L-Valine - UltraBio™, ≥99.5%(NT) , CAS No.72-18-4

CAS: 72-18-4 Cat. No.: L755656 分子式: C5H11NO2 分子量: 117.15 Beilstein Registry Number: 1721136 EC番号: 200-773-6
注文可能
グレード&純度 UltraBio™ ? UltraBio™ — Aladdin's line for molecular-biology applications. Use for nuclease-free, high-consistency reagents across molecular workflows. ≥99.5%(NT)
Synonyms
L-2-Aminoisovaleric Acid | val | valine | (S)-Valine | H-Val-OH | (S)-(+)-Valine
Storage
Room temperature
Shipped In
Normal
★
サイズ
USA
ドイツ (EU)*
価格
個数
5g
L755656-5g
2 在庫あり
—
$51.90
25g
L755656-25g
2 在庫あり
—
$151.90
100g
L755656-100g
2 在庫あり
1 在庫あり
$399.90
Enter a quantity for the sizes you want to add.
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このグレードを選ぶ理由

UltraBio™, ≥99.5%(NT) UltraBio™ ベースライン干渉を最小限に抑える必要がある、感度の高いクロマトグラフィーおよび分析ワークフロー向け。

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保管・配送

Room temperature Normal に出荷。正確な仕様については、ロット固有の COA をご確認ください。

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品質書類

SDS、COA、データシート、仕様書をダウンロードできます。ロット固有の COA はロット番号検索で入手可能です。

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文献的裏付け

クロマトグラフィー、有機合成、クロスカップリング反応に関する 280 件の査読済み論文で引用されています。

概要


  • Metabolomics reveals metabolites associated with hair follicle cycle in cashmere goats.: This study utilizes L-Valine as a standard for detecting, understanding, and enhancing hair follicle cycles in cashmere goats through metabolomic analysis, aiding in the improvement of fiber production and quality (Ma et al., 2024).

仕様

同義語
L-2-Aminoisovaleric Acid | val | valine | (S)-Valine | H-Val-OH | (S)-(+)-Valine
仕様と純度
UltraBio™, ≥99.5%(NT)
保管条件
Room temperature
入荷
Normal
等級
UltraBio™
純度
≥99.5%(NT)
名前と識別子
パブケム・シド
カノニカル・スマイル
CC(C)C(C(=O)O)N
IUPAC Name
(2S)-2-amino-3-methylbutanoic acid
InChIKey
KZSNJWFQEVHDMF-BYPYZUCNSA-N
INCHI
1S/C5H11NO2/c1-3(2)4(6)5(7)8/h3-4H,6H2,1-2H3,(H,7,8)/t4-/m0/s1
異性体SMILES
CC(C)[C@@H](C(=O)O)N
代替CAS番号
7004-03-7
分子量
117.15
Beilstein
1721136
Reaxy-Rn
506689
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=506689&ln=

ドキュメント

📋 安全データシート(SDS)

危険性、取扱い、保管、および規制遵守を網羅した包括的な文書。

<<<<<<< HEAD SDS をダウンロード → ======= SDS をダウンロード → >>>>>>> release248-p3

✅ 分析証明書(COA)

ロット固有の品質データ。ロット番号を入力して、正確な COA を取得してください。

COA を検索 →

📊 データシート

製品仕様と用途のクイックリファレンス概要。

データシートを見る →

🔬 仕様書

このグレードの完全な品質特性と合格基準。

仕様書を見る →

詳細データ

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
分類Carboxylic 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 L-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 - L-alpha-amino acid - Branched fatty acid - Methyl-branched fatty acid - Fatty acid - Fatty acyl - Amino acid - Monocarboxylic acid or derivatives - Carboxylic acid - Organic oxide - Organopnictogen compound - Primary amine - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Carbonyl group - Organic oxygen compound - Amine - Organic nitrogen compound - Hydrocarbon derivative - Aliphatic acyclic compound
説明This 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 Common amino acids
3 D構造
インタラクティブ化学構造モデル





証明書(CoA、COO、BSE/TSEと分析図)
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.

8 results found

Lot NumberCertificate Type日付商品
D2522382D2522382Certificate of AnalysisApr 28, 2025 L755656
D2522383D2522383Certificate of AnalysisApr 28, 2025 L755656
D2522392D2522392Certificate of AnalysisApr 28, 2025 L755656
D2522393D2522393Certificate of AnalysisApr 28, 2025 L755656
D2522398D2522398Certificate of AnalysisApr 28, 2025 L755656
D2522399D2522399Certificate of AnalysisApr 28, 2025 L755656
I2603456I2603456Certificate of AnalysisApr 28, 2025 L755656
K2528044K2528044Certificate of AnalysisApr 28, 2025 L755656
化学的性質と物理的性質
溶解度1 M HCl: 0.5 M at 20 °C, clear, colorless
比旋光度[α]28° (C=8,HCl(1+1))
融点(°C)315°C
分子量117.150 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 Count1
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
よくある質問と記事
UltraBio™: Defining Excellence in Molecular Biology Applications
β-Acyloxy Alkenyl Amides (AAAs): A New Approach to Amide Bond and Peptide Bond Construction Worth Attention
Silicon Reagent-Assisted Peptide Synthesis: Research Progress and Methodological Value of Peptide Bond Formation from Unprotected Substrates
From Analytical Instrument to Synthetic Platform: A New Strategy for Reconstructing Automated Flow Solid-Phase Peptide Synthesis with Standard Analytical HPLC
Reassessing Trimethylaluminum: Method Design and Experimental Value of One-Pot Peptide Elongation from Unprotected Amino Acids
Low-Racemization Control in Peptide Synthesis: An Inverse N→C Peptide Synthesis Strategy via Activated α-Aminoesters
Methods and Applications for the Determination of Amino Acid Content and Composition
Experimental Assessment of Fmoc Introduction Routes: Impurity Profile Differences, Raw Material Carryover, and Quality Control
Analysis of Hydrolyzed Pearl as a Cosmetic Raw Material: Preparation Process, Active Components, and Skincare Formulation Applications
Acetyl Tetrapeptide-2 and Elastic Fiber Formation: Research on Fibulin-5, LOXL1, and Skin Firmness
Sources, Host-Regulatory Mechanisms, and Tumor-Immune Effects of Gut Microbiota-Derived Metabolites
Catalytic Mechanisms of the Aminotransferase Family and Regulation of Amino Acid Metabolism
Citations of This Product
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