3-N-Methyl-L-histidine - ≥98% , CAS No.368-16-1

CAS: 368-16-1 Cat. No.: N137204 Molecular Weight: 169.18 EC Number: 206-704-6
AVAILABLE TO ORDER
GRADE & PURITY ≥98%
Synonyms
N3-Methyl-L-histidine | HY-W017007 | (2S)-2-amino-3-(1-methyl-1H-imidazol-5-yl)propanoic acid | 3-Methylhistidine | AKOS006274125 | DTXSID90920521 | 3-N-Methyl-L-histidine | EINECS 206-704-6 | Tau-methylhistidine | FD21706 | N(pros)-methyl-L-histidine | (
Storage
Room temperature
Shipped In
Normal
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Price
Qty
50mg
N137204-50mg
3

$55.90

$83.90
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100mg
N137204-100mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.

$98.90

$148.90
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250mg
N137204-250mg
3

$205.90

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1g
N137204-1g
3

$534.90

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5g
N137204-5g
1

$1,844.90

$2,767.90
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Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Room temperature Ships Normal Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 4 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyms
N3-Methyl-L-histidine | HY-W017007 | (2S)-2-amino-3-(1-methyl-1H-imidazol-5-yl)propanoic acid | 3-Methylhistidine | AKOS006274125 | DTXSID90920521 | 3-N-Methyl-L-histidine | EINECS 206-704-6 | Tau-methylhistidine | FD21706 | N(pros)-methyl-L-histidine | (
Specifications & Purity
≥98%
Biochemical and Physiological Mechanisms
3-Methyl-L-histidine is a non-proteinogenic amino acid and an index of muscle breakdown.
Storage
Room temperature
Shipped In
Normal
Purity
≥98%
Names and Identifiers
Pubchem Sid504753938
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504753938
Canonical SmilesCN1C=NC=C1CC(C(=O)O)N
IUPAC Name(2S)-2-amino-3-(3-methylimidazol-4-yl)propanoic acid
InChIKeyJDHILDINMRGULE-LURJTMIESA-N
INCHI1S/C7H11N3O2/c1-10-4-9-3-5(10)2-6(8)7(11)12/h3-4,6H,2,8H2,1H3,(H,11,12)/t6-/m0/s1
Isomeric SMILES CN1C=NC=C1C[C@@H](C(=O)O)N
WGK Germany 3
Molecular Weight 169.18
Reaxy-Rn 83652
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=83652&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

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🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
ClassCarboxylic acids and derivatives
SubclassAmino acids, peptides, and analogues
Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives
Direct ParentHistidine and derivatives
Alternative Parents L-alpha-amino acids  Imidazolyl carboxylic acids and derivatives  Aralkylamines  N-substituted imidazoles  Heteroaromatic compounds  Amino acids  Monocarboxylic acids and derivatives  Carboxylic acids  Azacyclic compounds  Organopnictogen compounds  Organic oxides  Monoalkylamines  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents Histidine or derivatives - Alpha-amino acid - L-alpha-amino acid - Imidazolyl carboxylic acid derivative - Aralkylamine - N-substituted imidazole - Azole - Imidazole - Heteroaromatic compound - Amino acid - Carboxylic acid - Azacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Primary amine - Primary aliphatic amine - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Carbonyl group - Organic oxygen compound - Amine - Aromatic heteromonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as histidine and derivatives. These are compounds containing cysteine or a derivative thereof resulting from reaction of cysteine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.
External Descriptors non-proteinogenic L-alpha-amino acid - L-histidine derivative
3D Structure
Interactive Chemical Structure Model





Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

13 results found

Lot NumberCertificate TypeDateItem
K2201597Certificate of AnalysisMay 11, 2026 N137204
K2201649Certificate of AnalysisMay 11, 2026 N137204
K2201652Certificate of AnalysisMay 11, 2026 N137204
F2206217Certificate of AnalysisDec 12, 2025 N137204
F2206218Certificate of AnalysisDec 12, 2025 N137204
F2206222Certificate of AnalysisDec 12, 2025 N137204
C2209192Certificate of AnalysisSep 09, 2025 N137204
L2402419Certificate of AnalysisDec 06, 2024 N137204
L2402445Certificate of AnalysisDec 06, 2024 N137204
K2201593Certificate of AnalysisAug 22, 2024 N137204
E1905164Certificate of AnalysisJan 15, 2023 N137204
I2503040Certificate of AnalysisMar 15, 2022 N137204
F2206216Certificate of AnalysisMar 09, 2022 N137204

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Chemical and Physical Properties
Melt Point(°C)254 °C
Molecular Weight169.180 g/mol
XLogP3-3.300
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count4
Rotatable Bond Count3
Exact Mass169.085 Da
Monoisotopic Mass169.085 Da
Topological Polar Surface Area81.100 Ų
Heavy Atom Count12
Formal Charge0
Complexity174.000
Isotope Atom Count0
Defined Atom Stereocenter Count1
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
References
1. Mingfa Sun, Hongchao Jiao, Jingpeng Zhao, Xiaojuan Wang, Haifang Li, Yunlei Zhou, Hai Lin.  (2022)  Research Note: Creatine monohydrate alleviates protein breakdown induced by corticosterone via inhibiting ubiquitin proteasome pathway in chicken myotubes.  POULTRY SCIENCE,      [PMID:36194918] [10.1016/j.psj.2022.102177]
2. Lili Zhang, Wen Duan, Yan Huang, Yuyu Zhang, Baoguo Sun, Dandan Pu, Yizhuang Tang, Chao Liu.  (2020)  Sensory taste properties of chicken (Hy-Line brown) soup as prepared with five different parts of the chicken.  INTERNATIONAL JOURNAL OF FOOD PROPERTIES,      [PMID:] [10.1080/10942912.2020.1828455]
3. Lu Wang, Limei Xiao, Shoujing Zheng, Jie Pang, Jiebo Chen.  (2024)  Characterization and assessment of free amino acids in different varieties of sugarcane.  INDUSTRIAL CROPS AND PRODUCTS,      [PMID:] [10.1016/j.indcrop.2024.118306]
4. Wenjun Zhang, Chuntao Dong, Zhaosheng Li, Huina Shi, Yijun Xu, Mingchen Zhu.  (2024)  Serum targeted metabolomics uncovering specific amino acid signature for diagnosis of intrahepatic cholangiocarcinoma.  JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS,      [PMID:39241676] [10.1016/j.jpba.2024.116457]
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