
底の開いたガラス瓶内容物は内部に挿入され接着された円錐部に入っています。
Other Notes
蛍光膜プローブ。
保管分類
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
資料
Nitric oxide (NO) as a signal transporter in neurons, endothelial cells and in the immune system.
Simmon Hofstetter et al.
Journal of microbiological methods, 91(1), 93-100 (2012-08-14)
A method for measuring the fluidity of inner membranes of populations of endospores of Clostridium spp. with a fluorescent dye was developed. Cells of Clostridium beijerinckii ATCC 8260 and Clostridium sporogenes ATCC 7955 were allowed to sporulate in the presence
L A Bagatolli et al.
Biochimica et biophysica acta, 1325(1), 80-90 (1997-04-03)
Laurdan (6-dodecanoyl-2-dimethylamine-naphthalene) is a fluorescent membrane probe of recent characterization. It was shown that this probe discriminates between phase transitions, phase fluctuations and the coexistence of phase domains in phospholipid multilamellar aggregates. We measured the excitation and emission generalized polarization
Adéla Melcrová et al.
Scientific reports, 6, 38035-38035 (2016-12-03)
Understanding interactions of calcium with lipid membranes at the molecular level is of great importance in light of their involvement in calcium signaling, association of proteins with cellular membranes, and membrane fusion. We quantify these interactions in detail by employing