MedPath

Sucrose

Generic Name
Sucrose
Drug Type
Small Molecule
Chemical Formula
C12H22O11
CAS Number
57-50-1
Unique Ingredient Identifier
C151H8M554

Overview

A nonreducing disaccharide composed of glucose and fructose linked via their anomeric carbons. It is obtained commercially from sugarcane, sugar beet (beta vulgaris), and other plants and used extensively as a food and a sweetener.

Indication

No indication information available.

Associated Conditions

No associated conditions information available.

Research Report

Published: Aug 27, 2025

A Comprehensive Monograph on Sucrose (DB02772): Physicochemical Properties, Metabolism, and Applications in Medicine and Pharmacology

Section 1: Compound Identification and Physicochemical Properties

Sucrose, a small molecule identified by DrugBank Accession Number DB02772 and CAS Registry Number 57-50-1, is one of the most well-known organic compounds in biology and commerce.[1] While universally recognized as table sugar, its roles extend far beyond simple nutrition, encompassing specific therapeutic applications and critical functions in advanced pharmaceutical manufacturing. This section provides a detailed characterization of its chemical identity and physicochemical properties, which form the basis for its behavior in biological and pharmaceutical systems.

1.1 Nomenclature and Chemical Structure

The compound is most commonly known by its generic name, Sucrose. However, it is referenced by a wide array of synonyms that reflect its natural sources and chemical nature. These include Saccharose, Sacarosa, Sacharose, cane sugar, and beet sugar.[1] In pharmaceutical and commercial contexts, it may also be referred to as confectioner's sugar, granulated sugar, or rock candy.[2]

From a chemical standpoint, sucrose is a disaccharide, meaning it is composed of two simpler monosaccharide units: glucose and fructose.[2] Specifically, it is formed from a molecule of α-D-glucopyranose and a molecule of β-D-fructofuranose.[5] The systematic IUPAC name precisely defines its stereochemistry and linkage: (2R,3R,4S,5S,6R)-2-oxy-6-(hydroxymethyl)oxane-3,4,5-triol.[2]

Continue reading the full research report

Clinical Trials

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
Deseret Biologicals, Inc.
43742-2276
ORAL
30 [hp_X] in 1 mL
5/7/2025
Deseret Biologicals, Inc.
43742-2185
ORAL
6 [hp_X] in 1 mL
5/27/2025

EMA Drug Approvals

Approved Product
Authorization Holder
Status
Issued Date
No EMA approvals found for this drug.

HSA Drug Approvals

Approved Product
Manufacturer
Approval Number
Dosage Form
Strength
Approval Date
No HSA approvals found for this drug.

NMPA Drug Approvals

Approved Product
Company
Approval Number
Drug Type
Dosage Form
Approval Date
No NMPA approvals found for this drug.

PPB Drug Approvals

Approved Product
Registration No.
Company
Licence No.
Strength
Registration Date
No PPB approvals found for this drug.

TGA Drug Approvals

Approved Product
ARTG ID
Sponsor
Registration Type
Status
Registration Date
No TGA approvals found for this drug.

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
SACCHARUM OFFICINALE GRAN (1CH-30CH)
homeocan inc.
01917889
Tablet - Oral
1 CH
12/31/1991
SACCHARUM OFFICINALE
dolisos canada inc.
02234717
Liquid ,  Granules ,  Globules - Oral
1 X
1/5/1998
SACCHARUM OFFICINALE
homeocan inc.
02234101
Granules ,  Globules ,  Drops - Oral
1 X
1/6/1998
UNDERBERG NATURAL HERBAL DIGESTIVE-LIQ
underberg ag
02138689
Liquid - Oral
.45 %
12/31/1995
SACCHARUM-INJEEL FORTE LIQ (6D,10D,30D,200D/1.1ML)
02071789
Liquid - Oral
6 D / 1.1 ML
12/31/1994
ALCOPT
terra botanica products ltd.
02233287
Liquid - Oral
30 X
5/25/1998
UNDERBERG BITTERS
underberg ag
00366730
Liquid - Oral
0.45 %
12/31/1972
HOMEOPATHIC MEDICINE (S71) DPS 30C
total health centre
02071290
Drops - Oral
30 C / ML
12/31/1994
SACCHARUM OFFICINALE LIQUID (S#71)-1,2X...CM
total health centre
02186233
Liquid ,  Drops - Sublingual
1 X / ML
6/1/1997
SACCHARUM-INJEEL LIQ (10D,30D,200D/1.1ML)
02071797
Liquid - Oral
10 D / 1.1 ML
12/31/1994

CIMA AEMPS Drug Approvals

Approved Product
Company
Registration Number
Pharmaceutical Form
Prescription Type
Status
No CIMA AEMPS (Spain) approvals found for this drug.

Philippines FDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Philippines FDA approvals found for this drug.

Saudi SFDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Saudi SFDA approvals found for this drug.

Malaysia NPRA Drug Approvals

Approved Product
Company
Registration Number
Dosage Form
Strength
Approval Date
No Malaysia NPRA approvals found for this drug.

UK EMC Drug Information

Medicine Name
MA Holder
MA Number
Pharmaceutical Form
Active Ingredient
Authorization Date
No UK EMC drug information found for this drug.

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