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5-Methyl-DL-tryptophan - 98%, high purity , CAS No.951-55-3

COA

Grade & Purity:

≥98%

Cas Number: 951-55-3
Molecular Weight: 218.26
Beilstein Registry Number: 20225
MDL number: MFCD00005652
PubChem CID: 92852
PubChem SID: 504756147

In stock

Item Number

M158068

Grouped product items
SKU	Size	Availability	Price
M158068-100mg	100mg	3	$59.90
M158068-250mg	250mg	3	$134.90
M158068-1g	1g	3	$484.90
M158068-5g	5g	2	$2,181.90

View related series

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

Basic Description

Synonyms	5-Methyl-DL-tryptophan (H-DL-Trp(5-Me)-OH) \| DL-2-Amino-3-(5-Methylindolyl) Propionic acid \| LIPOXINA4 \| SCHEMBL18029004 \| 5-Methyltryptophan \| 5-METHYL-TRYPTOPHAN \| 5-Methyl-DL-tryptophan \| (5Z,8Z,10E,12S,14Z)-12-hydroperoxyicosa-5,8,10,14-tetraenoic aci
Specifications & Purity	≥98%
Biochemical and Physiological Mechanisms	5-Methyl-DL-tryptophan inhibits the synthesis of anthranilate compounds that are the first steps in the biosynthesis of tryptophan in Neurospora crassa. 5-Methyl-DL-tryptophan is a corepressor of the E. coli trp repressor. 5-Methyl-DL-tryptophan may be us
Storage Temp	Store at 2-8°C,Protected from light
Shipped In	Wet ice This product requires cold chain shipping. Ground and other economy services are not available.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organoheterocyclic compounds
  - Class Indoles and derivatives
    - Subclass Indolyl carboxylic acids and derivatives

Kingdom	Organic compounds
Superclass	Organoheterocyclic compounds
Class	Indoles and derivatives
Subclass	Indolyl carboxylic acids and derivatives
Intermediate Tree Nodes	Not available
Direct Parent	Indolyl carboxylic acids and derivatives
Alternative Parents	Alpha amino acids 3-alkylindoles Aralkylamines Substituted pyrroles Benzenoids Heteroaromatic compounds Amino acids Monocarboxylic acids and derivatives Carboxylic acids Azacyclic compounds Organopnictogen compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds
Molecular Framework	Aromatic heteropolycyclic compounds
Substituents	Indolyl carboxylic acid derivative - Alpha-amino acid - Alpha-amino acid or derivatives - 3-alkylindole - Indole - Aralkylamine - Benzenoid - Substituted pyrrole - Heteroaromatic compound - Pyrrole - Amino acid or derivatives - Amino acid - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Azacycle - Amine - Primary aliphatic amine - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Organonitrogen compound - Organooxygen compound - Primary amine - Organopnictogen compound - Aromatic heteropolycyclic compound
Description	This compound belongs to the class of organic compounds known as indolyl carboxylic acids and derivatives. These are compounds containing a carboxylic acid chain (of at least 2 carbon atoms) linked to an indole ring.
External Descriptors	non-proteinogenic alpha-amino acid - tryptophan derivative
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	504756147
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/504756147
IUPAC Name	2-amino-3-(5-methyl-1H-indol-3-yl)propanoic acid
INCHI	InChI=1S/C12H14N2O2/c1-7-2-3-11-9(4-7)8(6-14-11)5-10(13)12(15)16/h2-4,6,10,14H,5,13H2,1H3,(H,15,16)
InChIKey	HUNCSWANZMJLPM-UHFFFAOYSA-N
Smiles	CC1=CC2=C(C=C1)NC=C2CC(C(=O)O)N
Isomeric SMILES	CC1=CC2=C(C=C1)NC=C2CC(C(=O)O)N
WGK Germany	3
Molecular Weight	218.26
Beilstein	20225
Reaxy-Rn	20225
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=20225&ln=

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

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Analytical Chart:

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6 results found

Lot Number	Certificate Type	Date	Item
F2520208	Certificate of Analysis	Jul 07, 2022	M158068
J2218066	Certificate of Analysis	Jul 07, 2022	M158068
J2218077	Certificate of Analysis	Jul 07, 2022	M158068
J2218008	Certificate of Analysis	Jul 07, 2022	M158068
J2218007	Certificate of Analysis	Jul 07, 2022	M158068
K2414018	Certificate of Analysis	Jul 07, 2022	M158068

Chemical and Physical Properties

Sensitivity	Light Sensitive
Specific Rotation[α]	0° (C=1,HCl)
Melt Point(°C)	275 °C(dec.)
Molecular Weight	218.250 g/mol
XLogP3	-0.700
Hydrogen Bond Donor Count	3
Hydrogen Bond Acceptor Count	3
Rotatable Bond Count	3
Exact Mass	218.106 Da
Monoisotopic Mass	218.106 Da
Topological Polar Surface Area	79.100 Å²
Heavy Atom Count	16
Formal Charge	0
Complexity	270.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	1
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

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