1-Pyrenemethylamine hydrochloride - CAS 93324-65-3

Name: 1-Pyrenemethylamine hydrochloride
Brand: BOC Sciences
Rating: 5 (1 reviews)

Catalog:	BB040850
Product Name:	1-Pyrenemethylamine hydrochloride
CAS:	93324-65-3
Synonyms:	pyren-1-ylmethanamine;hydrochloride

Technical Data

IUPAC Name:	pyren-1-ylmethanamine;hydrochloride
Description:	1-Pyrenemethylamine hydrochloride (CAS# 93324-65-3) is used for labelling of various biomolecules. It is used as a reactant in self-assembling vancomycin-pyrene derivatives as hydrogel with potential medical applications. Also used in the preparation of 25,27-bis(ethylacetoethoxy)-26,28-dipropyloxycalix[4]arene.
Molecular Weight:	267.75
Molecular Formula:	C17H13N · HCl
Canonical SMILES:	C1=CC2=C3C(=C1)C=CC4=C(C=CC(=C43)C=C2)CN.Cl
InChI:	InChI=1S/C17H13N.ClH/c18-10-14-7-6-13-5-4-11-2-1-3-12-8-9-15(14)17(13)16(11)12;/h1-9H,10,18H2;1H
InChI Key:	RGNMXKKNDSHTFD-UHFFFAOYSA-N
Boiling Point:	437.9 °C at 760 mmHg
Melting Point:	258 °C (dec.)(lit.)
Purity:	95 %
Appearance:	Off-white to beige, tan or yellow-tan powder
Storage:	Sealed in dry, Room Temperature
MDL:	MFCD00192425
LogP:	5.54500

GHS Hazard Statement:	H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]
Precautionary Statement:	P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501
Signal Word:	Warning

Publication Number	Title	Priority Date
CN-113433203-A	Method, device and substrate for preparing measurement samples for MALDI mass spectrometry	20200323
EP-3886141-A1	Method, device, and base for preparing measurement sample for maldi mass spectrometry	20200323
JP-2021153044-A	MALDI mass spectrometry measurement sample preparation method, MALDI mass spectrometry measurement sample preparation device, and MALDI mass spectrometry measurement sample preparation substrate	20200323
US-2021296109-A1	Method, device, and base for preparing measurement sample for maldi mass spectrometry	20200323
KR-102294709-B1	Method for preparing conductive polymer having dispersion stability and highly conductive, conductive polymer made therefrom and anti-static coating agent using the same	20191205

PMID	Publication Date	Title	Journal
21726056	20110905	Two-photon-absorption technique for selective detection of copper(II) ions in aqueous solution using a dansyl-pyrene conjugate	Chemistry, an Asian journal
20509021	20100701	Reagent peak-free liquid chromatography-fluorescence analysis of carboxylic acids using a fluorous scavenging-derivatization method	Analytical and bioanalytical chemistry
18610962	20080731	Effect of side-chain length on the side-chain dynamics of alpha-helical poly(L-glutamic acid) as probed by a fluorescence blob model	The journal of physical chemistry. B
16701937	20060920	Variable path length and counter-flow continuous variation methods for the study of the formation of high-affinity complexes by absorbance spectroscopy. An application to the studies of substrate binding in cytochrome P450	Biophysical chemistry
16566594	20060404	Resolution of multiple substrate binding sites in cytochrome P450 3A4: the stoichiometry of the enzyme-substrate complexes probed by FRET and Job's titration	Biochemistry

Complexity:	313
Compound Is Canonicalized:	Yes
Covalently-Bonded Unit Count:	2
Defined Atom Stereocenter Count:	0
Defined Bond Stereocenter Count:	0
Exact Mass:	267.0814771
Formal Charge:	0
Heavy Atom Count:	19
Hydrogen Bond Acceptor Count:	1
Hydrogen Bond Donor Count:	2
Isotope Atom Count:	0
Monoisotopic Mass:	267.0814771
Rotatable Bond Count:	1
Topological Polar Surface Area:	26 Å²
Undefined Atom Stereocenter Count:	0
Undefined Bond Stereocenter Count:	0