Alanine-15N

Modify Date: 2024-01-09 16:07:23

Alanine-15N structure	Common Name	Alanine-15N
	CAS Number	71261-64-8	Molecular Weight	89.093
	Density	1.2±0.1 g/cm3	Boiling Point	212.9±23.0 °C at 760 mmHg
	Molecular Formula	C₃H₇NO₂	Melting Point	289ºC (dec.)(lit.)
	MSDS	Chinese USA	Flash Point	82.6±22.6 °C

Use of Alanine-15N

DL-Alanine-15N is the 15N labeled DL-Alanine[1]. DL-alanine, an amino acid, is the racemic compound of L- and D-alanine. DL-alanine is employed both as a reducing and a capping agent, used with silver nitrate aqueous solutions for the production of nanoparticles. DL-alanine can be used for the research of transition metals chelation, such as Cu(II), Zn(II), Cd(11). DL-alanine, a sweetener, is classed together with glycine, and sodium saccharin. DL-alanine plays a key role in the glucose-alanine cycle between tissues and liver[2][3][4][5][6][7].

Name	2-azanylpropanoic acid
Synonym	More Synonyms

Description	DL-Alanine-15N is the 15N labeled DL-Alanine[1]. DL-alanine, an amino acid, is the racemic compound of L- and D-alanine. DL-alanine is employed both as a reducing and a capping agent, used with silver nitrate aqueous solutions for the production of nanoparticles. DL-alanine can be used for the research of transition metals chelation, such as Cu(II), Zn(II), Cd(11). DL-alanine, a sweetener, is classed together with glycine, and sodium saccharin. DL-alanine plays a key role in the glucose-alanine cycle between tissues and liver[2][3][4][5][6][7].
Related Catalog	Research Areas >> Metabolic Disease
In Vitro	Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs[1].
References	[1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019 Feb;53(2):211-216. [2]. Amrallah AH, et al. Mixed ligand complexes of benzimidazole and pyrimidine hydroxy azo dyes with some transition metals and glycine, dl-alanine or dl-leucine. Talanta. 1998 Aug;46(4):491-500. [3]. Eder José Guidelli, et, al. Synthesis of silver nanoparticles using dl-alanine for ESR dosimetry applications. Radiation Physics and Chemistry. Volume 81, Issue 3, 2012: Pages 301-307. [4]. Rashid M, et al. Biosynthesis of Self-Dispersed Silver Colloidal Particles Using the Aqueous Extract of P. peruviana for Sensing dl-Alanine[J]. Isrn Nanotechnology, 2014, 2014:1-7. [5]. Tapper DN, et al. Taste stimuli: a behavioral categorization. Science. 1968 Aug 16161(3842):708-10. [6]. Yamaguchi M, et al. Terahertz absorption spectra of L-, D-, and DL-alanine and their application to determination of enantiometric composition[J]. Applied Physics Letters, 2005, 86(5): 053903. [7]. Yamamoto T, et al. Gustatory reaction time to various sweeteners in human adults. Physiol Behav. 1985 Sep35(3):411-5.

Density	1.2±0.1 g/cm3
Boiling Point	212.9±23.0 °C at 760 mmHg
Melting Point	289ºC (dec.)(lit.)
Molecular Formula	C₃H₇NO₂
Molecular Weight	89.093
Flash Point	82.6±22.6 °C
Exact Mass	89.047676
PSA	63.32000
LogP	-0.68
Vapour Pressure	0.1±0.9 mmHg at 25°C
Index of Refraction	1.460

RIDADR	NONH for all modes of transport

(R,S)-Alanine

(±)-Alanine

Propanoic acid, 2-amino-

DL-Alanine-15N

DL-2-aminopropionic acid

α-Aminopropanoic acid

(15N)-dl-alanine

2-Aminopropanoic acid

(15)N-alanine

ZY1&VQ

Alanine

α-Aminopropionic acid

d,l-alanine

DL-15N-alanine

Alanine, DL-

UNII:1FU7983T0U

α-Alanine

MFCD00064409

2-Aminopropionic Acid

DL-α-Aminopropionic acid

H-DL-Ala-OH

DL-2-Aminopropanoic acid

DL-α-Alanine

DL-Aminopropanoic acid

Methyl glycine

Alanine-15N

Use of Alanine-15N

Names

Alanine-15N Biological Activity

Chemical & Physical Properties

Safety Information

Synonyms