1185-29-1

• 

• Basic information

  1. Product Name: 2-ETHYL-2-METHYLCAPROIC ACID
  2. Synonyms: 2-ETHYL-2-METHYLHEXANOIC ACID;2-ETHYL-2-METHYLCAPROIC ACID;2-methyl-2-ethylcaproic acid;2-METHYL-2-ETHYLHEXANOICACID;METHYL-ETHYL-HEXANOICACID;2-Ethyl-2-methylhexansaure;Isononansure (Isomerengemisch);33977-30-9 (Hydrochloride salt)
  3. CAS NO:1185-29-1
  4. Molecular Formula: C₉H₁₈O₂
  5. Molecular Weight: 158.24
  6. EINECS: 214-680-3
  7. Product Categories: N/A
  8. Mol File: 1185-29-1.mol
  9. Article Data: 10

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 246.9°Cat760mmHg
  3. Flash Point: 112.3°C
  4. Appearance: /
  5. Density: g/cm³
  6. Vapor Pressure: 0.00852mmHg at 25°C
  7. Refractive Index: 1.44
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. CAS DataBase Reference: 2-ETHYL-2-METHYLCAPROIC ACID(CAS DataBase Reference)
  11. NIST Chemistry Reference: 2-ETHYL-2-METHYLCAPROIC ACID(1185-29-1)
  12. EPA Substance Registry System: 2-ETHYL-2-METHYLCAPROIC ACID(1185-29-1)

• 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: 1185-29-1(Hazardous Substances Data)

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• SDS
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• Downstream Products
• Article

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• Pharmaceutical Grade CAS 1185-29-1 with competitive price

  Cas No: 1185-29-1

• USD $ 139.0-210.0 / Kilogram

• 1 Kilogram

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• Zhuozhou Wenxi import and Export Co., Ltd
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• 2-Ethyl-2-methylhexanoic acid

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• Dayang Chem (Hangzhou) Co.,Ltd.
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• Hexanoic acid,2-ethyl-2-methyl-

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• 2-ETHYL-2-METHYLHEXANOIC ACID

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• Hexanoic acid,2-ethyl-2-methyl-

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• 2-ETHYL-2-METHYLCAPROIC ACID

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• Hexanoic acid,2-ethyl-2-methyl-

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• 2-ETHYL-2-METHYLCAPROIC ACID

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• Shanghai Run-Biotech Co., Ltd.
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• 2-methyl-2-ethylcaproic acid

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1185-29-1 Usage

General Description

2-Ethyl-2-methylcaproic acid, also known as EMCA, is a chemical compound with the molecular formula C8H16O2. It is a carboxylic acid with a branched carbon chain and a methyl and an ethyl group attached to the second carbon atom. EMCA is used as a flavoring agent in the food industry, providing a fruity and pineapple-like aroma. It is also used in the production of fragrances and perfumes due to its pleasant and long-lasting scent. Additionally, EMCA has antimicrobial properties and is used in personal care products to inhibit the growth of bacteria and fungi. Overall, 2-ethyl-2-methylcaproic acid is a versatile compound with various industrial and commercial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1185-29-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,8 and 5 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1185-29:
(6*1)+(5*1)+(4*8)+(3*5)+(2*2)+(1*9)=71
71 % 10 = 1
So 1185-29-1 is a valid CAS Registry Number.

InChI:InChI=1/C9H18O2/c1-4-6-7-9(3,5-2)8(10)11/h4-7H2,1-3H3,(H,10,11)

1185-29-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name	2-ETHYL-2-METHYLCAPROIC ACID

1.2 Other means of identification

Product number	-
Other names	2-Ethyl-2-methylhexansaure

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:1185-29-1 SDS

1185-29-1Upstream product

• 13146-40-2 2-ethyl-2-methyl-hexanoic acid amide 
• 58308-70-6 2-ethyl-2-methyl-hexanoic acid ethyl ester 
• 111-87-5 octanol 
• 201230-82-2 carbon monoxide 
• 64-18-6 formic acid 
• 104-76-7 2-Ethylhexyl alcohol 
• 7452-79-1 ethyl 2-methylbutyrate 
• 15719-64-9 methylammonium carbonate 
• 111-66-0 oct-1-ene 
• 109-65-9 1-bromo-butane 
• 116-53-0 2-Methylbutanoic acid 
• 4128-31-8 rac-octan-2-ol 
• 3234-80-8 methyl 2-ethyl-2-methylhexanoate 
• 2177-81-3 methyl 2-methylcaproate 

1185-29-1Downstream Products

1185-29-1Relevant articles and documents

-

Souma et al.

, p. 2016 (1973)

-

Hexacarbonyldiplatinum(I) cation-catalyzed carbonylation of olefins in concentrated sulfuric acid

Xu,Fujiwara,Tanaka,Souma

, p. 8105 - 8107 (2000)

-

-

Creger,P.L.

, p. 2500 - 2501 (1967)

-

CARBONYLATION OF OLEFINS AND ALCOHOLS AT ATMOSPHERIC PRESSURE IN THE PRESENCE OF ACID CATALYSTS WITH ADDED Ag2O OR Cu2O

Pirozhkov, S. D.,Stepanyan, A. S.,Myshenkova, T. N.,Ordyan, M. B.,Lapidus, A. L.

, p. 1852 - 1858 (1982)

-

Method for the Production of Mixtures Containing Tertiary Isononanoic Acids Based on 2-Ethylhexanol

-

Paragraph 0038, (2017/07/14)

A process for producing a mixture comprising tertiary isononanoic acids proceeding from 2-ethylhexanol is characterized in that 2-ethylhexanol is (a) reacted at a temperature of 0° C. to 40° C. with a mixture of concentrated formic acid and a concentrated Br?nsted acid, wherein 2 to 10 mol of formic acid are used per mole of 2-ethylhexanol and the concentrated Br?nsted acid is used in an amount that corresponds to 6 to 90 mol of protons per mole of 2-ethylhexanol. The resulting reaction mixture from step (a) is subsequently (b) brought into contact with water, and the mixture comprising tertiary isononanoic acids formed according to step b) is removed.

Sulfoximine assisted Pd(II)-catalyzed bromination and chlorination of primary β-C(sp3)-H bond

Rit, Raja K.,Yadav, M. Ramu,Ghosh, Koushik,Shankar, Majji,Sahoo, Akhila K.

supporting information, p. 5258 - 5261 (2015/01/09)

S-Methyl-S-2-pyridyl-sulfoximine (MPyS) directed bromination and chlorination of the 1°-β-C(sp3)-H bond of MPyS-N-amides is realized under the influence of N-Br/Cl-phthalimides and a Pd(II)-catalyst. The sequential halogenation and acetoxylation of α-dimethyl MPyS-N-amides constructs highly functionalized α-trisubstituted aliphatic acid derivatives. The MPyS directing group is cleaved from the halogenated products and recovered. (Chemical Equation Presented).

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