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STACHYOSE

STACHYOSE Structure
CAS No.
470-55-3
Chemical Name:
STACHYOSE
Synonyms
LUPEOSE;Cicerose;Stachyos;STACHYOSE;STACHYOSE(SH);MANNOTETRAOSE;STACHYOSE N-HYDRATE;TRANS-4-TERT-BUTYLCYCLOHEXYL ACETIC ACID;stachyose hydrate from stachys tuberifera;.fwdarw.6)-o-alpha-d-galactopyranosyl-(1.fwdarw.6)-
CBNumber:
CB8412812
Molecular Formula:
C24H42O21
Molecular Weight:
666.58
MOL File:
470-55-3.mol
MSDS File:
SDS
Modify Date:
2024/7/2 8:55:32
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STACHYOSE Properties

Melting point 170°C
Boiling point 1044.2±65.0 °C(Predicted)
Density 1.84±0.1 g/cm3 (20 ºC 760 Torr)
solubility H2O: 50 mg/mL, clear, colorless
pka 12.81±0.70(Predicted)
form Solid
color White to off-white
LogP -2.880 (est)
EPA Substance Registry System .alpha.-D-Glucopyranoside, .beta.-D-fructofuranosyl O-.alpha.-D-galactopyranosyl-(1.fwdarw.6)-O-.alpha.-D-galactopyranosyl-(1.fwdarw.6)- (470-55-3)

SAFETY

Risk and Safety Statements

Safety Statements  22-24/25
WGK Germany  3
F  10

STACHYOSE Chemical Properties,Uses,Production

Uses

Stachyose is widely present in legumes and are indigestible by humans because of a lack of α-galactosidase. As a result, these compounds undergo fermentation in the colon with the concomitant production of CO2, H2, and CH4, commonly referred to as flatulence.

STACHYOSE Preparation Products And Raw materials

Raw materials

Preparation Products

STACHYOSE Suppliers

Global( 68)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
CLEARSYNTH LABS LTD. +91-22-45045900 Hyderabad, India 6351 58 Inquiry
Chengdu Biopurify Phytochemicals Ltd. +8618080483897 China 3424 58 Inquiry
BOC Sciences +1-631-485-4226 United States 19553 58 Inquiry
Hubei Ipure Biology Co., Ltd +8613367258412 China 10326 58 Inquiry
Dideu Industries Group Limited +86-29-89586680 +86-15129568250 China 26216 58 Inquiry
Finetech Industry Limited +86-27-87465837 +8618971612321 China 9626 58 Inquiry
ShenZhen Trendseen Biological Technology Co.,Ltd. 13417589054 China 11681 58 Inquiry
LEAPCHEM CO., LTD. +86-852-30606658 China 43348 58 Inquiry
Shanghai Acmec Biochemical Technology Co., Ltd. +undefined18621343501 China 33350 58 Inquiry
Aladdin Scientific +1-+1(833)-552-7181 United States 57511 58 Inquiry
Supplier Advantage
CLEARSYNTH LABS LTD. 58
Chengdu Biopurify Phytochemicals Ltd. 58
BOC Sciences 58
Hubei Ipure Biology Co., Ltd 58
Dideu Industries Group Limited 58
Finetech Industry Limited 58
ShenZhen Trendseen Biological Technology Co.,Ltd. 58
LEAPCHEM CO., LTD. 58
Shanghai Acmec Biochemical Technology Co., Ltd. 58
Aladdin Scientific 58

470-55-3(STACHYOSE)Related Search:

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STACHYOSE HYDRATE,STACHYOSE TETRAHYDRATE,STACHYOSE FROM STACHYS TUBERIFERA*HYDRAT E,Stachyose tetrahydrate, 98.50% METHYL-D-GALACTOPYRANOSIDE L-Arabinose 2,2'-Oxydipropanol D-Glucose monohydrate
Sucrose 2,5-Anhydro-D-mannitol (2S,4S)-(+)-PENTANEDIOL L-(+)-THREOSE L-(+)-ARABINOSE
ACETALDEHYDE DIPROPYL ACETAL 2-ETHOXYTETRAHYDROFURAN 2-(2-HEXYLOXYETHOXY)ETHANOL
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.fwdarw.6)-o-alpha-d-galactopyranosyl-(1.fwdarw.6)- alpha-d-glucopyranoside,beta-d-fructofuranosylo-alpha-d-galactopyranosyl-(1 STACHYOSE N-HYDRATE LUPEOSE MANNOTETRAOSE stachyose hydrate from stachys tuberifera TRANS-4-TERT-BUTYLCYCLOHEXYL ACETIC ACID (2S,3R,4S,5S,6R)-2-[[(2R,3R,4S,5R,6R)-6-[(2S,3S,4R,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy-3,4,5-trihydroxy-oxan-2-yl]methoxy]-6-[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxane-3,4,5-triol β-D-Fructofuranosyl 6-O-[6-O-(α-D-galactopyranosyl)-α-D-galactopyranosyl]-α-D-glucopyranoside STACHYOSE(SH) Cicerose STACHYOSE .alpha.-D-Glucopyranoside, .beta.-D-fructofuranosyl O-.alpha.-D-galactopyranosyl-(1.fwdarw.6)-O-.alpha.-D-galactopyranosyl-(1.fwdarw.6)- α-D-Glucopyranoside, β-D-fructofuranosyl O-α-D-galactopyranosyl-(1→6)-O-α-D-galactopyranosyl-(1→6)- Stachyos (2R,3R,4S,5S,6R)-2-(((2S,3S,4S,5R)-3,4-Dihydroxy-2,5-bis(hydroxymethyl)tetrahydrofuran-2-yl)oxy)-6-((((2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-((((2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)methyl)tetrahydro-2H-pyran-2-yl)oxy)methyl)tetrahydro-2H-pyran-3,4,5-triol 470-55-3 Oligosaccharide BioChemical Biochemicals and Reagents Carbohydrates