L-Glutamic acid:Hcl (17O4)

Modify Date: 2026-07-01 16:19:07

L-Glutamic acid:Hcl (17O4) Structure
L-Glutamic acid:Hcl (17O4) structure
Common Name L-Glutamic acid:Hcl (17O4)
CAS Number 138-15-8 Molecular Weight 183.590
Density 1.525 Boiling Point 333.8ºC at 760 mmHg
Molecular Formula C5H10ClNO4 Melting Point 214 °C (dec.)(lit.)
MSDS Chinese USA Flash Point 155.7ºC
Symbol GHS05
GHS05
Signal Word Danger

 Use of L-Glutamic acid:Hcl (17O4)


(S)-2-aminopentanedioic acid hydrochloride is a glutamic acid derivative[1].

 Names

Name L-(+)-Glutamic acid hydrochloride
Synonym More Synonyms

 L-Glutamic acid:Hcl (17O4) Biological Activity

Description (S)-2-aminopentanedioic acid hydrochloride is a glutamic acid derivative[1].
Related Catalog
In Vitro Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1].
References

[1]. Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1144.

 Chemical & Physical Properties

Density 1.525
Boiling Point 333.8ºC at 760 mmHg
Melting Point 214 °C (dec.)(lit.)
Molecular Formula C5H10ClNO4
Molecular Weight 183.590
Flash Point 155.7ºC
Exact Mass 183.029831
PSA 100.62000
LogP 0.76540
Vapour Pressure 2.55E-05mmHg at 25°C
Index of Refraction 24 ° (C=6, H2O)
InChIKey RPAJSBKBKSSMLJ-DFWYDOINSA-N
SMILES Cl.NC(CCC(=O)O)C(=O)O
Water Solubility 490 g/L (20 ºC)

 Safety Information

Symbol GHS05
GHS05
Signal Word Danger
Hazard Statements H314
Precautionary Statements P280-P305 + P351 + P338-P310
Personal Protective Equipment dust mask type N95 (US);Eyeshields;Gloves
Hazard Codes Xi:Irritant;
Risk Phrases R41
Safety Phrases S26-S39
RIDADR UN 1789 8/PG 3
WGK Germany 3
Hazard Class 8.0
HS Code 29224200

 Synthetic Route

 Customs

HS Code 2922499990
Summary HS:2922499990 other amino-acids, other than those containing more than one kind of oxygen function, and their esters; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward) MFN tariff:6.5% General tariff:30.0%

 Articles115

More Articles
Low resolution X-ray structure of γ-glutamyltranspeptidase from Bacillus licheniformis: opened active site cleft and a cluster of acid residues potentially involved in the recognition of a metal ion.

Biochim. Biophys. Acta 1844(9) , 1523-9, (2014)

γ-Glutamyltranspeptidases (γ-GTs) cleave the γ-glutamyl amide bond of glutathione and transfer the released γ-glutamyl group to water (hydrolysis) or acceptor amino acids (transpeptidation). These ubi...

γ-glutamyl transpeptidase 1 specifically suppresses green-light avoidance via GABAA receptors in Drosophila.

J. Neurochem. 130(3) , 408-18, (2014)

Drosophila larvae innately show light avoidance behavior. Compared with robust blue-light avoidance, larvae exhibit relatively weaker green-light responses. In our previous screening for genes involve...

Chemical genetics reveals a complex functional ground state of neural stem cells.

Nat. Chem. Biol. 3(5) , 268-273, (2007)

The identification of self-renewing and multipotent neural stem cells (NSCs) in the mammalian brain holds promise for the treatment of neurological diseases and has yielded new insight into brain canc...

 L-Glutamic acid:Hcl (17O4)Bioassay

View more

Name: Luminescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: mu-type opioid receptor isoform MOR-1 [Homo sapiens]
External Id: OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
Name: Inhibition of neurosphere proliferation of mouse neural precursor cells by MTT assay
Source: ChEMBL
Target: N/A
External Id: CHEMBL1266185
Name: Fluorescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id: CHRM1_AG_FLUO8_1536_1X%ACT PRUN
Name: Dicer-mediated maturation of pre-microRNA
Source: Center for Chemical Genomics, University of Michigan
Target: N/A
External Id: TargetID_659_CEMA
Name: Fluorescence-based cell-based primary high throughput screening assay to identify pos...
Source: The Scripps Research Institute Molecular Screening Center
Target: muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id: CHRM1_PAM_FLUO8_1536_1X%ACT PRUN
Name: Confirmed inhibitors of the Choline Transporter (CHT)
Source: 1043
Target: high affinity choline transporter 1 [Homo sapiens]
External Id: SAID_488997
Name: Fluorescence polarization-based biochemical high throughput primary assay to identify...
Source: The Scripps Research Institute Molecular Screening Center
Target: RecName: Full=Sialate O-acetylesterase; AltName: Full=H-Lse; AltName: Full=Sialic acid-specific 9-O-acetylesterase; Flags: Precursor [Homo sapiens]
External Id: SIAE_INH_FP_1536_1X%INH PRUN
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 Synonyms

acidulen
acidogen
acidulin
L-Glutamic acid hydrochloride (1:1)
L-GlutaMic Acid Hydrochloride
Glutamic acid, hydrochloride
L-glutamic acid hydrochloric salt
EINECS 205-315-9
MFCD00012619
Glutamic acid hydrochloride (1:1)
L-(+)-Glutamic Acid Hydrochloride
L-Glutamic acid, hydrochloride (1:1)
aclor
antalka
glutasin
L-GLUTAMIC ACID MONOHYDROCHLORIDE
Glutamic acid, hydrochloride (1:1)
muriamic
L(+)-Glutamic acid hydrochloride
H-Glu-OH·HCl
L-Glutamic acid, hydrochloride
glusatin
DL-GLUTAMIC ACID, HYDROCHLORIDE
pepsdol
(S)-2-Aminopentanedioic acid hydrochloride
acidalin
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