Feature reaction of phloroglucinol Chemical properties Uses Production method Hazards & Safety Information
ChemicalBook > CAS DataBase List > Phloroglucinol

Phloroglucinol

Feature reaction of phloroglucinol Chemical properties Uses Production method Hazards & Safety Information
Product Name
Phloroglucinol
CAS No.
108-73-6
Chemical Name
Phloroglucinol
Synonyms
Benzene-1,3,5-triol;1,3,5-TRIHYDROXYBENZENE;1,3,5-BENZENETRIOL;3,5-DIHYDROXYPHENOL;Nero;PHLOROGLUCIN;Floroglucinol;TRIHYDROXYBENZENE;1,3,5-trihydroxy-benzen;orog
CBNumber
CB0667672
Molecular Formula
C6H6O3
Formula Weight
126.11
MOL File
108-73-6.mol
More
Less

Phloroglucinol Property

Melting point:
215-220 °C
Boiling point:
194.21°C (rough estimate)
Density 
0.801 g/mL at 20 °C
vapor pressure 
0.001Pa at 25℃
refractive index 
n20/D 1.365
Flash point:
14 °C
storage temp. 
Store below +30°C.
solubility 
Soluble in diethyl ether, ethanol and pyridine.
form 
Crystalline Powder
pka
pK1:8.45(0);pK2:8.88(-1) (25°C)
color 
White to light beige
Water Solubility 
11.17g/L(room temperature)
Sensitive 
Light Sensitive & Hygroscopic
Merck 
14,7328
BRN 
1341907
InChIKey
QCDYQQDYXPDABM-UHFFFAOYSA-N
LogP
0.55 at 25℃
CAS DataBase Reference
108-73-6(CAS DataBase Reference)
NIST Chemistry Reference
1,3,5-Benzenetriol(108-73-6)
EPA Substance Registry System
1,3,5-Benzenetriol (108-73-6)
More
Less

Safety

Hazard Codes 
F,Xi
Risk Statements 
11-36/37/38-34-43
Safety Statements 
7-16-24/25-45-36/37/39-26-36/37-37/39
RIDADR 
UN 1170 3/PG 2
WGK Germany 
2
RTECS 
SY1050000
TSCA 
Yes
HS Code 
29072900
Toxicity
LD50 in mice, rats (g/kg): 4.7, 4.0 i.g. (Cahen)
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H317May cause an allergic skin reaction

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P271Use only outdoors or in a well-ventilated area.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
79330
Product name
Phloroglucinol
Purity
≥99.0% (HPLC)
Packaging
25g
Price
$35.5
Updated
2024/03/01
Sigma-Aldrich
Product number
8.18887
Product name
Phloroglucinol
Purity
for synthesis
Packaging
100g
Price
$116
Updated
2024/03/01
Sigma-Aldrich
Product number
79330
Product name
Phloroglucinol
Purity
≥99.0% (HPLC)
Packaging
100g
Price
$101
Updated
2024/03/01
Sigma-Aldrich
Product number
1.07069
Product name
Phloroglucinol
Purity
(1,3,5-trihydroxybenzene) for analysis
Packaging
25g
Price
$74.1
Updated
2024/03/01
TCI Chemical
Product number
P0249
Product name
Phloroglucinol Anhydrous
Purity
>99.0%(HPLC)
Packaging
25g
Price
$76
Updated
2024/03/01
More
Less

Phloroglucinol Chemical Properties,Usage,Production

Feature reaction of phloroglucinol

Reaction of formaldehyde with phloroglucinol under alkaline conditions generates orange compound. The colorimetric assay determination of this compound at the maximum absorption wavelength of 460 nm, can be used to detect low or trace formaldehyde in textile and garment.
Since phloroglucinol may occur enol and keto tautomers, it can react with ammonia according following reaction:

Under the influence of ammonia, 1,3,5-Benzenetriamine can be obtained by keto reaction of phloroglucinol, while this amine can also hydrolyze in aqueous acid to generate phloroglucinol. Besides phloroglucinol can also have enol reaction.

The information above is edited by Andy from Chemicalbook.

Chemical properties

This product is a white or light yellow crystal or crystalline powder with melting point of 218 ℃. Usually it carries two molecular crystallization water ([6099-90-7]) and converts into anhydrous at 110 ℃. It can be dissolved in 100 parts of water, 10 parts of ethanol, and 0.5 parts of pyridine and is soluble in ether. Besides It partially decomposes when sublimation, and changes its color when exposed to the light. In addition it tastes sweet.

Uses

Phloroglucinol can be used in verifications of antimony, arsenic, cerium, chromate, chromium, gold, iron, mercury, nitrites, osmium, palladium, tin, vanadium, vanillin and lignin, and measurement of furfural, pentose, pentosan, methanol, chloral hydrate, turpentine, Lignified cell tissues, free acid in gastric juice (HCl) and decalcified bone specimens. Besides it can also be used as biological reagent dyes.

Production method

2,4,6-aminobenzoic acid can be obtained by 2,4,6-trinitrobenzoic acid`s reduction of zinc particles. After its dilute solution was heated at reflux for 20h, acidified with hydrochloric acid, cooled and crystallized, phloroglucinol can be obtained with a yield of 46-53%.

Hazards & Safety Information

Category: Toxic substances
Toxicity grade: Moderate toxicity
Acute toxicity: oral-rat LD50: 4000 mg/kg; Oral-Mouse LD50: 4550 mg/kg
Flammability hazard characteristics: Combustible fire burning can cause smoke irritation
Storage characteristics: Ventilated, low-temperature and dry warehouse; and separately with oxidants
Extinguishing agents: Carbon dioxide, foam, sand and water mist

Description

Phloroglucinol is a naturally occurring phenol that exhibits diverse biological activities. Phloroglucinol protects V79-4 Chinese hamster lung fibroblast cells from oxidative stress and inhibits lipid peroxidation by scavenging reactive oxygen species (ROS). It induces apoptosis in HT-29 human colon cancer cells and inhibits metastasis of BT549 and MDA-MB-231 human breast cancer cells. Phloroglucinol protects primary neurons from β-amyloid-induced dendritic spine loss in vitro and shortens the latency to find the platform in a Morris water maze test in an Alzheimer’s disease (AD) mouse model. Phloroglucinol has been used to stain histological plant sections and in the synthesis of numerous natural products. Phloroglucinol slows the frequency and decreases the amplitude of contraction in isolated rabbit and rat intestine at a concentration of 100 and 1 μM, respectively. Formulations containing phloroglucinol have been used as antispasmodics.

Chemical Properties

white to light yellow crystal

Physical properties

Phloroglucinol crystallizes in the anhydrous form or as the dihydrate. Recrystallization from water gives the dihydrate, which is colorless, oderless, sweet in taste, and forms rhombic crystals. The dihydrate is converted into the anhydrous form by heating at 110 ℃. Phloroglucinol sublimes at higher temperatures with partial decomposition.

Uses

Phloroglucinol is mainly used as a coupling agent in printing. It is an active component of Tollen's reagent and Gunzburg reagent used to test pentoses and hydrochloric acid in gastric juice respectively. In analytical chemistry, it is used to study condensed tannins by means of depolymerization. It is also involved in the synthesis of 2,4,6-triamino-1,3,5- trinitrobenzene, trinitrophloroglucinol and pharmaceuticals like flopropione.

Uses

Phloroglucinol (1,3,5-trihydroxybenzene) is the core structure of a large family of substituted phenolics with broad, albeit weak, biological activity. Phloroglucinol is a useful metabolite for HPLC/DAD and bioassay dereplication.diagnostic aid growth hormone releasing factor. Antispasmodic.

Definition

ChEBI: Phloroglucinol is a benzenetriol with hydroxy groups at position 1, 3 and 5. It has a role as an algal metabolite.

Application

Phloroglucinol (phlo) is a phenol derivative that shows cyctoprotective effect from oxidative damage by enhancing the activity of cellular catalase.
It can react with benzaldehyde derivatives to form phloroglucinol-based microporous polymeric organic frameworks (phlo-POF) with potential applications in ion-exchange and gas adsorption.
Phlo can also be used to prepare synthetic analogs of A-type proanthocyanidins (PACs) such as 2,8-dioxabicyclo[3.3.1]nonane derivatives by reacting with the corresponding flavylium salts.

General Description

Phloroglucinol is a trihydroxybenzene with antithrombotic, profibrinolytic, antimicrobial, antimalarial, cancer chemopreventive, anti-HIV and anti-leishmanial activities. Phloroglucinol (PG) is a biosynthetic precursor of the 2,4-diacetylphloroglucinol (DAPG) an antibiotic against soil-borne diseases. Phloroglucinol is a useful intermediate because it is polyfunctional.

Flammability and Explosibility

Not classified

Safety Profile

Moderately toxic by subcutaneous and intraperitoneal routes. Mildly toxic by ingestion. Experimental reproductive effects. Mutation data reported. When heated to decomposition it emits acrid smoke and irritating fumes. Used in diazo-type printing and textile dyeing, in microscopy as a bone specimen decalcifier

Purification Methods

Crystallise the triol from water, and store it in the dark under nitrogen. [Beilstein 6 IV 7361.]

Phloroglucinol Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

Phloroglucinol Suppliers

HBCChem, Inc.
Tel
+1-510-219-6317
Fax
+1-650-486-1361
Email
sales@hbcchem.com
Country
United States
ProdList
10648
Advantage
60
Protheragen-ING
Tel
+16313385890
Email
info@protheragen-ing.com
Country
United States
ProdList
3868
Advantage
58
Aladdin Scientific
Tel
+1-+1(833)-552-7181
Email
sales@aladdinsci.com
Country
United States
ProdList
57505
Advantage
58
Alfa Chemistry
Tel
--
Fax
--
Email
info@Alfa-Chemistry.com
Country
United States
ProdList
6814
Advantage
0
Thoreau Chem Limited
Tel
--
Fax
--
Email
sales@thoreauchem.com
Country
United States
ProdList
483
Advantage
50
CarboMer, Inc.
Tel
--
Fax
--
Email
sales@carbomer.com
Country
United States
ProdList
4026
Advantage
67
Cayman Chemical Company
Tel
--
Fax
--
Email
cayman@caymanchem.com
Country
United States
ProdList
6213
Advantage
81
Redox Scientific
Tel
--
Fax
--
Email
info@redoxsci.com
Country
United States
ProdList
2380
Advantage
58
Aozeal Certified Standards (AOCS), Inc.
Tel
--
Fax
--
Email
info@aozeal.com
Country
United States
ProdList
504
Advantage
58
Parchem Fine & Specialty Chemicals
Tel
--
Fax
--
Email
info@parchem.com
Country
United States
ProdList
1031
Advantage
58
Penta Manufacturing Company (a division of Penta International Corporation)
Tel
--
Fax
--
Email
@pentamfg.com
Country
United States
ProdList
901
Advantage
58
CALSAK CORPORATION
Tel
--
Fax
--
Email
calsak@calsak.com
Country
United States
ProdList
430
Advantage
58
Barath Biosciences, Inc.
Tel
--
Fax
--
Email
barath@barathbiosciences.com
Country
United States
ProdList
203
Advantage
58
Glentham Life Sciences Ltd
Tel
--
Fax
--
Email
info@glentham.com
Country
United States
ProdList
2026
Advantage
58
Rochem International Inc.
Tel
--
Fax
--
Email
gcadioli@rochemintl.com
Country
United States
ProdList
80
Advantage
58
Voigt Global Distribution Inc
Tel
--
Fax
--
Email
Sales@Vgdusa.Com
Country
United States
ProdList
110
Advantage
58
MP Biomedicals, LLC. (Division of Valiant FC Co., Ltd.)
Tel
--
Fax
--
Email
serv@mpbio.com
Country
United States
ProdList
1854
Advantage
58
MilliporeSigma (Sigma-Aldrich Corp.)
Tel
--
Fax
--
Email
@sial.com
Country
United States
ProdList
5414
Advantage
58
Combi-Blocks, Inc.
Tel
--
Fax
--
Email
les@combi-blocks.com
Country
United States
ProdList
2555
Advantage
58
Beantown Chemical Corporation
Tel
--
Fax
--
Country
United States
ProdList
396
Advantage
58
Fluorochem Ltd.
Tel
--
Fax
--
Email
enquiries@fluorochem.co.uk
Country
United States
ProdList
4583
Advantage
58
TCI America, Inc. (part of Tokyo Chemical Industry)
Tel
--
Fax
--
Email
Angelina.Crew@tcichemicals.com
Country
United States
ProdList
2053
Advantage
58
Oakwood Products, Inc.
Tel
--
Fax
--
Email
sales@oakwoodchemical.com
Country
United States
ProdList
6193
Advantage
74
VWR International, LLC.
Tel
--
Fax
--
Email
@sargentwelch.com
Country
United States
ProdList
6262
Advantage
58
CJ Latta & Associates, LLC
Tel
--
Fax
--
Email
chiplatta@msn.com
Country
United States
ProdList
357
Advantage
58
Lluch Essence S.L.
Tel
--
Fax
--
Email
web@lluche.com
Country
United States
ProdList
2352
Advantage
58
Moellhausen S.P.A.
Tel
--
Fax
--
Country
United States
ProdList
1676
Advantage
58
Combi-Blocks Inc.
Tel
--
Fax
--
Email
sales@combi-blocks.com
Country
United States
ProdList
6618
Advantage
69
SynQuest Laboratories, Inc.
Tel
--
Fax
--
Email
info@synquestlabs.com
Country
United States
ProdList
6871
Advantage
62
Riedel-de Haen AG
Tel
--
Fax
--
Country
United States
ProdList
6773
Advantage
87
TCI America
Tel
--
Fax
--
Email
sales@tciamerica.com
Country
United States
ProdList
6909
Advantage
75
Frontier Scientific, Inc.
Tel
--
Fax
--
Email
sales@frontiersci.com
Country
United States
ProdList
6222
Advantage
86
Matrix Scientific
Tel
--
Fax
--
Email
sales@matrixscientific.com
Country
United States
ProdList
6632
Advantage
80
Ring Specialty Chemicals Inc.
Tel
--
Fax
--
Email
info@ringchemicals.com
Country
United States
ProdList
888
Advantage
39
Allweys LLC
Tel
--
Fax
--
Email
sales@allweysllc.com
Country
United States
ProdList
690
Advantage
30
HBCChem Inc.
Tel
--
Fax
--
Email
sales@hbcchem-inc.com
Country
United States
ProdList
4569
Advantage
30
Ivy Fine Chemicals
Tel
--
Fax
--
Email
sales@ivychem.com
Country
United States
ProdList
6493
Advantage
58
3B Scientific Corporation
Tel
--
Fax
--
Email
sales@3bsc.com
Country
United States
ProdList
6962
Advantage
56
AlliChem, LLC
Tel
--
Fax
--
Email
sales@allichemllc.com
Country
United States
ProdList
6516
Advantage
60
Lab Express
Tel
--
Fax
--
Email
sales@labexpress.com
Country
United States
ProdList
1577
Advantage
67
Advanced Synthesis Technologies
Tel
--
Fax
--
Email
sales@advancedsynthesis.com
Country
United States
ProdList
4775
Advantage
61
AK Scientific, Inc.
Tel
--
Fax
--
Email
sales@aksci.com
Country
United States
ProdList
6347
Advantage
65
Sinova Inc.
Tel
--
Fax
--
Email
sales@sinovainc.com
Country
United States
ProdList
4009
Advantage
58
Advance Scientific & Chemical
Tel
--
Fax
--
Email
sales@advance-scientific.com
Country
United States
ProdList
6419
Advantage
71
Leonid Chemicals Private Limited
Tel
--
Fax
--
Email
careers@leonidchemicals.com
Country
United States
ProdList
1700
Advantage
43
Pfaltz & Bauer, Inc.
Tel
--
Fax
--
Email
sales@pfaltzandbauer.com
Country
United States
ProdList
6828
Advantage
72
Spectrum Chemicals & Laboratory Products
Tel
--
Fax
--
Email
sales@spectrumchemical.com
Country
United States
ProdList
6699
Advantage
77
Penta Manufacturing Company
Tel
--
Fax
--
Email
sales@pentamfg.com
Country
United States
ProdList
5076
Advantage
65
Waterstone Technology, LLC
Tel
--
Fax
--
Email
sales@waterstonetech.com
Country
United States
ProdList
6786
Advantage
30
Naugra Export
Tel
--
Fax
--
Country
United States
ProdList
1332
Advantage
47
More
Less

View Lastest Price from Phloroglucinol manufacturers

Baoji Guokang Bio-Technology Co., Ltd.
Product
Phloroglucinol 108-73-6
Price
US $238.00/Kg/Bag
Min. Order
1KG
Purity
99%
Supply Ability
10T
Release date
2021-06-04
Hebei Weibang Biotechnology Co., Ltd
Product
Phloroglucinol 108-73-6
Price
US $10.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
10 mt
Release date
2024-10-31
Qingdao RENAS Polymer Material Co., Ltd.
Product
Phloroglucinol 108-73-6
Price
US $0.00/kg
Min. Order
20kg
Purity
99%
Supply Ability
20 tons
Release date
2024-09-29

108-73-6, PhloroglucinolRelated Search:


  • 6,17-alpha Epoxypregnenolone
  • Phloroglucinol >=99.0% (HPLC)
  • Floroglucin
  • Floroglucinol
  • Phloroglucine
  • Spasfon-Lyoc
  • s-Trihydroxybenzene
  • sym-Trihydroxybenzene
  • Phloroglucinol, >=98%
  • PHLOROGLUCINOL TS
  • PHLOROGLUCIN
  • PHLOROGLUCINOL
  • ?hloroglucin
  • 1,3,5-trihydroxy-benzen
  • 1,3,5-Trihydroxycyclohexatriene
  • 5-Oxyresorcinol
  • 5-Oxyresorcinolphloroglucin
  • Benzene, 1,3,5-trihydroxy-
  • Benzene, trihydroxy
  • Phloroglucinol Standard
  • Phloroglucin Anhydrous
  • Phloroglucinol, anhydrous, 99+% 25GR
  • 1,3,5-Trihydroxybenzene,Phloroglucinol Anhydrous and Dihydrate
  • 1,3,-Trihydroxybenzene
  • Anhydrous Phloroglucinol
  • benzene-1,3,5-triol(phloroglucinol)
  • orog
  • ucinoL
  • 1,2,5-TRIHYDROXYBENZENE
  • 1,3,5-TRIHYDROXYBENZENE
  • 1,3,5-TRIHYDROXYBENZENE ANH
  • 1,3,5-THB
  • 1,3,5-BENZENETRIOL
  • AKOS BBS-00004257
  • 5-HYDROXYRESORCINOL
  • 3,5-DIHYDROXYPHENOL
  • TRIHYDROXYBENZENE
  • Phlorogluctinol(Anhydrous)
  • phloroglucinol Anhy
  • phloroglucinol dihydrate MSDS
  • PHLOROGLUCINOL SOLUTION 1% IN ETHANOL
  • Phloroglucinol solution
  • PHLOROGLUCINOL, FREE OF DIRESORCIN
  • PhloroglucinolGr-(1,3,5-Trihydroxybenzene)
  • PhloroglucinolGr
  • 1,3,5-Trihydroxybenzene(Anhydrous)
  • Phloroglucinol, anhydrous, 99+%
  • benzene,trihydroxy
  • Benzene-1,3,5-triol
  • Benzene-s-triol
  • Dilospan S
  • dilospans
  • Phlorolglucine
  • 1,3,5-benzenetriol, anhydrous
  • 1.3.5-Trihydroxybenzene,Phloroglucinol
  • FLUOROGLUCINOL
  • 1,3,5-TRIHYDROXYBENZENE ANHYDRATE MIN 99%
  • Phloroglucinol, 99+%, anhydrous