Detail of > 1310-73-2
- MSDS Download

- CAS Number:
- 1310-73-2
- Name:
Sodium hydroxide
- Formula:
- NaOH
- Molecular Structure:

- Synonyms:
- Sodium oxidanide;Caustic soda;Lye;Ascarite;Aetznatron;Hydroxyde de sodium;Natrium causticum;Soda, hydrate;Soda lye;UN 1823 (solid);UN 1824 (solution);
- Molecular Weight:
- 40.00
- EINECS:
- 215-185-5
- Density:
- 2.13 g/cm3
- Melting Point:
- 318 °C, 591 K, 604 °F
- Boiling Point:
- 1388 °C, 1661 K, 2530 °F
- Flash Point:
- 176-178 °C
- Solubility:
- 1 M at 20 °C in water
- Appearance:
- White opaque crystals
- Hazard Symbols:
C,
Xi- Risk Codes:
- 36/38-35-34
- Safety:
- 26-45-37/39-24/25-36/37/39Details
- Transport Information:
- UN 1823 8/PG 2
- Deleted CAS:
- 8012-01-9
Related products
- 13010-37-2sodium hydroxide
- 8012-01-9Sodium Hydroxide
- 1310-73-2Sodium hydroxide
- 14014-06-3Sodium hydroxide(Na(OD)) (6CI,7CI,8CI,9CI)
- 1332-21-4Hydroxide, Sodium
- 168811-65-2Potassium silicon sodium titanium hydroxide oxide
- 8006-28-8Sodium hydroxide(Na(OH)), mixt. with lime
- 68608-66-2Aceticacid, 2-chloro-, sodium salt (1:1), reaction products with4,5-dihydro-2-undecyl-1H-imidazole-1-ethanol and sodium hydroxide
Other Products
- Titanium Dioxide Carbon black Glutathione Adenosine Cable pulling lubricant
- 108-46-3Resorcine
- 122-95-2Benzene, 1,4-diethoxy-
- 13028-62-1L-CYSTINE
- 13847-22-8Phosphoric acid, zinc salt
- 98-77-1Piperidine pentamethylenedithiocarbamate
- 54-21-7Sodium salicylate
- 68131-55-5Castor oil, polymer with glycerol and sebacic acid
- 7681-57-4Sodium metabisulfite
- 1310-73-2Sodium hydroxide
- 68611-23-4SYNTHETIC CAMPHOR
- 147-71-7Butanedioic acid, 2,3-dihydroxy-, (2S,3S)-
- 127906-38-1Phenol, 3-((2-((methylamino)methyl)phenyl)thio)-, (Z)-2-butenedioate(1:1) (salt)
- 32900-09-7Thiourea,N-ethyl-N'-2-propen-1-yl-
- 13463-67-7Titanium dioxide
- 1317-80-2Rutile
Refine Suppliers Do you want your product ranking ahead? Know what is 'Top Seller'!
- Supplier Location:
China (Mainland)(874)
India(75)
United States(58)
Canada(6)
United Kingdom(6)
Germany(5)
Hong Kong(4)
Malaysia(4)
China(Hongkong)(4)
Cameroon(3)
Japan(3)
France(3)
United Arab Emirates(3)
Turkey(3)
Russian Federation(2)
Pakistan(2)
South Africa(2)
Korea(2)
Netherlands(2)
Italy(2)
Australia(2)
Austria(1)
Belgium(1)
Egypt(1)
Finland(1)
Hungary(1)
Other Country(1)
Lebanon(1)
Spain(1)
Swaziland(1)
Switzerland(1)
Panama(1)
Poland(1)
Qatar(1)
Saudi Arabia(1)
Singapore(1)
Ukraine(1)
Uzbekistan(1)
Venezuela(1)More...
- Business Type:
- Importer/Exporter(750)Manufacturers(9)Other(6)Lab/Research institutions(3)
- Certificates:
- ISO(10)Production License(8)QS(2)
Please post your buying leads,so that our qualified suppliers
will soon contact you!
*Required Fields
Reference
- Effect of different solvents on the extraction of protein fractions of beans (Phaseolus vulgaris)
- Effect of different solvents on the extraction of protein fractions of beans (Phaseolus vulgaris). Gomez-Brenes, Roberto A.; Nunez, Elena Isabel; Bressani, Ricardo; Braham, J. Edgar (Inst. Nutr. Cent. America Panama, Guatemala, Guatemala). Arch. Latinoam. Nutr., 33(3), 503-18 (Spanish) 1983. CODEN: ALANBH. ISSN: 0004-0622. DOCUMENT TYPE: Journal CA Section: 17 (Food and Feed Chemistry) The effect of different solvents on the extn. of protein fractions in beans was studied. Black bean protein was extd. with distd. water, 0.01M NaOH, 0.05M NaCl, and 70% EtOH. 64-17-5 and 1310-73-2 which are cas registry numbers are also used here. Optimum conditions for the best extn. and fractionation of proteins were 1 h agitation at room temp., 3 successive extns. with the same solvent, and a ratio of solid to solvent of 1:20 wt./vol. The effect of 24 different sequences of solvents upon the extn. of protein was also investigated. The best sequence of solvents for extg. the protein was that where NaOH constituted the first solvent; this sequence, however, had the disadvantage of extg. all the protein from the seed, making it impossible to sep. other protein fractions by another solvent. If the purpose of the extn. was to sep. different protein fractions, the best sequence of solvents was distd. water or NaCl in the first place, followed by EtOH and NaOH. The need for using standardized methodol. for the fractionation of protein from seeds in order to obtain comparable data between research labs. is emphasized. .
- Poly(phenylene oxides)
- Poly(phenylene oxides). Burzin, Klaus; Bartmann, Martin; Bax, Hanns Joerg; Ribbing, Wilfried (Chemische Werke Huels A.-G. , Fed. Rep. Ger.). Ger. Offen. DE 3224692 A1 5 Jan 1984, 9 pp. (German). (Germany). CODEN: GWXXBX. CLASS: IC: C08G065-44. APPLICATION: DE 82-3224692 2 Jul 1982. DOCUMENT TYPE: Patent CA Section: 35 (Chemistry of Synthetic High Polymers) Polyoxyphenylenes with relative viscosity change (J-value) (CHCl3, 25°) >50 mL/g are prepd. 7447-39-4 and 1310-73-2 are also in the experiment. by polymg. 2,6-disubstituted phenols in the presence of Cu amine complexes and morpholine.HBr (I) [6377-82-8]-alkali metal or alk. earth hydroxide activators. Thus, passing 200 L/h air into a soln. of 2,6-dimethylphenol 100, CuCl2 2, morpholine [110-91-8] 200, I 5, 50% NaOH 4, and PhMe 900 g stirred at 30-35° for 90 min. gave a polymer [25134-01-4] with J-value 58 mL/g, compared with 35 with no activator. .
- 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


