Name: Dimethyl sulfoxide（DMSO） - Anhydrous Grade , CAS No.67-68-5
Brand: Aladdin Scientific
SKU: D103276
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

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Pourquoi cette qualité

Anhydrous Grade Anhydrous Grade pour les flux de travail chromatographiques et analytiques sensibles nécessitant une interférence de ligne de base minimale.

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Stockage & expédition

Room temperature,Argon charged,Desiccated Expédition Normal. Consultez le COA spécifique au lot pour les spécifications exactes.

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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.

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Preuve documentaire

Cité dans 5363 publications à comité de lecture couvrant la chromatographie, la synthèse organique et les réactions de couplage croisé.

Spécifications

Synonymes

Spécifications et pureté

Anhydrous Grade

Conditions de stockage de stockage

Room temperature,Argon charged,Desiccated

Expédié en

Normal

Grade

Anhydrous Grade

Noms et identifiants

Pubchem Sid

508812213

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/508812213

Sourires canoniques

CS(=O)C

IUPAC Name

methylsulfinylmethane

InChIKey

IAZDPXIOMUYVGZ-UHFFFAOYSA-N

INCHI

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

Isomères SMILES

CS(=O)C

WGK Allemagne

RTECS

PV6210000

Poids moléculaire

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=

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 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
Description	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

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

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

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

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

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.

209 results found

Lot Number	Certificate Type	Date	Article
J2620237	Certificate of Analysis	Oct 26, 2026	D103276
J2620292	Certificate of Analysis	Oct 14, 2026	D103276
J2620288	Certificate of Analysis	Oct 10, 2026	D103276
J2620290	Certificate of Analysis	Oct 10, 2026	D103276
J2620286	Certificate of Analysis	Oct 10, 2026	D103276
J2620496	Certificate of Analysis	Oct 10, 2026	D103276
J2620494	Certificate of Analysis	Oct 10, 2026	D103276
J2620495	Certificate of Analysis	Oct 10, 2026	D103276
J2620231	Certificate of Analysis	Sep 30, 2026	D103276
J2620232	Certificate of Analysis	Sep 30, 2026	D103276
J2620233	Certificate of Analysis	Sep 30, 2026	D103276
J2620235	Certificate of Analysis	Sep 30, 2026	D103276
J2620234	Certificate of Analysis	Sep 14, 2026	D103276
J2620238	Certificate of Analysis	Sep 14, 2026	D103276
J2620236	Certificate of Analysis	Sep 14, 2026	D103276
I2618473	Certificate of Analysis	Sep 09, 2026	D103276
I2618474	Certificate of Analysis	Sep 09, 2026	D103276
I2618469	Certificate of Analysis	Sep 04, 2026	D103276
I2618470	Certificate of Analysis	Sep 04, 2026	D103276
I2618471	Certificate of Analysis	Sep 04, 2026	D103276
I2618472	Certificate of Analysis	Sep 04, 2026	D103276
I2618467	Certificate of Analysis	Sep 03, 2026	D103276
I2618468	Certificate of Analysis	Sep 03, 2026	D103276
I2601452	Certificate of Analysis	Aug 25, 2026	D103276
I2601504	Certificate of Analysis	Aug 25, 2026	D103276
I2601505	Certificate of Analysis	Aug 25, 2026	D103276
I2601507	Certificate of Analysis	Aug 25, 2026	D103276
H2603362	Certificate of Analysis	Jul 13, 2026	D103276
H2603330	Certificate of Analysis	Jul 07, 2026	D103276
H2603332	Certificate of Analysis	Jul 02, 2026	D103276
H2603363	Certificate of Analysis	Jul 02, 2026	D103276
G2606301	Certificate of Analysis	Jun 24, 2026	D103276
G2606300	Certificate of Analysis	Jun 23, 2026	D103276
G2606299	Certificate of Analysis	Jun 17, 2026	D103276
G2606298	Certificate of Analysis	Jun 16, 2026	D103276
G2606297	Certificate of Analysis	Jun 12, 2026	D103276
F2611400	Certificate of Analysis	Jun 02, 2026	D103276
F2611397	Certificate of Analysis	May 28, 2026	D103276
F2611396	Certificate of Analysis	May 19, 2026	D103276
F2611398	Certificate of Analysis	May 13, 2026	D103276
E2614235	Certificate of Analysis	May 06, 2026	D103276
E2614234	Certificate of Analysis	Apr 24, 2026	D103276
E2614233	Certificate of Analysis	Apr 22, 2026	D103276
E2614231	Certificate of Analysis	Apr 21, 2026	D103276
E2614232	Certificate of Analysis	Apr 21, 2026	D103276
D2622268	Certificate of Analysis	Apr 09, 2026	D103276
D2622293	Certificate of Analysis	Apr 09, 2026	D103276
D2622294	Certificate of Analysis	Apr 09, 2026	D103276
D2603274	Certificate of Analysis	Mar 25, 2026	D103276
D2603288	Certificate of Analysis	Mar 25, 2026	D103276
D2603287	Certificate of Analysis	Mar 17, 2026	D103276
D2603289	Certificate of Analysis	Mar 17, 2026	D103276
C2625394	Certificate of Analysis	Mar 12, 2026	D103276
C2625408	Certificate of Analysis	Mar 12, 2026	D103276
L2508315	Certificate of Analysis	Dec 02, 2025	D103276
L2508318	Certificate of Analysis	Dec 02, 2025	D103276
L2508407	Certificate of Analysis	Dec 02, 2025	D103276
L2508316	Certificate of Analysis	Nov 24, 2025	D103276
L2508319	Certificate of Analysis	Nov 24, 2025	D103276
L2508317	Certificate of Analysis	Nov 24, 2025	D103276
L2508644	Certificate of Analysis	Nov 21, 2025	D103276
L2508675	Certificate of Analysis	Nov 21, 2025	D103276
L2508677	Certificate of Analysis	Nov 21, 2025	D103276
L2508678	Certificate of Analysis	Nov 21, 2025	D103276
K2518378	Certificate of Analysis	Nov 10, 2025	D103276
K2518403	Certificate of Analysis	Nov 10, 2025	D103276
K2518404	Certificate of Analysis	Nov 10, 2025	D103276
K2518407	Certificate of Analysis	Nov 10, 2025	D103276
K2518379	Certificate of Analysis	Nov 10, 2025	D103276
K2518406	Certificate of Analysis	Nov 10, 2025	D103276
K2518385	Certificate of Analysis	Nov 03, 2025	D103276
K2518405	Certificate of Analysis	Nov 03, 2025	D103276
J2517691	Certificate of Analysis	Oct 09, 2025	D103276
J2517715	Certificate of Analysis	Oct 09, 2025	D103276
J2517687	Certificate of Analysis	Oct 09, 2025	D103276
J2517689	Certificate of Analysis	Oct 09, 2025	D103276
I2529182	Certificate of Analysis	Sep 22, 2025	D103276
I2529183	Certificate of Analysis	Sep 22, 2025	D103276
I2529184	Certificate of Analysis	Sep 22, 2025	D103276
I2529187	Certificate of Analysis	Sep 22, 2025	D103276
I2529186	Certificate of Analysis	Sep 22, 2025	D103276
I2529188	Certificate of Analysis	Sep 22, 2025	D103276
I2529185	Certificate of Analysis	Sep 22, 2025	D103276
I2529189	Certificate of Analysis	Sep 22, 2025	D103276
I2522202	Certificate of Analysis	Sep 16, 2025	D103276
I2522203	Certificate of Analysis	Sep 16, 2025	D103276
I2502305	Certificate of Analysis	Aug 26, 2025	D103276
I2502306	Certificate of Analysis	Aug 26, 2025	D103276
H2504192	Certificate of Analysis	Jul 25, 2025	D103276
H2504214	Certificate of Analysis	Jul 25, 2025	D103276
G2529242	Certificate of Analysis	Jul 23, 2025	D103276
G2529243	Certificate of Analysis	Jul 23, 2025	D103276
G2503230	Certificate of Analysis	Jun 23, 2025	D103276
G2503231	Certificate of Analysis	Jun 23, 2025	D103276
F2523381	Certificate of Analysis	Jun 17, 2025	D103276
F2523382	Certificate of Analysis	Jun 17, 2025	D103276
F2510601	Certificate of Analysis	Jun 03, 2025	D103276
F2510602	Certificate of Analysis	Jun 03, 2025	D103276
D2525168	Certificate of Analysis	Apr 22, 2025	D103276
D2525169	Certificate of Analysis	Apr 22, 2025	D103276
C2513439	Certificate of Analysis	Mar 06, 2025	D103276
C2513440	Certificate of Analysis	Mar 06, 2025	D103276
B2508244	Certificate of Analysis	Jan 14, 2025	D103276
B2508262	Certificate of Analysis	Jan 14, 2025	D103276
L2420704	Certificate of Analysis	Oct 29, 2024	D103276
L2420705	Certificate of Analysis	Oct 29, 2024	D103276
L2420706	Certificate of Analysis	Oct 29, 2024	D103276
J2428616	Certificate of Analysis	Sep 12, 2024	D103276
J2428656	Certificate of Analysis	Sep 12, 2024	D103276
J2428563	Certificate of Analysis	Sep 12, 2024	D103276
J2428619	Certificate of Analysis	Aug 22, 2024	D103276
J2428617	Certificate of Analysis	Aug 22, 2024	D103276
H2401369	Certificate of Analysis	Jun 11, 2024	D103276
H2401342	Certificate of Analysis	Jun 11, 2024	D103276
H2401344	Certificate of Analysis	Jun 11, 2024	D103276
H2401343	Certificate of Analysis	Jun 11, 2024	D103276
H2401368	Certificate of Analysis	Jun 11, 2024	D103276
F2412198	Certificate of Analysis	May 07, 2024	D103276
F2412199	Certificate of Analysis	May 07, 2024	D103276
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Propriétés chimiques et physiques

Sensibilité	Hygroscopic.
Indice de réfraction	1.477-1.48
Point d'éclair (°F)	189 °F
Point d'éclair (°C)	87℃
Point d'ébullition (°C)	189°C
Point de fusion (°C)	16-19 °C (lit.)
Poids moléculaire	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

FAQ et articles

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

Amine-Reactive Probe Labeling Experimental Protocol

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Fluorescent dyes Amine probe Avidin Biomolecular marker Chemical probe Nucleic acid probe preparation Biomolecular tracking Cell surface labeling Affinity purification technology

The Guide to Anhydrous Grade for Reagents

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Anhydrous Grade

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

Application of the Na⁺-Sensitive Fluorescent Indicator SBFI AM in Intracellular Sodium Imaging and Experimental Procedures

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SBFI Na⁺-selective fluorescent indicator

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

Principles and Application Strategies of Common PCR Enhancers

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PCR PCR Enhancers

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: Structural Features, Preparation Routes, and Key Points for Research Applications

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ferulic acid 3-methoxy-4-hydroxycinnamic acid

Paeonol: Physicochemical Features, Uses, and Key Points for Research Applications

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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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Pepsin cAMP PK/PD famotidine H2-receptor antagonist gastric acid secretion pH-dependent absorption renal excretion histamine signaling

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

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

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

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DSC N,N′-disuccinimidyl carbonate

How to Construct Nitriles: Route Selection Across Direct Introduction, Precursor Dehydration, Oxidation/Dehydrogenation, and Cyanide-Free Processes

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Medicinal Chemistry Functional Group Synthetic Intermediate

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

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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

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

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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