Specifications Namen und Kennungen Documentation Advanced Data Taxonomic Classification 3D-Struktur Zugehörige Ziele (menschlich) Zugehörige Ziele (nicht menschlich) Wirkungsmechanismen Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm) Chemische und physikalische Eigenschaften FAQs und Artikel Citations of This Product Lösungsrechner Bewertungen

🧪

Why this grade

UltraPureChrom™, for GC-HS, ≥99.9%(GC) for GC-HS,UltraPureChrom™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature Ships FedEx DG Service 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 9428 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyme

Spezifikationen & Reinheit

UltraPureChrom™, for GC-HS, ≥99.9%(GC)

Storage

Room temperature

Verschickt in

FedEx DG Service

Note

for GC-HS, UltraPureChrom™

Reinheit

≥99.9%(GC)

Namen und Kennungen

Pubchem Sid

508811016

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/508811016

Kanonisches Lächeln

CN(C)C=O

IUPAC Name

N,N-dimethylformamide

InChIKey

ZMXDDKWLCZADIW-UHFFFAOYSA-N

INCHI

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

Isomere SMILES

CN(C)C=O

WGK Deutschland

RTECS

LQ2100000

UN-Nummer

2265

Verpackungsgruppe

III

Molekulargewicht

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

📋 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

Kingdom Organic compounds
- Superclass Organic acids and derivatives
  - Klasse Carboxylic acids and derivatives
    - Subclass Carboxylic acid derivatives
      - Ebene5 Carboxylic acid amides
        Ebene6 Tertiary carboxylic acid amides

Kingdom	Organic compounds
Superclass	Organic acids and derivatives
Klasse	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
Beschreibung	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

3D-Struktur

Zugehörige Ziele (menschlich)

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

Zugehörige Ziele (nicht menschlich)

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

Wirkungsmechanismen

Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)

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.

156 results found

Lot Number	Certificate Type	Datum	Artikel
J2609011	Certificate of Analysis	Oct 15, 2026	D112008
A2606200	Certificate of Analysis	Sep 02, 2026	D112008
H2304316	Certificate of Analysis	Sep 01, 2026	D112008
L2505417	Certificate of Analysis	Sep 01, 2026	D112008
J2511693	Certificate of Analysis	Jul 06, 2026	D112008
F2626503	Certificate of Analysis	Jun 08, 2026	D112008
F2626504	Certificate of Analysis	Jun 08, 2026	D112008
E2606173	Certificate of Analysis	Apr 16, 2026	D112008
E2606177	Certificate of Analysis	Apr 16, 2026	D112008
E2606178	Certificate of Analysis	Apr 16, 2026	D112008
E2606172	Certificate of Analysis	Mar 09, 2026	D112008
E2606258	Certificate of Analysis	Mar 09, 2026	D112008
E2606259	Certificate of Analysis	Mar 09, 2026	D112008
E2606179	Certificate of Analysis	Jan 30, 2026	D112008
E2606180	Certificate of Analysis	Jan 30, 2026	D112008
E2606181	Certificate of Analysis	Jan 30, 2026	D112008
A2629385	Certificate of Analysis	Jan 05, 2026	D112008
A2629387	Certificate of Analysis	Jan 05, 2026	D112008
A2629388	Certificate of Analysis	Jan 05, 2026	D112008
A2606199	Certificate of Analysis	Dec 30, 2025	D112008
A2606292	Certificate of Analysis	Dec 30, 2025	D112008
C2611140	Certificate of Analysis	Dec 30, 2025	D112008
L2505419	Certificate of Analysis	Dec 01, 2025	D112008
L2505420	Certificate of Analysis	Dec 01, 2025	D112008
J2516399	Certificate of Analysis	Oct 11, 2025	D112008
J2516400	Certificate of Analysis	Oct 11, 2025	D112008
J2516401	Certificate of Analysis	Oct 11, 2025	D112008
J2511727	Certificate of Analysis	Sep 22, 2025	D112008
J2511728	Certificate of Analysis	Sep 22, 2025	D112008
J2511730	Certificate of Analysis	Sep 22, 2025	D112008
I2510332	Certificate of Analysis	Aug 28, 2025	D112008
I2510392	Certificate of Analysis	Aug 28, 2025	D112008
I2510394	Certificate of Analysis	Aug 28, 2025	D112008
I2510409	Certificate of Analysis	Aug 28, 2025	D112008
H2514243	Certificate of Analysis	Jul 30, 2025	D112008
H2514291	Certificate of Analysis	Jul 30, 2025	D112008
H2514292	Certificate of Analysis	Jul 30, 2025	D112008
H2514293	Certificate of Analysis	Jul 30, 2025	D112008
G2528168	Certificate of Analysis	Jul 21, 2025	D112008
G2528169	Certificate of Analysis	Jul 21, 2025	D112008
G2528548	Certificate of Analysis	Jul 21, 2025	D112008
G2509302	Certificate of Analysis	Jul 02, 2025	D112008
F2525357	Certificate of Analysis	Jun 17, 2025	D112008
F2525358	Certificate of Analysis	Jun 17, 2025	D112008
F2525359	Certificate of Analysis	Jun 17, 2025	D112008
F2506392	Certificate of Analysis	May 19, 2025	D112008
F2506404	Certificate of Analysis	May 19, 2025	D112008
F2506405	Certificate of Analysis	May 19, 2025	D112008
E2523179	Certificate of Analysis	May 14, 2025	D112008
E2523270	Certificate of Analysis	May 14, 2025	D112008
E2523271	Certificate of Analysis	May 14, 2025	D112008
D2517428	Certificate of Analysis	Apr 10, 2025	D112008
D2517429	Certificate of Analysis	Apr 10, 2025	D112008
D2517430	Certificate of Analysis	Apr 10, 2025	D112008
C2512729	Certificate of Analysis	Mar 03, 2025	D112008
C2512730	Certificate of Analysis	Mar 03, 2025	D112008
C2512731	Certificate of Analysis	Mar 03, 2025	D112008
C2512732	Certificate of Analysis	Mar 03, 2025	D112008
E2520032	Certificate of Analysis	Mar 03, 2025	D112008
B2512201	Certificate of Analysis	Feb 06, 2025	D112008
B2512202	Certificate of Analysis	Feb 06, 2025	D112008
A2515365	Certificate of Analysis	Dec 30, 2024	D112008
A2515366	Certificate of Analysis	Dec 30, 2024	D112008
A2515367	Certificate of Analysis	Dec 30, 2024	D112008
L2410241	Certificate of Analysis	Dec 16, 2024	D112008
L2410602	Certificate of Analysis	Dec 04, 2024	D112008
L2410609	Certificate of Analysis	Dec 04, 2024	D112008
L2410610	Certificate of Analysis	Dec 04, 2024	D112008
L2410625	Certificate of Analysis	Dec 04, 2024	D112008
A2429261	Certificate of Analysis	Nov 07, 2024	D112008
K2408375	Certificate of Analysis	Nov 01, 2024	D112008
K2408376	Certificate of Analysis	Nov 01, 2024	D112008
K2408379	Certificate of Analysis	Nov 01, 2024	D112008
K2408380	Certificate of Analysis	Nov 01, 2024	D112008
J2421471	Certificate of Analysis	Oct 11, 2024	D112008
J2421475	Certificate of Analysis	Oct 11, 2024	D112008
J2421477	Certificate of Analysis	Oct 11, 2024	D112008
H2406394	Certificate of Analysis	Jul 31, 2024	D112008
H2406395	Certificate of Analysis	Jul 31, 2024	D112008
H2406396	Certificate of Analysis	Jul 31, 2024	D112008
H2406397	Certificate of Analysis	Jul 31, 2024	D112008
G2417213	Certificate of Analysis	Jul 10, 2024	D112008
G2417216	Certificate of Analysis	Jul 10, 2024	D112008
G2417219	Certificate of Analysis	Jul 10, 2024	D112008
F2412205	Certificate of Analysis	Jun 03, 2024	D112008
F2412206	Certificate of Analysis	Jun 03, 2024	D112008
F2412207	Certificate of Analysis	Jun 03, 2024	D112008
F2412257	Certificate of Analysis	Jun 03, 2024	D112008
E2413193	Certificate of Analysis	Apr 30, 2024	D112008
E2413194	Certificate of Analysis	Apr 30, 2024	D112008
E2413209	Certificate of Analysis	Apr 30, 2024	D112008
E2413210	Certificate of Analysis	Apr 30, 2024	D112008
D2408136	Certificate of Analysis	Mar 28, 2024	D112008
D2408152	Certificate of Analysis	Mar 28, 2024	D112008
D2408167	Certificate of Analysis	Mar 28, 2024	D112008
C2419085	Certificate of Analysis	Mar 11, 2024	D112008
C2419086	Certificate of Analysis	Mar 11, 2024	D112008
C2419087	Certificate of Analysis	Mar 11, 2024	D112008
C2419088	Certificate of Analysis	Mar 11, 2024	D112008
B2426063	Certificate of Analysis	Jan 30, 2024	D112008
B2426065	Certificate of Analysis	Jan 30, 2024	D112008
B2426066	Certificate of Analysis	Jan 30, 2024	D112008
B2426067	Certificate of Analysis	Jan 30, 2024	D112008
A2429161	Certificate of Analysis	Jan 15, 2024	D112008
A2429259	Certificate of Analysis	Jan 15, 2024	D112008
A2429262	Certificate of Analysis	Jan 15, 2024	D112008
A2429263	Certificate of Analysis	Jan 15, 2024	D112008
L2312330	Certificate of Analysis	Dec 05, 2023	D112008
L2312347	Certificate of Analysis	Dec 05, 2023	D112008
L2312348	Certificate of Analysis	Dec 05, 2023	D112008
K2309181	Certificate of Analysis	Oct 24, 2023	D112008
K2309182	Certificate of Analysis	Oct 24, 2023	D112008
K2309183	Certificate of Analysis	Oct 24, 2023	D112008
J2320238	Certificate of Analysis	Oct 10, 2023	D112008
J2320239	Certificate of Analysis	Oct 10, 2023	D112008
H2304305	Certificate of Analysis	Jul 13, 2023	D112008
H2304306	Certificate of Analysis	Jul 13, 2023	D112008
H2304307	Certificate of Analysis	Jul 13, 2023	D112008
F23161166	Certificate of Analysis	Jun 05, 2023	D112008
F23161169	Certificate of Analysis	Jun 05, 2023	D112008
E2318394	Certificate of Analysis	Apr 11, 2023	D112008
E2318453	Certificate of Analysis	Apr 11, 2023	D112008
E2318828	Certificate of Analysis	Apr 11, 2023	D112008
E2318882	Certificate of Analysis	Apr 11, 2023	D112008
D2303768	Certificate of Analysis	Mar 24, 2023	D112008
D2303774	Certificate of Analysis	Mar 24, 2023	D112008
D2303781	Certificate of Analysis	Mar 24, 2023	D112008
A2305297	Certificate of Analysis	Dec 18, 2022	D112008
A2305343	Certificate of Analysis	Dec 18, 2022	D112008
A2305344	Certificate of Analysis	Dec 18, 2022	D112008
A2305345	Certificate of Analysis	Dec 18, 2022	D112008
I2223387	Certificate of Analysis	Sep 15, 2022	D112008
I2223388	Certificate of Analysis	Sep 15, 2022	D112008
I2223389	Certificate of Analysis	Sep 15, 2022	D112008
I2223390	Certificate of Analysis	Sep 15, 2022	D112008
I2223391	Certificate of Analysis	Aug 24, 2022	D112008
H2211172	Certificate of Analysis	Jul 12, 2022	D112008
H2211173	Certificate of Analysis	Jul 12, 2022	D112008
H2211174	Certificate of Analysis	Jul 12, 2022	D112008
H2211175	Certificate of Analysis	Jul 12, 2022	D112008
G2205021	Certificate of Analysis	Jun 25, 2022	D112008
G2205022	Certificate of Analysis	Jun 25, 2022	D112008
G2205023	Certificate of Analysis	Jun 25, 2022	D112008
G2226167	Certificate of Analysis	Jun 25, 2022	D112008
G2205020	Certificate of Analysis	Jun 25, 2022	D112008
G2205024	Certificate of Analysis	Jun 25, 2022	D112008
G2205025	Certificate of Analysis	Jun 25, 2022	D112008
G2205026	Certificate of Analysis	Jun 25, 2022	D112008
G2205027	Certificate of Analysis	Jun 25, 2022	D112008
H2109120	Certificate of Analysis	Jun 21, 2022	D112008
E2211248	Certificate of Analysis	Apr 28, 2022	D112008
E2211256	Certificate of Analysis	Apr 28, 2022	D112008
E2211278	Certificate of Analysis	Apr 28, 2022	D112008
C2212489	Certificate of Analysis	Mar 31, 2022	D112008
D2101241	Certificate of Analysis	Feb 15, 2022	D112008
C2125229	Certificate of Analysis	Jan 18, 2022	D112008

Chemische und physikalische Eigenschaften

Empfindlichkeit	Moisture sensitive.
Brechungsindex	1.4269
Flammpunkt (°F)	136.4 °F
Flammpunkt (°C)	58℃
Siedepunkt (°C)	152.8°C
Schmelzpunkt (°C)	-61°C
Molekulargewicht	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

FAQs und Artikel

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

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

UltraPureChrom™: The Pinnacle of Purity for Chromatography

Categories: Reagent Specifications, Grading and Purity

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Specification Purity Grade UltraPureChrom for HPLC Suitable for HPLC

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

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

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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

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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

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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

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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

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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

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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

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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

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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

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–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

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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

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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

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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

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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

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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

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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

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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

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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

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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

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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

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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

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Peptide synthesis Liquid-phase peptide synthesis

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

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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

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carbamate Boc₂O Boc protection

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

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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

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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

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

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

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PEI Polyetherimide

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

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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

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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

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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

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Peptide synthesis TAG-LPP Peptide Intermediates

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

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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

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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

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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

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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

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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

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Cross-coupling lead compound

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

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

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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

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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

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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

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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

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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

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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

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Extracellular matrix Skin Repair ECM GHK-Cu

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

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–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

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

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

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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

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

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

Storage & shipping

Quality documents

Literature proof

Specifications

Documentation

📋 Safety Data Sheet (SDS)

✅ Certificate of Analysis (COA)

📊 Datasheet

🔬 Specification Sheet

Advanced Data

Molarity Calculator

Dilution Calculator

Reconstitution Calculator

Kundenbewertungen

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