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Sodium triacetoxyborohydride CAS 56553-60-7

Sodium triacetoxyborohydride CAS 56553-60-7

 

  • Lebitso la sehlahisoa:

    Sodium triacetoxyborohydride CAS 56553-60-7

  • Kereiti:

    Sehlopha sa meriana

  • Thepa:

    phofo e tšoeu

  • Ho paka:

    25kg / moropa

  • MOQ:

    1 kilo

  • Polokelo:Cool Dry Place
  • Shelf bophelo:lilemo tse 2


Lintlha

Li-tag

Tlhaloso ea Sehlahisoa

Sodium triacetyloxyborohydride is an organic boron compound with the chemical formula C6H10BNaO6.

Nature:
1. Appearance: Sodium triacetyloxyborohydride is usually a colorless crystalline solid.
2. Stability: It is relatively stable at room temperature and soluble in many organic solvents.
3. Toxicity: Compared with other boron compounds, sodium triacetyloxyborohydride has lower toxicity.


Preparation method:
The preparation method of sodium triacetoxyborohydride is generally obtained by the reaction of aluminum triacetoxyborohydride with sodium hydroxide. The specific process can be referred to relevant literature such as the Organic Chemical Synthesis Manual.

Security information:
Sodium triacetyloxyborohydride is irritating to the skin and eyes. During operation, be careful to avoid contact. If necessary, wear protective gloves and goggles.
2. During storage and handling, avoid contact with water vapor in the air as it is sensitive to water and may decompose.

Kopo

Purpose 1
The new type of catalyst for reduced-amination has excellent universality and selectivity. The reaction conditions are mild, the catalytic reduction performance is good, and it is easy to separate and purify. Both the catalyst itself and the by-products are non-toxic and cause no pollution to the environment, making it the preferred catalyst for reduced-amination reactions.
Use 2
Reagents, used for the reductive amination of ketones and aldehydes, the reductive amination/lactam of carbonyl complexes and amines, as well as the reductive amination of aryl aldehydes.
Purpose:
1. Reducing agent: Sodium triacetyloxyborohydride is a commonly used reducing agent in organic synthesis, which can effectively reduce aldehydes, ketones and other compounds to the corresponding alcohols.
2. Catalyst: Sodium triacetyloxyborohydride can be used as a catalyst in some organic synthesis reactions, such as the Bal-Fischer ester synthesis and the Swiss-Hausmann reaction, etc.

Melemo

Re na le lifeme tse ngata tsa boleng bo holimo tse nang le tšebelisano e tebileng, tse ka u fang lihlahisoa tsa boleng bo holimo le litheko tsa tlholisano. Hape re ka fana ka litheolelo bakeng sa ho reka ka bongata.'Me re sebelisana le lik'hamphani tse ngata tsa litsebi tse tsamaisang thepa, li ka isa lihlahisoa ka mokhoa o sireletsehileng le ka thelelo matsohong a hau. Nako ea ho fana e ka ba matsatsi a 3-20 ka mor'a hore ho netefatsoe tefo.

 

Tlhaloso
Molecular Formula C6H10BNaO6
Molar Mass 211.94
Density 1.36[at 20℃]
Melting Point 116-120 °C (dec.) (lit.)
Boling Point 111.1℃[at 101 325 Pa]
Ho qhibiliha ha Metsi reacts
Solubility Soluble in dimethyl sulfoxide, methanol, benzene, toluene, terahydrofuran, dioxane and methylene chloride.
Vapor Presure 0Pa at 25℃
Ponahalo Powder
Color White
Merck 14,8695

 

 

Ho romella le ho lefa

 

 

LBH

1. Na u feme kapa k'hamphani ea khoebo?
Re komnay e kopanyang indasteri le khoebo, ho fana ka ts'ebeletso e le 'ngoe.OEM e ka amoheloa.

2. O fana ka mehlala? Na ke mahala kapa ho feta?
Mehlala ea mahala. Tefiso ea thepa ea sampole e hloka ho lefuoa ka lehlakore la hau.

3. O na le litifikeiti tse amanang le taolo ea boleng?
Setifikeiti sa ISO 9001:2008 ho netefatsa boleng.

4. Ke fane ka eng ho fumana khotheishene?
Pls re tsebise ka mofuta oa sehlahisoa seo u se hlokang, bongata ba odara, aterese le litlhoko tse ikhethileng. Khotheishene e tla etsoa bakeng sa referense ea hau ka nako.

5. U khetha mofuta ofe oa mokhoa oa ho lefa? Ke mantsoe a mofuta ofe a amoheloang?
Melao e Amoheletsoeng ea Thomello: FOB,CFR,CIF,EXW;
Chelete ea Tefo e Amoheletsoeng: USD;
Accepted Payment Type: T/T,Western Union; Paypal,BTC
Puo e Builoeng: Senyesemane.

 

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