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BLOOD GROUP H DISACCHARIDE [FUC-ALPHA1-2)GAL], also known as Fuc-α1-2-Gal, is a carbohydrate structure found on the surface of red blood cells. It consists of a fucose molecule linked to a galactose molecule through an alpha 1-2 glycosidic bond. This disaccharide plays a crucial role in determining an individual's blood type and can influence the immune response to blood transfusions. It is also a target for certain antibodies in the immune system, which may be involved in diseases and conditions related to blood compatibility and organ transplantation.

16741-18-7

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16741-18-7 Usage

Uses

Used in Medical and Transfusion Purposes:
BLOOD GROUP H DISACCHARIDE [FUC-ALPHA1-2)GAL] is used as a key factor in determining an individual's blood group antigens for medical and transfusion purposes. The presence or absence of this disaccharide on red blood cells can have important implications for compatibility and safety during blood transfusions.
Used in Immunology Research:
BLOOD GROUP H DISACCHARIDE [FUC-ALPHA1-2)GAL] is used as a target for certain antibodies in the immune system for immunology research. Studying the interactions between this disaccharide and immune system components can provide insights into the mechanisms of blood compatibility and the role of antibodies in certain diseases and conditions.
Used in Organ Transplantation:
BLOOD GROUP H DISACCHARIDE [FUC-ALPHA1-2)GAL] is used as a factor in determining blood compatibility for organ transplantation. Understanding the presence or absence of this disaccharide on red blood cells can help in assessing the suitability of organ donors and recipients, reducing the risk of immune rejection and improving transplant outcomes.
Used in Pharmaceutical Development:
BLOOD GROUP H DISACCHARIDE [FUC-ALPHA1-2)GAL] is used as a potential target for the development of pharmaceuticals related to blood compatibility and immune response modulation. By studying the interactions between this disaccharide and the immune system, researchers can develop new therapies to improve blood transfusion safety and treat conditions related to blood compatibility.

Check Digit Verification of cas no

The CAS Registry Mumber 16741-18-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,7,4 and 1 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 16741-18:
(7*1)+(6*6)+(5*7)+(4*4)+(3*1)+(2*1)+(1*8)=107
107 % 10 = 7
So 16741-18-7 is a valid CAS Registry Number.

16741-18-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-6-[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxyoxane-3,4,5-triol

1.2 Other means of identification

Product number -
Other names Blood group H disaccharide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:16741-18-7 SDS

16741-18-7Relevant academic research and scientific papers

SYNTHESIS OF 2-O-α, 3-O-α, 3-O-β, AND 4-O-α-L-RHAMNOPYRANOSYL-D-GALACTOSE

Liptak Andras,Szurmai Zoltan,Nanasi Pal

, p. 13 - 22 (2007/10/02)

Condensation of benzyl 3-O-benzoyl-4,6-O-benzylidene-, benzyl 2-O-benzoyl-4,6-O-benzylidene- (2), and benzyl 2,3,6-tri-O-benzyl-β-D-galactopyranoside, separately, with tri-O-acetyl-α-L-rhamnopyranosyl bromide gave mainly α-linked disaccharide derivatives.An appreciable proportion of the β-linked disaccharide was also abtained from 2.An anomalous deacylation reaction was found for the (1-->3)-linked disaccharide, and the partially benzoylated products were isolated and characterised.The anomeric configuration of each disaccharide was established on the basis of JC-1,H-1 values.The chemical shifts for the galactose moieties of the α and β-L-rhamnopyranosyl derivatives differed in a systematic way.

Studies on the Constituents of Apocynacae Plants. Gas Chromatography-Mass Spectrometric Determination of New Flavanoid Triglycosides from the Leaves of Cerbera manghas L.

Sakushima, Akiyo,Hisada, Sueo,Ogihara, Yukio,Nishibe, Sansei

, p. 1219 - 1223 (2007/10/02)

Two new flavonol triglycosides, named manghaslin(I) and clitorin(II), were isolated from the leaves of Cerbera manghas L. (Apocynaceae).The structures of I and II were elucidated as quertecin-3-O-L-rhamnosyl-(12)-O6)> D-glucoside(I) and kaempferol-3-O-L-rhamnosyl-(12)-O-6)> D-glucoside(II), respectively, by chemical and gas chromatography-mass spectrometric studies.Keywords-Cerbera manghas L.; Apocynaceae; flavonol triglycerides; manghaslin; clitorin; gas chromatography-mass spectrometry; photohydrolysis; mass spectrum; methanolysis.

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