L-Carnosine CAS#: 305-84-0; ChemWhat Code: 354838

IdentificationPhysical DataSpectra
Route of Synthesis (ROS)Safety and HazardsOther Data

Identification

Product NameL-Carnosine
IUPAC Name(2S)-2-(3-aminopropanoylamino)-3-(1H-imidazol-5-yl)propanoic acid
Molecular StructureStructure of L-Carnosine CAS# 305-84-0
CAS Registry Number 305-84-0
EINECS Number206-169-9
MDL NumberMFCD00005207
Beilstein Registry Number87671
SynonymscarnosineL-carnosineCar
Molecular FormulaC9H14N4O3
Molecular Weight226.23
InChIInChI=1S/C9H14N4O3/c10-2-1-8(14)13-7(9(15)16)3-6-4-11-5-12-6/h4-5,7H,1-3,10H2,(H,11,12)(H,13,14)(H,15,16)/t7-/m0/s1
InChI KeyCQOVPNPJLQNMDC-ZETCQYMHSA-N
Canonical SMILESc1c(nc[nH]1)C[C@@H](C(=O)O)NC(=O)CCN
Patent Information
Patent IDTitlePublication Date
US2020/54061METHODS AND COMPOSITIONS FOR RAPIDLY DECREASING EPIGENETIC AGE AND RESTORATION OF MORE YOUTHFUL FUNCTION2020
WO2017/162267MEDICAMENT2017
US2016/166488MEDICAMENT2016

Physical Data

AppearanceWhite powder
Solubilityalmost transparency
Refractive index21 ° (C=2, H2O)
Melting Point, °C
258
251 – 252

Spectra

Description (NMR Spectroscopy)Nucleus (NMR Spectroscopy)Solvents (NMR Spectroscopy)Temperature (NMR Spectroscopy), °C Frequency (NMR Spectroscopy), MHz
Chemical shifts1Hwater-d2300
Chemical shifts15Nsolid30.412
Spectrum1HD2O
Spectrum1HD2O24.9
Description (IR Spectroscopy)Solvent (IR Spectroscopy)Comment (IR Spectroscopy)
Bandspotassium bromide
Bands, Spectrumpotassium bromide
BandsKBrpH dependence. Object(s) of Study: in the presence of inorganic compounds
Description (Mass Spectrometry)
high resolution mass spectrometry (HRMS), liquid chromatography mass spectrometry (LCMS), IT (ion trap), electrospray ionisation (ESI), fragmentation pattern, spectrum
liquid chromatography mass spectrometry (LCMS), electrospray ionisation (ESI), tandem mass spectrometry, fragmentation pattern, spectrum
electrospray ionisation (ESI), fragmentation pattern, spectrum
LCMS (Liquid chromatography mass spectrometry), Tandem mass spectrometry, Spectrum
Description (UV/VIS Spectroscopy)Absorption Maxima (UV/VIS), nm
Spectrum
Band assignment, Spectrum214, 264
Description (Raman Spectroscopy)Comment (Raman Spectroscopy)
BandspH dependence. Object(s) of Study: in the presence of inorganic compounds

Route of Synthesis (ROS)

Route-of-Synthesis-ROS-of-L-Carnosine-CAS-305-84-0
Route of Synthesis/ROS of L-Carnosine CAS 305-84-0
ConditionsYield
With water; sodium hydroxide In methanol at 25 – 60℃; for 3h; Solvent;99.7%
With sodium hydroxide In water at 23 – 83℃; for 3h; Solvent; Temperature;96.8%

Safety and Hazards

GHS Hazard StatementsNot Classified
SDS DownloadEnglish Version

Other Data

TransportationNONH for all modes of transport
Under the room temperature and away from light
HS Code293329
StorageStore at room temperature and away from light.
Shelf Life2 years
Market PriceUSD
Druglikeness
Lipinski rules component
Molecular Weight226.235
logP-4.099
HBA7
HBD4
Matching Lipinski Rules4
Veber rules component
Polar Surface Area (PSA)121.1
Rotatable Bond (RotB)7
Matching Veber Rules2
Quantitative Results
1 of 2Effectbehavioral symtoms
Route of Applicationintracerebroventricular
Kind of Dosing (Ecotoxicology)title comp. dissolved in 0.85percent saline containing 0.1percent Evans Blue solution; admin. in a volume of 10 ml using a microsyringe into lateral ventricle
Method (Ecotoxicology)layer chicks admin. with title comp. alone or in combination with HA; behavioral symptoms (active wakefulness (1), standing/sitting motionless with eyes opened (2), standing motionless with eyes closed (3), sleeping posture (4)) obsd. for 10 min
Resultstitle comp. showed significant effects in active wakefulness and sleeping posture; combination effects of title comp. and HA were similar to title comp. alone; table
2 of 2Effect (Ecotoxicology)behavioral symtoms
Further Details (Ecotoxicology)control: saline; further investigations with selective and non-selective nitric oxide synthase (NOS) inhibitors administered i.c.v.
Resultstitle comp. significantly induced spontaneous activity; effect may be linked to constitutive NOS rather than inducible NOS in brain
Use Pattern
preparation of antioxidant
preparation of whitening products
preparation of medicament for colon cancer metastasis
caring for lips
Cosmetics/dental/toilet

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