(S)-2-(Boc-amino)butyric acid - ≥97% , CAS No.34306-42-8

CAS: 34306-42-8 Cat. No.: A115872 Molecular Weight: 203.24 Beilstein Registry Number: 6801706 EC Number: 696-164-1
AVAILABLE TO ORDER
GRADE & PURITY ≥97%
Synonyms
(S)-2-(Tert-butoxycarbonylamino)butyric acid | Boc-Abu-OH | BOC-homoalanine | N-tert-Butoxycarbonyl-L-alpha-aminobutanoic acid | AKOS016842311 | (2S)-2-({[(1,1-dimethylethyl)oxy]carbonyl}amino)butanoic acid | Boc-L-Abu-OH | (2S)-2-[(tert-butoxycarbonyl)am
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
1g
A115872-1g
5

$9.90

$14.90
Save $5.00 (33.56%)
5g
A115872-5g
10

$12.90

$19.90
Save $7.00 (35.18%)
10g
A115872-10g
3

$17.90

$26.90
Save $9.00 (33.46%)
25g
A115872-25g
8

$35.90

$53.90
Save $18.00 (33.40%)
100g
A115872-100g
10

$54.90

$82.90
Save $28.00 (33.78%)
500g
A115872-500g
1

$71.90

$107.90
Save $36.00 (33.36%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥97% 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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

application:

It is employed as a intermediate for pharmaceutical.

Specifications

Synonyms
(S)-2-(Tert-butoxycarbonylamino)butyric acid | Boc-Abu-OH | BOC-homoalanine | N-tert-Butoxycarbonyl-L-alpha-aminobutanoic acid | AKOS016842311 | (2S)-2-({[(1, 1-dimethylethyl)oxy]carbonyl}amino)butanoic acid | Boc-L-Abu-OH | (2S)-2-[(tert-butoxycarbonyl)am
Specifications & Purity
≥97%
Storage
Room temperature
Shipped In
Normal
Purity
≥97%
Names and Identifiers
Pubchem Sid488192971
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488192971
Canonical SmilesCCC(C(=O)O)NC(=O)OC(C)(C)C
IUPAC Name(2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]butanoic acid
InChIKeyPNFVIPIQXAIUAY-LURJTMIESA-N
INCHI1S/C9H17NO4/c1-5-6(7(11)12)10-8(13)14-9(2,3)4/h6H,5H2,1-4H3,(H,10,13)(H,11,12)/t6-/m0/s1
Isomeric SMILES CC[C@@H](C(=O)O)NC(=O)OC(C)(C)C
WGK Germany 3
Molecular Weight 203.24
Beilstein 6801706
Reaxy-Rn 2366635
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2366635&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
Direct ParentAlpha amino acids and derivatives
Alternative Parents Branched fatty acids  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 Alpha-amino acid or derivatives - Branched fatty acid - Fatty acyl - Fatty acid - Carbamic acid ester - Carbonic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Carbonyl group - Organic oxygen compound - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as alpha amino acids and derivatives. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon), or a derivative thereof.
External Descriptors Not available
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.

14 results found

Lot NumberCertificate TypeDateItem
G2219038Certificate of AnalysisMay 08, 2026 A115872
G2219039Certificate of AnalysisMay 08, 2026 A115872
G2219040Certificate of AnalysisMay 08, 2026 A115872
G2219055Certificate of AnalysisMay 08, 2026 A115872
G2219056Certificate of AnalysisMay 08, 2026 A115872
G1818079Certificate of AnalysisFeb 05, 2026 A115872
A2125457Certificate of AnalysisDec 04, 2024 A115872
E1616027Certificate of AnalysisJan 15, 2024 A115872
E2312125Certificate of AnalysisMay 17, 2023 A115872
B2328288Certificate of AnalysisMar 07, 2023 A115872
E2312121Certificate of AnalysisJun 10, 2022 A115872
E2312145Certificate of AnalysisJun 10, 2022 A115872
G2502027Certificate of AnalysisJun 10, 2022 A115872
I2506048Certificate of AnalysisJun 10, 2022 A115872

Show more ⌵

Chemical and Physical Properties
SolubilitySlightly soluble in water
Specific Rotation[α]-19° (C=1,MeOH)
Melt Point(°C)70-74°C
Molecular Weight203.240 g/mol
XLogP31.500
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count4
Rotatable Bond Count5
Exact Mass203.116 Da
Monoisotopic Mass203.116 Da
Topological Polar Surface Area75.600 Ų
Heavy Atom Count14
Formal Charge0
Complexity219.000
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
Solution Calculators
Reviews

Customer Reviews

Shall we send you a message when we have discounts available?

Remind me later

Thank you! Please check your email inbox to confirm.

Oops! Notifications are disabled.