DL-Valine - ≥98% , CAS No.516-06-3

CAS: 516-06-3 Cat. No.: V104896 Molecular Weight: 117.15 Beilstein Registry Number: 506689 EC Number: 208-220-0
AVAILABLE TO ORDER
GRADE & PURITY ≥98%
Synonyms
(+/-)-2-AMINOISOVALERIC ACID | AKOS040764370 | HY-W012889 | NSC20654 | NSC-20654 | 8D785241-1AC3-4C14-8D43-308A8EA5169C | LMFA01100046 | 2-Amino-3-methylbutanoic acid, DL- | AS-11670 | L-VALINE-13C5, 15N | FT-0625632 | L-Valine-15N;59935-29-4;H-[15N]VAL-O
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
25g
V104896-25g
7

$9.90

$14.90
Save $5.00 (33.56%)
100g
V104896-100g
9

$15.90

$23.90
Save $8.00 (33.47%)
500g
V104896-500g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.

$65.90

$98.90
Save $33.00 (33.37%)
Enter a quantity for the sizes you want to add.
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Why this grade

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

🌡

Storage & shipping

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

📋

Quality documents

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

📚

Literature proof

Cited in 5 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyms
(+/-)-2-AMINOISOVALERIC ACID | AKOS040764370 | HY-W012889 | NSC20654 | NSC-20654 | 8D785241-1AC3-4C14-8D43-308A8EA5169C | LMFA01100046 | 2-Amino-3-methylbutanoic acid, DL- | AS-11670 | L-VALINE-13C5, 15N | FT-0625632 | L-Valine-15N;59935-29-4;H-[15N]VAL-O
Specifications & Purity
≥98%
Storage
Room temperature
Shipped In
Normal
Purity
≥98%
Names and Identifiers
Pubchem Sid488179608
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488179608
Canonical SmilesCC(C)C(C(=O)O)N
IUPAC Name2-amino-3-methylbutanoic acid
InChIKeyKZSNJWFQEVHDMF-UHFFFAOYSA-N
INCHI1S/C5H11NO2/c1-3(2)4(6)5(7)8/h3-4H,6H2,1-2H3,(H,7,8)
Isomeric SMILES CC(C)C(C(=O)O)N
WGK Germany 1
Molecular Weight 117.15
Beilstein 506689
Reaxy-Rn 506689
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=506689&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 ParentValine and derivatives
Alternative Parents Alpha amino acids  Methyl-branched fatty acids  Amino acids  Monocarboxylic acids and derivatives  Carboxylic acids  Organopnictogen compounds  Organic oxides  Monoalkylamines  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents Valine or derivatives - Alpha-amino acid - Branched fatty acid - Methyl-branched fatty acid - Fatty acid - Fatty acyl - Amino acid - Carboxylic acid - Monocarboxylic acid or derivatives - Organopnictogen compound - Primary amine - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Primary aliphatic amine - Carbonyl group - Organic oxygen compound - Amine - Organic oxide - Hydrocarbon derivative - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as valine and derivatives. These are compounds containing valine or a derivative thereof resulting from reaction of valine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.
External Descriptors Amino fatty acids
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
K2105413Certificate of AnalysisAug 12, 2025 V104896
C2414816Certificate of AnalysisMar 02, 2024 V104896
B2401045Certificate of AnalysisFeb 20, 2024 V104896
C2317024Certificate of AnalysisMar 29, 2023 V104896
E2308625Certificate of AnalysisMar 29, 2023 V104896
B2303928Certificate of AnalysisFeb 09, 2023 V104896
E2308608Certificate of AnalysisDec 08, 2022 V104896
K2230929Certificate of AnalysisDec 08, 2022 V104896
J1810093Certificate of AnalysisAug 08, 2022 V104896
K2320167Certificate of AnalysisAug 08, 2022 V104896
Chemical and Physical Properties
SensitivityMoisture sensitive.
Melt Point(°C)295°C
Molecular Weight117.150 g/mol
XLogP3-2.300
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count3
Rotatable Bond Count2
Exact Mass117.079 Da
Monoisotopic Mass117.079 Da
Topological Polar Surface Area63.300 Ų
Heavy Atom Count8
Formal Charge0
Complexity90.400
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count1
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. Yahui Yin, Weiping Liu, Xia Li, Yu Zhou, Xianzhen Xu.  (2023)  VLE determination and microscopic properties of amino acid aqueous solutions.  JOURNAL OF MOLECULAR LIQUIDS,      [PMID:] [10.1016/j.molliq.2023.122963]
2. Qing Xiong, Jing Jin, Liqiong Lv, Zhisi Bu, Shengqiang Tong.  (2018)  Chiral ligand exchange countercurrent chromatography: Enantioseparation of amino acids.  JOURNAL OF SEPARATION SCIENCE,  41  (6): (1479-1488).  [PMID:29323783] [10.1002/jssc.201701117]
3. Zhou Mengyan, Zhang Zhihui, Zheng Qi, Yu Mingdi, Si Mengxu, Wu Sirui, Zhang Yanan, Ding Shushu, Fu Ding-Yi.  (2025)  Ratiometric fluorescence quantification of folic acid utilizing D-penicillamine-based carbon dots in conjunction with glutathione S-transferase-Au nanoclusters.  MICROCHIMICA ACTA,  192  (4): (1-13).  [PMID:40080078] [10.1007/s00604-025-07062-8]
4. Xiaorong Hao, Zhehao Sun, Chen Hu, Ziyi Wang, Kangning Wang, Shaokun Chong, Zongyou Yin, Zhengqing Liu, Wei Huang.  (2025)  Chiral-driven synergistic electrolyte engineering for ultrastable aqueous zinc-ion batteries.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2025.166777]
5. Jian Zhang, Qi Zhang, Jiaxin Li, Zhihong Zheng, Yanqing Miao, Chunye Liu.  (2026)  Dual-modified gold nanoparticles with nitrogen-doped carbon quantum dots and aspartic acid as response system: A paper-based fluorescence sensing platform for selective cysteine identification.  TALANTA,      [PMID:] [10.1016/j.talanta.2026.129710]
Solution Calculators
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