Name: N,N-Dimethylformamide (DMF) - BioReagent, ≥99.9% , CAS No.68-12-2
Brand: Aladdin Scientific
SKU: D112007
Availability: InStock

Spécifications Noms et identifiants Documentation Données avancées Taxonomic Classification Structure 3D Cibles associées (humaines) Cibles associées (non humaines) Mécanismes d'action Certificats (CoA, COO, BSE/TSE et tableau d'analyse) Propriétés chimiques et physiques FAQ et articles Citations of This Product Calculateurs de solution Avis

🧪

Pourquoi cette qualité

BioReagent, ≥99.9% BioReagent pour les flux de travail chromatographiques et analytiques sensibles nécessitant une interférence de ligne de base minimale.

🌡

Stockage & expédition

Room temperature,Argon charged Expédition FedEx DG Service. Consultez le COA spécifique au lot pour les spécifications exactes.

📋

Documents qualité

SDS, COA, fiche technique et fiche de spécifications disponibles au téléchargement. COA spécifique au lot accessible via la recherche par numéro de lot.

📚

Preuve documentaire

Cité dans 9509 publications à comité de lecture couvrant la chromatographie, la synthèse organique et les réactions de couplage croisé.

Spécifications

Synonymes

Spécifications et pureté

BioReagent, ≥99.9%

Conditions de stockage de stockage

Room temperature,Argon charged

Expédié en

FedEx DG Service

Grade

BioReagent

Pureté

≥99.9%

Noms et identifiants

Pubchem Sid

508811024

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/508811024

Sourires canoniques

CN(C)C=O

IUPAC Name

N,N-dimethylformamide

InChIKey

ZMXDDKWLCZADIW-UHFFFAOYSA-N

INCHI

1S/C3H7NO/c1-4(2)3-5/h3H,1-2H3

Isomères SMILES

CN(C)C=O

WGK Allemagne

RTECS

LQ2100000

Numéro ONU

2265

Groupe d'emballage

III

Poids moléculaire

73.09

Beilstein

605365

Reaxy-Rn

605365

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=605365&ln=

Documentation

📋 Fiche de données de sécurité (FDS)

Document complet couvrant les dangers, la manipulation, le stockage et la conformité réglementaire.

<<<<<<< HEAD Télécharger la SDS → ======= Télécharger la SDS → >>>>>>> release248-p3

✅ Certificat d'analyse (COA)

Données qualité spécifiques au lot. Saisissez votre numéro de lot pour récupérer le COA exact.

Rechercher le COA →

📊 Fiche technique

Résumé de référence rapide des spécifications et applications du produit.

Voir la fiche technique →

🔬 Fiche de spécifications

Attributs de qualité complets et critères d'acceptation pour cette qualité.

Voir la fiche de spécifications →

Données avancées

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organic acids and derivatives
  - Classe Carboxylic acids and derivatives
    - Subclass Carboxylic acid derivatives
      - Level5 Carboxylic acid amides
        Level6 Tertiary carboxylic acid amides

Kingdom	Organic compounds
Superclass	Organic acids and derivatives
Classe	Carboxylic acids and derivatives
Subclass	Carboxylic acid derivatives
Intermediate Tree Nodes	Carboxylic acid amides
Direct Parent	Tertiary carboxylic acid amides
Alternative Parents	Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework	Aliphatic acyclic compounds
Substituents	Tertiary carboxylic acid amide - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - Aliphatic acyclic compound
Description	This compound belongs to the class of organic compounds known as tertiary carboxylic acid amides. These are compounds containing an amide derivative of carboxylic acid, with the general structure RN(R1)C(R2)=O (R1-R2 any atom but H).
External Descriptors	a small molecule
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Structure 3D

Cibles associées (humaines)

PDE5A Tclin Phosphodiesterase 5A (5113 Activities)

Discover Target: PDE5A

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

EGFR Tclin Epidermal growth factor receptor erbB1 (33727 Activities)

Discover Target: EGFR

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CA2 Tclin Carbonic anhydrase II (17698 Activities)

Discover Target: CA2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ESR1 Tclin Estrogen receptor alpha (17718 Activities)

Discover Target: ESR1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

HMGCR Tclin HMG-CoA reductase (2475 Activities)

Discover Target: HMGCR

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

NR3C1 Tclin Glucocorticoid receptor (14987 Activities)

Discover Target: NR3C1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

INSR Tclin Insulin receptor (5558 Activities)

Discover Target: INSR

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

PGR Tclin Progesterone receptor (8562 Activities)

Discover Target: PGR

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ADRB2 Tclin Beta-2 adrenergic receptor (11824 Activities)

Discover Target: ADRB2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CHRM2 Tclin Muscarinic acetylcholine receptor M2 (10671 Activities)

Discover Target: CHRM2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ADRB1 Tclin Beta-1 adrenergic receptor (6630 Activities)

Discover Target: ADRB1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

HTR1A Tclin Serotonin 1a (5-HT1a) receptor (14969 Activities)

Discover Target: HTR1A

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ADRA2A Tclin Alpha-2a adrenergic receptor (9450 Activities)

Discover Target: ADRA2A

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

AR Tclin Androgen Receptor (11781 Activities)

Discover Target: AR

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)

Discover Target: CHRM1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ACE Tclin Angiotensin-converting enzyme (1423 Activities)

Discover Target: ACE

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

DRD2 Tclin Dopamine D2 receptor (23596 Activities)

Discover Target: DRD2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

TSHR Tclin Thyroid stimulating hormone receptor (29986 Activities)

Discover Target: TSHR

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

MAOA Tclin Monoamine oxidase A (11911 Activities)

Discover Target: MAOA

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CNR1 Tclin Cannabinoid CB1 receptor (20913 Activities)

Discover Target: CNR1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

DRD1 Tclin Dopamine D1 receptor (9720 Activities)

Discover Target: DRD1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

DRD4 Tchem Dopamine D4 receptor (7907 Activities)

Discover Target: DRD4

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ACHE Tclin Acetylcholinesterase (18204 Activities)

Discover Target: ACHE

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

PTGS1 Tclin Cyclooxygenase-1 (9233 Activities)

Discover Target: PTGS1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

SLC6A2 Tclin Norepinephrine transporter (10102 Activities)

Discover Target: SLC6A2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

HRH2 Tclin Histamine H2 receptor (5428 Activities)

Discover Target: HRH2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ADRA1D Tclin Alpha-1d adrenergic receptor (4171 Activities)

Discover Target: ADRA1D

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

HTR1B Tclin Serotonin 1b (5-HT1b) receptor (2801 Activities)

Discover Target: HTR1B

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

HTR2A Tclin Serotonin 2a (5-HT2a) receptor (14758 Activities)

Discover Target: HTR2A

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

HTR2C Tclin Serotonin 2c (5-HT2c) receptor (11471 Activities)

Discover Target: HTR2C

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ADORA1 Tclin Adenosine A1 receptor (17603 Activities)

Discover Target: ADORA1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CALCR Tclin Calcitonin receptor (2215 Activities)

Discover Target: CALCR

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

SLC6A4 Tclin Serotonin transporter (12625 Activities)

Discover Target: SLC6A4

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ADRA1A Tclin Alpha-1a adrenergic receptor (8359 Activities)

Discover Target: ADRA1A

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

PTGS2 Tclin Cyclooxygenase-2 (13999 Activities)

Discover Target: PTGS2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

HRH1 Tclin Histamine H1 receptor (7573 Activities)

Discover Target: HRH1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ADRA1B Tclin Alpha-1b adrenergic receptor (2912 Activities)

Discover Target: ADRA1B

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

OPRM1 Tclin Mu opioid receptor (19785 Activities)

Discover Target: OPRM1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

DRD3 Tclin Dopamine D3 receptor (14368 Activities)

Discover Target: DRD3

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

AVPR1A Tclin Vasopressin V1a receptor (5412 Activities)

Discover Target: AVPR1A

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

OPRD1 Tclin Delta opioid receptor (15096 Activities)

Discover Target: OPRD1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

OPRK1 Tclin Kappa opioid receptor (16155 Activities)

Discover Target: OPRK1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

SLC6A3 Tclin Dopamine transporter (10535 Activities)

Discover Target: SLC6A3

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

KCNH2 Tclin HERG (29587 Activities)

Discover Target: KCNH2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

HTR4 Tclin Serotonin 4 (5-HT4) receptor (2068 Activities)

Discover Target: HTR4

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ESR2 Tclin Estrogen receptor beta (9272 Activities)

Discover Target: ESR2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CYSLTR1 Tclin Cysteinyl leukotriene receptor 1 (2118 Activities)

Discover Target: CYSLTR1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ERBB2 Tclin Receptor protein-tyrosine kinase erbB-2 (7851 Activities)

Discover Target: ERBB2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CHRM4 Tclin Muscarinic acetylcholine receptor M4 (6041 Activities)

Discover Target: CHRM4

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CHRM5 Tclin Muscarinic acetylcholine receptor M5 (4677 Activities)

Discover Target: CHRM5

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Cibles associées (non humaines)

Agtr2 Angiotensin II type 2 (AT-2) receptor (803 Activities)

Discover Target: Agtr2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mc4r Melanocortin receptor 4 (1205 Activities)

Discover Target: Mc4r

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Ltc4s Leukotriene C4 synthase (1 Activities)

Discover Target: Ltc4s

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Sigmar1 Sigma opioid receptor (160 Activities)

Discover Target: Sigmar1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Npy1r Neuropeptide Y receptor type 1 (8 Activities)

Discover Target: Npy1r

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Cckar Cholecystokinin A receptor (90 Activities)

Discover Target: Cckar

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Nos2 Nitric oxide synthase, inducible (3573 Activities)

Discover Target: Nos2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mapk1 MAP kinase ERK2 (650 Activities)

Discover Target: Mapk1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mmp9 Matrix metalloproteinase 9 (38 Activities)

Discover Target: Mmp9

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Pseudomonas aeruginosa (123386 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Staphylococcus aureus (210822 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Escherichia coli (133304 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Bacillus (868 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Aspergillus niger (16508 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Bacillus subtilis (32866 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Candida albicans (78123 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Fusarium oxysporum (3998 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mus musculus (284745 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Rattus norvegicus (775804 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Staphylococcus capitis (242 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Macrophomina phaseolina (474 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)

Discover Target: Nfe2l2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Impa1 Inositol monophosphatase 1 (16203 Activities)

Discover Target: Impa1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Glra2 Glycine receptor (1745 Activities)

Discover Target: Glra2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mécanismes d'action

Certificats (CoA, COO, BSE/TSE et tableau d'analyse)

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.

60 results found

Lot Number	Certificate Type	Date	Article
J2620824	Certificate of Analysis	Oct 15, 2026	D112007
J2620822	Certificate of Analysis	Oct 15, 2026	D112007
J2620820	Certificate of Analysis	Oct 15, 2026	D112007
J2610192	Certificate of Analysis	Sep 18, 2026	D112007
J2610193	Certificate of Analysis	Sep 18, 2026	D112007
J2616685	Certificate of Analysis	Sep 18, 2026	D112007
J2616684	Certificate of Analysis	Sep 18, 2026	D112007
J2610241	Certificate of Analysis	Sep 18, 2026	D112007
E2620200	Certificate of Analysis	May 15, 2026	D112007
E2620199	Certificate of Analysis	May 15, 2026	D112007
E2620198	Certificate of Analysis	May 15, 2026	D112007
E2620197	Certificate of Analysis	May 15, 2026	D112007
G2628122	Certificate of Analysis	Jan 22, 2026	D112007
A2627201	Certificate of Analysis	Jan 22, 2026	D112007
A2627204	Certificate of Analysis	Jan 22, 2026	D112007
A2627203	Certificate of Analysis	Jan 22, 2026	D112007
K2503685	Certificate of Analysis	Oct 30, 2025	D112007
K2503686	Certificate of Analysis	Oct 30, 2025	D112007
K2503687	Certificate of Analysis	Oct 30, 2025	D112007
K2503688	Certificate of Analysis	Oct 30, 2025	D112007
H2514242	Certificate of Analysis	Jul 04, 2025	D112007
H2514241	Certificate of Analysis	Jul 04, 2025	D112007
H2514166	Certificate of Analysis	Jul 04, 2025	D112007
H2514240	Certificate of Analysis	Jul 04, 2025	D112007
F2523144	Certificate of Analysis	May 29, 2025	D112007
F2523141	Certificate of Analysis	May 29, 2025	D112007
F2523138	Certificate of Analysis	May 29, 2025	D112007
C2504339	Certificate of Analysis	Feb 24, 2025	D112007
C2504598	Certificate of Analysis	Feb 24, 2025	D112007
C2504597	Certificate of Analysis	Feb 24, 2025	D112007
C2504596	Certificate of Analysis	Feb 24, 2025	D112007
L2424188	Certificate of Analysis	Dec 16, 2024	D112007
L2424187	Certificate of Analysis	Dec 16, 2024	D112007
L2424185	Certificate of Analysis	Dec 16, 2024	D112007
L2424183	Certificate of Analysis	Dec 16, 2024	D112007
E2521043	Certificate of Analysis	Dec 16, 2024	D112007
I2413098	Certificate of Analysis	Sep 06, 2024	D112007
I2413099	Certificate of Analysis	Sep 06, 2024	D112007
I2402670	Certificate of Analysis	Aug 30, 2024	D112007
I2402672	Certificate of Analysis	Aug 30, 2024	D112007
I2402671	Certificate of Analysis	Aug 30, 2024	D112007
I2402669	Certificate of Analysis	Aug 30, 2024	D112007
H2325385	Certificate of Analysis	Aug 17, 2023	D112007
K2303081	Certificate of Analysis	Aug 17, 2023	D112007
H2325388	Certificate of Analysis	Aug 17, 2023	D112007
H2325387	Certificate of Analysis	Aug 17, 2023	D112007
H2325386	Certificate of Analysis	Aug 17, 2023	D112007
K2223083	Certificate of Analysis	Nov 17, 2022	D112007
K2223084	Certificate of Analysis	Nov 17, 2022	D112007
K2223144	Certificate of Analysis	Nov 17, 2022	D112007
K2223145	Certificate of Analysis	Nov 17, 2022	D112007
E2319143	Certificate of Analysis	Nov 17, 2022	D112007
F2316135	Certificate of Analysis	Nov 17, 2022	D112007
F2326198	Certificate of Analysis	Nov 17, 2022	D112007
E2203174	Certificate of Analysis	Mar 12, 2022	D112007
E2203173	Certificate of Analysis	Mar 12, 2022	D112007
E2203172	Certificate of Analysis	Mar 12, 2022	D112007
E2203179	Certificate of Analysis	Mar 12, 2022	D112007
G2415344	Certificate of Analysis	Mar 12, 2022	D112007
H2219170	Certificate of Analysis	Mar 12, 2022	D112007

Propriétés chimiques et physiques

Sensibilité	Moisture sensitive.
Indice de réfraction	1.4269
Point d'éclair (°F)	136.4 °F
Point d'éclair (°C)	58℃
Point d'ébullition (°C)	152.8°C
Point de fusion (°C)	-61°C
Poids moléculaire	73.090 g/mol
XLogP3	-1.000
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	1
Rotatable Bond Count	0
Exact Mass	73.0528 Da
Monoisotopic Mass	73.0528 Da
Topological Polar Surface Area	20.300 Å²
Heavy Atom Count	5
Formal Charge	0
Complexity	33.900
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

FAQ et articles

Solid-Phase Peptide Synthesis (SPPS) — Efficient Strategies and Innovative Techniques

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Chemical synthesis Amino acids Protein Biology Acids Solvents Carbohydrates Peptides Peptide synthesis reagents Organic blocks SPPS Peptide synthesis Protection groups

Boc resin lysis protocol

Categories: Laboratory Protocols & SOPs Library

Tags:

Building Blocks peptide Protein Biology Solvents Peptides SPPS Peptide synthesis Protection groups Analytical standards

General Principles of Antibody Labeling with NHS-Activated Esters, F/P Calculation, and Troubleshooting Guide

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

NHS-Activated Esters

Applications of Nanoclay in Materials and Formulations: Dispersion Mechanisms, Performance Enhancement, and Product Selection

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Nanoclay

One-Stop Handbook for Palladium-Catalyzed Reactions: Catalytic Cycles, Deactivation Troubleshooting, Ligand/Precatalyst Selection, and an Aladdin Reference List

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Pd Palladium-Catalyzed Reactions

A Complete Guide to Choosing Resins for SPPS (Solid-Phase Peptide Synthesis): Fmoc/Boc Routes, C-Terminal Acid/Amide, and a Key-Parameter Navigator

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

SPPS Solid-Phase Peptide Synthesis

Installing a Redox Switch on Biomolecules: Principles, Conjugation Essentials, and an Application Guide for ATTO MB2 NHS ester

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

ATTO MB2 NHS ester Redox Switch

A Practical Guide to Small-Molecule Chemical Probes: Concept Clarification, Causal Validation, and Experimental Selection (with Product Navigation and Tables A–D)

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Chemical probe Small-Molecule Chemical Probes

Practical Guide to Carbon Nanotube (CNT) Dispersion: Three Key Knobs, SOP, and Selection Roadmap (Tables A–F)

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Carbon Nanotube

From Piperidine to Pyridine: The “Most Common N-Heterocycle” Shift in FDA Small-Molecule New Drugs (2013–2023) and a Selection Guide (Tables 1–4)

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

N-Heterocycle

Structural–Functional Analysis of the Methoxy Group (–OCH₃) in Approved Small-Molecule Drugs: Mechanisms, Evidence Chains, and Product-Selection Navigation (with Related Product Tables)

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

–OCH₃

A Practical Guide to Organozinc Reagents for Synthesis (Organozinc Reagents): Structural Features, Key Reactions, and a Practical Selection Navigation (Including Aladdin Product Tables)

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Organozinc reagents

Why Acridine Can Turn “Trace Molecules” into a Measurable Light Signal: A Mechanistic, Selection, and Troubleshooting Guide to Acridinium Ester Chemiluminescent Immunoassays (Including Product Tables 1–4)

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Nitrogen-containing heterocycles Polycyclic aromatic compounds aromatic compounds Chemiluminescence immunoassay

How to Make the Suzuki–Miyaura Reaction Robust: Pinpoint the Bottleneck and Lock in a Reproducible Operating Window (with Selection Navigation and Product Tables 1–5)

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Cross-coupling reactions Suzuki–Miyaura

β-Acyloxy Alkenyl Amides (AAAs): A New Approach to Amide Bond and Peptide Bond Construction Worth Attention

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

AAAs β-Acyloxy Alkenyl Amides

From Analytical Instrument to Synthetic Platform: A New Strategy for Reconstructing Automated Flow Solid-Phase Peptide Synthesis with Standard Analytical HPLC

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

HPLC Peptide synthesis coupling reagent Analytical Instrument

New Progress in the Solid-Phase Synthesis of Sterically Hindered Peptides: Background, Core Breakthroughs, and Implications for Automation Compatibility of the RMMR Strategy

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Tumors Peptides Solid-Phase Peptide Synthesis

Reassessing Trimethylaluminum: Method Design and Experimental Value of One-Pot Peptide Elongation from Unprotected Amino Acids

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Trimethylaluminum Unprotected amino acids One pot method for peptide chain elongation

What a Disagreement in Specific Rotation Results Reveals About Method Control: Why Specific Rotation Values for Chiral Samples Cannot Be Discussed Apart from Measurement Conditions

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Specific rotation measurement Specific rotation

Phthaloyl: Its Role in Primary Amine Protection and Practical Considerations for Experimental Selection

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Phthaloyl Phth

The Methodological Value of HATU in Difficult Couplings: Reactivity Advantages, Stereochemical Retention, and Condition Management

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

HATU

Low Racemization in Peptide Synthesis Is Not Just About Reagent Choice: Stereochemical Risk During the Activation Stage and Practical Strategies for Experimental Control

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Peptide synthesis Amide bond construction Racemic

The Methodological Value of DSC: Building NHS-Type Activated Intermediates and Deciding When to Use Them

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

DSC N,N′-disuccinimidyl carbonate

The Methodological Value of TCFH: Advantages in Challenging Amidation and the Switching Logic of Carboxylic Acid Activation Pathways

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

carboxylic acid TCFH coupling reagents Strong condensing reagent

Decision Logic for Peptide Synthesis Routes: Applicability and Criteria for Choosing among SPPS, LPPS, and Recombinant Expression

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Peptide synthesis Liquid-phase peptide synthesis

The Positioning of pNPP in ALP Testing: Quantitative Detection Logic, Application Scenarios, and Selection Criteria

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

pNPP ALP activity assays Chromogenic Substrate

Boc₂O Selection Cannot Be Judged by Protection Installation Alone: Experimental Decision-Making from Substrate Nucleophilicity and Medium Effects to Deprotection Pathways

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

carbamate Boc₂O Boc protection

DMAP Is More Than Just an Organic Base: Experimental Judgment from Nucleophilic Acyl Transfer to Esterification and Macrolactonization

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Organic synthesis Acyl transfer Organic base Esterification

Experimental Decision-Making for Introducing Aminoalkyl Side Chains Using N-Haloalkyl Phthalimides: Chain Length, Leaving Group, and Deprotection Choice

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

N-Haloalkyl Phthalimides Gabriel synthesis

Experimental Judgment in Oxyma Coupling Systems: Coupling Efficiency, Racemization Control, and the HCN Risk in DIC-Based Systems

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Coupling Oxyma Coupling Systems Oxyma ethyl 2-cyano-2-(hydroxyimino)acetate OxymaPure

Polyetherimide (PEI): Structural Features, Main Properties, and Typical Application Directions

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

PEI Polyetherimide

From Functional Groups to Experimental Decision-Making: Protein Crosslinker Selection and Experimental Essentials

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Functional Groups Crosslinkers

Metal Halide Perovskite Solar Cells: Sources of High Efficiency, Stability Bottlenecks, and Experimental Decision Logic

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

perovskite Solar cell Metal halides

How to Troubleshoot Abnormal Impurities in Peptide Synthesis? Locating Process Issues Through Amino-Related Side Reactions

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Peptide synthesis Abnormal impurities

Peptide Intermediates Difficult to Dissolve and Separate? Route Design and Workup Strategies for Tag-Assisted Liquid-Phase Peptide Synthesis (TAG-LPPS)

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Peptide synthesis TAG-LPP Peptide Intermediates

AITF-Mediated Carboxylic Acid Activation for the Synthesis of Amides, Peptides, and Esters: Activation Mechanism and Applicable Scenarios

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Peptides AITF Amides Esters

Formation and Control of Carboxyl- and Hydroxyl-Related Impurities in Peptide Synthesis — Using Asp/Glu and Ser/Thr Residue Side Reactions as Examples

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Peptide synthesis Functional Group Carboxyl group

CTSOBt Benzotriazole–Sulfonate Coupling Reagent: Carboxylic Acid Activation and Synthetic Application Value

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Peptide synthesis coupling reagent coupling reagents

From Photocatalytic Ring Opening to Skeletal Reconstruction: Reaction Logic and Synthetic Applications of Oxygen-Atom Replacement in Oxetanes

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Photocatalysts Saturated quaternary ring Skeleton

Logic for Selecting Amidation Reagents in Aqueous Media: Competing Reactions, Activated Intermediates, and Substrate Effects

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Amidation reaction

Sulfonyl Hydrazide-Mediated Introduction of Small C(sp³) Fragments: Nickel-Catalyzed Cross-Coupling, Medicinal Chemistry Applications, and Reagent Selection

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Cross-coupling lead compound

From Nucleophilic to Electrophilic BCB Synthetic Equivalents: Hypervalent-Iodine-Mediated Umpolung Design

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

BCB bicyclo[1.1.0]butane

From Functional-Group Transformation to Intramolecular Cyclization: Reaction-Pathway Analysis of TMSCl/DMF-Promoted Annulation and CuCN-Mediated Cascade Cyclization

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Organic synthesis trimethylsilyl chloride TMSCl N,N-dimethylformamide DMF

Medicinal Chemistry Design of the Indazole Scaffold: Tautomerism, Molecular Recognition, Substitution-Site Design, and Synthetic Strategies

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Indazole Nitrogen-containing aromatic heterocycles

Discovery and Structural Optimization of the Noncovalent 3CL Protease Inhibitor S-217622

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

3C-like protease main protease

How Cyclization Changes Peptide Behavior: Conformational Preorganization, Skin Delivery, and Integrin Binding, Using Cyclopeptide-5 as an Example

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Polypeptide Skincare

How to Bypass α-Fluoride Elimination: Bromine-Transfer Capture and Oxidative Coupling of α,α-Difluorobenzylic Anions

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Deprotonation

Reactions and Applications of 3,3-Difluoroallyl Sulfonium Salts (DFASs): Small-Molecule gem-Difluoroallylation, Selective Peptide Modification, and Subsequent Functionalization

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Polypeptide Fluorinated groups

Why Primary and Secondary Amines Have Difficulty Participating Directly in the Classical Mitsunobu Reaction: Mechanism, Inversion of Configuration, and Reaction Scope of BEHT-Mediated Alcohol Amination

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Mitsunobu Reaction BEHT Protonated Betaine Alcohol Activation Primary Amines Secondary Amines Bimolecular Nucleophilic Substitution Inversion Of Configuration Α-Chiral Amines

Mechanistic Basis of Acetyl Hexapeptide-8 in the Management of Expression Lines: SNARE Complex Interference, Constraints on Percutaneous Delivery, and Combination Strategies

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Retinol Acetyl Hexapeptide-8 Argireline SNAP-25 SNARE complex expression lines transdermal delivery anti-wrinkle combinations

Copper Tripeptide GHK-Cu and Skin Repair: From Copper Coordination Chemistry to Extracellular Matrix Remodeling

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Extracellular matrix Skin Repair ECM GHK-Cu

Direct Construction of Methylsulfonyl-Containing Heterocycles: Synthesis and Applications of Prefunctionalized Three-Carbon Vinamidinium Salts

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

–SO₂CH₃ –SO₂Me

Categories:

Tags:

Tether Effects in Intramolecular [2+2] Photocycloadditions: Straight and Crossed Regioselectivity and Stepwise C–C Bond Formation

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Screening and Replacement of Green Solvents in Metallaphotoredox Catalysis: Reaction Compatibility and Process Feasibility

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Photocatalytic

ACT-1014-6470 Kilogram-Scale Synthesis: N7-Selective Reductive Amination of an Unprotected Pyrazole, Subsequent N2 Alkylation, and Intramolecular Urea Formation

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

reductive amination Pyrazole

Bond-Formation Sequence and Process Improvement for 3-Bromo-6-alkyl-1,6-naphthyridin-5(6H)-ones: From Late-Stage N-Alkylation to Enamine Cyclization with Primary Amines

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Enamine cyclization 3-bromo-N-alkyl-1,6-naphthyridones

Citations of This Product

How to Cite Aladdin Scientific Products? Citations Search

Calculateurs de solution

Molarity Calculator

Determine the necessary mass, volume, or concentration for preparing a solution.

Dilution Calculator

Determine the dilution needed to prepare a stock solution.

Reconstitution Calculator

Avis

📚 Citations par application

Electrochemistry & battery electrolyte1877

Organic synthesis — reaction medium4600

Controlled-release & nanoparticle carrier474

Drug / compound screening618

Cancer cell line characterization101

Immune cell assay14

Other applications4976

IC50 determination28

Extraction & workup solvent1732

Spectroscopy sample preparation228

Crystallization & recrystallization221

Polymer synthesis & polymerization1465

Nanoparticle / material biocompatibility212

Chromatography (HPLC / GC / TLC)172

Thickener / viscosity modifier13

Industrial & non-pharma application680

Cross-coupling reactions153

Cell viability98

Cytotoxicity screening133

Film coating40

Stem cell research13

Cell proliferation42

Topical & ophthalmic formulation37

Sustained-release matrix5

Recrystallization & recrystallization1

Grignard & organometallic chemistry2

Mucoadhesive formulation3

Photothermal Therapy1

Inflammation response1

Angiogenesis1

Flotation reagent1

Catalysis1

Disintegrant / dissolution modifier1

Voir les 9509 citations →

Besoin d'aide pour choisir la qualité ?

Notre guide de sélection des qualités couvre la pureté, le statut du stabilisant et l'adéquation à l'application pour toutes les variantes de notre catalogue.

Voir le guide des qualités BioReagent →

Emballage en vrac & sur mesure Besoin de quantités plus importantes ou de spécifications personnalisées ? Contactez notre équipe pour un devis sur mesure.

Produits apparentés

N,N-Dimethylformamide (DMF) - Suitable for molecular biology, ≥99.9% , CAS No.68-12-2

N,N-Dimethylformamide (DMF) - Standard for GC, ≥99.9%(GC) , CAS No.68-12-2

N,N-Dimethylformamide (DMF) - UltraPureChrom™, for HPLC, ≥99.9% , CAS No.68-12-2

N,N-Dimethylformamide (DMF) - ≥99.9% , CAS No.68-12-2

N,N-Dimethylformamide (DMF) - Anhydrous Grade, ≥99.8% , CAS No.68-12-2

N,N-Dimethylformamide (DMF) - pesticide residue grade, ≥99.9% , CAS No.68-12-2

N,N-Dimethylformamide (DMF) - ≥99.9%(GC) , CAS No.68-12-2

N,N-Dimethylformamide (DMF) - AR, ≥99.5% , CAS No.68-12-2

N,N-Dimethylformamide (DMF) - UltraPureChrom™, for GC-HS, ≥99.9%(GC) , CAS No.68-12-2

N,N-Dimethylformamide (DMF) - PureSpectra™, ACS, Spectrum pure, ≥99.8% , CAS No.68-12-2

N,N-Dimethylformamide (DMF) - UltraPureChrom™, for GC-HS , CAS No.68-12-2

N,N-Dimethylformamide (DMF) - BioReagent, ≥99.9% , CAS No.68-12-2

Stockage & expédition

Documents qualité

Preuve documentaire

Spécifications

Documentation

📋 Fiche de données de sécurité (FDS)

✅ Certificat d'analyse (COA)

📊 Fiche technique

🔬 Fiche de spécifications

Données avancées

Molarity Calculator

Dilution Calculator

Reconstitution Calculator

Avis des clients

📚 Citations par application

Besoin d'aide pour choisir la qualité ?

View related series

Produits apparentés