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Octanohydroxamic Acid

CAS No.
7377-03-9
Chemical Name:
Octanohydroxamic Acid
Synonyms
CaprylhydroxaMic Acid;OCTANOHYDROXAMIC ACID;CAPRYLHYDROXAMIC;CAPRYLOHYDROXAMIC ACID;hydroximic acid;taselin;n-hydroxy-octanamid;N-HYDROXYOCTANAMIDE;OctanaMide, N-hydroxy-;HOHA
CBNumber:
CB9150582
Molecular Formula:
C8H17NO2
Molecular Weight:
159.23
MDL Number:
MFCD00143918
MOL File:
7377-03-9.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-08-04 11:17:55

Octanohydroxamic Acid Properties

Melting point 78°C
Density 0.970
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly)
form Solid
pka 9.56±0.20(Predicted)
color White to Off-White
Cosmetics Ingredients Functions CHELATING
Cosmetic Ingredient Review (CIR) Octanohydroxamic Acid (7377-03-9)
InChI InChI=1S/C8H17NO2/c1-2-3-4-5-6-7-8(10)9-11/h11H,2-7H2,1H3,(H,9,10)
InChIKey RGUVUPQQFXCJFC-UHFFFAOYSA-N
SMILES C(NO)(=O)CCCCCCC
EWG's Food Scores 1
FDA UNII UPY805K99W
EPA Substance Registry System Octanamide, N-hydroxy- (7377-03-9)
UNSPSC Code 12352111

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H319-H335-H315
Precautionary statements  P264-P280-P305+P351+P338-P337+P313P-P264-P280-P302+P352-P321-P332+P313-P362
Risk Statements  36/37/38
Safety Statements  26-36/37/39
WGK Germany  WGK 3
RTECS  RG9900500
TSCA  TSCA listed
HS Code  2928.00.5000
Storage Class 11 - Combustible Solids
REACH Registrations Active

Octanohydroxamic Acid price More Price(44)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TCI Chemical C1232 Octanohydroxamic Acid >99.0%(N) 7377-03-9 5g $80 2026-04-30 Buy
TCI Chemical C1232 Octanohydroxamic Acid >99.0%(N) 7377-03-9 25g $239 2026-04-30 Buy
Biosynth FC28962 Caprylohydroxamic acid 7377-03-9 50g $201 2026-06-04 Buy
Biosynth FC28962 Caprylohydroxamic acid 7377-03-9 100g $312 2026-06-04 Buy
Biosynth FC28962 Caprylohydroxamic acid 7377-03-9 250g $612.5 2026-06-04 Buy
Product number Packaging Price Buy
C1232 5g $80 Buy
C1232 25g $239 Buy
FC28962 50g $201 Buy
FC28962 100g $312 Buy
FC28962 250g $612.5 Buy

Octanohydroxamic Acid Chemical Properties, Uses, Production

Description

Octanohydroxamic acid (OHA), the more common hydroxamate collector, has both an acid group (single bondNHOH) and basic group (single bond CO). The hydrogen in the acid group can be replaced by a metal ion and a dative bond from the basic group to form a chelate. Improved monazite flotation performance was reported when using OHA compared to the results obtained with sodium oleate. Flotation separation of monazite and calcite using OHA has been described in previous publications. OHA was the most potent urease inhibitor among saturated hydroxamic acid (HAs) with a calculated IC50 of 0.25±0.1mM compared to 8.67±1.3 and 0.50±0.2mM for Acetohydroxamic acid and heptanohydroxamic acid, respectively. Further increase in the chain length from 8 to 12 carbons negatively affected the potency of HAs[1].

Uses

Octanohydroxamic Acid is used in preparation of Caprylohydroxamic Acid.

Synthesis

Ethyl caprylate

106-32-1

Octanohydroxamic Acid

7377-03-9

To a 1000 mL four-necked flask was added hydroxylamine hydrochloride (48.7 g, 0.70 mol, 1.4 eq.), water (50 g), and ethanol (200 g, 2.3 times the volume), and stirred at room temperature until hydroxylamine hydrochloride was completely dissolved. Ethyl octanoate (86.7 g, 0.5 mol, 1.0 eq.) was then added and stirred at room temperature to form a two-phase system. The reaction mixture was cooled to 5-10°C and 40% KOH solution (168 g, 1.2 mol, 2.4 eq.) was added slowly and dropwise. After the dropwise addition, the reaction system was heated to 50~55°C and the reaction was held for 3 hours and monitored by gas chromatography (GC) until the ethyl octanoate material completely disappeared. After the reaction was completed, cooled to 5~10°C, slowly added concentrated hydrochloric acid (90 mL) to adjust the pH to 6.4~6.7, at which time a large amount of white solid precipitated. The solid was collected by filtration and dried at 50°C for 8 hours. The crude product was recrystallized with benzene to give 78.8 g of white flocculent solid in 91.1% yield.

References

[1] Diana Evstafeva. “Inhibition of urease-mediated ammonia production by 2-octynohydroxamic acid in hepatic encephalopathy.” Nature Communications 15 1 (2024): 2226.

124-07-2
7377-03-9
Synthesis of Octanohydroxamic Acid from Octanoic acid

Octanohydroxamic Acid Preparation Products And Raw materials

Global Suppliers ( 418)
Supplier Tel Email Country ProdList Advantage
Weifang Runzhong Fine Chemical Co., LTD 18653686003 sq@runzhongchem.com China 81 58
Jinan Baozhao Pharmaceutical Technology Co., Ltd. 0531-82371868 13210529039 baozhaopharm@163.com China 160 58
Shandong Suihua Biotechnology Co. Ltd 15689727968 freesky2121@163.com China 987 58
Jiangyin Soteng Biotechnology Co., Ltd. 0510-86686637 13861630217 marketingb@suntonchem.com China 16 58
Shandong Lierbang New Material Co. LTD 15553337722 13964392203 1135818881@qq.com China 49 58
Wuhan penglei Biotechnology Co., Ltd 15871464247 17307245989 3471278124@qq.com China 4990 58
Guangzhou Hichvan Chemical Co., Ltd. 19128722614 hichvan@163.com China 103 58
Shandong Suihua Biotechnology Co., Ltd. 15169101773 15169101773 519904247@qq.com China 1077 58
J & K SCIENTIFIC LTD. 18210857532 18210857532 jkinfo@jkchemical.com China 96815 76
Meryer (Shanghai) Chemical Technology Co., Ltd. 4006356688 18621169109 market03@meryer.com China 40202 62

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