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Sodium-t-butoxide CAS: 865-48-5

NameSodium-t-butoxideSynonymsSTBNatBSodium-t-butoxideSodiuM tert-butoxisodium tertbutoxideSodium ter

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Contenu
NomSodium-t-butoxide
SynonymesSTB
NatB
Sodium-t-butoxide
SodiuM tert-butoxi
sodium tertbutoxide
Sodium tert Butoxide
sodiumt-butoxide,stb
sodium tert-butoxide
sodiumt-butoxide,stb,in
Sodium tertiary butoxide
Sodium tert-butyl alcohol
Sodium tert-butoxide (STB)
sodium 2-methylpropan-2-olate
sodiuM 2-Methyl-1-oxopropan-2-yl
SODIUM TERT-BUTYLATE FOR SYNTHESIS
CAS865-48-5
EINECS212-741-9
InChIInChI=1/C4H9O.Na/c1-4(2,3)5;/h1-3H3;/q-1;+1


Formule moléculaireC4H9NaO
Masse molaire96.1
Densité1,104 g/cm3
Point de fusion180 °C
point Boling180°C/1mmHg
Point d'éclair12°C
Solubilité dans l'eaureacts
Solubilitévery slightly in Tetrahydrofuran
pression vapeur0Pa at 20℃
Apparencepoudre
Gravité spécifique1.104
Couleurwhite to off-white
BRN3654215
Condition de stockageConserver à moins de +30°C.
Sensible7: reacts slowly with moisture/water
Indice de réfractionn20/D1.413
Propriétés physiques et chimiquesMelting point 180°C
water-soluble reactions
UtilisationFor organic synthesis intermediates, pharmaceutical intermediates


Codes de risqueR11 - hautement inflammable
R14 - Reacts violently with water
R34 - provoque des brûlures
R37 - stimulation du système respiratoire
R35 - Causes severe burns
R36/37/38 - Irritant pour les yeux, le système respiratoire et la peau.
R40 - Limited evidence of a carcinogenic effect
R19 - May form explosive peroxides
Description de la sécuritéS26 - En cas de contact avec les yeux, rincer immédiatement avec beaucoup d'eau et consulter un médecin.
S36 / 37 / 39 - porter des vêtements de protection appropriés, des gants et une protection oculaire / faciale.
S43 - In case of fire use ... (there follows the type of fire-fighting equipment to be used.)
S45 - en cas d'accident ou de malaise, consulter immédiatement un médecin (en montrant l'étiquette si possible).
S7/8 -
S8 - Keep container dry.
S16 - Éloigner les sources d'allumage.
S36 - porter des vêtements de protection appropriés.
Un idUN 3206 4.2/PG 2
Wgk Allemagne3
Code F de la marque Fluka1-3-10
TSCAOui
Code SH29051900
Classe de danger4.2
Catégorie d'emballageII



OverviewSodium tert-butoxide, also known as the third Sodium butoxide, English name Sodium tert-butoxide, white crystal, molecular formula C4H9NaO, molecular weight of 96.10, its stable nature at room temperature and atmospheric pressure, slightly harmful to water, used as intermediates in organic synthesis, pharmaceutical intermediates; Or as a strong alkali is widely used in chemical industry, medicine, pesticides and organic synthesis in the condensation, rearrangement and ring opening reaction, therefore, sodium tert-butoxide more and more by the fine chemical and pesticide, pharmaceutical industry.
Basicsodium tert-butoxide is an organic compound with chemical formula (CH3) 3con A, which is a strong base and has weak nucleophilic property, the chemical reaction is similar to potassium tert-butoxide.
Applicationsodium tert-butoxide white crystal, as a strong base widely used in chemical, pharmaceutical, pesticide and organic synthesis of condensation, rearrangement and ring-opening reactions. Stable under normal temperature and pressure, avoid strong reducing agent, moisture, air, acid contact. There is little harm to water, so as to avoid exposure of undiluted or large amount of products to groundwater, water channels or sewage systems; If there is no government permission, do not discharge the materials into the surrounding environment. Used as organic synthesis intermediates, pharmaceutical intermediates; As a strong base is widely used in chemical, pharmaceutical, pesticide and other organic synthesis of condensation, rearrangement and ring opening reaction.
Préparationsodium tert-butoxide is synthesized by using toluene or heptane as the solvent of the reaction system according to the following reaction formula, reflux condenser and thermometer in a 500mL reactor, add 240mL of toluene or heptane (moisture content less than 0.04%), add 9.8g 99% sodium amino acid (about 0.25mol) and 19.0g of 99% tert-butyl alcohol (about 0.254mol), the molar ratio of sodium amino acid and tert-butyl alcohol is 1:1.015, fully stirred to dissolve it completely, heated to 70 C to start the reaction, the released ammonia gas is absorbed with water or alkali solution, and the reaction is heated to 100~110 ℃ and then kept for 1H to stop the reaction. After the reaction is sufficient and complete, the reactants are cooled, atmospheric distillation of most of the reaction medium and reaction slightly excessive tert-butyl alcohol, and then vacuum distillation of the remaining small amount of reaction medium to obtain white solid powder about 25g, product content by acid-base titration analysis of more than 99%.
Utilisationas a strong base, it is widely used in condensation, rearrangement and ring opening reactions in chemical, pharmaceutical, pesticide and other organic synthesis.
used in organic synthesis
sodium tert-butoxide is used as an intermediate in organic synthesis and a pharmaceutical intermediate.

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