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Merck

W373011

L-Rhamnose

greener alternative

natural sourced, 99%, FG

Synonym(s):

L-Rhamnose, 6-Deoxy-L-mannose, 6-Deoxyhexopyranose, 6-Deoxymannose

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About This Item

Linear Formula:
C6H12O5 .H2O
CAS Number:
Molecular Weight:
182.17
PubChem Substance ID:
UNSPSC Code:
12164502
FEMA Number:
3730
NACRES:
NA.21
EC Number:
222-793-4
MDL number:
organoleptic:
odorless
grade:
FG
Halal
Kosher
food allergen:
no known allergens

Product Name

L-Rhamnose, natural sourced, 99%, FG

InChI key

CBDCDOTZPYZPRO-DEZHIRTDSA-N

InChI

1S/C6H12O5.H2O/c1-3(8)5(10)6(11)4(9)2-7;/h2-6,8-11H,1H3;1H2/t3-,4-,5-,6-;/m0./s1

SMILES string

O=C[C@H](O)[C@H](O)[C@@H](O)[C@@H](O)C.[H]O[H]

grade

FG
Halal
Kosher

reg. compliance

EU Regulation 178/2002

assay

99%

greener alternative product characteristics

Less Hazardous Chemical Syntheses
Use of Renewable Feedstocks
Learn more about the Principles of Green Chemistry.

mp

90-95 °C

application(s)

flavors and fragrances

documentation

see Safety & Documentation for available documents

food allergen

no known allergens

greener alternative category

organoleptic

odorless

Quality Level

Related Categories

General description

L-Rhamnose is a deoxy sugar mainly found in gums and plant mucilages. It is one of the structural units of complex polysaccharides such as pectin and sterculia gum. L-Rhamnose may react with aqueous ammonia to form volatile flavor compounds such as alkyl pyrazines.
We are committed to bringing you Greener Alternative Products, which adhere to one of the four categories of Greener Alternatives . This product is a Biobased products, showing key improvements in Green Chemistry Principles “Less Hazardous Chemical Syntheses” and “Use of Renewable Feedstock”.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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Encyclopedia of Food and Color Additives, 1, 2583-2583 (1997)
Claudius Marondedze et al.
Frontiers in molecular biosciences, 6, 163-163 (2020-02-11)
The spliceosome processes RNAs from a pre-RNA state to a mature mRNA thereby influencing RNA availability for translation, localization, and turnover. It consists of complex structures containing RNA-binding proteins (RBPs) essential for post-transcriptional gene expression control. Here we investigate the
Jun Liu et al.
Carbohydrate polymers, 172, 11-19 (2017-06-14)
Nanocellulose-based biomaterials for biomedical and pharmaceutical applications have been extensively explored. However, studies on different levels of impurities in the nanocellulose and their potential risks are lacking. This article is the most comprehensive to date survey of the importance and
Formation of heterocyclic compounds from the reaction of L-rhamnose with ammonia.
Shibamoto T & Bernhard RA
Journal of Agricultural and Food Chemistry, 26(1), 183-187 (1978)
Pauline van Nies et al.
Nature communications, 9(1), 1583-1583 (2018-04-22)
Replication of DNA-encoded information and its conversion into functional proteins are universal properties of life. In an effort toward the construction of a synthetic minimal cell, we implement here the DNA replication machinery of the Φ29 virus in a cell-free

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