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DIKEGULAC DIHYDRAT

CAS No.
18467-77-1
Chemical Name:
DIKEGULAC DIHYDRAT
Synonyms
diprogulic acid;dikegulac hydrate;DIKEGULAC DIHYDRAT;DIKEGULAC DIHYDRATE;DIACETONE-2-KETOGULONICACID;Oxogulonic acid diacetonide;Diacetone-2-oxo-L-gulonic acid;2,3,4,6-DIACETONE-2-KETOGULONIC ACID;Diprogulic acid (and its sodium salt);DIKEGULAC MONOHYDRATE PESTANAL 250 MG
CBNumber:
CB0464936
Molecular Formula:
C12H18O7
Molecular Weight:
274.27
MDL Number:
MFCD00150519
MOL File:
18467-77-1.mol
MSDS File:
SDS
Last updated:2026-07-31 15:25:13

DIKEGULAC DIHYDRAT Properties

Melting point 88-90 °C(lit.)
Boiling point 375℃
Density 1.281
Flash point 140℃
storage temp. 2-8°C
pka 1.77±0.60(Predicted)
Henry's Law Constant 5.2×1010 mol/(m3Pa) at 25℃, HSDB (2015)
FDA UNII 3981541LXD
EPA Substance Registry System .alpha.-L-xylo-2-Hexulofuranosonic acid, 2,3:4,6-bis-O-(1-methylethylidene)- (18467-77-1)

SAFETY

Risk and Safety Statements

Safety Statements  22-24/25
WGK Germany  3
TSCA  TSCA listed
HS Code  29329990

DIKEGULAC DIHYDRAT price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
American Custom Chemicals Corporation PST0000462 DIKEGULAC 98.00% 18467-77-1 1G $981.75 2021-12-16 Buy
Product number Packaging Price Buy
PST0000462 1G $981.75 Buy

DIKEGULAC DIHYDRAT Chemical Properties, Uses, Production

Definition

ChEBI: Dikegulac is a member of dioxanes.

Production Methods

The commercial production of dikegulac typically begins with 2-keto-L-gulonic acid. This precursor is reacted with 2,2-dimethoxypropane under elevated temperatures in the presence of a strong acid catalyst, such as sulphuric acid, to form a protected intermediate via acetal formation. This intermediate contains the diacetonide structure characteristic of dikegulac. The reaction mixture is then treated with a base, often sodium hydroxide, to hydrolyse residual esters and neutralise the acid, yielding dikegulac sodium, the usual marketed formulation.

Mechanism of action

Decreases RNA synthesis, rapidly inhibits amino-acid uptake by cells

Purification Methods

Dissolve -DAG in Et2O, filter, dry (MgSO4) it, filter it again and evaporate to give a yellow oil. Addition of one drop of H2O induces crystallisation to the monohydrate, which also forms rhombic crystals on recrystallisation from 95% EtOH/H2O at room temperature. [Flatt et al. Synthesis 815 1979, Reichstein & Grussner Helv Chim Acta 17 311 1934, Takagi & Jeffrey Acta Crystallogr Sect B 34 2932 1978, cf Org Synth 55 80 1976, Beilstein 19/12 V 520.]

Pesticide Type

Plant Growth Regulator

DIKEGULAC DIHYDRAT Preparation Products And Raw materials

Raw materials

Preparation Products

Global Suppliers ( 36)
Supplier Tel Email Country ProdList Advantage
Shenzhen Polymeri Biochemical Technology Co., Ltd. +86-400-002-6226 sales@rrkchem.com China 57336 58
Shanghai TenSus Biotechnology Co., Ltd. 021-50895067 18616507272;13681616114;15020344067 tensus@163.com China 8029 58
Shanghai Jiegu Biotechnology Co., Ltd. 021-51698675 sales@jiejiegroup.com China 8195 58
Mainchem Co., Ltd. -- sarah@mainchem.com China 6528 58
TCI (Shanghai) Chemical Trading Co., Ltd. 021-61109150 sales@tcisct.com China 29717 58
Beijing Qinling Pharmaceutical Co., Ltd. 010-61241352 18901327973 834537306@qq.com China 6234 58
Shanghai Yifei Biotechnology Co. , Ltd. 021-65675885 18964387627 customer_service@efebio.com China 11963 58
Shaanxi Didu Pharmaceutical Co., Ltd. 029-81124775 17791530730 1079@dideu.com China 10000 58
DAYANG CHEM (HANGZHOU) CO.,LTD +86-88938639 +86-17705817739 info@dycnchem.com China 53636 58
SUZHOU SENFEIDA CHEMICAL CO.,LTD +86-0512-83500002 +86-15195660023 3899766280@qq.com China 26349 58
DIKEGULAC DIHYDRAT DIKEGULAC DIHYDRATE 2,3:4,6-bis-o-(1-methylethylidene)-alpha-l-xylo-2-hexulofuranosonicaci L-Diacetoneketogulonic acid monohydrate (DAKS) DIKEGULAC MONOHYDRATE PESTANAL 250 MG 2,3:4,6-di-o-isopropyliden-2-oxo-l-gulonic acid dikegulac hydrate DIACETONE-2-KETOGULONICACID Diacetone-2-oxo-L-gulonic acid 2,3,4,6-DIACETONE-2-KETOGULONIC ACID Diprogulic acid (and its sodium salt) 2,3:4,6-Diisopropylidene-2-keto-L-gulonic acid Oxogulonic acid diacetonide α-L-xylo-2-Hexulofuranosonic acid, 2,3:4,6-bis-O-(1-methylethylidene)- diprogulic acid 18467-77-1 C12H18O7x2H2O Specialty Synthesis Monosaccharides Carbohydrate Synthesis