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L-Tryptophan methyl ester hydrochloride - 98%, high purity , CAS No.7524-52-9

3 Citations

COA

Grade & Purity:

≥98%

Cas Number: 7524-52-9
Molecular Weight: 254.71
Beilstein Registry Number: 4240280
EC Number: 231-385-5
MDL number: MFCD00066134
PubChem CID: 2734891
PubChem SID: 488192682

In stock

Item Number

T109009

Grouped product items
SKU	Size	Availability	Price
T109009-5g	5g	10	$28.90
T109009-10g	10g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$51.90
T109009-25g	25g	8	$92.90
T109009-100g	100g	10	$331.90
T109009-500g	500g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$1,492.90

View related series

azole (525) Five-Membered Heterocyclic Compounds (2064)

Basic Description

Synonyms	H-Trp-OMe•HCl \| methyl (2S)-2-amino-3-(1H-indol-3-yl)propanoate hydrochloride \| Q27274122 \| AC-8667 \| (L)-tryptophan methyl ester hydrochloride \| METHYL TRYPTOPHANATE HCL \| EINECS 231-385-5 \| Methyl L-Tryptophanate Hydrochloride \| T1657 \| MFCD00066134 \| N
Specifications & Purity	≥98%
Storage Temp	Protected from light,Argon charged
Shipped In	Normal
Product Description	L-Tryptophan Methyl Ester Hydrochloride an amino acid derivative.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organic acids and derivatives
  - Class Carboxylic acids and derivatives
    - Subclass Amino acids, peptides, and analogues
      - Level5 Amino acids and derivatives
        Level6 Alpha amino acids and derivatives
        Level7 Alpha amino acid esters

Kingdom	Organic compounds
Superclass	Organic acids and derivatives
Class	Carboxylic acids and derivatives
Subclass	Amino acids, peptides, and analogues
Intermediate Tree Nodes	Amino acids and derivatives - Alpha amino acids and derivatives
Direct Parent	Alpha amino acid esters
Alternative Parents	Indolyl carboxylic acids and derivatives 3-alkylindoles Aralkylamines Fatty acid esters Substituted pyrroles Benzenoids Methyl esters Heteroaromatic compounds Monocarboxylic acids and derivatives Azacyclic compounds Hydrocarbon derivatives Carbonyl compounds Hydrochlorides Monoalkylamines Organic oxides Organopnictogen compounds
Molecular Framework	Aromatic heteropolycyclic compounds
Substituents	Alpha-amino acid ester - Indolyl carboxylic acid derivative - 3-alkylindole - Indole - Indole or derivatives - Fatty acid ester - Aralkylamine - Substituted pyrrole - Benzenoid - Fatty acyl - Heteroaromatic compound - Methyl ester - Pyrrole - Carboxylic acid ester - Organoheterocyclic compound - Azacycle - Monocarboxylic acid or derivatives - Hydrochloride - Organooxygen compound - Organonitrogen compound - Primary amine - Primary aliphatic amine - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Amine - Aromatic heteropolycyclic compound
Description	This compound belongs to the class of organic compounds known as alpha amino acid esters. These are ester derivatives of alpha amino acids.
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

Pubchem Sid	488192682
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488192682
IUPAC Name	methyl (2S)-2-amino-3-(1H-indol-3-yl)propanoate;hydrochloride
INCHI	InChI=1S/C12H14N2O2.ClH/c1-16-12(15)10(13)6-8-7-14-11-5-3-2-4-9(8)11;/h2-5,7,10,14H,6,13H2,1H3;1H/t10-;/m0./s1
InChIKey	XNFNGGQRDXFYMM-PPHPATTJSA-N
Smiles	COC(=O)C(CC1=CNC2=CC=CC=C21)N.Cl
Isomeric SMILES	COC(=O)[C@H](CC1=CNC2=CC=CC=C21)N.Cl
WGK Germany	3
Molecular Weight	254.71
Beilstein	4240280
Reaxy-Rn	4035732
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4035732&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

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17 results found

Lot Number	Certificate Type	Date	Item
E2512108	Certificate of Analysis	May 17, 2025	T109009
K2217802	Certificate of Analysis	Mar 10, 2025	T109009
K2217801	Certificate of Analysis	Mar 10, 2025	T109009
E2305828	Certificate of Analysis	Feb 11, 2025	T109009
K2217799	Certificate of Analysis	Sep 19, 2024	T109009
K2217827	Certificate of Analysis	Sep 19, 2024	T109009
K2217800	Certificate of Analysis	Sep 19, 2024	T109009
K2217798	Certificate of Analysis	Sep 19, 2024	T109009
K2421097	Certificate of Analysis	Sep 19, 2024	T109009
B2526065	Certificate of Analysis	Jul 06, 2024	T109009
L2403003	Certificate of Analysis	Jul 06, 2024	T109009
L2403004	Certificate of Analysis	Jul 06, 2024	T109009
K2104554	Certificate of Analysis	Aug 04, 2023	T109009
K2104553	Certificate of Analysis	Aug 04, 2023	T109009
K1904088	Certificate of Analysis	Jun 08, 2023	T109009
K2005221	Certificate of Analysis	Sep 16, 2022	T109009
K2217803	Certificate of Analysis	Mar 07, 2022	T109009

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Chemical and Physical Properties

Sensitivity	Light & Moisture sensitive.
Specific Rotation[α]	19.5 ° (C=5, MeOH)
Melt Point(°C)	218-220°C
Molecular Weight	254.710 g/mol
XLogP3
Hydrogen Bond Donor Count	3
Hydrogen Bond Acceptor Count	3
Rotatable Bond Count	4
Exact Mass	254.082 Da
Monoisotopic Mass	254.082 Da
Topological Polar Surface Area	68.100 Å²
Heavy Atom Count	17
Formal Charge	0
Complexity	257.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	1
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	2

Citations of This Product

How to Cite Aladdin Scientific Products?

1. Jiansheng Liu,Yajing He,Jun Zhang,Jiajia Li,Xiangrong Yu,Zhonglian Cao,Fanmin Meng,Yuwu Zhao,Xunyi Wu,Teng Shen,Zhen Hong. (2015-10-09) Functionalized nanocarrier combined seizure-specific vector with P-glycoprotein modulation property for antiepileptic drug delivery.. Biomaterials, 74 (64-76).
2. Yufei Zhang, Yijie Cheng, Yunjian Yu, Jie Li, Yuqing Hu, Yingchao Gao, Siyuan Huang, Wenbo Wang, Xinge Zhang. (2022) Virus-like-inspired nanoparticles facilitate bacterial internalization for enhanced eradication of drug-resistant pathogens. NEW JOURNAL OF CHEMISTRY, 46 (30): (14410-14420).
3. Xufeng Qin, Weifeng Xu, Jiangnan Hu, Yong Dong, Renbo Ding, Shuheng Huang, Zhendong Zhao, Hong Chang, Xiaokun Wang, Shuai Dong. (2024) Structure-activity relationship study of Pseudellone C as anti-glioma agents by targeting TNF/TNFR signaling pathway. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 278 (116799).

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