Detail of > 13121-70-5
- MSDS Download

- CAS Number:
- 13121-70-5
- Name:
Stannane,tricyclohexylhydroxy-
- Superlist Name:
- Cyhexatin
- Formula:
- C18H34OSn
- Molecular Structure:

- Synonyms:
- Tin,tricyclohexylhydroxy- (7CI);Acarex;Acarstin;Acarstin L;Dowco213;Hokko Cyhexatin;Hydroxytricyclohexylstannane;M 3180;NSC 179742;Pennstyl;Plictran;Pliktran;Plyctran;Redran 25PB;Sipcatin;Tricyclohexylhydroxystannane;Tricyclohexylhydroxytin;Tricyclohexylstannanol;Tricyclohexylstannyl hydroxide;Tricyclohexyltin hydroxide;
- Molecular Weight:
- 385.21
- EINECS:
- 236-049-1
- Melting Point:
- 195-198 °C
- Boiling Point:
- 426.146 °C at 760 mmHg
- Flash Point:
- 211.526 °C
- Appearance:
- Colorless to white, nearly odorless, crystalline powder
- Hazard Symbols:
Xn,
N- Risk Codes:
- 20/21/22-50/53
- Safety:
- 13-60-61Details
- Transport Information:
- UN 2811
Related products
Other Products
- Titanium Dioxide Carbon black Glutathione Adenosine Cable pulling lubricant
- 13121-70-5Stannane,tricyclohexylhydroxy-
- 10510-54-0Cresyl Violet Acetate Certified
- 25837-05-2Benzene-1,2,3,4,5-d5,6-(ethyl-1,1,2,2,2-d5)-
- 326-66-9Acetamide,N-(4-bromo-2-fluorophenyl)-
- 4887-82-51H-Benzimidazole,6-chloro-
- 2873-74-7Pentanedioyl dichloride
- 999-21-3Diallyl maleate
- 53512-10-01,5-Naphthyridine-3-carboxylicacid, 4-hydroxy-
- 350-57-2Benzene,(1,1,2,2-tetrafluoroethoxy)-
- 103-99-1Octadecanamide,N-(4-hydroxyphenyl)-
- 53287-53-93-Thiophenamine,tetrahydro-N-methyl-, 1,1-dioxide, hydrochloride (1:1)
- 54903-50-3Thieno[3,2-c]pyridine,4,5,6,7-tetrahydro-
- 2239-24-91H-Cyclohepta[1,2-a:5,4-a']dinaphthalene-3,11-diol,2,3,4,4a,5,6,6a,7,9,9a,10,11,12,13,13a,13b,14,15,15a,15b-eicosahydro-4,4,6a,10,10,13a,15b-heptamethyl-,(3S,4aR,6aS,9aR,11S,13aR,13bS,15aS,15bR)-
- 4130-42-1Phenol,2,6-bis(1,1-dimethylethyl)-4-ethyl-
- 2687-12-9Benzene,(3-chloro-1-propen-1-yl)-
Refine Suppliers Do you want your product ranking ahead? Know what is 'Top Seller'!
- Supplier Location:
China (Mainland)(26)
Germany(1)
Italy(1)
United States(1)
- Business Type:
- Importer/Exporter(26)Lab/Research institutions(1)
Please post your buying leads,so that our qualified suppliers
will soon contact you!
*Required Fields
Reference
- Effect of tin on biological aspects of Cunninghamella echinulata and Fusarium oxysporum, under various cultural conditions
- Effect of tin on biological aspects of Cunninghamella echinulata and Fusarium oxysporum, under various cultural conditions. Naguib, Mohamed I.; Hamed, Aleya A.; Haikal, Nahed Z. (Fac. Sci., Cairo Univ., Cairo, Egypt). Arab Gulf J. Sci. Res., 1(2), 487-98 (English) 1983. CODEN: AGJRE8.Some commonly used reagents like 57-13-6 and 14797-55-8 are used in this experiment. DOCUMENT TYPE: Journal CA Section: 4 (Toxicology) Stannous ions, stannic ions, and Plictran (I) [13121-70-5] had no effect on C. echinulata growth when supplied with nitrate alone; however, stannous ions stimulated growth on either urea [57-13-6] on peptone media. On the other hand, the 3 compds. were toxic to F. oxysporum when supplied with urea. With an adequate supply of C, the inorg. Sn enhanced, but I inhibited, the growth of Cunninghamella. Nitrate favored greater absorption of sugar than either urea or peptone. Stannic and I were suppressive to glucose uptake by Cunninghamella when supplied with either N sources, whereas stannous exerted almost no effect with nitrate or urea but was suppressive with peptone. The Sn compds. also hindered glucose uptake by Fusarium, a phenomenon that was alleviated or even reversed with urea feeding. Inorg. Sn stimulated respiration of Cunninghamella in the presence of nitrate, whereas respiration was inhibited in the presence of urea. I inhibited respiration in media contg. either nitrate or urea. On the other hand, the 3 Sn-contg. compds. enhanced respiration of Fusarium, regardless of the N source. Further, the presence of glucose in media contg. Sn attenuated respiration of Cunninghamella, regardless of the N source. Glucose slightly suppressed N absorption from urea or peptone, but remarkably increased N uptake from nitrate media. In most cases, the various Sn compds. inhibited N absorption by Cunninghamella when glucose was supplied to the media. In the absence of glucose, the Sn compds. stimulated urea and peptone absorption. .
- Mechanism of action of the acaricide plictran
- Mechanism of action of the acaricide plictran. Tatevosyan, A. E.; Nagashyan, O. Z. (Vses. 9012-80-0 and 13121-70-5 are also occured in this study. Nauchno-Issled. Inst. Gig. Toksikol. Pestits., Polim. Plast. Mass, Yerevan, USSR). Gig. Sanit., (2), 74-5 (Russian) 1984. CODEN: GISAAA. ISSN: 0016-9900. DOCUMENT TYPE: Journal CA Section: 4 (Toxicology) Aniline p-hydroxylase [9012-80-0] activity in the liver of rats increased and reached a peak 5 days following the administration of 0.2 LD50 plictran [13121-70-5]. The activity remained high for 15 days (41% compared to the control). The enzyme activity was similar to the control in the hepatic postmitochondrial fraction by the 30th day after plictran intoxication. Plictran (45 mg/m3) inhalation, in contrast, decreased the enzyme activity (24 h), and it remained low for 15 days. The aniline hydroxylation increased by 28% in the postmitochondrial fraction of the exptl. animals, compared to the control. Thus, the effect of plictran on aniline hydroxylation varied with the route of administration. .
- About us
- |
- Payment
- |
- Contact us
- |
- Links
- |
- Help Center
- |
- Disclaimer
- |
- Add to favorite
- | SiteMap
- |
- Product SiteMap
- |
- Manufacturers
- |
- Suppliers
©2008 LookChem.com,License:ICP NO.:Zhejiang10014259
[Hangzhou]86-571-85317600,85317603,85317620

