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Methyl 3-Hydroxycyclopentanecarboxylate is a chemical compound characterized by the molecular formula C7H12O3. It is a colorless, oily liquid known for its sweet, fruity odor, and is widely recognized for its use as a flavoring ingredient in the food and beverage industry, as well as in the production of pharmaceuticals and fragrances.

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  • 101080-22-2 Structure
  • Basic information

    1. Product Name: Methyl 3-Hydroxycyclopentanecarboxylate
    2. Synonyms: Methyl 3-Hydroxycyclopentanecarboxylate;3-Hydroxycyclopentanecarboxylic acid
    3. CAS NO:101080-22-2
    4. Molecular Formula: C6H10O3
    5. Molecular Weight: 130.1418
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 101080-22-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 297.2±33.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.328±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: Sealed in dry,Room Temperature
    8. Solubility: N/A
    9. PKA: 4.59±0.40(Predicted)
    10. CAS DataBase Reference: Methyl 3-Hydroxycyclopentanecarboxylate(CAS DataBase Reference)
    11. NIST Chemistry Reference: Methyl 3-Hydroxycyclopentanecarboxylate(101080-22-2)
    12. EPA Substance Registry System: Methyl 3-Hydroxycyclopentanecarboxylate(101080-22-2)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 101080-22-2(Hazardous Substances Data)

101080-22-2 Usage

Uses

Used in Food and Beverage Industry:
Methyl 3-Hydroxycyclopentanecarboxylate is used as a flavoring ingredient for its ability to enhance the aroma and taste of various products. Its sweet, fruity scent makes it a valuable addition to a range of consumables, contributing to the overall sensory experience.
Used in Pharmaceutical Production:
In the pharmaceutical industry, Methyl 3-Hydroxycyclopentanecarboxylate is utilized in the development of medications, likely due to its properties that can contribute to the formulation of drugs with specific taste profiles or as part of the active ingredients themselves.
Used in Fragrance Industry:
Methyl 3-Hydroxycyclopentanecarboxylate is also employed in the creation of fragrances, capitalizing on its distinctive sweet and fruity scent to contribute to the composition of various olfactory products.
Regulatory Considerations:
It is considered safe for consumption when used in small quantities, and its use is regulated by food safety authorities to ensure that it meets safety standards and does not pose any health risks to consumers.

Check Digit Verification of cas no

The CAS Registry Mumber 101080-22-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,0,8 and 0 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 101080-22:
(8*1)+(7*0)+(6*1)+(5*0)+(4*8)+(3*0)+(2*2)+(1*2)=52
52 % 10 = 2
So 101080-22-2 is a valid CAS Registry Number.

101080-22-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Hydroxycyclopentanecarboxylic acid

1.2 Other means of identification

Product number -
Other names (+-)-cis-3-hydroxy-cyclohexanecarboxylic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:101080-22-2 SDS

101080-22-2Relevant articles and documents

CHEMOENZYMATIC SYNTHESIS OF CONFORMATIONALLY RIGID GLUTAMIC ACID ANALOGUES

Trigalo, F.,Buisson, D.,Azerad, R.

, p. 6109 - 6112 (2007/10/02)

All stereomers of cyclohexane cyclopentane-derived analogues of glutamic acid have been synthesized from the corresponding 3-keto-cycloalkyl carboxylic acid esters by a combination of microbial steps and standard chemical methods.

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