Boc-L-alanina - ≥98% , CAS No.15761-38-3

CAS: 15761-38-3 Cat. No.: B109000 Peso molecular: 189.21 Beilstein Registry Number: 1726365 Número EC: 239-847-8
Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
Boc-Ala-OH | EINECS 239-847-8 | N-t-butoxycarbonyl alanine | (S)-2-((tert-Butoxycarbonyl)amino)propanoic acid | (S)-2-((TERT-BUTOXYCARBONYL)AMINO)PROPIONIC ACID | 1-phenylsulphonylindole-3-carboxaldehyde | (2S)-2-[(tert-butoxycarbonyl)amino]propanoic acid
Storage
Conservar a 2-8°C
Shipped In
Hielo húmedo
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
5g
B109000-5g
1
9,90US$
10g
B109000-10g
2
10,90US$
25g
B109000-25g
1

11,90US$

17,90US$
Guardar 6,00 US$ (33.52%)
100g
B109000-100g
1

14,90US$

22,90US$
Guardar 8,00 US$ (34.93%)
250g
B109000-250g
3

32,90US$

49,90US$
Guardar 17,00 US$ (34.07%)
500g
B109000-500g
1

45,90US$

68,90US$
Guardar 23,00 US$ (33.38%)
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

Conservar a 2-8°C Ships Hielo húmedo 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 7 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
Boc-Ala-OH | EINECS 239-847-8 | N-t-butoxycarbonyl alanine | (S)-2-((tert-Butoxycarbonyl)amino)propanoic acid | (S)-2-((TERT-BUTOXYCARBONYL)AMINO)PROPIONIC ACID | 1-phenylsulphonylindole-3-carboxaldehyde | (2S)-2-[(tert-butoxycarbonyl)amino]propanoic acid
Especificaciones y pureza
≥98%
Condiciones de almacenamiento de almacenamiento
Conservar a 2-8°C
Enviado en
Hielo húmedo
Pureza
≥98%
Nombres e identificadores
Pubchem Sid504755789
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504755789
Sonrisas canónicasCC(C(=O)O)NC(=O)OC(C)(C)C
IUPAC Name(2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid
InChIKeyQVHJQCGUWFKTSE-YFKPBYRVSA-N
INCHI1S/C8H15NO4/c1-5(6(10)11)9-7(12)13-8(2,3)4/h5H,1-4H3,(H,9,12)(H,10,11)/t5-/m0/s1
Isómeros SMILES C[C@@H](C(=O)O)NC(=O)OC(C)(C)C
WGK Alemania 3
Peso molecular 189.21
Beilstein 1726365
Reaxy-Rn 1103973
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1103973&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
ClaseCarboxylic acids and derivatives
SubclassAmino acids, peptides, and analogues
Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives
Direct ParentAlanine and derivatives
Alternative Parents Carbamate esters  Organic carbonic acids and derivatives  Monocarboxylic acids and derivatives  Carboxylic acids  Organopnictogen compounds  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents Alanine or derivatives - Carbamic acid ester - Carbonic acid derivative - Monocarboxylic acid or derivatives - Carboxylic acid - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - Aliphatic acyclic compound
DescripciónThis compound belongs to the class of organic compounds known as alanine and derivatives. These are compounds containing alanine or a derivative thereof resulting from reaction of alanine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Certificados (CoA, COO, BSE/TSE y tabla de análisis)
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.

18 results found

Lot NumberCertificate TypeFechaArticulo
L2121373Certificate of AnalysisOct 13, 2025 B109000
L2121132Certificate of AnalysisOct 13, 2025 B109000
L2121130Certificate of AnalysisOct 13, 2025 B109000
L2121126Certificate of AnalysisOct 13, 2025 B109000
A1825043Certificate of AnalysisAug 18, 2025 B109000
E2128213Certificate of AnalysisMar 04, 2025 B109000
E2128214Certificate of AnalysisMar 04, 2025 B109000
G2416351Certificate of AnalysisApr 10, 2024 B109000
G2416352Certificate of AnalysisApr 10, 2024 B109000
G2416350Certificate of AnalysisApr 10, 2024 B109000
D2615138Certificate of AnalysisApr 10, 2024 B109000
G2425119Certificate of AnalysisApr 10, 2024 B109000
G2425120Certificate of AnalysisApr 10, 2024 B109000
G2425121Certificate of AnalysisApr 10, 2024 B109000
D2403018Certificate of AnalysisNov 11, 2021 B109000
D2403017Certificate of AnalysisNov 11, 2021 B109000
D2403016Certificate of AnalysisNov 11, 2021 B109000
D2403015Certificate of AnalysisNov 11, 2021 B109000

Show more ⌵

Propiedades químicas y físicas
Rotación específica [α]-25.5 ° (C=2, AcOH)
Punto de fusión (°C)79-83°C
Peso molecular189.210 g/mol
XLogP30.900
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count4
Rotatable Bond Count4
Exact Mass189.1 Da
Monoisotopic Mass189.1 Da
Topological Polar Surface Area75.600 Ų
Heavy Atom Count13
Formal Charge0
Complexity207.000
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
Preguntas frecuentes y artículos
Citations of This Product
Referencias
1. Lianjie Ren, Jingjing Li, Lisha Liu, Wantao Wu, Di Zhao, Kai Zhang, Xiaofei Xin, Lei Yang, Lifang Yin.  (2021)  Resolving hepatic fibrosis via suppressing oxidative stress and an inflammatory response using a novel hyaluronic acid modified nanocomplex.  Biomaterials Science,  (24): (8259-8269).  [PMID:34761752] [10.1039/D1BM01499D]
2. Lijie Yin, Huimin Duan, Tao Chen, Dongming Qi, Jianping Deng.  (2021)  Amino-acid-substituted polyacetylene-based chiral core–shell microspheres: helix structure induction and application for chiral resolution and adsorption.  Polymer Chemistry,  12  (44): (6404-6416).  [PMID:] [10.1039/D1PY01067K]
3. Yanli Zhou, Chunhong Zhang, Rui Ma, Lijia Liu, Hongxing Dong, Toshifumi Satoh, Yoshio Okamoto.  (2019)  Synthesis of helical poly(phenylacetylene) derivatives bearing diastereomeric pendants for enantioseparation by HPLC.  NEW JOURNAL OF CHEMISTRY,  43  (8): (3439-3446).  [PMID:] [10.1039/C8NJ05579C]
4. Huajun Huang, Yunbin Yuan, Jianping Deng.  (2015)  Helix-Sense-Selective Precipitation Polymerization of Achiral Monomer for Preparing Optically Active Helical Polymer Particles.  MACROMOLECULES,      [PMID:] [10.1021/acs.macromol.5b00811]
5. Huajun Huang, Wantai Yang, Jianping Deng.  (2015)  Chiral, fluorescent microparticles constructed by optically active helical substituted polyacetylene: preparation and enantioselective recognition ability.  RSC Advances,  (33): (26236-26245).  [PMID:] [10.1039/C4RA16466K]
6. Zhihuang Zhang, Yan Peng, Liyan Qiu.  (2024)  Rigid nanoparticles for efficient tumor immunotherapy through mechanical force mediated reprogramming of tumor-associated macrophages.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2024.152129]
7. Tong He, Gelin Liu, Wei Gao, Yafang Ding, Yu Qin, Jianzhong Shen, Zhanhui Wang, Kai Wen.  (2026)  Development of monoclonal antibody and immunoassays for determination of florylpicoxamid in foods: A sub-similarity principle for guiding the hapten design.  JOURNAL OF HAZARDOUS MATERIALS,      [PMID:41548306] [10.1016/j.jhazmat.2026.141167]
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