추천 제품
분석
≥99.995% trace metals basis
형태
crystalline
반응 적합성
reagent type: catalyst
core: titanium
mp
440 °C (dec.) (lit.)
SMILES string
Cl[Ti](Cl)Cl
InChI
1S/3ClH.Ti/h3*1H;/q;;;+3/p-3
InChI key
YONPGGFAJWQGJC-UHFFFAOYSA-K
유사한 제품을 찾으십니까? 방문 제품 비교 안내
애플리케이션
Used for the vapor-phase formation of intermetallic compounds with ultrafine particle size.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Pyr. Sol. 1 - Skin Corr. 1B
보충제 위험성
Storage Class Code
4.2 - Pyrophoric and self-heating hazardous materials
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
Gnana S Siluvai et al.
Biochemistry, 48(51), 12133-12144 (2009-11-20)
Sco-like proteins contain copper bound by two cysteines and a histidine residue. Although their function is still incompletely understood, there is a clear involvement with the assembly of cytochrome oxidases that contain the Cu(A) center in subunit 2, possibly mediating
Investigation into the effectiveness of surface treatment on poly(methyl methacrylate) when exposed in the mouth.
M D Murray
The Journal of prosthetic dentistry, 59(3), 368-373 (1988-03-01)
D J Kushner et al.
Analytical biochemistry, 133(1), 116-119 (1983-08-01)
Hydroxamic acid siderophores were observed to be inactivated by exposure to titanium(III) chloride. To study the reaction, a series of eight model hydroxamic acids were prepared and reacted with titanium(III) chloride. The products were shown by ir and NMR comparisons
Yan Zhang et al.
Organic & biomolecular chemistry, 9(13), 4977-4982 (2011-05-21)
N-N bond cleavage in hydrazines is widely used in the preparation of amines and thus occupies a significant place in organic synthesis. In this paper, we report a new method for the reductive cleavage of N-N bonds in hydrazines by
C P Offen et al.
Xenobiotica; the fate of foreign compounds in biological systems, 15(6), 503-511 (1985-06-01)
The metabolic fate of chlormethiazole in healthy male subjects has been investigated following the oral administration of a single dose of chlormethiazole edisylate. Five urinary C-oxidation metabolites were identified and shown to be identical with previously reported metabolites. A novel
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