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GF08507426

Titanium

foil, thickness 0.05 mm, 4 mm diameter, purity 99.6+%

Synonym(s):

TI000310

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About This Item

Empirical Formula (Hill Notation):
Ti
CAS Number:
Molecular Weight:
47.87
MDL number:
UNSPSC Code:
12141746
PubChem Substance ID:
NACRES:
NA.23
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Assay

≥99.6%

form

foil

autoignition temp.

860 °F

manufacturer/tradename

Goodfellow 085-074-26

resistivity

42.0 μΩ-cm, 20°C

diam.

4 mm

thickness

0.05 mm

diameter

4 mm

bp

3287 °C (lit.)

mp

1660 °C (lit.)

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GF59105189GF40852728GF49248490
manufacturer/tradename

Goodfellow 085-074-26

manufacturer/tradename

Goodfellow 591-051-89

manufacturer/tradename

Goodfellow 408-527-28

manufacturer/tradename

Goodfellow 492-484-90

form

foil

form

foil

form

foil

form

foil

assay

≥99.6%

assay

≥99.6%

assay

≥99.6%

assay

≥99.6%

bp

3287 °C (lit.)

bp

3287 °C (lit.)

bp

3287 °C (lit.)

bp

3287 °C (lit.)

density

4.5 g/mL at 25 °C (lit.)

density

4.5 g/mL at 25 °C (lit.)

density

4.5 g/mL at 25 °C (lit.)

density

4.5 g/mL at 25 °C (lit.)

resistivity

42.0 μΩ-cm, 20°C

resistivity

42.0 μΩ-cm, 20°C

resistivity

42.0 μΩ-cm, 20°C

resistivity

42.0 μΩ-cm, 20°C

General description

For updated SDS information please visit www.goodfellow.com

Legal Information

Product of Goodfellow

Storage Class Code

13 - Non Combustible Solids

WGK

nwg

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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    Magdalena Kotańska et al.
    Biochemical pharmacology, 168, 193-203 (2019-07-12)
    Histamine H3 receptors ligands act anorectic by blocking the H3 autoreceptors in the CNS, that results in increased synthesis and disinhibition of histamine release. Histamine further influencing H1 receptors participates in the leptin-dependent inhibition of food intake. It also affects
    Structure-activity relations of histamine analogs. XX. Absolute configuration and histamine-like activity of enantiomeric α-methyl histamines.
    Gerhard, et al.
    Archives of Pharmacal Research, 313, 709-709 (1980)
    J M Arrang et al.
    Nature, 327(6118), 117-123 (1987-05-14)
    New drugs selective for histamine H3-receptors can be used to establish that these receptors are involved in the feedback control of histamine synthesis and release, and to demonstrate their distribution in the brain and peripheral tissues. These drugs provide new
    R Oishi et al.
    Journal of neurochemistry, 52(5), 1388-1392 (1989-05-01)
    To study the feedback control by histamine (HA) H3-receptors on the synthesis and release of HA at nerve endings in the brain, the effects of a potent and selective H3-agonist, (R)-alpha-methylhistamine, and an H3-antagonist, thioperamide, on the pargyline-induced accumulation of
    Xu-Dong Wang et al.
    Nature communications, 10(1), 3201-3201 (2019-07-22)
    Pulmonary neuroendocrine (NE) cancer, including small cell lung cancer (SCLC), is a particularly aggressive malignancy. The lineage-specific transcription factors Achaete-scute homolog 1 (ASCL1), NEUROD1 and POU2F3 have been reported to identify the different subtypes of pulmonary NE cancers. Using a

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