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

사양 이름과 식별자 문서 고급 데이터 Taxonomic Classification 3D 구조 관련 대상(인간) 관련 대상(비인간) 작용 메커니즘 인증서(CoA, COO, BSE/TSE 및 분석 차트) 화학 및 물리적 특성 자주 묻는 질문과 기사 Citations of This Product 솔루션 계산기 리뷰

🧪

이 등급을 선택하는 이유

ACS, ≥99.9% ACS 최소한의 기준선 간섭이 필요한 민감한 크로마토그래피 및 분석 워크플로우용.

🌡

보관 및 배송

Argon charged,Desiccated,Room temperature Normal 출고. 정확한 사양은 로트별 COA를 확인하세요.

📋

품질 문서

SDS, COA, 데이터시트, 사양서를 다운로드할 수 있습니다. 로트별 COA는 로트 번호 조회를 통해 확인할 수 있습니다.

📚

문헌적 근거

크로마토그래피, 유기 합성 및 교차 커플링 반응 분야의 동료 심사 논문 5363편에서 인용되었습니다.

사양

동의어

사양 및 순도

ACS, ≥99.9%

보관 조건

Argon charged,Desiccated,Room temperature

배송

Normal

등급

ACS

순수함

≥99.9%

이름과 식별자

Pubchem Sid

508812221

정식 스마일

CS(=O)C

IUPAC Name

methylsulfinylmethane

InChIKey

IAZDPXIOMUYVGZ-UHFFFAOYSA-N

INCHI

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

이성체 SMILES

CS(=O)C

WGK 독일

RTECS

PV6210000

분자량

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=

문서

📋 안전 데이터 시트(SDS)

위험성, 취급, 보관 및 규제 준수를 포괄하는 종합 문서.

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

✅ 분석 성적서(COA)

로트별 품질 데이터. 로트 번호를 입력하여 정확한 COA를 확인하세요.

COA 조회 →

📊 데이터시트

제품 사양 및 응용 분야에 대한 빠른 참조 요약.

데이터시트 보기 →

🔬 사양서

이 등급의 전체 품질 특성 및 합격 기준.

사양서 보기 →

고급 데이터

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organosulfur compounds
  - 분류 Sulfoxides

Kingdom	Organic compounds
Superclass	Organosulfur compounds
분류	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
설명	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

3D 구조

관련 대상(비인간)

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)

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Klebsiella pneumoniae (43867 Activities)

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Micrococcus luteus (7463 Activities)

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Staphylococcus aureus (210822 Activities)

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Acinetobacter baumannii (41033 Activities)

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Escherichia coli (133304 Activities)

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Aspergillus niger (16508 Activities)

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Bacillus subtilis (32866 Activities)

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Enterococcus faecalis (29875 Activities)

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Bacillus cereus (7522 Activities)

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Candida albicans (78123 Activities)

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Trypanosoma cruzi (99888 Activities)

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Mus musculus (284745 Activities)

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Rattus norvegicus (775804 Activities)

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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)

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

작용 메커니즘

인증서(CoA, COO, BSE/TSE 및 분석 차트)

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	날짜	항목
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

화학 및 물리적 특성

감도	Hygroscopic.
굴절률	1.477-1.48
발화점(°F)	189 °F
발화점(°C)	87℃
끓는점(°C)	189°C
녹는점(°C)	16-19 °C (lit.)
분자량	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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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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Dimethyl sulfoxide(DMSO) - ACS, ≥99.9% , CAS No.67-68-5

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Dimethyl sulfoxide(DMSO) - ACS, ≥99.9% , CAS No.67-68-5

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고급 데이터

Molarity Calculator

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Reconstitution Calculator

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