Diethylphosphonoacetic acid - ≥95% , CAS No.3095-95-2

CAS: 3095-95-2 Cat. No.: D122564 Peso molecular: 196.14 Número EC: 608-560-3
Disponible para pedir
GRADE & PURITY ≥95%
Synonyms
AMY31094 | FT-0745335 | [bis(ethyloxy)phosphoryl]acetic acid | EN300-143507 | 2-(diethyl phosphono)acetic acid | Diethylphosphonoacetic acid, 95% | DIETHYL PHOSPHONOACETATE | Acetic acid, (diethoxyphosphinyl)- | NSC272281 | NSC-272281 | 2-(Diethoxyphospho
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1ml
D122564-1ml
5
9,90US$
5ml
D122564-5ml
3
10,90US$
25ml
D122564-25ml
2
39,90US$
100ml
D122564-100ml
1
73,90US$
Enter a quantity for the sizes you want to add.
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Why this grade

≥95% 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.

Descripción general

Acts as a nucleophile for nucleophilic addition reactions for synthesis of allene epoxides Reactant for: Stereoselectivity studies of the Staudinger reaction Enantioselective formation of diols via epoxidation and hydration reactions Horner-Wadsworth-Emmons reactions Remote chelation controlled Ireland-Claisen rearrangement Ugi-Dieckmann reactions for synthesis of tetramic acid derivatives


application:

Acts as a nucleophile for nucleophilic addition reactions for synthesis of allene epoxides

Reactant for:

Stereoselectivity studies of the Staudinger reaction

Enantioselective formation of diols via epoxidation and hydration reactions

Horner-Wadsworth-Emmons reactions

Remote chelation controlled Ireland-Claisen rearrangement

Ugi-Dieckmann reactions for synthesis of tetramic acid derivatives

Used to make phosphonoester intermediates for intramolecular HEW reactions.

Specifications

Sinónimos
AMY31094 | FT-0745335 | [bis(ethyloxy)phosphoryl]acetic acid | EN300-143507 | 2-(diethyl phosphono)acetic acid | Diethylphosphonoacetic acid, 95% | DIETHYL PHOSPHONOACETATE | Acetic acid, (diethoxyphosphinyl)- | NSC272281 | NSC-272281 | 2-(Diethoxyphospho
Especificaciones y pureza
≥95%
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
Normal
Pureza
≥95%
Nombres e identificadores
Pubchem Sid488183281
Sonrisas canónicasCCOP(=O)(CC(=O)O)OCC
IUPAC Name2-diethoxyphosphorylacetic acid
InChIKeyDVQMPWOLBFKUMM-UHFFFAOYSA-N
INCHI1S/C6H13O5P/c1-3-10-12(9,11-4-2)5-6(7)8/h3-5H2,1-2H3,(H,7,8)
Isómeros SMILES CCOP(=O)(CC(=O)O)OCC
WGK Alemania 3
Peso molecular 196.14
Reaxy-Rn 1239303
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1239303&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
ClaseOrganic phosphonic acids and derivatives
SubclassPhosphonic acid diesters
Intermediate Tree Nodes Not available
Direct ParentDialkyl alkylphosphonates
Alternative Parents Phosphonic acid esters  Monocarboxylic acids and derivatives  Carboxylic acids  Organopnictogen compounds  Organophosphorus compounds  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents Dialkyl alkylphosphonate - Phosphonic acid ester - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organophosphorus compound - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
DescripciónThis compound belongs to the class of organic compounds known as dialkyl alkylphosphonates. These are compounds containing a phosphonic acid that is diesterified with alkyl groups, and the phosphorus atom is also directly attached to an alkyl group.
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.

7 results found

Lot NumberCertificate TypeFechaArticulo
K2119282Certificate of AnalysisSep 09, 2025 D122564
K2119283Certificate of AnalysisSep 09, 2025 D122564
K2119302Certificate of AnalysisSep 09, 2025 D122564
K1928055Certificate of AnalysisSep 11, 2023 D122564
D2312243Certificate of AnalysisAug 31, 2021 D122564
E2308146Certificate of AnalysisAug 31, 2021 D122564
F2317941Certificate of AnalysisAug 31, 2021 D122564
Propiedades químicas y físicas
Índice de refracción1.445
Punto de inflamación (°F)>110℃
Punto de inflamación (°C)>110℃
Punto de ebullición (°C)150°C/0.05mmHg
Peso molecular196.140 g/mol
XLogP3-0.200
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count5
Rotatable Bond Count6
Exact Mass196.05 Da
Monoisotopic Mass196.05 Da
Topological Polar Surface Area72.800 Ų
Heavy Atom Count12
Formal Charge0
Complexity180.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Calculadoras de soluciones
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