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Maltotetraose

CAS No.
34612-38-9
Chemical Name:
Maltotetraose
Synonyms
Maltoteraose;AMYLOTETRAOSE;Fujioligo 450;Maltotetraose;Maltotetraose,97%;hydrolyzed starch;Maltotetraose CAS;MALTOTETRAOSE 95+%;maltotetraose, dp4;Maltotetraose,98+%
CBNumber:
CB4696652
Molecular Formula:
C24H42O21
Molecular Weight:
666.58
MDL Number:
MFCD00010576
MOL File:
34612-38-9.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-09-12 18:52:57

Maltotetraose Properties

Boiling point 597.68°C (rough estimate)
Density 1.3922 (rough estimate)
refractive index 170 ° (C=1, H2O)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
solubility H2O: 50 mg/mL, clear, colorless
form A crystalline solid
pka 12.39±0.20(Predicted)
color White to off-white
Cosmetics Ingredients Functions HUMECTANT
SKIN PROTECTING
SKIN CONDITIONING
Cosmetic Ingredient Review (CIR) MALTOTETRAOSE (34612-38-9)
InChIKey UYQJCPNSAVWAFU-KVXMBEGHSA-N
LogP -8.281 (est)
CAS DataBase Reference 34612-38-9(CAS DataBase Reference)
FDA UNII BO88JLT87R
UNSPSC Code 12352201
NACRES NA.25

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P271-P280
Safety Statements  24/25
WGK Germany  3
3-10
HS Code  29400090
Storage Class 11 - Combustible Solids

Maltotetraose price More Price(65)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich SMB01322 Maltotetraose 94% (HPLC) 34612-38-9 10MG $84 2026-04-30 Buy
Sigma-Aldrich SMB01322 Maltotetraose 94% (HPLC) 34612-38-9 50MG $323 2026-04-30 Buy
Cayman Chemical 24975 Maltotetraose ≥95% 34612-38-9 5mg $40 2026-04-30 Buy
Cayman Chemical 24975 Maltotetraose ≥95% 34612-38-9 10mg $73 2026-04-30 Buy
Cayman Chemical 24975 Maltotetraose ≥95% 34612-38-9 50mg $339 2026-04-30 Buy
Product number Packaging Price Buy
SMB01322 10MG $84 Buy
SMB01322 50MG $323 Buy
24975 5mg $40 Buy
24975 10mg $73 Buy
24975 50mg $339 Buy

Maltotetraose Chemical Properties, Uses, Production

Description

Maltotetraose is a tetrasaccharide that is composed of glucose molecules linked by α-1,4 glycosidic bonds and has been found in B. stearothermophilus. It increases the α-amylase synthesis rate in B. stearothermophilus 3-fold greater than sucrose or glucose when used at a concentration of 0.1 mM. Maltotetraose (750 μg/ml) inhibits the growth of E. carotovora in a cylinder-agar plate assay but does not affect the growth of several other microorganisms. It also inhibits TNF-α-induced expression of intercellular adhesion molecule-1 (ICAM-1) in MOVAS-1 mouse smooth muscle cells (VSMCs) transfected with an ICAM-1 luciferase reporter when used at a concentration of 20 μM.

Chemical Properties

white powder or crystals

Uses

Maltotetraose is a maltooligosaccharide that is used for research and diagnostic purposes. They can also be used in nutrients and healthcare.

Uses

inhibits AIDS virus infection in vitro and tumor necrosis factor-alpha (TNF), interleukin (IL)-1beta, and causes a marked depression of chemiluminescence activity

Definition

ChEBI: A maltotetraose tetrasaccharide in which the glucose residue at the reducing end is in the aldehydo open-chain form.

Synthesis

1. Preparation of maltotetrasaccharide by single enzyme method

Maltotetrasaccharide amylase is mainly used to decompose starch to get. Due to the unique molecular structure of the enzyme, the starch needs to be pre-treated, so that its DE value is controlled at 8~12, the amount of added maltotetrasaccharide enzyme should be controlled at 0.02%, the optimal reaction temperature is 58 , the optimal reaction pH is 6.8~7.0, and the optimal reaction time is 6~7 h, so as to obtain the crude hydrolyzed liquid of maltotetrasaccharide. The crude hydrolysate is then inactivated, cooled and clarified, filtered, concentrated in vacuum, spray-dried and finished as a solid product. The method is simple and easy to use, and the cost is not high, it is widely used.

2. Preparation of maltotetrasaccharide by synergistic action of Pullulanase

Pululanase is a branched-chain amylase, which has a strong hydrolysis effect on branched-chain starch and glycogen and other branched α-1,6 glycosidic bonds, the production of oligomeric isomaltose, most of the corn and tapioca starch as a raw material, starch liquefaction, saccharification or re-transglycosylation, and then by filtration, ion exchange and other treatments to get the syrup with a certain concentration of syrup or powdered sugar. Utilizing the enzyme method to produce malt tetrasaccharide, prulanase should be added appropriately as a synergistic enzyme. Because after adding Pullulanase most of the starch sugar filtration speed is slowed down, but the syrup transmittance ratio increases, which is conducive to improving the quality of sugar.

References

[1] JRGEN SAUER . Glucoamylase: structure/function relationships, and protein engineering[J]. Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology, 2000, 1543 2: Pages 275-293. DOI: 10.1016/s0167-4838(00)00232-6
[2] N E WELKER  L L C. INDUCTION OF ALPHA-AMYLASE OF BACILLUS STEAROTHERMOPHILUS BY MALTODEXTRINS.[J]. Journal of Bacteriology, 1963, 86: 687-691. DOI: 10.1128/jb.86.4.687-691.1963
[3] M FUJITA. Cloning and nucleotide sequence of the gene (amyP) for maltotetraose-forming amylase from Pseudomonas stutzeri MO-19.[J]. Journal of Bacteriology, 1989, 171 3: 1333-1339. DOI: 10.1128/jb.171.3.1333-1339.1989
[4] H KONDO. Isolation of maltotetraose from Streptomyces as an antibiotic against Erwinia carotovora.[J]. Journal of Antibiotics, 1975, 28 2: 157-160. DOI: 10.7164/antibiotics.28.157
[5] SOON YOUNG SHIN. Inhibition of PDGF-induced migration and TNF-α-induced ICAM-1 expression by maltotetraose from bamboo stem extract (BSE) in mouse vascular smooth muscle cells[J]. Molecular Nutrition & Food Research, 2016, 60 9: 2086-2097. DOI: 10.1002/mnfr.201500601

Maltotetraose Preparation Products And Raw materials

Raw materials

Preparation Products

Global Suppliers ( 253)
Supplier Tel Email Country ProdList Advantage
Shanghai Huicheng Biological Technology Co., Ltd. 60498804 18930850192 sales@e-biochem.com China 300 58
Chengdu Nakeli Biotechnology Co., Ltd. 028-61983833 19138982515 3265827856@qq.com China 1584 58
J & K SCIENTIFIC LTD. 18210857532 18210857532 jkinfo@jkchemical.com China 96815 76
Meryer (Shanghai) Chemical Technology Co., Ltd. 4006356688 18621169109 market03@meryer.com China 40202 62
Energy Chemical 400-0056266 sales8178@energy-chemical.com China 44850 61
Adamas Reagent, Ltd. 400-6009262 15618770481 yhx@titansci.com China 14098 59
Chemsky(shanghai)International Co.,Ltd. 021-50135380 shchemsky@sina.com China 32273 50
Syntechem Co.,Ltd info@syntechem.com China 12973 57
Sinopharm Chemical Reagent Co,Ltd. 86-21-63210123 sj_scrc@sinopharm.com China 9791 79
Hunan Hui Bai Shi Biotechnology Co., Ltd. 0731-85526065 13308475853 ivy@hnhbsj.com China 7236 62

View Latest Price from Maltotetraose manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Maltotetraose pictures 2026-09-16 Maltotetraose
34612-38-9
1g 99.4% 20g WUHAN FORTUNA CHEMICAL CO., LTD
MALTOTETRAOSE pictures 2026-03-20 MALTOTETRAOSE
34612-38-9
$1.00 1KG 99% 10 mt Hebei Chuanghai Biotechnology Co., Ltd
MALTOTETRAOSE pictures 2024-04-24 MALTOTETRAOSE
34612-38-9
$10.00 1kg 99.8% 10000ton Ouhuang Engineering Materials (Hubei) Co., Ltd
  • MALTOTETRAOSE pictures
  • MALTOTETRAOSE
    34612-38-9
  • $1.00
  • 99%
  • Hebei Chuanghai Biotechnology Co., Ltd
  • MALTOTETRAOSE pictures
  • MALTOTETRAOSE
    34612-38-9
  • $10.00
  • 99.8%
  • Ouhuang Engineering Materials (Hubei) Co., Ltd
O-ALPHA-D-GLUCOPYRANOSYL-[(1-4)-O-ALPHA-D-GLUCOPYRANOSYL]2(1-4)-D-GLUCOPYRANOSE O-alpha-D-glucopyranosyl-(1->4)-O-alpha-D-glucopyranosyl-(1->4)-O-alpha-D-glucopyranosyl-(1->4)-D-glucose MALTOTETRAOSE, DP4, 100MG NEAT MALTOTETRAOSE 95+% Maltotetraose, mixture of anomers, 97% D-Glucose, O-.alpha.-D-glucopyranosyl-(1?4)-O-.alpha.-D-glucopyranosyl-(1?4)-O-.alpha.-D-glucopyranosyl-(1?4)- maltotetraose, dp4 4-[5-[3,4-dihydroxy-6-(hydroxymethyl)-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-oxan-2-yl]oxy-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,5,6-tetrahydroxy-hexanal ALPHA-1,4-TETRAGLUCOSE AMYLOTETRAOSE ALPHA-D-GLUCOPYRANOSYL-(1->4)-O-ALPHA-D-GLUCOPYRANOSYL-(1->4)-O-ALPHA-D-GLUCOPYRANOSYL-(1->4)-D-GLUCOSE (+)-4-O-[4-O-[4-O-(α-D-gluco-Hexopyranosyl)-α-D-gluco-hexopyranosyl]-α-D-gluco-hexopyranosyl]-D-glucose Maltotetraose,97%,mixture of anomers Maltotetraose,97% Maltotetraose,98+% Maltoteraose (2R,3R,4R,5R)-4-(((2R,3R,4R,5S,6R)-5-(((2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxyMethyl)-5-(((2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxyMethyl)tetrahydro-2H-pyran-2-yl)oxy)tetrahydro-2H-pyran-2-yl)oxy)-3,4-dihydroxy-6-(hydroxyMethyl)tetrahydro-2H-pyran-2- alpha-D-Glucopyranosyl-1,4-O-alpha -D-glucopyranosyl-1,4-O-alpha -D-glucopyranosyl-1,4-D-glucopyranose Maltotraose - 100 mg Fujioligo 450 α-1,4-Tetraglucose MALTOTETRAOSE USP/EP/BP hydrolyzed starch -D-glucopyranosyl-(1→4)-D-glucose -D-glucopyranosyl-(1→4)-O-B1 Maltotetraose (DP4) extrapure, 97% (2R,3R,4R,5R)-4-(((2R,3R,4R,5S,6R)-5-(((2R,3R,4R,5S,6R)-3,4-Dihydroxy-6-(hydroxymethyl)-5-(((2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)tetrahydro-2H-pyran-2-yl)oxy)-3,4-dihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-2,3,5,6-tetrahydroxyhexanal Maltotetraose (Amylotetraose) UL-13C24]maltotetraose D-Glucose, O-α-D-glucopyranosyl-(1→4)-O-α-D-glucopyranosyl-(1→4)-O-α-D-glucopyranosyl-(1→4)- Maltotetraose((Glca1, 4) 3Glc) Maltotetraose CAS Maltotetraose DP4 grafted on OVA Maltotetraose DP4 with customizable dual functionalization Maltotetraose DP4 with stearic chain (Linker-STEA A) Maltotetraose DP4 with terminal alkyne (Linker-CΞCH A) Maltotetraose DP4 with terminal alkyne (Linker-CΞCH B) Maltotetraose DP4 with terminal alkyne (Linker-CΞCH C) Maltotetraose DP4 grafted on BSA Maltotetraose DP4 linked to biotin (Linker-BT A) Maltotetraose DP4 linked to biotin (Linker-BT B) Maltotetraose DP4 linked to biotin (Linker-BT C) Maltotetraose DP4 linked to biotin and fluorescein (Linker-BT-FLUO A) Maltotetraose DP4 linked to biotin and stearic chain (Linker-BT-STEA A) Maltotetraose DP4 grafted on CRM197 Maltotetraose DP4 with DBCO (Linker-DBCO A) Maltotetraose DP4 linked to desthiobiotin (Linker-DBT-A) Maltotetraose DP4 linked to fluorescein (Linker-FLUO A) Maltotetraose DP4 grafted on gel for affinity chromatography (Linker-GEL A) Maltotetraose DP4 grafted on gel for affinity chromatography (Linker-GEL B) Maltotetraose DP4 grafted on HSA Maltotetraose DP4 grafted on KLH Maltotetraose DP4 with cyclic di-thiol (Linker-LIPO A) Maltotetraose DP4 linked to maleimide (Linker-MAL A) Maltotetraose DP4 with terminal azide (Linker-N3 A) Maltotetraose DP4 with terminal azide (Linker-N3 B) Maltotetraose DP4 with free terminal amine (Linker-NH2 A) Hydrochloride form Maltotetraose DP4 with free terminal amine (Linker-NH2 B)