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Sodium hydroxide

CAS No.1310-73-2
Chemical Name:Sodium hydroxide
Synonyms:1L;5L;NaOH;Pels;Plung;3%pure;25%pure;20%p.A.;20%pure;30%pure
CBNumber:CB8105015
Molecular Formula:HNaO
Formula Weight:40
MOL File:1310-73-2.mol
Sodium hydroxide Property
mp : 681 °C(lit.)
bp : 145 °C
density : 1.515 g/mL at 20 °C
vapor density : <1 (vs air)
vapor pressure : 1 mm Hg ( 745 °C)
refractive index : 1,473-1,475
Fp : 176-178°C
storage temp. : 2-8°C
solubility : H2O: 1 M at 20 °C, clear, colorless
form : beads
Water Solubility : SOLUBLE
Decomposition : 176-178 ºC
Sensitive : Air Sensitive & Hygroscopic
Merck : 14,8627
CAS DataBase Reference: 1310-73-2(CAS DataBase Reference)
NIST Chemistry Reference: Sodium hydroxide(1310-73-2)
EPA Substance Registry System: Sodium hydroxide (Na(OH))(1310-73-2)
Safety
Hazard Codes : C,Xi
Risk Statements : 36/38-35-34
Safety Statements : 26-45-37/39-24/25-36/37/39
RIDADR : UN 1824 8/PG 2
WGK Germany : 1
RTECS : TT2975000
F : 8
HazardClass : 8
PackingGroup : II
Hazardous Substances Data: 1310-73-2(Hazardous Substances Data)

Sodium hydroxide Chemical Properties,Usage,Production

Chemical Properties
White solid
Usage
basic and important chemical feed.used asm textiles industry,printing, detergent,paper-making, soap-mak inmetallurgy, glass enamel,medica mentoil-refining and making synthetic fiber,plastics,and many kinds of organic-mediacy,
Usage
Choline acetyltransferase substrate.
General Description
A white solid. Corrosive to metals and tissue. Used in chemical manufacturing, petroleum refining, cleaning compounds, drain cleaners.
Air & Water Reactions
Soluble in water. Dissolution can liberate enough heat to cause steaming and spattering and ignite adjacent combustible material [Haz. Chem. Data 1966].
Reactivity Profile
CAUSTIC SODA (Sodium hydroxide) is a strong base. Reacts rapidly and exothermically with acids, both organic and inorganic. Readily absorbs moisture from the air to give caustic semi-solids that attack aluminum and zinc with the evolution of flammable hydrogen gas. Catalyzes the polymerization of acetaldehyde and other polymerizable compounds; these reactions can occur violently, for example, acrolein polymerizes with extreme violence when put in contact with alkaline materials such as sodium hydroxide [Chem. Safety Data Sheet SD-85 1961]. Reacts with great violence with phosphorus pentaoxide when initiated by local heating [Mellor 8 Supp.3:406 1971]. Contact (as a drying agent) with tetrahydrofuran, which often contains peroxides, may be hazardous---explosions have occurred in such a use of the chemically similar potassium hydroxide [NSC Newsletter Chem. Soc. 1967]. Mixing with any of the following substances in a closed container caused the temperature and pressure to increase: glacial acetic acid, acetic anhydride, acrolein, chlorohydrin, chlorosulfonic acid, ethylene cyanohydrin, glyoxal, hydrochloric acid (36%), hydrofluoric acid (48.7%), nitric acid (70%), oleum, propiolactone, sulfuric acid (96%) [NFPA 1991]. Accidental contact between a caustic cleaning solution (probably containing sodium hydroxide) and Pentol caused a violent explosion. [MCA Case History 363(1964)]. Heating with a mixture of methyl alcohol and trichlorobenzene during an attempted synthesis led to a sudden increase in pressure and an explosion [MCA Guide for Safety Appendix 3 1972]. Hot and/or concentrated NaOH can cause hydroquinone to decompose exothermically at elevated temperature. (NFPA Pub. 491M, 1975, 385)
Health Hazard
Strong corrosive action on contacted tissues. INHALATION: dust may cause damage to upper respiratory tract and lung itself, producing from mild nose irritation to pneumonitis. INGESTION: severe damage to mucous membranes; severe scar formation or perforation may occur. EYE CONTACT: produces severe damage.
Fire Hazard
Non-combustible, substance itself does not burn but may decompose upon heating to produce corrosive and/or toxic fumes. Some are oxidizers and may ignite combustibles (wood, paper, oil, clothing, etc.). Contact with metals may evolve flammable hydrogen gas. Containers may explode when heated.
Sodium hydroxide Preparation Products And Raw materials
Raw materials
Caustic Soda(liquid)30%-48%  CALCIUM CARBONATE Calcium oxide Barium chloride dihydrate Calcium chloride Sodium chloride Boron tribromide Barium chloride Calcium chloride hexahydrate Sodium polyacrylate Sodium carbonate
Preparation Products
Sodium pyroantimonate Disodium tartrate dihydrate dibenzyl biphenyl polyoxyethylene ether additive AC1210 2-(4,6-diamino-1,3,5-triazin-2-yl)acetic acid 2', 3'-ribonucleotide 3-(Acetylamino)thiophene-2-carboxylic acid 2-(1-Naphthalenyloxy)propanoic acid 3-Fluoro-4-hydroxybenzaldehyde emulsifier C^{8~10^} OPE-10 thiourea-formaldehyde resin 2-THIOPHENECARBOXYLIC ACID SODIUM SALT 11-Oxahexadecan-16-olide 4-METHYL-2-PHENYL-1,3-THIAZOLE-5-CARBOXYLIC ACID calcium disodium bis[2-chloro-5-[(2-hydroxy-1-naphthyl)azo]-4-sulphonatobenzoate] DL-4-HYDROXY-3-METHOXYMANDELIC ACID emulsifier SOPE-20 dodecyl phenyl polyoxyethylene (12) ether 6-AMINO-5-BROMOPYRIMIDIN-2(1H)-ONE C^{12~18^} fatty alcohol polyoxyethylene (35) ether Alkaline Treated Starch castor oil poloxyethylene (30) ether 5,5-DIETHYLBARBITURIC ACID SODIUM SALT Tricobalt tetraoxide Sodium lactate Sodium isoamylxanthate SODIUM PHOSPHOTUNGSTATE 2-HYDROXY-1-NAPHTHOIC ACID STRONTIUM HYDROXIDE OCTAHYDRATE C^{8~9^} alkyl phenyl polyoxyethylene (18) ether QUINUCLIDINE HYDROCHLORIDE SODA LIME SAFFLOWER YELLOW SODIUM STANNATE TRIHYDRATE 2,3-DIPHENYLPROPIONIC ACID Sodium O-isobutyl dithiocarbonate Peregal O-25 1-[(Benzyloxy)carbonyl]piperidine-4-carboxylic acid 2-AMINO-4,6-DIMETHOXY-1,3,5-TRIAZINE BENZYL 1-PIPERAZINECARBOXYLATE
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