Name: Dimethyl sulfoxide（DMSO） - AR, ≥99%(GC) , CAS No.67-68-5
Brand: Aladdin Scientific
SKU: D103272
Availability: InStock

Specifiche Nomi e identificatori Documentazione Dati avanzati Taxonomic Classification Struttura 3D Obiettivi associati (umani) Obiettivi associati (non umani) Meccanismi d'azione Certificati (CoA, COO, BSE/TSE e tabella di analisi) Proprietà chimiche e fisiche Domande frequenti e articoli Citations of This Product Calcolatori di soluzioni Recensioni

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Perché questa qualità

AR, ≥99%(GC) AR per flussi di lavoro cromatografici e analitici sensibili che richiedono un'interferenza minima della linea di base.

🌡

Stoccaggio e spedizione

Room temperature,Argon charged,Desiccated Spedizione Normal. Consultare il COA specifico del lotto per le specifiche esatte.

📋

Documenti di qualità

SDS, COA, scheda tecnica e scheda delle specifiche disponibili per il download. COA specifico del lotto accessibile tramite ricerca per numero di lotto.

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Prova documentale

Citato in 5363 pubblicazioni peer-reviewed su cromatografia, sintesi organica e reazioni di accoppiamento incrociato.

Specifiche

Sinonimi

Specifiche e purezza

AR, ≥99%(GC)

Condizioni di conservazione di stoccaggio

Room temperature,Argon charged,Desiccated

Spedito in

Normal

Grado

Purezza

≥99%(GC)

Nomi e identificatori

Pubchem Sid

508812210

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/508812210

Sorrisi canonici

CS(=O)C

IUPAC Name

methylsulfinylmethane

InChIKey

IAZDPXIOMUYVGZ-UHFFFAOYSA-N

INCHI

1S/C2H6OS/c1-4(2)3/h1-2H3

Isomeri SMILES

CS(=O)C

WGK Germania

RTECS

PV6210000

Peso molecolare

78.13

Beilstein

506008

Reaxy-Rn

506008

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=506008&ln=

Documentazione

📋 Scheda di dati di sicurezza (SDS)

Documento completo su pericoli, manipolazione, stoccaggio e conformità normativa.

<<<<<<< HEAD Scarica SDS → ======= Scarica SDS → >>>>>>> release248-p3

✅ Certificato di analisi (COA)

Dati di qualità specifici del lotto. Inserisci il numero di lotto per recuperare il COA esatto.

Cerca COA →

📊 Scheda tecnica

Riepilogo di riferimento rapido delle specifiche e applicazioni del prodotto.

Visualizza scheda tecnica →

🔬 Scheda delle specifiche

Attributi di qualità completi e criteri di accettazione per questa qualità.

Visualizza scheda delle specifiche →

Dati avanzati

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organosulfur compounds
  - Classe Sulfoxides

Kingdom	Organic compounds
Superclass	Organosulfur compounds
Classe	Sulfoxides
Subclass	Not available
Intermediate Tree Nodes	Not available
Direct Parent	Sulfoxides
Alternative Parents	Sulfinyl compounds Organic oxides Hydrocarbon derivatives
Molecular Framework	Aliphatic acyclic compounds
Substituents	Sulfoxide - Sulfinyl compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Aliphatic acyclic compound
Descrizione	This compound belongs to the class of organic compounds known as sulfoxides. These are compounds containing a sulfoxide functional group, with the structure RS(=O)R' (R,R' not 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

Struttura 3D

Obiettivi associati (umani)

PDE5A Tclin Phosphodiesterase 5A (5113 Activities)

Discover Target: PDE5A

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

ABL1 Tclin Tyrosine-protein kinase ABL (18331 Activities)

Discover Target: ABL1

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

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

Obiettivi associati (non umani)

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

Fgfr3 Fibroblast growth factor receptor 3 (21 Activities)

Discover Target: Fgfr3

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

Klebsiella pneumoniae (43867 Activities)

Explore this target

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

Micrococcus luteus (7463 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

Acinetobacter baumannii (41033 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

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

Enterococcus faecalis (29875 Activities)

Explore this target

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

Bacillus cereus (7522 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

Trypanosoma cruzi (99888 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

Ntrk2 BDNF/NT-3 growth factors receptor (124 Activities)

Discover Target: Ntrk2

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

Cereblon isoform 4 (52 Activities)

Explore this target

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

Meccanismi d'azione

Certificati (CoA, COO, BSE/TSE e tabella di analisi)

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.

224 results found

Lot Number	Certificate Type	Data	Oggetto
J2623300	Certificate of Analysis	Oct 26, 2026	D103272
J2623301	Certificate of Analysis	Oct 26, 2026	D103272
J2623302	Certificate of Analysis	Oct 26, 2026	D103272
J2623304	Certificate of Analysis	Oct 26, 2026	D103272
J2613367	Certificate of Analysis	Oct 22, 2026	D103272
J2613366	Certificate of Analysis	Oct 21, 2026	D103272
J2613370	Certificate of Analysis	Oct 21, 2026	D103272
J2613200	Certificate of Analysis	Oct 21, 2026	D103272
H2631408	Certificate of Analysis	Sep 02, 2026	D103272
H2631409	Certificate of Analysis	Sep 02, 2026	D103272
H2631410	Certificate of Analysis	Sep 02, 2026	D103272
H2631411	Certificate of Analysis	Sep 02, 2026	D103272
H2631412	Certificate of Analysis	Sep 02, 2026	D103272
H2611122	Certificate of Analysis	Aug 29, 2026	D103272
H2611125	Certificate of Analysis	Aug 29, 2026	D103272
H2611126	Certificate of Analysis	Aug 29, 2026	D103272
H2611121	Certificate of Analysis	Aug 19, 2026	D103272
G2628179	Certificate of Analysis	Jul 31, 2026	D103272
G2628180	Certificate of Analysis	Jul 31, 2026	D103272
G2628183	Certificate of Analysis	Jul 31, 2026	D103272
G2628184	Certificate of Analysis	Jul 31, 2026	D103272
G2628214	Certificate of Analysis	Jul 31, 2026	D103272
G2608141	Certificate of Analysis	Jul 18, 2026	D103272
G2608142	Certificate of Analysis	Jul 18, 2026	D103272
G2608143	Certificate of Analysis	Jul 18, 2026	D103272
G2608146	Certificate of Analysis	Jul 18, 2026	D103272
G2608147	Certificate of Analysis	Jul 18, 2026	D103272
F2626298	Certificate of Analysis	Jul 02, 2026	D103272
F2626614	Certificate of Analysis	Jun 29, 2026	D103272
F2626618	Certificate of Analysis	Jun 29, 2026	D103272
E2620236	Certificate of Analysis	Jun 06, 2026	D103272
D2609171	Certificate of Analysis	Apr 17, 2026	D103272
D2609172	Certificate of Analysis	Apr 17, 2026	D103272
D2609173	Certificate of Analysis	Apr 17, 2026	D103272
D2609174	Certificate of Analysis	Apr 17, 2026	D103272
E2620232	Certificate of Analysis	Apr 17, 2026	D103272
E2620234	Certificate of Analysis	Apr 17, 2026	D103272
E2620235	Certificate of Analysis	Apr 17, 2026	D103272
E2620237	Certificate of Analysis	Apr 17, 2026	D103272
A2630188	Certificate of Analysis	Feb 05, 2026	D103272
A2630189	Certificate of Analysis	Feb 05, 2026	D103272
A2630192	Certificate of Analysis	Feb 05, 2026	D103272
A2630193	Certificate of Analysis	Feb 05, 2026	D103272
A2630194	Certificate of Analysis	Feb 05, 2026	D103272
F2616047	Certificate of Analysis	Feb 05, 2026	D103272
A2607121	Certificate of Analysis	Jan 19, 2026	D103272
A2607134	Certificate of Analysis	Jan 19, 2026	D103272
L2508312	Certificate of Analysis	Dec 12, 2025	D103272
L2508313	Certificate of Analysis	Dec 12, 2025	D103272
L2508314	Certificate of Analysis	Dec 12, 2025	D103272
H2211120	Certificate of Analysis	Nov 06, 2025	D103272
J2524239	Certificate of Analysis	Oct 28, 2025	D103272
J2524252	Certificate of Analysis	Oct 28, 2025	D103272
J2524253	Certificate of Analysis	Oct 28, 2025	D103272
J2524301	Certificate of Analysis	Oct 28, 2025	D103272
J2524302	Certificate of Analysis	Oct 28, 2025	D103272
J2514191	Certificate of Analysis	Oct 20, 2025	D103272
J2514193	Certificate of Analysis	Oct 20, 2025	D103272
J2514194	Certificate of Analysis	Oct 20, 2025	D103272
I2509146	Certificate of Analysis	Sep 16, 2025	D103272
I2509152	Certificate of Analysis	Sep 16, 2025	D103272
I2509210	Certificate of Analysis	Sep 16, 2025	D103272
I2509216	Certificate of Analysis	Sep 16, 2025	D103272
I2509217	Certificate of Analysis	Sep 16, 2025	D103272
I2501108	Certificate of Analysis	Sep 09, 2025	D103272
I2501113	Certificate of Analysis	Sep 09, 2025	D103272
I2501124	Certificate of Analysis	Sep 09, 2025	D103272
I2501125	Certificate of Analysis	Sep 06, 2025	D103272
H2518201	Certificate of Analysis	Aug 21, 2025	D103272
G2525160	Certificate of Analysis	Aug 04, 2025	D103272
G2525161	Certificate of Analysis	Aug 04, 2025	D103272
G2525162	Certificate of Analysis	Aug 04, 2025	D103272
G2525163	Certificate of Analysis	Aug 04, 2025	D103272
H2518197	Certificate of Analysis	Aug 04, 2025	D103272
H2518199	Certificate of Analysis	Aug 04, 2025	D103272
H2518200	Certificate of Analysis	Aug 04, 2025	D103272
G2515115	Certificate of Analysis	Jul 29, 2025	D103272
G2515123	Certificate of Analysis	Jul 23, 2025	D103272
G2515124	Certificate of Analysis	Jul 23, 2025	D103272
G2515125	Certificate of Analysis	Jul 23, 2025	D103272
F2517077	Certificate of Analysis	Jul 08, 2025	D103272
F2513169	Certificate of Analysis	Jun 24, 2025	D103272
F2513171	Certificate of Analysis	Jun 24, 2025	D103272
F2513172	Certificate of Analysis	Jun 24, 2025	D103272
F2513173	Certificate of Analysis	Jun 23, 2025	D103272
E2526026	Certificate of Analysis	Jun 03, 2025	D103272
E2520045	Certificate of Analysis	May 29, 2025	D103272
F2512567	Certificate of Analysis	May 29, 2025	D103272
D2511305	Certificate of Analysis	Apr 22, 2025	D103272
D2511310	Certificate of Analysis	Apr 22, 2025	D103272
D2511388	Certificate of Analysis	Apr 22, 2025	D103272
C2504515	Certificate of Analysis	Mar 17, 2025	D103272
C2504521	Certificate of Analysis	Mar 17, 2025	D103272
B2522102	Certificate of Analysis	Mar 01, 2025	D103272
B2522103	Certificate of Analysis	Mar 01, 2025	D103272
B2522104	Certificate of Analysis	Mar 01, 2025	D103272
B2522106	Certificate of Analysis	Mar 01, 2025	D103272
B2522109	Certificate of Analysis	Mar 01, 2025	D103272
B2522098	Certificate of Analysis	Feb 28, 2025	D103272
B2522105	Certificate of Analysis	Feb 28, 2025	D103272
B2513319	Certificate of Analysis	Feb 20, 2025	D103272
B2513320	Certificate of Analysis	Feb 20, 2025	D103272
B2513321	Certificate of Analysis	Feb 20, 2025	D103272
B2513334	Certificate of Analysis	Feb 20, 2025	D103272
A2516049	Certificate of Analysis	Feb 10, 2025	D103272
A2516050	Certificate of Analysis	Feb 10, 2025	D103272
A2516051	Certificate of Analysis	Feb 10, 2025	D103272
A2516052	Certificate of Analysis	Feb 10, 2025	D103272
A2516053	Certificate of Analysis	Feb 10, 2025	D103272
J2415470	Certificate of Analysis	Oct 21, 2024	D103272
J2415471	Certificate of Analysis	Oct 21, 2024	D103272
J2415480	Certificate of Analysis	Oct 21, 2024	D103272
J2415481	Certificate of Analysis	Oct 21, 2024	D103272
J2415482	Certificate of Analysis	Oct 21, 2024	D103272
J2415485	Certificate of Analysis	Oct 21, 2024	D103272
I2424166	Certificate of Analysis	Sep 28, 2024	D103272
I2424167	Certificate of Analysis	Sep 28, 2024	D103272
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Proprietà chimiche e fisiche

Sensibilità	Hygroscopic.
Indice di rifrazione	1.477-1.48
Punto di infiammabilità (°F)	189 °F
Punto di infiammabilità (°C)	87℃
Punto di ebollizione (°C)	189°C
Punto di fusione (°C)	16-19 °C (lit.)
Peso molecolare	78.140 g/mol
XLogP3	-0.600
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	2
Rotatable Bond Count	0
Exact Mass	78.0139 Da
Monoisotopic Mass	78.0139 Da
Topological Polar Surface Area	36.300 Å²
Heavy Atom Count	4
Formal Charge	0
Complexity	29.000
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

Domande frequenti e articoli

Burgess reagent

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OxidizingAgents Organic Reaction Toolbox Burgess reagent

The Importance of L-Tyrosine in Laboratory Research and Cell Culture

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cell culture Amino acids Solvents Peptides Cell biology Metabolites Laboratory chemicals Medium component Liquid media

Formic Acid

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Organic Reaction Toolbox Reducing agents Oxidation Reagents Oxidation Reaction

Common Reducing Agents Used in Protein Experiments

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Reducing agents Protein Experiments

How do I load a hydrophobic drug into liposomes?

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liposomes

Differences Between Transformation and Transfection

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Transfection Transformation

How to Dissolve Biotin for Streptavidin Elution Buffers

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Buffer Streptavidin Biotin

CRISPR Gene-Editing Therapies

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CRISPR

How should laboratory strains be preserved?

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Microbial strains

Hoechst Staining for Apoptosis Detection: Experimental Workflow

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Fluorescent dyes Hoechst

What methods are used to measure cell proliferation?

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Cell Proliferation

FeRhoNox-1 (Fe²⁺ Indicator) Fluorescent Probe Instruction Manual — Practical Guide for Specific Detection of Intracellular Fe²⁺ in Live Cells

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FeRhoNox-1 Live cell fluorescent probe

Operational Guide for Fluorescent Labeling of Antibodies Using AF594 NHS Ester

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AF594 NHS Ester

Application Guide to Super Fluor 680 / 750 Near-Infrared Dyes for In Vivo Small-Animal Fluorescence Imaging

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Super Fluor 680 / 750 Near-Infrared Dyes

FAQ on Cell Culture Serum

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Serum

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

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NHS-Activated Esters

Mag-Fluo-4 AM Magnesium/Calcium Ion Fluorescent Probe: Properties, Experimental Use, and Aladdin Metal Ion Fluorescent Probe Selection Guide

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Fluorescent probes Fluorescent metal ion probe

Rapamycin: A Life-Balance Regulator Born from Easter Island Soil

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Rapamycin Sirolimus

Hesperidin: A Multifunctional Flavonoid Hidden in Citrus Peels

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Hesperidin

Protease & Phosphatase Inhibitor Cocktails: Research Applications and Principles

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Cell lysis Protein extraction Tissue homogenate

Carotenoids: Structural Features, Dietary Sources and Research Applications – With an Aladdin Natural Pigments Product Selection Guide

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Carotenoids

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

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Nanoclay

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

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Pd Palladium-Catalyzed Reactions

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

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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)

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Chemical probe Small-Molecule Chemical Probes

CCK-8 (WST-8) Colorimetric Cell Viability Assay: Principles, Experimental Design, and Typical Applications

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Cell Proliferation Cytotoxicity CCK-8 WST-8 cell viability drug sensitivity

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)

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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)

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–OCH₃

A Review of Ten Commonly Used Techniques for Detection, Quantification, and Interaction Analysis in Nucleic Acid Research

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PCR ChIP EMSA Nucleic acid detection Nucleic acid quantification RT-PCR Sequencing UV spectrophotometry Southern blot Northern blot Nucleic acid probes DNA footprinting

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)

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Nitrogen-containing heterocycles Polycyclic aromatic compounds aromatic compounds Chemiluminescence immunoassay

GelRed Nucleic Acid Stain: Frequently Asked Questions

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GelRed

Plant Omics Panorama: Workflow Frameworks and Multi-Omics Integration from Genomics to Transcriptomics, Proteomics, and Metabolomics

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Proteomics Plant omics Genomics Transcriptomics Metabolomics Multi-omics integration Phenomics Epigenomics

Diaphorase: NAD(P)H-Dependent Electron-Transfer Activity and Its Applications in Detection and Research

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NADH NADPH Formazan Diaphorase Flavin cofactor Tetrazolium salt Coupled-enzyme assay NADPH-diaphorase histochemistry Myocardial Enzyme

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)

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Cross-coupling reactions Suzuki–Miyaura

Angiotensin-Converting Enzyme (ACE): A Review of Molecular Features, Catalytic Functions, and Research and Translational Applications

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angiotensin-converting enzyme ACE RAAS

Fluconazole: Physicochemical Properties, Mechanism of Action, and Key Points for Clinical and Research Applications

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Triazole ergosterol Pharmacokinetics fluconazole CYP51 Candida Cryptococcus resistance PK/PD

AmpC β-Lactamases (Cephalosporinases): Mechanisms of Production, Diagnostic Pathways, and Research and Clinical Applications

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Azithromycin: Physicochemical Features, Mechanism of Action, and Key Points for Research Applications

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ferulic acid 3-methoxy-4-hydroxycinnamic acid

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HPLC Antioxidant anti-inflammatory skin barrier paeonol 2-hydroxy-4-methoxyacetophenone phenolic aromatic ketone analgesic anti-allergic formulation and delivery

Famotidine: Physicochemical Features, Mechanism of Action, and Key Points for Research Applications

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

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Trimethylaluminum Unprotected amino acids One pot method for peptide chain elongation

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Specific rotation measurement Specific rotation

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DSC N,N′-disuccinimidyl carbonate

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Medicinal Chemistry Functional Group Synthetic Intermediate

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N-Haloalkyl Phthalimides Gabriel synthesis

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

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PEI Polyetherimide

4-[(tert-Butyldimethylsilyl)oxy]butan-1-ol: Experimental Selection Logic as a Monoprotected 1,4-Butanediol Building Block and a Protected C4 Linker

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Organic synthesis Medicinal Chemistry Hydroxyl Protecting Groups

Application Comparison of the Neutral Red Assay and the MTT/CCK-8 Assays in Cytotoxicity Testing

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Cytotoxicity MTT CCK-8 method comparison Neutral Red assay lysosomal function dehydrogenase activity metabolic activity

Comparison of Principles, System Control, and Result Interpretation in Hydroxyl Radical Scavenging Capacity Assays

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Antioxidant Evaluation Chemiluminescence Hydroxyl Radical Scavenging Capacity Fenton Reaction Salicylic Acid Method Deoxyribose Assay Electron Spin Resonance

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

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perovskite Solar cell Metal halides

Mechanisms and Experimental Applications of β-GP, Ascorbic Acid, and Dexamethasone in Osteogenic Induction Systems

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ascorbic acid Dexamethasone Extracellular matrix β-GP ALP β-glycerophosphate Osteogenic induction Mineralized nodules

Avertin Anesthetic (Avertin, 2,2,2-Tribromoethanol): Overview, Applications, and Experimental Precautions

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Quality control Avertin tribromoethanol mouse anesthesi intraperitoneal injection peri-anesthetic management adverse reactions

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Peptide synthesis Abnormal impurities

Practical Guide to TSA Tyramide Signal Amplification: How to Select Reagents, Optimize the Workflow, and Reduce Background When Detection Signals Are Weak for Low-Abundance Targets

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ICC IHC Immunohistochemistry Horseradish peroxidase In situ hybridization TSA tyramide signal amplification Fluorescence In Situ Hybridization

What Is Synthetic Biology? The Industrialization Pathway from Upstream Reagent Toolchains to Biomanufacturing Applications

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Synthetic Biology SB

Rongalite, Sodium hydroxymethanesulfinate

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Chemical synthesis Reducing agent Selective reduction Efficient Reduction

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

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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

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Photocatalysts Saturated quaternary ring Skeleton

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

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Polypeptide Fluorinated groups

3,3-Spiro-α-Proline Building Blocks: Structural Features, Complementary Synthetic Routes, and Multigram-Scale Preparation

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Unnatural amino acids conformational restriction molecular building block 3,3-spiro-α-proline spiro quaternary carbon multigram-scale synthesis

Stereoretentive Decarboxylative Amidation with Dioxazolones: A Two-Electron Rearrangement Mechanism for Stereochemical Transfer from Chiral Carboxylic Acids

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Dioxazolone Decarboxylative Amidation Decarboxylation coupling

Reaction Logic of I₂/DMSO-Mediated Oxidation of Aryl Methyl Ketones: In Situ Generation, Trapping, and Heterocycle Construction of Aryl Glyoxals

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Dimethyl sulfoxide DMSO

Dual Role of NH₄SCN and CN Transfer: From Electrochemical Oxidation of SCN⁻ to the Construction of 1-Cyanoimidazo[1,5-a]pyridines

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NH₄SCN SCN⁻ Thiocyanation

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

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Photocatalytic

Rotary-Evaporation-Assisted Reversible Dehydration Reactions: Reduced-Pressure Evaporation, Removal of Volatile Components, and Equilibrium Response

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Rotary Evaporation

Fundamentals of the Reactivity of 9,10-Phenanthrenequinone and Its Derivatives: Vicinal Dicarbonyl Electronic Structure, Electron Transfer, and Photochemical Reactions

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9,10-phenanthrenequinone PQ

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

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

From Temporary Covalent Assembly to Intramolecular Smiles Aryl Migration: DCPDC-Mediated Phenol–Primary Amine C–N Cross-Coupling

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Drugs Aryl C–N

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IC50 determination50

Cell viability278

Industrial & non-pharma application353

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