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DL-Menthol

DL-Menthol Structure
CAS No.
89-78-1
Chemical Name:
DL-Menthol
Synonyms
89-78-1;Mentol;Racemic menthol;-MenthoL;I-menthol;Menthomenthol;p-Menthan-3-ol;component of Theragesic;DL - mint;DL-Menthol
CBNumber:
CB7498497
Molecular Formula:
C10H20O
Molecular Weight:
156.27
MOL File:
89-78-1.mol
MSDS File:
SDS
Modify Date:
2024/9/5 22:20:32

DL-Menthol Properties

Melting point 34-36 °C(lit.)
Boiling point 216 °C(lit.)
alpha -2 º (c=10, EtOH)
Density 0.89 g/mL at 25 °C(lit.)
vapor pressure 0.8 mm Hg ( 20 °C)
refractive index 1.4615
FEMA 2665 | MENTHOL RACEMIC
Flash point 200 °F
storage temp. Store below +30°C.
solubility 456mg/l
form Crystalline Solid
pka 15.30±0.60(Predicted)
color Colorless to white
Odor at 10.00 % in dipropylene glycol. peppermint cool woody
Odor Type mentholic
Water Solubility insoluble
Merck 14,5837
JECFA Number 427
BRN 3194263
LogP 3.4 at 37℃
CAS DataBase Reference 89-78-1(CAS DataBase Reference)
NIST Chemistry Reference DL-Menthol(89-78-1)
EPA Substance Registry System (1R,2S,5R)-Menthol (89-78-1)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H315-H319
Precautionary statements  P264-P280-P302+P352-P305+P351+P338-P332+P313-P337+P313
Hazard Codes  Xn,Xi
Risk Statements  37/38-41-36/37/38
Safety Statements  36/37/39-24/25-36-26-39
RIDADR  UN 1888 6.1/PG 3
WGK Germany  2
RTECS  OT0350000
Autoignition Temperature 405 °C
TSCA  Yes
HS Code  29061100
Toxicity LD50 orally in rats: 3180 mg/kg (Jenner)
NFPA 704
1
2 0

DL-Menthol price More Price(13)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) W266507 DL-Menthol ≥95%, FCC, FG 89-78-1 1SAMPLE-K ₹5141.88 2022-06-14 Buy
Sigma-Aldrich(India) W266507 DL-Menthol ≥95%, FCC, FG 89-78-1 250G ₹9233.73 2022-06-14 Buy
Sigma-Aldrich(India) W266507 DL-Menthol ≥95%, FCC, FG 89-78-1 1KG ₹13661.15 2022-06-14 Buy
Sigma-Aldrich(India) W266507 DL-Menthol ≥95%, FCC, FG 89-78-1 4KG ₹28145 2022-06-14 Buy
Sigma-Aldrich(India) M2772 Menthol 99% 89-78-1 100G ₹2089.23 2022-06-14 Buy
Product number Packaging Price Buy
W266507 1SAMPLE-K ₹5141.88 Buy
W266507 250G ₹9233.73 Buy
W266507 1KG ₹13661.15 Buy
W266507 4KG ₹28145 Buy
M2772 100G ₹2089.23 Buy

DL-Menthol Chemical Properties,Uses,Production

Description

Menthol has a mint-like odor and a fresh, cooling taste. It may be prepared by hydrogenation of thymol.

Chemical Properties

colorless to white crystalline solid

Physical properties

Appearance: colorless or white acicular prismatic crystals or white crystalline powder. Solubility: easily dissolved in ethanol, chloroform, ether, liquid paraffin, or volatile oil and soluble in water. Odor: a cool, refreshing, and pleasant mint aroma, sweet odor, and taste cool early after burning. Boiling point: 212?°C. Melting point: 41–43?°C. Specific optical rotation: ?49 to ?50°.

Occurrence

Reported found in peppermint and other mint oils (e.g., M. arvensis), lemon peel oil, cranberry, pineapple, cab bage, thymus, egg, rum, cocoa, tea, honey, avocado, coriander, mango, rice, litchi, dill herb, calamus, juniper berries, fennel, buchu oil, clam and Roman chamomile oil, Mentha species.

History

In the world of aromatic chemicals, menthol is often described as a unique source of skin and mucous membranes. Menthol is mainly extracted from natural plants. The vast majority of natural menthol in the global market is extracted from numerous Asian mint. In 2006, the world’s natural menthol production is 12,800?tons or more. However, due to various factors, the production of natural menthol is becoming less and less. Since the 1960s, Japan, Germany, and other countries had developed the synthetic menthol products. In 1974 the German company Symrise and Japan Takasago Fluidic Systems company launched chemical synthesis of menthol. At present, attention has been paid to the study of menthol analogy substances and the effect of the changes of molecular structure on the aroma and cool sensation. Some studies have shown that hydroxyl groups located in the branched or 1, 4 chain cannot show a sense of cool. The researchers believed that menthol analogy substances with optical activity should be able to show different, surprising cooling effect, and the structure of hydroxyl alkyl groups is the key point to have a cooling effect. The Japanese chemist Ryoji Noyo and his colleagues found that in BINAP and rhodium complexes as catalysts for asymmetric hydrogenation reaction, the synthesis of menthol is very effective. Because of the contribution of asymmetric organic synthesis, they won the 2001 Nobel Prize in Chemistry.

Uses

DL-Menthol may be used as an extraction solvent for the determination of parabens in food products, cosmetics and pharmaceuticals using liquid-liquid microextraction with high performance liquid chromatography-diode array detection (HPLC-DAD). It may also be used for the preparation of hydrophobic deep eutectic solvent (DES) in the extraction and determination of methylparaben, propylparaben, and butylparaben from cosmetics samples using syringe-to-syringe dispersive magnetic nanofluid microextraction procedure (SS-DMNF-ME) with high-performance liquid chromatography technique (HPLC).

Indications

For external application, it is applied locally and often used to relieve pain and itching. A nasal drip is used in the head cold. Inhalation or spray is used for sore throat. Oral administration can promote digestion.

Preparation

By hydrogenation of thymol.

General Description

White crystalline solid with a peppermint odor and taste.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

DL-Menthol is incompatible with butyl chloral hydrate, camphor, phenol, chloral hydrate, Exalgine, betanaphthol, resorcinol or thymol in triturations; potassium permanganate, chromium trioxide and pyrogallol. DL-Menthol is also incompatible with strong oxidizers.

Hazard

Irritant to mucous membranes on inhalation.

Fire Hazard

DL-Menthol is combustible.

Clinical Use

It can be clinically used to assist anesthesia, postoperative analgesia, intercostal nerve block, trigeminal nerve block, occipital nerve block, and so on. When applied locally, it can promote blood circulation, diminish inflammation, relieve itching, relieve pain, relieve edema, and so on.

Safety Profile

Poison by intravenous route. Moderately toxic by ingestion and intraperitoneal routes. A severe eye irritant. Incompatible with phenol, p-naphthol, resorcinol or thymol in trituration, potassium permanganate, chromium trioxide, pyrogallol. Combustible liquid. \When heated to decomposition it emits acrid smoke and irritating fumes.

Global( 768)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
Gansai International 91-40-27425615 Andhra Pradesh, India 159 58 Inquiry
Hemadri Chemicals 08047646492 Mumbai, India 17 58 Inquiry
Shreeji Pharma International 09824326039 Vadodara, India 166 58 Inquiry
CLEANCHEM LABORATORIES LLP +91 98921 69560 New Delhi, India 326 58 Inquiry
HRV Global Life Sciences Private Limited 91-40-23554991 Hyderabad, India 190 58 Inquiry
Pratham Texchem LLP 91-79-22144452 Gujarat, India 35 58 Inquiry
Nectar Lifesciences Ltd. (NLL) 91-172-3047713 Punjab, India 25 58 Inquiry
Global Chem Asia Pacific 91-9849161572 Hyderabad, India 255 58 Inquiry
Apara International 91-22-24306504 Mumbai, India 15 58 Inquiry
Nikunj Chemicals 08048967857 Vadodara, India 30 58 Inquiry

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