Name: Dimethyl sulfoxide(DMSO) - ACS, ≥99.9% , CAS No.67-68-5
Brand: Aladdin Scientific
SKU: D103281
Availability: InStock

Especificaciones Nombres e identificadores Documentación Datos avanzados Taxonomic Classification Estructura 3D Objetivos asociados (humanos) Objetivos asociados (no humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Preguntas frecuentes y artículos Citations of This Product Calculadoras de soluciones Reseñas

🧪

Por qué esta calidad

ACS, ≥99.9% ACS para flujos de trabajo cromatográficos y analíticos sensibles que requieren una interferencia mínima de la línea base.

🌡

Almacenamiento y envío

Argon charged,Desiccated,Room temperature Envío Normal. Consulte el COA específico del lote para conocer las especificaciones exactas.

📋

Documentos de calidad

SDS, COA, ficha técnica y hoja de especificaciones disponibles para descargar. COA específico del lote accesible mediante búsqueda por número de lote.

📚

Prueba documental

Citado en 5363 publicaciones revisadas por pares sobre cromatografía, síntesis orgánica y reacciones de acoplamiento cruzado.

Especificaciones

Sinónimos

Especificaciones y pureza

ACS, ≥99.9%

Condiciones de almacenamiento de almacenamiento

Argon charged,Desiccated,Room temperature

Enviado en

Normal

Grado

ACS

Pureza

≥99.9%

Nombres e identificadores

Pubchem Sid

508812221

Sonrisas canónicas

CS(=O)C

IUPAC Name

methylsulfinylmethane

InChIKey

IAZDPXIOMUYVGZ-UHFFFAOYSA-N

INCHI

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

Isómeros SMILES

CS(=O)C

WGK Alemania

RTECS

PV6210000

Peso molecular

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=

Documentación

📋 Hoja de datos de seguridad (SDS)

Documento completo sobre peligros, manipulación, almacenamiento y cumplimiento normativo.

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

✅ Certificado de análisis (COA)

Datos de calidad específicos del lote. Introduzca su número de lote para obtener el COA exacto.

Buscar COA →

📊 Ficha técnica

Resumen de referencia rápida de las especificaciones y aplicaciones del producto.

Ver ficha técnica →

🔬 Hoja de especificaciones

Atributos de calidad completos y criterios de aceptación para esta calidad.

Ver hoja de especificaciones →

Datos avanzados

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organosulfur compounds
  - Clase Sulfoxides

Kingdom	Organic compounds
Superclass	Organosulfur compounds
Clase	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
Descripción	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

Estructura 3D

Objetivos asociados (humanos)

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

Objetivos asociados (no humanos)

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

Mecanismos de acción

Certificados (CoA, COO, BSE/TSE y tabla de análisis)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

87 results found

Lot Number	Certificate Type	Fecha	Articulo
I2621641	Certificate of Analysis	Sep 18, 2026	D103281
I2621642	Certificate of Analysis	Sep 18, 2026	D103281
I2621643	Certificate of Analysis	Sep 18, 2026	D103281
I2621644	Certificate of Analysis	Sep 18, 2026	D103281
E2629152	Certificate of Analysis	May 18, 2026	D103281
G2630222	Certificate of Analysis	May 18, 2026	D103281
G2630221	Certificate of Analysis	May 18, 2026	D103281
G2630157	Certificate of Analysis	May 18, 2026	D103281
G2630223	Certificate of Analysis	May 18, 2026	D103281
G2630224	Certificate of Analysis	May 18, 2026	D103281
G2630225	Certificate of Analysis	May 18, 2026	D103281
E2629155	Certificate of Analysis	May 18, 2026	D103281
E2629150	Certificate of Analysis	May 18, 2026	D103281
C2623458	Certificate of Analysis	Mar 18, 2026	D103281
C2623459	Certificate of Analysis	Mar 18, 2026	D103281
A2605176	Certificate of Analysis	Jan 06, 2026	D103281
A2615176	Certificate of Analysis	Jan 06, 2026	D103281
A2615200	Certificate of Analysis	Jan 06, 2026	D103281
A2615201	Certificate of Analysis	Jan 06, 2026	D103281
A2615202	Certificate of Analysis	Jan 06, 2026	D103281
A2615203	Certificate of Analysis	Jan 06, 2026	D103281
C2603215	Certificate of Analysis	Jan 06, 2026	D103281
C2603216	Certificate of Analysis	Jan 06, 2026	D103281
C2603235	Certificate of Analysis	Jan 06, 2026	D103281
K2526258	Certificate of Analysis	Nov 15, 2025	D103281
K2526257	Certificate of Analysis	Nov 15, 2025	D103281
K2526229	Certificate of Analysis	Nov 15, 2025	D103281
K2526250	Certificate of Analysis	Nov 15, 2025	D103281
K2526251	Certificate of Analysis	Nov 15, 2025	D103281
F2517106	Certificate of Analysis	May 28, 2025	D103281
G2518125	Certificate of Analysis	May 28, 2025	D103281
G2518123	Certificate of Analysis	May 28, 2025	D103281
F2517144	Certificate of Analysis	May 28, 2025	D103281
F2517139	Certificate of Analysis	May 28, 2025	D103281
F2517137	Certificate of Analysis	May 28, 2025	D103281
F2517135	Certificate of Analysis	May 28, 2025	D103281
G2518182	Certificate of Analysis	May 28, 2025	D103281
G2524148	Certificate of Analysis	May 28, 2025	D103281
G2524149	Certificate of Analysis	May 28, 2025	D103281
D2521339	Certificate of Analysis	Apr 14, 2025	D103281
D2521361	Certificate of Analysis	Apr 14, 2025	D103281
D2521360	Certificate of Analysis	Apr 14, 2025	D103281
D2521340	Certificate of Analysis	Apr 14, 2025	D103281
D2521338	Certificate of Analysis	Apr 14, 2025	D103281
D2502103	Certificate of Analysis	Oct 30, 2024	D103281
K2407298	Certificate of Analysis	Oct 30, 2024	D103281
K2407295	Certificate of Analysis	Oct 30, 2024	D103281
K2407296	Certificate of Analysis	Oct 30, 2024	D103281
K2407297	Certificate of Analysis	Oct 30, 2024	D103281
K2407299	Certificate of Analysis	Oct 30, 2024	D103281
J2416182	Certificate of Analysis	Jul 05, 2024	D103281
G2411092	Certificate of Analysis	Jul 05, 2024	D103281
G2411091	Certificate of Analysis	Jul 05, 2024	D103281
G2411089	Certificate of Analysis	Jul 05, 2024	D103281
J2219065	Certificate of Analysis	Jul 05, 2024	D103281
F2217333	Certificate of Analysis	Mar 20, 2024	D103281
E2226039	Certificate of Analysis	Feb 20, 2024	D103281
K2309517	Certificate of Analysis	Oct 27, 2023	D103281
K2309529	Certificate of Analysis	Oct 27, 2023	D103281
K2309537	Certificate of Analysis	Oct 27, 2023	D103281
I2312261	Certificate of Analysis	Aug 30, 2023	D103281
I2312260	Certificate of Analysis	Aug 30, 2023	D103281
K2115027	Certificate of Analysis	Aug 07, 2023	D103281
F2308951	Certificate of Analysis	May 31, 2023	D103281
F2308950	Certificate of Analysis	May 31, 2023	D103281
F2308949	Certificate of Analysis	May 31, 2023	D103281
H2120213	Certificate of Analysis	May 12, 2023	D103281
E23251034	Certificate of Analysis	May 05, 2023	D103281
E23251025	Certificate of Analysis	May 05, 2023	D103281
F2110065	Certificate of Analysis	Mar 13, 2023	D103281
A2331321	Certificate of Analysis	Jan 10, 2023	D103281
A2331320	Certificate of Analysis	Jan 10, 2023	D103281
K2223064	Certificate of Analysis	Nov 05, 2022	D103281
K2223065	Certificate of Analysis	Nov 05, 2022	D103281
J2219089	Certificate of Analysis	Oct 12, 2022	D103281
J2219066	Certificate of Analysis	Oct 12, 2022	D103281
I2206576	Certificate of Analysis	Sep 09, 2022	D103281
I2206575	Certificate of Analysis	Sep 09, 2022	D103281
I2206572	Certificate of Analysis	Sep 09, 2022	D103281
H2211202	Certificate of Analysis	Aug 15, 2022	D103281
H2211114	Certificate of Analysis	Aug 15, 2022	D103281
F2217325	Certificate of Analysis	Jun 24, 2022	D103281
F2204742	Certificate of Analysis	Jun 09, 2022	D103281
E2226043	Certificate of Analysis	Jun 01, 2022	D103281
E2226042	Certificate of Analysis	Jun 01, 2022	D103281
G2129048	Certificate of Analysis	Aug 02, 2021	D103281
E2225004	Certificate of Analysis	Aug 02, 2021	D103281

Propiedades químicas y físicas

Sensibilidad	Hygroscopic.
Índice de refracción	1.477-1.48
Punto de inflamación (°F)	189 °F
Punto de inflamación (°C)	87℃
Punto de ebullición (°C)	189°C
Punto de fusión (°C)	16-19 °C (lit.)
Peso molecular	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

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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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β-lactamase AmpC cephalosporinase Ambler class C Bush group 1 inducible expression derepression cefoxitin hree-dimensional test carbapenems fourth-generation cephalosporins resistance surveillance

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

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Macrolides resistance PK/PD azithromycin 50S ribosome tissue distribution intracellular accumulation inflammation models antibacterial pharmacodynamics

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

Extraction Methods and Process Selection for Flavonoid Compounds

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flavonoid compounds extraction methods solvent extraction ultrasound-assisted extraction microwave-assisted extraction enzyme-assisted extraction supercritical fluid extraction process optimization

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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Especificaciones

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