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3302-03-2

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3302-03-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3302-03-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,0 and 2 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3302-03:
(6*3)+(5*3)+(4*0)+(3*2)+(2*0)+(1*3)=42
42 % 10 = 2
So 3302-03-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H16O2/c1-3-4-7(2)5-6-8(9)10/h7H,3-6H2,1-2H3,(H,9,10)

3302-03-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Methylheptanoic acid

1.2 Other means of identification

Product number -
Other names 4-Methyl-heptansaeure

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:3302-03-2 SDS

3302-03-2Relevant articles and documents

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Casey,C.P.,Cyr,C.R.

, p. 2240 - 2247 (1973)

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Identification and Synthesis of Branched Wax-type Esters, Novel Surface Lipids from the Spider Argyrodes?elevatus (Araneae: Theridiidae)

Chinta, Satya Prabhakar,Goller, Stephan,Uhl, Gabriele,Schulz, Stefan

, p. 1202 - 1220 (2016/10/03)

The analysis of cuticular extracts from the kleptoparasitic spider Argyrodes?elevatus revealed the presence of unusual esters, new for arthropods. These novel compounds proved to be methyl-branched long-chain fatty acid esters with methyl branches located either close or remote from the internally located ester group. The GC/MS analysis of the prosoma lipid blend from the male cuticle contained one major component, undecyl 2-methyltridecanoate (1). In contrast, four major wax-type esters, 2-methylundecyl 2,8-dimethylundecanoate (2), 2,8-dimethylundecyl 2,8-dimethylundecanoate (3), heptadecyl 4-methylheptanoate (4), and 14-methylheptadecyl 4-methylheptanoate (5), were identified in the lipid blend of female prosomata. Structure assignments were based on mass spectra, gas chromatographic retention indices, and microderivatization. Unambiguous proof of postulated structures was ensured by an independent synthesis of all five esters. Preferentially, odd-numbered carbon chains pointed to a distinct biosynthetic pathway, different from that of common fatty acids, because one or two C3 starter units are incorporated during the biosynthesis of all acid and alcohol building blocks present in the five esters. The striking sexual dimorphism together with the unique biosynthesis points to a function of the esters in chemical communication of the spiders, although no behavioral data are currently available to test this assumption.

Uropygial gland fat of the fulmar

Jacob,Zeman

, p. 33 - 40 (2007/10/12)

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