Sucrose Octaacetate(Usp/Nf/Chp)

Basic information

  • Product Name:Sucrose Octaacetate(Usp/Nf/Chp)
  • CasNo.:126-14-7
  • MF:C28H38O19
  • MW:678.598

Physical and Chemical Properties

  • Boiling Point:82-85 °C(lit.)
  • Packing:25kgs/drum or as required by the customer.
  • Throughput:
Inquiry

Product Details

CasNo: 126-14-7

MF: C28H38O19

Appearance: white to creamy white powder

Packing: 25kgs/drum or as required by the customer.

Sucrose Octaacetate(Usp/Nf/Chp) Good Supplier In Bulk Supply High Purity 126-14-7

Synonym: Octaacetyl Sucrose, Saccharose Octaacetate
Chemical Formula: C28H38O19    
Molecular Weight: 678.6    

CAS Number: 126-14-7

Molecular Structure:

 

 

Specification: ChP2025

Item

Specification

Appearance

White powder

         Related substance

Complies

Identification

Complies

Melting temperature,℃

≥78

Acidity,%

≤2drops

Water,%

≤1.0

Residue on ignition,%

≤0.5

Assay (HPLC), %

≥98.0

 

 

Properties: It is white powder with a strong bitter taste. It is easily soluble in methanol, soluble in ethanol , and very slightly soluble in water. The density is 1.28; boiling point is 250 °C.

Sucrose octaacetate(Cas 126-14-7) Usage

This product is used as alcohol denaturant. It also can be used for the treatment of gonarthromeningitis traditional Chinese medicine preparation placebo, coronary heart disease prescription placebo and the treatment of cardiovascular disease drugs.

 It is also a good remedy for thumb sucking and nail biting in children. This product can also be used for the synthesis of sucrose polyester.

Storage: Well closed and store in a dry place.

Package: 25kgs/drum or as required by the customer.

Expiration Date: 2 years

126-14-7 Relevant articles

A phenylpropanoid glycoside from Vaccaria segetalis

Sang, Shengmin,Lao, Aina,Wang, Hongcheng,Chen, Zhongliang,Uzawa, Jun,Fujimoto, Yasuo

, p. 569 - 571 (1998)

A new phenylpropanoid glycoside, named s...

-

Stanek,Cerna

, p. 329 (1963)

-

-

Cox et al.

, p. 968 (1933)

-

Isolation and synthesis of trans- and cis-(-)-clovamides and their deoxy analogues from the bark of Dalbergia melanoxylon

R. Van Heerden, Fanie,Vincent Brandt,G. Roux, David

, p. 2125 - 2129 (1980)

N-(3′,4′-Dihydroxy-trans-cinnamoyl)-3-(3...

-

Ness,Fletcher

, p. 465,467 (1971)

-

Rapid, clean, and mild O-acetylation of alcohols and carbohydrates in an ionic liquid

Forsyth, Stewart A.,MacFarlane, Douglas R.,Thomson, Robin J.,Von Itzstein, Mark

, p. 714 - 715 (2002)

Archetypal O-acetylation reactions of al...

Tandem acetalation-acetylation of sugars and related derivatives with enolacetates under solvent-free conditions

Mukherjee, Debaraj,Shah, Bhahwal Ali,Gupta, Pankaj,Taneja, Subhash Chandra

, p. 8965 - 8968 (2007)

(Chemical Equation Presented) Molecular ...

Cu(ClO4)2·6H2O catalyzed solvent free per-O-acetylation and sequential one-pot conversions of sugars to thioglycosides

Chatterjee, Debnath,Paul, Abhijit,Rajkamal,Yadav, Somnath

, p. 29669 - 29674 (2015/05/20)

The solvent free per-O-acetylation of va...

I2/ionic liquid as a highly efficient catalyst for per-O-acetylation of sugar under microwave irradiation

Xiong, Xingquan,Yi, Chao,Han, Qian,Shi, Lin,Li, Sizhong

, p. 237 - 243 (2015/09/28)

A practical and highly efficient approac...

H2SO4-SiO2: Highly efficient and reusable catalyst for per-O-acetylation of carbohydrates under solvent-free conditions

Zhang, Jianbo,Zhang, Bo,Zhou, Jiafen,Li, Juan,Shi, Chunjuan,Huang, Ting,Wang, Zhongfu,Tang, Jie

experimental part, p. 165 - 177 (2012/01/19)

Sulfuric acid immobilized on silica gel ...

Synthesis of (+)-sucrose via β-d-psicofuranosylation

Uenishi, Jun'ichi,Ueda, Atsushi

experimental part, p. 2210 - 2217 (2009/04/04)

Despite the difficulty of direct β-furan...

126-14-7 Process route

acetic anhydride
108-24-7

acetic anhydride

Sucrose
57-50-1

Sucrose

sucrose octaacetate
126-14-7

sucrose octaacetate

Conditions
Conditions Yield
With copper(II) perchlorate hexahydrate; In neat (no solvent); at 20 ℃; for 0.5h; Inert atmosphere;
97%
With iodine; at 50 ℃; for 0.166667h; Microwave irradiation;
96%
With butylmethylimidazolium dicyanamide; at 25 ℃; for 24h;
93%
perchloric acid; at 0 - 20 ℃; for 0.166667h;
92%
With sodium acetate; for 0.00972222h; microwave irradiation;
74%
iron(III) chloride; at 20 ℃; for 1h;
65%
With sodium acetate;
 
With pyridine;
 
With pyridine; N,N-dimethyl-formamide;
 
With pyridine; Yield given;
 
With pyridine; for 8h; Heating;
15 mg
With pyridine; at 20 ℃;
 
sucrose
57-50-1

sucrose

acetic anhydride
108-24-7

acetic anhydride

sucrose octaacetate
126-14-7

sucrose octaacetate

Conditions
Conditions Yield
With lithium perchlorate; for 5h; Heating;
98%
With 1H-imidazole; In acetonitrile; at 20 ℃; for 10h;
98%
With Sulfuric acid immobilized on silica gel; at 20 ℃; for 1h; neat (no solvent);
91%

126-14-7 Upstream products

  • 108-24-7
    108-24-7

    acetic anhydride

  • 57-50-1
    57-50-1

    Sucrose

  • 64-19-7
    64-19-7

    acetic acid

  • 52706-47-5
    52706-47-5

    1',2,3,3',4',6'-hexa-O-acetyl sucrose

126-14-7 Downstream products

  • 35520-98-0
    35520-98-0

    3,4,-di-O-acetyl-β-D-fructofuranosyl 2,3,4,6-tetra-O-acetyl-α-D-glucopyranoside

  • 30694-62-3
    30694-62-3

    1,3,4'-tri-O-acetyl-β-D-fructofuranosyl 2,3,4,6-tetra-O-acetyl-α-D-glucopyranoside

  • 35867-25-5
    35867-25-5

    2,3,6,3',4'-pentaacetyl sucrose (6-PAS)

  • 64644-60-6
    64644-60-6

    3,4,6-tri-O-acetyl-β-D-fructofuranosyl 2,3,4,6-tetra-O-acetyl-α-D-glucopyranoside