N-Acetyle-D-Leucine - ≥99% , CAS No.19764-30-8

CAS: 19764-30-8 Cat. No.: A106206 Molecular Weight: 173.21 EC Number: 896-508-2
AVAILABLE TO ORDER
GRADE & PURITY ≥99%
Synonyms
Ac-D-Leu-OH | Leucine, N-acetyl-, D- | HY-Y1080 | AC-22376 | Acetylleucine, D- | BRD-K05831461-001-01-8 | WXNXCEHXYPACJF-SSDOTTSWSA-N | EN300-321381 | NCGC00094935-02 | 91WU82GA22 | A20910 | (R)-acetylleucine | N-acetyl-(D)-leucine | SCHEMBL714003 | AKOS0
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
1g
A106206-1g
5
$9.90
5g
A106206-5g
4
$10.90
25g
A106206-25g
3

$28.90

$43.90
Save $15.00 (34.17%)
100g
A106206-100g
3

$34.90

$52.90
Save $18.00 (34.03%)
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Why this grade

≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -20°C Ships Ice chest + Ice pads 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.

📚

Literature proof

Cited in 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

N-Acetyl-D-leucine may be used with other D-aminoacylated amino acids as a substrate for the identification, differentiation and characterization of D-aminoacylase(s)/amidohydrolase(s).

Specifications

Synonyms
Ac-D-Leu-OH | Leucine, N-acetyl-, D- | HY-Y1080 | AC-22376 | Acetylleucine, D- | BRD-K05831461-001-01-8 | WXNXCEHXYPACJF-SSDOTTSWSA-N | EN300-321381 | NCGC00094935-02 | 91WU82GA22 | A20910 | (R)-acetylleucine | N-acetyl-(D)-leucine | SCHEMBL714003 | AKOS0
Specifications & Purity
≥99%
Biochemical and Physiological Mechanisms
N-Acetyl-D-leucine is a substrate for D-aminoacylase from Alcaligenes xylosoxydans subsp. xylosoxydans A-6. N-Acetyl-D-leucine is used to help differentiate members of the amidohydrolase enzyme superfamily. It is a preferred substrate of Gox1177 from Gluc
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Purity
≥99%
Names and Identifiers
Pubchem Sid504760430
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504760430
Canonical SmilesCC(C)CC(C(=O)O)NC(=O)C
IUPAC Name(2R)-2-acetamido-4-methylpentanoic acid
InChIKeyWXNXCEHXYPACJF-SSDOTTSWSA-N
INCHI1S/C8H15NO3/c1-5(2)4-7(8(11)12)9-6(3)10/h5,7H,4H2,1-3H3,(H,9,10)(H,11,12)/t7-/m1/s1
Isomeric SMILES CC(C)C[C@H](C(=O)O)NC(=O)C
WGK Germany 3
Molecular Weight 173.21
Reaxy-Rn 1724848
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1724848&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.

View datasheet →

🔬 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 ParentLeucine and derivatives
Alternative Parents N-acyl-alpha amino acids  Methyl-branched fatty acids  Acetamides  Secondary carboxylic acid amides  Monocarboxylic acids and derivatives  Carboxylic acids  Organopnictogen compounds  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents Leucine or derivatives - N-acyl-alpha-amino acid - N-acyl-alpha amino acid or derivatives - Branched fatty acid - Methyl-branched fatty acid - Fatty acyl - Fatty acid - Acetamide - Carboxamide group - Secondary carboxylic acid amide - Carboxylic acid - Monocarboxylic acid or derivatives - Organonitrogen compound - Organic oxide - Organopnictogen compound - Organic nitrogen compound - Organic oxygen compound - Carbonyl group - Organooxygen compound - Hydrocarbon derivative - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as leucine and derivatives. These are compounds containing leucine or a derivative thereof resulting from reaction of leucine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





Mechanisms of Action
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.

10 results found

Lot NumberCertificate TypeDateItem
G1817001Certificate of AnalysisFeb 05, 2026 A106206
J2121060Certificate of AnalysisAug 11, 2025 A106206
J2121061Certificate of AnalysisAug 11, 2025 A106206
J2121062Certificate of AnalysisAug 11, 2025 A106206
B1714042Certificate of AnalysisSep 03, 2024 A106206
A2513233Certificate of AnalysisJun 15, 2024 A106206
A2521191Certificate of AnalysisJun 15, 2024 A106206
B2324066Certificate of AnalysisMar 03, 2023 A106206
B2324089Certificate of AnalysisOct 11, 2021 A106206
B2324383Certificate of AnalysisOct 11, 2021 A106206
Chemical and Physical Properties
Specific Rotation[α]23 ° (C=4, EtOH)
Molecular Weight173.210 g/mol
XLogP30.500
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count3
Rotatable Bond Count4
Exact Mass173.105 Da
Monoisotopic Mass173.105 Da
Topological Polar Surface Area66.400 Ų
Heavy Atom Count12
Formal Charge0
Complexity177.000
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. Yaoguo Wang, Jie Sun, Weiwei Tang, Junbo Gong.  (2023)  Green chiral separation of racemic mixture via crystallization induced deracemization process synergistically intensified by ultrasound and temperature cycling.  CHEMICAL ENGINEERING SCIENCE,      [PMID:] [10.1016/j.ces.2023.119115]
Solution Calculators
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