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Merck
모든 사진(1)

주요 문서

357871

Sigma-Aldrich

5-Mercapto-1-methyltetrazole

98%

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About This Item

실험식(Hill 표기법):
C2H4N4S
CAS Number:
Molecular Weight:
116.14
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22
357871 제품과 관련한 질문은 현지 머크 영업소 또는 판매 사원에게 문의해 주십시오. 고객지원팀으로 연락바랍니다.

분석

98%

양식

powder

mp

125-128 °C (lit.)

SMILES string

Cn1nnnc1S

InChI

1S/C2H4N4S/c1-6-2(7)3-4-5-6/h1H3,(H,3,5,7)

InChI key

XOHZHMUQBFJTNH-UHFFFAOYSA-N

일반 설명

5-Mercapto-1-methyltetrazole is a heterocyclic thiol derivative. It forms dimeric or tetrameric complexes with trimethylgallium.[1]

애플리케이션

5-Mercapto-1-methyltetrazole may be employed as heterocyclic ligand to study the geometry and stereochemical activity of the lone pair at the lead atom in hemi- and holo-directed lead(II) complexes.[2] It may be used in the chemical modification of submicron particles of mesoporous MSU-2 silica[3] and SBA-15 mesoporous silica.[4]

픽토그램

Exclamation mark

신호어

Warning

유해 및 위험 성명서

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

표적 기관

Respiratory system

Storage Class Code

4.1A - Other explosive hazardous materials

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves


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문서 라이브러리 방문

Muhammad Imran et al.
Dalton transactions (Cambridge, England : 2003), 44(3), 924-937 (2014-08-12)
To investigate the geometry and stereochemical activity of the lone pair at the lead atom, lead(ii) complexes () with one tripodal (L(1)), one dipodal (L(2)) boron-centred soft ligand and eight other small soft heterocyclic ligands, 2-mercaptobenzimidazole (L(3)), 2-mercapto-5-methylbenzimidazole (L(4)), 3-mercapto-1,2,4-triazole
N Kanazumi et al.
Hepato-gastroenterology, 47(36), 1695-1699 (2001-01-10)
In this study, we examined the influence of clinical treatments in the perioperative period upon PIVKA-II (plasma levels of protein induced by vitamin K absence or antagonist-II) in patients with hepatocellular carcinoma and pancreatobiliary diseases. During a perioperative period, plasma
J J Lipsky
Biochemical pharmacology, 38(5), 773-779 (1989-03-01)
Antibiotics that contain the 1-methyltetrazole-5-thiol (MTT) leaving group are associated with an adverse effect when alcohol is ingested after their administration. Therefore, the ability of MTT to inhibit an enzyme in alcohol metabolism, aldehyde dehydrogenase (ALDH), was examined. In the
Damián Pérez-Quintanilla et al.
Journal of nanoscience and nanotechnology, 9(8), 4901-4909 (2009-11-26)
Submicron particles of mesoporous MSU-2 silica have been obtained by using Tergitol NP-9 as nonionic surfactant and TEOS as silica precursor. The material has been chemically modified with 5-mercapto-1-methyltetrazole and characterized by powder X-ray diffraction, TEM, SEM, N2 adsorption, FT-IR
K Kawamoto et al.
Japanese journal of pharmacology, 47(2), 169-178 (1988-06-01)
Liver microsomal vitamin K epoxide reductase activity was determined by measuring the formation of menaquinone-4 from the substrate menaquinone-4 2,3-epoxide. The enzyme was active when dithiothreitol (DTT) was used as a reducing agent, and the activity increased gradually with increasing

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