3785-01-1 Usage
Uses
Used in Biological Research:
DASPEI is used as a fluorescent dye for staining mitochondria, allowing researchers to visually examine cell energy production. This application is particularly beneficial in studies involving fish or aquatic invertebrates, where the dye's selective binding to actively respiring cells provides valuable insights into cellular processes.
Used in Cell Biology:
DASPEI is used as a staining agent in cell biology to facilitate the observation of mitochondrial activity. Its selective binding to actively respiring cells makes it an essential tool for studying various aspects of cellular metabolism and energy production.
Used in Toxicology:
DASPEI is used as a research tool in toxicology to investigate the effects of various substances on cell energy production and mitochondrial function. Its potential toxicity at high concentrations makes it a valuable compound for understanding the mechanisms of cellular damage and the development of potential therapeutic interventions.
Used in Aquatic Research:
DASPEI is used as a fluorescent dye in aquatic research, specifically for staining mitochondria in fish or aquatic invertebrates. This application aids in the study of the effects of environmental factors on the health and energy production of aquatic organisms.
Check Digit Verification of cas no
The CAS Registry Mumber 3785-01-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,8 and 5 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3785-01:
(6*3)+(5*7)+(4*8)+(3*5)+(2*0)+(1*1)=101
101 % 10 = 1
So 3785-01-1 is a valid CAS Registry Number.
InChI:InChI=1/C17H21N2.HI/c1-4-19-14-6-5-7-17(19)13-10-15-8-11-16(12-9-15)18(2)3;/h5-14H,4H2,1-3H3;1H/q+1;/p-1
3785-01-1Relevant academic research and scientific papers
Molecular Association of Water-Soluble Calixarenes with Several Stilbene Dyes and Its Application to the Facile Determination of Cationic Surfactant Concentrations
Nishida, Masashi,Ishii, Daido,Yoshida, Isao,Shinkai, Seiji
, p. 2131 - 2140 (2007/10/03)
The molecular association of water-soluble p-sulfonatocalix[n]arenes (1n; n = 4, 6, and 8) with several stilbene dyes (D) has been studied by spectrophotometric and 1HNMR methods. It was found that 1n reacts in 1: 1 stoichiometry with, D such as 4-[(4-dimethylamino)styryl]-1-methylpyridinium (St-4Me), 2-[(4-dimethylamino)styryl]-1-methylpyridinium (St-2Me) and 2-[(4-dimethylamino)styryl]-1-ethylpyridinium (St-2Et) iodides to form their complexes (1nD). The apparent association constants for 18-complexes are larger by about ten times than those of 14- and 16-complexes. Examinations of the CPK molecular models and the spectrophotometric studies suggested that 14 complexes D mainly with its 1-methyl- or 1-ethylpyridinium group, whereas 16 complexes D either with its pyridinium ring or with its protonated dimethylamino group in a similar probability, and in 18-complexes the molecule is wholly incorporated into the cavity of 18. The absorbance of D, which was decreased by association with 1n, was regenerated by the addition of other colorless cationic surfactants (A) such as cetylethyldimethylammonium ion. Studies on the substitution reaction of 1nD with A indicated that a 1 : 1 complex (1nA) is formed by releasing a free dye molecule (D). This was applied to a convenient determination of the cationic surfactant concentration in water.
