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Masoprocol

CAS 27686-84-6C18H22O4MW 302.4

Masoprocol (CAS 27686-84-6) — formula C18H22O4, molecular weight 302.4; category organic chemicals.

Product Description

Masoprocol (CAS 27686-84-6) is a chemical raw material in the organic chemicals category. Its molecular formula C18H22O4 comprises 18 C, 22 H, 4 O atoms. Its molecular weight is about 302.4. Reported physicochemical data: melting point around 185.5, LogP about 5.8. As a sourcing and distribution partner we help locate and compare this item across domestic and cross-border channels, arranging samples and batch orders with full COA and compliance files.

Product Overview

CAS Number27686-84-6
Molecular FormulaC18H22O4
Molecular Weight302.4
Melting Point185.5
LogP5.8
Applicationstreatment of actinic keratoses (precancerous skin growths that can become malignant if left untreated), 2-Benzenediol, 4'-[(2R, 3S)-2, 3-dimethyl-1, 4-butanediyl]bis
CategoryOrganic Chemicals

Applications

Documented applications: treatment of actinic keratoses (precancerous skin growths that can become malignant if left untreated), 2-Benzenediol, 4'-[(2R, 3S)-2, 3-dimethyl-1, 4-butanediyl]bis.

Technical Profile

What this product is

Masoprocol is a carbon-based organic compound with CAS registry number 27686-84-6 and molecular formula C18H22O4 (molecular weight 302.4), belonging to the organic chemicals segment of chemical raw materials.

Identification

CAS number: 27686-84-6

Its molecular formula C18H22O4 comprises 18 C, 22 H, 4 O atoms.

Also known as: Masoprocol · 马索普罗科尔

Category: organic chemicals

Frequently Asked Questions

What is the CAS number of Masoprocol?

The CAS registry number of Masoprocol is 27686-84-6.

What is the molecular formula and molecular weight of Masoprocol?

Molecular formula C18H22O4, molecular weight 302.4.

What other names is Masoprocol known by?

It is also registered under: Masoprocol, 马索普罗科尔.

What are the documented applications of Masoprocol?

Recorded applications: treatment of actinic keratoses (precancerous skin growths that can become malignant if left untreated), 2-Benzenediol, 4'-[(2R, 3S)-2, 3-dimethyl-1, 4-butanediyl]bis.

Which category does Masoprocol belong to?

Category: Organic Chemicals.

Packaging & documentation

Packaging is agreed per order, from lab-scale packs to bulk, and confirmed with each order rather than fixed on the page. A Certificate of Analysis (COA) ships with every batch and MSDS is available; where the end use carries a regulatory limit (food contact, pharmaceutical or cosmetic), state the standard at enquiry and the grade is set against it.

PubChem Public Data

Independent reference data for Masoprocol (CAS 27686-84-6), compiled from public chemistry databases.

Registry identifiers across databases

CAS Registry Number27686-84-6
PubChem CID71398
Molecular formulaC18H22O4
IUPAC name4-[(2S,3R)-4-(3,4-dihydroxyphenyl)-2,3-dimethylbutyl]benzene-1,2-diol
UNII (FDA)7BO8G1BYQU

Computed descriptors

Molecular Weight302.4
XLogP34.3
Hydrogen Bond Donor Count4
Hydrogen Bond Acceptor Count4
Rotatable Bond Count5
Exact Mass302.15180918
Monoisotopic Mass302.15180918
Topological Polar Surface Area80.9
Heavy Atom Count22

Physicochemical values on record

Melting Point185.5
Melting Point185.5 °C
Solubility1.36e-02 g/L
LogP5.8

Documented uses on record

    Used for the treatment of actinic keratoses (precancerous skin growths that can become malignant if left untreated).1,2-Benzenediol, 4,4'-[(2R,3S)-2,3-dimethyl-1,4-butanediyl]bis-, rel-: INACTIVE

    Synonyms and trade names

    Masoprocol; 27686-84-6; meso-NDGA; meso-Nordihydroguaiaretic acid; Actinex; Masoprocolum; CHX 100; CHX-100; meso-4,4'-(2,3-Dimethyltetramethylene)dipyrocatechol; 1,2-Benzenediol, 4,4'-(2,3-dimethyl-1,4-butanediyl)bis-, (R*,S*)-; ORISTAR NHGA; DTXSID5045178; 4-[(2S,3R)-4-(3,4-dihydroxyphenyl)-2,3-dimethylbutyl]benzene-1,2-diol; 7BO8G1BYQU; INSM-18; erythro-nordihydroguaiaretic acid

    What the public record says

    Masoprocol · CAS 27686-84-6 · C18H22O4. UNII 7BO8G1BYQU. Melting Point: 185.5; Melting Point: 185.5 °C; Solubility: 1.36e-02 g/L.

    Source: PubChem / Wikidata; the batch COA governs where values differ.

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