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Merck
모든 사진(3)

문서

296147

Sigma-Aldrich

Dimethyl sulfoxide-d6

99.9 atom % D, contains 0.03 % (v/v) TMS

동의어(들):

(Methyl sulfoxide)-d6, DMSO-d6, Hexadeuterodimethyl sulfoxide

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모든 사진(3)

About This Item

Linear Formula:
(CD3)2SO
CAS Number:
2206-27-1
Molecular Weight:
84.17
Beilstein:
1237248
EC Number:
218-617-0
MDL number:
MFCD00002090
UNSPSC 코드:
12191502
PubChem Substance ID:
24857840
NACRES:
NA.21

vapor pressure

0.42 mmHg ( 20 °C)

Quality Level

200

동위원소 순도

99.9 atom % D

분석

99% (CP)

형태

liquid

autoignition temp.

573 °F

포함

0.03 % (v/v) TMS

expl. lim.

42 %

기술

NMR: suitable

불순물

≤0.0250% water
water

refractive index

n20/D 1.476 (lit.)

bp

189 °C (lit.)

mp

20.2 °C (lit.)

density

1.190 g/mL at 25 °C (lit.)

질량 이동

M+6

SMILES string

[2H]C([2H])([2H])S(=O)C([2H])([2H])[2H]

InChI

1S/C2H6OS/c1-4(2)3/h1-2H3/i1D3,2D3

InChI key

IAZDPXIOMUYVGZ-WFGJKAKNSA-N

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관련 카테고리

일반 설명

Dimethyl sulfoxide-d6 is a deuterated NMR solvent that is useful in NMR-based research and analyses.

애플리케이션


  • Estimation of dissociation constants (pKa′s) of oximes from proton chemical shifts in dimethyl sulfoxide solution: This research utilizes Dimethyl sulfoxide-d₆ (DMSO-d₆) to determine pKa values of oximes, demonstrating its crucial role in enhancing the accuracy of proton NMR spectroscopy for chemical analysis and research within pharmaceutical contexts (Kurtz AP, D′Silva TD, 1987).

  • Proton nuclear magnetic resonance studies on methylthiohydantoins, thiohydantoins, and hydantoins of amino acids: DMSO-d₆ is extensively employed to investigate the structure and behavior of various hydantoin derivatives in amino acid research, proving essential for understanding protein structures and functions, with implications for both academic and pharmaceutical industries (Suzuki T, Tomioka T, Tuzimura K, 1977).

추천 제품

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Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point (°F)

190.4 °F

Flash Point (°C)

88 °C

개인 보호 장비

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)

시험 성적서(COA)

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문서 라이브러리 방문

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Acetonitrile-d3 99.8 atom % D, contains 0.03 % (v/v) TMS

Sigma-Aldrich

366544

Acetonitrile-d3

Methanol-d4 ≥99.8 atom % D, contains 0.05 % (v/v) TMS

Sigma-Aldrich

611646

Methanol-d4

M G Nair et al.
Applied and environmental microbiology, 57(2), 434-439 (1991-02-01)
Two isoflavonoids isolated from clover roots grown under phosphate stress were characterized as formononetin (7-hydroxy,4'-methoxy isoflavone) and biochanin A (5,7-dihydroxy,4'-methoxy isoflavone). At 5 ppm, these compounds stimulated hyphal growth in vitro and root colonization of an undescribed vesicular-arbuscular mycorrhiza, a
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Weber M, et al.
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Diode laser measurements of CD3 quantum yields and internal energy for the dissociation of dimethyl sulfoxide-d6.
Rudolph RN, et al.
J. Chem. Phys. , 106(4), 1346-1352 (1997)
Priya P Netalkar et al.
European journal of medicinal chemistry, 79, 47-56 (2014-04-12)
Air and moisture stable coordination compounds of late first row transition metals, viz. Co(II), Ni(II), Cu(II) and Zn(II), with a newly designed ligand, 2-(2-benzo[d]thiazol-2-yl)hydrazono)propan-1-ol (LH), were prepared and successfully characterized using various spectro-analytical techniques. The molecular structures of the ligand
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European journal of medicinal chemistry, 94, 367-377 (2015-03-18)
Three new ring systems, pyrido[2',3':3,4]pyrrolo[1,2-a]quinoxalines, pyrido[3',2':3,4]pyrrolo[1,2-a]quinoxalines and pyrido[2',3':5,6]pyrazino[2,1-a]isoindoles, were synthesized through an aza-substitution on the already active isoindolo-quinoxaline system and in particular in the position 7 or 4 of the isoindole moiety and in position 5 of the quinoxaline portion.
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관련 콘텐츠

Nuclear Magnetic Resonance (NMR)

NMR 분광법은 분자 구조, 화학 성분 및 순도를 측정하는 분석 기법입니다. NMR은 강한 자기장이 있는 경우 핵스핀 상태로 인해 흡수된 에너지를 검출합니다.

Nuclear Magnetic Resonance (NMR)

NMR spectroscopy elucidates molecular structure and purity via nuclear spin states in a strong magnetic field.

자사의 과학자팀은 생명 과학, 재료 과학, 화학 합성, 크로마토그래피, 분석 및 기타 많은 영역을 포함한 모든 과학 분야에 경험이 있습니다..

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